NsOSC2

Neopicrorhiza scrophulariiflora

Plantaginaceae

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

Substrate

2,3-oxidosqualene

PubChem ↗ CC(=CCC/C(=C/CC/C(=C/CC/C=C(\C)/CC/C=C(\C)/CCC1C(O1)(C)C)/C)/C)C

NsOSC2

ΔMass: +15.9949 Da fallback:~+16 Da (羟基化/氧化)

Product

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@…

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 ization; ization; Heterologous expression in yeast GIL77; GC-MS confirmed product.

Reaction & quality gates

Mechanism: Hydroxylation (+15.99 Da)
Evidence type: In vitro
Confidence: High
Data tier: Quarantine
non-CYP auxiliary enzyme (pathway partner, not cytochrome P450)
Substrate class: Other
Product class: Terpenoids

Literature & public identifiers

PubMed: PMID:40431127 ↗
DOI: 10.3390/plants14101562 ↗
UniProt: —
GenBank: —
NCBI TaxID: 470706 ↗

Multi-Omics and Functional Insights into Triterpenoid Biosynthesis Pathways in <i>Neopicrorhiza scrophulariiflora</i> (Pennell) D.Y.Hong.

Evidence trail

Reaction & quality gates

Literature & public identifiers

Other reactions by this enzyme