CYP96T6

Amaryllidaceae alkaloids CYP96T

Amaryllidaceae

Substrate reaction site Product reaction site MCS substructure diff highlighting · RDKit atom mapping

Substrate

4'-O-methylnorbelladine

PubChem ↗ COC1=C(C=C(C=C1)CNCCC2=CC=C(C=C2)O)O

CYP96T6

ΔMass: no_smiles Missing dual SMILES or RDKit not validated

Product

nornarwedine

PubChem ↗ Crowdsource product structure

Evidence trail

Excerpts are machine-extracted plain text for biochemical provenance. Follow DOI / PubMed links for the primary literature; publisher figures and PDF images are not displayed here.

Source text excerpt ation; ation; CYP96T6 proposed to catalyse para–ortho' phenol coupling leading to galanthamine-type AAs (Mehta et al., 2024).

Reaction & quality gates

Mechanism: Oxidation
Evidence type: In vitro
Confidence: High
Data tier: Silver
mass=no_smiles; incomplete_SMILES
Substrate class: Other
Product class: Other

Literature & public identifiers

PubMed: PMID:38652148 ↗
DOI: 10.1093/jxb/erae187 ↗
UniProt: —
GenBank: —
NCBI TaxID: 3062038 ↗

Navigating Amaryllidaceae alkaloids: bridging gaps and charting biosynthetic territories.