17 Results for "

cholesterol 7α-hydroxylase

" in MedChemExpress (MCE) Product Catalog:
Products (17)

17 Results for "cholesterol 7α-hydroxylase" in MCE Product Catalog:

9
9 Publications Verification
Cat. No.: HY-104081
CAS No.: 11041-12-6
Synonyms: Cholestyramine resin; Colestyramine
Cholestyramine (Cholestyramine resin) is an orally active bile acid sequestrant. Cholestyramine upregulates the expression of intestinal Apical sodium-dependent bile acid transporter and hepatic Cholesterol 7α-hydroxylase. Cholestyramine induces the expression of intestinal and hepatic cholesterol synthesis genes as well as hepatic lipogenesis genes, and promotes bile acid- and neutral sterol-mediated reverse cholesterol transport. Cholestyramine reduces intestinal cholesterol absorption and induces cholesterol efflux. Cholestyramine is applicable to research related to coronary artery disease, atherosclerotic cardiovascular disease and atherosclerosis .
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6
6 Cited Publications
Cat. No.: HY-113342
CAS No.: 566-28-9
Purity:  99.87%
7-Ketocholesterol is an oxidation product of cholesterol, widely present in atherosclerotic plaques, and has a stronger atherogenic effect than cholesterol. 7-Ketocholesterol can inhibit the rate-limiting enzymes involved in bile acid and cholesterol synthesis, such as cholesterol 7α-hydroxylase and HMG-CoA reductase. 7-Ketocholesterol exhibits pro-inflammatory effects both in vivo and in vitro and can induce cell apoptosis (apoptosis) .
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1
1 Cited Publications
Cat. No.: HY-117147A
CAS No.: 2517771-89-8
Purity:  99.69%
Target:  

REV-ERB Cytochrome P450

Research Areas:  

Metabolic Disease

GSK2945 hydrochloride is a class of tertiary amine, and is a highly specific Rev-erbα/REV-ERBα (mouse/human reverse erythroblastosis virus α) antagonist with EC50s of 21.5 μM and 20.8 μM, respectively. GSK2945 hydrochloride enhances cholesterol 7α-hydroxylase (CYP7A1) level and cholesterol metabolism .
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Cat. No.: HY-W008226
CAS No.: 480-66-0
Synonyms: 2,4,6-trihydroxyacetophenone; 1-(2,4,6-Trihydroxyphenyl)ethanone
Phloracetophenone (2,4,6-trihydroxyacetophenone) is the aglycone part of acetophenone glycoside obtained from Curcuma comosa Roxb, with cholesterol-lowering activity. Phloracetophenone enhances cholesterol 7α-hydroxylase (CYP7A1) activity . Phloracetophenone stimulats bile secretion mediated through Mrp2 .
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Cat. No.: HY-113259
CAS No.: 3862-25-7
Purity:  99.60%
7α-Hydroxy-4-cholesten-3-one is an intermediate in synthesis of bile acids from cholesterol. 7α-Hydroxy-4-cholesten-3-one is a pregnane X receptor (PXR) agonist. 7α-Hydroxy-cholest-4-en-3-one is a biomarker for bile acid loss, irritable bowel syndrome, and other diseases associated with defective bile acid biosynthesis. 7α-Hydroxy-cholest-4-en-3-one is the physiological substrate for CYP8B1 .
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Cat. No.: HY-B2012
CAS No.: 85509-19-9
Synonyms: DPX-H6573
Research Areas:  

Infection

Flusilazole (DPX-H6573) is a broad-spectrum fungicide and cytochrome P-450 inhibitor that can be used in studies related to fungal infections .
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Cat. No.: HY-130502
CAS No.: 4025-59-6
Purity:  ≥98.0%
Synonyms: cholesterol 5β,6β-epoxide; 5β,6β-Epoxycholesterol
Target:  

Apoptosis

Research Areas:  

Inflammation/Immunology Cancer

5β,6β-epoxycholestanol (Cholesterol 5β,6β-epoxide; 5β,6β-Epoxycholesterol) is an oxysterol. 5β,6β-epoxycholestanol induces cytotoxicity in bronchial epithelial cells. 5β,6β-epoxycholestanol induces lactate dehydrogenase (LDH) release and apoptosis in lymphoma cells undergoing macrophage differentiation . 5β,6β-epoxycholestanol is applicable to research related to atherosclerosis .
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Cat. No.: HY-117147
CAS No.: 1438071-12-5
Target:  

Cytochrome P450

Research Areas:  

Metabolic Disease

GSK2945 is a class of tertiary amine, and is a highly specific Rev-erbα/REV-ERBα (mouse/human reverse erythroblastosis virus α) antagonist with EC50s of 21.5 μM and 20.8 μM, respectively. GSK2945 enhances cholesterol 7α-hydroxylase (CYP7A1) level and cholesterol metabolism .
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Cat. No.: HY-105191
CAS No.: 143393-27-5
Synonyms: RS-21607
Research Areas:  

Metabolic Disease

Azalanstat (RS-21607) is an orally active lanosterol 14α-demethylase inhibitor. Azalanstat exerts a cholesterol-lowering effect by inhibiting cholesterol synthesis and regulating HMG-CoA Reductase (HMGCR), and shows an additive effect when used in combination with Cholestyramine (HY-104081). Azalanstat is used in the study of hypercholesterolemia .
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Cat. No.: HY-113342R
CAS No.: 566-28-9
7-Ketocholesterol (Standard) is the analytical standard of 7-Ketocholesterol. This product is intended for research and analytical applications. 7-Ketocholesterol is an oxidation product of cholesterol, widely present in atherosclerotic plaques, and has a stronger atherogenic effect than cholesterol. 7-Ketocholesterol can inhibit the rate-limiting enzymes involved in bile acid and cholesterol synthesis, such as cholesterol 7α-hydroxylase and HMG-CoA reductase. 7-Ketocholesterol exhibits pro-inflammatory effects both in vivo and in vitro and can induce cell apoptosis (apoptosis) .
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Cat. No.: HY-101812
CAS No.: 56488-59-6
Purity:  98.39%
Research Areas:  

Metabolic Disease

Terbufibrol is an orally active lipid-lowering agent. Terbufibrol inhibits hepatic Cholesterol 7 alpha-hydroxylase. Terbufibrol blocks a step between Acetate and HMG-CoA in the hepatic cholesterol synthesis process. Terbufibrol reduces serum total cholesterol, HDL, LDL, lipoprotein levels, and the cholesterol/phospholipid ratio, with dose- and sex-dependent changes in lipoprotein components. Terbufibrol exerts sustained cholesterol-lowering activity in baboons and rats. Terbufibrol can be used in research related to hypercholesterolemia .
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Cat. No.: HY-P702798
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CYP7A1; CYPVII; Prev. CYP7; Cytochrome P450, Subfamily VIIA Polypeptide 1; Cytochrome P450, Family 7, Subfamily A, Polypeptide 1; cholesterol 7 Alpha-Monooxygenase; 24-Hydroxycholesterol 7-Alpha-hydroxylase; cholesterol 7alpha-hydroxylase; cholesterol 7-A
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P81069
Synonyms: CYP7A1; CYP7; cholesterol 7-alpha-monooxygenase; CYPVII; cholesterol 7-alpha-hydroxylase; Cytochrome P450 7A1

Host:  

Rabbit

Application:  

WB

Reactivity:  

Human, Mouse

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Cat. No.: HY-P85425
Synonyms: CYP7A1; CYP7; cholesterol 7-alpha-monooxygenase; CYPVII; cholesterol 7-alpha-hydroxylase; Cytochrome P450 7A1

Host:  

Mouse

Application:  

WB

Reactivity:  

Human, Golden hamster

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Cat. No.: HY-101812R
CAS No.: 56488-59-6
Terbufibrol (Standard) is the analytical standard of Terbufibrol (HY-101812). This product is intended for research and analytical applications. Terbufibrol is an orally active lipid-lowering agent. Terbufibrol inhibits hepatic Cholesterol 7 alpha-hydroxylase. Terbufibrol blocks a step between Acetate and HMG-CoA in the hepatic cholesterol synthesis process. Terbufibrol reduces serum total cholesterol, HDL, LDL, lipoprotein levels, and the cholesterol/phospholipid ratio, with dose- and sex-dependent changes in lipoprotein components. Terbufibrol exerts sustained cholesterol-lowering activity in baboons and rats. Terbufibrol can be used in research related to hypercholesterolemia .
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Cat. No.: HY-105191A
CAS No.: 143484-82-6
Synonyms: RS-21607 dihydrochloride
Research Areas:  

Metabolic Disease

Azalanstat (RS-21607) dihydrochloride is an orally active lanosterol 14α-demethylase inhibitor. Azalanstat dihydrochloride exerts a cholesterol-lowering effect by inhibiting cholesterol synthesis and regulating HMG-CoA Reductase (HMGCR), and shows an additive effect when used in combination with Cholestyramine (HY-104081). Azalanstat dihydrochloride is used in the study of hypercholesterolemia .
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Cat. No.: HY-105191C
CAS No.: 143484-80-4
Synonyms: RS-21607 mesylate
Research Areas:  

Metabolic Disease

Azalanstat (RS-21607) mesylate is an orally active lanosterol 14α-demethylase inhibitor. Azalanstat mesylate exerts a cholesterol-lowering effect by inhibiting cholesterol synthesis and regulating HMG-CoA Reductase (HMGCR), and shows an additive effect when used in combination with Cholestyramine (HY-104081). Azalanstat mesylate is used in the study of hypercholesterolemia .
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