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Details

Stereochemistry ACHIRAL
Molecular Formula C13H12N2O2.ClH.H2O
Molecular Weight 282.723
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of OZAGREL HYDROCHLORIDE MONOHYDRATE

SMILES

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

InChI

InChIKey=OWIZTYOMGVTSDP-TXOOBNKBSA-N
InChI=1S/C13H12N2O2.ClH.H2O/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;1H2/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
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 MONOHYDRATE
Common Name English
OZAGREL HYDROCHLORIDE HYDRATE [JAN]
Common Name English
2-PROPENOIC ACID, 3-(4-(1H-IMIDAZOL-1-YLMETHYL)PHENYL)-, HYDROCHLORIDE, HYDRATE (1:1:1)
Common Name English
OZAGREL HYDROCHLORIDE HYDRATE
JAN  
Common Name English
Code System Code Type Description
SMS_ID
100000177063
Created by admin on Sat Dec 16 05:12:42 GMT 2023 , Edited by admin on Sat Dec 16 05:12:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID30232877
Created by admin on Sat Dec 16 05:12:42 GMT 2023 , Edited by admin on Sat Dec 16 05:12:42 GMT 2023
PRIMARY
CAS
83993-01-5
Created by admin on Sat Dec 16 05:12:42 GMT 2023 , Edited by admin on Sat Dec 16 05:12:42 GMT 2023
GENERIC (FAMILY)
FDA UNII
C0I3AF4OHV
Created by admin on Sat Dec 16 05:12:42 GMT 2023 , Edited by admin on Sat Dec 16 05:12:42 GMT 2023
PRIMARY
PUBCHEM
5282439
Created by admin on Sat Dec 16 05:12:42 GMT 2023 , Edited by admin on Sat Dec 16 05:12:42 GMT 2023
PRIMARY