R10663 |
5SrRNAmodificator |
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R10664 |
CM 346; Obenoxazine HCl |
CM 346 is an anxiolytic drug, produces anxiolytic and neuroprotective effects wi
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R10667 |
GBR12935 Dihydrochloride |
GBR 12935 dihydrochloride inhibits DAT (dopamine transporter) (Ki = 21.5 nM) and
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R10672 |
LH846 |
LH846 is a selective inhibitor of CK1δ (IC50 values are 290 nM, 1.3 uM and 2.5 u
|
R10675 |
B-RafIN1 |
B-Raf IN 1 is a highlt potent and selective B-Raf inhibitor with IC50 of 24 nM;
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R10678 |
ZLN005 |
ZLN005 is a potent and tissue-specific PGC-1α transcriptional activator.
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R10679 |
kobe2602 |
kobe2602 is a novel and effective small-molecule compound inhibiting Ras–Raf int
|
R10685 |
Nimorazole |
Nimorazole is a nitroimidazole anti-infective. It is also being investigated for
|
R10686 |
LB-100 |
LB-100 is a water soluble protein phosphatase 2A (PP2A) inhibitor. Phase 1.
|
R10689 |
ISRIB |
ISRIB (trans-isomer) is a potent and selective small molecule inhibitor of PERK
|
R10690 |
Clemizole.HCl |
Clemizole hydrochloride is an antagonist of H1 histamine receptor with an IC50 v
|
R10691 |
1443139-14-7 |
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R10693 |
Nicaraven |
Nicaraven is a hydroxyl radical scavenger with antivasospastic and neuroprotecti
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R10694 |
1350920-22-7 |
|
R10695 |
Bioymifi (DR5 Activator) |
Bioymifi is a potent and selective small molecule agonist of DR5 that directly t
|
R10696 |
2-Chloro-N-[[2'-[(cyanoamino)sulfonyl][1,1'-biphenyl]-4-yl]methyl]-N-[(4-methylphenyl)methyl]-benzamide |
S0859, an N-cyanosulphonamide compound, reversibly inhibit NBC-mediated pH(i) re
|
R10704 |
SRPIN340 |
SRPIN340 is a selective SRPK inhibitor with Ki of 0.89 μM for SRPK1, showing no
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R10718 |
kbNB142-70 |
kb NB 142-70 is a selective protein kinase D (PKD) inhibitor (IC50 values are 28
|
R10719 |
APY0201 |
APY0201 is a potent, highly selective, ATP-competitive PIKfyve inhibitor (IC50=5
|
R10721 |
ACT058362; Palosuran |
Palosuran is a new potent and specific antagonist of the human UT receptor with
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R10722 |
CASIN |
CASIN is a selective GTPase Cdc42 inhibitor with IC50 of 2 uM. In vitro: Treatme
|
R10728 |
BVT2733 |
BVT 2733 is a new, small molecule, non-steroidal, isoform-selective inhibitor of
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R10730 |
NSC-41589 |
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R10731 |
SKLB477;FLT3-IN-1 |
SKLB4771 is a novel potent and selective Flt3 inhibitor with IC50 of 10 nM; agai
|
R10734 |
TH588 |
TH588 is a potent and selective MTH1 (NUDT1) inhibitor with IC50 of 5 nM.
|