Dithiolopyrrolone natural products: isolation, synthesis and biosynthesis. - Test2 - elhamkhani - TriplyDB

Dithiolopyrrolone natural products: isolation, synthesis and biosynthesis.

Dithiolopyrrolone natural products: isolation, synthesis and biosynthesis.

http://www.wikidata.org/entity/Q37304033

about

Spotlight on Antimicrobial Metabolites from the Marine Bacteria Pseudoalteromonas: Chemodiversity and Ecological Significance Antibacterial products of marine organisms.Bioactive natural products from novel microbial sources.Evaluating Nitrogen-Containing Biosynthetic Products Produced by Saltwater Culturing of Several California Littoral Zone Gram-Negative Bacteria.Biosynthesis of polyketides by trans-AT polyketide synthases.Simple "on-demand" production of bioactive natural products.Action in pairs: two tandem genes in the fish pathogen Yersinia ruckeri are virulence factors.Derivatives of Holomycin and Cyclopropaneacetic Acid from Streptomyces sp. DT-A37.Antibiotics from Gram-negative bacteria: a comprehensive overview and selected biosynthetic highlights.

P2860

Q26741301-0A7557F0-37CB-4FB7-A7AC-007A6CE588C0 Q38421365-B4778FCD-DA45-4C69-9798-D102FEA522C2 Q38618414-ECBA8D1E-A9E0-45D9-AE5C-C4C0B7906F98 Q38640879-14A41817-D49D-4A15-B031-D9B79D37D76E Q38675125-7C0A0AD7-4316-449F-8896-5A610429532A Q38892548-0BB6753E-F944-4C14-986F-93DA081751F1 Q42741536-80DE037B-AA47-4A71-B28E-CEC8EAEF777B Q47825068-90CA706A-F0DB-4390-B385-50E84851F01E Q48223572-7AB54B1A-4C14-46A0-B4CA-B4DAC298B63F

P2860

Dithiolopyrrolone natural products: isolation, synthesis and biosynthesis.

http://www.wikidata.org/entity/Q37304033

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 17 October 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Dithiolopyrrolone natural products: isolation, synthesis and biosynthesis.

@en

Dithiolopyrrolone natural products: isolation, synthesis and biosynthesis.

@nl

type

label

Dithiolopyrrolone natural products: isolation, synthesis and biosynthesis.

@en

Dithiolopyrrolone natural products: isolation, synthesis and biosynthesis.

@nl

prefLabel

Dithiolopyrrolone natural products: isolation, synthesis and biosynthesis.

@en

Dithiolopyrrolone natural products: isolation, synthesis and biosynthesis.

@nl

P1433

Q37304033-0F7783B1-494C-4612-8102-99A921E7A67F

P1476

Q37304033-543AA9D7-0C31-4B7D-82A6-E941D74F9355

P2093

Q37304033-7CA29D79-4E95-4A9D-9E4C-23B0DE9B60B3

Q37304033-7FDFD48D-860B-4AC3-8102-9FAB280A336E

Q37304033-CA8F5FBE-932B-4E74-B14E-14F0DEA261CD

P2860

Q37304033-063F528B-96AA-44C5-ACDB-1EB1CAED07D1

Q37304033-078BA87F-F06A-44FF-B938-FCBE5C7EB3B8

Q37304033-0CD6A5B1-201E-4BF6-9FEB-FFF13D723007

Q37304033-0E9C2160-546B-4DF5-987A-14878DDCF236

Q37304033-0EB4CA66-189C-4732-BAFB-CCDF018A9FBF

Q37304033-177EA250-E16B-4076-851A-299207637ADE

Q37304033-18037EF8-DEB6-4F59-BF32-9715239EFA2C

Q37304033-1C80540D-393F-4D3B-BDF1-FDC4C396A2E9

Q37304033-1F6BCD8A-CCF1-4EFF-8819-5AF37F17D663

Q37304033-202A8148-5BB6-4B21-AD73-ACAE3EB1317A

P304

Q37304033-F1974D49-15EF-4BD0-9C37-737415A41F19

P31

Q37304033-B24DB750-F4C2-4620-8BAC-09309216155C

P356

Q37304033-9AA1721C-7D4D-4004-9B75-8CE79F00D16B

P433

Q37304033-F05DB48B-70C3-4B12-86FC-F58EC7788912

P478

Q37304033-5C1A5A86-C6E6-400C-A5CF-0CFCE08776A7

P50

Q37304033-3BBEFD4D-CF98-4484-85B0-B593C9059905

P577

Q37304033-BEDFD2BB-1280-4F93-845C-A2C0CDF925C9

P5875

Q37304033-6F8DE848-8641-458C-8D64-04A724ABC908

P698

Q37304033-6FAA1529-187C-458D-82B6-48C23B66373E

P932

Q37304033-500105E1-09F5-48F5-9957-93BFB7B8FD3D

P356

P1433

P1476

Dithiolopyrrolone natural products: isolation, synthesis and biosynthesis

@en

P2093

Hai Deng

http://www.w3.org/2001/XMLSchema#string

Sheng Huang

http://www.w3.org/2001/XMLSchema#string

Yi Yu

http://www.w3.org/2001/XMLSchema#string

P2860

The fish pathogen Yersinia ruckeri produces holomycin and uses an RNA methyltransferase for self-resistance

Rifamycin-mode of action, resistance, and biosynthesis

Exploiting adaptive laboratory evolution of Streptomyces clavuligerus for antibiotic discovery and overproduction

Antibiotics for emerging pathogens

Drug discovery and natural products: end of an era or an endless frontier?

Catalytic asymmetric synthesis of a potent thiomarinol antibiotic.

Cloning, overexpression, and purification of novobiocic acid synthetase from Streptomyces spheroides NCIMB 11891.

Thiolutin inhibits endothelial cell adhesion by perturbing Hsp27 interactions with components of the actin and intermediate filament cytoskeleton.

A natural plasmid uniquely encodes two biosynthetic pathways creating a potent anti-MRSA antibiotic

Biosynthesis of cephalosporin C from amino acids.

P304

3970-3997

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.3390/MD11103970

http://www.w3.org/2001/XMLSchema#string

P433

10

http://www.w3.org/2001/XMLSchema#string

P478

11

http://www.w3.org/2001/XMLSchema#string

P50

P577

2013-10-17T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

258060430

http://www.w3.org/2001/XMLSchema#string

P698

24141227

http://www.w3.org/2001/XMLSchema#string

P932

3826145

http://www.w3.org/2001/XMLSchema#string