<p style=/line-height:25px/>MMAF-OMe inhibits several tumor cell lines with IC50s of 0.056 nM, 0.166 nM, 0.183 nM, and 0.449 nM for MDAMB435/5T4, MDAMB361DYT2, MDAMB468, and Raji (5T4-) cell lines, respectively.<br>IC50:<br>Target:tubulin<br>In vitro:<br>In vivo: 2.5F-Fc and 2.5F-Fc-MMAF have similar IC50 values (6.9 ± 1.1 vs. 8.3 ± 1.3 nmol/L, respectively), indicating that MMAF conjugation has negligible impact on integrin-binding affinity[1].</p>
Catalog Number | I005184 |
CAS Number | 863971-12-4 |
Molecular Formula | C40H67N5O8 |
Purity | 95% |
Target | tubulin |
Solubility | DMSO |
Storage | -20°C |
Reference | <p style=/line-height:25px/> <br>[2]. Stephan JP, et al. Anti-CD22-MCC-DM1 and MC-MMAF conjugates: impact of assay format on pharmacokinetic parameters determination. Bioconjug Chem. 2008 Aug;19(8):1673-83. <br>[3]. Wils J, et al. MMAF for advanced gastric cancer. Eur J Cancer. 1992;28A(6-7):1299. <br>[4]. Anderson H, et al. MMAF for advanced gastric cancer. Eur J Cancer. 1991;27(10):1234-8. </p> |