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(S)-Pinocembrin, 98%, from Pinus cerebra|463196|480-39-7

(S)-Pinocembrin, 98%, from Pinus cerebra

Cat. No JK463196_25_MG
J&K Chemical

Product Information

Product Name
(S)-Pinocembrin, 98%, from Pinus cerebra
Brand Name
J&K
Product Number
463196
CAS
480-39-7
Molecular Formula
C15H12O4
Molecular Weight
256.25
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
  • (2S)-2,3-Dihydro-5,7-dihydroxy-2-phenyl-4H-1-benzopyran-4-one
  • (S)-2,3-dihydro-5,7-dihydroxy-2-phenyl-4H-1-benzopyran-4-one
  • (+)-Pinocembrin
  • Galangin Flavanone
PubChem CID
68071
IUPAC Name
(2S)-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one
InChI Key
URFCJEUYXNAHFI-ZDUSSCGKSA-N
SMILES
C1C@H(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3

Safety Information

Precautionary Statement
P262

References Data Source From Pubchem

The LOTUS Initiative for Open Natural Products Research: frozen dataset union wikidata (with metadata)
Publication Date: 2026
DOI: 10.5281/zenodo.5794106

Molecular Breeding Technologies in Ornithogalum (Star of Bethlehem)
Publication Name: Breeding of Ornamental Crops: Bulbous Flowers
Publication Date: 2025
DOI: 10.1007/978-3-031-77900-8_18

Microbial Production of Pinocembrin
Publication Name: Microbial Production of Food Bioactive Compounds
Publication Date: 2025
DOI: 10.1007/978-3-031-90974-0_18

Engineering an Escherichia coli strain for enhanced production of flavonoids derived from pinocembrin
Publication Name: Microbial Cell Factories
Publication Date: 2024-11-19
DOI: 10.1186/s12934-024-02582-z

Exercise activates interferon response of the liver via Gpld1 to enhance antiviral innate immunity
Publication Name: Science Advances
Publication Date: 2024-05-31
DOI: 10.1126/sciadv.adk5011

(S)-Pinocembrin, 98%, from Pinus cerebra

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