FLS

Panax notoginseng

Araliaceae

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

Substrate

dihydrokaempferol

PubChem ↗ C1=CC(=CC=C1[C@@H]2[C@H](C(=O)C3=C(C=C(C=C3O2)O)O)O)O

FLS

ΔMass: +13.9793 Da mismatch

Product

quercetin

PubChem ↗ C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O

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; Up-regulated in P. notoginseng after inflorescence removal; part of flavonoid pathway.

Reaction & quality gates

Mechanism: Oxidation
Evidence type: In vivo
Confidence: Medium
Data tier: Quarantine
non-CYP auxiliary enzyme (pathway partner, not cytochrome P450)
Substrate class: Phenylpropanoids
Product class: Phenylpropanoids

Literature & public identifiers

PubMed: PMID:34868157 ↗
DOI: 10.3389/fpls.2021.761821 ↗
UniProt: Q9XHG2 ↗
GenBank: —
NCBI TaxID: 44586 ↗

Transcriptomics and Metabolomics Changes Triggered by Inflorescence Removal in <i>Panax notoginseng</i> (Burk.).