武汉永璨生物科技有限公司
+86-17702719238 sales@sun-shinechem.com

产品目录

编号化学名称Cas号纯度化学结构
20641KP-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
20493KDM5-C491596348-16-198% Min.
KDM5-C49 is a potent and selective inhibitor of KDM5 (also known as JARID1). KDM5-C49
20472KSQ-42792446480-97-198% Min.
KSQ-4279 is a USP1 and PARP inhibitor. KSQ-4279 showed anti-proliferative effects in
L20334 KY193822226664-93-198% Min.
KY19382 is an orally active dual inhibitor of CXXC5-DVL and GSK3β
20277KPI-10888032-58-498% Min.
KPI-10 is a new compound currently being studied for its efficacy in the treatment of
21246KUN563211771756-32-198% Min.
KUN56321 is a luminescent agent. The application of KUN56321 comprises: coating the f
20122101 KO-9471695533-89-198% Min.
KO-947 is a potent and selective ERK inhibitor with slow dissociation kinetics. KO-94
2061304KY-22698% Min.
KY-226 is a protein tyrosine phosphatase 1B (PTP1B) inhibitor that protects neurons f
193203Kinesore 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
19362KH7330676-02-3>98%
KH7是一种新型的可溶性腺苷酸环化酶(Sac)抑制剂。
192152KINK-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
19123KU59403 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,
1810294KC011646795-59-6>98%
KC01是ABHD16A的共价抑制剂。ABHD16A是一种磷脂酰丝氨酸(PS)脂肪酶,
1810226KG-50118228-17-6>98%
KG-501是cAMP反应元件结合蛋白(CREB)抑制剂。
187124KYP-2047796874-99-2>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
3291806KGP-941131456-28-4>98%
KGP94 is a reversible, time-dependent and competitive inhibitor of human cathepsin L.
184121KIN-11481428729-56-9>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
184217KKL-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
1710132KI-6961799974-70-1>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
20178211KAF-1561261113-96-598% 
KAF-156,也称为GNF-156, 是一种可治疗疟疾的抗疟药。
17031301KM11060774549-97-298% 
KM11060是一种突变的F508del囊性纤维化跨膜电导调节器(CFTR)。CFTR基因
17031014KRIBB11342639-96-798% 
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
17022703Ki8751228559-41-998% 
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
16123029KN-93 phosphate1188890-41-698% 
KN-93 is a CaMKII inhibitor. KN-93 suppresses ventricular arrhythmia induced by LQT2
16123028K-7174191089-59-598% 
K-7174 is a novel orally active, potent proteasome inhibitor. K-7174 exerts anti-myel
16122827KC7F2927822-86-498% 
KC7F2 is a potent HIF-1 pathway inhibitor with potential anticancer activity. KC7F2 i
16122826KB-R7943 mesylate182004-65-598% 
KB-R7943 is a potent, selective inhibitor of the reverse mode of the Na+/Ca2+ exchang
16122824K-85872926-24-098% 
K-858 is a novel inhibitor of mitotic kinesin Eg5 and antitumor agent, induces cell d
16122711Kenpaullone142273-20-998% 
Kenpaullone is an ATP-competitive inhibitor of cyclin-dependent kinases (CDKs). It al