The discovery of a freezing-induced peptide ligation during the total chemical synthesis of human interferon-ε
文献情報
Yin-He Yang, Bin Di, Da-Song Yang
A counterintuitive freezing-induced peptide ligation was discovered during the total synthesis of human interferon-ε (hIFN-ε) which blocks HIV infection through unique mechanisms. The successful synthesis of hIFN-ε (187 amino acids) in this research laid the foundation for related anti-AIDS drug development. Moreover, alanine mutation based on sequence alignment to solve the maldistribution of the ligation site and freezing-induced dominant conformation that facilitates peptide ligation are expected to be helpful for the synthesis of macrobiomolecules.
おすすめジャーナル

Science Progress

European Journal of Wood and Wood Products

Molecular Pharmacology

Pure and Applied Chemistry

Journal of Organometallic Chemistry

Journal of Physics and Chemistry of Solids

Organic Preparations and Procedures International

Journal of Heterocyclic Chemistry

Journal of Medicinal Chemistry

Kinetics and Catalysis
関連文献
Microstructural dependent oxygen reduction reaction in a Ruddlesden–Popper perovskite (SmSr)NiO4−δ
Manisha Chauhan, Pardeep K. Jha, Ajay S. Bangwal, Priyanka A. Jha, Prabhakar Singh
DOI: 10.1039/D0CP00433B
Temperature effects on the ionic conductivity in concentrated alkaline electrolyte solutions
Yunqi Shao, Are Yllö, Jonas Mindemark, Kersti Hermansson, Jörg Behler, Chao Zhang
DOI: 10.1039/C9CP06479F
FB-REDA: fragment-based decomposition analysis of the reorganization energy for organic semiconductors
Kun-Han Lin, Clémence Corminboeuf
DOI: 10.1039/D0CP01722A
Charge fluctuations from molecular simulations in the constant-potential ensemble
Laura Scalfi, Sara Bonella, Paul A. Madden
DOI: 10.1039/C9CP06285H
Tailoring the protonic conductivity of porous yttria-stabilized zirconia thin films by surface modification
Erdogan Celik, Rajendra S. Negi, Michele Bastianello, Dominic Boll, Andrey Mazilkin, Torsten Brezesinski
DOI: 10.1039/D0CP01619E
A computational exploration of the 1D TiS2(en) nanostructure for lithium ion batteries
Chun-Hao Huang, Elise Y. Li
DOI: 10.1039/C9CP04675E
Ionization energies in solution with the QM:QM approach
Zsuzsanna Tóth, Jakub Kubečka, Eva Muchová, Petr Slavíček
DOI: 10.1039/C9CP06154A
Effect of strain and defects on the thermal conductance of the graphene/hexagonal boron nitride interface
Jieren Song, Chaocan Cai, Yujiao Bai, Linlin Miao, Rongguo Wang
DOI: 10.1039/D0CP01727B
こちらもおすすめ
「邻羟基阿托伐他汀内酯标准品」に適用される法規ガイドelinesは何ですか?
CAS番号163217-74-1の「邻羟基阿托伐他汀内酯标准品」は、GHS分類では危険物に分類されず、主にREACH規則とFDA/EPAの管理対象となります。R...
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩の主な用途は何ですか?
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩は、医薬品や合成化学の研究に広く用いられます。また、特定の薬物の前...
トランス-4-メチルピロリジン-3-オール塩酸塩はどのように合成されますか?
トランス-4-メチルピロリジン-3-オール塩酸塩は、4-メチルピロリジンの塩酸塩化によって合成されます。一般的な合成方法では、4-メチルピロリジンを塩酸に加えて...
硫雜環丁烷-1,1-二氧化物は安全ですか?
硫雜環丁烷-1,1-二氧化物は安全ではありません。毒性は報告されていませんが、高温下で分解し、可燃性があるため、高圧ガスは注意が必要です。密閉した容器で保管し、...
9-ヒドロキシエリプチシネ塩酸塩はどのように合成されますか?
9-ヒドロキシエリプチシネ塩酸塩は、エリプチシネから塩酸を添加することで合成されます。選択性は高いですが、収率は約70%です。
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮の物理化学的性質は何ですか?
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮のCAS番号は5621-86-3です。この化合物は白色の結晶性粉末で、分子量は415.03で...
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪はどのように保存すればよいですか?
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪は、直射日光を避けて暗所に、室温(15-25℃)で保管し、密閉容器に入れることで安定性を保つことができます。
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンの主な用途は何ですか?
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンは、医薬品の合成、有機合成化学、および新材料の研究で使用され...
掲載誌
Organic & Biomolecular Chemistry

Organic & Biomolecular Chemistry (OBC) publishes original and high impact research and reviews in organic chemistry. We welcome research that shows new or significantly improved protocols or methodologies in total synthesis, synthetic methodology or physical and theoretical organic chemistry as well as research that shows a significant advance in the organic chemistry or molecular design aspects of chemical biology, catalysis, supramolecular and macromolecular chemistry, theoretical chemistry, mechanism-oriented physical organic chemistry, medicinal chemistry or natural products. Articles published in the journal should report new work which makes a highly-significant impact in the field. Routine and incremental work is generally not suitable for publication in the journal. More details about key areas of our scope are below. In all cases authors should include in their article clear rationale for why their research has been carried out.

![(2E)-3-(3-Chlorophenyl)-N-{2-[4-(methylsulfonyl)-1-piperazinyl]-2-oxoethyl}acrylamide structure (2E)-3-(3-Chlorophenyl)-N-{2-[4-(methylsulfonyl)-1-piperazinyl]-2-oxoethyl}acrylamide structure](https://static.chemtradehub.com/structs/250/2505001-54-5-c1e9.webp)
![(3R,5R)-1-[(Benzyloxy)carbonyl]-5-methyl-3-piperidinecarboxylic acid structure (3R,5R)-1-[(Benzyloxy)carbonyl]-5-methyl-3-piperidinecarboxylic acid structure](https://static.chemtradehub.com/structs/126/1269757-29-0-c552.webp)

