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Irreversible enzyme inhibitors. CLXXIV. Metabolism of 4-(p-(4,6-diamino-1,2-dihydro-2,2-dimethyl-s-triazin-1-yl)hydrocinnamido)-o-toluenesulfonyl fluoride (NSC-113423), an active-site-directed irreversible inhibitor of dihydrofolic reductase.

作者信息

Ryan A J, Vermeulen N M, Baker B R

出版信息

J Med Chem. 1970 Nov;13(6):1140-2. doi: 10.1021/jm00300a027.

DOI:10.1021/jm00300a027
PMID:5479853
Abstract
摘要

相似文献

1
Irreversible enzyme inhibitors. CLXXIV. Metabolism of 4-(p-(4,6-diamino-1,2-dihydro-2,2-dimethyl-s-triazin-1-yl)hydrocinnamido)-o-toluenesulfonyl fluoride (NSC-113423), an active-site-directed irreversible inhibitor of dihydrofolic reductase.
J Med Chem. 1970 Nov;13(6):1140-2. doi: 10.1021/jm00300a027.
2
Irreversible enzyme inhibitors. CLIX. Effect of substitution on transport and isozyme specificity of p-(4,6-diamino-1,2-dihydro-2,2-dimethyl-s-triazin-1-yl)-o-chlorophenoxyacetamido-benzenesulfonyl fluoride, an active-site-directed irreversible inhibitor of dihydrofolic reductase.不可逆酶抑制剂。CLIX。取代基对p-(4,6-二氨基-1,2-二氢-2,2-二甲基-s-三嗪-1-基)-邻氯苯氧基乙酰氨基苯磺酰氟(一种二氢叶酸还原酶的活性位点导向不可逆抑制剂)的转运及同工酶特异性的影响。
J Med Chem. 1969 Sep;12(5):894-7. doi: 10.1021/jm00305a042.
3
Irreversible enzyme inhibitors. CXXXIX. p-(4,6-Diamino-1,2-dihydro-2,2-dimethyl-s-triazin-1-yl)phenylpropionylsulfanilyl fluoride, an active-site-directed irreversible inhibitor of dihydrofolic reductase. VI. Further studies on effects of substitution on the propionamide bridge on isozyme specificity.
J Med Chem. 1969 Jan;12(1):92-4. doi: 10.1021/jm00301a024.
4
Irreversible enzyme inhibitors. CLV. Active-site-directed irreversible inhibitors of dihydrofolic reductase derived from 1-[4-(omega-aminoalkoxy)-3-chlorophenyl]-4,6-diamino-1,2-dihydro-2,2-dimethyl-s-triazines bearing a terminal sulfonyl fluoride.不可逆酶抑制剂。CLV。源自带有末端磺酰氟的1-[4-(ω-氨基烷氧基)-3-氯苯基]-4,6-二氨基-1,2-二氢-2,2-二甲基-s-三嗪的二氢叶酸还原酶的活性位点定向不可逆抑制剂。
J Med Chem. 1969 Jul;12(4):672-6. doi: 10.1021/jm00304a025.
5
Irreversible enzyme inhibitors. CXXIX. p-(4,6-diamino-1,2-dihydro-2,2-dimethyl-s-triazin-1-yl)phenylpropionylsulfanilyl fluoride, an active-site-directed irreversible inhibitor of dihydrofolic reductase. V. Effects of substitution on the benzenesulfonyl fluoride moiety on isozyme specificity.不可逆酶抑制剂。CXXIX。对-(4,6-二氨基-1,2-二氢-2,2-二甲基-s-三嗪-1-基)苯基丙酰磺胺酰氟,二氢叶酸还原酶的活性位点定向不可逆抑制剂。V。苯磺酰氟部分取代对同工酶特异性的影响。
J Med Chem. 1968 Jul;11(4):677-82. doi: 10.1021/jm00310a009.
6
Irreversible enzyme inhibitors. CXXVII. p-(2,6-diamino-1,2-dihydro--2,2-dimethyl-s-triazin-1-yl)phenylpropionylsulfanilyl fluoride, an active-site-directed irreversible inhibitor of dihydrofolic reductase. 3. Effects of modification of the propionamide bridge on isozyme specificity.不可逆酶抑制剂。CXXVII。对-(2,6-二氨基-1,2-二氢- -2,2-二甲基-s-三嗪-1-基)苯基丙酰磺胺酰氟,一种二氢叶酸还原酶的活性位点导向不可逆抑制剂。3. 丙酰胺桥修饰对同工酶特异性的影响。
J Med Chem. 1968 Jul;11(4):666-72. doi: 10.1021/jm00310a007.
7
Irreversible enzyme inhibitors. 108. p-(4,6-diamino-1,2-dihydro-2,2-dimethyl-s-triazin-1-yl)phenylpropionylsulfanilyl fluoride, an active-site-directed irreversible inhibitor of dihydrofolic reductase. IV. Effects of substitution on the propionamide bridge on isozyme specificity.不可逆酶抑制剂。108. 对-(4,6-二氨基-1,2-二氢-2,2-二甲基-s-三嗪-1-基)苯丙酰基磺胺酰氟,二氢叶酸还原酶的活性位点导向不可逆抑制剂。IV. 丙酰胺桥上取代对同工酶特异性的影响。
J Med Chem. 1968 Jul;11(4):672-7. doi: 10.1021/jm00310a008.
8
Irreversible enzyme inhibitors. CLXXIX. Active-site-directed irreversible enzyme inhibitors of dihydrofolate reductase from 1-(3-chlorophenyl)-4,6-diamino-1,2-dihydro-2,2-dimethyl-s-triazine with oxyamide bridges to a terminal sulfonyl fluoride.不可逆酶抑制剂。CLXXIX。1-(3-氯苯基)-4,6-二氨基-1,2-二氢-2,2-二甲基-s-三嗪与末端磺酰氟通过氧酰胺桥连接的二氢叶酸还原酶的活性位点定向不可逆酶抑制剂。
J Med Chem. 1970 Nov;13(6):1165-70. doi: 10.1021/jm00300a032.
9
Irreversible enzyme inhibitors. CLXXVI. Active-site-directed irreversible inhibitors of dihydrofolate reductase derived from 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-phenyl-s-triazine by ether bridging to a terminal sulfonyl fluoride.不可逆酶抑制剂。CLXXVI. 通过醚桥连至末端磺酰氟由4,6-二氨基-1,2-二氢-2,2-二甲基-1-苯基-s-三嗪衍生而来的二氢叶酸还原酶的活性位点导向不可逆抑制剂。
J Med Chem. 1970 Nov;13(6):1149-54. doi: 10.1021/jm00300a029.
10
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.

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