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Chemical Compound Review

Pinoresinol     4-[(1S,4S,5S,8S)-4-(4- hydroxy-3-methoxy...

Synonyms: CHEBI:40, SureCN122105, CPD-8905, NSC-35444, MEGxp0_000829, ...
 
 
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Disease relevance of NSC 35444

 

High impact information on NSC 35444

 

Associations of NSC 35444 with other chemical compounds

 

Analytical, diagnostic and therapeutic context of NSC 35444

References

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  2. Biotransformation of pinoresinol diglucoside to mammalian lignans by human intestinal microflora, and isolation of Enterococcus faecalis strain PDG-1 responsible for the transformation of (+)-pinoresinol to (+)-lariciresinol. Xie, L.H., Akao, T., Hamasaki, K., Deyama, T., Hattori, M. Chem. Pharm. Bull. (2003) [Pubmed]
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  9. Identification and stereochemical characterization of lignans in flaxseed and pumpkin seeds. Sicilia, T., Niemeyer, H.B., Honig, D.M., Metzler, M. J. Agric. Food Chem. (2003) [Pubmed]
  10. Dirigent-mediated podophyllotoxin biosynthesis in Linum flavum and Podophyllum peltatum. Xia, Z.Q., Costa, M.A., Proctor, J., Davin, L.B., Lewis, N.G. Phytochemistry (2000) [Pubmed]
  11. Stability control of valerian ground material and extracts: a new HPLC-method for the routine quantification of valerenic acids and lignans. Goppel, M., Franz, G. Die Pharmazie. (2004) [Pubmed]
  12. Lignans from Strophanthus gratus. Cowan, S., Stewart, M., Abbiw, D.K., Latif, Z., Sarker, S.D., Nash, R.J. Fitoterapia (2001) [Pubmed]
  13. Pinoresinol-lariciresinol reductases with different stereospecificity from Linum album and Linum usitatissimum. von Heimendahl, C.B., Schäfer, K.M., Eklund, P., Sjöholm, R., Schmidt, T.J., Fuss, E. Phytochemistry (2005) [Pubmed]
 
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