74805-91-7

Methylophiopogonanone B Chemical Structure
74805-91-7

Chemical Structure

Methylophiopogonanone B

  • CAS No.: 74805-91-7
  • Formula:C19H20O5
  • Molecular Weight:328.36

IUPAC Name: (R)-5,7-dihydroxy-3-(4-methoxybenzyl)-6,8-dimethylchroman-4-one

InChIKey: UFMAZRUMVFVHLY-CYBMUJFWSA-N

SMILES: O=C1[C@H](CC2=CC=C(OC)C=C2)COC3=C(C)C(O)=C(C)C(O)=C13

Biological Activity: Methylophiopogonanone B is a homoisoflavonoid compound. Methylophiopogonanone B can be isolated from O. japonicus root. Methylophiopogonanone B promotes Rho activation and Tubulin depolymerization. Methylophiopogonanone B significantly increases GTP-Rho, but not GTP-Rac or GTP-CDC42. Methylophiopogonanone B induces cell morphological change via melanocyte dendrite retraction and stress fiber formation. Methylophiopogonanone B exhibits strong antioxidant activity. Methylophiopogonanone B can be used in the research of cervical cancer[1][2].

Cat. No. Product Name Purity Description Pricing
HY-N2438
Methylophiopogonanone B 99.84% Methylophiopogonanone B is a homoisoflavonoid compound. Methylophiopogonanone B can be isolated from O. japonicus root. Methylophiopogonanone B promotes Rho activation and Tubulin depolymerization. Methylophiopogonanone B significantly increases GTP-Rho, but not GTP-Rac or GTP-CDC42. Methylophiopogonanone B induces cell morphological change via melanocyte dendrite retraction and stress fiber formation. Methylophiopogonanone B exhibits strong antioxidant activity. Methylophiopogonanone B can be used in the research of cervical cancer.
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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References