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

Details

Stereochemistry ACHIRAL
Molecular Formula C13H12N2O2.ClH
Molecular Weight 264.708
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of OZAGREL HYDROCHLORIDE

SMILES

Cl.OC(=O)\C=C\C1=CC=C(CN2C=CN=C2)C=C1

InChI

InChIKey=CWKFWBJJNNPGAM-IPZCTEOASA-N
InChI=1S/C13H12N2O2.ClH/c16-13(17)6-5-11-1-3-12(4-2-11)9-15-8-7-14-10-15;/h1-8,10H,9H2,(H,16,17);1H/b6-5+;

HIDE SMILES / InChI
Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P24557|||Q8IUN1|||Q9HD82
Gene ID: 6916.0
Gene Symbol: TBXAS1
Target Organism: Homo sapiens (Human)
11.0 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
DOMENAN

Approved Use

Unknown
Primary
XANBON

Approved Use

Cerebral vasospasm and ischaemia following surgical management of subarachnoid haemorrhage.
PubMed

PubMed

TitleDatePubMed
Heparin-protamine complexes cause pulmonary hypertension in goats.
1995 Oct
Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome).
2008 Mar
Patents

Sample Use Guides

1 tablet (200 mg of the active ingredient) at a time, twice a day after breakfast and before bedtime (for asthma). Intravenous infusion of 80mg, twice a day, solute in 500ml normal saline or 5% glucose solution (cerebral vasospasm).
Route of Administration: Other
The influence of ozagrel on platelets aggregation was investigated. Platelet aggregation which was induced by ADP (5 uM) was inhibited by ozagrel. This inhibition was dependent on the concentration of the drug and was significant at 10(−6)–10(−3) M.
Name Type Language
OZAGREL HYDROCHLORIDE
MI   WHO-DD  
Common Name English
Ozagrel hydrochloride [WHO-DD]
Common Name English
OKY 046
Code English
OZAGREL HYDROCHLORIDE [MI]
Common Name English
(2E)-3-(4-(1H-IMIDAZOL-1-YLMETHYL)PHENYL)-2-PROPENOIC ACID HYDROCHLORIDE
Systematic Name English
OKY-046
Common Name English
Code System Code Type Description
CAS
78712-43-3
Created by admin on Fri Dec 15 18:17:35 GMT 2023 , Edited by admin on Fri Dec 15 18:17:35 GMT 2023
PRIMARY
SMS_ID
100000085534
Created by admin on Fri Dec 15 18:17:35 GMT 2023 , Edited by admin on Fri Dec 15 18:17:35 GMT 2023
PRIMARY
EVMPD
SUB03603MIG
Created by admin on Fri Dec 15 18:17:35 GMT 2023 , Edited by admin on Fri Dec 15 18:17:35 GMT 2023
PRIMARY
FDA UNII
W222U960HS
Created by admin on Fri Dec 15 18:17:35 GMT 2023 , Edited by admin on Fri Dec 15 18:17:35 GMT 2023
PRIMARY
MERCK INDEX
m8349
Created by admin on Fri Dec 15 18:17:35 GMT 2023 , Edited by admin on Fri Dec 15 18:17:35 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID9045506
Created by admin on Fri Dec 15 18:17:35 GMT 2023 , Edited by admin on Fri Dec 15 18:17:35 GMT 2023
PRIMARY
DRUG BANK
DBSALT002122
Created by admin on Fri Dec 15 18:17:35 GMT 2023 , Edited by admin on Fri Dec 15 18:17:35 GMT 2023
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PUBCHEM
6438130
Created by admin on Fri Dec 15 18:17:35 GMT 2023 , Edited by admin on Fri Dec 15 18:17:35 GMT 2023
PRIMARY