prudect name : TISSUE PLASMINOGEN ACTIVATOR, HUMANSynonyms: CAS NO: 189263-81-8Molecular Formula: C40H32N2Molecular Weight: Purity: 99%

June 21, 2017

prudect name : TISSUE PLASMINOGEN ACTIVATOR, HUMAN Synonyms: CAS NO: 189263-81-8Molecular Formula: C40H32N2Molecular Weight: Purity: 99% minSolubility: Storage: web site: www.medchemexpress.com

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prudect name : TAK-715Synonyms: CAS NO: 303162-79-0Molecular Formula: C24H21N3OSMolecular Weight: 399.51Purity: 98% minSolubility: In DMSOStorage:

prudect name : TAK-715 Synonyms: CAS NO: 303162-79-0Molecular Formula: C24H21N3OSMolecular Weight: 399.51Purity: 98% minSolubility: In DMSOStorage: -20°C web site: www.medchemexpress.com

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TSU-68 has significant antitumor activity against many types of tumor xenograft explants in athymic mice. TSU-68 inhibits angiogenesis through several mechanisms, including the induction of apoptosis in vascular endothelial cells and tumor cells, resulting in perturbing existing tumor vascular function and also inhibiting newly synthesis angiogenesis for the tumor growth.

prudect name : TSU-68 has significant antitumor activity against many types of tumor xenograft explants in athymic mice. TSU-68 inhibits angiogenesis through several mechanisms, including the induction of apoptosis in…

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prudect name : Tris(2-phenylpyridine)iridiumSynonyms: Ir(ppy)3CAS NO: 94928-86-6Molecular Formula: C33H27IrN3Molecular Weight: 657.80Purity: 99% minSolubility: Storage:

prudect name : Tris(2-phenylpyridine)iridium Synonyms: Ir(ppy)3CAS NO: 94928-86-6Molecular Formula: C33H27IrN3Molecular Weight: 657.80Purity: 99% minSolubility: Storage: web site: www.medchemexpress.com

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prudect name : Tris[1-phenylisoquinoline-C2,N]iridium(III)Synonyms: Ir(piq)3CAS NO: 435293-93-9Molecular Formula: C45H30IrN3Molecular Weight: 804.96Purity: 99% minSolubility: Storage:

prudect name : Tris[1-phenylisoquinoline-C2,N]iridium(III) Synonyms: Ir(piq)3CAS NO: 435293-93-9Molecular Formula: C45H30IrN3Molecular Weight: 804.96Purity: 99% minSolubility: Storage: web site: www.medchemexpress.com

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Telatinib has 0.66, 0.17, and 2.5 times higher IC50 values for VEGFR3, c-Kit, and PDGFRยฆร‚ than VEGFR2, respectively, while Vatalanib exhibits 18, 20, and 16 times higher IC50 values, respectively, indicating that Telatinib has potential benefit over Vatalanib. Telatinib inhibits VEGFR2 autophosphorylation in a whole-cell assay with an IC50 of 19 nM, suppresses VEGF-dependent proliferation of human umbilical vein endothelial cells with an IC50 of 26 nM, and blocks PDGF-stimulated growth of human aortic smooth muscle cells with an IC50 of 249 nM.Telatinib displays little inhibitory activity against the Raf kinase pathway, epidermal growth factor receptor family, the fibroblast growth factor receptor (FGFR) family, and the Tie-2 receptor.

prudect name : Telatinib has 0.66, 0.17, and 2.5 times higher IC50 values for VEGFR3, c-Kit, and PDGFRยฆร‚ than VEGFR2, respectively, while Vatalanib exhibits 18, 20, and 16 times higher…

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FK-506 inhibits Ca2+-dependent transcription of lymphokine genes in T cells. FK-506 (0.1 to 300 nM) concentration dependently inhibited histamine release from lung parenchymal mast cells activated by anti-IgE. FK-506 was more potent in lung mast cells than in basophils (IC50 = 1.13 +/- 0.46 nM vs 5.28 +/- 0.88 nM; p less than 0.001), whereas the maximal inhibitory effect was higher in basophils than in lung mast cells (88.4 +/- 2.5% vs 76.4 +/- 3.8%; p less than 0.01). FK-506 (1 to 300 nM) concentration dependently inhibited histamine release from basophils activated by Der p I Ag, anti-IgE, or compound A23187. FK-506 was more potent than CsA when basophils were challenged with Ag (IC50 = 25.5 +/- 9.5 vs 834.3 +/- 79.8 nM; p less than 0.001), anti-IgE (IC50 = 9.4 +/- 1.7 vs 441.3 +/- 106.7 nM; p less than 0.001), and A23187 (IC50 = 4.1 +/- 0.9 vs 36.7 +/- 3.8 nM; p less than 0.001). The maximal inhibitory effect of FK-506 was higher than that caused by CsA when basophils were activated by Der p I (80.0 +/- 3.6 vs 49.5 +/- 4.7%; p less than 0.001) and anti-IgE (90.4 +/- 1.8 vs 62.3 +/- 2.9%; p less than 0.001).

prudect name : FK-506 inhibits Ca2+-dependent transcription of lymphokine genes in T cells. FK-506 (0.1 to 300 nM) concentration dependently inhibited histamine release from lung parenchymal mast cells activated by…

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prudect name : Triethyl 3-bromopropane-1,1,1-tricarboxylateSynonyms: CAS NO: 71170-82-6Molecular Formula: C12H19BrO6Molecular Weight: 339.18Purity: 98%Solubility: Storage: −20°C

prudect name : Triethyl 3-bromopropane-1,1,1-tricarboxylate Synonyms: CAS NO: 71170-82-6Molecular Formula: C12H19BrO6Molecular Weight: 339.18Purity: 98%Solubility: Storage: −20°C 2 years web site: www.medchemexpress.com

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prudect name : TafluprostSynonyms: CAS NO: 209860-87-7Molecular Formula: C25H34F2O5Molecular Weight: C25H34F2O5Purity: 99%Solubility: Storage: −20°C

prudect name : Tafluprost Synonyms: CAS NO: 209860-87-7Molecular Formula: C25H34F2O5Molecular Weight: C25H34F2O5Purity: 99%Solubility: Storage: −20°C web site: www.medchemexpress.com

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prudect name : Treprostinil sodiumSynonyms: Uniprost,LRX-15,U-62840CAS NO: 289480-64-4Molecular Formula: C23H33NaO5Molecular Weight: 412.4987Purity: 99%Solubility: Storage: -20°C

prudect name : Treprostinil sodium Synonyms: Uniprost,LRX-15,U-62840CAS NO: 289480-64-4Molecular Formula: C23H33NaO5Molecular Weight: 412.4987Purity: 99%Solubility: Storage: -20°C web site: www.medchemexpress.com

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