Silver
no_smiles
Hydroxylation
Substrate reaction site
Product reaction site
MCS substructure diff highlighting · RDKit atom mapping
Substrate
7β-hydroxy-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@…
CYP714A1
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 AtCYP714A1; product 32 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
- A0A8F0K7Q1 ↗
- GenBank
- —
- NCBI TaxID
- —
Chemoenzymatic Synthesis with Plant Oxidases and Metabolic Engineering Enable Rapid Access to Rare Gibberellins.