Caldarchaeol

Caldarchaeol
Skeletal formula of caldarchaeol
Space-filling model of the caldarchaeol molecule
Names
IUPAC name
[(2R,7R,11R,15S,19S, 22S,26S,30R,34R,38R,43R,47R, 51S,55S,58S,62S,66R,70R)- 38-(Hydroxymethyl)- 7,11,15,19,22,26,30,34,43,47,51,55,58,62,66,70-hexadecamethyl- 1,4,37,40-tetraoxacyclodoheptacont-2-yl]methanol
Other names
Dibiphytanyldiglycerol tetraether
Identifiers
99529-31-4 YesY
3D model (Jmol) Interactive image
ChemSpider 4696841 YesY
PubChem 5771745
Properties
C86H172O6
Molar mass 1302.28 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Caldarchaeol is a membrane-spanning lipid found in hyperthermophilic archaea. Membranes made up of caldarchaeol are more stable since the hydrophobic chains are linked together, allowing the microorganisms to withstand high temperatures. It is also known as dibiphytanyldiglycerol tetraether. Two glycerol units are linked together by two strains which consist of two phytanes linked together to form a linear chain of 32 carbon atoms (40 carbons including methyl sidechains).

The configuration of the macrocyclic tetraether has been determined by total synthesis of the C40-diol and comparison with a sample of obtained by degradation of natural tetraether.[1] A synthesis of tetraether has also been carried out.[2]

Notes

  1. C. H. Heathcock; B. L. Finkelstein; E. T. Jarvi; P. A. Radel; C. R. Hadley (1988). "Acyclic stereoselection. Part 42. 1,4- and 1,5-Stereoselection by sequential aldol addition to a .alpha.,.beta.-unsaturated aldehydes followed by Claisen rearrangement. Application to total synthesis of the vitamin E side chain and the archaebacterial C40 diol". J. Org. Chem. 53 (9): 1922–1942. doi:10.1021/jo00244a017.
  2. T. Eguchi; K. Ibaragi; K. Kakinuma (1998). "Total Synthesis of Archaeal 72-Membered Macrocyclic Tetraether Lipids". J. Org. Chem. 63 (8): 2689–2698. doi:10.1021/jo972328p. PMID 11672138.

Additional references

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