Molecule

(1S,4R,5R,6S)-N-(2-methylpropyl)-6-[(1E)-2-[(2-methylpropyl)carbamoyl]eth-1-en-1-yl]-4,5-dipentylcyclohex-2-ene-1-carboxamide

AlkaPlorer ID: AK073241

Synonym: None

IUPAC Name: (1S,4R,5R,6S)-N-(2-methylpropyl)-6-[(E)-3-(2-methylpropylamino)-3-oxoprop-1-enyl]-4,5-dipentylcyclohex-2-ene-1-carboxamide

Structure

SMILES: CCCCC[C@H]1[C@H](/C=C/C(=O)NCC(C)C)[C@@H](C(=O)NCC(C)C)C=C[C@H]1CCCCC

InChI: InChI=1S/C28H50N2O2/c1-7-9-11-13-23-15-16-26(28(32)30-20-22(5)6)25(24(23)14-12-10-8-2)17-18-27(31)29-19-21(3)4/h15-18,21-26H,7-14,19-20H2,1-6H3,(H,29,31)(H,30,32)/b18-17+/t23-,24-,25+,26+/m1/s1

InChIKey: WPDPJKDSGPYRKL-DHEXJBJSSA-N

Reference

Novel dimeric amide alkaloids from Piper chaba Hunter: isolation, cytotoxic activity, and their biomimetic synthesis

PubChem CID: 53243800

LOTUS: LTS0262661

SuperNatural Ⅲ: SN0416256-01

NPASS: NPC105550

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
Didymosphaeria enalia	Didymosphaeria	Didymosphaeriaceae	Pleosporales	Dothideomycetes	Ascomycota	Fungi	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
Piper retrofractum	Piper	Piperaceae	Piperales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Verbesina virginica	Verbesina	Asteraceae	Asterales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Mycoplasma mycoides	Mycoplasma	Mycoplasmataceae	Mycoplasmatales	Mollicutes	Mycoplasmatota	None	Bacteria
Penicillium tardum	Penicillium	Aspergillaceae	Eurotiales	Eurotiomycetes	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: 446.72000000000025

TPSA？: 58.2

MolLogP？: 6.282200000000007

Number of H-Donors: 2

Number of H-Acceptors: 2

RingCount: 1

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi