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HMN176 Chemical Structure

HMN176

Data Sheet For research use only. Not for human use.
Cat. No. :BCP19302CAS No. :173529-10-7Purity:98%
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  • Chemical Properties&Biological Activity
CAS No. 173529-10-7 Cat. No. BCP19302
Name HMN176
Synonyms HMN-176;HMN 176;
SMILES COC1=CC=C(C=C1)S(=O)(=O)N=C2C=CC=CC2=CC=C3C=CN(C=C3)O
Chemical Name
Formula C20H18N2O4S M. Wt 382.43
Purity 98% Storage Store at 4-8°C
Description In vitro: HMN-176 (2.5 μM) greatly increases the duration of mitosis in hTERT-RPE1 and CFPAC-1 Cell lines. The effect of HMN-176 on spindle morphology does not appear to be related to effects on microtubule polymerization. HMN-176 (2.5, 0.25, and 0.025 μM) inhibits aster formation in a concentration dependent manner. HMN-176 (0.1, 1.0, or 10.0 μg/ml) demonstrates inhibitory effects in multiple tumors, with notable activity seen in breast, nonsmall-cell lung, and ovarian cancer specimens. HMN-176 demonstrates activity towards 63% of the breast (5/8), 67% of the non-small cell lung (4/6), and 57% of the ovarian (4/7) tumor specimens treated with 10.0 μg/ml. HMN-176 shows potent cytotoxicity, with a mean IC50 value of 118 nM. HMN-176 displays similar cytotoxicity against tumors with various characteristics from different organs. Treatment with 3 μM HMN-176 suppresses the expression of MDR1 mRNA by 56%. HMN-176 has no significant effect on the residual promoter activity. In vivo: HMN-176 p
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