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Details

Stereochemistry ABSOLUTE
Molecular Formula C9H12FN2O9P
Molecular Weight 342.1717
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 5-FLUOROURIDINE MONOPHOSPHATE

SMILES

O[C@H]1[C@@H](O)[C@@H](O[C@@H]1COP(O)(O)=O)N2C=C(F)C(=O)NC2=O

InChI

InChIKey=RNBMPPYRHNWTMA-UAKXSSHOSA-N
InChI=1S/C9H12FN2O9P/c10-3-1-12(9(16)11-7(3)15)8-6(14)5(13)4(21-8)2-20-22(17,18)19/h1,4-6,8,13-14H,2H2,(H,11,15,16)(H2,17,18,19)/t4-,5-,6-,8-/m1/s1

HIDE SMILES / InChI

Molecular Formula C9H12FN2O9P
Molecular Weight 342.1717
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Flosfluridine tidoxil, a thymidylate synthase inhibitor that was developed for the treatment of actinic keratosis and solid tumors, e.g. breast and colorectal cancers. These studies were suspended and information about the further development of this drug is not available.

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 20:06:20 GMT 2025
Edited
by admin
on Mon Mar 31 20:06:20 GMT 2025
Record UNII
BMW6RNK254
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5'-URIDYLIC ACID, 5-FLUORO-
Preferred Name English
5-FLUOROURIDINE MONOPHOSPHATE
Systematic Name English
5-FLUOROURIDINE 5'-MONOPHOSPHATE
Systematic Name English
5-FLUOROURIDYLIC ACID
Common Name English
Code System Code Type Description
PUBCHEM
150856
Created by admin on Mon Mar 31 20:06:20 GMT 2025 , Edited by admin on Mon Mar 31 20:06:20 GMT 2025
PRIMARY
FDA UNII
BMW6RNK254
Created by admin on Mon Mar 31 20:06:20 GMT 2025 , Edited by admin on Mon Mar 31 20:06:20 GMT 2025
PRIMARY
MESH
C016462
Created by admin on Mon Mar 31 20:06:20 GMT 2025 , Edited by admin on Mon Mar 31 20:06:20 GMT 2025
PRIMARY
EPA CompTox
DTXSID601000617
Created by admin on Mon Mar 31 20:06:20 GMT 2025 , Edited by admin on Mon Mar 31 20:06:20 GMT 2025
PRIMARY
CHEBI
40101
Created by admin on Mon Mar 31 20:06:20 GMT 2025 , Edited by admin on Mon Mar 31 20:06:20 GMT 2025
PRIMARY
CAS
796-66-7
Created by admin on Mon Mar 31 20:06:20 GMT 2025 , Edited by admin on Mon Mar 31 20:06:20 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
PRODRUG -> METABOLITE ACTIVE