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| Product | Description | |
|---|---|---|
| [4, 8'-Bi-2H-1-benzopyran]-3, 3', 5, 5', 7, 7'-hexol, 3, 3', 4, 4'-tetrahydro-2, 2'-bis(4-hydroxyphenyl)-, (2r, 2'r, 3s, 3's, 4s)- | Heterocyclic Organic Compound. Alternative Names: Afzelechin-(4alpha->8)-afzelechin, CID442671, C10209, 101339-37-1. CAS No. 101339-37-1. Molecular formula: C30H26O10. Mole weight: 546.5214. Purity: 0.96. IUPACName: (2R,3S)-2-(4-hydroxyphenyl)-8-[(2R,3S,4S)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol. Canonical SMILES: C1C (C (OC2=C1C (=CC (=C2C3C (C (OC4=CC (=CC (=C34)O)O)C5=CC=C (C=C5)O)O)O)O)C6=CC=C (C=C6)O)O. Density: 1.596g/cm³. Catalog: ACM101339371. |  |
| leucoanthocyanidin reductase | The enzyme catalyses the synthesis of catechin, catechin-4β-ol (leucocyanidin) and the related flavan-3-ols afzelechin and gallocatechin, which are initiating monomers in the synthesis of plant polymeric proanthocyanidins or condensed tannins. While 2,3-trans-3,4-cis-leucocyanidin is the preferred flavan-3,4-diol substrate, 2,3-trans-3,4-cis-leucodelphinidin and 2,3-trans-3,4-cis-leucopelargonidin can also act as substrates, but more slowly. NADH can replace NADPH but is oxidized more slowly. Group: Enzymes. Synonyms: leucocyanidin reductase. Enzyme Commission Number: EC 1.17.1.3. CAS No. 776323-46-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1081; leucoanthocyanidin reductase; EC 1.17.1.3; 776323-46-7; leucocyanidin reductase. Cat No: EXWM-1081. |  |
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