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Pseudoaspidin
CAS No. 478-28-4
Pseudoaspidin( —— )
Catalog No. M18600 CAS No. 478-28-4
Pseudoaspidin is isolated from the ferns of the class Pterophyta or Filicinae.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NamePseudoaspidin
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NoteResearch use only, not for human use.
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Brief DescriptionPseudoaspidin is isolated from the ferns of the class Pterophyta or Filicinae.
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DescriptionPseudoaspidin is isolated from the ferns of the class Pterophyta or Filicinae.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number478-28-4
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Formula Weight460.52
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Molecular FormulaC25H32O8
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Purity>98% (HPLC)
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Solubility——
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SMILESCCCC(=O)C1=C(C(=C(C(=C1O)CC2=C(C(=C(C(=C2O)C)OC)C(=O)CCC)O)O)C)OC
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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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CRF, bovine TFA (923...
CRF, bovine (TFA) is a potent agonist of CRF receptor, and displaces [125I-Tyr]ovine CRF with a Ki of 3.52 nM.CRF, bovine is a potent agonist of CRF receptor, and displaces [125I-Tyr]ovine CRF with a Ki of 3.52 nM. CRF shows pEC50s of 11.16, 8.53 and 8.70 for human CRF1, human CRF2 and rat CRF2α.
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Fumonisin B1
Fumonisin B1 is a mycotoxin produced from Fusarium moniliforme. Fumonisin B1 is a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase) and disrupts de novo sphingolipid biosynthesis.Fumonisin B1 is the most abundant and toxic fumonisin.
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McN3716
Inhibition of brain mitochondrial β-oxidation by McN3716 (Methyl palmoxirate, MEP) significantly reduces the levels of all measured HETE and epoxytrienoic acids (EET), nonenzymatic auto-oxidative metabolites of ARA.
