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Microtubule

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Microtubule

Chemical Structure Cat. No. Product Name CAS No.
Cephalomannine Chemical Structure
BCP28192 Cephalomannine 71610-00-9
Cephalomannine is a taxol derivative with antitumor, antiproliferative properties.
TAI-1 Chemical Structure
BCP24407 TAI-1 1334921-03-7
TAI-1 is a potent and specific Hec1 inhibitor, which disrupts Hec1-Nek2 protein interaction.
Netobimin Chemical Structure
BCP29587 Netobimin 88255-01-0
Netobimin is an anthelmintic from the group of sample zimidazoles.Netobimin is a prodrug of albendazole .
Ombrabulin hydrochloride Chemical Structure
BCP29573 Ombrabulin hydrochloride 253426-24-3
Ombrabulin hydrochloride is a derivative of CA-4 phosphate, which is known to exhibit antivascular effects through selective disruption of the tubulin cytoskeleton of endothelial cells.
Taltobulin Chemical Structure
BCP29188 Taltobulin 228266-40-8
Taltobulin (HTI-286; SPA-110) is an analogue of Hemiasterlin; potent tubulin inhibitor; ADCs cytotoxin.
OXi-4503 sodium Chemical Structure
BCP29540 OXi-4503 sodium 288847-34-7
OXi-4503 is the diphosphate prodrug of the stilbenoid combretastatin A1, originally isolated from the plant Combretum caffrum, with vascular-disrupting and antineoplastic activities.
Cevipabulin Chemical Structure
BCP28162 Cevipabulin 849550-05-6
Cevipabulin(TTI-237) is a novel, potent, synthetic small molecule, inhibits binding of vinblastine at the Vinca alkaloid site of the αβ-tubulin heterodimer.
Thiocolchicine Chemical Structure
BCP28813 Thiocolchicine 2730-71-4
Thiocolchicine is a potent tubulin polymerization and microtubule assembly inhibitor, a axonal cytoskeleton modulator and apoptosis inducer.
DM1-SMe Chemical Structure
BCP16660 DM1-SMe 138148-68-2
DM1-SMe is a potent maytansinoid microtubular inhibitor and an unconjugated DM1 as a mixed disulfide with thiomethane to cap its sulfhydryl group. DM1-SMe can be readily conjugate to the SH group of an antibody to form antibody-drug conjugate (ADC).
McMMAE Chemical Structure
BCP24644 McMMAE 863971-24-8
Mc-MMAE is a protective group (maleimidocaproyl)-conjugated monomethyl auristatin E (MMAE), which is a potent tubulin inhibitor, is a toxin payload in antibody drug conjugate (ADC).
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