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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H12FN5O4
Molecular Weight 285.2318
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLUDARABINE

SMILES

NC1=NC(F)=NC2=C1N=CN2[C@@H]3O[C@H](CO)[C@@H](O)[C@@H]3O

InChI

InChIKey=HBUBKKRHXORPQB-FJFJXFQQSA-N
InChI=1S/C10H12FN5O4/c11-10-14-7(12)4-8(15-10)16(2-13-4)9-6(19)5(18)3(1-17)20-9/h2-3,5-6,9,17-19H,1H2,(H2,12,14,15)/t3-,5-,6+,9-/m1/s1

HIDE SMILES / InChI
Molecular Formula C10H12FN5O4
Molecular Weight 285.2318
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 Fri Dec 15 16:20:07 UTC 2023
Edited
by admin
on Fri Dec 15 16:20:07 UTC 2023
Record UNII
P2K93U8740
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLUDARABINE
HSDB   INN   MI   VANDF   WHO-DD  
INN  
Official Name English
FLURADOSA
Brand Name English
FLUDARABINE PHOSPHATE IMPURITY, 2-FLUORO-ARA-ADENINE- [USP IMPURITY]
Common Name English
NSC-118218
Code English
9-.BETA.-D-ARABINOFURANOSYL-2-FLUOROADENINE
Common Name English
FLUDARABINE [HSDB]
Common Name English
2-F-ARAA
Common Name English
2-FLUORO-9-.BETA.-D-ARABINOFURANOSYLADENINE
Common Name English
FLUDARABINE [VANDF]
Common Name English
fludarabine [INN]
Common Name English
Fludarabine [WHO-DD]
Common Name English
2-FLUOROVIDARABINE
Common Name English
FLUDARABINE [MI]
Common Name English
9-.BETA.-D-ARABINOFURANOSYL-2-FLUORO-9H-PURIN-6-AMINE
Common Name English
FLUDARABINE PHOSPHATE IMPURITY E [EP IMPURITY]
Common Name English
2-FLUORO ARA-A
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C2150
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
NDF-RT N0000000233
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
WHO-VATC QL01BB05
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
NDF-RT N0000175595
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
LIVERTOX NBK548845
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
NCI_THESAURUS C1556
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
WHO-ATC L01BB05
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C1094
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
DAILYMED
P2K93U8740
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
HSDB
6964
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
MERCK INDEX
m5427
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY Merck Index
DRUG BANK
DB01073
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
SMS_ID
100000081235
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
ECHA (EC/EINECS)
244-525-5
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
NSC
118218
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
EVMPD
SUB07678MIG
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
RXCUI
24698
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY RxNorm
WIKIPEDIA
FLUDARABINE
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
ChEMBL
CHEMBL1096882
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
EPA CompTox
DTXSID4039657
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
PUBCHEM
657237
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
INN
5214
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
MESH
C024352
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
CAS
21679-14-1
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
FDA UNII
P2K93U8740
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
IUPHAR
4802
Created by admin on Fri Dec 15 16:20:07 UTC 2023 , Edited by admin on Fri Dec 15 16:20:07 UTC 2023
PRIMARY
Related Record Type Details
Structure of FLUDARABINE TRIPHOSPHATE
METABOLITE ACTIVE -> PARENT
Structure of FLUDARABINE PHOSPHATE
PRODRUG -> METABOLITE ACTIVE
Structure of FLUDARABINE DIPHOSPHATE
METABOLITE ACTIVE -> PARENT
Related Record Type Details
Structure of FLUDARABINE PHOSPHATE
PARENT -> IMPURITY
For the calculation of contents, multiply the peak areas by 0.6
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
Structure of FLUDARABINE
ACTIVE MOIETY
NIH
NCATS
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