5 Results for "

B0AT1

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "B0AT1" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-B1274
CAS No.: 58473-74-8
Synonyms: trans-3-Bromo-N-ethylcinnamamide
Cinromide is an anticonvulsant agent. Cinromide inhibits epithelial neutral amino acid transporter B 0AT1 (SLC6A19) with an IC50 of 0.5 μM .
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Cat. No.: HY-162864
CAS No.: 1021125-90-5
Research Areas:  

Metabolic Disease

JX237 is an inhibitor of the epithelial neutral amino acid transporter B 0AT1 (SLC6A19) with an IC50 value of 31 nM. SLC6A19 is the main transporter for the absorption of neutral amino acids in the intestines and their reabsorption in the kidneys. By inhibiting B 0AT1, JX237 can be used for the study of disorders of amino acid metabolism .
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Cat. No.: HY-187959
CAS No.: 851269-95-9
Research Areas:  

Metabolic Disease

SLC6A19-IN-6 is a B0AT1 (SLC6A19) inhibitor. SLC6A19-IN-6 inhibits sodium-dependent neutral amino acid transport. SLC6A19-IN-6 can be used for research on non-alcoholic steatohepatitis .
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Cat. No.: HY-RS13305
Research Areas:  

Others

SLC6A19 Human Pre-designed siRNA Set A contains three designed siRNAs for SLC6A19 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-179581
CAS No.: 2962069-39-0
Research Areas:  

Metabolic Disease

SLC6A19-IN-4 is an allosteric-competitive and orally active B 0AT1 inhibitor. SLC6A19-IN-4 inhibits both human and mouse B 0AT1 with IC50 values of 513 nM and 295 nM, respectively. SLC6A19-IN-4 exhibits excellent metabolic stability. SLC6A19-IN-4 significantly increases urinary phenylalanine (Phe) excretion and reduces plasma Phe levels through dual inhibition of B 0AT1 in both the intestine (reducing absorption) and kidney (promoting excretion) in vivo. SLC6A19-IN-4 can be used for phenylketonuria (PKU) and other disorders involving SLC6-family transporters research .
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