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Chemical Structure Cat. No. Product Name CAS No.
Leucomethylene blue Chemical Structure
BCP42937 Leucomethylene blue 613-11-6
Leucomethylene blue is a second-generation tau protein aggregation inhibitor currently in development for the treatment of Alzheimer's disease (AD) and frontotemporal dementia.
OUN10989 HCl Chemical Structure
BCP42739 OUN10989 HCl 915413-40-0
OUN10989, an analogue compound of LP-261, is a Potent Antimitotic Agent.
OUN10989 Chemical Structure
BCP42738 OUN10989 915410-98-9
OUN10989, an analogue compound of LP-261, is a Potent Antimitotic Agent.
Parbendazole Chemical Structure
BCP39884 Parbendazole 14255-87-9
Parbendazole, a benzimidazole carbamat used as an antinematodal agent, is a potent inhibitor of microtubule assembly and functions.
KX2-391 Mesylate Chemical Structure
BCP25173 KX2-391 Mesylate 1080645-95-9
Tirbanibulin, also known as KX-01 and KX2-391, is the first clinical Src inhibitor of the novel peptidomimetic class that targets the peptide substrate site of Src providing more specificity toward Src kinase.
Takeda103A Chemical Structure
BCP37916 Takeda103A 865609-72-9
Takeda103A is a potent inhibitor of the GRK2--​dependent bovine tubulin oxidation.
Tubulin inhibitor 6 Chemical Structure
BCP35744 Tubulin inhibitor 6 105925-39-1
Tubulin inhibitor 6 is a tubulin inhibitor and a potent inhibitor of multiple cancer cell lines.
Flubendazole Chemical Structure
BCP34258 Flubendazole 31430-15-6
Flubendazole is a safe and efficacious anthelmintic drug, which is widely used for anthelmintic to human, rodents and ruminants. Flubendazole exerts anticancer activities by mechanisms including inhibition of microtubule function. Flubendazole induces p53-mediated apoptosis and arrests G2/M cell cycle.
Indibulin Chemical Structure
BCP33949 Indibulin 204205-90-3
Indibulin, an orally applicable inhibitor of tubulin assembly, shows potent anticancer activity with a minimal neurotoxicity. Indibulin reduces inter-kinetochoric tension, produces aberrant spindles, activates mitotic checkpoint proteins Mad2 and BubR1, and induces mitotic arrest and apoptosis.
Vc-MMAD Chemical Structure
BCP32929 Vc-MMAD 1401963-17-4
Vc-MMAD consists the ADCs linker (Val-Cit) and potent tubulin inhibitor (MMAD). Vc-MMAD is a drug-linker conjugate for ADC.
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