A total synthesis of actinomycin D (C1) via peptide cyclization between proline and sarcosine.
作者信息
Meienhofer J
出版信息
Experientia. 1968 Aug 15;24(8):776-7. doi: 10.1007/BF02144860.
PMID:5683160
Abstract
摘要
相似文献
1
A total synthesis of actinomycin D (C1) via peptide cyclization between proline and sarcosine.通过脯氨酸和肌氨酸之间的肽环化反应全合成放线菌素D（C1）。
Experientia. 1968 Aug 15;24(8):776-7. doi: 10.1007/BF02144860.
2
Syntheses of actinomycin and analogs. 3. A total synthesis of actinomycin D (Cl) via peptide cyclization between proline and sarcosine.放线菌素及其类似物的合成。3. 通过脯氨酸和肌氨酸之间的肽环化反应全合成放线菌素D（C1）。
J Am Chem Soc. 1970 Jun 17;92(12):3771-7. doi: 10.1021/ja00715a039.
3
Synthesis of peptide analogs of actinomycin D (NSC-3053).
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4
Origin of the sarcosine molecules of actinomycins.放线菌素中肌氨酸分子的起源。
Biochem J. 1965 Sep;96(3):853-61. doi: 10.1042/bj0960853.
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Refinement of the molecular structure of actinomycin D by energy minimization.通过能量最小化对放线菌素D分子结构的优化。
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[New actinomycin from Actinomyces sp. No. 2].[来自放线菌属2号菌株的新型放线菌素]
Antibiotiki. 1981 Jan;26(1):5-7.
7
[Total synthesis of the actinomycins C1, C2, i-C 2, and C3 by way of N-(2-amino-3-hydroxy-4-methyl-benzoyl)-pentapeptide lactone; a further proof for the bis-pentapeptide structure for actinomycin].通过N-(2-氨基-3-羟基-4-甲基苯甲酰基)-五肽内酯全合成放线菌素C1、C2、异-C2和C3；放线菌素双五肽结构的进一步证据
Chem Ber. 1968;101(6):2231-43. doi: 10.1002/cber.19681010643.
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[A new producer of actinomycin D (Actinomyces olivobrunneus Krassilnikov, 1970)].[放线菌素D的一种新产生菌（橄榄褐色放线菌，克拉西里尼科夫，1970年）]
Antibiotiki. 1970 Aug;15(8):718-21.
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Synthesis of (4',4'-bis(glycine),5',5'-bis(valine))actinomycin D, a tetra-N-demethylactinomycin.（4',4'-双（甘氨酸），5',5'-双（缬氨酸））放线菌素D（一种四-N-去甲基放线菌素）的合成
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Syntheses of actinomycin and analogs. 8. A synthesis of actinomycin D lactam.放线菌素及其类似物的合成。8. 放线菌素D内酰胺的合成。
J Am Chem Soc. 1972 Jun 28;94(13):4759-61. doi: 10.1021/ja00768a070.
本文引用的文献
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STUDIES ON POLYPEPTIDES. XXIX. SYNTHETIC PEPTIDES RELATED TO THE N-TERMINUS OF BOVINE PANCREATIC RIBONUCLEASE A (POSITIONS 1-7).多肽研究。二十九。与牛胰核糖核酸酶A N端相关的合成肽（第1 - 7位）。
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A comparative study of the use of microorganisms in the screening of potential antitumor agents.微生物在潜在抗肿瘤药物筛选中的应用比较研究。
Ann N Y Acad Sci. 1958 Dec 5;76(3):413-38; discussion 438-41. doi: 10.1111/j.1749-6632.1958.tb54862.x.
3
Paper chromatographic identification of the actinomycins.放线菌素的纸色谱鉴定
Science. 1954 Sep 3;120(3114):389-90. doi: 10.1126/science.120.3114.389.
4
Synthesis of peptide derivatives with actinomycin D sequence.
J Org Chem. 1967 Apr;32(4):1143-5. doi: 10.1021/jo01279a064.
5
Analysis of N-methylamino acids by automatic amino acid analyzer and gas-liquid chromatography.用自动氨基酸分析仪和气液色谱法分析N-甲基氨基酸
J Chromatogr. 1966 Nov;25(1):1-10. doi: 10.1016/s0021-9673(01)98210-x.
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[Improved synthesis of etert-butyloxycarbonyl-amino acids through pH stable reactions].[通过pH稳定反应改进叔丁氧羰基氨基酸的合成]
Justus Liebigs Ann Chem. 1967;702:188-96. doi: 10.1002/jlac.19677020123.
7
[The building up of actinomycins by way of actinomycin acids; a second way of synthesis].通过放线菌素酸合成放线菌素；第二种合成方法
Chem Ber. 1968;101(4):1312-40. doi: 10.1002/cber.19681010425.
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