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1、Hotline: 400-820-3792Inhibitors Agonists Screening Librarieswww.MedChemESHIN1Cat. No.: HY-112066CAS No.: 2146095-85-2Synonyms: RZ-2994分式: CHNO分量: 400.47作靶點(diǎn): Others作通路: Others儲(chǔ)存式: Powder -20C 3 years4C 2 yearsIn solvent -80C 6 months-20C 1 month溶解性數(shù)據(jù)體外實(shí)驗(yàn) DMSO : 50 mg/mL (124.85 mM)* means soluble, bu

2、t saturation unknown.Mass Solvent1 mg 5 mg 10 mg Concentration制備儲(chǔ)備液1 mM 2.4971 mL 12.4853 mL 24.9707 mL5 mM 0.4994 mL 2.4971 mL 4.9941 mL10 mM 0.2497 mL 1.2485 mL 2.4971 mL請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度,選擇合適的溶劑配制儲(chǔ)備液,并請(qǐng)注意儲(chǔ)備液的保存式和期限。BIOLOGICAL ACTIVITY物活性 SHIN1 (RZ-2994)絲氨酸羥甲轉(zhuǎn)移酶1和2 (SHMT1/2) 抑制劑,體外實(shí)驗(yàn)中的其IC50 值分別為5和13

3、nM。IC50 & Target IC50: 5 nM (SHMT1), 13 nM (SHMT1) 11/2 Master of Small Molecules 您邊的抑制劑師www.MedChemE體外研究 SHIN1 (RZ-2994) inhibits human SHIN1 SHMT1/2 with IC50s of 5 and 13 nM, respectively in an in vitroassay. SHIN1 inhibits the growth of SHMT2 deletion HCT-116 cells with an IC50 of 10 nM. SHIN1 (

4、RZ-2994)inhibits SHMT1/2 in HCT-116 cells. SHIN1 (RZ-2994) is particularly active against B-cell malignancies.SHIN1 blocks cell growth through a progressive depletion of purines, leading to loss of nucleotidetriphosphates 1.PROTOCOLCell Assay 1 For proliferation assays, HCT-116 cells are treated wit

5、h SHIN1 (1, 10, 100, 1000, 10000 nM) for 24-72 hours.Cell number was counted directly using Trypan blue and the Countess system 1.MCE has not independently confirmed the accuracy of these methods. They are for reference only. Mol Cell. 2019 Jul 23. pii: S1097-2765(19)30496-4.See more customer valida

6、tions on HYPERLINK / www.MedChemEREFERENCES1. Ducker GS, et al. Human SHMT inhibitors reveal defective glycine import as a targetable metabolic vulnerability of diffuse large B-celllymphoma. Proc Natl Acad Sci U S A. 2017 Oct 24;114(43):11404-11409.McePdfHeightCaution: Product has not been fully validated for medical applications.For research use only.Tel: 400-

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