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?-L-Gulopyranosyl-caldarchaetidyl-glycerol

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    ?-L-Gulopyranosyl-<wbr/>caldarchaetidyl-<wbr/>glycerol
  • ?-L-Gulopyranosyl-<wbr/>caldarchaetidyl-<wbr/>glycerol
Cat No: 27203
Biochemicals - Lipids
Cayman

β-L-Gulopyranosyl-caldarchaetidyl-glycerol is the main polar lipid of the archaeon T. acidophilum.{42663} Cellular levels of β-L-gulopyranosyl-caldarchaetidyl-glycerol in T. acidophilum HO-62 positively and negatively correlate with increases in cultu...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • [(2S,7R,11R,15S,19S,22S,26S,30R,34R,38S,43R,47R,51S,55S,58S,62S,66R,70R)-38-[[[(2,3-dihydroxypropoxy)hydroxyphosphinyl]oxy]methyl]-7,11,15,19,22,26,30,34,43,47,51,55,58,62,66,70-hexadecamethyl-1,4,37,40-tetraoxacyclodoheptacont-2-yl]methyl ?-L-gulopyranoside
Correlated keywords:
  • 194805-31-7 776306-78-6 Gulopyranosylcaldarchaetidylglycerol Thermoplasma HO62 MPL Gu CGp CG p ?-1 Archaebacteria
Product Overview:
β-L-Gulopyranosyl-caldarchaetidyl-glycerol is the main polar lipid of the archaeon T. acidophilum.{42663} Cellular levels of β-L-gulopyranosyl-caldarchaetidyl-glycerol in T. acidophilum HO-62 positively and negatively correlate with increases in culture pH and temperature, respectively. β-L-gulopyranosyl-caldarchaetidyl-glycerol has been used as a standard for the quantification of polar lipids extracted from T. acidophilum HO-62. [Matreya, LLC. Catalog No. 1303]
Size 1 mg
Shipping dry ice
CAS Number 416880-23-4
Molecular Formula C95H189O16P
SMILES C[C@H]1CCC[C@@H](C)CCOC[C@@H](COP(OCC(O)CO)(O)=O)OCC[C@H](C)CCC[C@H](C)CCC[C@H](C)CCC[C@H](C)CC[C@@H](C)CCC[C@@H](C)CCC[C@@H](C)CCC[C@@H](C)CCOC[C@@H](CO[C@@H]2[C@@H](O)[C@@H](O)[C@H](O)[C@H](CO)O2)OCC[C@H](C)CCC[C@H](C)CCC[C@H](C)CCC[C@H](C)CC[C@@H](C)CC
Molecular Weight 1618,5
Formulation A solid
Purity ≥95%
Custom Code 2932.99
UNSPSC code 12352100

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Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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