Molecule

Acetyllycopsamine

AlkaPlorer ID: AK011822

Synonym: 'Acetyllycopsamine', 'O-Acetylintermedine', '7-Acetylintermedine', 'Acetylintermedine', '7-Acetyllycopsamine', 'Intermedine 1-acetate', 'Lycopsamine 1-acetate', '7-Acetylechinatine', 'Echinatine 1-acetate', '7-O-Acetylechinatine'

IUPAC Name: [(7S,8R)-7-acetyloxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-hydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoate

Structure

SMILES: CC(=O)O[C@H]1CCN2CC=C(COC(=O)[C@](O)(C(C)C)[C@@H](C)O)[C@H]12

InChI: InChI=1S/C17H27NO6/c1-10(2)17(22,11(3)19)16(21)23-9-13-5-7-18-8-6-14(15(13)18)24-12(4)20/h5,10-11,14-15,19,22H,6-9H2,1-4H3/t11-,14+,15-,17+/m1/s1

InChIKey: RKDOFSJTBIDAHX-MVQRFQBOSA-N

Reference

Pyrrolizidine alkaloids from eupatorium fortunei

PubChem CID: 185847

CAS: 63450-95-3

LOTUS: LTS0145192

SuperNatural Ⅲ: SN0327611-04

NPASS: NPC179897

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Moringa stenopetala	Moringa	Moringaceae	Brassicales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Achillea pannonica	Achillea	Asteraceae	Asterales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Mimosa tenuiflora	Mimosa	Fabaceae	Fabales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Asclepias speciosa	Asclepias	Apocynaceae	Gentianales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Manilkara hexandra	Manilkara	Sapotaceae	Ericales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Polyopes affinis	Polyopes	Halymeniaceae	Halymeniales	Florideophyceae	Rhodophyta	None	Eukaryota
Paeonia delavayi	Paeonia	Paeoniaceae	Saxifragales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Ricciocarpos natans	Ricciocarpos	Ricciaceae	Marchantiales	Marchantiopsida	Streptophyta	Viridiplantae	Eukaryota
Senna sophera	Senna	Fabaceae	Fabales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Diospyros crassiflora	Diospyros	Ebenaceae	Ericales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Lysimachia clethroides	Lysimachia	Primulaceae	Ericales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Phaulopsis imbricata	Phaulopsis	Acanthaceae	Lamiales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Alloascoidea hylecoeti	Alloascoidea	Alloascoideaceae	Saccharomycetales	Saccharomycetes	Ascomycota	Fungi	Eukaryota
Dichapetalum madagascariense	Dichapetalum	Dichapetalaceae	Malpighiales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Callicarpa bodinieri	Callicarpa	Lamiaceae	Lamiales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Teucrium trifidum	Teucrium	Lamiaceae	Lamiales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Eupatorium fortunei	Eupatorium	Asteraceae	Asterales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Piper sintenense	Piper	Piperaceae	Piperales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Aphanamixis polystachya	Aphanamixis	Meliaceae	Sapindales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Erica carnea	Erica	Ericaceae	Ericales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Doriopsilla albopunctata	Doriopsilla	Dendrodorididae	Nudibranchia	Gastropoda	Mollusca	Metazoa	Eukaryota
Annulusmagnus triseptatus	Annulusmagnus	Annulatascaceae	Annulatascales	Sordariomycetes	Ascomycota	Fungi	Eukaryota
Medicago truncatula	Medicago	Fabaceae	Fabales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Sarcophyton glaucum	Sarcophyton	Alcyoniidae	Malacalcyonacea	Anthozoa	Cnidaria	Metazoa	Eukaryota
Mourera fluviatilis	Mourera	Podostemaceae	Malpighiales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Huperzia lucidula	Huperzia	Lycopodiaceae	Lycopodiales	Lycopodiopsida	Streptophyta	Viridiplantae	Eukaryota

Properties Information

Molecule Weight: 341.40400000000005

TPSA？: 96.3

MolLogP？: 0.2435000000000003

Number of H-Donors: 2

Number of H-Acceptors: 7

RingCount: 2

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi