Levistilide A
CAS No. 88182-33-6
Levistilide A( Levistilide A | Levistilide-A )
Catalog No. M19222 CAS No. 88182-33-6
Levistilide A inhibits liver fibrosis and angiogenesis.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 126 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameLevistilide A
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NoteResearch use only, not for human use.
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Brief DescriptionLevistilide A inhibits liver fibrosis and angiogenesis.
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DescriptionLevistilide A is a P-gp modulator. It acts by overcoming P-glycoprotein-mediated drug resistance in human breast carcinoma cells.
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In Vitro——
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In Vivo——
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SynonymsLevistilide A | Levistilide-A
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research AreaOthers-Field
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Indication——
Chemical Information
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CAS Number88182-33-6
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Formula Weight380.48
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Molecular FormulaC24H28O4
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (262.83 mM)
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SMILESCCCC=C1C2=C(C3C(CC2)C4CCC35C(=C4)C(=O)OC5=CCCC)C(=O)O1
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Chemical Name(1Z,5S,5aS,8Z,10bS,10cS)-1,8-Dibutylidene-5,5a,6,7-tetrahydro-1H-5,10c-ethanonaphtho[1,2-c:7,8-c']difuran-3,10(8H,10bH)-dione
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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Ethyl potassium malo...
Ethyl potassium malonate, a competitive inhibitor of the enzyme succinate dehydrogenase, acts as a precursor to produce (trimethylsilyl)ethyl malonate, which is utilized to prepare beta-ketoesters by acylation and serves as an intermediate for the preparation of ethyl tert-butyl malonate.
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Somatostatin-25
Somatostatin is an endogenous neuropeptide hormone found in the brain and pancreas. Somatostatin binds several isoforms of the somatostatin receptor, exhibiting anxiolytic, antiepileptic/anticonvulsant, and anorexigenic activities.
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7-Methyl-6-mercaptop...
7-Methyl-6-mercaptopurine is an inhibitor of PRPP aminotransferase, inhibits IMP metabolism and prevents purine, DNA and RNA synthesis.
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