نتایج جستجو برای: keywordscyp2a6coumarinfluorometryiranpolymorphism7 hydroxycoumarin

تعداد نتایج: 505  

Journal: :The Journal of organic chemistry 2014
Kaitlyn M Mahoney Pratik P Goswami Aleem Syed Patrick Kolker Brian Shannan Emily A Smith Arthur H Winter

Self-immolative aryl phthalate esters were conjugated with cleavable masking groups sensitive to light and hydrogen peroxide. The phthalate linker releases the fluorescent dye 7-hydroxycoumarin upon exposure to light or H2O2, respectively, leading to an increase in fluorescence. The light-sensitive aryl phthalate ester is demonstrated as a pro-fluorophore in cultured S2 cells.

Journal: :Zeitschrift fur Naturforschung. C, Journal of biosciences 2001
A Ivanova B Mikhova T Stambolijska I Kostova

Two new lignan glycosides of dibenzylbutyrolactol type (haplomarin) and arylnaphthalene type (haploborin) were isolated from the aerial parts of Haplophyllumn suaveolens together with the known arylnaphthalene lignan glycoside arabelline and hydroxycoumarin glycoside xeroboside. So far arabelline is found only in H. buxbaunii. This is the first report of the isolation of xeroboside from Haploph...

2012
Johannes Reisch Ranjith W. Dharmaratne

2-Dimethyl-2H-Chromenes, Coumarin Derivatives, Phase-Transfer Catalysis 2,2-Dimethyl-5H-pyrano(3,2-c)-l-benzopyrano-5-one(2) and 4H-2,3-dihydro-3-methyl-2methylene-furan-l-benzopyran-4-one (3), two new coumarin derivatives were synthesised from 4-hydroxycoumarin by treating with 3-chloro-3-methylbut-l-yne and 3-chlorobut-l-yne respectively, both reactions progressing via the phase-transfer cata...

Journal: :Physical chemistry chemical physics : PCCP 2013
Caroline M Krauter Jens Möhring Tiago Buckup Markus Pernpointner Marcus Motzkus

In the present work we have explored the ultrafast relaxation network of coumarin and umbelliferone (7-hydroxy-coumarin) using time-resolved femtosecond spectroscopy and quantum chemical calculations. Despite the importance of the photophysical properties of coumarin derivatives for applications in biomedicine, the low fluorescence quantum yield of coumarin itself has not been fully understood ...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 1997
S L Born P A Rodriguez C L Eddy L D Lehman-McKeeman

Coumarin is used widely as a fragrance constituent and is administered clinically in the treatment of certain lymphedemas and malignancies. Although toxicity occurs only rarely in humans treated clinically with high-dose coumarin, it is well established that coumarin is hepatotoxic in the rat. This species difference in susceptibility to toxicity reflects the disparate metabolic processes occur...

Journal: :Journal of Pharmaceutical and Biomedical Analysis 1996

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2010
Sun-Ha Park Dong-Hyun Kim Dooil Kim Dae-Hwan Kim Heung-Chae Jung Jae-Gu Pan Taeho Ahn Donghak Kim Chul-Ho Yun

Human cytochrome P450 (P450) enzymes metabolize a variety of endogenous and xenobiotic compounds, including steroids, drugs, and environmental chemicals. In this study, we examine the possibility that bacterial P450 BM3 (CYP102A1) mutants with indole oxidation activity have the catalytic activities of human P450 enzymes. Error-prone polymerase chain reaction was carried out on the heme domain-c...

Journal: :Molecules 2011
Ahmed A Al-Amiery Ahmed Y Musa Abdul Amir H Kadhum Abu Bakar Mohamad

New coumarin derivatives, namely 7-[(5-amino-1,3,4-thiadiazol-2-yl)methoxy]-2H-chromen-2-one, 5-[(2-oxo-2H-chromen-7-yloxy)methyl]-1,3,4-thiadiazol-2(3H)-one, 2-[2-(2-oxo-2H-chromen-7-yloxy)acetyl]-N-phenylhydrazinecarbothioamide, 7-[(5-(phenylamino)-1,3,4-thiadiazol-2-yl)methoxy]-2H-chromen-2-one and 7-[(5-mercapto-4-phenyl-4H-1,2,4-triazol-3-yl)methoxy]-2H-chromen-2-one were prepared starting...

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