Molecule

(2E,4E)-5-(2H-1,3-benzodioxol-5-yl)-N-[(5E)-10-methylundec-5-en-1-yl]penta-2,4-dienamide

AlkaPlorer ID: AK325496

Synonym: None

IUPAC Name: (2E,4E)-5-(1,3-benzodioxol-5-yl)-N-[(E)-10-methylundec-5-enyl]penta-2,4-dienamide

Structure

SMILES: CC(C)CCC/C=C/CCCCN=C(O)/C=C/C=C/C1=CC=C2OCOC2=C1

InChI: InChI=1S/C24H33NO3/c1-20(2)12-8-6-4-3-5-7-11-17-25-24(26)14-10-9-13-21-15-16-22-23(18-21)28-19-27-22/h3-4,9-10,13-16,18,20H,5-8,11-12,17,19H2,1-2H3,(H,25,26)/b4-3+,13-9+,14-10+

InChIKey: URFYPQQKBYOWIX-UDNGMWKQSA-N

Reference

Isolation of N-isobutyl deca-trans-2-trans-4-dienamide fromPiper sylvaticum Roxb

PubChem CID: 90472536

CAS: 42438-80-2

LOTUS: LTS0042729

SuperNatural Ⅲ: SN0378019-02

NPASS: NPC99298

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Crocus corsicus	Crocus	Iridaceae	Asparagales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Brickellia longifolia	Brickellia	Asteraceae	Asterales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Silene banksia	Silene	Caryophyllaceae	Caryophyllales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Cochlearia officinalis	Cochlearia	Brassicaceae	Brassicales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Frullania brasiliensis	Frullania	Frullaniaceae	Porellales	Jungermanniopsida	Streptophyta	Viridiplantae	Eukaryota
Hippocrepis emerus	Hippocrepis	Fabaceae	Fabales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Didymosphaeria enalia	Didymosphaeria	Didymosphaeriaceae	Pleosporales	Dothideomycetes	Ascomycota	Fungi	Eukaryota
Plenckia populnea	Plenckia	Celastraceae	Celastrales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Matsumurella chinensis	Matsumurella	Lamiaceae	Lamiales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Dichotomanthes tristaniicarpa	Dichotomanthes	Rosaceae	Rosales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Agaricus xanthodermus	Agaricus	Agaricaceae	Agaricales	Agaricomycetes	Basidiomycota	Fungi	Eukaryota
Pinus aristata	Pinus	Pinaceae	Pinales	Pinopsida	Streptophyta	Viridiplantae	Eukaryota
Dryopteris arguta	Dryopteris	Dryopteridaceae	Polypodiales	Polypodiopsida	Streptophyta	Viridiplantae	Eukaryota
Piper longum	Piper	Piperaceae	Piperales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Piper retrofractum	Piper	Piperaceae	Piperales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Verbesina virginica	Verbesina	Asteraceae	Asterales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Bellardia viscosa	Bellardia	Orobanchaceae	Lamiales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Mycoplasma mycoides	Mycoplasma	Mycoplasmataceae	Mycoplasmatales	Mollicutes	Mycoplasmatota	None	Bacteria
Penicillium tardum	Penicillium	Aspergillaceae	Eurotiales	Eurotiomycetes	Ascomycota	Fungi	Eukaryota
Gyalolechia fulgida	Gyalolechia	Teloschistaceae	Teloschistales	Lecanoromycetes	Ascomycota	Fungi	Eukaryota
Bupleurum rigidum	Bupleurum	Apiaceae	Apiales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Palisota barteri	Palisota	Commelinaceae	Commelinales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Carpesium longifolium	Carpesium	Asteraceae	Asterales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Photorhabdus luminescens	Photorhabdus	Morganellaceae	Enterobacterales	Gammaproteobacteria	Pseudomonadota	None	Bacteria
Leifsonia aquatica	Leifsonia	Microbacteriaceae	Micrococcales	Actinomycetes	Actinomycetota	None	Bacteria
Coelogyne nitida	Coelogyne	Orchidaceae	Asparagales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota

Properties Information

Molecule Weight: 383.53200000000015

TPSA？: 51.05000000000001

MolLogP？: 6.494000000000007

Number of H-Donors: 1

Number of H-Acceptors: 3

RingCount: 2

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi