CYP96T1

Progress in CYP96T

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

CYP96T1

ΔMass: -1.0084 Da mismatch

Product

(10bR,4aS)-noroxomaritidine

PubChem ↗ COC1=C(C=C2C[NH+]3CC[C@]4([C@@H]3CC(=O)C=C4)C2=C1)O

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; CYP96T1 catalyzes para-para' phenol coupling of 4'-O-methylnorbelladine to form (10bR,4aS)-noroxomaritidine; enzyme characterized in monocots (Amaryllidaceae).

Reaction & quality gates

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

Literature & public identifiers

PubMed: PMID:33066212 ↗
DOI: 10.3390/molecules25204670 ↗
UniProt: A0A346TLF6 ↗
GenBank: —
NCBI TaxID: —

Recent Progress in Amaryllidaceae Biotechnology.

Evidence trail

Reaction & quality gates

Literature & public identifiers

Other reactions by this enzyme