Molecule

(2E)-2-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)but-2-enenitrile

AlkaPlorer ID: AK092788

Synonym: None

IUPAC Name: (E)-2-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]but-2-enenitrile

Structure

SMILES: C/C=C(\C#N)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI: InChI=1S/C11H17NO6/c1-2-6(3-12)5-17-11-10(16)9(15)8(14)7(4-13)18-11/h2,7-11,13-16H,4-5H2,1H3/b6-2+/t7-,8-,9+,10-,11-/m1/s1

InChIKey: UMDGSPMIRLGQIM-ZCIPGPJXSA-N

Reference

Bioactive Constituents of Chinese Natural Medicines. IV. Rhodiolae Radix. (2).: On the Histamine Release Inhibitors from the Underground Part of Rhodiola sacra (PRAIN ex HAMET) S. H. Fu (Crassulaceae): Chemical Structures of Rhodiocyanoside D and Sacranosides A and B.

PubChem CID: 6442230

LOTUS: LTS0018061

SuperNatural Ⅲ: SN0374070-02

NPASS: NPC148358

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Pieris napi	Pieris	Pieridae	Lepidoptera	Insecta	Arthropoda	Metazoa	Eukaryota
Sextonia rubra	Sextonia	Lauraceae	Laurales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Lotus japonicus	Lotus	Fabaceae	Fabales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Senna siamea	Senna	Fabaceae	Fabales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Triaenophora rupestris	Triaenophora	Orobanchaceae	Lamiales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Bartramia pomiformis	Bartramia	Bartramiaceae	Bartramiales	Bryopsida	Streptophyta	Viridiplantae	Eukaryota
Streptomyces paulus	Streptomyces	Streptomycetaceae	Kitasatosporales	Actinomycetes	Actinomycetota	None	Bacteria
Cerinthe minor	Cerinthe	Boraginaceae	Boraginales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Dioscorea japonica	Dioscorea	Dioscoreaceae	Dioscoreales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Ehretia dicksonii	Ehretia	Ehretiaceae	Boraginales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Cedrus libani	Cedrus	Pinaceae	Pinales	Pinopsida	Streptophyta	Viridiplantae	Eukaryota
Ixeris stolonifera	Ixeris	Asteraceae	Asterales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Khaya senegalensis	Khaya	Meliaceae	Sapindales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Balanophora involucrata	Balanophora	Balanophoraceae	Santalales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Rhodiola crenulata	Rhodiola	Crassulaceae	Saxifragales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Craspidospermum verticillatum	Craspidospermum	Apocynaceae	Gentianales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Hypericum ascyron	Hypericum	Hypericaceae	Malpighiales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Aristolochia zollingeriana	Aristolochia	Aristolochiaceae	Piperales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Khaya ivorensis	Khaya	Meliaceae	Sapindales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota
Larix cajanderi	Larix	Pinaceae	Pinales	Pinopsida	Streptophyta	Viridiplantae	Eukaryota
Penicillium paxilli	Penicillium	Aspergillaceae	Eurotiales	Eurotiomycetes	Ascomycota	Fungi	Eukaryota

Properties Information

Molecule Weight: 259.258

TPSA？: 123.17000000000002

MolLogP？: -1.7272200000000006

Number of H-Donors: 4

Number of H-Acceptors: 7

RingCount: 1

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi