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Lomitapide
Cat. No.:
0225LY-1235
Purity:
≥99%
Identity:
Confirmed by NMR, and LC-MS.
Size:
Add to basket
Product Overview
Description:
Lomitapide acts as a small molecule inhibitor of microsomal triglyceride transfer protein (MTP), preventing the assembly of very-low-density lipoproteins by blocking lipid absorption and triglyceride transfer.
Synonym:
AEGR-733; BMS-201038; 182431-12-5; Juxtapid; AEGR-733; Lojuxta; AEGR 733; AEGR733; BMS 201038; BMS201038; Lomitapidum; BMS 201238; Lomitapide free base; 9H-Fluorene-9-carboxamide, N-(2,2,2-trifluoroethyl)-9-[4-[4-[[[4'-(trifluoromethyl)[1,1'-biphenyl]-2-yl]carbonyl]amino]-1-piperidinyl]butyl]-; DTXSID50171294; 182431-12-5 (free base); N-(2,2,2-trifluoroethyl)-9-[4-[4-[[2-[4-(trifluoromethyl)phenyl]benzoyl]amino]piperidin-1-yl]butyl]fluorene-9-carboxamide; 9H-Fluorene-9-carboxamide, N-(2,2,2-trifluoroethyl)-9-(4-(4-(((4'-(trifluoromethyl)(1,1'-biphenyl)-2-yl)carbonyl)amino)-1-piperidinyl)butyl)-
CAS No.:
182431-12-5
Compound CID:
9853053
Formula:
C39H37F6N3O2
Formula Weight:
693.72
Specification
Targets&IC50:
MTP: 8 nM
Relative Density:
1.34 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Lomitapide can be used in metabolic pharmacology to investigate the regulation of cholesterol levels through the targeted inhibition of MTP.
Library Information
Target:
MTP
Receptor:
MTTP
Pathways:
Metabolism
Plate Number:
AOCL-16
Plate Location:
h2
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
242 mg/mL; 348.84 mM
Water Max Solubility:
<1 mg/mL (insoluble or slightly soluble)
Ethanol Max Solubility:
93 mg/mL; 134.06 mM





