119 Results for "

destabilizing

" in MedChemExpress (MCE) Product Catalog:
Products (119)

119 Results for "destabilizing" in MCE Product Catalog:

Cat. No.: HY-179695
Research Areas:  

Cancer

Microtubule destabilizing agent-3, a B32B3 (HY-12240) analog, is a microtubule destabilizing agent. Microtubule destabilizing agent-3 exerts its antimyeloma phenotypes by destabilizing microtubules and promoting mitotic arrest, leading to cell death. Microtubule destabilizing agent-3 induces G2/M phase arrest and caspase-dependent apoptosis. Microtubule destabilizing agent-3 can be used for the research of multiple myeloma .
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Cat. No.: HY-P10443
CAS No.: 380480-75-1
Target:  

Inhibitory Antibodies

Research Areas:  

Others

ppTG20 is an amphiphilic cell penetrating peptide (KALA) that can be used for gene transfection. ppTG20 can bind to DNA, destabilize membranes, and mediate DNA transfection .
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Cat. No.: HY-118748
CAS No.: 1477482-50-0
Purity:  ≥98.0%
Synonyms: SRF
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Suprafenacine is a cell permeable, tubulin-destabilizing molecule which bind microtubules at the colchicine-binding site and inhibit polymerization. Suprafenacine can induce G2/M cell cycle arrest and apoptosis, and can be used for cancer research .
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Cat. No.: HY-118295
CAS No.: 441742-93-4
Target:  

Endogenous Metabolite

Research Areas:  

Cancer

Pyrimidine-indole hybrid is a compound that inhibits ciliogenesis and has the activity of antagonizing the Hedgehog signaling pathway by destabilizing microtubules. Pyrimidine-indole hybrid exerts its biological effects by inhibiting ciliogenesis and deconstructing the stable form of α-tubulin. Pyrimidine-indole hybrid has shown its unique mechanism of action in in vitro cell experiments and zebrafish embryo models, interfering with microtubule dynamics .
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Cat. No.: HY-159987
CAS No.: 2848560-66-5
Target:  

HBV

Research Areas:  

Infection

AB-161 is an orally active HBV RNA destabilizer and a PAPD5/7 inhibitor, with its primary action focused in the liver. AB-161 treats Hepatitis B Virus (HBV) infection by lowering the levels of Hepatitis B surface antigen (HBsAg), with an EC50 value of 2.2 nM for HBsAg. AB-161 can be used in the field of HBV infection research .
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Cat. No.: HY-173361
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Anticancer agent 270 (Compound 8e) is an inhibitor that acts on tubulin. Its IC50 value against MCF-7 breast cancer cells is 1.02 μM. Through a dual mechanism of action, namely inducing Apoptosis and destabilizing microtubules, it exerts significant anti-proliferative activity against breast cancer cells. Anticancer agent 270 can be applied to research in the field of cancer .
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Cat. No.: HY-B1864C
CAS No.: 78822-08-9
Synonyms: Ksg sulfate
Target:  

Antibiotic Bacterial

Research Areas:  

Infection

Kasugamycin (Ksg) sulfate is an aminoglycoside antibiotic (antibiotic) that binds to the bacterial 30S ribosomal subunit and inhibits canonical translation initiation. Kasugamycin sulfate binds to the P-site and E-site codon regions in the mRNA channel and interferes with mRNA-tRNA codon-anticodon interactions, thereby destabilizing initiator tRNA binding. Kasugamycin sulfate possesses anti-infective activity. Kasugamycin sulfate is used in research on bacterial translation and Pseudomonas infection .
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Cat. No.: HY-176762
CAS No.: 67047-17-0
Target:  

Topoisomerase

Research Areas:  

Infection Cancer

TOP3B-IN-1 (NSC-260610) is a Topoisomerase IIIβ (TOP3B) inhibitor. TOP3B-IN-1 fails to induce the formation of TOP3B cleavage complexes (TOP3Bccs) with both DNA and RNA, and destabilizes TOP3Bccs. TOP3B-IN-1 can be used as a control compound for the development of inhibitors targeting TOP3B .
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Cat. No.: HY-163270
CAS No.: 2446376-25-4
Research Areas:  

Cancer

PM534 is a potent tubulin inhibitor (KD = 20 nM). PM534 targets and binds to the entire colchicine-binding domain (CBD) of tubulin, thereby inhibiting tubulin assembly; this leads to cell cycle arrest at the G2-M phase and induces multinucleation and apoptosis. PM534 exhibits microtubule-destabilizing agent (MDA) activity, potent broad-spectrum antitumor activity, and anti-angiogenic effects. PM534 can be used in research concerning human non-small cell lung cancer (NSCLC), breast cancer, ovarian cancer, and prostate cancer .
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Cat. No.: HY-B1864AR
CAS No.: 19408-46-9
Synonyms: Ksg hydrochloride (Standard)
Kasugamycin hydrochloride (Standard) (Ksg hydrochloride (Standard)) is the analytical standard of Kasugamycin hydrochloride (HY-B1864A). This product is intended for research and analytical applications. Kasugamycin (Ksg) hydrochloride is an aminoglycoside antibiotic (antibiotic) that binds to the bacterial 30S ribosomal subunit and inhibits canonical translation initiation. Kasugamycin hydrochloride binds to the P-site and E-site codon regions in the mRNA channel and interferes with mRNA-tRNA codon-anticodon interactions, thereby destabilizing initiator tRNA binding. Kasugamycin hydrochloride possesses anti-infective activity. Kasugamycin hydrochloride is used in research on bacterial translation and Pseudomonas infection .
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Cat. No.: HY-B1864BR
CAS No.: 200132-83-8
Synonyms: Ksg hydrochloride hydrate (Standard)
Research Areas:  

Infection

Kasugamycin hydrochloride hydrate (Standard) (Ksg hydrochloride hydrate (Standard)) is the analytical standard of Kasugamycin hydrochloride hydrate (HY-B1864B). This product is intended for research and analytical applications. Kasugamycin (Ksg) hydrochloride hydrate is an aminoglycoside antibiotic (antibiotic) that binds to the bacterial 30S ribosomal subunit and inhibits canonical translation initiation. Kasugamycin hydrochloride hydrate binds to the P-site and E-site codon regions in the mRNA channel and interferes with mRNA-tRNA codon-anticodon interactions, thereby destabilizing initiator tRNA binding. Kasugamycin hydrochloride hydrate possesses anti-infective activity. Kasugamycin hydrochloride hydrate is used in research on bacterial translation and Pseudomonas infection .
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Cat. No.: HY-121634
CAS No.: 794466-17-4
Research Areas:  

Others

DAP-81 is an inhibitory agent targeting Polo-like kinases (Plks), a class of evolutionarily conserved serine/threonine kinases. DAP-81 dose-dependently increases the number of monopolar spindles in treated cells. High-resolution live-cell microscopy revealed that Plk activity is required for the assembly and maintenance of bipolar mitotic spindles. Plk inhibition destabilizes centromeric microtubules while stabilizing other spindle microtubules, leading to the formation of monopolar spindles. Further testing of compounds based on "privileged scaffolds" such as the DAP scaffold may lead to the discovery of new cell division probes and anti-microtubule agents.
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Cat. No.: HY-149918
CAS No.: 3049213-47-7
Research Areas:  

Cancer

Antiproliferative agent-23 is a microtubule-destabilizing agent (MDA) and efficiently disturbes the tubulin-microtubule system. Antiproliferative agent-23 induces apoptosis via a mitochondrion-dependent pathway by downregulating the Bcl-2 protein, upregulating Bax and Cyt c proteins, and activating the caspase cascade. Antiproliferative agent-23 initiates reactive oxygen species (ROS)-mediated endoplasmic reticulum stress in A549/CDDP cells (cisplatin resistant cancer cell line) via the PERK/ATF4/CHOP signaling pathway. Antiproliferative agent-23 has anti-tumor activity .
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Cat. No.: HY-185284
Target:  

Liposome

Research Areas:  

Others

MeDZ lipid is a zwitterion-type ionizable endosomal membrane destabilizer and anti-inflammatory agent that promotes endosomal escape. When incorporated into LNP formulations, MeDZ lipid enhances mRNA expression in lymph node antigen-presenting cells and promotes cytotoxic T cell activation. MeDZ lipid is compatible with existing targeted nanoparticle formulations to improve mRNA delivery efficiency .
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Cat. No.: HY-179114
CAS No.: 1211788-57-6
Research Areas:  

Others

VU0519975 is a raft destabilizing compound. VU0519975 reduces PMP22 raft partitioning and destabilizes ordered domains. VU0519975 significantly decreases the fraction of phase separated GPMVs .
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Cat. No.: HY-P700312
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: gp32, Helix-destabilizing protein; Single-stranded DNA-binding protein; SSB protein; 32; ssb
Species:  
Others
Source:  
E. coli
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Cat. No.: HY-P11006A
Target:  

Bacterial

Research Areas:  

Infection

Onc112 acetate is a proline-rich antimicrobial peptide that displays potent activity against Gram-negative bacteria. Onc112 acetate inhibits translation by blocking and destabilizing the initiation complex .
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Cat. No.: HY-160125
CAS No.: 2154373-61-0
Research Areas:  

Others

25,25-Difluoro-27-norcholestenoic acid is an LXRb ligand that disrupts the His435-Trp457 aromatic-aromatic interaction, destabilizing the H11-H12 region and favoring corepressor binding .
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Cat. No.: HY-102028R
CAS No.: 292168-79-7
Research Areas:  

Cancer

KY1220 (Standard) is the analytical standard of KY1220 (HY-102028). This product is intended for research and analytical applications. KY1220 is a compound that destabilizes both β-catenin and Ras, via targeting the Wnt/β-catenin pathway, with an IC50 of 2.1 μM in HEK293 reporter cells .
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