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DL-эритро-Dihydrosphingosine структурированное изображение

DL-эритро-Dihydrosphingosine

  • английское имяDL-erythro-Dihydrosphingosine
  • CAS №3102-56-5
  • CBNumberCB6139144
  • ФормулаC18H39NO2
  • мольный вес301.51
  • EINECS608-571-3
  • номер MDLMFCD00079141
  • файл Mol3102-56-5.mol
химическое свойство
Температура плавления 70-72°C
Температура кипения 446.2±25.0 °C(Predicted)
плотность 0.927±0.06 g/cm3(Predicted)
температура хранения −20°C
растворимость chloroform/methanol (9:1): 20 mg/mL, clear, colorless to faintly yellow
форма Solid
пка 12.57±0.45(Predicted)
цвет white
Растворимость в воде Soluble in water (partly miscible), chloroform, 100% warm ethanol (25 mg/ml), warm DMSO (25 mg/ml), and methanol.
InChI InChI=1/C18H39NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(21)17(19)16-20/h17-18,20-21H,2-16,19H2,1H3/t17-,18+/s3
ИнЧИКей OTKJDMGTUTTYMP-LHIQYTEENA-N
SMILES C(O)[C@@H](N)[C@@H](O)CCCCCCCCCCCCCCC |&1:2,4,r|
Справочник по базе данных CAS 3102-56-5(CAS DataBase Reference)
Заявления об опасности и безопасности
WGK Германия 3

DL-эритро-Dihydrosphingosine химические свойства, назначение, производство

Описание

DL-erythro Sphinganine (d18:0) is a precursor of ceramide and sphingosine as well as a substrate of sphingosine kinases, which generate sphinganine-1-phosphate . Sphinganine levels increase significantly in response to certain mycotoxins, including fumonisins as well as in some cancers. This product is a mixture of sphinganine (d18:0) , L-erythro sphinganine (d18:0) , D-threo sphinganine (d18:0) , and L-threo sphinganine (d18:0). [Matreya, LLC. Catalog No. 1324]

Химические свойства

White Powder

Использование

DL-erythro-Dihydrosphingosine is an inhibitor of PKC (protein kinase C). This compound also blocks PLA2 (phospholipases A2) and the D-sphingosine precursor.

Биологические функции

Sphingosine (Sph) is emerging as an intracellular regulator of cellular differentiation and apoptosis. Three stereoisomers,d-erythro-Sph,l-threo-Sph, and dl-erythro-dihydrosphingosine, were tested in the induction of apoptosis and inhibition of MAPK activity in three different kinds of solid tumour cell lines. d-erythro-Sph was strongest in these effects among the three compounds. l-threo-Sphingosine was partly active. On the other hand,dl-erythro-dihydrosphingosine was inactive[1].

Биологическая активность

Protein kinase C inhibitor.

Методы очистки

Purify it by recrystallisation from pet ether/EtOAc or CHCl3. The (±)-N-dichloroacetyl derivative has m 142-144o (from MeOH). [Shapiro et al. J Am Chem Soc 80 2170 1958, Shapiro & Sheradsky J Org Chem 28 2157 1963.] The D-isomer crystallises from pet ether/Et2O and has m 78.5-79o, [] 28 +6o (CHCl3/MeOH, 10:1). [Grob & Jenny Helv Chim Acta 35 2106 1953, Jenny & Grob Helv Chim Acta 36 1454 1953, Beilstein 4 I 448, 4 II 757, 4 III 854, 4 IV 1887.]

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DL-эритро-Dihydrosphingosine Обзор)