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Chemical Structure
Chemical Structure
Chemical Structure

Calpinactam [1205538-83-5]

Research Use Only
AG-CN2-0131
AdipoGen Life Sciences
CAS Number1205538-83-5
Product group Chemicals
Estimated Purity>95%
Molecular Weight767.9
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Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    Calpinactam
  • Delivery Days Customer
    10
  • CAS Number
    1205538-83-5
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Hazard Information
    Warning
  • Molecular Formula
    C38H57N9O8
  • Molecular Weight
    767.9
  • Scientific Description
    Chemical. CAS: 1205538-83-5. Formula: C38H57N9O8. MW: 767.9. Synthetic. Originally isolated from Mortierella alpina. Specific anti-mycobacterial. Inhibits growth of Mycobacteria smegmatis but also Mycobacteria tuberculosis. M. smegmatis is used as a model for mycobacterial species. It is useful for the research analysis of other Mycobacteria species in laboratory experiments. M. smegmatis is commonly used in work on the mycobacterium species, since it is a fast grower and non-pathogenic. - Specific anti-mycobacterial. Inhibits growth of Mycobacteria smegmatis but also Mycobacteria tuberculosis. M. smegmatis is used as a model for mycobacterial species. It is useful for the research analysis of other Mycobacteria species in laboratory experiments. M. smegmatis is commonly used in work on the mycobacterium species, since it is a fast grower and non-pathogenic.
  • SMILES
    [H][C@@](NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@H](CC1=CNC=N1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](N)CC1=CC=CC=C1)([C@@H](C)CC)C(=O)N[C@@]1([H])CCCCNC1=O
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352200

References

  • Structure and total synthesis of fungal calpinactam, a new antimycobacterial agent: N. Koyama, et al.; Org. Lett. 12, 432 (2010)
  • Calpinactam, a new anti-mycobacterial agent, produced by Mortierella alpina FKI-4905: N. Koyama, et al.; J. Antibiot. (Tokyo) 63, 183 (2010)
  • Synthesis and antimycobacterial activity of calpinactam derivatives: K. Nagai, et al.; Bioorg. Med. Chem. Lett. 22, 7739 (2012)