Results 121 to 130 of about 2,743 (163)

Influence of the Solvent and the Harvesting Site on the Content of Phenolic Compounds and the in Vitro Antidiabetic Potential of Leafy Stems and Roots of <i>Phyllanthus amarus Schum. and Thonn</i>. [PDF]

J Exp Pharmacol
Zanté AA, Zoungo D, Sanou Y, Kabré P, Ouédraogo RJ, Belemnaba L, Ouattara L, Ouoba P, Ouédraogo GA.   +8 more
europepmc   +1 more source

Comparative evaluation of volatile compounds and lipidomic profile in different cuts of Gangba sheep. [PDF]

Food Chem X
Xie Y, Zhang H, Shui Y, Gu X, Tang H, Cheng L, Wang J, Geng F.   +7 more
europepmc   +1 more source

Marine-Derived Defenses Against HIV: Emerging Bioactive Molecules from the Seas. [PDF]

Mar Drugs
Santos T, Pintão A, Marques CS, Brandão P.   +3 more
europepmc   +1 more source

[Pharmacological properties of certain thiazoline derivatives].

Medycyna doswiadczalna i mikrobiologia, 1998
D, DARZYNKIEWICZ-CZERNIK, P, POLAKOWSKI, A, SZADOWSKA   +2 more
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GlcNAc-Thiazoline conformations

Bioorganic & Medicinal Chemistry, 2009
The title compound, a powerful inhibitor of retaining N-acetylhexosaminidases, can move freely among three pyranose solution conformations of similar energy-two twist boats and the (4)C(1) chair-as revealed by NMR, calculational, and crystallographic studies.
Knapp, S., Fash, D., Abdo, M., Emge, T. J., Rablen, Paul R.   +4 more
openaire   +3 more sources

ChemInform Abstract: N‐Acyl‐4‐thiazolines from 3‐Thiazolines.

ChemInform, 1991
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
J. MARTENS, H.‐H. JANKNECHT
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D3-Thiazolines, D4-Thiazolines and Thiazoles from Penem Antibiotics

HETEROCYCLES, 1992
Upon cleavage of the β-lactam ring, penems are converted to unstable Δ 4 -thiazolines, which epimerize at the ex-C-5 position, lose a nucleofugal group at C-2' (if originally present), tautomerize to Δ 3 -thiazolines, or suffer hydrolytic decomposition.
Ugo Chiacchio, Giuseppina Visentin, Ettore Perrone, Daniela Borghi, Vincenzo Rizzo, Marco Alpegiani, Angelo Bedeschi, Riccardo Corigli Giovanni Rivola, Giovanni Franceschi   +8 more
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Thiazoline carboxylic acid from formylcysteine

Experientia, 1957
La formilcisteina in HCl 12N da un assorbimento nell'ultravioletto indicante la formazione di un anello tiazolinico. La reazione e piu rapida per la formilcisteina che per il glutatione e dipende dalla concentrazione dell'acido. Trattando la formicilsteina con HCl 12N, e stato preparato un composto avente le proprieta dell'acido tiazolin carbossilico ...
D, CAVALLINI, B, MONDOVI, C, DE MARCO
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Infrarotspektren einiger Thiazoline

Chemische Berichte, 1955
AbstractDie Infrarotspektren von 15 in 2‐Stellung substituierten Thiazolinen wurden aufgenommen. Folgende charakteristische Frequenzen treten auf: a) 6.1–6.45 μ (stark), b) 8.0–8.4 μ (mittelstark bis schwach) und c) 9.8–10.5 μ (stark). Thiazole absorbieren im Bereich a) (6.1–6.45 μ) nur schwach, Thiazolidine nicht.
Otting, W., Drawert, F.
openaire   +2 more sources