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

Details

Stereochemistry RACEMIC
Molecular Formula C15H12ClNO2
Molecular Weight 273.714
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARPROFEN

SMILES

CC(C(O)=O)C1=CC2=C(C=C1)C3=C(N2)C=CC(Cl)=C3

InChI

InChIKey=PUXBGTOOZJQSKH-UHFFFAOYSA-N
InChI=1S/C15H12ClNO2/c1-8(15(18)19)9-2-4-11-12-7-10(16)3-5-13(12)17-14(11)6-9/h2-8,17H,1H3,(H,18,19)

HIDE SMILES / InChI
Carprofen is an anti-inflammatory drug developed in Japan by Nippon Roche Research Center. Carprofen, as many NSAIDs, selectively inhibits COX-2 and was shown to suppress inflammation in vitro, using osteoarthritis models. The drug was approved by FDA for human use under the name Ridamyl, however, now it is sold only for veterinary purposes and prescribed for the treatment of postoperative pain and the relief of pain and inflammation associated with osteoarthritis in dogs.

Originator

Curator's Comment: The full version can be found here: https://www.jstage.jst.go.jp/article/fpj1944/73/7/73_7_757/_pdf

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.102 µM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
RIMADYL

Approved Use

Rimadyl is indicated for the relief of pain and inflammation associated with osteoarthritis and for the control of postoperative pain associated with soft tissue and orthopedic surgeries in dogs.

Launch Date

1996
Primary
RIMADYL

Approved Use

Rimadyl is indicated for the relief of pain and inflammation associated with osteoarthritis and for the control of postoperative pain associated with soft tissue and orthopedic surgeries in dogs.

Launch Date

1996
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
10.2 μg/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CARPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
10.4 μg/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CARPROFEN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
52.4 μg × h/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CARPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
57.8 μg × h/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CARPROFEN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
9.4 h
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CARPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
10.5 h
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CARPROFEN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
1%
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CARPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
1%
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CARPROFEN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer

Drug as victim

Drug as victim

TargetModalityActivityMetaboliteClinical evidence
yes
PubMed

PubMed

TitleDatePubMed
Determination of expression of cyclooxygenase-1 and -2 isozymes in canine tissues and their differential sensitivity to nonsteroidal anti-inflammatory drugs.
2004 Jun
SAR studies of acidic dual γ-secretase/PPARγ modulators.
2011 Sep 15
Patents

Sample Use Guides

The recommended dosage for oral administration to dogs is 2 mg/lb (4.4 mg/kg) of body weight daily. The total daily dose may be administered as 2 mg/lb of body weight once daily or divided and administered as 1 mg/lb (2.2 mg/kg) twice daily. For the control of postoperative pain, administer approximately 2 hours before the procedure.
Route of Administration: Oral
Canine chondrocytes isolated from normal canine articular cartilage were used to create an in vitro model of osteoarthritis. Cells were incubated at 37C in a 5% CO2 atmosphere for 72 h and then treated with 500 uL of the pro-inflammatory cytokine, interleukin-1b (IL-1b) (10 ng/mL in serum-free medium) to induce inflammatory conditions and incubated at 37C in 5% CO2 atmosphere for 2 h. Carprofen was added to the cells at concentration from 0.1 to 250 ug/mL.
Name Type Language
CARPROFEN
GREEN BOOK   INN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN   INN  
Official Name English
CARPROFEN [USP MONOGRAPH]
Common Name English
RO-20-5720/000
Code English
CARPROFEN [GREEN BOOK]
Common Name English
CARPROFEN [MI]
Common Name English
(±)-6-CHLORO-.ALPHA.-METHYLCARBAZOLE-2-ACETIC ACID
Systematic Name English
CARPROFEN [MART.]
Common Name English
9H-CARBAZOLE-2-ACETIC ACID, 6-CHLORO-.ALPHA.-METHYL, (±)-
Common Name English
RO 20-5720/000
Code English
Carprofen [WHO-DD]
Common Name English
carprofen [INN]
Common Name English
RIMADYL
Brand Name English
CARPROFEN [ORANGE BOOK]
Common Name English
CARPROFEN [USP IMPURITY]
Common Name English
CARPROFEN FOR VETERINARY USE
EP  
Common Name English
CARPROFEN FOR VETERINARY USE [EP MONOGRAPH]
Common Name English
CARPROFEN [USAN]
Common Name English
CARPROFEN [USP-RS]
Common Name English
CARPROFEN [VANDF]
Common Name English
NSC-297935
Code English
Classification Tree Code System Code
CFR 21 CFR 520.304
Created by admin on Sat Dec 16 17:18:28 GMT 2023 , Edited by admin on Sat Dec 16 17:18:28 GMT 2023
NCI_THESAURUS C257
Created by admin on Sat Dec 16 17:18:28 GMT 2023 , Edited by admin on Sat Dec 16 17:18:28 GMT 2023
WHO-VATC QM01AE91
Created by admin on Sat Dec 16 17:18:28 GMT 2023 , Edited by admin on Sat Dec 16 17:18:28 GMT 2023
CFR 21 CFR 522.304
Created by admin on Sat Dec 16 17:18:28 GMT 2023 , Edited by admin on Sat Dec 16 17:18:28 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C65290
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PRIMARY
DRUG BANK
DB00821
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INN
3980
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PRIMARY
PUBCHEM
2581
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DRUG CENTRAL
518
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CAS
53716-49-7
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PRIMARY
MERCK INDEX
m3132
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PRIMARY Merck Index
RXCUI
20343
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PRIMARY RxNorm
ECHA (EC/EINECS)
258-712-4
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PRIMARY
DAILYMED
FFL0D546HO
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PRIMARY
MESH
C007005
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PRIMARY
RS_ITEM_NUM
1096699
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PRIMARY
CHEBI
364453
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PRIMARY
EVMPD
SUB06144MIG
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PRIMARY
SMS_ID
100000081327
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PRIMARY
FDA UNII
FFL0D546HO
Created by admin on Sat Dec 16 17:18:28 GMT 2023 , Edited by admin on Sat Dec 16 17:18:28 GMT 2023
PRIMARY
NSC
297935
Created by admin on Sat Dec 16 17:18:28 GMT 2023 , Edited by admin on Sat Dec 16 17:18:28 GMT 2023
PRIMARY
IUPHAR
7141
Created by admin on Sat Dec 16 17:18:28 GMT 2023 , Edited by admin on Sat Dec 16 17:18:28 GMT 2023
PRIMARY
ChEMBL
CHEMBL1316
Created by admin on Sat Dec 16 17:18:28 GMT 2023 , Edited by admin on Sat Dec 16 17:18:28 GMT 2023
PRIMARY
WIKIPEDIA
CARPROFEN
Created by admin on Sat Dec 16 17:18:28 GMT 2023 , Edited by admin on Sat Dec 16 17:18:28 GMT 2023
PRIMARY
EPA CompTox
DTXSID1045871
Created by admin on Sat Dec 16 17:18:28 GMT 2023 , Edited by admin on Sat Dec 16 17:18:28 GMT 2023
PRIMARY