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59995-64-1,MFCD00072032
Catalog No.:AA00EJM3

59995-64-1 | Thienamycin

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1mg
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$1,225.00   $858.00
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  • Technical Information
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Technical Information
Catalog Number:
AA00EJM3
Chemical Name:
Thienamycin
CAS Number:
59995-64-1
Molecular Formula:
C11H16N2O4S
Molecular Weight:
272.3207
MDL Number:
MFCD00072032
SMILES:
NCCSC1=C(C(=O)O)N2[C@H](C1)[C@H](C2=O)[C@H](O)C
Properties
Computed Properties
 
Complexity:
423  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
3  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
5  
XLogP3:
-3  

Literature

Title: Autoproteolytic activation of ThnT results in structural reorganization necessary for substrate binding and catalysis.

Journal: Journal of molecular biology 20120928

Title: Comparative analysis of a cryptic thienamycin-like gene cluster identified in Streptomyces flavogriseus by genome mining.

Journal: Archives of microbiology 20120601

Title: Radical-mediated enzymatic methylation: a tale of two SAMS.

Journal: Accounts of chemical research 20120417

Title: Novel carbon-carbon bond formations for biocatalysis.

Journal: Current opinion in biotechnology 20111201

Title: Definition of the common and divergent steps in carbapenem β-lactam antibiotic biosynthesis.

Journal: Chembiochem : a European journal of chemical biology 20110919

Title: Discovery of 3-formyl-tyrosine metabolites from Pseudoalteromonas tunicata through heterologous expression.

Journal: Journal of the American Chemical Society 20100127

Title: Non-heme iron oxygenases generate natural structural diversity in carbapenem antibiotics.

Journal: Journal of the American Chemical Society 20100113

Title: Current status of carbapenem antibiotics.

Journal: Current topics in medicinal chemistry 20100101

Title: Synthesis of regio- and stereoselectively deuterium-labelled derivatives of L-glutamate semialdehyde for studies on carbapenem biosynthesis.

Journal: Organic & biomolecular chemistry 20090707

Title: Evidence that thienamycin biosynthesis proceeds via C-5 epimerization: ThnE catalyzes the formation of (2S,5S)-trans-carboxymethylproline.

Journal: Chembiochem : a European journal of chemical biology 20090126

Title: Identification of transcriptional activators for thienamycin and cephamycin C biosynthetic genes within the thienamycin gene cluster from Streptomyces cattleya.

Journal: Molecular microbiology 20080801

Title: Genome-wide transcriptome analysis reveals that a pleiotropic antibiotic regulator, AfsS, modulates nutritional stress response in Streptomyces coelicolor A3(2).

Journal: BMC genomics 20080101

Title: Empirical antibacterial drug discovery--foundation in natural products.

Journal: Biochemical pharmacology 20060330

Title: Involvement of nitrogen-containing compounds in beta-lactam biosynthesis and its control.

Journal: Critical reviews in biotechnology 20060101

Title: Secretion systems for secondary metabolites: how producer cells send out messages of intercellular communication.

Journal: Current opinion in microbiology 20050601

Title: Regulation and biosynthesis of carbapenem antibiotics in bacteria.

Journal: Nature reviews. Microbiology 20050401

Title: Carboxymethylproline synthase (CarB), an unusual carbon-carbon bond-forming enzyme of the crotonase superfamily involved in carbapenem biosynthesis.

Journal: The Journal of biological chemistry 20040220

Title: The biosynthetic gene cluster for the beta-lactam carbapenem thienamycin in Streptomyces cattleya.

Journal: Chemistry & biology 20030401

Title: Recent developments in carbapenems.

Journal: Expert opinion on investigational drugs 20020401

Title: Antibiotic resistance and molecular typing of Pseudomonas aeruginosa: focus on imipenem.

Journal: The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases 20020201

Title: Carbapenems, a new class of beta-lactam antibiotics. Discovery and development of imipenem/cilastatin.

Journal: The American journal of medicine 19850607

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