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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
22 Results for "
atrio-His bundle
" in MedChemExpress (MCE) Product Catalog:
Products (22)
22 Results for "atrio-His bundle" in MCE Product Catalog:
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Plant Taxus chinensis (Pilger) Rehd. Extract Taxaceae Extract Terpenoids Diterpenoids Disease Research Fields Cancer
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1 Cited Publications
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BRD9876 is the “rigor” inhibitor that locks kinesin-5 (Eg5) in a state with enhanced microtubules (MTs) binding, leading to bundling and stabilization of MTs. BRD9876 interacts with the tyrosine 104 residue that is part of the α4-α6 allosteric binding pocket. BRD9876 specifically targets microtubule-bound Eg5 and selectively inhibits myeloma over CD34 cells. BRD9876 has the potential for multiple myeloma (MM) research .
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1 Cited Publications
Cat. No.: HY-N4208
CAS No.: 2230777-09-8
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Taccalonolide AJ is a microtubule stabilizer and antiproliferative agent with an IC50 of 4.2 nM against β-tubulin (β-tubulin) D226. Taccalonolide AJ increases cellular microtubule density, induces microtubule bundling, triggers G2/M cell cycle arrest with abnormal mitotic spindles, and inhibits cancer cell proliferation. Taccalonolide AJ can be used in the research of oral cancer, breast cancer, solid tumors, as well as tumors resistant to Paclitaxel (HY-B0015) and Doxorubicin (HY-15142A) .
Cat. No.: HY-134200
CAS No.: 29541-66-0
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Gamendazole, an indazole carboxylic acid (ICA), is an orally active, selective HSP90AB1 (HSP90BETA) and EEF1A1 (eEF1A) inhibitor. Gamendazole binds to the C-terminal nucleotide binding pocket of HSP90 and cause downregulation of clients AKT1 and ERBB2, but stabilizes the HSP90 heterocomplex. Gamendazole specifically inhibits the actin bundling function of EEF1A1, but does not bind to the nucleotide docking pocket nor inhibits the ribosome charging or protein translation functions of EEF1A1. Gamendazole, an antispermatogenic compound with antifertility effects, has the potential for reversible non-hormonal male contraceptive agent research .
Cat. No.: HY-N6701
CAS No.: 39156-67-7
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Dihydrocytochalasin B is an Actin disruptor. Dihydrocytochalasin B disrupts actin microfilament bundles, inhibits actin polymerization, and alters intracellular actin cytoskeletal structures. Dihydrocytochalasin B blocks the initiation of DNA synthesis. Dihydrocytochalasin B inhibits Calcium transport. Dihydrocytochalasin B inhibits cytokinesis and alters cell morphology. Dihydrocytochalasin B can be used in studies related to rickets .
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Cat. No.: HY-121242
CAS No.: 55511-98-3
Synonyms: VEL-5026
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Buthidazole (VEL-5026) is a Herbicide. Buthidazole targets photosynthesis as its most sensitive and first-inhibited process, and inhibits RNA synthesis, lipid synthesis, and anthocyanin biosynthesis, while transiently stimulating dark respiration. Buthidazole reduces or prevents starch accumulation in bundle sheath chloroplasts, causing swelling and ultrastructural damage of mesophyll chloroplasts. Buthidazole damages corn seedlings at high doses .
Synonyms: Disodium sulfate, meets analytical specification of Ph. Eur. BP USP
Cat. No.: HY-175753
CAS No.: 2094958-44-6
Z17544625 is a Fascin inhibitor. Z17544625 has a strong binding capacity to fascin and inhibits Actin bundling. Z17544625 significantly reduces proliferation and impairs migration of CRC cells. Z17544625 can be used for cancer, especially colorectal cancer (CRC) research .
Cat. No.: HY-P11012
Cat. No.: HY-116915
CAS No.: 257612-36-5
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Synstab A is a mitosis modulator to promote interactions between α- and β-tubulin. Synstab A can polymerizes microtubules from purified tubulin, and produces microtubule bundles in interphase cells .
Cat. No.: HY-135746R
CAS No.: 220246-81-1
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7-epi-Taxol (Standard) is the analytical standard of 7-epi-Taxol. This product is intended for research and analytical applications. 7-epi-Taxol is an active metabolite of taxol, with activity comparable to that of taxol against cell replication, promoting microtubule bundle formation and against microtubule depolymerization.
Cat. No.: HY-157808
Antibacterial agent 185 (compound IP-01) is a potent antibacterial agent. Antibacterial agent 185 inhibits filamentous temperature-sensitive mutant Z (FtsZ) polymerization and bundling by increasing GTP hydrolysis. Antibacterial agent 185 inhibits Streptococcus pneumoniae and shows narrow-spectrum activity .
Cat. No.: HY-N0227R
CAS No.: 105454-04-4
Synonyms: 7-epi-Paclitaxel (Standard)
Cat. No.: HY-175762
Z118298144 is a Fascin inhibitor. Z118298144 has a strong binding capacity to fascin and inhibits Actin bundling. Z118298144 significantly reduces proliferation and impairs migration of CRC cells. Z118298144 can be used for cancer, especially colorectal cancer (CRC) research .
Cat. No.: HY-187686
CAS No.: 2606843-12-1
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UA49 is a plasma membrane voltage-dependent potassium channel inhibitor. UA49 inhibits the phosphorylation of plasma membrane H +-ATPase, reduces potassium ion levels in guard cells, increases calcium ion concentrations in the cytoplasm and endoplasmic reticulum, induces actin filament bundling, and triggers SLAC1-dependent stomatal closure through a pathway distinct from that of ABA. UA49 can be used in studies related to plant drought stress .
Cat. No.: HY-165369
CAS No.: 1192754-38-3
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IBPR002 is an inhibitor of Aurora kinase A and Aurora kinase B, with IC50 values of 41 nM and 17 nM, respectively. IBPR002 disrupts the nucleation and bundling of kinetochore microtubules, impairs the bipolarity of mitotic spindles, and promotes the binding of non-phosphorylated hepatoma up-regulated protein (HURP) to microtubules derived from the mother centrosome. IBPR002 reduces tumorigenesis levels in a colorectal cancer xenograft model using athymic nude mice. IBPR002 is applicable for research related to colorectal cancer .
Cat. No.: HY-183584
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ARN25699 is a kinase inhibitor with an IC50 of 5.5 nM against GSK-3β, 2.2 nM against FYN-α, and 242.3 nM against DYRK1A, and it exhibits oral bioavailability. ARN25699 reduces hyperphosphorylation of tau protein and promotes microtubule bundle formation. ARN25699 has a broader kinome inhibitory profile and targets kinases associated with the pathogenic mechanisms linked to Alzheimer's disease. ARN25699 can be used in the research of Alzheimer's disease and related tauopathies .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
