3'-AMINO-3'-DEOXYTHYMIDINE

CC1=CN([C@H]2C[C@H](N)[C@@H](CO)O2)C(=O)NC1=O

InChIKey=ADVCGXWUUOVPPB-XLPZGREQSA-N

InChI=1S/C10H15N3O4/c1-5-3-13(10(16)12-9(5)15)8-2-6(11)7(4-14)17-8/h3,6-8,14H,2,4,11H2,1H3,(H,12,15,16)/t6-,7+,8+/m0/s1

PubMed

Title	Date	PubMed
Synthesis and antiviral activity of various 3'-azido, 3'-amino, 2',3'-unsaturated, and 2',3'-dideoxy analogues of pyrimidine deoxyribonucleosides against retroviruses.	1987 Feb	3643284
Enhanced in vitro inhibition of HIV-1 replication by 3'-fluoro-3'-deoxythymidine compared to several other nucleoside analogs.	1988 Dec	3219235
Aryl phosphate derivatives of bromo-methoxy-azidothymidine are dual-function spermicides with potent anti-human immunodeficiency virus.	1998 Sep	9716547
Prophylactic contraceptives for HIV/AIDS.	1999 Sep-Oct	10582788
Thymidine and thymidine-5'-O-monophosphate analogues as inhibitors of Mycobacterium tuberculosis thymidylate kinase.	2003 Sep 15	12941330
3D-QSAR studies on antitubercular thymidine monophosphate kinase inhibitors based on different alignment methods.	2006 Feb 15	16290929

Name

Type

Language

3'-AMINO-3'-DEOXYTHYMIDINE

Systematic Name

English

3'-DEOXY-3'-AMINOTHYMIDINE

Systematic Name

English

THYMIDINE, 3'-AMINO-3'-DEOXY-

Systematic Name

English

Code System Code Type Description

CAS

52450-18-7

Created by admin on Sat Dec 16 05:53:57 GMT 2023 , Edited by admin on Sat Dec 16 05:53:57 GMT 2023

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EPA CompTox

DTXSID00966879

Created by admin on Sat Dec 16 05:53:57 GMT 2023 , Edited by admin on Sat Dec 16 05:53:57 GMT 2023

PRIMARY

FDA UNII

7W21M0C25B

Created by admin on Sat Dec 16 05:53:57 GMT 2023 , Edited by admin on Sat Dec 16 05:53:57 GMT 2023

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PUBCHEM

108074

Created by admin on Sat Dec 16 05:53:57 GMT 2023 , Edited by admin on Sat Dec 16 05:53:57 GMT 2023

PRIMARY

PARENT (METABOLITE TOXIC)


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SUBSTANCE RECORD


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