Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Alamethicin

Base Information Edit
  • Chemical Name:Alamethicin
  • CAS No.:59588-86-2
  • Deprecated CAS:66473-80-1
  • Molecular Formula:C92H150 N22 O25
  • Molecular Weight:1964.31
  • Hs Code.:
  • European Community (EC) Number:608-040-6
  • ChEMBL ID:CHEMBL438243
  • Metabolomics Workbench ID:144418
  • Wikidata:Q4705902
  • Wikipedia:Alamethicin
  • Mol file:59588-86-2.mol
Alamethicin

Synonyms:Alamethicin

Suppliers and Price of Alamethicin
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Alamethicin
  • 1mg
  • $ 262.00
  • Alfa Aesar
  • Alamethicin
  • 5mg
  • $ 557.00
  • Alfa Aesar
  • Alamethicin
  • 1mg
  • $ 138.00
Total 13 raw suppliers
Chemical Property of Alamethicin Edit
Chemical Property:
  • Appearance/Colour:Tan or light brown solid 
  • Melting Point:277-278ºC 
  • PSA:708.13000 
  • LogP:3.96740 
  • Storage Temp.:2-8°C 
  • Solubility.:Soluble in DMSO and ethanol. 
  • Water Solubility.:Soluble in DMSO and ethanol 
  • XLogP3:-1.8
  • Hydrogen Bond Donor Count:22
  • Hydrogen Bond Acceptor Count:25
  • Rotatable Bond Count:53
  • Exact Mass:1963.11424836
  • Heavy Atom Count:139
  • Complexity:4520
Purity/Quality:

99% *data from raw suppliers

Alamethicin *data from reagent suppliers

Safty Information:
  • Pictogram(s): Toxic
  • Hazard Codes:
  • Statements: 25 
  • Safety Statements: 45 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)CC(C(=O)NC(C)(C)C(=O)N1CCCC1C(=O)NC(C(C)C)C(=O)NC(C)(C)C(=O)NC(C)(C)C(=O)NC(CCC(=O)O)C(=O)NC(CCC(=O)N)C(=O)NC(CC2=CC=CC=C2)CO)NC(=O)CNC(=O)C(C)(C)NC(=O)C(C(C)C)NC(=O)C(C)(C)NC(=O)C(CCC(=O)N)NC(=O)C(C)NC(=O)C(C)(C)NC(=O)C(C)NC(=O)C(C)(C)NC(=O)C3CCCN3C(=O)C(C)(C)NC(=O)C
  • Isomeric SMILES:C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)NC(C)(C)C(=O)N[C@@H](C(C)C)C(=O)NC(C)(C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)NC(C)(C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(=O)NC(C)(C)C(=O)NC(C)(C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC2=CC=CC=C2)CO)NC(=O)C(C)(C)NC(=O)[C@H](C)NC(=O)C(C)(C)NC(=O)[C@@H]3CCCN3C(=O)C(C)(C)NC(=O)C
  • Uses Alamethicin is used as a channel-forming ionophore that activates membrane enzymes, membrane channel-forming peptide. It is a 20-amino acid channel-forming peptide antibiotic that can function as a monovalent cation ionophore. Alamethicin has been used to develop methods for the routine assessment of potential new drug candidates to elicit their pharmacokinetic drug interactions.
Technology Process of Alamethicin

There total 3 articles about Alamethicin 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:
Guidance literature:
With sodium tetrahydroborate; water; In isopropyl alcohol; at 0 ℃; for 0.333333h;
DOI:10.1002/ejoc.201601102
Guidance literature:
With chlorotriisopropylsilane; water; trifluoroacetic acid; resin
Guidance literature:
With palladium; cyclohexene; In ethanol; for 1h; Yield given; Heating;
DOI:10.1016/S0040-4020(01)92061-7
upstream raw materials:

C99H156N22O25

Refernces Edit
Post RFQ for Price