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Details

Stereochemistry ABSOLUTE
Molecular Formula C9H13N3O5
Molecular Weight 243.2166
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CYTARABINE

SMILES

NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)[C@@H]2O

InChI

InChIKey=UHDGCWIWMRVCDJ-CCXZUQQUSA-N
InChI=1S/C9H13N3O5/c10-5-1-2-12(9(16)11-5)8-7(15)6(14)4(3-13)17-8/h1-2,4,6-8,13-15H,3H2,(H2,10,11,16)/t4-,6-,7+,8-/m1/s1

HIDE SMILES / InChI
Molecular Formula C9H13N3O5
Molecular Weight 243.2166
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:40:24 UTC 2023
Edited
by admin
on Sat Dec 16 16:40:24 UTC 2023
Record UNII
04079A1RDZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CYTARABINE
EMA EPAR   EP   HSDB   INN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD   WHO-IP  
USAN   INN  
Official Name English
CYTARABINE [USP-RS]
Common Name English
CYTARABINE [HSDB]
Common Name English
CYTOSAR-U
Brand Name English
CYTARABINE [EP MONOGRAPH]
Common Name English
CYTARABINE [WHO-IP]
Common Name English
CYTARABINUM [WHO-IP LATIN]
Common Name English
DEPOCYT
Brand Name English
ARACYTIN
Common Name English
U-19,920
Code English
CYTARABINE [USAN]
Common Name English
CYTARABINE LIPOSOME
VANDF  
Common Name English
CYTARABINE [VANDF]
Common Name English
ARACYTIDINE
Common Name English
SPONGOCYTIDINE
Common Name English
CYTARABINE [MI]
Common Name English
ARABINOCYTOSINE
Common Name English
CYTARABINE [ORANGE BOOK]
Common Name English
ARA-C
Common Name English
CYTARABINE LIPOSOME [VANDF]
Common Name English
CYTARABINE [USP IMPURITY]
Common Name English
1-.BETA.-D-ARABINOFURANOSYLCYTOSINE
Common Name English
Cytarabine [WHO-DD]
Common Name English
VYXEOS COMPONENT CYTARABINE
Brand Name English
NSC-287459
Code English
U 19920A
Common Name English
CYTARABINE [MART.]
Common Name English
CYTARABINOSIDE
Common Name English
CYTARABINE [JAN]
Common Name English
U-19920
Code English
ARACYTINE
Common Name English
cytarabine [INN]
Common Name English
CYTARABINE [EMA EPAR]
Common Name English
2(1H)-PYRIMIDINONE, 4-AMINO-1-.BETA.-D-ARABINOFURANOSYL-
Common Name English
CYTARABINE [USP MONOGRAPH]
Common Name English
Classification Tree Code System Code
WHO-ATC L01XY01
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
FDA ORPHAN DRUG 234806
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
NDF-RT N0000175595
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
NDF-RT N0000000233
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
EMA ASSESSMENT REPORTS DEPOCYT (AUTHORIZED: MENINGEAL NEOPLASMS)
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
FDA ORPHAN DRUG 265808
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
NCI_THESAURUS C1557
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
WHO-ESSENTIAL MEDICINES LIST 8.2
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
FDA ORPHAN DRUG 73393
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
LIVERTOX NBK548291
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
WHO-ATC L01BC01
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
EU-Orphan Drug EU/3/11/942
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
WHO-VATC QL01BC01
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
Code System Code Type Description
RXCUI
968804
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
ALTERNATIVE
ECHA (EC/EINECS)
205-705-9
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
EPA CompTox
DTXSID3022877
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
DRUG BANK
DB00987
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
EVMPD
SUB06880MIG
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
NCI_THESAURUS
C408
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
RXCUI
3041
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
DAILYMED
04079A1RDZ
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
MERCK INDEX
m4051
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY Merck Index
PUBCHEM
6253
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
WIKIPEDIA
CYTARABINE
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
ChEMBL
CHEMBL803
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
RS_ITEM_NUM
1162002
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
FDA UNII
04079A1RDZ
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
IUPHAR
4827
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
DRUG CENTRAL
770
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
CAS
147-94-4
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
MESH
D003561
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
CHEBI
28680
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
SMS_ID
100000089874
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
INN
1709
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
HSDB
3049
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
NSC
287459
Created by admin on Sat Dec 16 16:40:27 UTC 2023 , Edited by admin on Sat Dec 16 16:40:27 UTC 2023
PRIMARY
Related Record Type Details
DEOXYCYTIDINE KINASE
METABOLIC ENZYME -> SUBSTRATE
kcat
DEOXYCYTIDINE KINASE
METABOLIC ENZYME -> SUBSTRATE
Km
PLASMA PROTEIN FRACTION (HUMAN)
BINDER->LIGAND
BINDING
Structure of CYTARABINE HYDROCHLORIDE
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of ASPACYTARABINE
PRODRUG -> METABOLITE ACTIVE
Structure of URACIL ARABINOSIDE
METABOLITE INACTIVE -> PARENT
Produced via Cytidine deaminase exposure.
PLASMA
Structure of CYTIDINE TRIPHOSPHATE
METABOLITE ACTIVE -> PARENT
PLASMA
Structure of ELACYTARABINE
PRODRUG -> METABOLITE ACTIVE
Structure of CYTARABINE TRIPHOSPHATE
METABOLITE ACTIVE -> PARENT
Structure of URACIL ARABINOTIDE
METABOLITE ACTIVE -> PARENT
PLASMA
Structure of CYTARABINE 5'-PHOSPHATE
METABOLITE -> PARENT
Related Record Type Details
Structure of CYTIDINE
IMPURITY -> PARENT
Structure of CYTOSINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of URACIL
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of URACIL ARABINOSIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of URACIL ARABINOSIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of URACIL
IMPURITY -> PARENT
Structure of 5-METHYLCYTIDINE
IMPURITY -> PARENT
Structure of ANCITABINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of URIDINE
IMPURITY -> PARENT
Structure of URACIL
IMPURITY -> PARENT
Related Record Type Details
Structure of CYTARABINE
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Volume of Distribution PHARMACOKINETIC
Biological Half-life PHARMACOKINETIC
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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