WS

Gumlich aldehyde

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

Substrate

18-OH-norfluorocurarine

PubChem ↗ Crowdsource substrate structure

ΔMass: no_smiles Missing dual SMILES or RDKit not validated

Product

Wieland-Gumlich aldehyde

PubChem ↗ C1CN2CC3=CCO[C@H]([C@@H]4[C@H]3C[C@H]2[C@@]15[C@H]4NC6=CC=CC=C5…

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 ion; ion; SnvWS catalyzes 1,2-iminium reduction of 18-OH-norfluorocurarine to Wieland-Gumlich aldehyde.

Reaction & quality gates

Mechanism: Reduction
Evidence type: In vitro
Confidence: High
Data tier: Silver
mass=no_smiles; incomplete_SMILES
Substrate class: Other
Product class: Other

Literature & public identifiers

PubMed: PMID:40536199 ↗
DOI: 10.1021/acs.biochem.5c00234 ↗
UniProt: OM304294 ↗
GenBank: OM304294 ↗
NCBI TaxID: —

A Tight-Knit Family: The Medium-Chain Dehydrogenase/Reductases of Monoterpene Indole Alkaloid Biosynthesis.