R10018 |
GMX1778;CHS828 |
GMX1778(CHS-828) is a potent inhibitor of NAD+ biosynthesis enzyme NAMPT with IC
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R10338 |
CIQ |
CIQ is a subunit-selective potentiator of NMDA receptors containing the NR2C or
|
R10615 |
MDL29951 |
MDL-29951 is a novel glycine antagonist of NMDA receptor activation (Ki=0.14 mM,
|
R10089 |
Ralimetinib dimesylate; LY2228820 dimesylate |
LY2228820 is a novel and potent inhibitor of p38 MAPK with IC50 of 7 nM in a cel
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R10196 |
SB203580 |
SB203580 is a p38 MAPK inhibitor with IC50 of 0.3-0.5 μM in THP-1 cells, 10-fold
|
R10670 |
kb-NB77-78 |
kb-NB77-78 is an analog of CID797718, which is a by-product of the synthesis of
|
R10142 |
Tariquidar;XR9576 |
Tariquidar is a potent and selective noncompetitive inhibitor of P-glycoprotein
|
R10017 |
CGI1746 |
CGI1746 is a potent and highly selective small-molecule inhibitor of the Btk wit
|
R10173 |
R406 tosilate |
R406 is a potent Syk inhibitor with IC50 of 41 nM in cell-free assays, strongly
|
R10021 |
CK-1827452 |
Omecamtiv mecarbil (CK-1827452) is a specific cardiac myosin activator and a cli
|
R10886 |
Domatinostat (4SC-202 free base) |
Domatinostat (4SC-202 free base) is a selective class I HDAC inhibitor with IC50
|
R10888 |
Cefditoren Pivoxil (Cefditoren pivoxyl; Cefditoren pivaloyloxymethyl ester; ME1207) |
Cefditoren Pivoxil is a broad-spectrum antibiotic against Gram-negative and Gram
|
R10873 |
CNX-774 |
CNX-774 is an irreversible, orally active, and highly selective BTK inhibitor wi
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R10852 |
Daunorubicin hydrochloride |
Daunorubicin HCl inhibits both DNA and RNA synthesis and inhibits DNA synthesis
|
R10839 |
Doramectin |
Doramectin is an antiparasitic agent.
|
R10871 |
Dorsomorphin (Synonyms: BML-275; Compound C) |
Dorsomorphin (Compound C) 2HCl is a potent, reversible, selective AMPK inhibitor
|
R10872 |
Dorsomorphin dihydrochloride (Synonyms: BML-275 dihydrochloride; Compound C dihydrochloride) |
Dorsomorphin (Compound C) 2HCl is a potent, reversible, selective AMPK inhibitor
|
R10875 |
Entospletinib (GS-9973) |
Entospletinib (GS-9973) is an orally bioavailable, selective Syk inhibitor with
|
R10853 |
Epirubicin hydrochloride |
Epirubicin HCl, a semisynthetic L-arabino derivative of doxorubicin, is an antin
|
R10848 |
Ki16198 |
Ki16198 is the methyl ester of Ki16425, which is a LPA antagonist and inhibits L
|
R10880 |
Lapatinib (GW572016; GW2016) |
Lapatinib, used in the form of Lapatinib Ditosylate, is a potent EGFR and ErbB2
|
R10867 |
LDC1267 |
LDC1267 is a highly selective TAM kinase inhibitor with IC50 of <5 nM, 8 nM,
|
R10870 |
LDN-193189 HCl |
LDN193189 HCl is the hydrochloride salt of LDN193189, which is a selective BMP s
|
R10869 |
LDN-193189 |
LDN-193189 is a selective BMP signaling inhibitor, inhibits the transcriptional
|
R10868 |
MK-2206 dihydrochloride |
MK-2206 2HCl is a highly selective inhibitor of Akt1/2/3 with IC50 of 8 nM/12 nM
|