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Tashfeen Akhtar 《Tetrahedron letters》2007,48(49):8673-8677
Six tail-to-tail amine-linked neodisaccharides were synthesised as potential glycomimetics. Primary-primary linked compounds were synthesised using Mitsunobu chemistry with glucose-6-sulfonamides as nucleophiles and primary carbohydrate alcohols as electrophiles. Primary-secondary linked compounds were synthesised by epoxide ring opening with carbohydrate 6-amines. Deprotection of all neodisaccharides was carried out using dissolving metal reduction. 相似文献
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Bello D Aslam T Bultynck G Slawin AM Roderick HL Bootman MD Conway SJ 《The Journal of organic chemistry》2007,72(15):5647-5659
The design of a range of 4-position-modified D-myo-inositol 1,4,5-trisphosphate derivatives is described. The enantioselective synthesis of these compounds is reported, along with initial biological analysis, which indicates that these compounds do not act as D-myo-inositol 1,4,5-trisphosphate receptor agonists or antagonists. 相似文献
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Keddie NS Ye Y Aslam T Luyten T Bello D Garnham C Bultynck G Galione A Conway SJ 《Chemical communications (Cambridge, England)》2011,47(1):242-244
The syntheses of four D-myo-inositol 1,4,5-trisphosphate (InsP(3)) derivatives, incorporating phosphate bioisosteres at the 5-position, are reported. The methyl phosphate ester and sulfate derivatives retain InsP(3) receptor (InsP(3)R) agonist activity; the compounds that possess a methylphosphonate or a carboxymethyl moiety are InsP(3)R antagonists. 相似文献
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Tashfeen Akhtar Shahid Hameed Najim A. Al‐Masoudi Khalid M. Khan 《Heteroatom Chemistry》2007,18(3):316-322
5‐substituted 4‐(4‐chlorophenyl)‐4H‐1,2,4‐triazol‐3‐thiones 3 and 2‐substituted 5‐(4‐chlorophenylamino)‐1,3,4‐thiadiazoles 4 were prepared from the intermediate thiosemicarbazides 2 under basic and acidic conditions, respectively. The thiosemicarbazides, in turn, were prepared by the reaction of hydrazides 1 with 4‐chlorophenylisothiocyanate in MeOH. Some of the new synthesized compounds were assayed against HIV‐1 and HIV‐2 in MT‐4 cells. All the compounds were inactive except 3f , which showed an EC50 value of 23.9 μg/mL and 9.9 μg/mL against HIV‐1 and HIV‐2 with a therapeutic index of 3 and 7, respectively. It means that compound 3f was cytotoxic to MT‐4 cells at CC50 of 72.7 μg/mL in both strains. © 2007 Wiley Periodicals, Inc. Heteroatom Chem 18:316–322, 2007; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20282 相似文献
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Iftikhar Ahmad Hassan Adnan Anjum Muneeb Ullah Malik Sohail Ali Tashfeen 《Acoustical Physics》2019,65(5):471-477
Acoustical Physics - In this article, an acoustic energy harvester (AEH) is conceptualized, designed, fabricated and tested. The developed AEH (DAEH) consists of two Helmholtz cavities (HCs) and a... 相似文献
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Tashfeen Aslam 《Tetrahedron letters》2005,46(18):3249-3252
Two C-glycosides related to the recurrent α-d-arabinofuranosyl-(1→5)-α-d-arabinofuranosyl structural motif of mycobacterial arabinan have been prepared by routes involving acetylenic intermediates. 相似文献
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