![]()
产品详情
产品名称 英文名称:Tyrphostin AG 879 同义词 Tyrphostin AG 879、148741-30-4、AG 879、AG-879、AG879、alpha-Cyano-(3,5-di-t-butyl-4-hydroxy)thiocinnamide、Tyrphostin Ag-879、(2E)-2-cyano-3-(3,5-di-tert-butyl-4-hydroxyphenyl)prop-2-enethioamide、(E)-2-cyano-3-(3,5-di-tert-butyl-4-hydroxyphenyl)prop-2-enethioam 产品性质 CAS编号:148741-30-4 分子式:C18H24N2OS 分子量:316.46 MDL号:MFCD00236450 PubChem编号:135419190 英文别名:Tyrphostin AG 879|148741-30-4|AG 879|AG-879|AG879|alpha-Cyano-(3,5-di-t-butyl-4-hydroxy)thiocinnamide|Tyrphostin Ag-879|(2E)-2-cyano-3-(3,5-di-tert-butyl-4-hydroxyphenyl)prop-2-enethioamide|(E)-2-cyano-3-(3,5-di-tert-butyl-4-hydroxyphenyl)prop-2-enethioam 规格或纯度:≥98% 英文名称:Tyrphostin AG 879 生化机理:Tyrphostin AG 879 is a protein tyrosine kinase inhibitor with potent effects on TrkA. This product reportedly inhibits NGF-induced PLC-γ 1 phosphorylation and phosphatidylinositol-3 kinase activation. Has been shown in lab studies to disrupt Sertoli cell aggregation and stop androgen-induced cell proliferation. AG 879 also displays anti-cancer effects by inhibiting the expression of RAF-1 gene encoding MAP kinase activity necessary for human breast cancer cell proliferation. Shown to inhibit Neu (HER-2 or ERBB2) expression and reduced tumor sizes in mice leukemia cells. Tyrphostin AG 879 is an inhibitor of Flk-1.Selective TrkA receptor inhibitor. Inhibits NGF-dependent TrkA phosphorylation (IC 50 = 40 μM). Additionally inhibits ErbB2 and the VEGF receptor FLK-1 (IC 50 = ~1 μM). Active in vitro and in vivo . Shows antitumor activity. 储存温度:-20°C储存 运输条件:超低温冰袋运输 备注:如果有可能,您尽量在使用的当天配置溶液,并在当天使用完它。但是,如果您需要预先配制储备溶液,我们建议您将溶液等份保存在-20°C的密封小瓶中。通常,它们最多可以使用一个月。在使用前和打开样品瓶之前,我们建议您让您的产品在室温下平衡至少1小时。需要更多关于溶解度,用法和处理的建议吗?请访问我们的常见问题(FAQ)页面以获取更多详细信息。 产品介绍:AG879是酪氨酸激酶的抑制剂,能够抑制TrKA的磷酸化,但不能抑制TrKB 和TrKC,也是高选择性的ErbB2激酶抑制剂。A protein tyrosine kinase inhibitor with potent effects on TrkATyrphostinAG879 is a tyrosine kinase inhibitor that inhibits TrKA phosphorylation, but not TrKB and TrKC.[1] also a ErbB2 kinase inhibitor, has at least 500-fold higher selectivity to ErbB2 (IC50 = 1 μmol/L) than EGFR (IC50 >500 μmol/L).A protein tyrosine kinase inhibitor with potent effects on TrkA IUPAC Name:(E)-2-cyano-3-(3,5-ditert-butyl-4-hydroxyphenyl)prop-2-enethioamide INCHI:InChI=1S/C18H24N2OS/c1-17(2,3)13-8-11(7-12(10-19)16(20)22)9-14(15(13)21)18(4,5)6/h7-9,21H,1-6H3,(H2,20,22)/b12-7+ InChi Key:XRZYELWZLNAXGE-KPKJPENVSA-N Canonical SMILES:CC(C)(C)C1=CC(=CC(=C1O)C(C)(C)C)C=C(C#N)C(=S)N Isomeric SMILES:CC(C)(C)C1=CC(=CC(=C1O)C(C)(C)C)/C=C(\C#N)/C(=S)N WGK Germany:3 PubChem CID:135419190 CAS Registry No.:148741-30-4 ChEMBL Ligand:CHEMBL539947 溶解性:DMSO 36 mg/mL Water <1 mg/mL Ethanol 3 mg/mL 折光率:1.61 沸点:~443.81° C at 760 mmHg 熔点:219-220°C 个人防护装备:Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter 产品包装
免责声明:以上所展示的信息由企业自行提供,内容的真实性
、准确性和合法性由发布企业负责,chemdig对此不承担任何保证责任。 同时我们郑重提醒各位买/卖家,
交易前 请详细核实对方身份,切勿随意打款或发货,谨防上当受骗。如发现虚假信息,请向chemdig举报。 |
上海阿拉丁生化科技股份有限公司
|
上海阿拉丁生化科技股份有限公司
邮箱 | market@aladdin-e.com |
联系人 | 18521732826 |
咨询请告知是在ChemDig上看到的,有助于交易达成。