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Silver no_smiles Hydroxylation

CYP714A2

Preparative leaf CYP714A

Substrate reaction site Product reaction site MCS substructure diff highlighting · RDKit atom mapping
Substrate
6β,7β-dihydroxy-ent-kaurenoic acid
PubChem ↗ [H][C@@]12CC/C(=C(\C)C#CCC(O)(CC)CC)[C@@]1(C)CCC/C2=C\C=C1\C[C@…
CYP714A2
ΔMass: no_smiles Missing dual SMILES or RDKit not validated

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; Preparative leaf disk assay with AtCYP714A2; product 34 isolated and characterized by NMR and HRMS.

Reaction & quality gates

Mechanism
Hydroxylation
Evidence type
In vitro
Confidence
High
Data tier
Silver
mass=no_smiles; incomplete_SMILES
Substrate class
Organic acids
Product class
Other

Literature & public identifiers

PubMed
PMID:42054221 ↗
DOI
10.1021/jacs.6c06067 ↗
UniProt
A0A438HY93 ↗
GenBank
NCBI TaxID

Chemoenzymatic Synthesis with Plant Oxidases and Metabolic Engineering Enable Rapid Access to Rare Gibberellins.