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RK-682 (calcium salt) Sale

(Synonyms: CI-010, TAN 1364B) 目录号 : GC44846

An inhibitor of PTPs

RK-682 (calcium salt) Chemical Structure

Cas No.:332131-32-5

规格 价格 库存 购买数量
500μg
¥3,409.00
现货
2.5mg
¥16,189.00
现货

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Sample solution is provided at 25 µL, 10mM.

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产品描述

Protein tyrosine phosphatases (PTPs) remove phosphate from tyrosine residues of cellular proteins. Reversible phosphorylation catalyzed by the coordinated actions of protein tyrosine kinases and phosphatases is key to the regulation of the signaling events that control cell growth and proliferation, differentiation, and survival or apoptosis, as well as adhesion and motility. RK-682, a bioactive compound originally isolated from the fermentation of Streptomyces sp. 88-682, is an inhibitor of the PTPs. It inhibits the phosphorylation of CD45 and VHR with IC50 values of 54 and 2 µM, respectively, and arrests cell cycle progress at the G1/S transition. It is also reported to inhibit heparanase (IC50 = 17 µM), an endo-β-D-glucuronidase involved in tumor cell invasion and angiogenesis. RK-682 (calcium salt) is a less soluble version of the free acid.

Chemical Properties

Cas No. 332131-32-5 SDF
别名 CI-010, TAN 1364B
Canonical SMILES O=C1C(C(CCCCCCCCCCCCCCC)=O)=C([O-])[C@@H](CO)O1.O=C2C(C(CCCCCCCCCCCCCCC)=O)=C([O-])[C@@H](CO)O2.[Ca+2]
分子式 [C21H35O5]2•Ca 分子量 775.1
溶解度 DMF: soluble,DMSO: soluble,Ethanol: soluble,Methanol: soluble 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 1.2902 mL 6.4508 mL 12.9016 mL
5 mM 0.258 mL 1.2902 mL 2.5803 mL
10 mM 0.129 mL 0.6451 mL 1.2902 mL
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Research Update

Asymmetric synthesis of a 3-acyltetronic acid derivative, RK-682, and formation of its calcium salt during silica gel column chromatography

Chem Pharm Bull (Tokyo) 2001 Feb;49(2):206-12.PMID:11217111DOI:10.1248/cpb.49.206.

RK-682 was reported to be a potent protein tyrosine phosphatase inhibitor. We found that (R)-3-hexadecanoyl-5-hydroxymethyltetronic acid (1) was easily converted to its calcium salt during column chromatography on Silica gel 60, and this calcium salt was identical to RK-682 originally isolated from a natural source. Here we report details of the asymmetric synthesis of (R)-1 and its conversion to the calcium salt. Fast atom bombardment mass spectrometric (FAB-MS) analysis of the free and calcium salt forms of RK-682 is also reported.

Conversion of Ca2+ salt of an organic compound to its Li+ salt to simplify the fast atom bombardment mass spectrum

Chem Pharm Bull (Tokyo) 2003 Nov;51(11):1341-4.PMID:14600389DOI:10.1248/cpb.51.1341.

The FAB mass spectrum of the Ca(2+) salt of RK-682 (1, MW 368), a potent protein tyrosine phosphatase inhibitor, shows a complex pattern due to Ca(2+) adduct ions with multimers of 1 and their decomposition ions. Addition of LiCl greatly simplified the FAB mass spectrum, providing a prominent Li(+) adduct ion of 1 at m/z 381 [M+2Li-H](+). The addition of LiCl also greatly simplified the FAB mass spectrum of calcium pantothenate. This approach may be generally useful for molecular weight determination of multivalent metal salts of organic compounds, or organic compounds that can form Li salts, by FAB mass spectrometry.