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Details

Stereochemistry ACHIRAL
Molecular Formula C14H16N2O4
Molecular Weight 276.2878
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 5-BENZYLACYCLOURIDINE

SMILES

OCCOCN1C=C(CC2=CC=CC=C2)C(=O)NC1=O

InChI

InChIKey=SPJAGILXQBHHSZ-UHFFFAOYSA-N
InChI=1S/C14H16N2O4/c17-6-7-20-10-16-9-12(13(18)15-14(16)19)8-11-4-2-1-3-5-11/h1-5,9,17H,6-8,10H2,(H,15,18,19)

HIDE SMILES / InChI

Molecular Formula C14H16N2O4
Molecular Weight 276.2878
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Different effect of benzylacyclouridine on the toxic and therapeutic effects of azidothymidine in mice.
1990 Dec 1
Modulation of uridine phosphorylase gene expression by tumor necrosis factor-alpha enhances the antiproliferative activity of the capecitabine intermediate 5'-deoxy-5-fluorouridine in breast cancer cells.
2006 Apr
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:29:43 GMT 2023
Edited
by admin
on Fri Dec 15 15:29:43 GMT 2023
Record UNII
0H851I3O9D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5-BENZYLACYCLOURIDINE
Common Name English
BENZYLACYCLOURIDINE
Common Name English
5-BACU
Common Name English
2,4(1H,3H)-PYRIMIDINEDIONE, 1-((2-HYDROXYETHOXY)METHYL)-5-(PHENYLMETHYL)-
Systematic Name English
BAU
Common Name English
5-BENZYL-1-(2-HYDROXYETHOXYMETHYL)URACIL
Systematic Name English
Code System Code Type Description
DRUG BANK
DB07437
Created by admin on Fri Dec 15 15:29:43 GMT 2023 , Edited by admin on Fri Dec 15 15:29:43 GMT 2023
PRIMARY
CAS
82857-69-0
Created by admin on Fri Dec 15 15:29:43 GMT 2023 , Edited by admin on Fri Dec 15 15:29:43 GMT 2023
PRIMARY
CHEBI
41037
Created by admin on Fri Dec 15 15:29:43 GMT 2023 , Edited by admin on Fri Dec 15 15:29:43 GMT 2023
PRIMARY
FDA UNII
0H851I3O9D
Created by admin on Fri Dec 15 15:29:43 GMT 2023 , Edited by admin on Fri Dec 15 15:29:43 GMT 2023
PRIMARY
EPA CompTox
DTXSID30232034
Created by admin on Fri Dec 15 15:29:43 GMT 2023 , Edited by admin on Fri Dec 15 15:29:43 GMT 2023
PRIMARY
PUBCHEM
54929
Created by admin on Fri Dec 15 15:29:43 GMT 2023 , Edited by admin on Fri Dec 15 15:29:43 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY