VD/VDR-vd-vdr.com

prudect name : TeniposideSynonyms: CAS NO: 29767-20-2Molecular Formula: C32H32O13SMolecular Weight: 656.66Purity: 98% minSolubility: In DMSOStorage:

June 21, 2017

prudect name : Teniposide Synonyms: CAS NO: 29767-20-2Molecular Formula: C32H32O13SMolecular Weight: 656.66Purity: 98% minSolubility: In DMSOStorage: −20°C web site: www.medchemexpress.com

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liquid crystal intermediates

prudect name : liquid crystal intermediatestrans-(4-Propylcyclohexyl)benzene Synonyms: CAS NO: 61203-94-9Molecular Formula: C15H22Molecular Weight: 202.34Purity: 99% minSolubility: Storage: web site: www.medchemexpress.com

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Trelagliptin is a long acting dipeptidyl peptidase-4 (DPP-4) inhibitor that is being developed for the treatment of type 2 diabetes (T2D). Two Phase II clinical studies have been completed with Efficacy and Safety of SYR-472 in Subjects With Type 2 Diabetes Mellitus. Phase III clinical studies with trelagliptin in Japan to evaluate its safety and efficacy in a once-weekly oral treatment regimen. Currently, all available DPP-4 inhibitors are dosed once-daily. A once-weekly treatment, such as trelagliptin, would provide patients with a convenient treatment alternative and has the potential to improve treatment compliance.

prudect name : Trelagliptin is a long acting dipeptidyl peptidase-4 (DPP-4) inhibitor that is being developed for the treatment of type 2 diabetes (T2D). Two Phase II clinical studies have…

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TGR-1202, also known as RP5264 , is a highly specific, orally available, PI3K delta inhibitor, targeting the delta isoform with nanomolar potency and several fold selectivity over the alpha, beta, and gamma isoforms of PI3K. Inhibition of PI3K delta signaling with TGR-1202 has demonstrated robust activity in numerous pre-clinical models and primary cells from patients with hematologic malignancies.

prudect name : TGR-1202, also known as RP5264 , is a highly specific, orally available, PI3K delta inhibitor, targeting the delta isoform with nanomolar potency and several fold selectivity over…

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N-[2-[2-(Hydroxyamino)-2-oxoethyl]-4-methyl-1-oxopentyl]-3-(2-naphthalenyl)-L-alanyl-N-(2-aminoethyl)-L-alaninamide

prudect name : N-[2-[2-(Hydroxyamino)-2-oxoethyl]-4-methyl-1-oxopentyl]-3-(2-naphthalenyl)-L-alanyl-N-(2-aminoethyl)-L-alaninamideTAPI-1 Synonyms: CAS NO: 171235-71-5Molecular Formula: C26H37N5O5Molecular Weight: 499.60Purity: 98% minSolubility: In DMSOStorage: -20 oC web site: www.medchemexpress.com

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N-[(5-Bromo-2-thienyl)sulfonyl]-2,4-dichlorobenzamide sodium salt; LY 573636Na

prudect name : N-[(5-Bromo-2-thienyl)sulfonyl]-2,4-dichlorobenzamide sodium salt; LY 573636NaTasisulam sodium LY-573636 Synonyms: CAS NO: 519055-63-1Molecular Formula: C11H6BrCl2NO3S2.NaMolecular Weight: 438.09Purity: 98% minSolubility: In DMSOStorage: -20°C web site: www.medchemexpress.com

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TAK-901 is a small-molecule inhibitor of the serine-threonine kinase Aurora B with potential antineoplastic activity. Aurora B is a positive regulator of mitosis that functions in the attachment of the mitotic spindle to the centromere. This serine/threonine kinase may be amplified and overexpressed by a variety of cancer cell types. After binding of TAK-901 to Aurora B, it inhibits the activity of Aurora B, which may result in a reduction in the proliferation of tumor cells that overexpress Aurora B. TAK-901 is originally developed by Millennium Pharmaceuticals, Inc.. And TAK-901 is been performed phase I clinical trials for the treatment of advanced solid tumors and lymphoma.

prudect name : TAK-901 is a small-molecule inhibitor of the serine-threonine kinase Aurora B with potential antineoplastic activity. Aurora B is a positive regulator of mitosis that functions in the…

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Tenovin-6 is the water soluble analog of Tenovin-1 (HY-13423) and acts as a potent SIRT1 (IC50=21 uM) and SIRT2 (IC50= 10 uM) inhibitor as well as p53 activator.

prudect name : Tenovin-6 is the water soluble analog of Tenovin-1 (HY-13423) and acts as a potent SIRT1 (IC50=21 uM) and SIRT2 (IC50= 10 uM) inhibitor as well as p53…

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TAK-700 is a type of selective effect of oral non-steroidal androgen synthesis inhibitors. Pre-clinical results show that it can selectively lock and inhibit the testes and adrenal glands among the 17, 20 carbon chain cleavage enzyme

prudect name : TAK-700 is a type of selective effect of oral non-steroidal androgen synthesis inhibitors. Pre-clinical results show that it can selectively lock and inhibit the testes and adrenal…

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Tigecycline is a glycylcycline antibiotic. It was developed in response to the growing prevalence of antibiotic resistance in bacteria such as Staphylococcus aureus and acinetobacter baumanii.

prudect name : Tigecycline is a glycylcycline antibiotic. It was developed in response to the growing prevalence of antibiotic resistance in bacteria such as Staphylococcus aureus and acinetobacter baumanii.Tigecycline Synonyms:…

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