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name Structure Reference Source Properties Activities Metabolism

2,4,8,10,12-Tetradecapentaenoic acid; (2E,4E,8Z,10Z,12E)-form, 2-Methylpropylamide 

AlkaPlorer ID: AK315204

Synonym: None

IUPAC Name: (2E,4E,8E,10E,12E)-N-(2-methylpropyl)tetradeca-2,4,8,10,12-pentaenamide

Structure

SMILES: C/C=C/C=C/C=C/CC/C=C/C=C/C(O)=NCC(C)C

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InChI: InChI=1S/C18H27NO/c1-4-5-6-7-8-9-10-11-12-13-14-15-18(20)19-16-17(2)3/h4-9,12-15,17H,10-11,16H2,1-3H3,(H,19,20)/b5-4+,7-6+,9-8+,13-12+,15-14+

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InChIKey: KVUKDCFEXVWYBN-FMBIJHKPSA-N

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Source

Species Genus Family Order Class Phylum Kingdom Domain
Trapa japonica Trapa Lythraceae Myrtales Magnoliopsida Streptophyta Viridiplantae Eukaryota
Archaster typicus Archaster Archasteridae Valvatida Asteroidea Echinodermata Metazoa Eukaryota
Zanthoxylum bungeanum Zanthoxylum Rutaceae Sapindales Magnoliopsida Streptophyta Viridiplantae Eukaryota
Cratystylis conocephala Cratystylis Asteraceae Asterales Magnoliopsida Streptophyta Viridiplantae Eukaryota
Beaucarnea recurvata Beaucarnea Asparagaceae Asparagales Magnoliopsida Streptophyta Viridiplantae Eukaryota
Mikania scandens Mikania Asteraceae Asterales Magnoliopsida Streptophyta Viridiplantae Eukaryota
Zanthoxylum piperitum Zanthoxylum Rutaceae Sapindales Magnoliopsida Streptophyta Viridiplantae Eukaryota
Diospyros abyssinica Diospyros Ebenaceae Ericales Magnoliopsida Streptophyta Viridiplantae Eukaryota
Phaeotremella fagi Phaeotremella Phaeotremellaceae Tremellales Tremellomycetes Basidiomycota Fungi Eukaryota
Gutenbergia cordifolia Gutenbergia Asteraceae Asterales Magnoliopsida Streptophyta Viridiplantae Eukaryota
Cotylelobium scabriusculum Cotylelobium Dipterocarpaceae Malvales Magnoliopsida Streptophyta Viridiplantae Eukaryota
Diospyros elliptifolia Diospyros Ebenaceae Ericales Magnoliopsida Streptophyta Viridiplantae Eukaryota
Phyllodium pulchellum Phyllodium Fabaceae Fabales Magnoliopsida Streptophyta Viridiplantae Eukaryota
Centaurea arenaria Centaurea Asteraceae Asterales Magnoliopsida Streptophyta Viridiplantae Eukaryota

Properties Information

Molecule Weight: 273.42

TPSA？: 32.59

MolLogP？: 5.180000000000005

Number of H-Donors: 1

Number of H-Acceptors: 1

RingCount: 0

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi
Homo sapiens Cannabinoid CB1 receptor Activity 5.0 % 10.1021/np400478c
Homo sapiens Cannabinoid CB1 receptor IC50 100.0 nM 10.1021/np400478c
Homo sapiens Cannabinoid CB1 receptor Inhibition 15.0 % 10.1021/np400478c
Homo sapiens Cannabinoid CB1 receptor Inhibition 37.0 % 10.1021/np400478c
Homo sapiens Cannabinoid CB2 receptor EC50 41.7 nM 10.1021/np400478c
Homo sapiens Cannabinoid CB2 receptor IC50 664.0 nM 10.1021/np400478c
Homo sapiens Cannabinoid CB2 receptor Inhibition 57.0 % 10.1021/np400478c
Homo sapiens Cannabinoid CB2 receptor Inhibition 64.0 % 10.1021/np400478c
Homo sapiens Cannabinoid CB2 receptor Inhibition 72.0 % 10.1021/np400478c
Homo sapiens Follicle stimulating hormone receptor Activity 5.0 % 10.1021/np400478c
Homo sapiens Follicle stimulating hormone receptor Inhibition 68.0 % 10.1021/np400478c
Homo sapiens G-protein coupled receptor 55 Activity 67.0 % 10.1021/np400478c
Homo sapiens Histamine H4 receptor Activity 18.0 % 10.1021/np400478c
Homo sapiens Histamine H4 receptor Inhibition -54.0 % 10.1021/np400478c
Homo sapiens Probable G-protein coupled receptor 132 Activity 61.0 % 10.1021/np400478c
Homo sapiens Probable G-protein coupled receptor 151 Activity 76.0 % 10.1021/np400478c
Homo sapiens Prolactin-releasing peptide receptor Activity 5.0 % 10.1021/np400478c
Homo sapiens Prolactin-releasing peptide receptor Inhibition 52.0 % 10.1021/np400478c
Homo sapiens Prostanoid EP2 receptor Activity 7.0 % 10.1021/np400478c
Homo sapiens Prostanoid EP2 receptor Inhibition -52.0 % 10.1021/np400478c
Homo sapiens Relaxin-3 receptor 1 Activity 18.0 % 10.1021/np400478c
Homo sapiens Relaxin-3 receptor 1 Inhibition -81.0 % 10.1021/np400478c
None Unchecked Ratio IC50 0.15 None 10.1021/np400478c

Metabolism Information