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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H24N2O
Molecular Weight 284.396
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VINTOPEROL

SMILES

[H][C@]12N(CCC[C@]1(CC)CO)CCC3=C2NC4=CC=CC=C34

InChI

InChIKey=BKRBRZLECKMEBD-QZTJIDSGSA-N
InChI=1S/C18H24N2O/c1-2-18(12-21)9-5-10-20-11-8-14-13-6-3-4-7-15(13)19-16(14)17(18)20/h3-4,6-7,17,19,21H,2,5,8-12H2,1H3/t17-,18-/m1/s1

HIDE SMILES / InChI

Molecular Formula C18H24N2O
Molecular Weight 284.396
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Vintoperol (also known as RGH 2981), a peripheral circulation-enhancing compound that was developed as a moderate serotonin and calcium channel antagonist. Vintoperol was studied for the treatment of arterial occlusive disease and peripheral vascular disorders. It was shown that this compound interfered with platelet aggregation both in vitro and in vivo and possessed potent antithrombotic effects in thrombosis models in which platelet activation was mainly involved. Vintoperol participated in phase II clinical trials in Japan for the treatment patients with arterial occlusive disorders, peripheral vascular disorders, and thrombosis. However, because of its toxic side effects, vintoperol was discontinued from the clinical practice.

Approval Year

PubMed

PubMed

TitleDatePubMed
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:46:41 GMT 2023
Edited
by admin
on Fri Dec 15 15:46:41 GMT 2023
Record UNII
IS7C3GTW01
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VINTOPEROL
INN  
INN  
Official Name English
vintoperol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C333
Created by admin on Fri Dec 15 15:46:41 GMT 2023 , Edited by admin on Fri Dec 15 15:46:41 GMT 2023
Code System Code Type Description
CAS
106498-99-1
Created by admin on Fri Dec 15 15:46:41 GMT 2023 , Edited by admin on Fri Dec 15 15:46:41 GMT 2023
PRIMARY
NCI_THESAURUS
C76585
Created by admin on Fri Dec 15 15:46:41 GMT 2023 , Edited by admin on Fri Dec 15 15:46:41 GMT 2023
PRIMARY
MESH
C066359
Created by admin on Fri Dec 15 15:46:41 GMT 2023 , Edited by admin on Fri Dec 15 15:46:41 GMT 2023
PRIMARY
INN
6467
Created by admin on Fri Dec 15 15:46:41 GMT 2023 , Edited by admin on Fri Dec 15 15:46:41 GMT 2023
PRIMARY
PUBCHEM
6917973
Created by admin on Fri Dec 15 15:46:41 GMT 2023 , Edited by admin on Fri Dec 15 15:46:41 GMT 2023
PRIMARY
EPA CompTox
DTXSID001030624
Created by admin on Fri Dec 15 15:46:41 GMT 2023 , Edited by admin on Fri Dec 15 15:46:41 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105559
Created by admin on Fri Dec 15 15:46:41 GMT 2023 , Edited by admin on Fri Dec 15 15:46:41 GMT 2023
PRIMARY
FDA UNII
IS7C3GTW01
Created by admin on Fri Dec 15 15:46:41 GMT 2023 , Edited by admin on Fri Dec 15 15:46:41 GMT 2023
PRIMARY
EVMPD
SUB00074MIG
Created by admin on Fri Dec 15 15:46:41 GMT 2023 , Edited by admin on Fri Dec 15 15:46:41 GMT 2023
PRIMARY
SMS_ID
100000079136
Created by admin on Fri Dec 15 15:46:41 GMT 2023 , Edited by admin on Fri Dec 15 15:46:41 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY