997-55-7Relevant articles and documents
Synthetic strategy of new powerful tris-bisphosphonic ligands for chelation of uranyl, iron, and cobalt cations
Burgada, Ramon,Bailly, Théodorine,Prangé, Thierry,Lecouvey, Marc
, p. 2315 - 2319 (2007)
New tripodal uranyl ion chelators containing gem-bisphosphonic units have been synthesized. All bisphosphonic units present a side chain with 0, 1, or 2 methylene group terminated by -NH2 or -CO2H group. These units were respectively coupled with a -CO2H or -NH2 functions of a suitable tri-functional platform. The shape and size of the new designed ligands were selected and validated through computer molecular modelization.
Peptide Tyrosinase Activators
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, (2015/06/10)
Peptides that increase melanin synthesis are provided. These peptides include pentapeptides YSSWY, YRSRK, and their variants. The peptides may activate the enzymatic activity of tyrosinase to increase melanin synthesis. The pharmaceutical, cosmetic, and other compositions including the peptides are also provided. The methods of increasing melanin production in epidermis of a subject are provided where the methods include administering compositions comprising an amount of one or more peptides effective to increase the melanin production. The methods also include treating vitiligo or other hypopigmentation disorders with compositions including one or more peptides.
Reactions of substituted aspirins with amino acids
Orth, Elisa S.,Medeiros, Michelle,Souza, Bruno S.,Caon, Natalia B.,Kirby, Anthony J.,Nome, Faruk
supporting information, p. 939 - 945 (2014/01/06)
Acyl transfers are key reactions in biology and in the laboratory. In biological systems they are involved in energy transport, in the assembly of complex molecules and in the mechanisms of efficient action of many hydrolytic enzymes. We report a mechanistic and calculational study of the selective N-acylation reactions of amino acids by substituted aspirins, under mild conditions, in water at 25 °C. The acetylated amino-acid products of the reactions were identified by nuclear magnetic resonance, and the reaction steps were studied by density functional theory. Copyright
Detection of enzyme activity through catalytic signal amplification with functionalized gold nanoparticles
Bonomi, Renato,Cazzolaro, Alessandro,Sansone, Anna,Scrimin, Paolo,Prins, Leonard J.
supporting information; scheme or table, p. 2307 - 2312 (2011/04/21)
A cascade of two catalytic events was used to detect enzyme activity: When a peptide substrate acting as an inhibitor for a catalytic gold nanoparticle was hydrolyzed by an enzyme, the catalytic activity of the nanoparticle was restored, and a large amount of a yellow reporter molecule was produced (see picture; S=substrate, P=product). The assay can be made selective for a particular enzyme by changing the inhibitory peptide. (Chemical Equation Presented).
Peculiar stability of amino acids and peptides from a radical perspective
Watts, Zachary I.,Easton, Christopher J.
supporting information; experimental part, p. 11323 - 11325 (2011/03/19)
(Chemical Equation Presented) Photochemical reactions of free and N-acetyl α-amino acids with chlorine and deuterium labeled hydrogen peroxide have been used to determine both the relative rates of reaction of molecules of these classes and the relative reactivity of their different types of hydrogen toward abstraction by chlorine and oxygen centered radicals. The relative rates of reaction of these species range over more than 3 orders of magnitude; however, where data are available from more than one amino acid for a particular type of group at a specific position on the side chain, the values are remarkably similar. The predictive utility of these results has been demonstrated for the regioselective chlorination of tripeptides. More generally this analysis shows that the backbone and adjacent side chain positions of amino acids and peptides are peculiarly resistant to hydrogen atom transfer, and a similar pattern of reactivity has been noted from earlier studies of reactions of modified substrates catalyzed by isopenicillin-N-synthetase. Such resistance stands out in contrast to the common occurrence of free radical reactions of α-amino acids, peptides, and proteins and their importance in biology. Nevertheless, it provides a reason for the ability of amino acids and their derivatives to avoid degradation in Nature where they are constantly exposed to radicals, and it accounts, at least in part, for the anomalous ability of enzymes to catalyze free radical reactions without being broken down by the radical intermediates.
Cosmetic composition
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, (2008/06/13)
A composition suitable for topical application to mammalian skin and hair for inducing, maintaining or increasing hair growth comprises a hair growth promoter chosen from glutamine derivatives and salts thereof. The composition preferably also comprises an activity enhancer which may be chosen from hair growth stimulants, penetration enhancers and cationic polymers.
Cosmetic composition containing DOPA derivatives
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, (2008/06/13)
A composition for topical application to human hair or skin contains a chemical analogue of dihydroxyphenyl alanine (DOPA). This chemical analogue can be absorbed by skin or by a hair follicle and metabolised in-vivo, thus leading to the formation of melanin in skin or to the growth of melanin-pigmented hair. Consequently the composition can give controlled skin darkening to mimic sun-induced tanning or can bring about the growth of dar hair in place of the grey or white hair.
Cosmestic composition
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, (2008/06/13)
A composition suitable for topical application to mammalian skin and hair for inducing, maintaining or increasing hair growth comprises a hair growth promoter chosen from glutamic acid derivatives and salts thereof. The composition preferably also comprises an activity enhancer which may be chosen from hair growth stimulants, penetration enhancers and cationic polymers.
Acetylation under ultrasonic conditions: Convenient preparation of N-acetylamino acids
Veera Reddy,Ravindranath
, p. 257 - 264 (2007/10/02)
An efficient and simple method of preparation of acetylamino acids from amino acids under ultrasonic conditions is described. The reactions proceed without racemization and the yields are almost quantitative.
Hair growth composition containing citric acid esters
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, (2008/06/13)
Triesters of citric acid are used for inducing, maintaining or increasing hair growth. Compositions for topical application to mammalian hair or scalp comprise an effective amount of from 1% to 99% by weight of an ester of citric acid having the structure (1): where, R1, R2 and R3 each independently represent a branched or unbranched alkyl, alkenyl, aryl, alkylaryl or arylalkyl group, each said group having from 1 to 18 carbon atoms, R4 represents -H, or a branched or unbranched saturated or unsaturated acyl, alkyl, aryl, alkylaryl or aylalkyl group having from 1 to 18 carbon atoms, in the presence of a cosmetically acceptable vehicle for the citric acid ester and in the absence of solid absorbent for the ester;, said effective amount of said ester being sufficient to increase hair growth in the rat, when said composition is applied topically thereto over a period of no more than three months, by at least 10% more than that obtainable using a control composition from which the said ester has been omitted, in accordance with the Rat Hair Growth Test.
