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Antibiotics from Streptomyces coeruleorubidus

Base Information
  • Chemical Name:Antibiotics from Streptomyces coeruleorubidus
  • CAS No.:71214-33-0
  • Molecular Formula:C27H30NO10*Cl
  • Molecular Weight:563.989
  • Hs Code.:
  • European Community (EC) Number:245-723-4
  • NSC Number:301724,257457,249333,83142,304419,82151
  • UN Number:2811
  • NCI Thesaurus Code:C1583
  • RXCUI:81992
  • ChEMBL ID:CHEMBL158918
Antibiotics from Streptomyces coeruleorubidus

Synonyms:Cerubidine;Dauno Rubidomycine;Dauno-Rubidomycine;Daunoblastin;Daunoblastine;Daunomycin;Daunorubicin;Daunorubicin Hydrochloride;Hydrochloride, Daunorubicin;NSC 82151;NSC-82151;NSC82151;Rubidomycin;Rubomycin

Suppliers and Price of Antibiotics from Streptomyces coeruleorubidus
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
Total 2 raw suppliers
Chemical Property of Antibiotics from Streptomyces coeruleorubidus
Chemical Property:
  • Vapor Pressure:6.13E-25mmHg at 25°C 
  • Boiling Point:770°C at 760 mmHg 
  • Flash Point:419.5°C 
  • Hydrogen Bond Donor Count:6
  • Hydrogen Bond Acceptor Count:11
  • Rotatable Bond Count:4
  • Exact Mass:563.1558238
  • Heavy Atom Count:39
  • Complexity:960
  • Transport DOT Label:Poison
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1C(C(CC(O1)OC2CC(CC3=C2C(=C4C(=C3O)C(=O)C5=C(C4=O)C(=CC=C5)OC)O)(C(=O)C)O)N)O.Cl
  • Isomeric SMILES:CC1C(C(CC(O1)O[C@H]2C[C@@](CC3=C2C(=C4C(=C3O)C(=O)C5=C(C4=O)C(=CC=C5)OC)O)(C(=O)C)O)N)O.Cl
  • Recent ClinicalTrials:Selinexor With Combination With Induction/Consolidation Therapy in Acute Myeloid Leukemia Patients
  • Recent EU Clinical Trials:A Phase 1B/2 Study To Evaluate The Safety And Efficacy of PF-04449913, An Oral Hedgehog Inhibitor, In Combination With Intensive Chemotherapy, Low Dose ARA-C Or Decitabine In Patients With Acute Myeloid Leukemia Or High-Risk Myelodysplastic Syndrome
Technology Process of Antibiotics from Streptomyces coeruleorubidus

There total 6 articles about Antibiotics from Streptomyces coeruleorubidus 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:
Multi-step reaction with 5 steps
1: 92 percent / barium hydroxide hydrate / H2O / 20 h / Heating
2: 77 percent / CH2Cl2 / 1 h / 20 °C
3: 81 percent / pyridine / 3 h / 0 °C
4: acetic acid / H2O / 24 h / Heating
With pyridine; barium hydroxide monohydrate; acetic acid; In dichloromethane; water;
DOI:10.1016/S0008-6215(00)84673-X
Guidance literature:
Multi-step reaction with 4 steps
1: 77 percent / CH2Cl2 / 1 h / 20 °C
2: 81 percent / pyridine / 3 h / 0 °C
3: acetic acid / H2O / 24 h / Heating
With pyridine; acetic acid; In dichloromethane; water;
DOI:10.1016/S0008-6215(00)84673-X
Guidance literature:
Multi-step reaction with 3 steps
1: 81 percent / pyridine / 3 h / 0 °C
2: acetic acid / H2O / 24 h / Heating
With pyridine; acetic acid; In water;
DOI:10.1016/S0008-6215(00)84673-X
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