R2304273 |
Merafloxacin |
Merafloxacin (CI-934), a fluoroquinolone antibacterial agent, is a selective pro
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R2304274 |
CK1-IN-1 |
CK1-IN-1 is a casein kinase 1 (CK1) inhibitor extracted from patent WO2015119579
|
R2304275 |
Pizuglanstat |
Pizuglanstat (compound 3) is a prostaglandin D synthase inhibitor with an IC50 o
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R2304276 |
MS402 |
MS402 is a BD1-selective BET BrD inhibitor with Kis of 77 nM, 718 nM, 110 nM, 20
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R2304277 |
Antifungal agent 6 |
Antifungal agent 6 is an antifungal agent.
|
R2304278 |
Vodobatinib |
Vodobatinib (K0706) is a potent, third generation and orally active Bcr-Abl1 tyr
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R2304279 |
GR125743 |
GR 125743 is a selective 5-HT1B/1D receptor antagonist, with pKis of 8.85 and 8.
|
R2304280 |
(Rac)-Benpyrine |
(Rac)-Benpyrine, a racemate of Benpyrine, is a potent and orally active TNF-α in
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R2304281 |
Diphenylterazine |
Diphenylterazine (DTZ) is a bioluminescence agent. Diphenylterazine alone yielde
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R2304282 |
ROCK inhibitor-2 |
ROCK inhibitor-2 is a selective dual ROCK1 and ROCK2 inhibitor with IC50s of 17
|
R2304283 |
NLX-204HCl |
NLX-204 is a potent, selective agonist of ERK1/2 phosphorylation-preferring sero
|
R2304284 |
Practolol |
Practolol is a potent and selective β1-adrenergic receptor antagonist. Practolol
|
R2304285 |
Bisindolylmaleimide VIII acetate |
Bisindolylmaleimide VIII acetate (Ro 31-7549 acetate) is a potent and selective
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R2304286 |
Ro0335 |
RO-0335 is a novel and potent diphenylether nonnucleoside reverse transcriptase
|
R2304287 |
CITCO |
CITCO, an imidazothiazole derivative, is a selective Constitutive androstane rec
|
R2304288 |
JNJ-18038683 |
JNJ-18038683 is a 5-Hydroxytryptamine Type 7 (5-HT7) receptor antagonist, with p
|
R2304289 |
Aumitin |
Aumitin is a diaminopyrimidine-based autophagy inhibitor which inhibits mitochon
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R2304290 |
RAD51-IN-1 |
RAD51-IN-1, a derivative of B02, is a potent inhibitor of RAD51. RAD51-IN-1 can
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R2304291 |
MRGPRX1 agonist 1 |
MRGPRX1 agonist 1 is a highly potent agonist of MRGPRX1 (Mas-related G-protein-c
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R2304292 |
Menin-MLL inhibitor 20 |
Menin-MLL inhibitor 20 is an irreversible menin-MLL interaction inhibitor with a
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R2304293 |
SMS1-IN-1 |
SMS1-IN-1, compound SAPA 1j, is a novel and the most potent sphingomyelin syntha
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R2304294 |
LMPTP INHIBITOR 1 dihydrochloride |
LMPTP INHIBITOR 1 (dihydrochloride) is a selective inhibitor of low molecular we
|
R2304295 |
Gemfibrozil 1-O-β-glucuronide |
Gemfibrozil 1-O-β-Glucuronide, a metabolite of Gemfibrozil (CI-719; HY-B0258), i
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R2304296 |
SN-38 glucuronide (SN-38G) |
SN-38 glucuronide is an inactive metabolite of the cancer drug Irinotecan. Irino
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R2304297 |
PF-06821497 |
PF-06821497 is a selective inhibitor of EZH2 with significant tumor growth inhib
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