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
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
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.
Originator
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:46:41 GMT 2023
by
admin
on
Fri Dec 15 15:46:41 GMT 2023
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Record UNII |
IS7C3GTW01
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Record Status |
Validated (UNII)
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Record Version |
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-
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Official Name | English | ||
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Common Name | English |
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NCI_THESAURUS |
C333
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admin on Fri Dec 15 15:46:41 GMT 2023 , Edited by admin on Fri Dec 15 15:46:41 GMT 2023
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106498-99-1
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C76585
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C066359
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6467
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6917973
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DTXSID001030624
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CHEMBL2105559
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IS7C3GTW01
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SUB00074MIG
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100000079136
Created by
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Related Record | Type | Details | ||
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ACTIVE MOIETY |