2. Natural Products
  3. Plants Flavonoids
  4. Lauraceae Flavanols
  5. Machilus thunbergii Sieb. et Zucc.
  6. 5,7,3'-Tri-O-methyl (-)-epicatechin

5,7,3' -tri-O-Methyl (-)-epicatechin (Compound 13) is a phospholipase Cγ1 (PLCγ1) inhibitor. 5,7,3' -tri-o-methyl (-)-epicatechin has a methylene dioxy benzene ring and can express inhibitory activity against PLCγ1. 5,7,3' -tri-O-Methyl (-)-epicatechin can be used in the study of chemotherapy and chemopexic agents for cancer .

For research use only. We do not sell to patients.

5,7,3'-Tri-O-methyl (-)-epicatechin Chemical Structure

5,7,3'-Tri-O-methyl (-)-epicatechin Chemical Structure

CAS No. : 97914-19-7

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Based on 1 publication(s) in Google Scholar

5,7,3'-Tri-O-methyl (-)-epicatechin Related Antibodies

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Description

5,7,3' -tri-O-Methyl (-)-epicatechin (Compound 13) is a phospholipase Cγ1 (PLCγ1) inhibitor. 5,7,3' -tri-o-methyl (-)-epicatechin has a methylene dioxy benzene ring and can express inhibitory activity against PLCγ1. 5,7,3' -tri-O-Methyl (-)-epicatechin can be used in the study of chemotherapy and chemopexic agents for cancer [1].

Molecular Weight

332.35

Formula

C18H20O6
CAS No.
SMILES

O[C@H]1[C@@H](C2=CC=C(O)C(OC)=C2)OC3=CC(OC)=CC(OC)=C3C1
Structure Classification
Initial Source
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Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
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5,7,3'-Tri-O-methyl (-)-epicatechin Related Classifications

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

5,7,3'-Tri-O-methyl (-)-epicatechin97914-19-7Othersmachilus thunbergfilauraceaephospholipase Cγ1lignanflavanmethylene dioxy groupantiproliferation of human cancer cellsInhibitorinhibitorinhibit

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