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61.
Three-dimensional quantitative structure-activity relationship (3D-QSAR) studies for a series of arylsulfonylimidazolidinone derivatives having antitumor activity were conducted using comparative molecular field analysis (CoMFA) and comparative molecular similarity indices analysis (CoMSIA). The in vitro cytotoxicity against human lung carcinoma (A549) exhibited a strong correlation with steric and electrostatic factors of the molecules. Four different types of models have been built using CoMFA and CoMSIA method with AM1 charge or Gasteiger-Huckel charge. By comparison of the statistical results of these models, model I obtained by CoMFA study with AM1 showed the best predictability of the antitumor activities based on the cross-validated value (0.642), conventional r2 (0.981), standard error of estimate (0.106) and PRESS value (0.170). 相似文献
62.
Doddareddy MR Lee YJ Cho YS Choi KI Koh HY Pae AN 《Bioorganic & medicinal chemistry》2004,12(14):3815-3824
Predictive hologram quantitative structure activity relationship (HQSAR) models were developed for a series of arylsulfonamide compounds acting as specific 5-HT6 antagonists. A training set containing 48 compounds served to establish the model. The best HQSAR model was generated using atoms, bond, and connectivity as fragment distinction and 4-7 as fragment size showing cross-validated r2(q2) value of 0.702 and conventional r2 value of 0.971. The predictive ability of the model was validated by an external test set of 20 compounds giving satisfactory predictive r2 value of 0.678. The efficiency of HQSAR approach was further evidenced by the generation of predictive models for a training set containing 30 highly diverse, both specific and nonspecific 5-HT6 antagonists. The best HQSAR model for this training set was generated using atoms, bond, and connectivity as fragment distinction and 4-7 as fragment size showing cross-validated r2(q2) value of 0.693 and conventional r2 value of 0.923. This model was also validated by using an external test set of 10 compounds giving satisfactory predictive r2 value of 0.692. The contribution maps obtained from these models were used to explain the individual atomic contributions to the overall activity. 相似文献
63.
Volsurf analysis of carbapenem antibiotics 总被引:3,自引:0,他引:3
Doddareddy MR Cha JH Cho YS Koh HY Yoo KH Kim DJ Pae AN 《Bioorganic & medicinal chemistry》2005,13(10):3339-3349
64.
Park JH Choi JK Lee E Lee JK Rhim H Seo SH Kim Y Doddareddy MR Pae AN Kang J Roh EJ 《Bioorganic & medicinal chemistry》2007,15(3):1409-1419
A series of compounds were designed as T-type calcium channel blocker containing 6 or 5 pharmacophore features from structure-based virtual screening. To optimize the suggested structure, over 130 derivatives were synthesized and their inhibitory activities on T-type calcium channel were assayed using in vitro screening system with alpha1(G) and alpha1(H) clones. For the compounds with higher activities in FDSS assay system, the efficacy was measured by patch-clamp method. Among the library with 5 features, alkaneamide derivatives (7b, 9j, 11b, 11g, 11h) with 4-arylsubstituted piperazine showed better IC(50) values than Mibefradil. 相似文献
65.
The bacteria Orientia tsutsugamushi is the causative agent of scrub typhus, a prevalent disease in Asian countries that can affect humans and which shows an alarming increase of cases during the last years, especially in rural areas. Unfortunately, there is no vaccine for scrub typhus, and antibiotic treatments successfully used in the past appear to be inefficient to treat some strains of O. tsutsugamushi. We introduce a mathematical model that approximates the dynamics of the bacteria among its natural reservoirs. After computing the basic reproductive number from the proposed model, we explore its sensitivity to the parameter values that may be affected by application of control measures. This theoretical model may be of interest to pest managers as well as health authorities interested in gaining insight into the public management of the disease, through a better understanding of its qualitative dynamics. 相似文献
66.
Boksik Cha Yaerin Park Byul Nim Hwang So-young Kim Eek-hoon Jho 《Molecules and cells》2015,38(8):723-728
Smurf2, a member of the HECT domain E3 ligase family, is well known for its role as a negative regulator of TGF-β signaling by targeting Smads and TGF-β receptor. However, the regulatory mechanism of Smurf2 has not been elucidated. Arginine methylation is a type of post-translational modification that produces monomethylated or dimethylated arginine residues. In this report, we demonstrated methylation of Smurf2 by PRMT1. In vitro methylation assay showed that Smurf2, not Smurf1, was methylated by PRMT1. Among the type I PRMT family, only PRMT1 showed activity for Smurf2. Transiently expressed Smurf2 was methylated by PRMT1, indicating Smurf2 is a novel substrate of PRMT1. Using deletion constructs, methylation sites were shown to be located within amino acid region 224–298 of Smurf2. In vitro methylation assay following point mutation of putative methylation sites confirmed the presence of Arg232, Arg234, Arg237, and Arg239. Knockdown of PRMT1 resulted in increased Smurf2 expression as well as inhibition of TGF-β-mediated reporter activity. Although it is unclear whether or not increased Smurf2 expression can be directly attributed to lack of methylation of arginine residues, our results suggest that methylation by PRMT1 may regulate Smurf2 stability and control TGF-β signaling. 相似文献
67.
68.
Yoon J Yoo EA Kim JY Pae AN Rhim H Park WK Kong JY Park Choo HY 《Bioorganic & medicinal chemistry》2008,16(10):5405-5412
Twenty-four compounds of 4-methoxy-N-[3-(4-substituted phenyl-piperazine-1-yl)propyl] benzene sulfonamides and N-[3-(4-substituted phenyl-piperazine-1-yl)propyl] naphthyl sulfonamides were prepared and evaluated as 5-HT(7) receptor antagonists. Most of the compounds showed the IC(50) values of 12-580nM. Four methyl branched analogues were also obtained, but the activity for methyl branched analogues was almost same as its straight chain congeners. Among the synthesized compounds, 3c showed a good activity on 5-HT(7) receptors and a good selectivity on 5-HT(1a), 5-HT(2a), 5-HT(2c), and 5-HT(6) receptors. 相似文献
69.
Choi JY Seo HN Lee MJ Park SJ Park SJ Jeon JY Kang JH Pae AN Rhim H Lee JY 《Bioorganic & medicinal chemistry letters》2007,17(2):471-475
3,4-Dihydroquinazoline analogues substituted by N-methyl-N-(5-pyrrolidinopentyl)amine at the 2-position were synthesized and their blocking effects were evaluated for T- and N-type calcium channels. Compound 11b (KYS05080), compared to mibefradil (IC50=1.34+/-0.49 microM), was about 5-fold potent (IC50=0.26+/-0.01 microM) for T-type calcium channel (alpha1G) blocking and its selectivity of T/N-type was also improved (7.5 versus 1.4 of mibefradil). 相似文献
70.
Jo MN Seo HJ Kim Y Seo SH Rhim H Cho YS Cha JH Koh HY Choo H Pae AN 《Bioorganic & medicinal chemistry》2007,15(1):365-373
T-type calcium channel is one of therapeutic targets for the treatment of cardiovascular diseases and neuropathic pains. Since the withdrawal of mibefradil, a T-type calcium channel blocker, there have been a lot of efforts to develop T-type calcium channel blockers. A small molecule library of dioxoquinazoline carboxamide derivatives containing 155 compounds was designed, synthesized, and biologically evaluated for T-type calcium channel blocking activity. Among those compounds synthesized, the compound 1n shows the most potent T-type calcium current blocking activity with an IC(50) value of 1.52 microM, which is comparable to that of mibefradil. 相似文献