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Brevianamide F

Base Information
  • Chemical Name:Brevianamide F
  • CAS No.:38136-70-8
  • Molecular Formula:C16H17N3O2
  • Molecular Weight:283.33
  • Hs Code.:
  • UNII:76XZ426FPP
  • DSSTox Substance ID:DTXSID10959075
  • Nikkaji Number:J17.960D
  • Wikipedia:Brevianamide_F
  • Wikidata:Q25323862
  • Metabolomics Workbench ID:63425
  • ChEMBL ID:CHEMBL563557
  • Mol file:38136-70-8.mol
Brevianamide F

Synonyms:brevianamide F

Suppliers and Price of Brevianamide F
Supply Marketing:
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
  • TRC
  • BrevianamideF
  • 50mg
  • $ 250.00
  • DC Chemicals
  • BrevianamideF >98%
  • 1 g
  • $ 1800.00
  • DC Chemicals
  • BrevianamideF >98%
  • 250 mg
  • $ 900.00
  • Crysdot
  • BrevianamideF 98+%
  • 50mg
  • $ 432.00
  • Crysdot
  • BrevianamideF 98+%
  • 100mg
  • $ 671.00
  • ChemScene
  • BrevianamideF 99.49%
  • 50mg
  • $ 540.00
  • ChemScene
  • BrevianamideF 99.49%
  • 100mg
  • $ 840.00
  • ChemScene
  • BrevianamideF 99.49%
  • 5mg
  • $ 120.00
  • ChemScene
  • BrevianamideF 99.49%
  • 10mg
  • $ 180.00
  • Chemenu
  • BrevianamideF 98%
  • 100mg
  • $ 628.00
Total 18 raw suppliers
Chemical Property of Brevianamide F
Chemical Property:
  • Vapor Pressure:6.11E-16mmHg at 25°C 
  • Melting Point:165-167 °C 
  • Boiling Point:633.2°C at 760 mmHg 
  • PKA:13.20±0.40(Predicted) 
  • Flash Point:336.8°C 
  • PSA:68.69000 
  • Density:1.37g/cm3 
  • LogP:1.41360 
  • Storage Temp.:2-8°C 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly) 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:283.132076794
  • Heavy Atom Count:21
  • Complexity:453
Purity/Quality:

97% *data from raw suppliers

BrevianamideF *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC2C(=O)NC(C(=O)N2C1)CC3=CNC4=CC=CC=C43
  • Isomeric SMILES:C1C[C@H]2C(=O)N[C@H](C(=O)N2C1)CC3=CNC4=CC=CC=C43
  • Description Brevianamide F is an alkaloid metabolite produced by various Streptomyces, Actinomycetes, and Aspergillus strains that has diverse biological activities. It inhibits growth of M. luteus and S. aureus in an inhibitory disc assay when used at a concentration of 30 μg/disc as well as the Bacille Calmette-Guerin M. bovis strain (MIC = 12.5 μg/ml). Brevianamide F has antifouling activity, inhibiting attachment of B. neritina larvae to PVC plates without inducing lethality (EC50 = 6.35 μg/ml; LC50 = >200 μg/ml in paint used to coat PVC plates).
  • Uses Brevianamide F is used in the preparation, reactions, medicinal and cheical propreties of diketopiperazines as bioactive natural products. Acts as a reagent in the total synthesis and antitumor activity in vitro of glioperazine C and its derivatives, synthesis and biological evaluation of a post-synthetically trp-based diketopiperazine and it’s antitumor structure-activity relationship.
Technology Process of Brevianamide F

There total 39 articles about Brevianamide F 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:
D-proline methyl ester hydrochloride; N-carbobenzyloxy-L-tryptophane; With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 2h;
With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃;
DOI:10.1039/c3md20353k
Guidance literature:
N-tert-butyloxycarbonyl-L-tryptophan-L-proline methyl ester; With formic acid; methoxybenzene; at 20 ℃; for 3h;
In toluene; iso-butanol; for 3h; Further stages.; Heating;
DOI:10.1016/j.tetlet.2008.04.156
Guidance literature:
With ammonium hydroxide; In water; at 0 - 23 ℃; for 14h; diastereoselective reaction;
DOI:10.1021/ja4023557
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