Details
Stereochemistry | ACHIRAL |
Molecular Formula | C17H17F3N6O2 |
Molecular Weight | 394.3511 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1(C)CN(C(=O)N1)C2=NC=C(C(=O)NC3=CC=CC(=C3)C(F)(F)F)C(N)=N2
InChI
InChIKey=FUSNOPLQVRUIIM-UHFFFAOYSA-N
InChI=1S/C17H17F3N6O2/c1-16(2)8-26(15(28)25-16)14-22-7-11(12(21)24-14)13(27)23-10-5-3-4-9(6-10)17(18,19)20/h3-7H,8H2,1-2H3,(H,23,27)(H,25,28)(H2,21,22,24)
Molecular Formula | C17H17F3N6O2 |
Molecular Weight | 394.3511 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Imanixil (also known as HOE-402) was developed as a potent cholesterol-lowering compound, which inhibits VLDL production, and consequently attenuates atherosclerosis development. This drug participated in phase I clinical trial for the treatment of hyperlipidemia, however, this study was discontinued.
Originator
Approval Year
PubMed
Title | Date | PubMed |
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Hypolipidemic activity of HOE-402 is mediated by stimulation of the LDL receptor pathway. | 1993 Jul |
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Cholesterol lowering action of HOE 402 in the normolipidemic and hypercholesterolemic golden Syrian hamster. | 1996 Jan 5 |
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HOE 402 lowers serum cholesterol levels by reducing VLDL-lipid production, and not by induction of the LDL receptor, and reduces atherosclerosis in wild-type and LDL receptor-deficient mice. | 2002 May 1 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 16:48:32 GMT 2023
by
admin
on
Sat Dec 16 16:48:32 GMT 2023
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Record UNII |
8892KM4U61
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C29703
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Related Record | Type | Details | ||
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