96089-43-9Relevant academic research and scientific papers
Aldehydes can switch the chemoselectivity of electrophiles in protein labeling
Adusumalli, Srinivasa Rao,Rawale, Dattatraya Gautam,Rai, Vishal
, p. 9377 - 9381 (2018)
We show that the chemoselectivity of an electrophile in protein labeling can be promiscuous. An aldehyde enables switching of chemoselectivity of an epoxide and a sulfonate ester along with an enhanced rate of reaction. The chemical technology renders single-site installation of diverse probes on a protein and delivers analytically pure tagged proteins.
Ag+-induced reverse vesicle to helical fiber transformation in a self-assembly by adjusting the keto-enol equilibrium of a chiral salicylideneaniline
Datta, Sougata,Bhattacharya, Santanu
, p. 13929 - 13932 (2015)
A new chiral amphiphilic salicylideneaniline bearing a terminal pyridine was synthesized. It formed reverse vesicles in toluene. The addition of Ag+, however, reversibly transforms these reverse vesicles into left-handed nanohelices accompanied by spontaneous gel formation at room temperature.
Preparation method of 4-hydroxymethyl-3-methoxyphenoxyacetic acid
-
Paragraph 0053, (2018/05/16)
The invention discloses a preparation method of 4-hydroxymethyl-3-methoxyphenoxyacetic acid, comprising the steps of a) subjecting the start material 2,4-dihydroxybenzaldehyde and halogenated ethyl acetate to nucleophilic substitution reaction under the a
MULTI-FUNCTIONAL CHEMICAL AGENTS, AND THE METHOD FOR PROTEIN MODIFICATION
-
Page/Page column 23, (2017/10/11)
A multifunctional chemical agents comprising functional agents Fn1, Fn2 and linkers, for the linchpin directed (LDM), protein directed (PDPM) modifications of proteins, and Fn1 accelerated kinetic labeling by Fn2.
Evidence of aggregation induced emission enhancement and keto-enol-tautomerism in a gallic acid derived salicylideneaniline gel
Datta, Sougata,Bhattacharya, Santanu
supporting information; scheme or table, p. 877 - 879 (2012/02/14)
A novel salicylideneaniline type fluorescent organogelator based on a 3,4,5-(tri-dodecyloxy)benzoyl group immobilizes aromatic solvents. The resulting gels show enhancement in emission and thermochromic/non-photochromic behaviour during sol-to-gel transit
A series of 2(Z)-2-benzylidene-6,7-dihydroxybenzofuran-3[2H]-ones as inhibitors of chorismate synthase
Thomas, Michael G.,Lawson, Chris,Allanson, Nigel M.,Leslie, Bruce W.,Bottomley, Joanna R.,McBride, Andrew,Olusanya, Oyinkan A.
, p. 423 - 426 (2007/10/03)
A series of 2(Z)-2-benzylidene-6,7-dihydroxybenzofuran-3[2H]-ones was identified as potent inhibitors of bacterial chorismate synthase. The 2′-hydroxy-4′-pentoxy analogue 33 is a potent inhibitor of Streptococcus pneumoniae chorismate synthase.
8-Aryl- and 8-cycloalkyl-1,3-dipropylxanthines: Further potent and selective antagonists for A1-adenosine receptors
Shamim,Ukena,Padgett,Hong,Daly
, p. 613 - 617 (2007/10/02)
A series of 1,3-dipropylxanthines were prepared with a variety of substituents at the 8-position. These included 8-aryl and 8-cycloalkyl groups. Polar carboxylate and carboxamide moieties were introduced as aryl substituents to increase water solubility.
