7 Results for "

MDR2

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "MDR2" in MCE Product Catalog:

6
6 Cited Publications
Cat. No.: HY-D0217
CAS No.: 71-67-0
Synonyms: Bromosulfophthalein disodium salt
Sulfobromophthalein (Bromosulfophthalein) disodium salt is an organic anion dye used in the study of a variety of membrane carriers expressed in animal tissues and involved in transport of agents and metabolites .
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Cat. No.: HY-148795
CAS No.: 2460667-52-9
Ritivixibat is an apical sodium-dependent bile acid transporter (ASBT/IBAT) inhibitor. Ritivixibat blocks ASBT/IBAT function, thereby reducing bile acid reabsorption, regulating bile acid homeostasis and alleviating liver injury. Ritivixibat protects cholangiocytes from damage caused by cytotoxic bile acids. Ritivixibat is applicable to research related to primary sclerosing cholangitis .
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Cat. No.: HY-RS21466
Research Areas:  

Others

Abcb4 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Abcb4 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS27984
Research Areas:  

Others

Abcb4 Rat Pre-designed siRNA Set A contains three designed siRNAs for Abcb4 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Cat. No.: HY-RS00051
Research Areas:  

Others

ABCB4 Human Pre-designed siRNA Set A contains three designed siRNAs for ABCB4 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-154979
CAS No.: 2380421-60-1
Target:  

DNA/RNA Synthesis

Research Areas:  

Inflammation/Immunology

Anti-hepatic fibrosis agent 2 (Compound 6k) is an orally active COL1A1 inhibitor. Anti-hepatic fibrosis agent 2 is an anti-fibrogenic agent targeting ewing sarcoma breakpoint region 1 (EWSR1) .
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Cat. No.: HY-180131
CAS No.: 1312993-34-2
Synonyms: ASB17061
Target:  

Proteasome

Research Areas:  

Inflammation/Immunology

INVA8001 (ASB17061) is a highly selective and orally active chymase inhibitor with IC50 values for human chymase and mouse mast cell proteinase 4 (mMCP-4) of 0.02 and 0.03 μM, respectively. INVA8001 exhibits IC50 values for bovine α-chymotrypsin and human cathesin G of 3.4 and 32.1 μM, respectively, and it shows over 1000-fold selectivity for other related serine proteases. INVA8001 inhibits mast cells in a mouse primary sclerosing cholangitis (PSC) model, improves bile duct pathology, and alleviates bile stasis, demonstrating anti-inflammatory and anti-fibrotic effects .
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