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- MPC 6827 hydrochloride
- CW069
- MMAD
- CYT997 (Lexibulin)
- Monomethyl auristatin E
D-64131Tubulin polymerization inhibitor |
Sample solution is provided at 25 µL, 10mM.
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Quality Control & MSDS
- View current batch:
- Purity = 98.00%
- COA (Certificate Of Analysis)
- MSDS (Material Safety Data Sheet)
Chemical structure
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D-64131 Dilution Calculator
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D-64131 Molarity Calculator
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Cas No. | 74588-78-6 | SDF | Download SDF |
Synonyms | D 64131;D64131 | ||
Chemical Name | (5-methoxy-1H-indol-2-yl)(phenyl)methanone | ||
Canonical SMILES | COC1=CC2=C(C=C1)NC(=C2)C(=O)C3=CC=CC=C3 | ||
Formula | C16H13NO2 | M.Wt | 251.28 |
Solubility | Soluble in DMSO | Storage | Store at -20°C |
Physical Appearance | Yellow crystalline solid | Shipping Condition | Evaluation sample solution : ship with blue ice.All other available size:ship with RT , or blue ice upon request |
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. |
D-64131 is a tubulin polymerization inhibitor with an IC50 value of 0.53 μM. [1]
The polymerization of bovine brain tubulin as well as binding of [3H] colchicine to biotinylated αβ-tubulin was dose-dependently inhibited by D-64131. Many cancer cells display abnormal microtubule structures, such as fragmented mitotic spindles or multiple spindle poles after treatment with D-64131. Nuclear blebbing and abnormal nuclear structures typical for apoptotic cells are detectable in many cells treated with D-64131. In nude mice, D-64131 proved to be well tolerated and highly active against the human amelanoic melanoma MEXF 989 tumor xenograft. D-64131 treatment resulted in significant tumor growth inhibition during treatment. [1]
Reference:1. Beckers T, Reissmann T, Schmidt M et al. 2-aroylindoles, a novel class of potent, orally active small molecule tubulin inhibitors. Cancer Res. 2002 Jun 1;62(11):3113-9.