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Gold ΔMass ✓ Hydroxylation

CYP76M6

Oryza sativa CYP76M

Poaceae

Substrate reaction site Product reaction site MCS substructure diff highlighting · RDKit atom mapping
Substrate
3α-Hydroxy-ent-sandaracopimaradiene
PubChem ↗ C[C@]1(CC[C@@H]2C(=C1)CC[C@H]3[C@]2(CC[C@H](C3(C)C)O)C)C=C
CYP76M6
ΔMass: +15.9949 Da hydroxylation(+15.9949)
Product
oryzalexin E
PubChem ↗ C[C@]1(CC[C@@]2(C(=C1)CC[C@H]3[C@]2(CC[C@H](C3(C)C)O)C)O)C=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; CYP76M6 hydroxylates C-9β position leading to oryzalexin E; reference [78].

Reaction & quality gates

Mechanism
Hydroxylation (+15.99 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:39329985 ↗
DOI
10.3390/cimb46090634 ↗
UniProt
Q6Z5I7 ↗
GenBank
NCBI TaxID
4530 ↗

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