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

Encyclopedia

BLASTICIDIN S

Base Information Edit
  • Chemical Name:BLASTICIDIN S
  • CAS No.:2079-00-7
  • Deprecated CAS:11002-92-9,11028-10-7,12767-55-4,13184-51-5,7562-21-2
  • Molecular Formula:C17H26N8O5
  • Molecular Weight:422.444
  • Hs Code.:29349990
  • European Community (EC) Number:606-640-2
  • ICSC Number:1758
  • UN Number:2588
  • UNII:83U64J9U23
  • Wikipedia:Blasticidin_S
  • ChEMBL ID:CHEMBL511116
  • Mol file:2079-00-7.mol
BLASTICIDIN S

Synonyms:BlasticidinS (6CI,8CI);D-erythro-Hex-2-enopyranuronic acid,4-[3-amino-5-(1-methylguanidino)valeramido]-1-(4-amino-2-oxo-1(2H)-pyrimidinyl)-1,2,3,4-tetradeoxy-(7CI);Bla-S;

Suppliers and Price of BLASTICIDIN S
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
  • American Custom Chemicals Corporation
  • BLASTICIDIN S 95.00%
  • 50MG
  • $ 759.41
  • American Custom Chemicals Corporation
  • BLASTICIDIN S 95.00%
  • 250MG
  • $ 1086.86
  • American Custom Chemicals Corporation
  • BLASTICIDIN S 95.00%
  • 100MG
  • $ 839.45
  • AHH
  • BlasticidinS 98%
  • 0.5g
  • $ 770.00
Total 7 raw suppliers
Chemical Property of BLASTICIDIN S Edit
Chemical Property:
  • Appearance/Colour:Colourless needles 
  • Vapor Pressure:Low 
  • Melting Point:235-236ºC 
  • Refractive Index:1.707 
  • Boiling Point:°Cat760mmHg 
  • PKA:2.4 (carboxyl), 4.6,8.0 and>12.5 (three bases) 
  • Flash Point:°C 
  • PSA:215.67000 
  • Density:1.61 g/cm3 
  • LogP:0.25370 
  • Water Solubility.:>30 g l-1(20 °C) 
  • XLogP3:-5.2
  • Hydrogen Bond Donor Count:6
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:9
  • Exact Mass:422.20261596
  • Heavy Atom Count:30
  • Complexity:795
Purity/Quality:

98%, *data from raw suppliers

BLASTICIDIN S 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s): VeryT+ 
  • Hazard Codes:T+ 
  • Statements: 28 
  • Safety Statements: 24/25-36/37-45 
MSDS Files:

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Pesticides -> Fungicides
  • Canonical SMILES:CN(CCC(CC(=O)NC1C=CC(OC1C(=O)O)N2C=CC(=NC2=O)N)N)C(=N)N
  • Isomeric SMILES:CN(CC[C@@H](CC(=O)N[C@@H]1C=C[C@H](O[C@H]1C(=O)O)N2C=CC(=NC2=O)N)N)C(=N)N
  • Inhalation Risk:A harmful concentration of airborne particles can be reached quickly when dispersed, especially if powdered.
  • Effects of Short Term Exposure:The substance is severely irritating to the eyes. The substance is irritating to the respiratory tract and skin. Corrosive on ingestion. Exposure at high levels could cause death.
  • Description Nucleoside antibiotic produced by Streptomyces griseochromogenes (1). Biosynthesized from cytosine, glucose, arginine, and methionine (2).
  • Uses Blasticidin S is a nucleoside produced by several species of Streptomyces, first reported in the late 1950s. Blasticidin S is an antifungal agent with particularly potent activity against the rice pathogen, Piricularia oryzae, for which it was used commercially for some time in Japan. Blasticidin S inhibits protein synthesis and is active against bacteria, tumour cell lines and nematodes. More recently, blasticidin S has been used as a marker for strain manipulations. Blasticidin S provided by BioAustralis is presented as the free base to avoid problems associated with the use of the hydrochloride. Blasticidin-S is used for the control of rice blast (PyricuZuria oryzae) by foliar application.
Technology Process of BLASTICIDIN S

There total 6 articles about BLASTICIDIN S 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 Streptomyces griseochromogenes cell-free extract; In phosphate buffer; at 30 ℃; pH=7.0; Enzymatic reaction;
DOI:10.1016/S0040-4020(99)01060-1
upstream raw materials:

D-Glucose

L-methionine

L-arginine

Cytosine

Downstream raw materials:

cytosinine

Post RFQ for Price