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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H22O11
Molecular Weight 342.2965
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MELIBIOSE

SMILES

OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O)[C@H](O)[C@@H](O)[C@H]1O

InChI

InChIKey=AYRXSINWFIIFAE-GFRRCQKTSA-N
InChI=1S/C12H22O11/c13-1-4(15)7(17)8(18)5(16)3-22-12-11(21)10(20)9(19)6(2-14)23-12/h1,4-12,14-21H,2-3H2/t4-,5+,6+,7+,8+,9-,10-,11+,12-/m0/s1

HIDE SMILES / InChI

Molecular Formula C12H22O11
Molecular Weight 342.2965
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Isolation and characterization of lactic acid bacteria strains with ornithine producing capacity from natural sea salt.
2010-08
Complete genome sequence of Meiothermus silvanus type strain (VI-R2).
2010-07-29
Biochemical and functional properties of a lectin purified from korean large black soybeans--a cultivar of glycine max.
2010-06
Complete genome sequence of Kribbella flavida type strain (IFO 14399).
2010-03-30
A novel lectin with antiproliferative and HIV-1 reverse transcriptase inhibitory activities from dried fruiting bodies of the monkey head mushroom Hericium erinaceum.
2010
Complete genome sequence of Actinosynnema mirum type strain (101).
2009-07-20
Evidence of different fermentation behaviours of two indigenous strains of Saccharomyces cerevisiae and Saccharomyces uvarum isolated from Amarone wine.
2009-07
Purification and characterization of a novel lectin from the toxic wild mushroom Inocybe umbrinella.
2009-03-01
Glycosylated neurotensin analogues exhibit sub-picomolar anticonvulsant potency in a pharmacoresistant model of epilepsy.
2009-03
Purification and characterization of a lectin from Phaseolus vulgaris cv. (Anasazi beans).
2009
Virulent clones of Klebsiella pneumoniae: identification and evolutionary scenario based on genomic and phenotypic characterization.
2009
Utilisation of carbon sources by pythium, phytophthora and fusarium species as determined by biolog® microplate assay.
2009
Hydration index--a better parameter for explaining small molecule hydration in inhibition of ice recrystallization.
2008-12-24
[Intracellular lectins of Lentinus edodes at various developmental stages of the fungus].
2008-10-02
The taxonomy of Enterobacter sakazakii: proposal of a new genus Cronobacter gen. nov. and descriptions of Cronobacter sakazakii comb. nov. Cronobacter sakazakii subsp. sakazakii, comb. nov., Cronobacter sakazakii subsp. malonaticus subsp. nov., Cronobacter turicensis sp. nov., Cronobacter muytjensii sp. nov., Cronobacter dublinensis sp. nov. and Cronobacter genomospecies 1.
2007-04-17
Lactobacillus tucceti sp. nov., a new lactic acid bacterium isolated from sausage.
2006-07
Substrate-induced conformational changes of melibiose permease from Escherichia coli studied by infrared difference spectroscopy.
2005-03-08
Boronic acid based modular fluorescent sensors for glucose.
2004-09
Synthesis and hemolytic activity of some hederagenin diglycosides.
2004-08
Taxonomic study of sucrose-positive Aeromonas jandaei-like isolates from faeces, water and eels: emendation of A. jandaei Carnahan et al. 1992.
2003-09
Specificity of human anti-NOR antibodies, a distinct species of "natural" anti-alpha-galactosyl antibodies.
2003-04
Purification and physicochemical characterization of a cotyledonary lectin from Luetzelburgia auriculata.
2002-10
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:00:10 GMT 2025
Edited
by admin
on Mon Mar 31 19:00:10 GMT 2025
Record UNII
9B1VBE526I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MELIBIOSE
INCI   MI  
INCI  
Official Name English
NSC-2028
Preferred Name English
(3R,4S,5S,6R)-6-((((2S,3R,4S,5R,6R)-3,4,5-TRIHYDROXY-6-(HYDROXYMETHYL)TETRAHYDRO-2H-PYRAN-2-YL)OXY)METHYL)TETRAHYDRO-2H-PYRAN-2,3,4,5-TETRAOL
Systematic Name English
(2R,3S,4R,5R)-2,3,4,5-TETRAHYDROXY-6-(((2S,3R,4S,5R,6R)-3,4,5-TRIHYDROXY-6-(HYDROXYMETHYL)TETRAHYDRO-2H-PYRAN-2-YL)OXY)HEXANAL
Systematic Name English
MELIBIOSE [MI]
Common Name English
D-GLUCOSE, 6-O-.ALPHA.-D-GALACTOPYRANOSYL-
Common Name English
Code System Code Type Description
CHEBI
28053
Created by admin on Mon Mar 31 19:00:10 GMT 2025 , Edited by admin on Mon Mar 31 19:00:10 GMT 2025
PRIMARY
MERCK INDEX
m7158
Created by admin on Mon Mar 31 19:00:10 GMT 2025 , Edited by admin on Mon Mar 31 19:00:10 GMT 2025
PRIMARY Merck Index
NSC
2028
Created by admin on Mon Mar 31 19:00:10 GMT 2025 , Edited by admin on Mon Mar 31 19:00:10 GMT 2025
PRIMARY
PUBCHEM
5460027
Created by admin on Mon Mar 31 19:00:10 GMT 2025 , Edited by admin on Mon Mar 31 19:00:10 GMT 2025
PRIMARY
EPA CompTox
DTXSID101014653
Created by admin on Mon Mar 31 19:00:10 GMT 2025 , Edited by admin on Mon Mar 31 19:00:10 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-568-6
Created by admin on Mon Mar 31 19:00:10 GMT 2025 , Edited by admin on Mon Mar 31 19:00:10 GMT 2025
PRIMARY
WIKIPEDIA
MELIBIOSE
Created by admin on Mon Mar 31 19:00:10 GMT 2025 , Edited by admin on Mon Mar 31 19:00:10 GMT 2025
PRIMARY
CAS
585-99-9
Created by admin on Mon Mar 31 19:00:10 GMT 2025 , Edited by admin on Mon Mar 31 19:00:10 GMT 2025
PRIMARY
FDA UNII
9B1VBE526I
Created by admin on Mon Mar 31 19:00:10 GMT 2025 , Edited by admin on Mon Mar 31 19:00:10 GMT 2025
PRIMARY