نتایج جستجو برای: 8 tetrahydro 1 benzothieno2

تعداد نتایج: 3083482  

Journal: :Acta Crystallographica Section E Structure Reports Online 2010

A quantitative structure-activity relationship (QSAR) study was conducted for the prediction of inhibitory activity of 1-phenyl[2H]-tetrahydro-triazine-3-one analogues as inhibitors of 5-Lipoxygenase. The inhibitory activities of the 1-phenyl[2H]-tetrahydro-triazine-3-one analogues modeled as a function of molecular structures using chemometrics methods such as multiple linear regression (MLR) ...

Journal: :Oman medical journal 2012
Gollapalle L Viswanatha Shylaja Hanumanthappa Srinath Rangappa Saravanan Janardhanan

OBJECTIVES The present study was aimed to evaluate the anti-hyperlipidemic activity of newly synthesized tricyclic benzothieno 1, 2, 3-triazine derivatives namely CP-1 (3-(methyl)- 5,6,7,8-tetrahydro,3H-benzo[4,5] thieno [2,3-d][1,2,3] triazin-4-one), CP-2 (3-(ethyl)- 5,6,7,8-tetrahydro,3H-benzo[4,5] thieno [2,3-d][1,2,3] triazin-4-one) and CP-6 (3-(2-chloro phenyl)-5,6,7,8-tetrahydro,3H-benzo[...

2010
Hironori Tsuchiya Shuichi Ohmoto

The effects of 14 -carbolines on human platelet aggregability were comparatively studied, and the effects on lipid membranes were determined. Several -carbolines inhibited platelet aggregation induced by collagen, epinephrine, adenosine 5’-diphosphate, platelet-activating factor and thrombin. This activity was structure-dependent. Of all the compounds examined, 1-methyl-1,2,3,4tetrahydro-carbol...

Journal: :Cancer research 1984
F L Chung R Young S S Hecht

Acrolein reacted with deoxyguanosine at pH 7 and 37 degrees to give three major products, Adducts 1 to 3, which were separated by high-performance liquid chromatography. They were identified by their ultraviolet, mass, and nuclear magnetic resonance spectra, by the spectra of the corresponding guanine derivatives, and by chemical transformations. Adducts 1 and 2 were two rapidly equilibrating d...

Journal: :Chemical & pharmaceutical bulletin 2008
Yu-Lin Feng He-Ran Li Yi Rao Xiao-Jian Luo Li-Zhen Xu Yue-Sheng Wang Shi-Lin Yang Susumu Kitanaka

Two new sulfated triterpenoid saponins, zygophylosides Q (1) and R (2), have been isolated from the barks of Zygophyllum fabago L. Their structures were elucidated as 3beta,24,28,30-tetrahydro-urs-20-ene-24-O-sulphonyl-3-O-[beta-D-glucopyranosyl]-30-O-beta-D-glucopyranoside and 3beta,24,28,30-tetrahydro-urs-20-ene-24-O-sulphonyl-3-O-[beta-D-xylopyranosyl]-30-O-beta-D-glucopyranoside, respective...

2009
Md Salahuddin Sanjay Singh

Cyclization and chlorination of 2-amino-5-benzyl-4, 5, 6, 7-tetrahydro hydro thieno [3, 2c] pyridine-3carboxamide yielded (3 a-b). Reaction with different substituted pyridines of [3 a-b] yielded 4a (1-4) and 4b (1-2). However reaction of 3a with different substituted 2-amino phenols yielded 4a (5-6). Further 3a yields 4a (7) & 4a (8) from different substituents like o-phenylene diamine and 4-c...

Journal: :Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 2001
E Kendi Z Ates-Alagoz S Suzen E Buyukbingol

retinoids with a tetrahydronaphthalene structure (Fig. 1), was synthesized using an NaHSO3 addition product of 5,6,7,8tetrahydro-5,5,8,8-tetramethyl-2-naphthalene-carboxaldehyde (compound I) as a starting material, which was prepared as described.1 The condensation of compound I and 4-ethylamino3-amino-ethylbenzoate (mp: 73 ̊C) in DMF for 70 h gave the title compound (recrystallized from hexane/...

2016
Sreekanth Kokkonda Xiaoyi Deng Karen L. White Jose M. Coteron Maria Marco Laura de las Heras John White Farah El Mazouni Diana R. Tomchick Krishne Manjalanagara Kakali Rani Rudra Gong Chen Julia Morizzi Eileen Ryan Werner Kaminsky Didier Leroy María Santos Martínez-Martínez Maria Belen Jimenez-Diaz Santiago Ferrer Bazaga Iñigo Angulo-Barturen David Waterson Jeremy N. Burrows Dave Matthews Susan A. Charman Margaret A. Phillips Pradipsinh K. Rathod

Malaria persists as one of the most devastating global infectious diseases. The pyrimidine biosynthetic enzyme dihydroorotate dehydrogenase (DHODH) has been identified as a new malaria drug target, and a triazolopyrimidine-based DHODH inhibitor 1 (DSM265) is in clinical development. We sought to identify compounds with higher potency against Plasmodium DHODH while showing greater selectivity to...

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