| R2032558 |
VE-821 |
VE-821 is a potent ATP-competitive inhibitor of ATR with Ki/IC50 of 13 nM/26 nM.
|
| R2032559 |
Verdinexor(KPT-335) |
Verdinexor(KPT-335) is a novel, orally bioavailable selective inhibitor of nucle
|
| R2032560 |
VS-5584 |
VS-5584 is a pan-PI3K/mTOR kinase inhibitor with IC50s of 16 nM, 68 nM, 42 nM, 2
|
| R2032561 |
VX-702 |
VX-702 is a highly selective inhibitor of p38α MAPK, 14-fold higher potency agai
|
| R2032562 |
VX745;Neflamapimod(VX-745) |
Neflamapimod (VX-745) is a potent, blood-brain barrier penetrant, highly selecti
|
| R2032563 |
Belnacasan(VX-765) |
Belnacasan (VX-765) is an orally bioactive prodrug of VRT-043198, which is a pot
|
| R2032564 |
Walrycin B |
Walrycin B is a novel antibacterial compound specifically targeting the essentia
|
| R2032565 |
WAY100635 |
WAY-100635 maleate is a potent and selective 5-hydroxytryptamine 1A (5-HT1A) rec
|
| R2032566 |
WHI-P154 |
WHI-P154 is a potent EGFR inhibitor, and also modestly blocks JAK3, with IC50s o
|
| R2032567 |
Wnt-c59 |
Wnt-C59 (C59) is a highly potent and oral porcupine (PORCN) inhibitor with an IC
|
| R2032568 |
WYE125132(WYE-132) |
WYE-132 (WYE-125132) is a highly potent, ATP-competitive, and specific mTOR kina
|
| R2032569 |
XCT790 |
XCT-790 is a potent and selective inverse agonist for ERRα with an IC50 value of
|
| R2032570 |
XL388 |
XL388 is a highly potent and ATP-competitive mTOR inhibitor with an IC50 of 9.9
|
| R2032571 |
XMD17-109 |
XMD17-109 is a novel, specific ERK-5 inhibitor, with an IC50 of 162 nM.
|
| R2032572 |
YH239-EE |
YH239-EE, ethyl ester of the free carboxylic acid compound YH239, is a potent p5
|
| R2032573 |
YM155 |
YM-155 is a survivin inhibitor with an IC50 of 0.54 nM.
|
| R2032574 |
z-fa-fMk |
Z-FA-FMK is an irreversible cysteine protease inhibitor, and also inhibits effec
|
| R2032575 |
ZK-811752 hydrochloride(BX471 hydrochloride) |
BX471 hydrochloride (ZK-811752 hydrochloride) is a potent, selective non-peptide
|
| R2032576 |
ZM39923 hydrochloride |
ZM 39923 HCl is an JAK1/3 inhibitor with pIC50 of 4.4/7.1, almost no activity to
|
| R2032577 |
z-vad -fMk |
Z-VAD(OMe)-FMK (Z-Val-Ala-Asp(OMe)-FMK) is a cell-permeable and irreversible pan
|
| R2032578 |
AS602801(BentaMapiMod) |
Bentamapimod (AS 602801) is an ATP-competitive JNK inhibitor with IC50 of 80 nM,
|
| R2032579 |
PF670462 |
PF-670462 is a potent and selective inhibitor of casein kinase (CK1ε and CK1δ),
|
| R2032580 |
SBC110,736 |
SBC-110736 is a proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitor
|
| R2032581 |
Y-27632 |
Y-27632 dihydrochloride is a cell-permeable, ATP-competitive inhibitor of ROCK-I
|
| R2032582 |
BRL54443 |
BRL 54443 is a potent 5-HT1E/1F receptor agonist (pKi values are 8.7 and 8.9 res
|