Name | (2S)-1-benzyl-N-[(2S)-2-[[(2S)-2-(dimethylamino)-3-methylbutanoyl]amino]-3-methylbutanoyl]-N-[(2S)-1-[(2S)-3-methyl-2-(methylamino)butanoyl]pyrrolidine-2-carbonyl]pyrrolidine-2-carboxamide |
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Synonyms |
UNII-6SQ8M7ZSFV
N,N-Dimethyl-L-valyl-L-valyl-N-methyl-L-valyl-L-prolyl-N-benzyl-L-prolinamide Cemadotin N,N-dimethyl-L-valyl-L-valyl-N-methyl-L-valyl-L-prolyl-N-(phenylmethyl)-L-prolinamide L-Prolinamide,N,N-dimethyl-L-valyl-L-valyl-N-methyl-L-valyl-L-prolyl-N-(phenylmethyl) |
Description | Cemadotin (LU103793) is an analogue of Dolastatin 15 (HY-P1126) which is naturally occurring cytotoxic peptides. Cemadotin blocks cells at mitosis, and exhibits Ki value of 1 μM for inhibiting tubulin. Cemadotin can be used to research anticancer[1]. |
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Related Catalog | |
Target |
Ki: 1 μM (tubulin)[1] |
In Vitro | Cemadotin (0-100 μM; 35 min) inhibits polymerization dose-dependently in Tubulin-treated Strongylocentrotus purpuratus[1]. Cemadotin (0-1000 nM) preferentially suppresses the rate and extent of growing excursions of tubulin, and suppression is dependent upon the drug concentration[1]. Cemadotin (0-1 μM) markedly increases the rescue frequency but had little effect on the catastrophe frequency[1]. Cemadotin (400 pM~300 nM; 72 h) inhibits cancer cells HEK 293, F9 and HL60[2]. Cell Proliferation Assay[2] Cell Line: HEK 293, F9 and HL60 Concentration: 400 pM~300 nM Incubation Time: 72 h Result: Exhibited cytotoxicity against HEK 293, F9 and HL60 with IC50s of 0.7 nM, 14.8 nM and 0.5 nM, respectively. |
Density | 1.138g/cm3 |
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Boiling Point | 857.7ºC at 760mmHg |
Molecular Formula | C35H56N6O5 |
Molecular Weight | 640.85600 |
Flash Point | 472.5ºC |
Exact Mass | 640.43100 |
PSA | 122.37000 |
LogP | 3.15240 |
Vapour Pressure | 0mmHg at 25°C |
Index of Refraction | 1.545 |