Molecule

(2R)-N-[(2S,3S,4R)-3,4-dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexadecan-2-yl]-2-hydroxytricosanamide

AlkaPlorer ID: AK073785

Synonym: None

IUPAC Name: (2R)-N-[(2S,3S,4R)-3,4-dihydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexadecan-2-yl]-2-hydroxytricosanamide

Structure

SMILES: CCCCCCCCCCCCCCCCCCCCC[C@@H](O)C(O)=N[C@@H](CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@H](O)[C@H](O)CCCCCCCCCCCC

InChI: InChI=1S/C45H89NO10/c1-3-5-7-9-11-13-15-16-17-18-19-20-21-22-23-25-27-29-31-33-38(49)44(54)46-36(35-55-45-43(53)42(52)41(51)39(34-47)56-45)40(50)37(48)32-30-28-26-24-14-12-10-8-6-4-2/h36-43,45,47-53H,3-35H2,1-2H3,(H,46,54)/t36-,37+,38+,39+,40-,41+,42-,43+,45+/m0/s1

InChIKey: OYZFUZFOAATCER-XKFNKPFMSA-N

Reference

Biologically active glycosides from asteroidea, XX. Glycosphingolipids from the starfish <i>Asterina pectinifera</i>,1. Isolation and characterization of acanthacerebroside B and structure elucidation of related, nearly homogeneous cerebrosides

PubChem CID: 14586577

LOTUS: LTS0146651

SuperNatural Ⅲ: SN0278878-04

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Patiria pectinifera	Patiria	Asterinidae	Valvatida	Asteroidea	Echinodermata	Metazoa	Eukaryota

Properties Information

Molecule Weight: 804.2039999999997

TPSA？: 192.66

MolLogP？: 8.343600000000013

Number of H-Donors: 8

Number of H-Acceptors: 10

RingCount: 1

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi