| Cas No.: | 105925-39-1 |
| Chemical Name: | 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)- |
| SMILES: | COC1=CC=C(C=C1)C(=O)N2C3=C(C=CC(Cl)=C3)SC4C2=CC=CC=4 |
| Formula: | C20H14NO2Scl |
| M.Wt: | 367.84866 |
| Purity: | >98% |
| Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
| Publication: | [1]. Prinz H, et al. N-benzoylated phenoxazines and phenothiazines: synthesis, antiproliferative activity, and inhibition of tubulin polymerization. J Med Chem. 2011 Jun 23;54(12):4247-63. |
| Description: | Tubulin inhibitor 6 (Compound 14b) is a tubulin inhibitor and a potent inhibitor of multiple cancer cell lines. Tubulin inhibitor 6 inhibits tubulin polymerization with an IC50 of 0.87 μM. Tubulin inhibitor 6 inhibits K562 cell growth with an IC50 of 840 nM[1]. |
| Target: | IC50: 0.87 μM (tubulin polymerization)[1] |
| In Vitro: | Tubulin inhibitor 6 displays submicromolar antiproliferative activity[1]. |
| References: | [1]. Prinz H, et al. N-benzoylated phenoxazines and phenothiazines: synthesis, antiproliferative activity, and inhibition of tubulin polymerization. J Med Chem. 2011 Jun 23;54(12):4247-63. |

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