通过将1-取代腺嘌呤重排为6-取代氨基嘌呤来产生细胞分裂素活性：N6,1-环化导致失活。 - Suppr

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超能文献

Development of cytokinin activity by rearrangement of 1-substituted adenines to 6-substituted aminopurines: inactivation by N6, 1-cyclization.

作者信息

Leonard N J, Achmatowicz S, Loeppky R N, Carraway K L, Grimm W A, Szweykowska A, Hamzi Q H, Skoog F

出版信息

Proc Natl Acad Sci U S A. 1966 Aug;56(2):709-16. doi: 10.1073/pnas.56.2.709.

DOI:10.1073/pnas.56.2.709

PMID:5229988

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC224430/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a90/224430/7cfb008c2eeb/pnas00147-0406-a.jpg

相似文献

Development of cytokinin activity by rearrangement of 1-substituted adenines to 6-substituted aminopurines: inactivation by N6, 1-cyclization.通过将1-取代腺嘌呤重排为6-取代氨基嘌呤来产生细胞分裂素活性：N6,1-环化导致失活。

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本文引用的文献

Cytokinins.细胞分裂素

Science. 1965 Apr 23;148(3669):532-3. doi: 10.1126/science.148.3669.532-a.

PURINE NUCLEOSIDES. VI. FURTHER METHYLATION STUDIES OF NATURALLY OCCURRING PURINE NUCLEOSIDES.嘌呤核苷。VI. 天然存在的嘌呤核苷的进一步甲基化研究。

Biochemistry. 1964 Apr;3:494-500. doi: 10.1021/bi00892a005.

KINETIN-LIKE GROWTH-PROMOTING ACTIVITY OF 1-SUBSTITUTED ADENINES (1-BENZYL-6-AMINOPURINE AND 1-(GAMMA, GAMMA-DIMETHYLALLYL)-6-AMINOPURINE.1-取代腺嘌呤（1-苄基-6-氨基嘌呤和1-（γ，γ-二甲基烯丙基）-6-氨基嘌呤）的类激动素促生长活性

Proc Natl Acad Sci U S A. 1964 Jan;51(1):76-83. doi: 10.1073/pnas.51.1.76.

THE SYNTHESIS OF COMPOUNDS POSSESSING KINETIN ACTIVITY. THE USE OF A BLOCKING GROUP AT THE 9-POSITION OF ADENINE FOR THE SYNTHESIS OF 1-SUBSTITUTED ADENINES.具有激动素活性的化合物的合成。在腺嘌呤9位使用保护基用于合成1-取代腺嘌呤。

Proc Natl Acad Sci U S A. 1964 Jan;51(1):73-5. doi: 10.1073/pnas.51.1.73.

The preparation of 6-N-methyldeoxyadenosine.6-N-甲基脱氧腺苷的制备

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[Identity of triacanthine, togholamine and chidlovine].[三刺棘碱、托戈拉明和奇德洛文的特性]

Ann Pharm Fr. 1962 Mar;20:285-92.

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