CSNpharm
Tuberostemonine is a natural product isolated from the roots of Stemona japonica, which shows therapeutic effects against cigarette smoke-induced acute lung inflammation in mice and acts as an open-channel blocker at the crayfish neuromuscular junction.
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CSNpharm
Tuberostemonine is a natural product isolated from the roots of Stemona japonica, which shows therapeutic effects against cigarette smoke-induced acute lung inflammation in mice and acts as an open-channel blocker at the crayfish neuromuscular junction.
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CSNpharm
Tuberostemonine is a natural product isolated from the roots of Stemona japonica, which shows therapeutic effects against cigarette smoke-induced acute lung inflammation in mice and acts as an open-channel blocker at the crayfish neuromuscular junction.
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CSNpharm
Tuberostemonine is a natural product isolated from the roots of Stemona japonica, which shows therapeutic effects against cigarette smoke-induced acute lung inflammation in mice and acts as an open-channel blocker at the crayfish neuromuscular junction.
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CSNpharm
Tubulin inhibitor 6 (Compound 14b) is a tubulin inhibitor and a potent inhibitor of multiple cancer cell lines. Tubulin inhibitor 6 inhibits tubulin polymerization with an IC50 of 0.87 μM. Tubulin inhibitor 6 inhibits K562 cell growth with an IC50 of 840 nM[1].
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CSNpharm
Tubulin inhibitor 6 (Compound 14b) is a tubulin inhibitor and a potent inhibitor of multiple cancer cell lines. Tubulin inhibitor 6 inhibits tubulin polymerization with an IC50 of 0.87 μM. Tubulin inhibitor 6 inhibits K562 cell growth with an IC50 of 840 nM[1].
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CSNpharm
Tuftsin is a macrophage/microglial activator that dramatically improves the clinical course of experimental autoimmune encephalomyelitis.
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CSNpharm
Tuftsin is a macrophage/microglial activator that dramatically improves the clinical course of experimental autoimmune encephalomyelitis.
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CSNpharm
Tuftsin is a macrophage/microglial activator that dramatically improves the clinical course of experimental autoimmune encephalomyelitis.
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Tylosin is a macrolide antibiotic and a bacteriostatic feed additive used in veterinary medicine with a broad spectrum of activity against Gram-positive organisms and a limited range of Gram-negative organisms.
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CSNpharm
Tylosin is a macrolide antibiotic and a bacteriostatic feed additive used in veterinary medicine with a broad spectrum of activity against Gram-positive organisms and a limited range of Gram-negative organisms.
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CSNpharm
Tylosin Tartrate is a macrolide antibiotic and a bacteriostatic feed additive used in veterinary medicine with a broad spectrum of activity against Gram-positive organisms and a limited range of Gram-negative organisms.
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CSNpharm
Tylosin Tartrate is a macrolide antibiotic and a bacteriostatic feed additive used in veterinary medicine with a broad spectrum of activity against Gram-positive organisms and a limited range of Gram-negative organisms.
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CSNpharm
Typhaneoside, extracted from Typha angustifolia L., Typhaneoside can inhibit the excessive autophagy of hypoxia/reoxygenation cells and increase the phosphorylation of Akt and mTOR. Typhaneoside has certain effects on the cardiovascular system, including lowering blood lipid levels, promoting antiatherosclerosis activities, as well as improving immune and coagulation function[1].
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CSNpharm
Typhaneoside, extracted from Typha angustifolia L., Typhaneoside can inhibit the excessive autophagy of hypoxia/reoxygenation cells and increase the phosphorylation of Akt and mTOR. Typhaneoside has certain effects on the cardiovascular system, including lowering blood lipid levels, promoting antiatherosclerosis activities, as well as improving immune and coagulation function[1].
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CSNpharm
Typhaneoside, extracted from Typha angustifolia L., Typhaneoside can inhibit the excessive autophagy of hypoxia/reoxygenation cells and increase the phosphorylation of Akt and mTOR. Typhaneoside has certain effects on the cardiovascular system, including lowering blood lipid levels, promoting antiatherosclerosis activities, as well as improving immune and coagulation function[1].
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CSNpharm
Typhaneoside, extracted from Typha angustifolia L., Typhaneoside can inhibit the excessive autophagy of hypoxia/reoxygenation cells and increase the phosphorylation of Akt and mTOR. Typhaneoside has certain effects on the cardiovascular system, including lowering blood lipid levels, promoting antiatherosclerosis activities, as well as improving immune and coagulation function[1].
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CSNpharm
Tyrphostin A1 inhibits CD40L-stimulated IL-12 production in macrophage cultures and antigen-induced generation of Th1 cells.
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CSNpharm
Tyrphostin A1 inhibits CD40L-stimulated IL-12 production in macrophage cultures and antigen-induced generation of Th1 cells.
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CSNpharm
Tyrphostin AG 30 is an antimicrobial peptide with angiogenic properties. It activates human mast cells through the MAPK and NF-κB pathways.
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CSNpharm
Tyrphostin AG 30 is an antimicrobial peptide with angiogenic properties. It activates human mast cells through the MAPK and NF-κB pathways.
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CSNpharm
Tyrphostin AG 30 is an antimicrobial peptide with angiogenic properties. It activates human mast cells through the MAPK and NF-κB pathways.
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CSNpharm
Tyrphostin AG 879 potently inhibits HER2/ErbB2 with IC50 of 1 μM, 100- and 500-fold higher selective to ErbB2 than PDGFR and EGFR.
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CSNpharm
Tyrphostin AG 879 potently inhibits HER2/ErbB2 with IC50 of 1 μM, 100- and 500-fold higher selective to ErbB2 than PDGFR and EGFR.
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CSNpharm
Tyrphostin AG 879 potently inhibits HER2/ErbB2 with IC50 of 1 μM, 100- and 500-fold higher selective to ErbB2 than PDGFR and EGFR.
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CSNpharm
Tyrphostin AG 879 potently inhibits HER2/ErbB2 with IC50 of 1 μM, 100- and 500-fold higher selective to ErbB2 than PDGFR and EGFR.
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CSNpharm
Tyrphostin AG 879 potently inhibits HER2/ErbB2 with IC50 of 1 μM, 100- and 500-fold higher selective to ErbB2 than PDGFR and EGFR.
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CSNpharm
Tyrphostin AG1433 is a tyrosine kinases inhibitor and also a selective PDGFRβ and VEGFR-2 (Flk-1/KDR) inhibitor with IC50s of 5.0 μM and 9.3 μM, respectively.
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CSNpharm
Tyrphostin AG1433 is a tyrosine kinases inhibitor and also a selective PDGFRβ and VEGFR-2 (Flk-1/KDR) inhibitor with IC50s of 5.0 μM and 9.3 μM, respectively.
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CSNpharm
Tyrphostin AG1433 is a tyrosine kinases inhibitor and also a selective PDGFRβ and VEGFR-2 (Flk-1/KDR) inhibitor with IC50s of 5.0 μM and 9.3 μM, respectively.
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CSNpharm
Tyrphostin AG1433 is a tyrosine kinases inhibitor and also a selective PDGFRβ and VEGFR-2 (Flk-1/KDR) inhibitor with IC50s of 5.0 μM and 9.3 μM, respectively.
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U-104
50mg
| ≥99%
CSNpharm
U-104 is a potent carbonic anhydrase (CA) inhibitor with Ki of 45.1 nM and 4.5 nM for CA IX and CA XII, respectively.
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U-104
10mg
| ≥99%
CSNpharm
U-104 is a potent carbonic anhydrase (CA) inhibitor with Ki of 45.1 nM and 4.5 nM for CA IX and CA XII, respectively.
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U-104
5mg
| ≥99%
CSNpharm
U-104 is a potent carbonic anhydrase (CA) inhibitor with Ki of 45.1 nM and 4.5 nM for CA IX and CA XII, respectively.
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U-74389G is an antioxidant which prevents iron-dependent lipid peroxidation. It protects against ischemia-reperfusion injury in animal heart, liver, and kidney models.
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CSNpharm
U-74389G is an antioxidant which prevents iron-dependent lipid peroxidation. It protects against ischemia-reperfusion injury in animal heart, liver, and kidney models.
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CSNpharm
U-74389G is an antioxidant which prevents iron-dependent lipid peroxidation. It protects against ischemia-reperfusion injury in animal heart, liver, and kidney models.
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CSNpharm
Bunaprolast is a potent inhibitor of LTB4 production in human whole blood and also exhibits significant inhibition of lipoxygenase and TXB2 release.
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