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Gold ΔMass ✓ Oxidation

CYP71

Catharanthus roseus

Apocynaceae

Substrate reaction site Product reaction site MCS substructure diff highlighting · RDKit atom mapping
Substrate
19E-geissoschizine
PubChem ↗ C/C=C\1/CN2CCC3=C([C@@H]2C[C@@H]1/C(=C/O)/C(=O)OC)NC4=CC=CC=C34
CYP71
ΔMass: -2.0157 Da ketone_formation(-2.0157)
Product
rhazimal
PubChem ↗ C/C=C\1/CN2CC[C@@]34C5=CC=CC=C5N=C3[C@@H]2C[C@@H]1[C@@]4(C=O)C(…

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; CrRS (rhazimal synthase) catalyzes C7-C16 oxidative coupling; rhazimal spontaneously deformylates to strictamine.

Reaction & quality gates

Mechanism
Ketone formation (-2.02 Da)
Evidence type
In vitro
Confidence
High
Data tier
Gold
Latin binomial + experiment + dual SMILES + ΔMass pass
Substrate class
Other
Product class
Other

Literature & public identifiers

PubMed
PMID:40202182 ↗
DOI
10.1002/anie.202501323 ↗
UniProt
W8JDE2 ↗
GenBank
NCBI TaxID
4058 ↗

Oxidative Rearrangements of the Alkaloid Intermediate Geissoschizine.