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Details

Stereochemistry RACEMIC
Molecular Formula C18H19N3O5S
Molecular Weight 389.426
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ONDANSETRON 8-SULFATE

SMILES

CN1C2=C(C3=CC=CC(OS(O)(=O)=O)=C13)C(=O)C(CN4C=CN=C4C)CC2

InChI

InChIKey=FKMUSAHZDJNPJY-UHFFFAOYSA-N
InChI=1S/C18H19N3O5S/c1-11-19-8-9-21(11)10-12-6-7-14-16(18(12)22)13-4-3-5-15(17(13)20(14)2)26-27(23,24)25/h3-5,8-9,12H,6-7,10H2,1-2H3,(H,23,24,25)

HIDE SMILES / InChI
Ondansetron 8-sulfate is a metabolite of the ondansetron, a drug which is used to prevent nausea and vomiting caused by cancer chemotherapy, radiation therapy, or surgery. Ondansetron is extensively metabolized in humans; the primary metabolic pathway is hydroxylation on the indole ring followed by glucuronide or sulfate conjugation.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Ondansetron metabolism and pharmacokinetics.
1992 Aug

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Name Type Language
ONDANSETRON 8-SULFATE
Common Name English
4H-CARBAZOL-4-ONE, 1,2,3,9-TETRAHYDRO-9-METHYL-3-((2-METHYL-1H-IMIDAZOL-1-YL)METHYL)-8-(SULFOOXY)-
Systematic Name English
Code System Code Type Description
FDA UNII
59D7QNM478
Created by admin on Sat Dec 16 10:50:48 GMT 2023 , Edited by admin on Sat Dec 16 10:50:48 GMT 2023
PRIMARY
PUBCHEM
15700432
Created by admin on Sat Dec 16 10:50:48 GMT 2023 , Edited by admin on Sat Dec 16 10:50:48 GMT 2023
PRIMARY
CAS
126671-73-6
Created by admin on Sat Dec 16 10:50:48 GMT 2023 , Edited by admin on Sat Dec 16 10:50:48 GMT 2023
PRIMARY