Cas No.: | 108212-76-6 |
Chemical Name: | N-Acetyl-Calicheamicin |
Synonyms: | N-Acetyl-Calicheamicin;N-Acetyl-Calicheamicin γ;N-Acetyl-γ-calicheamicin;N-Acetyl-y-calicheamicin;N-Acetyl-Calicheamicin y |
SMILES: | IC1C(C)=C(C(=C(C=1O[C@H]1[C@@H]([C@@H]([C@H]([C@H](C)O1)O)OC)O)OC)OC)C(=O)S[C@@H]1[C@@H](C)O[C@H](C[C@@H]1O)ON[C@@H]1[C@@H](C)O[C@H]([C@@H]([C@H]1O)O[C@H]1C[C@@H]([C@H](CO1)N(C(C)=O)CC)OC)O[C@H]1C#CC=CC#C[C@@]2(CC(C(=C1/C/2=C\CSSSC)NC(=O)OC)=O)O |c:69| |
Formula: | C57H76In3O22S4 |
M.Wt: | 1410.38472557068 |
Purity: | >98% |
Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
Description: | N-Acetyl-Calicheamicin is a potent enediyne antitumor antibiotic.N-Acetyl-Calicheamicin is a a derivative of Calicheamicin. Calicheamicin is a naturally occurring hydrophobic enediyne antibiotic that was isolated from the actinomycete Micromonospora echinospora calichensis. Calicheamicin can interfere with biological processes not simply by cleaving free DNA but also by displacing a DNA-binding protein through competition or modulation of DNA structure. |
Target: | Antibacterial |
References: | [1]. Stasi R, et al. Gemtuzumab ozogamicin in the treatment of acute myeloid leukemia. Cancer Treat Rev. 2008 Feb;34(1):49-60. |