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Details

Stereochemistry ABSOLUTE
Molecular Formula C8H12N4O5
Molecular Weight 244.2047
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AZACITIDINE

SMILES

NC1=NC(=O)N(C=N1)[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O

InChI

InChIKey=NMUSYJAQQFHJEW-KVTDHHQDSA-N
InChI=1S/C8H12N4O5/c9-7-10-2-12(8(16)11-7)6-5(15)4(14)3(1-13)17-6/h2-6,13-15H,1H2,(H2,9,11,16)/t3-,4-,5-,6-/m1/s1

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
AZACITIDINE
EMA EPAR   HSDB   INN   JAN   MART.   MI   ORANGE BOOK   USAN   USP-RS   VANDF   WHO-DD  
USAN   INN  
Official Name English
AZACITIDINE [ORANGE BOOK]
Common Name English
Azacitidine [WHO-DD]
Common Name English
5-AZACYTIDINE
Systematic Name English
AZACITIDINE [VANDF]
Common Name English
ONUREG
Brand Name English
azacitidine [INN]
Common Name English
AZACITIDINE [MI]
Common Name English
AZACITIDINE [HSDB]
Common Name English
AZACITIDINE [JAN]
Common Name English
VIDAZA
Brand Name English
AZACITIDINE [IARC]
Common Name English
5-AZACITIDINE
Common Name English
4-AMINO-1-.BETA.-D-RIBOFURANOSYL-S-TRIAZIN-2(1H)-ONE
Common Name English
U-18,496
Code English
1,3,5-TRIAZIN-2(1H)-ONE, 4-AMINO-1-.BETA.-D-RIBOFURANOSYL-
Common Name English
AZACYTIDINE
Systematic Name English
AZACITIDINE [EMA EPAR]
Common Name English
AZACITIDINE [MART.]
Common Name English
NSC-102816
Code English
AZACITIDINE [USP-RS]
Common Name English
U-18496
Code English
AZACITIDINE [USAN]
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 150101
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
WHO-ATC L01BC07
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
FDA ORPHAN DRUG 257008
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
NDF-RT N0000000233
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
EMA ASSESSMENT REPORTS VIDAZA (AUTHORIZED: MYELODYPLASTIC SYNDROMES)
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
LIVERTOX NBK548363
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
WHO-VATC QL01BC07
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
NCI_THESAURUS C2083
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
NDF-RT N0000175595
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
NCI_THESAURUS C1557
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
FDA ORPHAN DRUG 829021
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
EU-Orphan Drug EU/3/01/084
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
Code System Code Type Description
ChEMBL
CHEMBL1489
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
ECHA (EC/EINECS)
206-280-2
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
SMS_ID
100000086905
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
IUPHAR
6796
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
EPA CompTox
DTXSID9020116
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
RS_ITEM_NUM
1045520
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
CHEBI
2038
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
RXCUI
1251
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY RxNorm
WIKIPEDIA
AZACITIDINE
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
DAILYMED
M801H13NRU
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
HSDB
6879
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
NSC
102816
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
PUBCHEM
9444
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
INN
4520
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
MESH
D001374
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
EVMPD
SUB05624MIG
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
MERCK INDEX
m2154
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY Merck Index
LACTMED
Azacitidine
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
FDA UNII
M801H13NRU
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
NCI_THESAURUS
C288
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
DRUG CENTRAL
25
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
CAS
320-67-2
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
DRUG BANK
DB00928
Created by admin on Sat Dec 16 05:11:30 UTC 2023 , Edited by admin on Sat Dec 16 05:11:30 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of AZACITIDINE
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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