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Cephalostatin 1

Base Information
  • Chemical Name:Cephalostatin 1
  • CAS No.:112088-56-9
  • Molecular Formula:C54H74 N2 O10
  • Molecular Weight:911.1728
  • Hs Code.:
  • Wikidata:Q27137715
  • Metabolomics Workbench ID:129948
  • ChEMBL ID:CHEMBL269081
Cephalostatin 1

Synonyms:cephalostatin 1;cephalostatin I

Suppliers and Price of Cephalostatin 1
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 Cephalostatin 1
Chemical Property:
  • XLogP3:3.7
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:12
  • Rotatable Bond Count:1
  • Exact Mass:910.53434656
  • Heavy Atom Count:66
  • Complexity:2170
Purity/Quality:

85.0-99.8% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1C2CC=C3C2(COC14C(CC(O4)(C)C)O)C(=O)CC5C3CCC6C5(CC7=NC8=C(CC9(C(C8)CCC1C9CC(C2(C1=CC1C2(C(C2(O1)C(CC(O2)(C)CO)O)C)O)C)O)C)N=C7C6)C
  • Isomeric SMILES:C[C@H]1[C@H]2CC=C3[C@]2(CO[C@]14[C@@H](CC(O4)(C)C)O)C(=O)C[C@H]5[C@H]3CC[C@@H]6[C@@]5(CC7=NC8=C(C[C@]9([C@H](C8)CC[C@@H]1[C@@H]9C[C@H]([C@]2(C1=C[C@H]1[C@@]2([C@@H]([C@@]2(O1)[C@@H](C[C@@](O2)(C)CO)O)C)O)C)O)C)N=C7C6)C
Refernces

Selective synthesis of bissteroidal compounds by multifold Heck reactions

10.1055/s-2001-12438

The research focuses on the selective synthesis of bissteroidal compounds, which are simplified analogs of cephalostatins, through multifold Heck reactions. The purpose of this study was to develop a facile and convergent strategy for the synthesis of these compounds, which exhibit high cytostatic activity against human cancer cell lines. The researchers successfully synthesized a simplified analog of cephalostatins by replacing the central octahydrophenazine moiety with a benzene ring through a twofold intramolecular Heck reaction. Key chemicals used in the process include hexahydro-1H-indene, dibromoterephthalaldehyde derivative, palladacycle catalyst, and various reagents for selective debromination and protection/deprotection steps. The synthesis allowed for the preparation of both symmetrical and unsymmetrical analogs of cephalostatins, providing a short and efficient route to structurally simplified analogs, with potential applications in the preparation of a variety of cephalostatin analogs.

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