Epigenetics
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TC-A-2317 HCl
Catalog No. A13567 Aurora kinase A 抑制剂TC-A-2317 HCl是一种有效的Aurora激酶A抑制剂(Ki = 1.2 nM,而抑制Aurora激酶B则为101 nM)。选择性超过60种其他激酶(IC50值> 1000 nM)。表现出良好的细胞通透性和抗肿瘤活性。 了解更多 -
SCH-1473759
Catalog No. A14059 -
AAPK-25
Catalog No. A19085 Aurora/PLK dual 抑制剂AAPK-25 is a potent and selective Aurora/PLK dual inhibitor with anti-tumor activity, which can cause mitotic delay and arrest cells in a prometaphase, reflecting by the biomarker histone H3Ser10 phosphorylation and followed by a surge in apoptosis. 了解更多 -
SCH-1473759 hydrochloride
Catalog No. A21711 Aurora inhibitorSCH-1473759 hydrochloride is an aurora inhibitor with IC50s of 4 and 13 nM for aurora A and B, respectively. 了解更多 -
Aurora Kinase Inhibitor 3
Catalog No. A19448 Aurora A kinase inhibitorAurora Kinase Inhibitor 3 is a strong and selective Aurora A kinase inhibitor with an IC50 of 42 nM, and weakly inhibits EGFR with an IC50>10 μM. 了解更多 -
Aurora inhibitor 1
Catalog No. A19637 Aurora inhibitorAurora inhibitor 1 is a potent Aurora inhibitor with an IC50 of ?? 4 nM and ??13 nM for Aurora A and Aurora B kinase, respectively. 了解更多 -
MLN8237 (Alisertib)
Catalog No. A10004 Aurora A Kinase 抑制剂MLN8237 (Alisertib)是一种选择性Aurora A抑制剂,在无细胞分析中的IC50为1.2 nM。它对Aurora A的选择性比Aurora B高200倍以上。 了解更多 -
Hesperadin
Catalog No. A10448 Aurora B Kinase 抑制剂Hesperadin是一种人极光B抑制剂,IC50为40 nM,用于防止底物磷酸化。它显著降低AMPK、Lck、MKK1、MAPKAP-K1、CHK1和PHK的活性,而不抑制MKK1在体内的活性。 了解更多 -
AZD1152-HQPA (Barasertib)
Catalog No. A10109 Aurora Kinase B 抑制剂AZD1152-HQPA (Barasertib)是Aurora B的高效抑制剂,Ki值分别为0.36(Aurora B)和1369 nM(Aurora A),与一组其他50种激酶相比具有很高的特异性。 了解更多 -
VX-680 (MK-0457, Tozasertib)
Catalog No. A10981 Aurora Kinase 抑制剂VX-680 (MK-0457,Tozasertib)是一种有效的选择性Aurora激酶小分子抑制剂。 了解更多 -
Danusertib (PHA-739358)
Catalog No. A10715 Aurora 抑制剂Danusertib (PHA-739358)是Aurora A/B/C的Aurora激酶抑制剂,在无细胞分析中的IC50为13 nM/79nM/61 nM,对Abl,TrkA,c-RET和FGFR1以及更低的浓度具有中等效力 对Lck,VEGFR2/3,c-Kit,CDK2等有效。 了解更多 -
JNJ-7706621
Catalog No. A10494 CDK/Aurora A/B 抑制剂JNJ-7706621是对CDK1/2具有最高效力的pan-CDK抑制剂,IC50为9 nM/4 nM,并且在无细胞分析中对CDK1/2的选择性是CDK3/4/6的6倍以上。它还能有效抑制极光A/B,对Plk1和Wee1没有活性。 了解更多 -
TC-S 7010 (Aurora A Inhibitor I)
Catalog No. A10100 Aurora A 抑制剂TC-S 7010 (Aurora A Inhibitor I)是Aurora A激酶(AurA)的有效和选择性抑制剂,IC50值为3.4 nM(Aurora A),对Aurora B具有极高的选择性1000倍; 用于研究Aurora A激酶的细胞作用的有用工具化合物。 了解更多 -
GSK1070916
Catalog No. A11168 Aurora Kinase B/C 抑制剂GSK1070916是一种有效的Aurora B/C激酶抑制剂(IC50为3.5 nM/6.5 nM),在组织培养细胞和人肿瘤异种移植模型中具有广泛的抗肿瘤活性。 了解更多 -
PF-03814735
Catalog No. A11171 Aurora A/B Kinase 抑制剂PF-03814735是一种新颖,有效且可逆的Aurora A/B抑制剂,IC50为0.8 nM/5 nM,对Flt3,FAK,TrkA的效力较低,对Met和FGFR1的活性最低。 了解更多 -
PHA-680632
Catalog No. A10714 Aurora 抑制剂PHA-680632是Aurora A,Aurora B和Aurora C的有效抑制剂,IC50分别为27 nM,135 nM和120 nM。对于FGFR1,FLT3,LCK,PLK1,STLK2和VEGFR2/3,它的IC50高10到200倍。 了解更多 -
MK-5108 (VX-689)
Catalog No. A11410 Aurora A Kinase 抑制剂MK-5108,也称为VX-689,是Aurora A激酶ATP结合位点的竞争性抑制剂。 了解更多 -
CYC116 (CYC-116)
Catalog No. A10248 Aurora Kinase 抑制剂CYC116 (CYC-116)是一种有效的Aurora A/B抑制剂,Ki为8.0 nM/9.2 nM,对VEGFR2(Ki为44 nM)作用稍弱。 了解更多 -
MK-8745
Catalog No. A13396 -
PIM447 (LGH447)
Catalog No. A16807 Pim 抑制剂PIM447 (LGH447)是一种新型的pan-PIM激酶抑制剂,其PIM1,PIM2,PIM3的Ki值分别为6 pM,18 pM,9 pM。它也抑制GSK3β,PKN1和PKCτ,但效力显着降低,IC50在1-5μM之间(相对于PIM上Ki的差异> 105倍)。 了解更多 -
AZD1208 HCl
Catalog No. A16927 -
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SMI-16a
Catalog No. A17157 -
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INCB053914 phosphate
Catalog No. A21444 Pim inhibitorINCB053914 phosphate is an inhibitor of Pim extracted from patent WO 2017044730 A1, compound 1; has an IC50 of less than 35 nM. 了解更多 -
SGI-1776 (free base)
Catalog No. A10838 PIM1 抑制剂SGI-1776 (free base)是Pim1的一种新型ATP竞争性抑制剂,在无细胞试验中的IC50为7 nM,选择性是Pim2和Pim3的50倍和10倍,对Flt3和haspin也有效。阶段1。 了解更多