Home   >  
Cell Cycle/DNA Damage
  >  
Microtubule

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

Microtubule

Chemical Structure Cat. No. Product Name CAS No.
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.
VAL-CIT-PAB-MMAD Chemical Structure
BCP32931 VAL-CIT-PAB-MMAD 1415329-13-3
VAL-CIT-PAB-MMAD is a drug-linker conjugate for ADC with potent antitumor activity by using Monomethyl Dolastatin 10 (a potent tubulin inhibitor), linked via the ADC linker Vat-Cit-PAB.
123下一页末页共 85 条记录 1 / 9 页 
0086-15971444841