Chemical Name: 1-[8-(2-Chlorophenyl)-9-(4-chlorophenyl)-9H-purin-6-yl]-4-(ethylamino)piperidine-4-carboxamide hydrochloride

 June 21, 2017

prudect name : Chemical Name: 1-[8-(2-Chlorophenyl)-9-(4-chlorophenyl)-9H-purin-6-yl]-4-(ethylamino)piperidine-4-carboxamide hydrochlorideCP-945598 hydrochloride Synonyms: CAS NO: 686347-12-6Molecular Formula: C25H25Cl2N7O.HClMolecular Weight: 546.88Purity: 98% minSolubility: In DMSOStorage: −20°C KB-R7943 References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/18507836

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CP 673451 is a selective inhibitor of PDGFR¦Á/¦Â with IC50 of 10 nM/1 nM, exhibits >450-fold selectivity over other angiogenic receptors, has antiangiogenic and antitumor activity.

prudect name : CP 673451 is a selective inhibitor of PDGFR¦Á/¦Â with IC50 of 10 nM/1 nM, exhibits >450-fold selectivity over other angiogenic receptors, has antiangiogenic and antitumor activity.CP 673451…

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Cimetidine is a histamine-2 (H2) receptor antagonist.

prudect name : Cimetidine is a histamine-2 (H2) receptor antagonist.Cimetidine Synonyms: CAS NO: 51481-61-9Molecular Formula: C10H16N6SMolecular Weight: 252.34Purity: 98% minSolubility: DMSOStorage: -20¡æ GBR-12909 References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/18507566

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prudect name : Carfilzomib (PR-171)Synonyms: Carfilzomib (PR-171)CAS NO: 868540-17-4Molecular Formula: C40H57N5O7Molecular Weight: 719.91Purity: 98%Solubility: In

prudect name : Carfilzomib (PR-171) Synonyms: Carfilzomib (PR-171)CAS NO: 868540-17-4Molecular Formula: C40H57N5O7Molecular Weight: 719.91Purity: 98%Solubility: In DMSOStorage: −20°C Vistusertib References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/18507540

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prudect name : CDDO-Methyl ester,TP-155CSynonyms: CAS NO: 218600-53-4Molecular Formula: C32H43NO4Molecular Weight: 505.69Purity: 98% minSolubility: In

prudect name : CDDO-Methyl ester,TP-155C Synonyms: CAS NO: 218600-53-4Molecular Formula: C32H43NO4Molecular Weight: 505.69Purity: 98% minSolubility: In DMSOStorage: -20°C BI-2536 References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/18507499

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prudect name : c-FMS inhibitorSynonyms: 4-Cyano-N-[4-(4-methyl-1-piperazinyl)-2-(4-methyl-1-piperidinyl)phenyl]-1H-pyrrole-2-carboxamideCAS NO: 885704-21-2Molecular Formula: C23H30N6OMolecular Weight: 406.52Purity: 98% minSolubility: In

prudect name : c-FMS inhibitor Synonyms: 4-Cyano-N-[4-(4-methyl-1-piperazinyl)-2-(4-methyl-1-piperidinyl)phenyl]-1H-pyrrole-2-carboxamideCAS NO: 885704-21-2Molecular Formula: C23H30N6OMolecular Weight: 406.52Purity: 98% minSolubility: In DMSOStorage: -20°C Ricolinostat References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/1850745

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Clarithromycin for the semi-synthetic macrolide antibiotic, with bacterial 50S ribosomal subunits, thus inhibiting its role in protein synthesis and antibiotic production

prudect name : Clarithromycin for the semi-synthetic macrolide antibiotic, with bacterial 50S ribosomal subunits, thus inhibiting its role in protein synthesis and antibiotic productionClarithromycin Synonyms: CAS NO: 81103-11-9Molecular Formula: C38H69NO13Molecular…

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Cobicistat is a drug under experimental investigation for use in the treatment of infection with the human immunodeficiency virus (HIV). Like ritonovir (Norvir), cobicistat is of interest not for its anti-HIV properties, but rather its ability to inhibit liver enzymes that metabolize other medications used to treat HIV, notably elvitegravir, an HIV integrase inhibitor currently under investigation itself. By combining cobicistat with elvitegravir, higher concentrations of elvitgravir are achieved in the body with lower dosing, theoretically enhancing elvitgravir¡¯s viral suppression while diminishing its adverse side-effects. In contrast with ritonavir, the only currently approved booster, cobicistat has no anti-HIV activity of its own¡­From Wikipedia.

prudect name : Cobicistat is a drug under experimental investigation for use in the treatment of infection with the human immunodeficiency virus (HIV). Like ritonovir (Norvir), cobicistat is of interest…

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CH5132799 is a novel and selective class I PI3K inhibitor with IC50 of 0.014, 0.12, 0.5, 0.036, 5.3 and 1.6 ¦ÌM for PI3K¦Á, PI3K¦Â, PI3K¦Ä, PI3K¦Ã, PI3K C2¦Â and mTOR, respectively.

prudect name : CH5132799 is a novel and selective class I PI3K inhibitor with IC50 of 0.014, 0.12, 0.5, 0.036, 5.3 and 1.6 ¦ÌM for PI3K¦Á, PI3K¦Â, PI3K¦Ä, PI3K¦Ã, PI3K…

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Department of the Swiss Sandoz clozapine (the predecessor of Novartis) in 1961 and the successful development of antipsychotic drugs and are diphenyl compounds of nitrous Zhuoyan Sheng property

prudect name : Department of the Swiss Sandoz clozapine (the predecessor of Novartis) in 1961 and the successful development of antipsychotic drugs and are diphenyl compounds of nitrous Zhuoyan Sheng…

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