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1821908-48-8

中文名稱 SGC2085
英文名稱 SGC2085
CAS 1821908-48-8
分子式 C19H24N2O2
分子量 312.41
MOL 文件 1821908-48-8.mol
更新日期 2024/11/13 09:55:58
1821908-48-8 結(jié)構(gòu)式 1821908-48-8 結(jié)構(gòu)式

基本信息

中文別名
(S)-2-氨基-N-((4-(3,5-二甲基苯氧基)-3-甲基苯基)甲基)丙酰胺
英文別名
CS-2688
CS-2529
SGC-2085
SGC 2085
Propanamide, 2-amino-N-[[4-(3,5-dimethylphenoxy)-3-methylphenyl]methyl]-, (2S)-

物理化學(xué)性質(zhì)

沸點(diǎn)498.3±45.0 °C(Predicted)
密度1.097±0.06 g/cm3(Predicted)
儲(chǔ)存條件Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
溶解度DMSO : ≥ 32 mg/mL (102.43 mM)
酸度系數(shù)(pKa)14.83±0.46(Predicted)
形態(tài)Solid
顏色White to off-white

常見(jiàn)問(wèn)題列表

生物活性
SGC2085是一種具有高效性和選擇性的CARM1抑制劑, IC50值為50 nM。
靶點(diǎn)

IC50: 50 nM (CARM1)

體外研究

SGC2085 which features a methyl at position R1 and a 3,5-dimethylphenoxy at R2 has an IC 50 of 50 nM for CARM1 and is over 100-fold selective for CARM1 over PRMT6. These results indicate that the presence of a substituent at R1 is essential for potent and selective inhibition of CARM1. With the exception of PRMT6 (IC 50 =5.2 μM), SGC2085 does not inhibit other PRMTs. Considering its small size (MW=312.4 Da), SGC2085 has an excellent selectivity profile, which can probably be further improved by exploiting differences in the binding sites of the two enzymes outside the arginine binding pocket. Compound SGC2085 also shows complete selectivity against a panel of 21 human protein methyltrans- ferases tested at three different concentrations (1,10, and 50 μM). To characterize the mechanism of action of SGC2085 in solution, IC 50 values are determined at various concentrations of SAM and peptide substrate. Increasing concentration of substrate peptide or cofactor does not affect IC 50 values, indicative of a noncompetitive mechanism of inhibition, which has been previously shown for other protein methyltransferase inhibitors binding at the substrate pocket. No cellular activity is observed for SGC2085 when tested up to 10 μM (48 h exposure in HEK293 cells), while methylation of BAF155 is abrogated by 10 μM of the dual CARM1/PRMT6 inhibitor MS049. We assume that the absence of cellular activity for SGC2085 is due to poor permeability.

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