磺酰

The biodegradation behaviors of six kinds of fatliquors have been researched including sulphated castor sulphated neatsfoot oil, sulphated fish oils, lecithin, chlorinated paraffin and alkyl sulfonyl chloride.

基于活性污泥处理，对制革生产中6种典型加脂剂（硫酸化牛蹄油、硫酸化蓖麻油、硫酸化鱼油、卵磷脂、氯化石蜡和烷基磺酰氯）的生物降解特性进行了系统研究。

MSMstands for Methyl Sulphonyl Methane – a naturally occurring organic sulphur compound that provides building blocks for the production of joint cartilage.

的MSM代表甲基磺酰甲烷-一种天然的有机硫化合物，提供积木生产关节软骨。

By the nucleophilic substitution reaction of 6-O-tosyl-l,2:3,4-di-O- isopropylidene-a-Z-galactopyranose (3) with some substituted 1, 2,4- triazole-3-thiols (4a ~ 4c) or 1, 2, 3,4-tetrazole-5-thiols (5a~5f), nine 6-S-(substituted triazolyl or tetrazolyl)-l,2 : 3,4-di-O- isopropylidene-a-D-galactopyranoses (6a ~ 6i) were prepared in high yields. Their structures and configurations were analyzed and established by elemental analysis, IR, NMR, MS spectra.

报道了6－O－对甲苯磺酰基－1，2：3，4－二－O－异亚丙基－α-D吡喃型半乳糖（3）与取代的3－巯基三唑或5－巯基四唑4a-4c或5a-5f的亲核取代反应，合成了9个6－S－－1，2：3，4－二－O－异亚丙基－α- D吡喃型半乳糖（6a-6i），通过元素分析，IR，NMR和MS确证了上述化合物的结构，并经分子模型计算进行了其构象分析。

Of thiazoles, sub-Sulfonamide, guanidine type, thiuram type accelerator has activation.

对噻唑类、次磺酰胺类、胍类、秋兰姆类促进剂有活化作用。

Herein, using grafting strategy we have developed a new kind of sulfamide-amine alcohol ligands by grafting a activator to the traditional aminoalcohols, which led to more rigid tridentate coordination model and benefit to the control of chiral surrounding.

本文提出一种嫁接策略设计新的手性配体，即在传统的氨醇配体上嫁接上一个活化剂就可以得到一类新型的手性磺酰胺-氨醇配体。

A readily available β-sulfonamide alcohol-titanium complex was found to be effective on promoting the asymmetric addition reaction of an alkynylzinc reagent to unactivated simple ketones under very mild conditions.

为此我们合成了一系列β-磺酰胺基醇，并将其作为配体与Ti4一起催化炔基锌对简单非活化酮的不对称加成反应。

PBMC treated with inhibitor N-tosyl phenylalanine chlormethyl ketone, Astragalus can increase the activity of NF-κ B and the concentration of IL-8 in patients with PNS. it also increases the the activity of NF-κ B in normal children , but can ' t affected the concentration of IL-8 in normal children. ConclusionIn patients with PNS , the activity of NF-κ B was up-regulated and the level of IL-8 was significantly elevated.

结果肾病患儿 NF-κ B 活性及 IL-8含量增高，2者呈正相关； IL-1β刺激后，黄芪降低肾病患儿 NF-κ B 活性及 IL-8含量、降低正常儿童 NF-κ B 活性而不影响 IL-8含量；用对甲苯磺酰-L-苯丙氨酸氯甲基甲酮抑制后，黄芪可提高肾病患儿 NF-κ B 活性及 IL-8含量、提高正常儿童 NF-κ B 活性；而不影响 IL-8含量。

It is shown that the optimal conditions for the reaction of CADB with SESA are pH 12.0 and m:m=6:1.The product p-aminobenzart sulfanily ethyl CADBwas diazotized and linked with lipase.The optimal pH for lipase linked to diao-compound is 7.5.The link time is at last 12h.

试验结果表明：CADB与SESA反应的最适条件是pH＝12.0，SESA与CADB质量比为6：1，反应生成的对氨基苯磺酰乙基交联烯丙基葡聚糖凝胶经重氮化后与脂肪酶偶联的最适条件是pH7.5，偶联时间≥12h。

The alkylation of a-methylene of PhSO2CH2COPh with alkyl halides catalyzed by quaternary ammonium base resin in 50% aqueous sodium hydroxide solution was investigated.

本文以季铵碱树脂作为聚合物固载的相转移催化剂，在50%氢氧化钠水溶液中催化α-苯磺酰基苯乙酮(1)的α-亚甲基的烷基化反应。

The PCR products were examined by agarose gel electrophoresis. The target gene fragments were purified by gel extraction kit and ligated to cloning vector pMD18-T. The recombinant vectors were transformed into host strain E. coli K802 by lithium chloride method, screened and identified with PCR and restrictive enzymatic digestion. Their sequences were confirmed by DNA sequencing.(2) sTWEAK1 gene was subcloned into expression vector pProEx HTb and transformed into E. coli BL21. sTWEAK2 gene was subcloned into expression vector pMAL-C2x and transformed into E. coli TB1. The recombinant vectors were screened and identified with PCR and restrictive enzymatic digestion. The recombinant fusion proteins were induced to express with IPTG, detected by coomassie brilliant blue-stained SDS-polyacrylamide gel electrophoresis , and confirmed by Western blot analysis.(3) The sTWEAK1 fusion protein was purified with Ni-NTA Spin Kit.(4) The biological activity was assayed on transformed and tumor cells by microplate photometer after crystal violet or sulfur rodamine B staining.(5) The contents of IL-8 in the supernatant of 1990 cell cultures were determined by ELISA.(6) The morphological changes of the sensitive cells were observed by light and transmission electron microscopies.(7) The cell cycle and apoptotic rate were assayed by flow cytometry in 1990 and M85 cells.(8) The effect of fusion proteins on induction of NF-κB in 1990 and LOVO cells was detected with Dual-Luciferase Reporter Assay system.(9) The TWEAK gene was subcloned into Adeno-X Viral DNA with pShuttle vector and transfected into HEK293 cells by lipofectamine method.

(1)本研究用RT-PCR方法，从人组织细胞总RNA中扩增可溶性TWEAK胞外区（sTWEAK1和sTWEAK2）的cDNA序列及全长编码序列，用琼脂糖凝胶电泳分析PCR产物，胶回收目的基因片段，连接到pMD18-T克隆载体中，转化大肠杆菌K802，PCR和酶切筛选阳性克隆，全自动DNA测序验证序列；(2)sTWEAK1和sTWEAK2分别亚克隆到pProEx HTb和pMAL-C2x表达载体中，分别转化大肠杆菌BL21和TB1，PCR筛选和酶切鉴定，阳性克隆用IPTG诱导表达，表达产物用SDS-PAGE分析和Western blot验证融合蛋白；(3)用NTA-Ni Spin试剂盒初步分离纯化sTWEAK1融合蛋白；(4)用体外培养的肿瘤细胞和正常对表达产物进行活性检测，贴壁细胞用结晶紫染色法，悬浮细胞用磺酰罗丹明B染色法，酶标仪检测OD值；(5)敏感细胞用ELISA法检测细胞培养上清中IL-8的含量；(6)用光镜和电镜观察敏感细胞死亡和细胞凋亡情况；(7)用流式细胞仪分析表达产物对敏感细胞凋亡率和细胞周期的影响；(8)用双荧光素酶报告基因检测法，测定表达产物对敏感细胞NF-κB的影响；(9)用pShuttle穿梭质粒将TWEAK重组到腺病毒载体上，用脂质体转染法转染HEK293细胞，PCR鉴定重组质粒。

Plunder melds and run with this jewel!

掠夺melds和运行与此宝石！

My dream is to be a crazy growing tree and extend at the edge between the city and the forest.

此刻，也许正是在通往天国的路上，我体验着这白色的晕旋。