Differential binding to the hydrophobic bonding region of T2 phage induced, Escherichia coli B, and pigeon liver dihydrofolic reductases. - Suppr | 超能文献

Differential binding to the hydrophobic bonding region of T2 phage induced, Escherichia coli B, and pigeon liver dihydrofolic reductases.

作者信息

Baker B R

出版信息

J Med Chem. 1967 Sep;10(5):912-7. doi: 10.1021/jm00317a035.

DOI:10.1021/jm00317a035

Abstract

摘要

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1

Differential binding to the hydrophobic bonding region of T2 phage induced, Escherichia coli B, and pigeon liver dihydrofolic reductases.

J Med Chem. 1967 Sep;10(5):912-7. doi: 10.1021/jm00317a035.

2

Irreversible enzyme inhibitors. CV. Differential irreversible inhibition of vertebrate dihydrofolic reductases by derivatives of 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-phenyl-s-triazines substituted with a terminal sulfonyl fluoride.

J Med Chem. 1967 Nov;10(6):1113-22. doi: 10.1021/jm00318a029.

3

Dihydrofolate reductases of Escherichia coli and bacteriophage Tr. A spectrofluorometric study.

Biochemistry. 1973 Jan 30;12(3):372-80. doi: 10.1021/bi00727a002.

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Irreversible enzyme inhibitors. CX. Candidate irreversible inhibitors of dihydrofolic reductase derived from 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-phenyl-s-triazine. IV.不可逆酶抑制剂。CX。源自4,6-二氨基-1,2-二氢-2,2-二甲基-1-苯基-s-三嗪的二氢叶酸还原酶的候选不可逆抑制剂。IV。

J Med Chem. 1968 Jan;11(1):34-7. doi: 10.1021/jm00307a006.

5

Irreversible enzyme inhibitors. CIX. Candidate irreversible inhibitors of dihydrofolic reductase derived from 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-phenyl-s-triazine. 3.不可逆酶抑制剂。CIX。源自4,6-二氨基-1,2-二氢-2,2-二甲基-1-苯基-s-三嗪的二氢叶酸还原酶候选不可逆抑制剂。3。

J Med Chem. 1968 Jan;11(1):26-33. doi: 10.1021/jm00307a005.

6

Irreversible enzyme inhibitors. CXII. Active-site-directed irreversible inhibitors of dihydrofolic reductase derived from 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-phenyl-s-triazine substituted with a terminal sulfonyl fluoride. II.不可逆酶抑制剂。CXII。源自4,6-二氨基-1,2-二氢-2,2-二甲基-1-苯基-s-三嗪并被末端磺酰氟取代的二氢叶酸还原酶的活性位点导向不可逆抑制剂。II。

J Med Chem. 1968 Jan;11(1):38-41. doi: 10.1021/jm00307a007.

7

Irreversible enzyme inhibitors. CXVII. Hydrophobic bonding to dihydrofolic reductase. XI. Comparison of the enzyme from Walker 256, rat liver, and L1210 mouse leukemia.不可逆酶抑制剂。CXVII。与二氢叶酸还原酶的疏水键合。XI。来自Walker 256、大鼠肝脏和L1210小鼠白血病的酶的比较。

J Med Chem. 1968 May;11(3):483-6. doi: 10.1021/jm00309a016.

8

T4 bacteriophage-specific dihydrofolate reductase: purification to homogeneity by affinity chromatography.T4噬菌体特异性二氢叶酸还原酶：通过亲和层析纯化至均一性。

Biochem Biophys Res Commun. 1971 Jun 4;43(5):1164-70. doi: 10.1016/0006-291x(71)90585-7.

9

Folate inhibitors: a structure-activity analysis using linear modeling.叶酸抑制剂：使用线性模型的构效关系分析

Ann N Y Acad Sci. 1971 Nov 30;186:235-47.

10

Inhibitor binding analysis of dihydrofolate reductases from various species.不同物种二氢叶酸还原酶的抑制剂结合分析

Mol Pharmacol. 1965 Sep;1(2):126-36.

引用本文的文献

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The temporal expression of T2r + bacteriophage genes in vivo and in vitro.T2r + 噬菌体基因在体内和体外的时序表达。

Proc Natl Acad Sci U S A. 1972 Jul;69(7):1659-63. doi: 10.1073/pnas.69.7.1659.

2

Interaction of methotrexate, folates, and pyridine nucleotides with dihydrofolate reductase: calorimetric and spectroscopic binding studies.甲氨蝶呤、叶酸和吡啶核苷酸与二氢叶酸还原酶的相互作用：量热法和光谱结合研究。

Proc Natl Acad Sci U S A. 1978 Jul;75(7):3201-5. doi: 10.1073/pnas.75.7.3201.