| Weight | 501.733 g/mol |
|---|---|
| Formula | C29H43NO4S |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 10 |
Avasimibe (166518-60-1)
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- Effects of the Acyl Coenzyme A:Cholesterol Acyltransferase Inhibitor Avasimibe on Human Atherosclerotic Lesions (Circulation, 2004)
- The ACAT Inhibitor Avasimibe Reduces Macrophages and Matrix Metalloproteinase Expression in Atherosclerotic Lesions of Hypercholesterolemic Rabbits (Arteriosclerosis, Thrombosis, and Vascular Biology, 2000)
- Acyl-CoA:Cholesterol Acyltransferase Inhibitor Avasimibe Reduces Atherosclerosis in Addition to Its Cholesterol-Lowering Effect in ApoE*3-Leiden Mice (Circulation, 2001)
- Efficacy and short-term safety of a new ACAT inhibitor, avasimibe, on lipids, lipoproteins, and apolipoproteins, in patients with combined hyperlipidemia (Atherosclerosis, 2001)
- Inhibition of ACAT by avasimibe decreases both VLDL and LDL apolipoprotein B production in miniature pigs (Journal of Lipid Research, 1999)
- Avasimibe induces CYP3A4 and multiple drug resistance protein 1 gene expression through activation of the pregnane X receptor (Journal of Pharmacology and Experimental Therapeutics, 2003)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)C1=C(C(=CC=C1)C(C)C)OS(=O)(=O)NC(=O)CC2=C(C=C(C=C2C(C)C)C(C)C)C(C)C
-
InChIKeyPTQXTEKSNBVPQJ-UHFFFAOYSA-N
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Synthesis
Benzeneacetyl chloride, 2,4,6-tris(1-methylethyl)-
+
Reactant
(Schotten-Baumann amide from acid)
1,3,5-TRIISOPROPYLBENZENE
+
Reactant
(Friedel-Crafts alkylation)
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Avasimibe
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