Thuringiensin

Base Information

• Chemical Name: Thuringiensin
• CAS No.: 23526-02-5
• Molecular Formula: C₂₂H₃₂N₅O₁₉P
• Molecular Weight: 701.492
• NSC Number: 197177
• DSSTox Substance ID: DTXSID00860303
• ChEMBL ID: CHEMBL1988470
• Mol file: 23526-02-5.mol

Synonyms:Exotoxin;Exotoxins

Chemical Property of Thuringiensin

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Boiling Point: 1263.8°Cat760mmHg
• PKA: 1.69±0.10(Predicted)
• Flash Point: 718.1°C
• PSA: 399.32000
• Density: 2.27g/cm³
• LogP: -5.81280
• XLogP3: -7
• Hydrogen Bond Donor Count: 12
• Hydrogen Bond Acceptor Count: 23
• Rotatable Bond Count: 14
• Exact Mass: 701.14291081
• Heavy Atom Count: 47
• Complexity: 1140

Purity/Quality:

99% ^*data from raw suppliers

β-Exotoxin ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Biological Agents -> Bacterial Toxins
• Canonical SMILES: C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COC4C(OC(C(C4O)O)OC(C(C(C(C(=O)O)O)OP(=O)(O)O)O)C(=O)O)CO)O)O)N
• Uses: 2-[5-[[5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy]-3,4-di hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,5-dihydroxy-4-phosphonooxy-he xanedioic acid is a thermostable metabolite produced by some strains of Bacillus thuringiensis. 2-[5-[[5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy]-3,4-di hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,5-dihydroxy-4-phosphonooxy-he xanedioic acid can be used to screen and quantify indigenous thuringiensin-producing Bacillus thuringiensis isolates. β-Exotoxin can cause damage to the host by destroying cells or disrupting normal cellular metabolism.

Technology Process of Thuringiensin

There total 4 articles about Thuringiensin 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:

Reference yield:

→ β-exotoxin (52520-32-8,63267-74-3,23526-02-5)

Guidance literature:

Lacton VIII;

Reference yield:

→ D-O2-(O4-adenosin-5'-yl-α-D-glucopyranosyl)-O4-phosphono-allaric acid (52520-32-8,63267-74-3,23526-02-5)

Guidance literature:

Aus XXXVII,POCl3, Py u. NaOH;

Reference yield:

→ O2-(O4-adenosin-5'-yl-D-glucopyranosyl)-O4-phosphono-allaric acid (52520-32-8,63267-74-3,23526-02-5)

Guidance literature:

asu Allarat LIX, POCl3, methanolischem CH3ONa, H2O;