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 About 21 results found for searched term "CP-10" (0.054 seconds)

Cat.No.  Name Target
M2202 CPI-0610 Epigenetic Reader Domain
Pelabresib
CPI-0610 is a novel BET protein bromodomain inhibitor.
M2899 Orbifloxacin Antibiotic
CP-104354
Orbifloxacin is a synthetic broad-spectrum fluoroquinolone antibiotic.
M3659 Pimavanserin 5-HT Receptor
ACP-103
Pimavanserin is a selective serotonin 5-HT2A inverse agonist.
M5369 Fenclonine (4-Chloro-DL-phenylalanine) 5-HT Receptor
PCPA; CP-10188; 4-Chloro-DL-phenylalanine; p-Chlorophenylalanine
Fenclonine (4-Chloro-DL-phenylalanine) is a selective and irreversible inhibitor of tryptophan hydroxylase, a rate-limiting enzyme in the biosynthesis of serotonin. Fenclonine (4-Chloro-DL-phenylalanine) acts pharmacologically to deplete endogenous levels of serotonin.
M6628 CP 809101 hydrochloride Others
CP 809101 hydrochloride is a potent and selective 5-HT 2C agonist.
M7451 UCPH 101 Others
UCPH 101 is a selective non-substrate EAAT1 inhibitor.
M8041 CP-101537 MMP
Cp-101537 is an MMP inhibitor, a candidate compound for the treatment of myocardial infarction, and an antibacterial compound.
M8062 CP-100356 monohydrochloride BCRP/ABCG2/MXR/ABCP
CP-100356 is a specific inhibitor of MDR1 (P-Gp), the protypical ABC transporter.
M8076 CP-101606 mesylate Others
CP-101606 mesylate (Traxoprodil mesylate) is a potent noncompetitive antagonist of N-methyl-D-aspartate (NMDA) receptors, selective for the NR2B subunit.
M8116 CP-105,696 Leukotriene Receptor
CP-105,696 is an orally active, potent and selective leukotriene B4 receptor (LTB4R) antagonist (IC50 against [3H]LTB4 = 5.
M8215 CP-101,606 Others
Traxoprodil (CP-101,606) is a potent noncompetitive antagonist of N-methyl-D-aspartate (NMDA) receptors, selective for the NR2B subunit.
M8671 UCPH-102 Others
UCPH-102 is a selective inhibitor of the Excitatory Amino Acid Transporter subtype-1 (EAAT1, GLAST) with an IC50 value of 420 nM for EAAT1 and >300 μM for EAAT2-5.
M10084 AMY-101 acetate Complement System
Cp40; AMY101 acetate
AMY-101 acetate is a peptidic inhibitor of the central complement component C3 (KD = 0.5 nM).
M13701 Gemcitabine elaidate Others
CP-4126; CO-101; Gemcitabine 5'-elaidate
Gemcitabine elaidate (CP-4126) is lipophilic pro-drug of Gemcitabine. Gemcitabine elaidate is converted to Gemcitabine by esterases in order to be phosphorylated. Gemcitabine elaidate exhibits anti-tumor activity.
M13702 Gemcitabine elaidate hydrochloride Others
CP-4126 hydrochloride; CO-101 hydrochloride; Gemcitabine 5'-elaidate hydrochloride
Gemcitabine elaidate (CP-4126) hydrochloride is lipophilic pro-drug of Gemcitabine. Gemcitabine elaidate hydrochloride is converted to Gemcitabine by esterases in order to be phosphorylated. Gemcitabine elaidate hydrochloride exhibits anti-tumor activity.
M13873 Pimavanserin hemitartrate 5-HT Receptor
ACP-103 hemitartrate
Pimavanserin (ACP-103) hemitartrate is a potent 5-HT 2A receptor inverse agonist with pIC50 and pKi of 8.73 and 9.3, respectively.
M14614 ACP-105 Androgen Receptor
ACP-105 is an orally available, selective amd potent androgen receptor modulator (SARM), with pEC50s of 9.0 and 9.3 for AR wild type and T877A mutant, respectively.
M14869 CP-10 PROTAC
CP-10 is a PROTAC connected by ligands for Cereblon and CDK, with highly selective, specific, and remarkable CDK6 degradation (DC50=2.1 nM).
M20725 MCP110 Ras
MCP110 is an inhibitor of Ras/Raf-1 interaction. MCP110 disrupts the interaction of activated Ras with Raf and is potential for the treatment of human tumors.
M22016 CP-809101 Others
CP-809101
M49361 Cpd10 RIPK
Cpd10 is a type II RIPK1 inhibitor that binds to the ATP site in the inactive conformation of the kinase.



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