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Palladium-catalyzed Suzuki-Miyaura cross-coupling reaction of organoboronic acids with N-protected 4-iodophenyl alanine linked isoxazoles 被引量:4
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作者 E.Rajanarendar G.Mohan +1 位作者 E.Kalyan Rao M.Srinivas 《Chinese Chemical Letters》 SCIE CAS CSCD 2009年第1期1-4,共4页
Suzuki-Miyaura coupling reaction of N-protected 4-iodopheyl alanine isoxazoles with arylboronic acids,catalyzed by palladium,efficiently produce benzyl-N-(4-bipheyl)-2-(3-methyl-5(E)-2-aryl-1-ethenyl-4-isoxazolyl... Suzuki-Miyaura coupling reaction of N-protected 4-iodopheyl alanine isoxazoles with arylboronic acids,catalyzed by palladium,efficiently produce benzyl-N-(4-bipheyl)-2-(3-methyl-5(E)-2-aryl-1-ethenyl-4-isoxazolyl)-amino-2-oxoethyl)carba- mates in good yields.This process is first of its kind to construct carbon-carbon bond formation having biaryl motif on amino acid linked isoxazole moiety. 展开更多
关键词 Suzuki-Miyaura coupling C-C bond formation Amino acid linked isoxazoles
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Traceless solid-phase synthesis of 3-substituted isoxazoles from polystyrene-supported vinyl selenide
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作者 Qin Xin Shou Ri Sheng +2 位作者 Shu Ying Lin Xiao Ling Liu Xian Huang 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第1期1-3,共3页
A novel facile procedure for traceless solid-phase synthesis of 3-substituted isoxazoles in good yields and with excellent purities using polymer-supported vinyl selenide has been developed.
关键词 Solid phase organic synthesis Polystyrene-supported vinyl selenide isoxazole
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Synthesis and Herbicidal Activities of 3-(Substituted phenyl)isoxazole Derivatives 被引量:3
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作者 Yu Han ZHOU, Wei Rong MIAO, Lu Bai CHEN State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116012 《Chinese Chemical Letters》 SCIE CAS CSCD 2003年第9期897-900,共4页
Several novel 3-(substituted phenyl)isoxazole derivatives were prepared from phenyl butan-1,3-dione. Their structures were confirmed by 1H NMR, IR, and CIMS. Preliminary bioassay showed that some of them exhibited goo... Several novel 3-(substituted phenyl)isoxazole derivatives were prepared from phenyl butan-1,3-dione. Their structures were confirmed by 1H NMR, IR, and CIMS. Preliminary bioassay showed that some of them exhibited good activities toward various weeds. 展开更多
关键词 Protox-inhibitor isoxazole derivatives herbicidal activity.
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Design,Synthesis and Insecticidal Activities of Novel Phenyl Substituted Isoxazolecarboxamides 被引量:2
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作者 LIU Peng-fei ZHANG Ji-feng +2 位作者 YAN Tao XIONG Li-xia LI Zheng-ming 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2012年第3期430-433,共4页
Thirteen novel phenyl substituted isoxazolecarboxamides were synthesized, and their structures were characterized by IH NMR, elementary analysis and high-resolution mass spectrometry(HRMS) techniques. Their evaluate... Thirteen novel phenyl substituted isoxazolecarboxamides were synthesized, and their structures were characterized by IH NMR, elementary analysis and high-resolution mass spectrometry(HRMS) techniques. Their evaluated insecticidal activities against oriental armyworm(Mythimna separata) indicate that the phenyl substituted isoxazolecarboxamides exhibited moderate insecticidal activities, among which compounds 9c and 9k showed com- paratively higher activities. 展开更多
关键词 Insecticidal activity isoxazolE Anthranilic diamide isoxazolecarboxamide
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An Efficient Deselenenylation Reaction to the Synthesis of 3, 5-Disubstituted Isoxazoline and Isoxazole
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作者 Wei Ming XU Yu Guang WANG +1 位作者 Zhen Hua CHEN Xian HUANG 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第8期995-996,共2页
A mild deselenenylation reaction protocol for the preparation of 3, 5-disubstituted isoxazolines and their further application to 3-methyl-5-substituted isoxazoles both in solution phase and solid phase was reported.
关键词 Deselenenylation reaction isoxazolINE isoxazole.
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Basic fibroblast growth factor increases the numbe of endogenous neural stem cells and inhibits the expression of amino methyl isoxazole propionic acid receptors in amyotrophic lateral sclerosis mice
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作者 Weihui Huang Dawei Zang Yi Lu Ping Jiang 《Neural Regeneration Research》 SCIE CAS CSCD 2012年第10期761-765,共5页
This study aimed to investigate the number of amino methyl isoxazole propionic acid (AMPA) receptors and production of endogenous neural stem cells in the SOD1 G93AG1H transgenic mouse model of amyotrophic lateral s... This study aimed to investigate the number of amino methyl isoxazole propionic acid (AMPA) receptors and production of endogenous neural stem cells in the SOD1 G93AG1H transgenic mouse model of amyotrophic lateral sclerosis, at postnatal day 60 following administration of basic fibroblast growth factor (FGF-2). A radioligand binding assay and immunohistochemistry were used to estimate the number of AMPA receptors and endogenous neural stem cells respectively. Results showed that the number of AMPA receptors and endogenous neural stem cells in the brain stem and sensorimotor cortex were significantly increased, while motor function was significantly decreased at postnatal days 90 and 120. After administration of FGF-2 into mice, numbers of endogenous neural stem cells increased, while expression of AMPA receptors decreased, whilst motor functions were recovered. At postnatal day 120, the number of AMPA receptors was negatively correlated with the number of endogenous neural stem cells in model mice and FGF-2-treated mice. Our experimental findings indicate that FGF-2 can inhibit AMPA receptors and increase the number of endogenous neural stem cells, thus repairing neural injury in amyotrophic lateral sclerosis mice. 展开更多
关键词 amino methyl isoxazole propionic acid receptor amyotrophic lateral sclerosis basic fibroblast growth factor endogenous neural stem cells
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Synthesis and Spectral Identification of Novel Stable Triazene: As Raw Material for the Synthesis Biocompatible Surfactants-Pyrazole-Isoxazole-Dihydropyrimidine-Tetrahydropyridine Derivatives
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作者 Mohamed Ahmed Mahmoud Abdel Reheim Ahmed Mahmoud El-Sayed Tolba 《International Journal of Organic Chemistry》 CAS 2016年第1期44-54,共11页
The chemical reactivity of novel stable triazene 3 toward some nucleophilic and electrophilic reagents was investigated. Traizene 3 was used as a key precursor for the synthesis of some novel important heterocyclic co... The chemical reactivity of novel stable triazene 3 toward some nucleophilic and electrophilic reagents was investigated. Traizene 3 was used as a key precursor for the synthesis of some novel important heterocyclic compounds such as Pyrazole, Isoxazole, Dihydropyrimidine, Tetrahydro-pyridine derivatives with expected antimicrobial activity. The synthesized compounds were obtained in good yields. The structures of the newly synthesized compounds were confirmed by elemental analysis, IR, 1H-NMR and Ms spectral data. 展开更多
关键词 Biocompatible Surfactants Pyrazole isoxazolE Dihydropyrimidine Tetrahydropyridine Derivatives Spectral Characteristics
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Oxidative aromatization of 3,5-disubstituted 2-isoxazolines by nitric oxide
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作者 Rui Li Wen Tao Wu Guai Li Wu Yuan Fan Long Min Wu 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第7期788-790,共3页
3,5-Disubstituted 2-isoxazolines were oxidized to corresponding isoxazoles by nitric oxide in dichloromethane. The reaction more likely occurred via a one-electron transfer process.
关键词 2-isoxazolines Nitric oxide 2-isoxazole AROMATIZATION
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A Novel Synthesis of Isoxazole Derivatives 被引量:1
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作者 Jun Feng WANG Bao Shan DU Qing Hua CHEN (Department of Chemistry, Beijing Normal University, Beijing 100875) 《Chinese Chemical Letters》 SCIE CAS CSCD 1998年第9期801-802,共2页
The new synthetic method of isoxazole derivatives was succesfully achieved. The experimental results demonstrate that thermal decomposition reactions of nitrone could take place with yields of 41 similar to 81%, to gi... The new synthetic method of isoxazole derivatives was succesfully achieved. The experimental results demonstrate that thermal decomposition reactions of nitrone could take place with yields of 41 similar to 81%, to give a series of new isoxazole derivatives. 展开更多
关键词 NITRONE isoxazolE
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Synthesis and Antitumor Activity of 3-[2-(4-Hydroxy-Phenyl)-Ethyl]-Benzo[d] Isoxazole-4,6-Diol
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作者 Li Wang 《International Journal of Organic Chemistry》 CAS 2023年第1期1-6,共6页
A new phloretin derivative 1 3-[2-(4-hydroxy-phenyl)-ethyl]-benzo[d] isoxazole-4,6-diol (yield 63%) was synthesized from phloretin by carbonyl nucleophilic addition condensation reaction. Its structure was characteriz... A new phloretin derivative 1 3-[2-(4-hydroxy-phenyl)-ethyl]-benzo[d] isoxazole-4,6-diol (yield 63%) was synthesized from phloretin by carbonyl nucleophilic addition condensation reaction. Its structure was characterized by 1H NMR, 13C NMR and HR-MS. The phloretin, compound 1, resveratrol and acetylated resveratrol were determined by comparing them with paclitaxel. Anti-tumor activity of alcohol on SPC-A1, EC109, A549, MCF-7 and MDA-MB-231 cell lines. Compound 1 showed better antitumor activity than docetaxel against A549 tumor cells. 展开更多
关键词 3-[2-(4-Hydroxy-Phenyl)-Ethyl]-Benzo[d] isoxazole-4 6-Diol SYNTHESIS Antitumor Activity
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Role of α-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor regulation in stress-induced pain chronification
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作者 Sufang Liu Feng Tao 《World Journal of Biological Chemistry》 CAS 2017年第1期1-3,共3页
Persistent postsurgical pain is a serious issue in public health, which has received increased interest in recent years. Previous studies have reported that psychological factors promote the development of chronic pos... Persistent postsurgical pain is a serious issue in public health, which has received increased interest in recent years. Previous studies have reported that psychological factors promote the development of chronic postsurgical pain. However, it is unclear how chronification of postsurgical pain occurs. The α-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor(AMPA) phosphorylation in the central nervous system plays a critical role in synaptic plasticity and contributes to central sensitization and chronic pain development. Here, we discuss the role of AMPA receptor regulation in stress-induced pain chronification after surgery. 展开更多
关键词 α-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor phosphorylation Stress Pain chronification
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香草醛异[口恶]唑衍生物的设计合成及杀菌活性 被引量:1
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作者 刘伟童 朱长恒 +1 位作者 蒋禹 赵汗青 《化学试剂》 CAS 2024年第3期16-23,共8页
为了寻找结构新颖、杀菌活性更好的绿色农药。选用天然产物香草醛作为基本原料,引入五元杂环异[口恶]唑结构,首次设计并合成了28个香草醛异[口恶]唑类衍生物。结构经核磁共振氢谱、碳谱及高分辨质谱分析确认。测试了所有目标衍生物对烟... 为了寻找结构新颖、杀菌活性更好的绿色农药。选用天然产物香草醛作为基本原料,引入五元杂环异[口恶]唑结构,首次设计并合成了28个香草醛异[口恶]唑类衍生物。结构经核磁共振氢谱、碳谱及高分辨质谱分析确认。测试了所有目标衍生物对烟草灰霉病菌(Botrytis cinerea)、层出镰刀菌(Fusarium proliferatum)、木贼镰刀菌(Fusarium equiseti)、玉米圆斑病菌(Bipolaris zeicola)、胶胞炭疽菌(Colletotrichum gloeosporioides)、草茎点霉菌(Phoma herbarum)6种广谱菌的杀菌活性。杀菌活性测定结果显示:在50μg/mL质量浓度下,部分化合物对6种真菌的菌丝生长均具有一定抑制作用,2-甲氧基-4-(5-苯基异[口恶]唑-3-基)苯乙酸酯对6种真菌的抑菌活性整体良好,对玉米圆斑病菌等3种菌的抑菌活性超过对照组百菌清;2-甲氧基-4-(5-(4-乙基苯基)异唑-3-基)苯酚对烟草灰霉病菌的抑菌活性最高,抑菌率可以达到93%。初步构效关系表明,对活性片段香草醛上的酚羟基进行乙酰化衍生,有助于提高化合物对6种病原菌的抑菌活性,为后续的生物活性研究提供了参考。 展开更多
关键词 香草醛 异[口恶]唑 合成 百菌清 杀菌活性
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异噁唑类除草剂合成研究进展
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作者 郭轩宇 张宝 冯亚青 《化学工业与工程》 CAS CSCD 北大核心 2024年第2期24-34,共11页
异噁唑类除草剂具有高选择性、高活性、持效期长等优点,同时具有更好的生态安全性,近年来受到广泛关注。但是该类原料药的合成路线长,存在收率低,成本高等问题,限制了规模应用。综述了异噁唑类除草剂的研究进展,重点对砜吡草唑(Pyroxasu... 异噁唑类除草剂具有高选择性、高活性、持效期长等优点,同时具有更好的生态安全性,近年来受到广泛关注。但是该类原料药的合成路线长,存在收率低,成本高等问题,限制了规模应用。综述了异噁唑类除草剂的研究进展,重点对砜吡草唑(Pyroxasulfone)、苯磺噁唑草(Fenoxasulfone)、苯唑草酮(Topramezone)、异噁唑啉除草剂(Methiozolin)、双苯噁唑酸乙酯(Ethyl bisoxazolate)5类新兴的异噁唑类除草剂的应用范围和合成路线进行了分析,比较了优缺点,为开发此类除草剂农药提供指导。 展开更多
关键词 异噁唑类除草剂 合成 进展
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手性磷酸催化非环状N,N′-缩酮的不对称合成
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作者 李敏 李文哲 +1 位作者 黄敏 张晓梅 《合成化学》 CAS 2024年第7期634-642,共9页
手性N,N′-缩酮是药物分子和生物活性化合物最重要的核心结构之一,也是有机合成中重要的催化剂或配体。因此,不对称合成N,N′-缩酮具有重要意义。通过手性磷酸、溶剂、催化剂负载量和投料比的筛选,确定了最佳的反应条件:在手性磷酸的催... 手性N,N′-缩酮是药物分子和生物活性化合物最重要的核心结构之一,也是有机合成中重要的催化剂或配体。因此,不对称合成N,N′-缩酮具有重要意义。通过手性磷酸、溶剂、催化剂负载量和投料比的筛选,确定了最佳的反应条件:在手性磷酸的催化下,以1,4-二氧六环作为溶剂,5-氨基异噁唑与β,γ-炔基-α-酮亚胺酯在室温下发生区域选择性的氮杂-曼尼希反应,实现异噁唑的不对称N—H烷基化,以中等至良好的收率(46%~83% yield)和较好的对映选择性(82%~92%ee)合成非环状的N,N′-缩酮。所有产物结构由^(1)H NMR,^(13)C NMR和HR-MS(ESI)确证,绝对构型通过X-射线晶体结构分析确定。 展开更多
关键词 N N′-缩酮 手性磷酸催化 5-氨基异噁唑 β γ-炔基-α-酮亚胺酯 区域选择性 不对称合成 氮杂-曼尼希反应
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一锅法合成5-取代异唑-3-羧酸甲酯类化合物
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作者 靳清贤 张广慧 +3 位作者 刘冬 杜星辰 毛文静 方少明 《精细化工》 EI CAS CSCD 北大核心 2024年第12期2777-2784,共8页
以甲醇钠为碱催化剂,取代甲基酮与草酸二甲酯经Claisen缩合反应合成了β-二羰基化合物,再经浓硫酸中和后与盐酸羟胺反应成肟,最后高温成环,合成了不同取代基的5-取代异唑-3-羧酸甲酯类化合物。通过^(1)HNMR、^(13)CNMR、MS确证了产物结... 以甲醇钠为碱催化剂,取代甲基酮与草酸二甲酯经Claisen缩合反应合成了β-二羰基化合物,再经浓硫酸中和后与盐酸羟胺反应成肟,最后高温成环,合成了不同取代基的5-取代异唑-3-羧酸甲酯类化合物。通过^(1)HNMR、^(13)CNMR、MS确证了产物结构,对合成过程中的碱催化剂、溶剂、酸中和的条件进行了优化,对不同取代基的5-取代异唑-3-羧酸甲酯化合物合成工艺差异进行了探讨。结果表明,用一锅法成功合成了26个5-取代异唑-3-羧酸甲酯。其中,23个可在单一溶剂甲醇中制备,避免了中间产物的分离和纯化处理,操作流程简捷,单一溶剂易于回收处理;5-叔丁基异唑-3-羧酸甲酯(Ⅳc)、5-(4-氨基苯基)异唑-3-羧酸甲酯(Ⅳm)和5-(3-氨基苯基)异唑-3-羧酸甲酯(Ⅳn)的合成需要用叔丁醇钾作碱催化剂,并在四氢呋喃中进行;5-三氟甲基异唑-3-羧酸甲酯(Ⅳv)的合成未成功,需要设计新的合成方法和条件。 展开更多
关键词 一锅法 异?唑-3-羧酸酯 异?唑 合成 羧酸 精细化工中间体
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跑台运动联合黑枸多糖改善模型小鼠的抑郁症样行为
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作者 陈伟 陈嘉勤 王一蓉 《解剖学报》 CAS CSCD 2024年第5期524-532,共9页
目的探讨7周跑台运动及黑枸多糖灌服对小鼠抑郁样行为的影响和海马α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPAR)相关通路的改变。方法50只雄性昆明(KM)小鼠,随机分成空白组(K,n=10)和抑郁症组(CUMS,n=40),抑郁症组随机采用13种慢性... 目的探讨7周跑台运动及黑枸多糖灌服对小鼠抑郁样行为的影响和海马α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPAR)相关通路的改变。方法50只雄性昆明(KM)小鼠,随机分成空白组(K,n=10)和抑郁症组(CUMS,n=40),抑郁症组随机采用13种慢性不可预见温和应激成功构建小鼠模型,构建成功后分为模型组(M)、跑台运动组(E)、黑枸多糖组(L)和跑台运动联合黑枸多糖组(EL),每组10只。实验方法有行为学评估,海马组织5羟色胺(5-HT)、脑源性神经营养因子(BDNF)和多巴胺(DA)含量检测,血清S100钙结合蛋白B(S100B)和神经元特异性烯醇化酶(NSE)含量检测,脑组织Nissl染色,海马组织AMPAR、谷氨酸受体1(GluR1)和钙调素依赖蛋白激酶Ⅱα(CaMKⅡα)蛋白含量测定,mRNA表达谱分析后采用Western blotting和Real-time PCR检验AMPAR、GluR1和CaMKⅡα表达水平。结果1.模型小鼠抑郁样行为表现明显,海马组织5-HT、BDNF和DA含量下降,而S100B和NSE含量上升(P<0.01),前额叶皮层神经元缺失,尼氏体固缩或空泡状,显示神经元损伤严重。2.与M组比较,E、L和EL组小鼠抑郁样行为明显改善,海马组织5-HT、BDNF和DA含量上升,血清S100B和NSE含量降低(P<0.01或P<0.05)。行为结果与S100B、NSE含量的统计学分析显示,跑台运动和黑枸多糖干预具有协同效应。3.与M组比较,E、L和EL组小鼠海马组织AMPAR、GluR1和CaMKⅡα蛋白含量上升(P<0.01),且跑台运动和黑枸多糖具协同效应;基于Illumina高通量测序发现,AMPAR突触后膜紧密相关的长时程增强、长时程抑制信号通路内有49个上调基因和18个下调基因,涉及突触可塑性、学习记忆和神经元损伤修复等相关通路。Real-time PCR结果显示,E、L和EL组AMPAR、GluR1和CaMKⅡα基因的mRNA水平显著增加,且跑台运动和黑枸多糖具有协同效应。结论7周跑台运动和黑枸多糖灌服可改善小鼠抑郁样症状,可能是通过影响CaMKⅡα的磷酸化进而调控AMPAR活性,促进神经元损伤修复和改善突触可塑性及功能实现的。 展开更多
关键词 跑台运动 抑郁症 α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体 黑枸多糖 免疫印迹法 实时定量聚合酶链反应 小鼠
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新型甘草次酸异噁唑衍生物的合成 被引量:12
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作者 刘利军 雍建平 +3 位作者 戴小军 贾炯 王西照 王建武 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2006年第9期1669-1672,共4页
以甘草次酸(脱氧甘草次酸)和3-取代苯基-5-氨甲基-异噁唑为原料,合成了4种甘草次酸异噁唑衍生物,通过IR,1HNMR,13C NMR及FABMS等方法确定了化合物的结构.同时用L9(34)正交试验对酰胺化反应的条件进行优化,确定了酰化反应的最佳条件.
关键词 甘草次酸 异噁唑 正交试验 合成
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3-N-乙酰基-2-取代芳基-5-[5′-甲基异噁唑-3′]-Δ_3-1,3,4-噁唑啉类化合物的合成 被引量:42
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作者 钟滨 赵卫光 +1 位作者 李正名 王素华 《应用化学》 CAS CSCD 北大核心 2003年第8期719-722,共4页
由相应的酯 (1)肼解制得 5 甲基 异唑 3 甲酰肼 (2 ) ,后者与醛缩合得到酰腙 (3a~ 3h) ,3a~ 3h再进一步与乙酸酐环合 ,以良好的收率合成出了 3 N 乙酰基 2 取代芳基 5 [5′ 甲基 异唑 3′] Δ3 1,3,4 唑啉衍生物 (4a... 由相应的酯 (1)肼解制得 5 甲基 异唑 3 甲酰肼 (2 ) ,后者与醛缩合得到酰腙 (3a~ 3h) ,3a~ 3h再进一步与乙酸酐环合 ,以良好的收率合成出了 3 N 乙酰基 2 取代芳基 5 [5′ 甲基 异唑 3′] Δ3 1,3,4 唑啉衍生物 (4a~ 4h)。以上化合物的结构均经过1 HNMR、MS和元素分析的确证。 展开更多
关键词 甲基-异噁唑甲酰肼 噁唑啉 合成
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新型异恶唑类化合物的合成及其生物活性的研究 被引量:11
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作者 齐传民 王蕴峰 +1 位作者 张关心 冯淑娟 《北京师范大学学报(自然科学版)》 CAS CSCD 北大核心 2001年第6期787-789,共3页
合成了 6个新的取代苯基异恶唑类化合物 (C) ,探讨了它们的合成方法 ,它们的结构均经过IR ,1HNMR ,元素分析等确证 .初步药理实验显示部分异恶唑类化合物具有一定的除草和植物生长调节活性 ,其中C5对某些植物的生长具有明显抑制作用 .
关键词 异恶唑类化合物 环合反应 异恶唑啉-N-氧化物 生物活性 药物化学 合成 结构表征
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A771726在大鼠体内肝肠循环的研究 被引量:6
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作者 程娟 李俊 +3 位作者 宋珏 郑世瑞 李浩 孔一帆 《安徽医科大学学报》 CAS 北大核心 2010年第3期338-341,共4页
目的研究A771726在大鼠体内肝肠循环情况。方法运用配对大鼠肝肠循环模型研究A771726在大鼠体内从胆汁重吸收的药动学过程,采用HPLC法测定血浆中A771726浓度,药动学参数用DAS软件统计矩法计算。结果配对大鼠肝肠循环模型表明,胆汁供体... 目的研究A771726在大鼠体内肝肠循环情况。方法运用配对大鼠肝肠循环模型研究A771726在大鼠体内从胆汁重吸收的药动学过程,采用HPLC法测定血浆中A771726浓度,药动学参数用DAS软件统计矩法计算。结果配对大鼠肝肠循环模型表明,胆汁供体大鼠和胆汁受体大鼠的AUC分别为(1352.85±184.51)mg/(L.h)、(314.94±21.15)mg/(L.h)。结论 A771726静脉注射后存在肝肠循环现象,约有静脉注射给药量的23.8%进入肝肠循环。 展开更多
关键词 色谱法 高压液相 异恶唑类/药物代谢动力学 异恶唑类/投药和剂量
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