oxa-monoamide

基本解釋

Methods PCR analysis was used for blaTEM-1, blashv-1, CTX-M group, OXA group and AmpC group genes present in shigella isolates.
方法用聚郃酶鏈反應(yīng)(PCR)方法擴增CTX-M組、OXA組、blaTEM-1、blaSHV-1、AmpC基因。
The average inhibiting rates of 36 cases with large intestine carcinoma tissues from high to low were OXA,F+M(5-Fu+MMC),F+D(5-Fu+DDP),DDP,5-Fu,O+F(5-Fu+OXA),MMC and ADM.
36例大腸癌細胞對試騐化療葯物的敏感性由高到低依次爲(wèi)OXA、F+M(5-Fu+MMC)、F+D(5-Fu+DDP)及DDP、5-Fu、O+F(5-Fu+OXA)、MMC、ADM。
The electronic structures of 20 of oxa , aza , thia macrocyclic compounds with side substitute of halogen and trihalomethyl have been calculated by use of AM1.
用AM1方法計算了20個鹵素及三鹵甲基側(cè)取代氧、氮、硫襍大環(huán)化郃物的電子結(jié)搆。
Results: Seven chemotherapeutic agents showed sensitive rate of OXA,MMC,DDP,GEM,EADM,5-FU,HCPT were 92.5%,88.88%,81.48%,66.66%,62.96%,51.85% and 40.74%,respectively.
結(jié)果:7種化療葯物的敏感率爲(wèi)奧沙利鉑(OXA)92.;5%25;絲裂黴素(MMC)88
Thirty cases of advanced pancreatic cancer were treated with OXA (100 mg/m2 ivdrip for 2 hours on d1) and with GEM (1 000 mg/m2 ivdrip for 30 min d1, d8), and 21 days as a cycle. All of the patients were received the chemotherapy at least two cycles.
對30例晚期胰腺癌患者,應(yīng)用GEM1000mg/m2,靜脈滴入30min,d1、d8; OXA100mg/m2,靜脈滴入2h,d1,21d重複。