132 Results for "

chaperones

" in MedChemExpress (MCE) Product Catalog:
Products (132)

132 Results for "chaperones" in MCE Product Catalog:

Cat. No.: HY-173150
CAS No.: 106928-29-4
Hapalindole Q (Compound (+)-1) is an autophagy (Autophagy) inhibitor targeting YAP1. Hapalindole Q binds to the Hippo pathway transcription factor YAP1 with a Kd of 9.13 μM and induces its degradation via the chaperone-mediated autophagy (CMA) pathway. This process inhibits Rab7-mediated fusion of autophagosomes and lysosomes, thereby reducing overall autophagy levels without affecting lysosomal function. Hapalindole Q holds promise for research in cancer (e.g., liver cancer, breast cancer, etc.) .
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Cat. No.: HY-W728096
Synonyms: GR181413A-d5 free base
Migalastat-d5 (GR181413A-d5 (free base)) is deuterium labeled Migalastat. Migalastat (GR181413A free base) is an orally active α-galactosidase A molecular chaperone, with an IC50 value of 0.04 μM for human α-Gal A. Migalastat binds to the active site of certain unstable mutant forms of α-galactosidase A, facilitating their transport to the lysosome. After dissociation in the acidic environment, Migalastat enables the mutant α-galactosidase A to exhibit biological activity .
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Cat. No.: HY-176951
CAS No.: 3048497-50-0
Research Areas:  

Cancer

Chaperone complex ligand 1 is a chaperone ligand for HSP90. Chaperone complex ligand 1 can be connected to the MET ligand (HY-50878) by a linker to synthesis of MET degrader OZD-MET 01 (HY-177893) .
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Cat. No.: HY-107636R
CAS No.: 497061-48-0
Research Areas:  

Cancer

DC_AC50 (Standard) is the analytical standard of DC_AC50 (HY-107636). This product is intended for research and analytical applications. DC_AC50 is a dual inhibitor of Atox1 and CCS (copper chaperones). Inhibiting intracellular copper chaperones as a means of reducing/preventing acquired chemotherapy resistance .
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Cat. No.: HY-187920
CAS No.: 3084683-45-1
Target:  

Others

Research Areas:  

Others

Rexipictor is a small molecule compound that can be used as a molecular chaperone for polycystin 1 (PC1) .
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Cat. No.: HY-W015787
CAS No.: 7768-28-7
2-Hydroxyphenylethanol is a molecular chaperone that rescues misfolded P123S mutant pendrin, promoting translocation from the cytoplasm to the plasma membrane. 2-Hydroxyphenylethanol can be used for the research of pendred syndrome .
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Cat. No.: HY-Y0999
CAS No.: 821-55-6
2-Nonanone is a ketone compound that inhibits the DnaKJE-ClpB bichaperone de-pendent refolding of heat-inactivated bacterial luciferases. 2-Nonanone interacts with hydrophobic segments of heat-inactivated substrates, and competes with chaperones IbpAB. 2-Nonanone can be used for the research of infection .
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Cat. No.: HY-117192
CAS No.: 1052515-37-3
Target:  

HSP Fungal

Research Areas:  

Infection

NSC145366 monohydrochloride is a Hsp90 C-terminal inhibitor. NSC145366 monohydrochloride directly interacts with the C-terminus of Hsp90 and inhibits its chaperone activity. NSC145366 monohydrochloride strongly inhibits the growth of Saccharomyces cerevisiae cog7Δ and cog8Δ strains .
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Cat. No.: HY-100437R
CAS No.: 1609402-14-3
Research Areas:  

Cancer

HA15 (Standard) is the analytical standard of HA15 (HY-100437). This product is intended for research and analytical applications. HA15 is a potent and specific inhibitor of ER chaperone BiP/GRP78/HSPA5, inhibits the ATPase activity of BiP, with anti-cancerous activity .
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Cat. No.: HY-101106R
CAS No.: 80306-38-3
Research Areas:  

Neurological Disease Cancer

AR7 (Standard) is the analytical standard of AR7 (HY-101106). This product is intended for research and analytical applications. AR7 is an atypical RARA/RARα (retinoic acid receptor, alpha) antagonist. AR7 specifically activates chaperone-mediated-autophagy (CMA) activity without affecting macroautophagy .
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Cat. No.: HY-FLB1039A
CAS No.: 23828-92-4
Synonyms: NA-872 hydrochloride solution
Ambroxol hydrochloride solution is mainly composed of Ambroxol hydrochloride (HY-B1039A). Ambroxol hydrochloride (NA-872 hydrochloride), an active metabolite of the proagent Bromhexine, has potent expectorant effects. Ambroxol hydrochloride is a glucocerebrosidase (GCase) chaperone and increases glucocerebrosidase activity. Ambroxol hydrochloride induces lung autophagy and has the potential for Parkinson disease and neuronopathic Gaucher disease research .
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Cat. No.: HY-120227
CAS No.: 1610546-52-5
Target:  

HSP Apoptosis Caspase ERK Akt CDK

Research Areas:  

Cancer

SM253 is an Hsp90 inhibitor that inhibits Hsp90-dependent protein folding. SM253 blocks chaperone function by binding to the N-middle linker region and the C-terminal M domain, reducing co-chaperone and client protein binding and activation. SM253 induces cancer cell apoptosis, activates caspase 3/7, causes cell cycle arrest and reduces cell proliferation, while decreasing Hsp90 client proteins such as AR, FKBP51, PSA, Cdk4, AKT, ERK, and p23, and reducing Hsp27/Hsp70 expression without inducing heat shock proteins. SM253 causes dose-dependent fibronectin loss in cells expressing LRP1. SM253 can be used for research on colon cancer, pancreatic cancer, and prostate cancer .
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Cat. No.: HY-187106
CAS No.: 874968-47-5
Research Areas:  

Infection

Antibacterial agent 361 is an antibacterial agent as well as a membrane-permeable prodrug. Antibacterial agent 361 binds to subsite I of the linear motif binding pocket of the Escherichia coli sliding clamp, disrupts the interaction between the sliding clamp and its chaperone protein, and inhibits sliding clamp-dependent in vitro DNA replication. Antibacterial agent 361 can be used in the research of bacterial infections .
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Cat. No.: HY-187645
CAS No.: 22044-58-2
Target:  

HSP

Derrubone is a prenylated isoflavone Hsp90 inhibitor that binds to the C-terminal ATP site of Hsp90α, stabilizes the Hsp90-client protein co-chaperone complex, and induces client protein degradation, thereby inhibiting cancer cell proliferation. Derrubone can be used for research on breast cancer, colon cancer, Alzheimer's disease, and type 2 diabetes .
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Cat. No.: HY-181062
Research Areas:  

Cancer

VWK147 is a second-generation HSP90 C-terminal domain (CTD) inhibitor. VWK147 targets the CTD dimerization interface, prevents HSP90 CTD dimerization, disrupts co-chaperone PPID binding to HSP90 CTD, and inhibits HSP90 chaperone function dependent on dimerization. VWK147 reduces protein levels of HSP90 client proteins ULK1, RIPK1, and CDK4 without inducing a heat shock response. VWK147 induces cell death, including apoptosis, in Cisplatin (HY-17394)-sensitive and -resistant urothelial carcinoma cells. VWK147 induces LC3-II accumulation, inhibits autophagosome-lysosome fusion to block canonical autophagy, and induces non-canonical LC3 lipidation independent of ULK1 and PIK3C3 complexes. VWK147 can be used for the research of urothelial carcinoma .
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Cat. No.: HY-153922
CAS No.: 942065-96-5
Target:  

Glycosidase

Research Areas:  

Neurological Disease

N-Octyl-α-4-epivalienamine is an orally active and CNS-penetrant molecular chaperone that induces high expression of the deficient β-galactosidase activity. N-Octyl-α-4-epivalienamine ameliorates symptoms and increase survival rate in a mouse model of GM1-gangliosidosis. N-Octyl-α-4-epivalienamine can be used for neurogenetic disease research .
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Cat. No.: HY-119732
CAS No.: 2134571-29-0
Target:  

HSP

Research Areas:  

Neurological Disease Cancer

KUNG94 is a selective Grp94/HSP90B inhibitor (IC50=8 nM). By inhibiting the chaperone function of Grp94, KUNG94 reduces the maturation and cell surface trafficking of its specific client proteins. KUNG94 can be used for studies on Grp94-related biological mechanisms, as well as diseases including cancer and primary open-angle glaucoma .
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Cat. No.: HY-182938
CAS No.: 1111050-17-9
Target:  

Autophagy

Research Areas:  

Metabolic Disease

Autophagy activator-2 is a potent autophagy activator with EC50 values of 14.33 μM. Autophagy activator-2 acts as a proteostasis modulator and small-molecule chaperone that upregulates I1061T mutant NPC1 expression and facilitates cholesterol efflux. Autophagy activator-2 reduces lysosomal hydrolase levels. Autophagy activator-2 can be used for the study of Niemann-Pick Type C disease .
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Cat. No.: HY-182809
CAS No.: 1372688-55-5
Target:  

Androgen Receptor HSP

Research Areas:  

Neurological Disease Cancer

Androgen receptor degrader-6 is a blood-brain barrier-permeable AR degrader. Androgen receptor degrader-6 inhibits the chaperone activity of HSP27 and disrupts the HSP27-AR complex. Androgen receptor degrader-6 promotes the degradation of wild-type and mutant AR, reduces AR protein levels, and inhibits the growth of glioblastoma cells. Androgen receptor degrader-6 can be used in glioblastoma research .
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Cat. No.: HY-P2961A
Research Areas:  

Cancer

Glutathione-S-Transferase, Rat is a glutathione S-transferase derived from the rat. Glutathione-S-Transferase, Rat is a phase II metabolic enzyme composed of three superfamilies: cytosolic, mitochondrial, and microsomal. Glutathione-S-Transferase, Rat possesses multiple catalytic activities, including catalytic detoxification and thiol transfer, as well as molecular chaperone functions. The Glutathione-S-Transferase, Rat isoform GSTP1 is highly expressed in malignant tumors and serves as a tumor biomarker .
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