Structure and Anti-HIV Activity of Betulinic Acid Analogues

Summary Firstly discovered in 1980s, human immunodeficiency virus (HIV) continues to affect more and more people. However, there is no effective drug available for the therapy of HIV infection. Betulinic acid existing in various medicinal herbs and fruits exhibits multiple biological effects, especi...

Full description

Saved in:
Bibliographic Details
Published inCurrent medical science Vol. 38; no. 3; pp. 387 - 397
Main Authors Huang, Qiu-xia, Chen, Hong-fei, Luo, Xing-rui, Zhang, Yin-xiang, Yao, Xu, Zheng, Xing
Format Journal Article
LanguageEnglish
Published Wuhan Huazhong University of Science and Technology 01.06.2018
University of South China, Hengyang 421001, China
Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, Hengyang 421001, China
Subjects
Online AccessGet full text
ISSN2096-5230
2523-899X
1672-0733
2523-899X
DOI10.1007/s11596-018-1891-4

Cover

Abstract Summary Firstly discovered in 1980s, human immunodeficiency virus (HIV) continues to affect more and more people. However, there is no effective drug available for the therapy of HIV infection. Betulinic acid existing in various medicinal herbs and fruits exhibits multiple biological effects, especially its outstanding anti-HIV activity, which has drawn the attentions of many pharmacists. Among the derivatives of betulinic acid, some compounds exhibited inhibitory activities at the nanomolar concentration, and have entered phase II clinical trials. This paper summarizes the current investigations on the anti-HIV activity of betulinic acid analogues, and provides valuable data for subsequent researches.
AbstractList Summary Firstly discovered in 1980s, human immunodeficiency virus (HIV) continues to affect more and more people. However, there is no effective drug available for the therapy of HIV infection. Betulinic acid existing in various medicinal herbs and fruits exhibits multiple biological effects, especially its outstanding anti-HIV activity, which has drawn the attentions of many pharmacists. Among the derivatives of betulinic acid, some compounds exhibited inhibitory activities at the nanomolar concentration, and have entered phase II clinical trials. This paper summarizes the current investigations on the anti-HIV activity of betulinic acid analogues, and provides valuable data for subsequent researches.
Firstly discovered in 1980s, human immunodeficiency virus (HIV) continues to affect more and more people. However, there is no effective drug available for the therapy of HIV infection. Betulinic acid existing in various medicinal herbs and fruits exhibits multiple biological effects, especially its outstanding anti-HIV activity, which has drawn the attentions of many pharmacists. Among the derivatives of betulinic acid, some compounds exhibited inhibitory activities at the nanomolar concentration, and have entered phase II clinical trials. This paper summarizes the current investigations on the anti-HIV activity of betulinic acid analogues, and provides valuable data for subsequent researches.Firstly discovered in 1980s, human immunodeficiency virus (HIV) continues to affect more and more people. However, there is no effective drug available for the therapy of HIV infection. Betulinic acid existing in various medicinal herbs and fruits exhibits multiple biological effects, especially its outstanding anti-HIV activity, which has drawn the attentions of many pharmacists. Among the derivatives of betulinic acid, some compounds exhibited inhibitory activities at the nanomolar concentration, and have entered phase II clinical trials. This paper summarizes the current investigations on the anti-HIV activity of betulinic acid analogues, and provides valuable data for subsequent researches.
Firstly discovered in 1980s,human immunodeficiency virus (HIV) continues to affect more and more people.However,there is no effective drug available for the therapy of HIV infection.Betulinic acid existing in various medicinal herbs and fruits exhibits multiple biological effects,especially its outstanding anti-HIV activity,which has drawn the attentions of many pharmacists.Among the derivatives of betulinic acid,some compounds exhibited inhibitory activities at the nanomolar concentration,and have entered phase Ⅱ clinical trials.This paper summarizes the current investigations on the anti-HIV activity of betulinic acid analogues,and provides valuable data for subsequent researches.
Firstly discovered in 1980s, human immunodeficiency virus (HIV) continues to affect more and more people. However, there is no effective drug available for the therapy of HIV infection. Betulinic acid existing in various medicinal herbs and fruits exhibits multiple biological effects, especially its outstanding anti-HIV activity, which has drawn the attentions of many pharmacists. Among the derivatives of betulinic acid, some compounds exhibited inhibitory activities at the nanomolar concentration, and have entered phase II clinical trials. This paper summarizes the current investigations on the anti-HIV activity of betulinic acid analogues, and provides valuable data for subsequent researches.
Author Yao, Xu
Chen, Hong-fei
Zhang, Yin-xiang
Luo, Xing-rui
Huang, Qiu-xia
Zheng, Xing
AuthorAffiliation University of South China, Hengyang 421001, China;Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, Hengyang 421001, China
AuthorAffiliation_xml – name: University of South China, Hengyang 421001, China;Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, Hengyang 421001, China
Author_xml – sequence: 1
  givenname: Qiu-xia
  surname: Huang
  fullname: Huang, Qiu-xia
  organization: University of South China, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study
– sequence: 2
  givenname: Hong-fei
  surname: Chen
  fullname: Chen, Hong-fei
  organization: University of South China, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study
– sequence: 3
  givenname: Xing-rui
  surname: Luo
  fullname: Luo, Xing-rui
  organization: University of South China, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study
– sequence: 4
  givenname: Yin-xiang
  surname: Zhang
  fullname: Zhang, Yin-xiang
  organization: University of South China, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study
– sequence: 5
  givenname: Xu
  surname: Yao
  fullname: Yao, Xu
  email: 355938360@qq.com
  organization: University of South China, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study
– sequence: 6
  givenname: Xing
  surname: Zheng
  fullname: Zheng, Xing
  email: zhengxing5018@yahoo.com
  organization: University of South China, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30074203$$D View this record in MEDLINE/PubMed
BookMark eNp9kU9rGzEQxUVJqJPUH6CXssdC2EQj7a4kenJC_hgCPTQpvQlZKxm5a20qaZP420dmbQKB9CRp9HuPNzPH6MD33iD0FfAZYMzOI0AtmhIDL4ELKKtP6IjUhJZciD8H-Y7zb37jCZrG6BaYAmkocPIZTWg2qAimR-jHrxQGnYZgCuXbYuaTK2_nv4uZTu7JpU3R2-LCpKFz3ulcdVtGdf1yMPELOrSqi2a6O0_Qw_XV_eVteffzZn45uys15TiVRtS1aGvCKOEKqkoYzVSrOTSctQKEIbWxZIFtA8pYrpkGohreWsuAKiHoCTodfZ-Vt8ov5aofQg4RZVpt_rYvLwtpSJ4Dzm1Bpr-P9GPo_-WUSa5d1KbrlDf9ECXBnDIsWEUz-m2HDou1aeVjcGsVNnI_ngywEdChjzEYK7VLKrnep6BcJwHL7S7kuAuZM8jtLmSVlfBOuTf_n4aMmphZvzThrdGPRa_qU5jM
CitedBy_id crossref_primary_10_4028_www_scientific_net_KEM_884_282
crossref_primary_10_1002_cbdv_202301275
crossref_primary_10_3390_ijms24021430
crossref_primary_10_1111_nyas_14623
crossref_primary_10_2174_1573407219666230705160027
crossref_primary_10_1021_acs_jmedchem_0c01348
crossref_primary_10_3390_ijms251910366
crossref_primary_10_3390_biom11121805
crossref_primary_10_2174_0122113525305139240629084443
crossref_primary_10_3390_plants12061214
crossref_primary_10_1016_j_bmcl_2022_128768
crossref_primary_10_3390_molecules26051381
crossref_primary_10_1007_s00709_019_01411_0
crossref_primary_10_3390_ph15101169
crossref_primary_10_3389_fphar_2023_1254317
crossref_primary_10_4103_jrptps_JRPTPS_60_18
crossref_primary_10_1021_acsomega_8b03691
crossref_primary_10_1039_C9NP00030E
crossref_primary_10_1016_j_ejmech_2022_114850
crossref_primary_10_3390_biomedicines12061168
crossref_primary_10_1111_cbdd_13685
crossref_primary_10_1021_acs_jnatprod_8b00830
crossref_primary_10_1155_2022_1148874
crossref_primary_10_1039_D3MD00560G
crossref_primary_10_3390_molecules26216356
crossref_primary_10_1016_j_ejmech_2023_115472
crossref_primary_10_3390_ijms23020736
crossref_primary_10_1016_j_bjp_2018_10_006
crossref_primary_10_3390_molecules26041081
crossref_primary_10_14258_jcprm_2019045419
Cites_doi 10.1073/pnas.2234683100
10.1073/pnas.91.9.3564
10.1021/cr900019j
10.1128/AAC.00737-07
10.2174/1874104501408010023
10.1016/j.bmc.2016.03.001
10.1016/j.ejps.2006.04.006
10.1128/AAC.02560-15
10.1016/j.bmc.2005.11.016
10.3390/ijms9061096
10.2165/11633630-000000000-00000
10.1016/j.bmcl.2016.03.019
10.1016/j.bmc.2010.06.092
10.1021/acs.jmedchem.5b00497
10.3109/14756366.2011.611134
10.1016/j.bmcl.2012.06.080
10.1016/j.bmcl.2009.06.100
10.1021/jm3016969
10.1016/j.bmcl.2007.09.081
10.1016/j.virol.2004.04.009
10.1016/j.ejmech.2017.04.062
10.1101/cshperspect.a007161
10.1038/srep27403
10.1016/j.steroids.2017.04.002
10.1128/AAC.02121-15
10.1016/j.bmcl.2017.04.042
10.1128/AAC.01391-06
10.1371/journal.pone.0027234
10.1016/j.bmcl.2015.11.029
10.3390/v6104095
10.1016/j.drudis.2006.11.008
10.3109/13880209.2011.559476
10.1016/S1359-6446(04)03163-0
10.1016/j.ejmech.2013.01.013
10.2165/00003088-200746070-00004
10.1128/AAC.00152-07
10.1128/AAC.48.2.663-665.2004
10.1021/acs.jmedchem.6b00461
ContentType Journal Article
Copyright Huazhong University of Science and Technology 2018
Copyright © Wanfang Data Co. Ltd. All Rights Reserved.
Copyright_xml – notice: Huazhong University of Science and Technology 2018
– notice: Copyright © Wanfang Data Co. Ltd. All Rights Reserved.
DBID AAYXX
CITATION
NPM
7X8
2B.
4A8
92I
93N
PSX
TCJ
DOI 10.1007/s11596-018-1891-4
DatabaseName CrossRef
PubMed
MEDLINE - Academic
Wanfang Data Journals - Hong Kong
WANFANG Data Centre
Wanfang Data Journals
万方数据期刊 - 香港版
China Online Journals (COJ)
China Online Journals (COJ)
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList
MEDLINE - Academic

PubMed
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 2523-899X
EndPage 397
ExternalDocumentID tjykdxxb_e201803001
30074203
10_1007_s11596_018_1891_4
Genre Journal Article
GrantInformation_xml – fundername: This research was supported by the National Natural Science Foundation of China; Scientific Research Fund of Education Department of Hunan Province; the Key Project of Science and Technology Department of Hunan Province; the Key Disciplines of Hunan Province and the Zhengxing Scholar Program of the University of South China
  funderid: (81273537); (17A190); (2016DK2001); the Key Disciplines of Hunan Province and the Zhengxing Scholar Program of the University of South China
GroupedDBID -05
-0E
-EM
-SE
-S~
.VR
0R~
2J2
2JN
2JY
2KG
2LR
30V
406
408
5VR
92M
95-
96X
9D9
9DE
AAAVM
AACDK
AAHNG
AAIAL
AAJBT
AANZL
AASML
AATNV
AAUYE
AAXDM
AAYZH
ABAKF
ABDZT
ABECU
ABFTV
ABHQN
ABJNI
ABKCH
ABKZE
ABMQK
ABNWP
ABSXP
ABTEG
ABTKH
ABTMW
ABWNU
ABXPI
ACAOD
ACDTI
ACHSB
ACMDZ
ACMLO
ACOKC
ACZOJ
ADKNI
ADRFC
ADTPH
ADURQ
ADYFF
AEFQL
AEJRE
AEMSY
AESKC
AEVLU
AEXYK
AFBBN
AFLOW
AFQWF
AFUIB
AGDGC
AGJBK
AGMZJ
AGQEE
AGRTI
AHSBF
AIAKS
AIGIU
AILAN
AITGF
AJRNO
ALMA_UNASSIGNED_HOLDINGS
AMKLP
AMXSW
AMYLF
AMYQR
AOCGG
AXYYD
B-.
BA0
BDATZ
BGNMA
CAJEE
CSCUP
DDRTE
DNIVK
DPUIP
EBLON
EBS
EIOEI
EJD
FERAY
FFXSO
FIGPU
FINBP
FNLPD
FSGXE
G-Y
G-Z
GGCAI
GNWQR
GQ7
GRRUI
IKXTQ
IWAJR
IXD
I~Z
J-C
JZLTJ
KOV
LLZTM
M4Y
MA-
NPVJJ
NQJWS
NU0
O9J
PF0
PT4
Q--
QOR
QOS
RHV
ROL
RSV
RT5
S16
S37
S3B
SAP
SCLPG
SDE
SDH
SHX
SISQX
SJYHP
SNE
SNPRN
SNX
SOHCF
SOJ
SRMVM
SSLCW
STPWE
SZN
T8U
TCJ
TGQ
TSG
TUC
U1F
U1G
U2A
U5E
U5O
UOJIU
UTJUX
UZXMN
VC2
VFIZW
YLTOR
Z87
ZMTXR
~A9
AAPKM
AAYXX
ABBRH
ABDBE
ABFSG
ABRTQ
ACSTC
AEZWR
AFDZB
AFHIU
AFOHR
AHPBZ
AHWEU
AIXLP
ATHPR
AYFIA
CITATION
NPM
7X8
-Y2
.86
06C
06D
0VY
1N0
29K
29~
2B.
2KM
2~H
4.4
40D
40E
4A8
53G
5GY
5VS
6NX
8TC
8UJ
92F
92I
93N
95.
95~
AABHQ
AAJKR
AANXM
AARHV
AARTL
AAYIU
AAYQN
AAYTO
ABJOX
ABMNI
ABQBU
ABQSL
ACGFS
ACHXU
ACKNC
ACOMO
ACSNA
ACUDM
ADHIR
ADHKG
ADKPE
ADZKW
AEBTG
AEGNC
AEJHL
AEKMD
AEOHA
AEPYU
AETLH
AFWTZ
AFZKB
AGAYW
AGQMX
AGQPQ
AGWIL
AGWZB
AGYKE
AHAVH
AHBYD
AHKAY
AHYZX
AIIXL
AJBLW
ALWAN
ARMRJ
AZFZN
CAG
CCEZO
CHBEP
CIEJG
COF
CS3
CW9
D-I
ESBYG
FA0
FEDTE
FRRFC
FWDCC
GGRSB
GJIRD
H13
HF~
HMJXF
HRMNR
HVGLF
HZ~
IJ-
I~X
JBSCW
JUIAU
N2Q
NDZJH
O9-
O93
O9I
P9S
PSX
R-E
R89
R9I
RIG
RPX
S..
S1Z
S27
SCL
SMD
SPISZ
SZ9
T13
TT1
U9L
UG4
W48
WK8
ZOVNA
ID FETCH-LOGICAL-c380t-e9559d527328a1449ec7adc81687d919e25ef2b0f61aef8c7c12a68dff713a993
IEDL.DBID U2A
ISSN 2096-5230
2523-899X
1672-0733
IngestDate Thu May 29 04:06:48 EDT 2025
Fri Sep 05 14:49:41 EDT 2025
Wed Feb 19 02:42:16 EST 2025
Wed Oct 01 04:53:51 EDT 2025
Thu Apr 24 22:58:54 EDT 2025
Fri Feb 21 02:37:17 EST 2025
IsPeerReviewed true
IsScholarly true
Issue 3
Keywords structure activity relationship
HIV
structural modification
betulinic acid analogues
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c380t-e9559d527328a1449ec7adc81687d919e25ef2b0f61aef8c7c12a68dff713a993
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
ObjectType-Review-3
content type line 23
PMID 30074203
PQID 2083709743
PQPubID 23479
PageCount 11
ParticipantIDs wanfang_journals_tjykdxxb_e201803001
proquest_miscellaneous_2083709743
pubmed_primary_30074203
crossref_citationtrail_10_1007_s11596_018_1891_4
crossref_primary_10_1007_s11596_018_1891_4
springer_journals_10_1007_s11596_018_1891_4
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2018-06-01
PublicationDateYYYYMMDD 2018-06-01
PublicationDate_xml – month: 06
  year: 2018
  text: 2018-06-01
  day: 01
PublicationDecade 2010
PublicationPlace Wuhan
PublicationPlace_xml – name: Wuhan
– name: China
PublicationTitle Current medical science
PublicationTitleAbbrev CURR MED SCI
PublicationTitleAlternate Curr Med Sci
PublicationTitle_FL Journal of Huazhong University of Science and Technology(Medical Science)
PublicationYear 2018
Publisher Huazhong University of Science and Technology
University of South China, Hengyang 421001, China
Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, Hengyang 421001, China
Publisher_xml – name: Huazhong University of Science and Technology
– name: University of South China, Hengyang 421001, China
– name: Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, Hengyang 421001, China
References Iyidogan, Anderson (CR4) 2014; 6
Kuttan, Pratheeshkumar, Manu (CR6) 2011; 49
Li, Goila-Gaur, Salzwedel (CR13) 2003; 100
Martin, Blum, Wilton (CR11) 2007; 51
Mayaux, Bousseau, Pauwels (CR18) 1994; 91
Yuan, Huang, Ho (CR19) 2004; 324
Zimmermann, Lehár, Keith (CR27) 2007; 12
Smith, Ogundele, Forrest (CR15) 2007; 51
Nowicka-Sans, Protack, Lin (CR37) 2016; 60
Li, Goto, Yang (CR42) 2016; 26
Tang, Jones, Jeffery (CR41) 2014; 8
Qian, Bori, Chen (CR22) 2012; 55
Qian, Nakagawa-Goto, Yu (CR38) 2007; 17
Zhan, Pannecouque, Clercq (CR3) 2016; 59
Martin, Blum, Doto (CR16) 2007; 46
Urano, Ablan, Mandt (CR23) 2015; 60
Dang, Qian, Ho (CR21) 2012; 22
Coric, Turcaud, Souquet (CR33) 2013; 62
Bori, Hung, Qian (CR30) 2012; 53
Swidorski, Liu, Sit (CR36) 2016; 26
Lai, Huang, Ho (CR17) 2008; 52
Timilsina, Ghimire, Timalsina (CR24) 2016; 6
Tang, Shafer (CR2) 2012; 72
Gupta, Rath, Singh (CR9) 2017; 135
Huang, Ho, Lee (CR25) 2006; 14
Liu, Swidorski, Nowicka-Sans (CR40) 2016; 24
Tang, Jones, Jeffrey (CR43) 2017; 27
Huang, Yuan, Aiken (CR26) 2004; 48
Morphy, Kay, Rankovic (CR28) 2004; 9
Altmann (CR12) 2009; 90
Zhao, Holmes, Baker (CR35) 2012; 27
Li, Goila-Gaur, Salzwedel (CR14) 2003; 100
Fulda (CR7) 2008; 9
Alakurtti, Makela, Koskimies (CR8) 2006; 29
Qian, Kuo, Chen (CR39) 2010; 53
Cragg, Grothaus, Newman (CR5) 2009; 109
Wang, Liu, Sanches (CR31) 2009; 19
Dangroo, Singh, Rath (CR10) 2017; 123
Arts, Hazuda (CR1) 2012; 2
Zhao, Gu, Morris-Natschke (CR32) 2016; 59
Dang, Ho, Zhu (CR20) 2013; 56
Gonzalez, DaFonseca, Errazuriz (CR34) 2011; 6
Xiong, Kashiwada, Chen (CR29) 2010; 18
DE Martin (1891_CR11) 2007; 51
Z Dang (1891_CR20) 2013; 56
ID Bori (1891_CR30) 2012; 53
P Iyidogan (1891_CR4) 2014; 6
NA Dangroo (1891_CR10) 2017; 123
L Huang (1891_CR26) 2004; 48
E Urano (1891_CR23) 2015; 60
B Nowicka-Sans (1891_CR37) 2016; 60
EJ Arts (1891_CR1) 2012; 2
GR Zimmermann (1891_CR27) 2007; 12
N Gupta (1891_CR9) 2017; 135
W Lai (1891_CR17) 2008; 52
J Tang (1891_CR41) 2014; 8
H Zhao (1891_CR35) 2012; 27
JF Mayaux (1891_CR18) 1994; 91
F Li (1891_CR13) 2003; 100
J Li (1891_CR42) 2016; 26
G Gonzalez (1891_CR34) 2011; 6
K Qian (1891_CR38) 2007; 17
P Coric (1891_CR33) 2013; 62
GM Cragg (1891_CR5) 2009; 109
K Qian (1891_CR39) 2010; 53
PF Smith (1891_CR15) 2007; 51
MW Tang (1891_CR2) 2012; 72
J Xiong (1891_CR29) 2010; 18
L Huang (1891_CR25) 2006; 14
JJ Swidorski (1891_CR36) 2016; 26
S Alakurtti (1891_CR8) 2006; 29
K Qian (1891_CR22) 2012; 55
G Kuttan (1891_CR6) 2011; 49
R Morphy (1891_CR28) 2004; 9
Z Liu (1891_CR40) 2016; 24
F R Li (1891_CR14) 2003; 100
X Yuan (1891_CR19) 2004; 324
J Tang (1891_CR43) 2017; 27
P Zhan (1891_CR3) 2016; 59
U Timilsina (1891_CR24) 2016; 6
DE Martin (1891_CR16) 2007; 46
Y Zhao (1891_CR32) 2016; 59
KH Altmann (1891_CR12) 2009; 90
S Fulda (1891_CR7) 2008; 9
Z Dang (1891_CR21) 2012; 22
P Wang (1891_CR31) 2009; 19
15279847 - Drug Discov Today. 2004 Aug 1;9(15):641-51
25341668 - Viruses. 2014 Oct 24;6(10):4095-139
21985312 - J Enzyme Inhib Med Chem. 2012 Oct;27(5):715-21
19325847 - Int J Mol Sci. 2008 Jun;9(6):1096-107
25250097 - Open Med Chem J. 2014 Sep 03;8:23-7
26598461 - Bioorg Med Chem Lett. 2016 Jan 1;26(1):68-71
8170948 - Proc Natl Acad Sci U S A. 1994 Apr 26;91(9):3564-8
17596104 - Clin Pharmacokinet. 2007;46(7):589-98
15207637 - Virology. 2004 Jul 1;324(2):525-30
26509831 - J Med Chem. 2016 Apr 14;59(7):2849-78
19625188 - Bioorg Med Chem Lett. 2009 Aug 15;19(16):4574-8
26482309 - Antimicrob Agents Chemother. 2015 Oct 19;60(1):190-7
27264714 - Sci Rep. 2016 Jun 06;6:27403
28454672 - Bioorg Med Chem Lett. 2017 Jun 15;27(12):2689-2694
23399723 - Eur J Med Chem. 2013 Apr;62:453-65
22818973 - Bioorg Med Chem Lett. 2012 Aug 15;22(16):5190-4
21936626 - Pharm Biol. 2011 Oct;49(10):995-1007
16314103 - Bioorg Med Chem. 2006 Apr 1;14(7):2279-89
20329730 - J Med Chem. 2010 Apr 22;53(8):3133-41
23379607 - J Med Chem. 2013 Mar 14;56(5):2029-37
22474613 - Cold Spring Harb Perspect Med. 2012 Apr;2(4):a007161
14742233 - Antimicrob Agents Chemother. 2004 Feb;48(2):663-5
14573704 - Proc Natl Acad Sci U S A. 2003 Nov 11;100(23):13555-60
17576843 - Antimicrob Agents Chemother. 2007 Sep;51(9):3063-6
26988305 - Bioorg Med Chem Lett. 2016 Apr 15;26(8):1925-30
26968652 - Bioorg Med Chem. 2016 Apr 15;24(8):1757-70
20673723 - Bioorg Med Chem. 2010 Sep 1;18(17):6451-69
28435038 - Steroids. 2017 Jul;123:1-12
17935987 - Bioorg Med Chem Lett. 2007 Dec 1;17(23):6553-7
17198971 - Drug Discov Today. 2007 Jan;12(1-2):34-42
16716572 - Eur J Pharm Sci. 2006 Sep;29(1):1-13
27090171 - Antimicrob Agents Chemother. 2016 Jun 20;60(7):3956-69
19422222 - Chem Rev. 2009 Jul;109(7):3012-43
22711941 - Tetrahedron Lett. 2012 Apr 11;53(15):1987-1989
22978745 - J Med Chem. 2012 Sep 27;55(18):8128-36
28500966 - Eur J Med Chem. 2017 Jul 28;135:517-530
19209842 - Fortschr Chem Org Naturst. 2009;90:135-56
22686620 - Drugs. 2012 Jun 18;72(9):e1-25
27676157 - J Med Chem. 2016 Oct 13;59(19):9262-9268
17954689 - Antimicrob Agents Chemother. 2008 Jan;52(1):128-36
22073298 - PLoS One. 2011;6(11):e27234
17638699 - Antimicrob Agents Chemother. 2007 Oct;51(10):3574-81
References_xml – volume: 100
  start-page: 13555
  issue: 23
  year: 2003
  end-page: 13560
  ident: CR13
  article-title: PA-457: a potent HIV inhibitor that disrupts core condensation by targeting a late step in Gag processing
  publication-title: Proc Natl Acad Sci USA.
  doi: 10.1073/pnas.2234683100
– volume: 91
  start-page: 3564
  issue: 9
  year: 1994
  end-page: 3568
  ident: CR18
  article-title: Triterpene derivatives that block entry of human immunodeficiency virus type 1 into cells
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.91.9.3564
– volume: 90
  start-page: 135
  year: 2009
  end-page: 156
  ident: CR12
  article-title: Semisynthetic derivatives of epothilones
  publication-title: Fortschr Chem Org Naturst
– volume: 109
  start-page: 3012
  issue: 7
  year: 2009
  end-page: 3043
  ident: CR5
  article-title: Impact of natural products on developing new anti-cancer agents
  publication-title: Chem Rev
  doi: 10.1021/cr900019j
– volume: 52
  start-page: 128
  issue: 1
  year: 2008
  end-page: 136
  ident: CR17
  article-title: Betulinic acid derivatives that target gpl20 and inhibit multiple genetic subtypes of human immunodeficiency virus type 1
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.00737-07
– volume: 8
  start-page: 23
  year: 2014
  end-page: 27
  ident: CR41
  article-title: Synthesis and biological evaluation of macrocyclized betulin derivatives as a novel class of anti-HIV-1 maturation inhibitors
  publication-title: Open Med Chem J
  doi: 10.2174/1874104501408010023
– volume: 24
  start-page: 1757
  issue: 8
  year: 2016
  end-page: 1770
  ident: CR40
  article-title: C-3 benzoic acid derivatives of C-3 deoxybetulinic acid and deoxybetulin as HIV-l maturation inhibitors
  publication-title: Bioorg Med Chem
  doi: 10.1016/j.bmc.2016.03.001
– volume: 29
  start-page: 1
  issue: 1
  year: 2006
  end-page: 13
  ident: CR8
  article-title: Pharmacological properties of the ubiquitous natural product betulin
  publication-title: Eur J Pharm Sci
  doi: 10.1016/j.ejps.2006.04.006
– volume: 53
  start-page: 3133
  issue: 8
  year: 2010
  end-page: 3141
  ident: CR39
  article-title: Anti-AIDS agents 81
  publication-title: Design, synthesis, and structure-activity relationship study of betulinic acid and moronic acid derivatives as potent HIV maturation inhibitors. J Med Chem
– volume: 60
  start-page: 3956
  issue: 7
  year: 2016
  end-page: 3969
  ident: CR37
  article-title: Identification and characterization of BMS-955176, a secondgeneration HIV-l maturation inhibitor with improved potency, antiviral spectrum, and gag polymorphic coverage
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.02560-15
– volume: 14
  start-page: 2279
  issue: 7
  year: 2006
  end-page: 2289
  ident: CR25
  article-title: Synthesis and anti-HIV activity of bi-functional betulinic acid derivatives
  publication-title: Bioorg Med Chem
  doi: 10.1016/j.bmc.2005.11.016
– volume: 9
  start-page: 1096
  issue: 6
  year: 2008
  end-page: 1107
  ident: CR7
  article-title: Betulinic Acid for cancer treatment and prevention
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms9061096
– volume: 72
  start-page: el
  issue: 9
  year: 2012
  end-page: 25
  ident: CR2
  article-title: HIV-1 antiretroviral resistance: scientific principles and clinical applications
  publication-title: Drugs
  doi: 10.2165/11633630-000000000-00000
– volume: 26
  start-page: 1925
  issue: 8
  year: 2016
  end-page: 1930
  ident: CR36
  article-title: Inhibitors of HIV-1 maturation: Development of structure-activity relationship for C-28 amides based on C-3 benzoic acid-modified triterpenoids
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2016.03.019
– volume: 18
  start-page: 6451
  issue: 17
  year: 2010
  end-page: 6469
  ident: CR29
  article-title: Conjugates of betulin derivatives with AZT as potent anti-HIV agents
  publication-title: Bioorg Med Chem
  doi: 10.1016/j.bmc.2010.06.092
– volume: 100
  start-page: 13555
  year: 2003
  end-page: 13560
  ident: CR14
  article-title: PA-457: a potent HIV inhibitor that disrupts core condensation by targeting a late step in Gag processing
  publication-title: Proc Natl Acad Sci
  doi: 10.1073/pnas.2234683100
– volume: 59
  start-page: 2849
  issue: 7
  year: 2016
  end-page: 2878
  ident: CR3
  article-title: Anti-HIV Drug Discovery and Development: Current Innovations and Future Trends
  publication-title: J Med Chem
  doi: 10.1021/acs.jmedchem.5b00497
– volume: 27
  start-page: 715
  issue: 5
  year: 2012
  end-page: 721
  ident: CR35
  article-title: Ionic derivatives of betulinic acid as novel HIV-l protease inhibitors
  publication-title: J Enzyme Inhib Med Chem
  doi: 10.3109/14756366.2011.611134
– volume: 22
  start-page: 5190
  issue: 16
  year: 2012
  end-page: 5194
  ident: CR21
  article-title: Synthesis of betulinic acid derivatives as entry inhibitors against HIV-1 and bevirimat-resistant HIV-1 variants
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2012.06.080
– volume: 19
  start-page: 4574
  issue: 16
  year: 2009
  end-page: 4578
  ident: CR31
  article-title: Design and synthesis of novel nitrogen-containing polyhydroxylated aromatics as HIV-l integrase inhibitors from caffeic acid phenethyl ester
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2009.06.100
– volume: 56
  start-page: 2029
  issue: 5
  year: 2013
  end-page: 2037
  ident: CR20
  article-title: New betulinic acid derivatives for bevirimat-resistant human immunodeficiency virus type-1
  publication-title: J Med Chem
  doi: 10.1021/jm3016969
– volume: 17
  start-page: 6553
  issue: 23
  year: 2007
  end-page: 6557
  ident: CR38
  article-title: Anti-AIDS agents 73: structure-activity relationship study and asymmetric synthesis of 3-O-monomethylsuccinylbetulinic acid derivatives
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2007.09.081
– volume: 324
  start-page: 525
  issue: 2
  year: 2004
  end-page: 530
  ident: CR19
  article-title: Conformation of gpl20 determines the sensitivity of HIV-1 DH012 to the entry inhibitor IC9564
  publication-title: Virology
  doi: 10.1016/j.virol.2004.04.009
– volume: 135
  start-page: 517
  year: 2017
  end-page: 530
  ident: CR9
  article-title: Synthesis of novel benzylidene analogues of betulinic acid as potent cytotoxic agents
  publication-title: Eur J Med Chem
  doi: 10.1016/j.ejmech.2017.04.062
– volume: 2
  start-page: a007161
  year: 2012
  ident: CR1
  article-title: HIV-1 antiretroviral drug therapy
  publication-title: Cold Spring Harb Perspect Med
  doi: 10.1101/cshperspect.a007161
– volume: 6
  start-page: 27403
  year: 2016
  ident: CR24
  article-title: Identification of potent maturation inhibitors against HIV-1 clade C
  publication-title: Sci Rep
  doi: 10.1038/srep27403
– volume: 123
  start-page: 1
  year: 2017
  end-page: 12
  ident: CR10
  article-title: A convergent synthesis of novel alkyne-azide cycloaddition congeners of betulinic acid as potent cytotoxic agent
  publication-title: Steroids
  doi: 10.1016/j.steroids.2017.04.002
– volume: 60
  start-page: 190
  issue: 1
  year: 2015
  end-page: 197
  ident: CR23
  article-title: Alkyl amine bevirimat derivatives are potent and broadly active HIV-1 maturation inhibitors
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.02121-15
– volume: 27
  start-page: 2689
  issue: 12
  year: 2017
  end-page: 2694
  ident: CR43
  article-title: Discovery of a novel and potent class of anti-HIV-1 maturation inhibitors with improved virology profile against gag polymorphisms
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2017.04.042
– volume: 51
  start-page: 3063
  issue: 9
  year: 2007
  end-page: 3066
  ident: CR11
  article-title: Safety and pharmacokinetics of Bevirimat (PA-457), a novel inhibitor of human immunodeficiency virus maturation, in healthy volunteers
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.01391-06
– volume: 6
  start-page: e27234
  issue: 11
  year: 2011
  ident: CR34
  article-title: Characterization of a novel type of HIV-l particle assembly inhibitor using a quantitative luciferase-Vpr packaging-based assay
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0027234
– volume: 26
  start-page: 68
  issue: 1
  year: 2016
  end-page: 71
  ident: CR42
  article-title: Fluorinated betulinic acid derivatives and evaluation of their anti-HIV activity
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2015.11.029
– volume: 6
  start-page: 4095
  issue: 10
  year: 2014
  end-page: 4139
  ident: CR4
  article-title: Current perspectives on HIV-1 antiretroviral drug resistance
  publication-title: Viruses
  doi: 10.3390/v6104095
– volume: 12
  start-page: 34
  year: 2007
  end-page: 42
  ident: CR27
  article-title: Multi-target therapeutics: when the whole is greater than the sum of the parts
  publication-title: Drug Discov Today
  doi: 10.1016/j.drudis.2006.11.008
– volume: 49
  start-page: 995
  issue: 10
  year: 2011
  end-page: 1007
  ident: CR6
  article-title: Inhibition of tumor progression by naturally occurring terpenoids
  publication-title: Pharm Biol
  doi: 10.3109/13880209.2011.559476
– volume: 9
  start-page: 641
  year: 2004
  end-page: 651
  ident: CR28
  article-title: From magic bullets to designed multiple ligands
  publication-title: Drug Discov Today
  doi: 10.1016/S1359-6446(04)03163-0
– volume: 62
  start-page: 453
  year: 2013
  end-page: 465
  ident: CR33
  article-title: Synthesis and biological evaluation of a new derivative of bevirimat that targets the Gag CA-SP1 cleavage site
  publication-title: Eur J Med Chem
  doi: 10.1016/j.ejmech.2013.01.013
– volume: 46
  start-page: 589
  issue: 7
  year: 2007
  end-page: 598
  ident: CR16
  article-title: Multiple-dose pharmacokinetics and safety of bevirimat, a novel inhibitor of HIV maturation, in healthy volunteers
  publication-title: Clin Pharmacokinet
  doi: 10.2165/00003088-200746070-00004
– volume: 53
  start-page: 1987
  issue: 15
  year: 2012
  end-page: 1989
  ident: CR30
  article-title: Anti-AIDS agents 88
  publication-title: Anti-HIV conjugates of betulin and betulinic acid with AZT prepared via click chemistry. Tetrahedron Lett
– volume: 51
  start-page: 3574
  issue: 10
  year: 2007
  end-page: 3581
  ident: CR15
  article-title: Phase I and II study of the safety, virologie effect, and pharmacokinetics/pharmacodynamics of singledose 3-o-(3',3'-dimethylsuccinyl) betulinic acid (bevirimat) against human immunodeficiency virus infection
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.00152-07
– volume: 48
  start-page: 66366
  issue: 2
  year: 2004
  end-page: 66275
  ident: CR26
  article-title: Bifimctional antihuman immunodeficiency virus type 1 small molecules with two novel mechanisms of action
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.48.2.663-665.2004
– volume: 55
  start-page: 8128
  issue: 18
  year: 2012
  end-page: 8136
  ident: CR22
  article-title: Anti-AIDS agents 90
  publication-title: Novel C-28 modified bevirimat analogues as potent HIV maturation inhibitors. J Med Chem
– volume: 59
  start-page: 9262
  issue: 19
  year: 2016
  end-page: 9268
  ident: CR32
  article-title: Incorporation of Privileged Structures into Bevirimat Can Improve Activity against Wild-Type and Bevirimat-Resistant HIV-l
  publication-title: J Med Chem
  doi: 10.1021/acs.jmedchem.6b00461
– volume: 9
  start-page: 1096
  issue: 6
  year: 2008
  ident: 1891_CR7
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms9061096
– volume: 6
  start-page: 4095
  issue: 10
  year: 2014
  ident: 1891_CR4
  publication-title: Viruses
  doi: 10.3390/v6104095
– volume: 123
  start-page: 1
  year: 2017
  ident: 1891_CR10
  publication-title: Steroids
  doi: 10.1016/j.steroids.2017.04.002
– volume: 17
  start-page: 6553
  issue: 23
  year: 2007
  ident: 1891_CR38
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2007.09.081
– volume: 60
  start-page: 3956
  issue: 7
  year: 2016
  ident: 1891_CR37
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.02560-15
– volume: 90
  start-page: 135
  year: 2009
  ident: 1891_CR12
  publication-title: Fortschr Chem Org Naturst
– volume: 62
  start-page: 453
  year: 2013
  ident: 1891_CR33
  publication-title: Eur J Med Chem
  doi: 10.1016/j.ejmech.2013.01.013
– volume: 53
  start-page: 3133
  issue: 8
  year: 2010
  ident: 1891_CR39
  publication-title: Design, synthesis, and structure-activity relationship study of betulinic acid and moronic acid derivatives as potent HIV maturation inhibitors. J Med Chem
– volume: 24
  start-page: 1757
  issue: 8
  year: 2016
  ident: 1891_CR40
  publication-title: Bioorg Med Chem
  doi: 10.1016/j.bmc.2016.03.001
– volume: 135
  start-page: 517
  year: 2017
  ident: 1891_CR9
  publication-title: Eur J Med Chem
  doi: 10.1016/j.ejmech.2017.04.062
– volume: 6
  start-page: e27234
  issue: 11
  year: 2011
  ident: 1891_CR34
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0027234
– volume: 22
  start-page: 5190
  issue: 16
  year: 2012
  ident: 1891_CR21
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2012.06.080
– volume: 53
  start-page: 1987
  issue: 15
  year: 2012
  ident: 1891_CR30
  publication-title: Anti-HIV conjugates of betulin and betulinic acid with AZT prepared via click chemistry. Tetrahedron Lett
– volume: 72
  start-page: el
  issue: 9
  year: 2012
  ident: 1891_CR2
  publication-title: Drugs
  doi: 10.2165/11633630-000000000-00000
– volume: 48
  start-page: 66366
  issue: 2
  year: 2004
  ident: 1891_CR26
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.48.2.663-665.2004
– volume: 27
  start-page: 715
  issue: 5
  year: 2012
  ident: 1891_CR35
  publication-title: J Enzyme Inhib Med Chem
  doi: 10.3109/14756366.2011.611134
– volume: 14
  start-page: 2279
  issue: 7
  year: 2006
  ident: 1891_CR25
  publication-title: Bioorg Med Chem
  doi: 10.1016/j.bmc.2005.11.016
– volume: 18
  start-page: 6451
  issue: 17
  year: 2010
  ident: 1891_CR29
  publication-title: Bioorg Med Chem
  doi: 10.1016/j.bmc.2010.06.092
– volume: 2
  start-page: a007161
  year: 2012
  ident: 1891_CR1
  publication-title: Cold Spring Harb Perspect Med
  doi: 10.1101/cshperspect.a007161
– volume: 55
  start-page: 8128
  issue: 18
  year: 2012
  ident: 1891_CR22
  publication-title: Novel C-28 modified bevirimat analogues as potent HIV maturation inhibitors. J Med Chem
– volume: 26
  start-page: 1925
  issue: 8
  year: 2016
  ident: 1891_CR36
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2016.03.019
– volume: 6
  start-page: 27403
  year: 2016
  ident: 1891_CR24
  publication-title: Sci Rep
  doi: 10.1038/srep27403
– volume: 27
  start-page: 2689
  issue: 12
  year: 2017
  ident: 1891_CR43
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2017.04.042
– volume: 49
  start-page: 995
  issue: 10
  year: 2011
  ident: 1891_CR6
  publication-title: Pharm Biol
  doi: 10.3109/13880209.2011.559476
– volume: 100
  start-page: 13555
  year: 2003
  ident: 1891_CR14
  publication-title: Proc Natl Acad Sci
  doi: 10.1073/pnas.2234683100
– volume: 91
  start-page: 3564
  issue: 9
  year: 1994
  ident: 1891_CR18
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.91.9.3564
– volume: 26
  start-page: 68
  issue: 1
  year: 2016
  ident: 1891_CR42
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2015.11.029
– volume: 46
  start-page: 589
  issue: 7
  year: 2007
  ident: 1891_CR16
  publication-title: Clin Pharmacokinet
  doi: 10.2165/00003088-200746070-00004
– volume: 52
  start-page: 128
  issue: 1
  year: 2008
  ident: 1891_CR17
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.00737-07
– volume: 56
  start-page: 2029
  issue: 5
  year: 2013
  ident: 1891_CR20
  publication-title: J Med Chem
  doi: 10.1021/jm3016969
– volume: 19
  start-page: 4574
  issue: 16
  year: 2009
  ident: 1891_CR31
  publication-title: Bioorg Med Chem Lett
  doi: 10.1016/j.bmcl.2009.06.100
– volume: 59
  start-page: 9262
  issue: 19
  year: 2016
  ident: 1891_CR32
  publication-title: J Med Chem
  doi: 10.1021/acs.jmedchem.6b00461
– volume: 324
  start-page: 525
  issue: 2
  year: 2004
  ident: 1891_CR19
  publication-title: Virology
  doi: 10.1016/j.virol.2004.04.009
– volume: 8
  start-page: 23
  year: 2014
  ident: 1891_CR41
  publication-title: Open Med Chem J
  doi: 10.2174/1874104501408010023
– volume: 59
  start-page: 2849
  issue: 7
  year: 2016
  ident: 1891_CR3
  publication-title: J Med Chem
  doi: 10.1021/acs.jmedchem.5b00497
– volume: 109
  start-page: 3012
  issue: 7
  year: 2009
  ident: 1891_CR5
  publication-title: Chem Rev
  doi: 10.1021/cr900019j
– volume: 51
  start-page: 3063
  issue: 9
  year: 2007
  ident: 1891_CR11
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.01391-06
– volume: 60
  start-page: 190
  issue: 1
  year: 2015
  ident: 1891_CR23
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.02121-15
– volume: 12
  start-page: 34
  year: 2007
  ident: 1891_CR27
  publication-title: Drug Discov Today
  doi: 10.1016/j.drudis.2006.11.008
– volume: 100
  start-page: 13555
  issue: 23
  year: 2003
  ident: 1891_CR13
  publication-title: Proc Natl Acad Sci USA.
  doi: 10.1073/pnas.2234683100
– volume: 9
  start-page: 641
  year: 2004
  ident: 1891_CR28
  publication-title: Drug Discov Today
  doi: 10.1016/S1359-6446(04)03163-0
– volume: 29
  start-page: 1
  issue: 1
  year: 2006
  ident: 1891_CR8
  publication-title: Eur J Pharm Sci
  doi: 10.1016/j.ejps.2006.04.006
– volume: 51
  start-page: 3574
  issue: 10
  year: 2007
  ident: 1891_CR15
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.00152-07
– reference: 25250097 - Open Med Chem J. 2014 Sep 03;8:23-7
– reference: 19325847 - Int J Mol Sci. 2008 Jun;9(6):1096-107
– reference: 16314103 - Bioorg Med Chem. 2006 Apr 1;14(7):2279-89
– reference: 19422222 - Chem Rev. 2009 Jul;109(7):3012-43
– reference: 15279847 - Drug Discov Today. 2004 Aug 1;9(15):641-51
– reference: 17638699 - Antimicrob Agents Chemother. 2007 Oct;51(10):3574-81
– reference: 27676157 - J Med Chem. 2016 Oct 13;59(19):9262-9268
– reference: 26968652 - Bioorg Med Chem. 2016 Apr 15;24(8):1757-70
– reference: 21985312 - J Enzyme Inhib Med Chem. 2012 Oct;27(5):715-21
– reference: 8170948 - Proc Natl Acad Sci U S A. 1994 Apr 26;91(9):3564-8
– reference: 26482309 - Antimicrob Agents Chemother. 2015 Oct 19;60(1):190-7
– reference: 22978745 - J Med Chem. 2012 Sep 27;55(18):8128-36
– reference: 28500966 - Eur J Med Chem. 2017 Jul 28;135:517-530
– reference: 15207637 - Virology. 2004 Jul 1;324(2):525-30
– reference: 22073298 - PLoS One. 2011;6(11):e27234
– reference: 25341668 - Viruses. 2014 Oct 24;6(10):4095-139
– reference: 23379607 - J Med Chem. 2013 Mar 14;56(5):2029-37
– reference: 22711941 - Tetrahedron Lett. 2012 Apr 11;53(15):1987-1989
– reference: 22474613 - Cold Spring Harb Perspect Med. 2012 Apr;2(4):a007161
– reference: 28454672 - Bioorg Med Chem Lett. 2017 Jun 15;27(12):2689-2694
– reference: 28435038 - Steroids. 2017 Jul;123:1-12
– reference: 27264714 - Sci Rep. 2016 Jun 06;6:27403
– reference: 17935987 - Bioorg Med Chem Lett. 2007 Dec 1;17(23):6553-7
– reference: 20329730 - J Med Chem. 2010 Apr 22;53(8):3133-41
– reference: 23399723 - Eur J Med Chem. 2013 Apr;62:453-65
– reference: 16716572 - Eur J Pharm Sci. 2006 Sep;29(1):1-13
– reference: 22686620 - Drugs. 2012 Jun 18;72(9):e1-25
– reference: 27090171 - Antimicrob Agents Chemother. 2016 Jun 20;60(7):3956-69
– reference: 26598461 - Bioorg Med Chem Lett. 2016 Jan 1;26(1):68-71
– reference: 14573704 - Proc Natl Acad Sci U S A. 2003 Nov 11;100(23):13555-60
– reference: 17576843 - Antimicrob Agents Chemother. 2007 Sep;51(9):3063-6
– reference: 26509831 - J Med Chem. 2016 Apr 14;59(7):2849-78
– reference: 22818973 - Bioorg Med Chem Lett. 2012 Aug 15;22(16):5190-4
– reference: 21936626 - Pharm Biol. 2011 Oct;49(10):995-1007
– reference: 19209842 - Fortschr Chem Org Naturst. 2009;90:135-56
– reference: 26988305 - Bioorg Med Chem Lett. 2016 Apr 15;26(8):1925-30
– reference: 17198971 - Drug Discov Today. 2007 Jan;12(1-2):34-42
– reference: 20673723 - Bioorg Med Chem. 2010 Sep 1;18(17):6451-69
– reference: 19625188 - Bioorg Med Chem Lett. 2009 Aug 15;19(16):4574-8
– reference: 14742233 - Antimicrob Agents Chemother. 2004 Feb;48(2):663-5
– reference: 17954689 - Antimicrob Agents Chemother. 2008 Jan;52(1):128-36
– reference: 17596104 - Clin Pharmacokinet. 2007;46(7):589-98
SSID ssib031263182
ssj0002039635
ssib051367596
ssib034325102
ssj0057624
Score 2.2770224
SecondaryResourceType review_article
Snippet Summary Firstly discovered in 1980s, human immunodeficiency virus (HIV) continues to affect more and more people. However, there is no effective drug available...
Firstly discovered in 1980s, human immunodeficiency virus (HIV) continues to affect more and more people. However, there is no effective drug available for the...
Firstly discovered in 1980s,human immunodeficiency virus (HIV) continues to affect more and more people.However,there is no effective drug available for the...
SourceID wanfang
proquest
pubmed
crossref
springer
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 387
SubjectTerms Medicine
Medicine & Public Health
Title Structure and Anti-HIV Activity of Betulinic Acid Analogues
URI https://link.springer.com/article/10.1007/s11596-018-1891-4
https://www.ncbi.nlm.nih.gov/pubmed/30074203
https://www.proquest.com/docview/2083709743
https://d.wanfangdata.com.cn/periodical/tjykdxxb-e201803001
Volume 38
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVLSH
  databaseName: SpringerLink Journals
  customDbUrl:
  mediaType: online
  eissn: 2523-899X
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0002039635
  issn: 2096-5230
  databaseCode: AFBBN
  dateStart: 19970301
  isFulltext: true
  providerName: Library Specific Holdings
– providerCode: PRVAVX
  databaseName: SpringerLINK - Czech Republic Consortium
  customDbUrl:
  eissn: 2523-899X
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0057624
  issn: 2096-5230
  databaseCode: AGYKE
  dateStart: 19970101
  isFulltext: true
  titleUrlDefault: http://link.springer.com
  providerName: Springer Nature
– providerCode: PRVAVX
  databaseName: SpringerLink Journals (ICM)
  customDbUrl:
  eissn: 2523-899X
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0057624
  issn: 2096-5230
  databaseCode: U2A
  dateStart: 20020101
  isFulltext: true
  titleUrlDefault: http://www.springerlink.com/journals/
  providerName: Springer Nature
– providerCode: PRVAVX
  databaseName: SpringerLink Journals (ICM)
  customDbUrl:
  eissn: 2523-899X
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0002039635
  issn: 2096-5230
  databaseCode: U2A
  dateStart: 20180101
  isFulltext: true
  titleUrlDefault: http://www.springerlink.com/journals/
  providerName: Springer Nature
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1LS8NAEF60gngR38YXEXpSArubRxM8VbFUoV600tuy2Ye0Sio2hfrvncmjrSiC17A7gZnZzHyZnW8IaQaBleC71NOJH3mBZpGXBr7xVBJSaTinaUHX1HuIuv3gfhAOqj7uSX3bvS5JFl_qRbMbRF5Ev4B64gSAzypZC9F_wIn7vF07kc94BH46j9nYOBkucWSFyFEWVhxzo7ISB0LwqiOHdB6B2bz6-dtbv8evH0npUkG1aAPKrMxeliJWZ4tsVqmm2y59Y5usmGyHrPeqYvouuXosuGOnH8aVmXbbWT70unfPbluVEyXcsXWvTT4teifh6RDXlP96Jnuk37l9uul61SwFT_kxzT2DTHMa2dZ4LAFEJUa1pFY4daOlE5YYHhrLU2ojJo2NVUsxLqNYWwsoVkISs08a2Tgzh8RlgYk0JE4hRTTTopJxZWGzZtREgYodQmsNCVURjeO8izexoEhGpQpQqkClisAhF_Mt7yXLxl-Lz2u1CzgLWOCQmRlPJ4JTpPIBhOQ75KC0x1ycj8kS2Nohl7WBRHVcJ3-9q1nZcLE4H32-6tksFYYj-xkIZkf_EnpMNnBneeHshDTA2OYUUps8PStc-QufuuWf
linkProvider Springer Nature
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1Lb9NAEB7RIFEuFRQoKY-6Uk4gS7vrR2xxCogqoUkuJFVuq_U-qqbIQdiRwr9nxo8kqCgSV2s9K83Meubz7HwD0AtDp9B3mW_SIPZDw2M_CwPr6zRiygrBsoquaTKNh_Pw2yJaNH3cRXvbvS1JVl_qXbMbRl5Cv4h6khSBzxE8piojufVcDFonCriI0U-3MZsaJ6M9jqyIOMqihmNuWVfi0AnpqqPAdJ6A2bb6-a9d_45fD5LSvYJq1QaUO5Xf7kWsq2dw0qSa3qD2jefwyOan8GTSFNNfwKfvFXfs-pf1VG68QV7e-cPRjTfQ9UQJb-W8z7ZcV72T-PSO1tT_eoqXML_6Ovsy9JtZCr4OElb6lpjmDLGtiUQhiEqt7iujaepG36Q8tSKyTmTMxVxZl-i-5kLFiXEOUazCJOYVdPJVbl-Dx0MbG0ycIkZops8UF9rhy4YzG4c66QJrNSR1QzRO8y5-yB1FMilVolIlKVWGXfiwfeVnzbJxaPFlq3aJZ4EKHCq3q3UhBSMqH0RIQRfOantsxQWULKGtu_CxNZBsjmtxaK9eY8Pd4nL5-95sNpm0gtjPUDA__y-hF3A8nE3GcjyaXr-BpySlvnz2FjpoePsO05wye1-59R9xWuiC
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1ZaxsxEB6aFEJeSo8kdXptIU8pSyStdr1Ln9zDOCeBxCVvQqujOA1yqNeQ_vvO7GE7pAT6ukgjmBkx8-1ovgHYk9Jr9F0W2yLJYml5FpcycbEpUqadEKys6ZpOz7LRWB5dpVftnNNZ99q9K0k2PQ3E0hSqg1vrD5aNbxiFCQkjAsoLBEFr8FRiqCb0NRaDzqESLjL02UX8pibKdIUvKyW-srTlm7tuqnLokPTsUWBqTyBtUQn916n3Y9mDBHWluFq3BAWvw8-V6DV8Ds_atDMaNH7yAp648BI2TtvC-iv4fFHzyM5_u0gHGw1CNYlHhz-igWmmS0RTH31x1bzuo8SvE1rT_PeZbcF4-P3y6yhu5yrEJslZFTtinbPEvCZyjYCqcKavraEJHH1b8MKJ1HlRMp9x7Xxu-oYLneXWe0S0GhOabVgP0-BeQ8SlyywmUSkjZNNnmgvjcbPlzGXS5D1gnYaUaUnHafbFjVrSJZNSFSpVkVKV7MH-Ysttw7jx2OKPndoV3gsqdujgpvOZEoxofRAtJT3YaeyxEJdQ4oS27sGnzkCqvbqzx87aa224XFxd__ll7-5K5QQxoaFgvvtfQj_Axvm3oTo5PDt-A5skpHmH9hbW0e7uHWY8Vfm-9uq_gYnsxw
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Structure+and+Anti-HIV+Activity+of+Betulinic+Acid+Analogues&rft.jtitle=%E5%8D%8E%E4%B8%AD%E7%A7%91%E6%8A%80%E5%A4%A7%E5%AD%A6%E5%AD%A6%E6%8A%A5%EF%BC%88%E5%8C%BB%E5%AD%A6%E8%8B%B1%E5%BE%B7%E6%96%87%E7%89%88%EF%BC%89&rft.au=Qiu-xia+HUANG&rft.au=Hong-fei+CHEN&rft.au=Xing-rui+LUO&rft.au=Yin-xiang+ZHANG&rft.date=2018-06-01&rft.pub=University+of+South+China%2C+Hengyang+421001%2C+China&rft.issn=1672-0733&rft.volume=38&rft.issue=3&rft.spage=387&rft.epage=397&rft_id=info:doi/10.1007%2Fs11596-018-1891-4&rft.externalDocID=tjykdxxb_e201803001
thumbnail_s http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=http%3A%2F%2Fwww.wanfangdata.com.cn%2Fimages%2FPeriodicalImages%2Ftjykdxxb-e%2Ftjykdxxb-e.jpg