编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
6111506 | JAK3-IN-1 | 1805787-93-2 | 98% | |
JAK3-IN-1 is a potent JAK3 inhibitor with IC50 of 4.8 nM, also inhibits JAK1 (IC50 = | ||||
6111109 | JWH-133 | 259869-55-1 | 98% | |
JWH 133 is a potent CB2 selective agonist with Ki of 3.4 nM, 200-fold selective over | ||||
16070105 | (+)-JQ1 | 1268524-70-4 | 98% by HPLC | |
(+)-JQ1 is a BET potent BET bromodomain Inhibitor. Bromodomain and extra terminal dom | ||||
031401 | JNJ-42041935 | 1193383-09-3 | 98% | |
JNJ-42041935 is a potent (pKi = 7.3-7.9), 2-oxoglutarate competitive, reversible, and | ||||
62103 | JH-VIII-157-02 | 1639422-97-1 | 98% by HPLC | |
JH-VIII-157-02, a structural analogue of alectinib, is potent against the G1202R muta | ||||
012010 | JH-II-127 | 1700693-08-8 | 98% | |
JH-II-127 is a potent and selective inhibitor of both wild-type and G2019S mutant LRR | ||||
122939 | JNJ 40411813 | 1127498-03-6 | 98% | |
JNJ-40411813 is a novel positive allosteric modulator of the metabotropic Glutamate 2 | ||||
122938 | JNJ 303 | 878489-28-2 | 98% | |
Coming soon! | ||||
111007 | JZL195 | 1210004-12-8 | 98% | |
JZL195 is a selective and efficacious dual FAAH/MAGL inhibitor with IC50 of 13 nM and | ||||
100903 | JNJ-31020028 | 1094873-14-9 | 98% | |
JNJ-31020028 is a selective brain penetrant small molecule antagonist of the neuropep | ||||
52729 | JSH-23 | 749886-87-1 | 98% | |
JSH-23 is an inhibitor of NF-B transcriptional activity with IC50 of 7.1 M. | ||||
52522 | JNJ-26854165 (Serdemetan) | 881202-45-5 | 98% | |
JNJ-26854165 (Serdemetan) acts as a HDM2 ubiquitin ligase antagonist and also induces | ||||
52505 | J-147 | 1146963-51-0 | 98% | |
J-147 is a broad spectrum neuroprotective phenyl hydrazide compound(EC50=60-115 nM) w | ||||
52220 | JANEX-1 | 202475-60-3 | 98% | |
Janex-1 is a cell-permeable, reversible, potent, ATP-competitive, and specific inhibi | ||||
52225 | JIB-04 | 199596-05-9 | 98% | |
JIB-04 is a pan-selective Jumonji histone demethylase inihibitor with IC50 of 230, 34 |