CYP716A278

Aesculus wilsonii CYP716A

Sapindaceae

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

Substrate

β-amyrin

PubChem ↗ [H][C@]12[C@H](O)C=C3[C@]4([H])CC(C)(C)CC[C@]4(C)CC[C@@]3(C)[C@…

CYP716A278

ΔMass: no_smiles Missing dual SMILES or RDKit not validated

Product

21β-hydroxyl-β-amyrin

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; 酵母异源表达验证

Reaction & quality gates

Mechanism: Hydroxylation
Evidence type: In vivo
Confidence: High
Data tier: Silver
mass=no_smiles; incomplete_SMILES
Substrate class: Terpenoids
Product class: Terpenoids

Literature & public identifiers

PubMed: PMID:41536068 ↗
DOI: 10.1016/j.xplc.2026.101715 ↗
UniProt: —
GenBank: —
NCBI TaxID: 531827 ↗

Multi-omics and functional analyses in Aesculus wilsonii elucidate the biosynthetic pathways of moretane- and oleanane-type triterpenoids.