GLPG0187 10 mg | 100.00%
TargetMol
GLPG0187, a broad spectrum integrin receptor antagonist, inhibits αvβ1-integrin (IC50: 1.3 nM).
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GLPG0187 5 mg | 100.00%
TargetMol
GLPG0187, a broad spectrum integrin receptor antagonist, inhibits αvβ1-integrin (IC50: 1.3 nM).
More Information Supplier PageGLPG0187
GLPG0187 1 mg | 100.00%
TargetMol
GLPG0187, a broad spectrum integrin receptor antagonist, inhibits αvβ1-integrin (IC50: 1.3 nM).
More Information Supplier PageGLPG0187
BQR-695 25 mg | 100.00%
TargetMol
BQR-695 (NVP-BQR695) is a phosphatidylinositol 4-kinase (PI4K) inhibitor with IC50s of 80 and 3.5 nM for human PI4KIIIβ and Plasmodium variant of PI4KIIIβ, respectively.
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Neoandrographolide 25 mg | 98.52%
TargetMol
Neoandrographolide has potent hypolipidemic effect and protects the cardiovascular without significant liver damage.Neoandrographolide has anti-inflammatory effect, might result from inhibition of iNOS and COX-2 expression through inhibiting p38 MAPKs activation.Neoandrographolide as chemosensitizer in S-Jurkat and X chromosome-linked inhibitor of apoptosis protein (XIAP)-overexpressing Jurkat cells, a model for chemoresistance.
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Verbenalin 25 mg | 99.88%
TargetMol
Verbenalin induces angiogenesis via a programmed PI3K/Akt/eNOS/VEGF signaling axis.
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Angoroside C 25 mg | 98.27%
TargetMol
Angoroside C is a Potential anti-inflammatory compound. Inhibitor of prostaglandin E2 release in mouse peritoneal macrophages in vitro. Shows potent antioxidative activity in reducing the oxidized OH adducts of dAMP and dGMP. Reveals some trypanocidal potential.
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Ginsenoside Rb3 25 mg | 99.98%
TargetMol
Ginsenoside Rb3 is a natural triterpenoid saponin, exhibiting inhibition effect on TNFα-induced NF-κB transcriptional activity. It also inhibits the induction of COX-2 and iNOS mRNA.
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Complanatoside A 25 mg | Purity Not Available
TargetMol
Complanatoside A is a flavonol glycoside isolated from Astragalus complanatus.
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Jatrorrhizine 10 mg | 98.59%
TargetMol
Jatrorrhizine is a protoberberine alkaloid isolated from Enantia chlorantha (Annonaceae) and other species. It was found to have antimicrobial and antifungal activity. It binds and noncompetitively inhibits monoamine oxidase (IC50 4 micromolar for MAO-A and 62 for MAO-B).
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