Design and Synthesis of Novel Quinazoline Derivatives as Tyrosine Kinase Chemical Inhibitors 新型喹唑啉类酪氨酸激酶化学抑制剂的设计与合成
Tryptanthrin is a kind of indole quinazoline alkaloid. 色胺酮属吲哚喹唑啉类生物碱。
The electron impact and field desorption mass spectra of 10 2,4-diamino-6-substituted quinazoline sulfonamides were investigated. 研究了10种2,4-二氨基-6-取代磺酰胺喹唑啉类药物的电子电离及场解吸质谱。
Studies on antimalarials ⅵ. synthesis and antimalarial activities of some 2,4-di amino-6-substituted amino sulfonyl quinazoline derivatives 疟疾防治药物的研究&Ⅵ.2,4-二氨基-6-取代氨基-磺酰基喹唑啉衍生物的合成及其抗疟作用
3D-QSAR Study of a Series of Indolo [ 1,2-b] quinazoline Derivatives with Antitumor Activity and their Molecular Design 抗癌性吲哚喹唑啉衍生物3D-QSAR研究及其分子设计
Synthesis and Crystal Structure of the Fused Quinazoline Spiro-heterocyclic Compounds 喹唑啉稠合螺杂环化合物的合成及晶体结构
Study of Binding Characteristics of Quinazoline Molecularly Imprinted Polymeric Microspheres 喹唑啉分子印迹聚合物微球的吸附特性
It has been demonstrated that the models are successfully used for predicting the GC retention indices of quinazoline derivatives. 表明该模型可用于对喹唑啉类衍生物的气相色谱保留值的预测。
Quantitative Structure-activity Relationship of Quinazoline Derivatives with Antitumor Activity 二环己基二甲氧基硅烷的合成抗肿瘤喹唑啉衍生物的定量构效关系
On quantitative structure-retention relationship for quinazoline derivatives 喹唑啉类衍生物定量结构保留关系的研究
Antimalarial activity of some 2,4-di amino-6-substituted amino sulfonyl quinazoline derivatives 2,4-二氨基-6-取代氨基磺酰喹唑啉类化合物抗鼠疟作用的研究
Chemistry of the quinazoline series ⅲ. molecular rearrangement of 4-hydroxy quinazoline di-N-oxide 喹唑啉类杂环化合物的化学&Ⅲ.N~1,N~3-二氧化-4-羟基喹唑啉的分子重排反应
Seventeen 2,4-diamino-6-substituted amino sulfonyl quinazoline derivatives were tested for antimalarial activity on mice infected with several strains of Plasmodium berghei. 用伯氏鼠疟模型筛选了17个2,4-二氨基-6-取代氨基磺酰喹唑啉类化合物。
Antitumor effects of 2,4-diamino-6-( n-substituted amino) quinazoline derivatives 具有抗肿瘤作用的2,4-二氨基-6-取代氨基喹唑啉类化合物
Synthesis of 2-Amino-benzo [ h] quinazoline Derivatives under Microwave Irradiation 微波辐射下2-氨基苯并[h]喹唑啉衍生物的合成
Studies on antimalarial agents ⅳ& synthesis of 2, 4-di amino-6-substituted amino sulfonyl quinazoline 抗疟药的研究Ⅳ&2,4-二氨基-6-取代氨基磺酰喹唑啉的合成
In medicine aspect, quinazoline compounds have inhibition on EGF receptor ( EGFR), and then demonstrate the anticancer activation. 在医药方面,其对EGF受体(EGFR)产生抑制作用,进而表现出抗癌活性。
The effect of new quinazoline and sulfoxide derivatives were tested against pathogenic fungi bv using the mycelial growth rate method in the laboratory. 本论文采用室内生长速率法对本课题组合成的新型亚砜类和喹唑啉类化合物进行了抑菌活性初步筛选。
Indole and quinazoline derivatives are two kinds of important nitrogen-containing heterocyclic compounds, The cores of them are privileged structural motifs found in both designed medicinal agents and in natural products. 吲哚类化合物和喹唑啉类化合物是非常重要的两类氮杂环化合物,是很多天然产物及药物的母核结构。