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• 1346528-50-4 | JNJ-42165279 (Catalog# : 16123025)JNJ-42165279 is a potent and selective fatty acid amide hydrolase (FAAH) inhibitor. J
• 1037592-40-7 | JPH203(KYT-0353) (Catalog# : 6112701)JPH203(also known as KYT-0353) is a potent and selective LAT1 selective ( L-type amin
• 1805787-93-2 | JAK3-IN-1 (Catalog# : 6111506)JAK3-IN-1 is a potent JAK3 inhibitor with IC50 of 4.8 nM, also inhibits JAK1 (IC50 =
• 1268524-70-4 | (+)-JQ1 (Catalog# : 16070105)(+)-JQ1 is a BET potent BET bromodomain Inhibitor. Bromodomain and extra terminal dom
• 1193383-09-3 | JNJ-42041935 (Catalog# : 031401)JNJ-42041935 is a potent (pKi = 7.3-7.9), 2-oxoglutarate competitive, reversible, and
• 1639422-97-1 | JH-VIII-157-02 (Catalog# : 62103)JH-VIII-157-02, a structural analogue of alectinib, is potent against the G1202R muta
• 1700693-08-8 | JH-II-127 (Catalog# : 012010)JH-II-127 is a potent and selective inhibitor of both wild-type and G2019S mutant LRR
• 1127498-03-6 | JNJ 40411813 (Catalog# : 122939)JNJ-40411813 is a novel positive allosteric modulator of the metabotropic Glutamate 2
• 1210004-12-8 | JZL195 (Catalog# : 111007)JZL195 is a selective and efficacious dual FAAH/MAGL inhibitor with IC50 of 13 nM and
• 1094873-14-9 | JNJ-31020028 (Catalog# : 100903)JNJ-31020028 is a selective brain penetrant small molecule antagonist of the neuropep
• 1146963-51-0 | J-147 (Catalog# : 52505)J-147 is a broad spectrum neuroprotective phenyl hydrazide compound(EC50=60-115 nM) w
• 199596-05-9 | JIB-04 (Catalog# : 52225)JIB-04 is a pan-selective Jumonji histone demethylase inihibitor with IC50 of 230, 34
• 1215115-03-9 | KH-3 (Catalog# : 24143)KH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC50 value
• 1357164-52-3 | KUS121 (Catalog# : 20676)KUS-121 是一种过渡内质网 ATP 酶（含缬氨肽蛋白 [VCP]；p97）的小分
• 1596348-16-1 | KDM5-C49 (Catalog# : 20493)KDM5-C49 is a potent and selective inhibitor of KDM5 (also known as JARID1). KDM5-C49
• 1771756-32-1 | KUN56321 (Catalog# : 21246)KUN56321 is a luminescent agent. The application of KUN56321 comprises: coating the f
• 1695533-89-1 | KO-947 (Catalog# : 20122101)KO-947 is a potent and selective ERK inhibitor with slow dissociation kinetics. KO-94
• 1784282-12-7 | KHS101盐酸盐 (Catalog# : 191281)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
• 1646795-59-6 | KC01 (Catalog# : 1810294)KC01是ABHD16A的共价抑制剂。ABHD16A是一种磷脂酰丝氨酸(PS)脂肪酶，
• 18228-17-6 | KG-501 (Catalog# : 1810226)KG-501是cAMP反应元件结合蛋白(CREB)抑制剂。
• 1131456-28-4 | KGP-94 (Catalog# : 3291806)KGP94 is a reversible, time-dependent and competitive inhibitor of human cathepsin L.
• 1428729-56-9 | KIN-1148 (Catalog# : 184121)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
• 1799974-70-1 | KI-696 (Catalog# : 1710132)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
• 1261113-96-5 | KAF-156 (Catalog# : 20178211)KAF-156，也称为GNF-156, 是一种可治疗疟疾的抗疟药。
• 1188890-41-6 | KN-93 phosphate (Catalog# : 16123029)KN-93 is a CaMKII inhibitor. KN-93 suppresses ventricular arrhythmia induced by LQT2
• 191089-59-5 | K-7174 (Catalog# : 16123028)K-7174 is a novel orally active, potent proteasome inhibitor. K-7174 exerts anti-myel
• 182004-65-5 | KB-R7943 mesylate (Catalog# : 16122826)KB-R7943 is a potent, selective inhibitor of the reverse mode of the Na+/Ca2+ exchang
• 142273-20-9 | Kenpaullone (Catalog# : 16122711)Kenpaullone is an ATP-competitive inhibitor of cyclin-dependent kinases (CDKs). It al
• 1309444-75-4 | K145 (Catalog# : 6111523)K145 is a selective SphK2 inhibitor with an IC50 of 4.300.06 M , while no inhibition
• 1253452-78-6 | KS176 (Catalog# : 6111510)KS176 is a potent and selective inhibitor of the breast cancer resistance protein (BC