gelomulide M (BioCAD00000536951)

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Metabolite Card

Formula: C24H30O7 (430.1991)
SMILES: [H][C@@]12C[C@@]3([H])[C@]4(C)[C@H](OC(C)=O)C=CC(C)(C)[C@@]4([H])C[C@H](OC(C)=O)[C@]33O[C@]3([H])C1=C(C)C(=O)O2

Synonyms [en]

Gelomulide M; 7-diyl diacetate; [(1~{R},3~{R},8~{R},10~{S},11~{R},12~{R},16~{R},18~{S})-12-acetoxy-5,11,15,15-tetramethyl-6-oxo-2,7-dioxapentacyclo[8.8.0.0^{1,3}.0^{4,8}.0^{11,16}]octadeca-4,13-dien-18-yl] acetate; (2~{R})-2-(2,5-dimethoxyphenyl)-5,7-dimethyl-5,7,9-triazatetracyclo[8.7.0.0^{3,8}.0^{11,16}]heptadeca-1(10),3(8),11,13,15-pentaene-4,6,17-trione; 9-triazatetracyclo8.7.0.03; CHEBI:65956

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

gelomulide M. 数据之源，洞见之始. SMRUCC genomics institute, a synthetic life researcher from China. https://biocad_registry.innovation.ac.cn/s/(-)-arctiin (retrieved 2026-01-03) (CAD Registry RN: BioCAD00000536951). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

An abietane diterpenoid that is ent-abieta-2(3),13(15)-diene-16,12-olide substituted by beta-acetoxy groups at positions 1 and 7 and a beta-epoxy group across positions 8 and 14. Isolated from the leaves of Gelonium aequoreum, it exhibits moderate cytotoxicity against lung (A549), breast (MDAMB-231 and MCF7), and liver (HepG2) cancer cell lines." []

Entity Information

DBLinks

  • CAS Registry Number:
  • PubChem CID:
  • ChEBI: 65956
  • HMDB:
  • LipidMaps:
  • KEGG:
  • BioCyc:
  • NCBI MeSH:
  • Wikipedia:
Other DBLinks
  • ChEBI: ChEBI:65956
  • Coconut NaturalProduct: CNP0045196.2
  • Coconut NaturalProduct: CNP0291263.1
  • Coconut NaturalProduct: CNP0496861.1
  • Coconut NaturalProduct: CNP0496861.2

Class / Ontology

Metabolic Network
ID EC Number Name
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Organism Source

Taxonomy Source

  1. Gelonium aequoreum [ncbi taxid: ]

Pathway Synthetic

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