CYP716C1

Eriobotrya japonica CYP716C

Rosaceae

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

Substrate

oleanolic acid

PubChem ↗ C[C@]12CC[C@@H](C([C@@H]1CC[C@@]3([C@@H]2CC=C4[C@]3(CC[C@@]5([C…

CYP716C1

ΔMass: +15.9949 Da hydroxylation(+15.9949)

Product

maslinic acid

PubChem ↗ C[C@@]12CC[C@@H]3[C@@]([C@H]1CC=C4[C@]2(CC[C@@]5([C@H]4CC(CC5)(…

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; C-2α hydroxylation of oleanolic acid to maslinic acid; previously characterized in loquat (ref 14).

Reaction & quality gates

Mechanism: Hydroxylation (+15.99 Da)
Evidence type: In vitro
Confidence: High
Data tier: Quarantine
PDF audit quarantine (enzyme_miss_in_pdf;two_core_fields_in_text;review_structured_partial_core). pdf=41897800.pdf; enzyme_in_pdf=miss; issue=review_structured…
Substrate class: Organic acids
Product class: Organic acids

Literature & public identifiers

PubMed: PMID:41897800 ↗
DOI: 10.3390/foods15061078 ↗
UniProt: —
GenBank: —
NCBI TaxID: 32224 ↗

Exogenous Methyl Jasmonate Promotes Triterpene Accumulation in Loquat Callus.