对氨基苯甲酰谷氨酸
- 网络P-aminobenzoyl glutamate;p-aminobenzoylglutamic acid
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本研究为进行MTX的结构修饰开辟了新途径,2-氨基-4-[N-(对氨基苯甲酰谷氨酸)-基]-6-取代基蝶啶衍生物可成为潜在的抗肿瘤候选药物被进一步研究。
These studies show that we open up a new pathway of the structural modifi - cation of MTX , and 2-amino-4 - [ N - ( p-aminobenzoyl glutamic acid ) - yl ] - 6-alkyl / arylpteridine derivatives may be brought to potential antineoplastic candidates for further studies .
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催化加氢合成对氨基苯甲酰谷氨酸新工艺
New Synthesis of P-Amino-benzoyl Glutamic Acid by Catalytically Hydrogenation