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prudect name : Ceftibuten SidechainSynonyms: CAS NO: 115065-79-7Molecular Formula: C21H22N2O6SMolecular Weight: 430.47Purity: 98%Solubility: Storage: −20°C

June 21, 2017

prudect name : Ceftibuten Sidechain Synonyms: CAS NO: 115065-79-7Molecular Formula: C21H22N2O6SMolecular Weight: 430.47Purity: 98%Solubility: Storage: −20°C 2 years TMC207 References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/18506316

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prudect name : Cyclophosphamide monohydrateSynonyms: CAS NO: 6055-19-2Molecular Formula: C7H15Cl2N2O2P.H2OMolecular Weight: 279.10Purity: 99%Solubility: Storage: −20°C

prudect name : Cyclophosphamide monohydrate Synonyms: CAS NO: 6055-19-2Molecular Formula: C7H15Cl2N2O2P.H2OMolecular Weight: 279.10Purity: 99%Solubility: Storage: −20°C 2 years AZD6244 References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/18506208/

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prudect name : Cytarabini HydrochloridumSynonyms: CAS NO: 69-74-9Molecular Formula: C9H14ClN3O5Molecular Weight: 279.68Purity: 99%Solubility: Storage: −20°C

prudect name : Cytarabini Hydrochloridum Synonyms: CAS NO: 69-74-9Molecular Formula: C9H14ClN3O5Molecular Weight: 279.68Purity: 99%Solubility: Storage: −20°C 2 years SCH 727965 References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/1850616

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CCG-1423 is a novel inhibitor of RhoA/C-mediated gene transcription that is capable of inhibiting invasion of PC-3 prostate cancer cells in a Matrigel model of metastasis.

prudect name : CCG-1423 is a novel inhibitor of RhoA/C-mediated gene transcription that is capable of inhibiting invasion of PC-3 prostate cancer cells in a Matrigel model of metastasis.CCG1423;CCG-1423 Synonyms:…

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Cinaciguat (BAY 58-2667) is the first of a new class of soluble guanylate cyclase (sGC) activators in clinical development for acute decompensated heart failure. Cinaciguat has potent preload- and afterload-reducing effects, increasing cardiac output. Cinaciguat causes potent and sustained fetal pulmonary vasodilation that is augmented in the presence of oxidized sGC and speculate that Cinaciguat may have therapeutic potential for severe neonatal pulmonary hypertension.

prudect name : Cinaciguat (BAY 58-2667) is the first of a new class of soluble guanylate cyclase (sGC) activators in clinical development for acute decompensated heart failure. Cinaciguat has potent…

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Chidamide(CS055; HBI-8000) is a class I HDAC inhibitor with IC50s of 95/160/67/733 nM for HDAC1/2/3/8; also inhibits HDAC10/11(IC50=78/432 nM); no inhibition on HDAC4/5/7/9/6(IC50>30 uM).

prudect name : Chidamide(CS055; HBI-8000) is a class I HDAC inhibitor with IC50s of 95/160/67/733 nM for HDAC1/2/3/8; also inhibits HDAC10/11(IC50=78/432 nM); no inhibition on HDAC4/5/7/9/6(IC50>30 uM).Chidamide(CS055; HBI-8000) Synonyms: CAS…

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Clemizole Hcl is a H1 histamine receptor antagonist. Recently, researchers have identified that clemizole hydrochloride can inhibit NS4B¡¯s RNA binding and hepatitis C virus (HCV) replication.

prudect name : Clemizole Hcl is a H1 histamine receptor antagonist. Recently, researchers have identified that clemizole hydrochloride can inhibit NS4B¡¯s RNA binding and hepatitis C virus (HCV) replication.Clemizole hydrochloride…

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prudect name : Calcium folinateSynonyms: CAS NO: 1492-18-8Molecular Formula: C20H21CaN7O7Molecular Weight: 511.5Purity: 99%Solubility: Storage: −20°C

prudect name : Calcium folinate Synonyms: CAS NO: 1492-18-8Molecular Formula: C20H21CaN7O7Molecular Weight: 511.5Purity: 99%Solubility: Storage: −20°C 2 years CB5083 References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/18505993

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RAF265 (CHIR-265) is a derivative of Raf265 that is an oral, highly selective RAF and VEGFR kinase inhibitor with IC50 of of 5 to 10 ¦ÌM. RAF is a key component of the RAS/RAF/MEK/ERK signal-transduction pathway, which controls cell proliferation, differentiation, and apoptosis in mammalian cells. Raf265 also has anti-angiogenic activity through inhibition of vascular endothelial growth factor receptor 2 (VEGFR-2).

prudect name : RAF265 (CHIR-265) is a derivative of Raf265 that is an oral, highly selective RAF and VEGFR kinase inhibitor with IC50 of of 5 to 10 ¦ÌM. RAF…

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CL-387785(EKI785; WAY-EKI 785) is an irreversible inhibitor of EGFR with IC50 of 370+/-120 pM; is able to overcome resistance caused by the T790M mutation on a functional level.

prudect name : CL-387785(EKI785; WAY-EKI 785) is an irreversible inhibitor of EGFR with IC50 of 370+/-120 pM; is able to overcome resistance caused by the T790M mutation on a functional…

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