Monogalactosil Diglicérido - ≥95% , CAS No.41670-62-6

CAS: 41670-62-6 Cat. No.: M338950 Peso molecular: 787.16

GRADE & PURITY ≥95%

Synonyms

3-(((2R,3R,4S,5R,6R)-3,4,5-Trihidroxi-6-(hidroximetil)tetrahidro-2H-piran-2-il)oxi)diestearato de propano-1,2-diilo | Mezcla de monogalactosil diglicéridos | 1,2-Distearoilmonoglactosilglicérido | MGDG (hidrogenado) | DTXSID70961896 | 3-(Hexopiranosiloxi)

Storage

Conservar a -20°C

Shipped In

Hielera + almohadillas de hielo

Specifications

Sinónimos

3-(((2R, 3R, 4S, 5R, 6R)-3, 4, 5-Trihidroxi-6-(hidroximetil)tetrahidro-2H-piran-2-il)oxi)diestearato de propano-1, 2-diilo | Mezcla de monogalactosil diglicéridos | 1, 2-Distearoilmonoglactosilglicérido | MGDG (hidrogenado) | DTXSID70961896 | 3-(Hexopiranosiloxi)

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

Conservar a -20°C

Enviado en

Hielera + almohadillas de hielo

Pureza

≥95%

Nombres e identificadores

• Pubchem Sid: 504757771
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504757771
• Sonrisas canónicas: CCCCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCCCCCCCCCCC
• IUPAC Name: [2-octadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] octadecanoate
• InChIKey: DCLTVZLYPPIIID-XMGVTQGESA-N
• INCHI: 1S/C45H86O10/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-40(47)52-36-38(37-53-45-44(51)43(50)42(49)39(35-46)55-45)54-41(48)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h38-39,42-46,49-51H,3-37H2,1-2H3/t38?,39-,42+,43+,44-,45-/m1/s1
• Isómeros SMILES: CCCCCCCCCCCCCCCCCC(=O)OCC(CO[C@H]1[C@@H]([C@H]([C@H]([C@H](O1)CO)O)O)O)OC(=O)CCCCCCCCCCCCCCCCC
• Peso molecular: 787.16
• Reaxy-Rn: 26338197
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=26338197&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Glycerolipids
      • Subclass Glycosylglycerols
        • Level5 Glycosyldiradylglycerols
          • Level6 Glycosyldiacylglycerols
            • Level7 1,2-diacyl-3-O-beta-D-galactosyl-sn-glycerols

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Glycerolipids
• Subclass: Glycosylglycerols
• Intermediate Tree Nodes: Glycosyldiradylglycerols - Glycosyldiacylglycerols
• Direct Parent: 1,2-diacyl-3-O-beta-D-galactosyl-sn-glycerols
• Alternative Parents: Fatty acyl glycosides of mono- and disaccharides Hexoses O-glycosyl compounds Fatty acid esters Oxanes Dicarboxylic acids and derivatives Secondary alcohols Carboxylic acid esters Polyols Oxacyclic compounds Acetals Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: 1,2-diacyl-3-o-beta-d-galactosyl-sn-glycerol - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Fatty acid ester - Fatty acyl - Dicarboxylic acid or derivatives - Monosaccharide - Oxane - Carboxylic acid ester - Secondary alcohol - Polyol - Acetal - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary alcohol - Carbonyl group - Alcohol - Organooxygen compound - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as 1,2-diacyl-3-o-beta-d-galactosyl-sn-glycerols. These are glycosyldiacylglycerols carrying a beta-D-galactose at the 3-position of the glycerol moiety.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (no humanos)

Pseudomonas aeruginosa (123386 Activities)

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Staphylococcus aureus (210822 Activities)

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Escherichia coli (133304 Activities)

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Bacillus subtilis (32866 Activities)

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Mycobacterium tuberculosis (203094 Activities)

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Enterococcus faecalis (29875 Activities)

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Kluyveromyces marxianus (909 Activities)

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Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water (partly), and chloroform:methanol:water( 4:1:0.1).
• Peso molecular: 787.200 g/mol
• XLogP3: 14.600
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 41
• Exact Mass: 786.622 Da
• Monoisotopic Mass: 786.622 Da
• Topological Polar Surface Area: 152.000 Ų
• Heavy Atom Count: 55
• Formal Charge: 0
• Complexity: 873.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 5
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1