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Cas Index 1

• 1380392-05-1 | JMS-17-2 (Catalog# : 2071624)JMS-17-2 is a potent and selective antagonist of CX3CR1.
• 1443235-95-7 | JAK3-IN-2 (Catalog# : 2071551)JAK3-IN-2 is a potent and highly selective JAK3 inhibitor.
• 1572510-42-9 | JNJ-632 (Catalog# : 2071507)JNJ-632 is a potent HVV capsid assembly modulator and HBV replication inhibitor with
• 1408064-71-0 | JNK-IN-7 (Catalog# : 2061305)JNK-IN-7 is a relatively selective JNKs inhibitor(IC50= 1.54/1.99/0.75 for JNK1/2/3);
• 1408064-71-0 | JNK-IN-7 (Catalog# : 2061305)
• 1597402-27-1 | JPH203 HCl ( Nanvuranlat ) (Catalog# : 18381)JPH203, also known as KYT-0353, is a potent and selective LAT1 selective ( L-type ami
• 1142363-52-7 | JNJ-40346527 (Catalog# : 1711221)JNJ-40346527 is a small molecule and orally available inhibitor of colony-stimulating
• 1254977-87-1 | JNJ-42153605 (Catalog# : 1791311)JNJ-42153605 is a potent and selective mGlu2 receptor PAM with an acceptable pharmaco
• 1346528-51-5 | JNJ-42165279(2HCl salt) (Catalog# : 1783012)JNJ-42165279 exhibited excellent ADME and pharmacodynamic properties as evidenced by
• 1346528-52-6 | JNJ-42165279(mono HCl salt) (Catalog# : 1783011)JNJ-42165279 is a potent and selective fatty acid amide hydrolase (FAAH) inhibitor. J
• 1913252-04-6 | JQ-EZ-05 (Catalog# : 2017871)JQ-EZ-05, also known as JQEZ5, is a bio active chemical. 
• 1410880-22-6 | JNK-IN-8 (Catalog# : 16123027)JNK-IN-8, also known as JNK Inhibitor XVI, is a selective JNK inhibitor that inhibits
• 1802326-66-4 | JNJ 63533054 (Catalog# : 16123026)JNJ 63533054 is a potent and selective GPR139 agonist (EC50 = 16 nM) that is brain an
• 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
• 1800405-30-4 | KL1333 (Catalog# : 25201)KL1333 is an orally available, small organic molecule that reacts with NAD(P)H:quinon
• 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 is a small-molecule inhibitor of the transitional endoplasmic reticulum ATPas
• 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