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Name Index C

• Cefozopran (Catalog# : 17032402, Cas# : 113359-04-9)Cefozopran(SCE 2787) is a fourth-generation cephalosporin. 
• Cefoselis (Catalog# : 17032401, Cas# : 122841-10-5)Cefoselis is a widely used beta-lactam antibiotic. 
• CC-122 (Catalog# : 17030313, Cas# : 1015474-32-4)CC-122 is an orally available pleiotropic pathway modulator with potential antineopla
• CP21R7 (Catalog# : 17022715, Cas# : 125314-13-8)CP21R7, also known CP21, is a potent and selective GSK-3 inhibitor. 
• Citarinostat (Catalog# : 17022701, Cas# : 1316215-12-9)Citarinostat is a HDAC6 specific inhibitor, with IC50 of 4 nM and 76 nM for HDAC6 and
• (+)-Camphor (Catalog# : 17021401, Cas# : 464-49-3)(+)-Camphor is an ingredient in cooking, and as an embalming fluid for medicinal purp
• CeMMEC1 (Catalog# : 17021308, Cas# : 440662-09-9)CeMMEC1 is an N-methylisoquinolinone derivative that inhibits the second bromodomain
• CA-074 methyl ester (CA-074 Me) (Catalog# : 17011104, Cas# : 147859-80-1)CA-074 Me is a membrane-permeable derivative of CA-074 and acts as an irreversible c
• CZ415 (Catalog# : 17011101, Cas# : 1429639-50-8)CZ415, a potent ATP-competitivemTORinhibitor with very good cell permeability.
• CPI-455 (Catalog# : 17109005, Cas# : 1628208-23-0)CPI-455 is a specific KDM5 inhibitor, elevating global levels of H3K4 trimethylation
• Cytosporone B (Catalog# : 16122924, Cas# : 321661-62-5)Cytosporone B is the first naturally occurring agonist for nuclear orphan receptor Nu
• CVT-313 (Catalog# : 16122923, Cas# : 199986-75-9)CVT-313 is a potent and selective inhibitor of CDK2 that prevents neointimal prolifer
• CTP354 (Catalog# : 16122922, Cas# : 1213669-91-0)CTP354, also known as C-21191, a novel deuterated subtype-selective GABA(A) modulator
• Ciliobrevin A (Catalog# : 16122921, Cas# : 302803-72-1)Ciliobrevin A, also known as HPI-4 and Hedgehog Pathway Inhibitor 4, is a Hedgehog pa
• CID5721353 (Catalog# : 16122920, Cas# : 301356-95-6)CID5721353 is a B-Cell Lymphoma 6 Inhibitor (BCL6 inhibitor).
• Cetilistat (Catalog# : 16122918, Cas# : 282526-98-1)Cetilistat, also known as ATL-962, is a drug designed to treat obesity. It acts in th
• Cerdulatinib (PRT062070) (Catalog# : 16122917, Cas# : 1198300-79-6)Cerdulatinib, also known as PRT2070 and PRT062070, is a n ovel, oral, dual spleen tyr
• Cefotetan Sodium (Catalog# : 16122916, Cas# : 74356-00-6)Cefotetan Sodium, also known as ICI-156834 and YM-09330, is a second-generation cepha
• C-DIM12 (Catalog# : 16122915, Cas# : 178946-89-9)C-DIM12 is a novel synthetic activator of Nurr1. C-DIM12 induces dopaminergic gene ex
• CCG215022 (Catalog# : 16122914, Cas# : 1813527-81-9)CCG215022 is a potent GRK2 and GRK5 inhibitor. CCG215022 exhibited nanomolar IC50 val
• CB-839 (Catalog# : 16122913, Cas# : 1439399-58-2)CB-839 an is orally bioavailable inhibitor of glutaminase, with potential antineoplas
• CAY10683 (Catalog# : 16122912, Cas# : 1477949-42-0)CAY10683, also known as Santacruzamate A, is a potent and selective histone deacetyla
• Cardiogenol C HCl (Catalog# : 16122911, Cas# : 1049741-55-0)Cardiogenol C is a diaminopyrimidine compound that induces the differentiation of MHC
• Capromorelin tartrate (Catalog# : 16122910, Cas# : 193273-69-7)Capromorelin, also known as CP-424,391, is a growth hormone secretagogue and ghrelin
• Canertinib (Catalog# : 16122909, Cas# : 289499-45-2)Canertinib dihydrochloride is the hydrochloride salt of an orally bio-available quina
• Camostat Mesilate (Catalog# : 16122806, Cas# : 59721-29-8)Camostat Mesilate, also known as FOY 305, is a serine protease inhibitor. Serine prot
• CPI-0610 (Catalog# : 16122738, Cas# : 1380087-89-7)CPI-0610 is a potent and selective benzoisoxazoloazepine BET bromodomain inhibitor an
• CPI-637 (Catalog# : 16122737, Cas# : 1884712-47-3)CPI-637 is a selective and cell-active benzodiazepinone CBP/EP300 bromodomain inhibit
• CeMMEC13 (Catalog# : 6111701, Cas# : 1790895-25-8)CeMMEC13 is an isoquinolinone that selectively inhibits the second bromodomain of TAF
• CB1-IN-1 (Catalog# : 6111108, Cas# : 1429239-98-4)CB1-IN-1 is a peripherally restricted CB1R antagonist, with Ki of 0.3 nM and 21 nM fo