>>(+/-) RK-682

(+/-) RK-682 (Synonyms: (±)-3-Hexadecanoyl-5-hydroxymethyltetronic acid)

Catalog No.GB40043

(±)-RK-682 (150627-37-5) is a protein tyrosine phosphatase inhibitor (IC50's = 54 7 µM for CD45, 2.0 μM for VHR; did not inhibit cdc25B) originally isolated from the fermentation of Streptomyces sp. 88-682. Inhibits cell cycle at G1/S. RK-682 has also been shown to inhibit PLA2 (IC50 = 16 μM), HIV-1 protease (IC50 = 84 μlM), and heparanase (IC50 = 17 μM). Natural RK-682 (R-isomer) and synthetic racemic material have identical phosphatase activity. Care should be taken when using RK-682 in the presence of metal salts - because it readily forms metal complexes that affects its phosphatase inhibitory activity. RK-682 has been identified as a potential promiscuous inhibitor.

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(+/-) RK-682 Chemical Structure

Cas No.: 150627-37-5

Size 가격 재고 수량
200µg,1mg
US$225.00
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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

(±)-RK-682 (150627-37-5) is a protein tyrosine phosphatase inhibitor (IC50's = 54 7 µM for CD45, 2.0 μM for VHR; did not inhibit cdc25B) originally isolated from the fermentation of Streptomyces sp. 88-682. Inhibits cell cycle at G1/S. RK-682 has also been shown to inhibit PLA2 (IC50 = 16 μM), HIV-1 protease (IC50 = 84 μlM), and heparanase (IC50 = 17 μM). Natural RK-682 (R-isomer) and synthetic racemic material have identical phosphatase activity. Care should be taken when using RK-682 in the presence of metal salts - because it readily forms metal complexes that affects its phosphatase inhibitory activity. RK-682 has been identified as a potential promiscuous inhibitor.

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Average Rating: 5 ★★★★★ (Based on Reviews and 30 reference(s) in Google Scholar.)

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