U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C10H14N2O5
Molecular Weight 242.2286
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Doxribtimine

SMILES

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

InChI

InChIKey=IQFYYKKMVGJFEH-XLPZGREQSA-N
InChI=1S/C10H14N2O5/c1-5-3-12(10(16)11-9(5)15)8-2-6(14)7(4-13)17-8/h3,6-8,13-14H,2,4H2,1H3,(H,11,15,16)/t6-,7+,8+/m0/s1

HIDE SMILES / InChI
Molecular Formula C10H14N2O5
Molecular Weight 242.2286
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:21:10 UTC 2023
Edited
by admin
on Fri Dec 15 15:21:10 UTC 2023
Record UNII
VC2W18DGKR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
THYMIDINE
INCI   MART.   MI   WHO-DD   WHO-IP  
INCI  
Preferred Name English
Doxribtimine
INN   USAN  
Official Name English
MT-1621 COMPONENT 2'-DEOXYTHYMIDINE
Code English
1-(2-Deoxy-β-D-erythro-pentofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione
Common Name English
ZIDOVUDINE RELATED COMPOUND D
USP-RS  
Common Name English
STAVUDINE IMPURITY C [EP IMPURITY]
Common Name English
ZIDOVUDINE RELATED COMPOUND D [USP IMPURITY]
Common Name English
THYMIDINE [MART.]
Common Name English
THYMIDINE [MI]
Common Name English
DOXRIBTIMINE [USAN]
Common Name English
THYMIDINE [WHO-IP]
Common Name English
Thymidine [WHO-DD]
Common Name English
IMPURITY C [EP IMPURITY]
Common Name English
ZIDOVUDINE RELATED COMPOUND D [USP-RS]
Common Name English
NSC-21548
Code English
THYMIDINE [INCI]
Common Name English
5-Methyl-2′-deoxyuridine
Systematic Name English
ZIDOVUDINE IMPURITY E [EP IMPURITY]
Common Name English
1-(2-DEOXY-.BETA.-D-ERYTHRO-PENTOFURANOSYL)-5-METHYLPYRIMIDINE-2,4(1H,3H)-DIONE [WHO-IP]
Systematic Name English
2,4(1H,3H)-Pyrimidinedione, 1-(2-deoxy-β-D-erythro-pentofuranosyl)-5-methyl-
Systematic Name English
THYMINE-2-DESOXYRIBOSIDE
Common Name English
DEOXYRIBOTHYMIDINE
Common Name English
STAVUDINE IMPURITY C [WHO-IP]
Common Name English
doxribtimine [INN]
Common Name English
2′-Deoxythymidine
Common Name English
Classification Tree Code System Code
LOINC 59215-4
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
EU-Orphan Drug EU/3/17/1870
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
LOINC 48162-2
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
NCI_THESAURUS C707
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
LOINC 75156-0
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
Code System Code Type Description
USAN
KL-167
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
INN
11756
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
MESH
D013936
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-070-4
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
PUBCHEM
5789
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
CHEBI
17748
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
WIKIPEDIA
THYMIDINE
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
CAS
50-89-5
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
RS_ITEM_NUM
1724543
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
NCI_THESAURUS
C880
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
EVMPD
SUB15554MIG
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
NSC
21548
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
MERCK INDEX
m10822
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY Merck Index
DRUG BANK
DB04485
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
DAILYMED
VC2W18DGKR
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
FDA UNII
VC2W18DGKR
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
RXCUI
1372538
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID5023661
Created by admin on Fri Dec 15 15:21:10 UTC 2023 , Edited by admin on Fri Dec 15 15:21:10 UTC 2023
PRIMARY
Related Record Type Details
Structure of ZIDOVUDINE
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of STAVUDINE
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of STAVUDINE
PARENT -> IMPURITY
Amount Not Specified
INTERNATIONAL PHARMACOPEIA
Related Record Type Details
Structure of Doxribtimine
ACTIVE MOIETY
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966