Isolation and Synthesis of Laxaphycin B-Type Peptides: A Case Study and Clues to Their Biosynthesis
出版年份 2015 全文链接
标题
Isolation and Synthesis of Laxaphycin B-Type Peptides: A Case Study and Clues to Their Biosynthesis
作者
关键词
-
出版物
Marine Drugs
Volume 13, Issue 12, Pages 7285-7300
出版商
MDPI AG
发表日期
2015-12-09
DOI
10.3390/md13127065
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Trichormamides C and D, antiproliferative cyclic lipopeptides from the cultured freshwater cyanobacterium cf. Oscillatoria sp. UIC 10045
- (2015) Shangwen Luo et al. BIOORGANIC & MEDICINAL CHEMISTRY
- Straightforward strategy to substitute amide bonds by 1,2,3-triazoles in peptaibols analogs using Aibψ[Tz]-Xaa dipeptides
- (2015) Khoubaib Ben Haj Salah et al. BIOPOLYMERS
- Trichormamides A and B with Antiproliferative Activity from the Cultured Freshwater Cyanobacterium Trichormus sp. UIC 10339
- (2014) Shangwen Luo et al. JOURNAL OF NATURAL PRODUCTS
- High-Efficiency Solid Phase Peptide Synthesis (HE-SPPS)
- (2014) Jonathan M. Collins et al. ORGANIC LETTERS
- Efficient Microwave-Assisted One Shot Synthesis of Peptaibols Using Inexpensive Coupling Reagents
- (2014) Khoubaib Ben Haj Salah et al. ORGANIC LETTERS
- A Hybrid Non-Ribosomal Peptide/Polyketide Synthetase Containing Fatty-Acyl Ligase (FAAL) Synthesizes the β-Amino Fatty Acid Lipopeptides Puwainaphycins in the Cyanobacterium Cylindrospermum alatosporum
- (2014) Jan Mareš et al. PLoS One
- Cytochrome P450sky Interacts Directly with the Nonribosomal Peptide Synthetase to Generate Three Amino Acid Precursors in Skyllamycin Biosynthesis
- (2013) Stefanie Uhlmann et al. ACS Chemical Biology
- Heating and microwave assisted SPPS of C-terminal acid peptides on trityl resin: the truth behind the yield
- (2013) Cécile Echalier et al. AMINO ACIDS
- First Total Synthesis and Stereochemical Revision of Laxaphycin B and Its Extension to Lyngbyacyclamide A
- (2013) France Boyaud et al. ORGANIC LETTERS
- In Vitro Characterization of Echinomycin Biosynthesis: Formation and Hydroxylation of L-Tryptophanyl-S-Enzyme and Oxidation of (2S,3S) β-Hydroxytryptophan
- (2013) Chen Zhang et al. PLoS One
- Structure and noncanonical chemistry of nonribosomal peptide biosynthetic machinery
- (2012) Heather L. Condurso et al. NATURAL PRODUCT REPORTS
- Enzymatic resistance to the lipopeptide surfactin as identified through imaging mass spectrometry of bacterial competition
- (2012) B. C. Hoefler et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Synthesis of a protected derivative of (2R,3R)-β-hydroxyaspartic acid suitable for Fmoc-based solid phase synthesis
- (2012) Boyaud France et al. TETRAHEDRON LETTERS
- Microwave heating in solid-phase peptide synthesis
- (2011) Søren L. Pedersen et al. CHEMICAL SOCIETY REVIEWS
- Underestimated biodiversity as a major explanation for the perceived rich secondary metabolite capacity of the cyanobacterial genusLyngbya
- (2011) Niclas Engene et al. ENVIRONMENTAL MICROBIOLOGY
- Contemporary strategies for peptide macrocyclization
- (2011) Christopher J. White et al. Nature Chemistry
- Filamentous tropical marine cyanobacteria: a rich source of natural products for anticancer drug discovery
- (2010) Lik Tong Tan JOURNAL OF APPLIED PHYCOLOGY
- Structural Characterization of OxyD, a Cytochrome P450 Involved in β-Hydroxytyrosine Formation in Vancomycin Biosynthesis
- (2010) Max J. Cryle et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Lyngbyacyclamides A and B, novel cytotoxic peptides from marine cyanobacteria Lyngbya sp.
- (2010) Norihito Maru et al. TETRAHEDRON LETTERS
- COMU: A Safer and More Effective Replacement for Benzotriazole-Based Uronium Coupling Reagents
- (2009) Ayman El-Faham et al. CHEMISTRY-A EUROPEAN JOURNAL
- Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole-Based HOBt and HOAt with a Lower Risk of Explosion[1]
- (2009) Ramon Subirós-Funosas et al. CHEMISTRY-A EUROPEAN JOURNAL
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