scholarly journals Identification of ecdysone 22-long-chain fatty acyl esters in newly laid eggs of the cattle tick Boophilus microplus

1986 ◽  
Vol 240 (1) ◽  
pp. 131-138 ◽  
Author(s):  
T Crosby ◽  
R P Evershed ◽  
D Lewis ◽  
K P Wigglesworth ◽  
H H Rees

The five major apolar ecdysone esters present in newly laid eggs of the cattle tick Boophilus microplus have been purified by h.p.l.c. The quantities of the apolar esters present in the eggs were increased by administration of ecdysone to the mature females. G.c.-m.s. analysis, as their methyl esters, of the fatty acids released from the apolar ecdysone derivatives by alkali, coupled with positive-ion fast-atom-bombardment m.s. of the intact ecdysone esters, showed that the compounds consisted of a series of fatty acyl esters of ecdysone. The position of esterification of the ecdysone was established by p.m.r. spectroscopy. The combined data show that the novel apolar derivatives of ecdysone consist of the 22-palmitate, -palmitoleate, -stearate, -oleate, and -linoleate esters respectively. Confirmation was obtained by comparison with synthetic ecdysone 22-palmitate. The significance of the ecdysone fatty acyl esters as a possible source of free hormone during embryogenesis is discussed.

1989 ◽  
Vol 24 (8) ◽  
pp. 679-688 ◽  
Author(s):  
Russell P. Newton ◽  
Terence J. Walton ◽  
Salem A. Basaif ◽  
Andrea M. Jenkins ◽  
A. Gareth Brenton ◽  
...  

2010 ◽  
Vol 428-429 ◽  
pp. 132-134
Author(s):  
Xu Ying Liu ◽  
Wen Guang Wang ◽  
Jia Ling Pu

Due to hexa-peri-hexabenzocoronene (HBC)’s perfect structural and their promising electronic and optoelectronic properties, the novel derivatives of HBC have continuously attracted interest. Hexaphenylbenene, as a necessary precursor to synthesize HBC, is affected by the substituents during dehydrocyclization. New synthetic strategy of some HPC derivatives with long-chain ester groups is described. Their structures were established by 1H nuclear magnetic resonance (1HNMR) and infrared spectrometry (IR), ultraviolet-visible spectrograph (UV-vis). The results indicate that the substituents play an important role on oxydehydrogenation of HPCs.


2005 ◽  
Vol 60 (4) ◽  
pp. 471-475 ◽  
Author(s):  
Barbara Orzeszko ◽  
Tomasz Świtaj ◽  
Anna B. Jakubowska-Mućka ◽  
Witold Lasek ◽  
Andrzej Orzeszko ◽  
...  

Certain adamantylated heterocycles were previously shown to enhance the secretion of tumor necrosis factor alpha (TNF-α) by murine melanoma cells that have been transduced with the gene for human TNF-α and constitutively expressed this cytokine. The stimulatory potency of those compounds depended, among other factors, on the structure of the linker between the adamantyl residue and the heterocyclic core. In the present study, a series of (1-adamantyl)alkylsulfanyl derivatives of heterocyclic compounds was prepared by alkylation of the corresponding thioheterocyles. Of the novel adamantylalkylthio compounds tested in the aforementioned cell line, 2-(2-adamantan-1-ylethylsulfanyl)- 4-methyl-pyrimidine was found to be the most active


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