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
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)
| 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
| Title | Date | PubMed |
|---|---|---|
| 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
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8430060
250, 500, and 1000 mg every 12 hr for 28 days to healthy male volunteers.
Route of Administration:
Oral
| Substance Class |
Chemical
Created
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admin
on
Edited
Mon Mar 31 17:51:07 GMT 2025
by
admin
on
Mon Mar 31 17:51:07 GMT 2025
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| Record UNII |
6NHC09L02I
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| Record Status |
Validated (UNII)
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| Record Version |
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Official Name | English | ||
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Preferred Name | English | ||
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Common Name | English |
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NCI_THESAURUS |
C257
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CHEMBL2111033
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C052921
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60352
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100000081088
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C73833
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DTXSID40868449
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6NHC09L02I
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77639-66-8
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6045
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SUB10047MIG
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |