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cephamycin C

Base Information
  • Chemical Name:cephamycin C
  • CAS No.:38429-35-5
  • Molecular Formula:C16H22N4O9S
  • Molecular Weight:446.438
  • Hs Code.:
  • NSC Number:179170
  • DSSTox Substance ID:DTXSID301100850
  • Nikkaji Number:J3.030.642B
  • Wikidata:Q105159121
  • Mol file:38429-35-5.mol
cephamycin C

Synonyms:A 16886B;A-16886B;A16886B;cephamycin C;cephamycin C sodium;cephamycin C, (6R)-isomer;cephamycin C, (6R-(6alpha,7alpha,7(R*)))-isomer;cephamycin C, (6R-(6alpha,7alpha,7(S*)))-isomer;cephamycin C, monosodium salt;cephamycin C, sodium salt

Suppliers and Price of cephamycin C
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 29 raw suppliers
Chemical Property of cephamycin C
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:898.2°Cat760mmHg 
  • Flash Point:497°C 
  • PSA:241.36000 
  • Density:1.61g/cm3 
  • LogP:0.36890 
  • XLogP3:-4.3
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:11
  • Rotatable Bond Count:11
  • Exact Mass:446.11074947
  • Heavy Atom Count:30
  • Complexity:802
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1(C2N(C1=O)C(=C(CS2)COC(=O)N)C(=O)O)NC(=O)CCCC(C(=O)O)N
  • General Description Cephamycin, also known as A16886b, is a β-lactam antibiotic structurally related to cephalosporins but distinguished by the presence of a 7α-methoxy group, which enhances its stability against β-lactamases. The synthesized derivatives in this study, particularly those with a five-membered heterocyclic ring in the acylamido side chain, demonstrated potent antibacterial activity, with some compounds rivaling or surpassing the efficacy of cefoxitin and cephalothin against gram-negative bacteria. This highlights the potential of cephamycin derivatives as promising candidates for combating resistant bacterial infections.
Technology Process of cephamycin C

There total 1 articles about cephamycin C which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Refernces

Synthesis of 7α methoxy 7 [2 (substituted thio)acetamido]cephalosporin derivatives and their antibacterial activities

10.1248/cpb.24.2629

The research focused on the synthesis and antibacterial activities of 7a-methoxy-7-[2-(substituted thio)acetamido]cephalosporin derivatives. The purpose was to develop more active cephalosporin derivatives by nucleophilic displacement of the halogen atom of 7β-(2-halogenoacetamido)-7-methoxy cephalosporanic acid derivatives with various mercapto compounds. The study concluded that the synthesized compounds, particularly those with a five-membered heterocyclic ring in the acylamido group, exhibited potent antibacterial activities, with compound (6) showing activities comparable to the semi-synthetic antibiotic cefoxitin and superior to cephalothin against gram-negative bacteria. Key chemicals used in the process included cephamycin C, tert-butoxycarbonyl azide, diphenyldiazomethane, chloroacetyl chloride, bis(trimethylsilyl)trifluoroacetamide, and various mercapto compounds for the nucleophilic displacement reaction.

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