Compound CL0485 1 mg | >95%
Creative Biolabs
ADCs Toxins, HCT-116: IC50=0,86 µM; PSN1 : IC50=0,86 µM; T98G : IC50=>8,62 µM; A549 : IC50=>8,62 µM (preliminary laboratory results).
More Information Supplier PageADCs Toxins, HCT-116: IC50=0,86 µM; PSN1 : IC50=0,86 µM; T98G : IC50=>8,62 µM; A549 : IC50=>8,62 µM (preliminary laboratory results).
More Information Supplier PageADCs Toxins, Combretastatin-A4 is a potent tubulin polymerization inhibitor. Comretastatin-A4 displays a strong inhibition on tumor cell growth.
More Information Supplier PageADCs Toxins, Colchicine is a mitosis inhibitor useful in cell division studies.
More Information Supplier PageADCs Toxins, Cinerubin B is described as an antibiotic compound. HCT-116: IC50=0,0006 uM; PSN1 : IC50=0,0012 uM; T98G : IC50=0,0012 uM; A549 : IC50=0,0006 uM (preliminary laboratory results). Biological & Pharmaceutical Bulletin (2006), 29(10), 1999-2003, Journal of Antibiotics (1981),34(12), 1596-1607.
More Information Supplier PageADCs Toxins, Nemorubicin is a morpholinyl analog of doxorubicin. It is more cytotoxic and less cardiotoxic against multidrug-resistant tumor cells. IC50= 0.08 µM.
More Information Supplier PageADCs cytotoxin, Daunorubicin Hcl inhibits both DNA and RNA synthesis and inhibits DNA synthesis with Ki of 0.02 μM.
More Information Supplier PageADCs cytotoxin, Daunorubicin(RP13057) inhibits both DNA and RNA synthesis and inhibits DNA synthesis with Ki of 0.02 μM.
More Information Supplier PageADCs cytotoxin, Daun02 is a daunorubicin b-galactoside prodrug for use in conjunction.
More Information Supplier PageADCs cytotoxin, Calicheamicin is a potent DNA-binding cytotoxic antibiotic.
More Information Supplier PageADCs cytotoxin, Auristatin F is a cytotoxic tubulin modifier with potent and selective antitumor activity; MMAF analog and cytotoxin in Antibody-drug conjugates.
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