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Methyl gypsogenin 3-O-beta-D-glucuronopy
Methyl gypsogenin 3-O-beta-D-glucuronopy
CAS No. 96553-02-5
Methyl gypsogenin 3-O-beta-D-glucuronopy( —— )
Catalog No. M19287 CAS No. 96553-02-5
Gypsogenin 3-O-beta-D-glucuronopyranoside shows inhibitory activity toward pancreatic lipase with IC5 value of .29 mM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 85 | In Stock |
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| 2MG | 33 | In Stock |
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| 5MG | 53 | In Stock |
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| 10MG | 93 | In Stock |
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| 25MG | 154 | In Stock |
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| 50MG | 221 | In Stock |
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| 100MG | 332 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameMethyl gypsogenin 3-O-beta-D-glucuronopy
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NoteResearch use only, not for human use.
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Brief DescriptionGypsogenin 3-O-beta-D-glucuronopyranoside shows inhibitory activity toward pancreatic lipase with IC5 value of .29 mM.
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DescriptionGypsogenin 3-O-beta-D-glucuronopyranoside shows inhibitory activity toward pancreatic lipase with IC5 value of .29 mM, and the free carboxylic acid groups in position 28 within its chemical structures are required for enhancement of pancreatic lipase inhibition.
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In VitroTreatment of suspended G. paniculata cells with Methyl gypsogenin-3-O-glucuronide (Gypsogenin-3-O-(6-O-methyl)-glucoside) 24 hours before administration of [14C]acetate results in a marked reduction in the incorporation of radioactivity into saponins and their precursors but not into sterols and steryl glucosides.
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In Vivo——
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Synonyms——
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PathwayCell Cycle/DNA Damage
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TargetPotassium Channel
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Recptorpancreatic lipase
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Research AreaMetabolic Disease
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Indication——
Chemical Information
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CAS Number96553-02-5
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Formula Weight660.84
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Molecular FormulaC37H56O10
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (151.32 mM)
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SMILESCC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C=O)OC6C(C(C(C(O6)C(=O)OC)O)O)O)C)C)C2C1)C)C(=O)O)C
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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5-Hydroxydecanoate s...
5-Hydroxydecanoate sodium is a selective ATP-sensitive K+ (KATP) channel blocker with an IC50 of approximately 30 μM and a substrate for mitochondrial outer membrane acyl-CoA synthetase, possessing antioxidant properties.
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Linoleoyl glycine
Linoleoyl glycine, a modified polyunsaturated fatty acid, is an endogenous homologue of linoleoyl glycine. Linoleoyl glycine activates human KCNQ1/KCNE1 (hKCNQ1/hKCNE1) channels expressed in xenopus oocytes from mammalian skin.
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VU591
VU591 is the first reported selective, small-molecule ROMK inhibitor(IC50 of 0.24 μM).?It inhibits potassium transport in isolated perfused rat collecting duct tubules with no effect on sodium transport.
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