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GYKI53655 Hydrochloride
Catalog No. A17032 -
PHTPP
Catalog No. A17035 -
Nedisertib
Catalog No. A17055 DNA-PK 抑制剂Nedisertib (M-3814,MSC2490484A)是一种可口服的DNA依赖性蛋白激酶（DNA-PK）抑制剂，具有潜在的抗肿瘤和化学/放射增敏活性。 了解更多 -
SR9238
Catalog No. A15763 -
KDU691
Catalog No. A17066 -
PF-06855800
Catalog No. A16860 PRMT5 抑制剂PF-06855800 (PF06855800)是一种有效的，选择性的，SAM竞争性，BBB渗透性，口服活性的蛋白精氨酸甲基转移酶PRMT5抑制剂，Ki为0.02 nM。 了解更多 -
GSK-3326595 (EPZ015938)
Catalog No. A16862 PRMT5 抑制剂GSK-3326595 (EPZ015938)是一种有效的，选择性的，可逆的蛋白精氨酸甲基转移酶5（PRMT5）抑制剂，IC50为6.2 nM。 了解更多 -
CB-1158
Catalog No. A16864 -
AZD3229 Tosylate
Catalog No. A16867 -
PF-06873600
Catalog No. A16875 CDK 抑制剂PF-06873600是一种口服生物利用型，细胞周期蛋白依赖性激酶（CDK）抑制剂，其对 CDK2、CDK4和CDK6的Ki值分别为 0.09 nM、0.13 nM 和 0.16 nM。具有潜在的抗肿瘤活性。 了解更多 -
NSC117079
Catalog No. A16894 -
ICEC0942 HCl
Catalog No. A16903 CDK7 抑制剂ICEC0942 HCl，也称为CT7001，是CDK7的口服生物利用选择性抑制剂。它选择性抑制CDK7，IC50为40nM。CDK1，CDK2，CDK5和CDK9的IC50值分别高45倍，15倍，230倍和30倍。 了解更多 -
Vorasidenib
Catalog No. A16908 IDH1 抑制剂Vorasidenib (AG-881)是一种有效且选择性的口服抑制剂，可抑制细胞质中异柠檬酸脱氢酶1型(IDH1，IDH1 [NADP+]可溶)和2型（IDH2异柠檬酸脱氢酶[NADP+]）的突变形式。线粒体中的线粒体，具有潜在的抗肿瘤活性。 了解更多 -
Oxyclozanide
Catalog No. A16979 -
KIN001-051
Catalog No. A16923 Lck 抑制剂KIN001-051是一种有效的、选择性的Lck抑制剂。淋巴细胞特异性蛋白酪氨酸激酶（Lck）是非受体蛋白酪氨酸激酶Src家族的成员，在触发细胞因子产生的T细胞受体信号转导的初始步骤中起着至关重要的作用。 了解更多 -
CB-1158
Catalog No. A16929 -
CAY10566
Catalog No. A16936 -
LF3
Catalog No. A16851 -
LXH254
Catalog No. A16841 -
Ruxolitinib Phosphate
Catalog No. A11552 JAK 抑制剂Ruxolitinib Phosphate是ruxolitinib的磷酸盐形式，ruxolitinib是一种口服生物可利用的Janus相关激酶(JAK)抑制剂，具有潜在的抗肿瘤和免疫调节活性。 了解更多 -
Albiglutide
Catalog No. A16823 -
IL 1RA Mouse, His
Catalog No. AP5306 Interleukin-1 Receptor Antagonist Mouse Recombinant, His Tag 了解更多
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