U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C15H13N3O2
Molecular Weight 267.2826
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PRINOMIDE

SMILES

CN1C=CC=C1C(=O)C(C#N)C(=O)NC2=CC=CC=C2

InChI

InChIKey=KBQUAIAGRLAZGP-UHFFFAOYSA-N
InChI=1S/C15H13N3O2/c1-18-9-5-8-13(18)14(19)12(10-16)15(20)17-11-6-3-2-4-7-11/h2-9,12H,1H3,(H,17,20)

HIDE SMILES / InChI

Molecular Formula C15H13N3O2
Molecular Weight 267.2826
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Prinomide is a carbamoylpyrrolepropionitrile derivative patented by Ciba-Geigy A.-G. as a nonsteroidal anti-inflammatory drug that has disease-modifying activity in rheumatoid arthritis. In clinical trials, Prinomide demonstrate significant improvement in symptom score and laboratory variables.

Approval Year

PubMed

PubMed

TitleDatePubMed
Prinomide tromethamine pharmacokinetics: mutually dependent saturable and competitive protein binding between prinomide and its own metabolite.
1993-01
Effect of a new antirheumatic drug (CGS10787B) on antibody formation and delayed-type hypersensitivity in BALB/c mice.
1988
Patents

Patents

Sample Use Guides

250, 500, and 1000 mg every 12 hr for 28 days to healthy male volunteers.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:51:07 GMT 2025
Edited
by admin
on Mon Mar 31 17:51:07 GMT 2025
Record UNII
6NHC09L02I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PRINOMIDE
INN   WHO-DD  
INN  
Official Name English
Prinomide [WHO-DD]
Preferred Name English
prinomide [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Mon Mar 31 17:51:07 GMT 2025 , Edited by admin on Mon Mar 31 17:51:07 GMT 2025
Code System Code Type Description
ChEMBL
CHEMBL2111033
Created by admin on Mon Mar 31 17:51:07 GMT 2025 , Edited by admin on Mon Mar 31 17:51:07 GMT 2025
PRIMARY
MESH
C052921
Created by admin on Mon Mar 31 17:51:07 GMT 2025 , Edited by admin on Mon Mar 31 17:51:07 GMT 2025
PRIMARY
PUBCHEM
60352
Created by admin on Mon Mar 31 17:51:07 GMT 2025 , Edited by admin on Mon Mar 31 17:51:07 GMT 2025
PRIMARY
SMS_ID
100000081088
Created by admin on Mon Mar 31 17:51:07 GMT 2025 , Edited by admin on Mon Mar 31 17:51:07 GMT 2025
PRIMARY
NCI_THESAURUS
C73833
Created by admin on Mon Mar 31 17:51:07 GMT 2025 , Edited by admin on Mon Mar 31 17:51:07 GMT 2025
PRIMARY
EPA CompTox
DTXSID40868449
Created by admin on Mon Mar 31 17:51:07 GMT 2025 , Edited by admin on Mon Mar 31 17:51:07 GMT 2025
PRIMARY
FDA UNII
6NHC09L02I
Created by admin on Mon Mar 31 17:51:07 GMT 2025 , Edited by admin on Mon Mar 31 17:51:07 GMT 2025
PRIMARY
CAS
77639-66-8
Created by admin on Mon Mar 31 17:51:07 GMT 2025 , Edited by admin on Mon Mar 31 17:51:07 GMT 2025
PRIMARY
INN
6045
Created by admin on Mon Mar 31 17:51:07 GMT 2025 , Edited by admin on Mon Mar 31 17:51:07 GMT 2025
PRIMARY
EVMPD
SUB10047MIG
Created by admin on Mon Mar 31 17:51:07 GMT 2025 , Edited by admin on Mon Mar 31 17:51:07 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY