9 Results for "

Rat hepatic microsomes

" in MedChemExpress (MCE) Product Catalog:
Products (9)

9 Results for "Rat hepatic microsomes" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-W010981
CAS No.: 77-90-7
Synonyms: Tributyl O-acetylcitRate; ATBC
Acetyl tributyl citrate (Tributyl O-acetylcitrate) is a pharmaceutical excipient and biodegradable hydrophobic plasticizer. Acetyl tributyl citrate can be used in cosmetics, food packaging, and as a flavoring substance for food .
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Cat. No.: HY-W006230
CAS No.: 84-60-6
Target:  

Cytochrome P450

Research Areas:  

Cancer

Anthraflavic acid specifically inhibits the activity of cytochrome P-448 without affecting phenobarbital-induced cytochrome P-450 or NADPH-dependent cytochrome c reduction. Anthraflavic acid inhibits cytosolic metabolic pathways, blocks the microsomal and cytosolic activation of IQ, and reduces the metabolic activation level of Glu-P-I. Anthraflavic acid may exert anticancer activity by inhibiting the metabolic activation of chemical carcinogens. Anthraflavic acid is applicable to cancer-related research .
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Cat. No.: HY-119879
CAS No.: 108437-28-1
Synonyms: CP-73049
Target:  

Antibiotic Bacterial

Research Areas:  

Infection

Binfloxacin (CP-73049) is a fluoroquinolone antibiotic. Binfloxacin does not inhibit the metabolism of theophylline, so it is safer to be used in combination with theophylline and other drugs metabolized by P450 1A2. Binfloxacin can be used in studies of bacterial infections .
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Cat. No.: HY-118178
CAS No.: 26766-35-8
Purity:  99.76%
Research Areas:  

Cardiovascular Disease

LY43578 is an orally active aromatase inhibitor. LY43578 inhibits P-450-dependent p-nitroanisole O-demethylation and ethylmorphine N-demethylation in hepatic microsomes isolated from rat, with the IC50 of 0.3 and 5 μΜ, respectively. LY43578 can be used for neurological disorder study .
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Cat. No.: HY-118407
CAS No.: 26766-37-0
Research Areas:  

Neurological Disease

LY56110 is an orally active aromatase inhibitor. LY56110 inhibits P-450-dependent p-nitroanisole O-demethylation and ethylmorphine N-demethylation in hepatic microsomes isolated from rat, with the IC50 of 2.5 and 11 μΜ, respectively. LY56110 can be used for neurological disorder study .
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Cat. No.: HY-182585
CAS No.: 150490-85-0
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Berupipam is a benzazepine-selective dopamine D1 receptor antagonist. Berupipam is used in the research of mental disorders .
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Cat. No.: HY-181792
Target:  

STAT

Research Areas:  

Inflammation/Immunology

ZDZ-553 is an orally active STAT1 inhibitor with an IC50 value of 0.87 μM. ZDZ-553 modulates STAT1 signaling to affect downstream lipid metabolism and inflammatory pathways. ZDZ-553 attenuates hepatic steatosis in NASH mouse models. ZDZ-553 reduces inflammatory responses in NASH mouse models. ZDZ-553 can be used for the research of nonalcoholic steatohepatitis .
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Cat. No.: HY-130203
CAS No.: 1379510-21-0
Target:  

Dopamine Receptor

Research Areas:  

Others

Dopamine D4R antagonist-1 is a blood-brain barrier-permeable antagonist of dopamine D4 receptor. Dopamine D4R antagonist-1 functionally inhibits dopamine D4 receptor, exhibits only weak activity against dopamine D3 receptor, and shows no activity against dopamine D1 and D2 receptors .
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Cat. No.: HY-182060
CAS No.: 3064814-26-9
PDE4B/D-IN-5 (Compound P32) is a peripherally restricted, oral active inhibitor of PDE4B and PDE4D with extremely low blood-brain barrier penetration, with IC50 values of 3.4 nM and 2.2 nM, respectively. PDE4B-IN-8 inhibits the production of TNF-α. PDE4B/D-IN-5 significantly reduces the Bax/Bcl2 ratio, and alleviates oxidative stress by decreasing MPO activity and NO levels. PDE4B/D-IN-5 exhibits anti-inflammatory, antioxidant, and anti-apoptotic activities. PDE4B/D-IN-5 can be used for the research of acute lung injury .
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