| Cat.No. | Name | Information |
|---|---|---|
| M39159 | Epitheaflagallin 3-O-gallate | Epitheaflagallin 3-O-gallate is a minor polyphenol in black tea. Epitheaflagallin 3-O-gallate exhibits antioxidative activity, pancreatic lipase inhibition, and an inhibiting effect on the activity of matrix metalloprotease-1 and -3 and their synthesis by human gingival fibroblasts. |
| M39158 | Genistein 8-c-glucoside | Genistein 8-c-glucoside (G8CG) is a glucoside. Genistein 8-c-glucoside induces mitochondrial membrane depolarization and induces apoptosis. |
| M39157 | Plathymenin | Plathymenin is a flavonoid that can be isolated from Nepalese propolis. Plathymenin is a potent inhibitor of 5-LOX. |
| M39156 | 2,3,4'-Trihydroxy-3',5'-dimethoxypropiophenone | 2,3,4'-Trihydroxy-3',5'-dimethoxypropiophenone, isolated from Parinari hypochrysea (Chrysobalanaceae), exhibits antioxidant and lipoxygenase inhibition. |
| M39155 | Linoleyl methane sulfonate | Linoleyl methane sulfonate is a selective lipid-based vehicle for use in drug delivery systems. |
| M39153 | Integracin B | Integracin B is a potent dimeric alkyl aromatic inhibitor of HIV-1 integrase discovered from the screening of fungal extracts using an in vitro assay. Integracin B inhibits both coupled and strand transfer activity of HIV-1 integrase. |
| M39152 | Anonaine | Anonaine is an antiparasitic agent. Anonaine also is a glutathione S-transferase (GST) inhibitor. |
| M39150 | Kojibiose | Kojibiose can specifically inhibit the activity of α-glucosidase I. Kojibiose exhibits antitoxic activity. Kojibiose reduces hepatic expression of inflammatory markers in vivo. |
| M39149 | Terphenyllin | Terphenyllin is a naturally abundant p-terphenyl metabolite isolated from the coral derived fungus Aspergillus candidus, has significant α-glucosidase inhibitory activity. |
| M39147 | β-Hydroxypropiovanillone | β-Hydroxypropiovanillone, a natural compound, shows significant concentration-dependent inhibitory effects on α-glucosidase with an IC50 of 257.8 μg/mL. |
| M39146 | 6-Prenylquercetin-3-Me ether | 6-Prenylquercetin-3-Me ether is a natural product that can be extracted from G. uralensis leaves. 6-Prenylquercetin-3-Me ether has radical scavenging activity toward DPPH. 6-Prenylquercetin-3-Me ether also has inhibitory activity against α-glucosidase. |
| M39145 | Prunetin 5-O-β-D-glucopyranoside | Prunetin 5-O-β-D-glucopyranoside is a potent and uncompetitive inhibitor of α-glucosidase, with an IC50 of 56.05 μg/mL. Prunetin 5-O-β-D-glucopyranoside can be used for the research of type-2 diabetes. |
| M39144 | 4-Nitrophenyl a-D-glucopyranoside | 4-Nitrophenyl a-D-glucopyranoside is a chromogenic substrate for α-glucosidase. 4-Nitrophenyl a-D-glucopyranoside can be used to measure of α-glucosidase activity. |
| M39143 | Chrysin 6-C-arabinoside 8-C-glucoside | Chrysin 6-C-arabinoside 8-C-glucoside is a α±-glucosidase inhibitors which are widely used in the study for type 2 diabetes. |
| M39142 | (-)-6β-Hydroxy-5β,8β,9β,10α-cleroda-3,13-dien-16,15-olid-18-oic acid | (-)-6β-Hydroxy-5β,8β,9β,10α-cleroda-3,13-dien-16,15-olid-18-oic acid (compound 4) is a α-Glucosidase inhibitor with an IC50 value of 577.7 µM. |
| M39141 | Nelumol A | Nelumol A is a farnesoid X receptor (FXR) agonist. |
| M39140 | Fargesone A | Fargesone A is a potent and selective FXR agonist. Fargesone A shows anti-inflammatory activity. |
| M39139 | Andrastin A | Andrastin A meroterpenoid compound, is a farnesyltransferase inhibitor. Andrastin A inhibits the efflux of anticancer compounds from multidrug-resistant cancer cells. Andrastin A can be isolated from Penicillium species. |
| M39138 | 5-R-Rivaroxaban | 5-R-Rivaroxaban is (R)-enantiomer of Rivaroxaban. Rivaroxaban (BAY 59-7939) is a highly potent and selective, direct Factor Xa (FXa) inhibitor, achieving a strong gain in anti-FXa potency (IC50 0.7 nM; Ki 0.4 nM). |
| M39136 | D-Lysine | D-Lysine decreases renal uptake of radioactivity during scintigraphy and PRRT with low toxicity. D-Lysine not interferes with the natural amino acid metabolic balance. |
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