编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
20641 | KP-302 ( Synonyms: Lucid-21-302 ; Lucid-MS ) | 2082765-42-0 | ≧98.0% | |
KP-302 ( Synonyms: Lucid-21-302 ; Lucid-MS ) 是一种蛋白质精氨酸脱亚胺酶的 | ||||
20493 | KDM5-C49 | 1596348-16-1 | 98% Min. | |
KDM5-C49 is a potent and selective inhibitor of KDM5 (also known as JARID1). KDM5-C49 | ||||
20472 | KSQ-4279 | 2446480-97-1 | 98% Min. | |
KSQ-4279 is a USP1 and PARP inhibitor. KSQ-4279 showed anti-proliferative effects in | ||||
L20334 | KY19382 | 2226664-93-1 | 98% Min. | |
KY19382 is an orally active dual inhibitor of CXXC5-DVL and GSK3β | ||||
20277 | KPI-10 | 888032-58-4 | 98% Min. | |
KPI-10 is a new compound currently being studied for its efficacy in the treatment of | ||||
21246 | KUN56321 | 1771756-32-1 | 98% Min. | |
KUN56321 is a luminescent agent. The application of KUN56321 comprises: coating the f | ||||
20122101 | KO-947 | 1695533-89-1 | 98% Min. | |
KO-947 is a potent and selective ERK inhibitor with slow dissociation kinetics. KO-94 | ||||
2061304 | KY-226 | 98% Min. | ||
KY-226 is a protein tyrosine phosphatase 1B (PTP1B) inhibitor that protects neurons f | ||||
193203 | Kinesore | 363571-83-9 | >98% | |
Kinesore是肌动蛋白-1在细胞微管动力学调控中的激活因子。它已被 | ||||
19362 | KH7 | 330676-02-3 | >98% | |
KH7是一种新型的可溶性腺苷酸环化酶(Sac)抑制剂。 | ||||
192152 | KINK-1 | 600734-06-3 | >98% | |
IKKßKINK-1是一种抑制剂,阻止NF-kappaB激活。 | ||||
191281 | KHS101盐酸盐 | 1784282-12-7 | >98% | |
KHS101 HCl是一种转化酸性卷曲蛋白3 (TACC3)的抑制剂。它的作用是通 | ||||
19123 | KU59403 | 845932-30-1 | >98% | |
KU59403是一种有效的选择性ATM(共济失调毛细血管扩张突变)抑制剂, | ||||
1810294 | KC01 | 1646795-59-6 | >98% | |
KC01是ABHD16A的共价抑制剂。ABHD16A是一种磷脂酰丝氨酸(PS)脂肪酶, | ||||
1810226 | KG-501 | 18228-17-6 | >98% | |
KG-501是cAMP反应元件结合蛋白(CREB)抑制剂。 | ||||
187124 | KYP-2047 | 796874-99-2 | >98% | |
KYP-2047是一种非常有效的、选择性的Prolyl寡肽酶(POP)抑制剂,也被 | ||||
3291806 | KGP-94 | 1131456-28-4 | >98% | |
KGP94 is a reversible, time-dependent and competitive inhibitor of human cathepsin L. | ||||
184121 | KIN-1148 | 1428729-56-9 | >98% | |
KIN-1148是一个IRF3激动剂。KIN1148诱导剂量依赖性IRF3核易位和特异性 | ||||
184217 | KKL-10 | 952849-76-2 | >98% | |
KKL-10是一种抗菌药物。KKL-10在体外和体外感染中均表现出了对弱毒 | ||||
1710132 | KI-696 | 1799974-70-1 | >98% | |
ki-696代表一个优良的低分子量的工具来研究体内Keap1与Nrf2-Nrf2的相 | ||||
20178211 | KAF-156 | 1261113-96-5 | 98% | |
KAF-156,也称为GNF-156, 是一种可治疗疟疾的抗疟药。 | ||||
17031301 | KM11060 | 774549-97-2 | 98% | |
KM11060是一种突变的F508del囊性纤维化跨膜电导调节器(CFTR)。CFTR基因 | ||||
17031014 | KRIBB11 | 342639-96-7 | 98% | |
KRIBB11废除了热触觉荧光素酶活动的IC50 1.2μM。它是转录因子热休克 | ||||
17022703 | Ki8751 | 228559-41-9 | 98% | |
Ki8751是一种强力的、选择性的VEGFR- 2酪氨酸激酶(IC50 = 0.9 nM)的抑制 | ||||
16123029 | KN-93 phosphate | 1188890-41-6 | 98% | |
KN-93 is a CaMKII inhibitor. KN-93 suppresses ventricular arrhythmia induced by LQT2 | ||||
16123028 | K-7174 | 191089-59-5 | 98% | |
K-7174 is a novel orally active, potent proteasome inhibitor. K-7174 exerts anti-myel | ||||
16122827 | KC7F2 | 927822-86-4 | 98% | |
KC7F2 is a potent HIF-1 pathway inhibitor with potential anticancer activity. KC7F2 i | ||||
16122826 | KB-R7943 mesylate | 182004-65-5 | 98% | |
KB-R7943 is a potent, selective inhibitor of the reverse mode of the Na+/Ca2+ exchang | ||||
16122824 | K-858 | 72926-24-0 | 98% | |
K-858 is a novel inhibitor of mitotic kinesin Eg5 and antitumor agent, induces cell d | ||||
16122711 | Kenpaullone | 142273-20-9 | 98% | |
Kenpaullone is an ATP-competitive inhibitor of cyclin-dependent kinases (CDKs). It al |