CYP701A8

Oryza sativa CYP701A

Poaceae

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

Substrate

(9β-H)-pimara-7,15-diene

PubChem ↗ C[C@]1(CC[C@@H]2C(=CC[C@@H]3[C@@]2(CCCC3(C)C)C)C1)C=C

CYP701A8

ΔMass: no_smiles Missing dual SMILES or RDKit not validated

Product

3β-hydroxy-(9β-H)-pimara-7,15-dien-19,6β-olide

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; CYP76M8 and CYP701A8 catalyze conversion of (9β-H)-pimara-7,15-diene into 3β-hydroxy-(9β-H)-pimara-7,15-dien-19,6β-olide; reference [68].

Reaction & quality gates

Mechanism: Hydroxylation
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:39329985 ↗
DOI: 10.3390/cimb46090634 ↗
UniProt: Q0DBF4 ↗
GenBank: —
NCBI TaxID: 4530 ↗

Enhancing Crop Resilience: Insights from Labdane-Related Diterpenoid Phytoalexin Research in Rice (<i>Oryza sativa</i> L.).

Evidence trail

Reaction & quality gates

Literature & public identifiers

Other reactions by this enzyme