11 Results for "

CYP4A1

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "CYP4A1" in MCE Product Catalog:

6
6 Cited Publications
Cat. No.: HY-124527
CAS No.: 339068-25-6
Purity:  99.69%
Target:  

Cytochrome P450

Research Areas:  

Cardiovascular Disease Cancer

HET0016 is a potent and selective 20-hydroxyeicosatetraenoic acid (20-HETE) synthase inhibitor, with IC50 values of 17.7 nM, 12.1 nM and 20.6 nM for recombinant CYP4A1-, CYP4A2- and CYP4A3-catalyzed 20-HETE synthesis, respectively. HET0016 also is a selective CYP450 inhibitor, which has been shown to inhibit angiogenesis and tumor growth .
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Cat. No.: HY-78086
CAS No.: 620-23-5
Synonyms: 3-Methylbenzaldehyde
m-Tolualdehyde (3-Methylbenzaldehyde) is an aldehyde metabolite produced by m-xylene metabolism, and it bidirectionally regulates the CYP 2B1, CYP 2E1, and CYP 4B1 isoenzymes in the respiratory tract of rats. m-Tolualdehyde serves as an oxidation substrate and carbon source for Pseudomonas Pxy, and it can be oxidized to m-toluic acid in an NAD + -dependent manner. m-Tolualdehyde exerts a dose-dependent inhibitory effect on CYP 2B1 and CYP 2E1 in the nasal mucosa and lungs of rats, and a dose-dependent activating effect on pulmonary CYP 4B1. m-Tolualdehyde can form aldehyde-heme adducts with the heme group of cytochrome P450. m-Tolualdehyde can be used in studies related to metabolic enzymes in the respiratory tract of rats .
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Cat. No.: HY-152159
CAS No.: 2760611-38-7
Target:  

Cytochrome P450

Research Areas:  

Cancer

CYP4Z1-IN-1 (compound 7c) is a potent CYP4Z1 inhibitor, with an IC50 of 41.8 nM. CYP4Z1-IN-1 decreases the expression of breast CSCs stemness markers, spheroid formation, and metastatic ability as well as tumor-initiation capability in a concentration-dependent manner in vitro and in vivo .
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Cat. No.: HY-124527R
CAS No.: 339068-25-6
Target:  

Cytochrome P450

Research Areas:  

Cardiovascular Disease Cancer

HET0016 (Standard) is the analytical standard of HET0016. This product is intended for research and analytical applications. HET0016 is a potent and selective 20-hydroxyeicosatetraenoic acid (20-HETE) synthase inhibitor, with IC50 values of 17.7 nM, 12.1 nM and 20.6 nM for recombinant CYP4A1-, CYP4A2- and CYP4A3-catalyzed 20-HETE synthesis, respectively. HET0016 also is a selective CYP450 inhibitor, which has been shown to inhibit angiogenesis and tumor growth .
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Cat. No.: HY-139002
CAS No.: 2428734-45-4
Target:  

Cytochrome P450

Research Areas:  

Cancer

CYP4Z1-IN-2 (compound 7) is a reversible inhibitor of CYP4Z1 (Ki=2.2 μM), which inhibits the production of 14,15-EET in breast cancer cells. CYP4Z1-IN-2 inhibits the CYP4Z1-mediated Luc-BE O-debenzylation reaction with an IC50 of 5.9 μM .
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Cat. No.: HY-RS03477
Research Areas:  

Others

CYP4B1 Human Pre-designed siRNA Set A contains three designed siRNAs for CYP4B1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS03484
Research Areas:  

Others

CYP4X1 Human Pre-designed siRNA Set A contains three designed siRNAs for CYP4X1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS03485
Research Areas:  

Others

CYP4Z1 Human Pre-designed siRNA Set A contains three designed siRNAs for CYP4Z1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-106315
CAS No.: 32954-58-8
Target:  

Cytochrome P450

Research Areas:  

Inflammation/Immunology

4-Ipomeanol is a pneumotoxin. 4-Ipomeanol can be produced by the common sweet potato, Ipomoea batatas, in the presence of Fusarium solani. 4-Ipomeanol can be bioactivated by CYP4B1 .
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Cat. No.: HY-78086R
CAS No.: 620-23-5
Synonyms: 3-Methylbenzaldehyde (Standard)
m-Tolualdehyde (Standard) is the analytical standard of m-Tolualdehyde (HY-78086). This product is intended for research and analytical applications. m-Tolualdehyde (3-Methylbenzaldehyde) is an aldehyde metabolite produced by m-xylene metabolism, and it bidirectionally regulates the CYP 2B1, CYP 2E1, and CYP 4B1 isoenzymes in the respiratory tract of rats. m-Tolualdehyde serves as an oxidation substrate and carbon source for Pseudomonas Pxy, and it can be oxidized to m-toluic acid in an NAD + -dependent manner. m-Tolualdehyde exerts a dose-dependent inhibitory effect on CYP 2B1 and CYP 2E1 in the nasal mucosa and lungs of rats, and a dose-dependent activating effect on pulmonary CYP 4B1. m-Tolualdehyde can form aldehyde-heme adducts with the heme group of cytochrome P450. m-Tolualdehyde can be used in studies related to metabolic enzymes in the respiratory tract of rats .
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Cat. No.: HY-183756
CAS No.: 3106166-49-5
Research Areas:  

Cancer

CYP4Z1-IN-3 is a selective CYP4Z1 inhibitor with a human IC50 of 55.3 nM. CYP4Z1-IN-3 inhibits breast cancer cell migration and induces apoptosis. CYP4Z1-IN-3 can be used for the research of breast cancer .
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