Cell Chemical Biology
基本信息
Cell Chemical Biology (originally Chemistry & Biology) is a Cell Press journal that aims to publish and promote the most important advances in chemical biology with integrity, responsiveness, fairness, and friendliness. Chemical biology is a unique discipline that harnesses the power of chemistry to deliver profound molecular insights into biological function and disease etiology and develop solutions for life sciences, biotechnology, and human health. Cell Chemical Biology encourages submission of basic, translational, and clinical research articles that provide significant conceptual advancements of broad general interest to researchers within the biological sciences, the biomedical sciences, and associated fields. Research areas that we consider within our scope include but are not limited to cancer biology, immunology, cell biology, microbiology, virology, RNA biology, synthetic biology, protein engineering, genome editing, drug discovery, metabolism, and physiology. We are interested in papers that report molecular mechanisms underlying cellular processes or disease biology; those that report new therapeutics derived from utilizing chemical biology tools; and those that report technologies that perturb, visualize, or measure biological processes. Examples of chemical or molecular tools include but are not confined to nucleic acids and/or their modifications, small molecules, antibodies, biologics, probes, engineered proteins, metabolites, lipids, sugars, and post-translational modifications. We also welcome submissions reporting significant technical advancements in molecular probes, sensors, tools, and technologies, including a proof-of-principle demonstration that the new methodology/tool will help address important questions in biomedical research that are of interest to our broad readership (from basic scientists to clinicians).
CiteScore
| 学科 | 排名 | 百分位 |
|---|---|---|
Biochemistry, Genetics and Molecular BiologyClinical Biochemistry |
7 / 117 | 94% |
期刊统计
投稿信息
投稿网址:
https://www.editorialmanager.com/CELL-CHEMICAL-BIOLOGY收录体裁:
Brief Communication
Resource
Matters Arising
Minireview
Review
Perspective
Meeting Report
Preview
相关文献
Palladium-catalysed direct synthesis of benzo[b]thiophenes from thioenols
Kiyofumi Inamoto, Yukari Arai, Kou Hiroya, Takayuki Doi
DOI: 10.1039/B811362A
A robust strategy for the preparation of libraries of metallopeptides. A new paradigm for the discovery of targeted molecular imaging and therapy agents
Andrea F. Armstrong, Nick Oakley, Shannon Parker, Patrick W. Causey, Jennifer Lemon, Alfredo Capretta, Craig Zimmerman, John Joyal, Francis Appoh, Jon Zubieta, John W. Babich, Gurmit Singh, John F. Valliant
DOI: 10.1039/B810706H
Chemiluminescence thrombin aptasensor using high-activity DNAzyme as catalytic label
DOI: 10.1039/B809296F
New 6-oxa-2-silabicyclo[2.2.0]hexanes by photochemical conversion of acyl(allyl)(dimethyl)silanes
Catherine Hammaecher, Charles Portella
DOI: 10.1039/B812550C
The doping effect of fluorinated aromatic hydrocarbon solvents on the performance of common olefin metathesis catalysts: application in the preparation of biologically active compounds
Cezary Samojłowicz, Michał Bieniek, Andrzej Zarecki, Renat Kadyrov, Karol Grela
DOI: 10.1039/B816567J
Synthesis of tri- and tetraynes using a butadiynyl synthon
Khalid Azyat, Eike Jahnke, Trent Rankin, Rik R. Tykwinski
DOI: 10.1039/B816177A
Rapid analysis of isotopically unmodified amino acids by high-resolution 14N-edited 1H–13C correlation NMR spectroscopy
Jean-Paul Amoureux, Bingwen Hu, Olivier Lafon, Julien Trébosc, Feng Deng
DOI: 10.1039/B816362F
One-phase synthesis of small gold nanoparticles coated by a horizontal porphyrin monolayer
Junya Ohyama, Yasuhiro Higuchi, Masashi Shinagawa, Hidefumi Mukai, Masahito Kodera, Kentaro Teramura, Tetsuya Shishido, Tsunehiro Tanaka
DOI: 10.1039/B815100H
Reactions over catalysts confined in carbon nanotubes
Xiulian Pan, Xinhe Bao
DOI: 10.1039/B810994J
An approach to biodegradable star polymeric architectures using disulfide coupling
Jingquan Liu, Huiyun Liu, Zhongfan Jia, Volga Bulmus, Thomas P. Davis
DOI: 10.1039/B817037A
您可能还喜欢
4-[4-三氟甲基苯基]恶唑(CAS号:1126636-40-5)通常如何合成?
4-[4-三氟甲基苯基]恶唑通常通过将4-三氟甲基苯酚与异硫氰酸苯酯在有机溶剂中进行酯化反应合成。该反应可在无水条件下,使用适当的催化剂,如四丁基氢氧化铵,以提...
RockPhos Pd G3(CAS号:2009020-38-4)通常如何合成?
RockPhos Pd G3 通常通过钯催化偶联反应合成,使用配体 (2'-Amino-2-biphenylyl)(methanesulfonato-kappa...
1-哌啶甲酰胺(CAS号:2158-03-4)的市场或研究趋势如何?
1-哌啶甲酰胺作为有机合成中的重要中间体,其市场需求主要受医药、农药、染料等行业推动。近年来,随着新药开发和绿色化学的发展,该化合物的研究趋势集中在开发更高效、...
2-(二苯基膦基)乙胺(CAS号:4848-43-5)适用哪些法规指南?
2-(二苯基膦基)乙胺适用于多种法规指南,包括但不限于《全球化学品统一分类和标签制度》(GHS),欧盟《化学品注册、评估、授权和限制》法规(REACH),以及美...
如何储存间苯二甲酸二烯丙酯(CAS号:1087-21-4)?
间苯二甲酸二烯丙酯应储存在阴凉、干燥、通风良好的地方,远离火源和热源。储存容器应密封,避免光照和高温。储存温度应控制在25℃以下,相对湿度应低于80%。避免与其...
什么是间甲苯异硫代异氰酸酯(CAS号:621-30-7)?
间甲苯异硫代异氰酸酯是一种有机化合物,分子式为C7H7NO2S,具有刺激性气味。它是一种重要的有机合成中间体,在合成其他化合物时广泛应用。
在合成中是否有N-Boc-D-苯丙氨醇(CAS号:106454-69-7)的替代品?
在合成中,可以考虑使用N-Cbz-D-苯丙氨醇或N-Fmoc-D-苯丙氨醇作为替代品。这些化合物同样具有保护氨基的功能,且在合成过程中表现出良好的反应性能。
3-羟甲基-2-氧异丙基吡啶(CAS号:954240-50-7)的主要用途是什么?
3-羟甲基-2-氧异丙基吡啶主要用于有机合成领域,可以作为合成其他药物、农药或精细化学品的中间体。此外,它还可能在实验室研究中作为特定反应的前体或溶剂。
6-氨基-9-甲基嘌呤(CAS号:700-00-5)应用于哪些行业?
6-氨基-9-甲基嘌呤目前主要应用于医药行业,作为某些药物的中间体。此外,它还可能用于聚合物、传感器和半导体的某些领域,作为功能性单体或掺杂剂。












![Bis[(1,2,3,4,5-eta)-1-(diphenylphosphino)cyclopentadienyl]iron structure Bis[(1,2,3,4,5-eta)-1-(diphenylphosphino)cyclopentadienyl]iron structure](https://cnstatic.chemtradehub.com/structs/121/12150-46-8-ecd2.webp)




