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[Synthesis of methyl-transferase inhibitors: analogs of S-adenosyl homocysteine].

作者信息

Hildesheim J, Hildesheim R, Lederer E

出版信息

Biochimie. 1971;53(10):1067-71. doi: 10.1016/s0300-9084(71)80194-3.

DOI:10.1016/s0300-9084(71)80194-3
PMID:5150737
Abstract
摘要

相似文献

1
[Synthesis of methyl-transferase inhibitors: analogs of S-adenosyl homocysteine].[甲基转移酶抑制剂的合成:S-腺苷高半胱氨酸类似物]
Biochimie. 1971;53(10):1067-71. doi: 10.1016/s0300-9084(71)80194-3.
2
[Inhibition of a t-RNA N 2 -guanine methyl transferase from rabbit liver by analogs of S-adenosyl homocysteine].[S-腺苷同型半胱氨酸类似物对兔肝t-RNA N2-鸟嘌呤甲基转移酶的抑制作用]
Biochimie. 1972;54(8):989-95. doi: 10.1016/s0300-9084(72)80049-x.
3
Analogs of S-adenosylhomocysteine as potential inhibitors of biological transmethylation. Specificity of the S-adenosylhomocysteine binding site.S-腺苷同型半胱氨酸类似物作为生物甲基化潜在抑制剂。S-腺苷同型半胱氨酸结合位点的特异性。
J Med Chem. 1973 May;16(5):460-3. doi: 10.1021/jm00263a008.
4
Potential inhibitors of S-adenosylmethionine-dependent methyltransferases. 3. Modifications of the sugar portion of S-adenosylhomocysteine.S-腺苷甲硫氨酸依赖性甲基转移酶的潜在抑制剂。3. S-腺苷同型半胱氨酸糖部分的修饰。
J Med Chem. 1975 Mar;18(3):300-4. doi: 10.1021/jm00237a018.
5
Speculations about the binding sites of S-adenosyl-L-homocysteine and some of its synthetic analogues to histamine methyltransferase.关于S-腺苷-L-同型半胱氨酸及其一些合成类似物与组胺甲基转移酶结合位点的推测。
Agents Actions. 1974 Aug;4(3):186-8. doi: 10.1007/BF01970266.
6
Affinity labeling of histamine N-methyltransferase by 2',3'-dialdehyde derivatives of S-adenosylhomocysteine and S-adenosylmethionine. Kinetics of inactivation.S-腺苷同型半胱氨酸和S-腺苷甲硫氨酸的2',3'-二醛衍生物对组胺N-甲基转移酶的亲和标记。失活动力学。
Biochemistry. 1978 Oct 3;17(20):4145-52. doi: 10.1021/bi00613a007.
7
Analogs of S-adenosylhomocysteine as potential inhibitors of biological transmethylation. Inhibition of several methylases by S-tubercidinylhomocysteine.S-腺苷高半胱氨酸类似物作为生物转甲基作用的潜在抑制剂。S-杀结核菌素基高半胱氨酸对几种甲基化酶的抑制作用。
J Med Chem. 1974 Dec;17(12):1286-9. doi: 10.1021/jm00258a011.
8
Inhibition of catechol-O-methyltransferase by S-adenosylhomocysteine and S-adenosylhomocysteine sulfoxide, a potential transition-state analog.S-腺苷同型半胱氨酸和S-腺苷同型半胱氨酸亚砜对儿茶酚-O-甲基转移酶的抑制作用,一种潜在的过渡态类似物。
Biochem Pharmacol. 1972 Apr 15;21(8):1200-3. doi: 10.1016/0006-2952(72)90114-1.
9
Potential inhibitors of S-adenosylmethionine-dependent methyltransferases. 10. Base- and amino acid modified analogues of S-aristeromycinyl-L-homocysteine.S-腺苷甲硫氨酸依赖性甲基转移酶的潜在抑制剂。10. S-阿瑞吡坦基-L-高半胱氨酸的碱基和氨基酸修饰类似物。
J Med Chem. 1985 Apr;28(4):478-82. doi: 10.1021/jm00382a016.
10
[New syntheses of S-adenosyl homocysteine analogues, potential methyltransferase inhibitors].
Biochimie. 1972;54(4):431-7. doi: 10.1016/s0300-9084(72)80226-8.

引用本文的文献

1
Effect of 5'-deoxy-5'-isobutylthioadenosine on putrescine uptake and polyamine biosynthesis by chick embryo fibroblasts.5'-脱氧-5'-异丁硫基腺苷对鸡胚成纤维细胞腐胺摄取和多胺生物合成的影响。
Biochem J. 1982 Jun 15;204(3):853-9. doi: 10.1042/bj2040853.
2
A base-pairing hypothesis for t-RNA methylation.一种关于转运核糖核酸甲基化的碱基配对假说。
Experientia. 1974 Aug 15;30(8):884-6. doi: 10.1007/BF01938339.
3
Speculations about the binding sites of S-adenosyl-L-homocysteine and some of its synthetic analogues to histamine methyltransferase.
关于S-腺苷-L-同型半胱氨酸及其一些合成类似物与组胺甲基转移酶结合位点的推测。
Agents Actions. 1974 Aug;4(3):186-8. doi: 10.1007/BF01970266.
4
Inhibition of viral RNA methylation in herpes simplex virus type 1-infected cells by 5' S-isobutyl-adenosine.5'-S-异丁基腺苷对单纯疱疹病毒1型感染细胞中病毒RNA甲基化的抑制作用。
J Virol. 1977 Apr;22(1):160-7. doi: 10.1128/JVI.22.1.160-167.1977.