HSP
Gli inibitori delle proteine da shock termico (HSP) prendono di mira le HSP, una famiglia di chaperoni molecolari che assistono nel ripiegamento delle proteine, nella stabilità e nella protezione contro i danni indotti dallo stress. Le HSP sono spesso sovraregolate nelle cellule tumorali, aiutandole a sopravvivere in condizioni stressanti come l'ipossia e la chemioterapia. L'inibizione delle HSP può interrompere questi meccanismi protettivi, portando alla morte cellulare. Gli inibitori delle HSP sono quindi preziosi nella terapia del cancro e nella ricerca sulle risposte allo stress. Presso CymitQuimica, offriamo una gamma completa di inibitori delle HSP di alta qualità per supportare la tua ricerca nell'omeostasi delle proteine, nelle risposte allo stress e nell'oncologia.
Trovati 176 prodotti per "HSP".
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Alvespimycin hydrochloride
CAS:Alvespimycin hydrochloride (BMS 826476) is a potent HSP90 inhibitor with IC50 of 62 nM. Phase 2.Formula:C32H48N4O8·HClPurezza:99.85% - 99.94%Colore e forma:Purple SolidPeso molecolare:653.21Feretoside
CAS:Feretoside is a natural product extracted from the barks of E. ulmoides. Feretoside shows inducible activity on the heat shock factor 1 (HSF1).Formula:C17H24O11Purezza:99.85%Colore e forma:SolidPeso molecolare:404.37Ref: TM-TQ0280
1mg73,00€5mg167,00€1mL*10mM (DMSO)190,00€10mg260,00€25mg440,00€50mg628,00€100mg872,00€200mg1.153,00€Apoptozole
CAS:Apoptozole (Apoptosis Activator VII) is an inhibitor of the ATPase domain of Hsc70 and Hsp70, and can induce apoptosis.Formula:C33H25F6N3O3Purezza:99.75%Colore e forma:SolidPeso molecolare:625.56Ref: TM-T3293
2mg34,00€5mg48,00€1mL*10mM (DMSO)63,00€10mg79,00€25mg130,00€50mg222,00€100mg331,00€200mg489,00€VER-50589
CAS:VER-50589 is a potent HSP90 inhibitor.Formula:C19H17ClN2O5Purezza:99.96% - >99.99%Colore e forma:SolidPeso molecolare:388.8Ref: TM-T2258
1mg39,00€5mg92,00€1mL*10mM (DMSO)92,00€10mg150,00€25mg250,00€50mg384,00€100mg557,00€200mg787,00€Teprenone
CAS:Teprenone (Geranylgeranylacetone) is a anti-ulcer drug, and works as an inducer of heat shock proteins (HSPs).Formula:C23H38OPurezza:99.1% - 99.96%Colore e forma:SolidPeso molecolare:330.55Alvespimycin
CAS:Alvespimycin (17-DMAG) is a potent Hsp90 inhibitor with potential anticancer activity, which acts by binding to Hsp90.Formula:C32H48N4O8Purezza:99.88%Colore e forma:SolidPeso molecolare:616.75Calenduloside E
CAS:Calenduloside E (Silphioside F) exhibits hypoglycemic activities by suppressing the transfer of glucose from the stomach to the small intestine and byFormula:C36H56O9Purezza:96.16% - 98.99%Colore e forma:SolidPeso molecolare:632.82HSP90-IN-20
CAS:HSP90-IN-20, a potent inhibitor of HSP90, exhibits an IC50 of ≤10 μM, indicating its potential application in cancer research.Formula:C26H32N4O4Colore e forma:SolidPeso molecolare:464.56HSP90-IN-12
CAS:VAC, a potent anti-cancer vibsanin A analog, inhibits cell proliferation and affects HSP90 protein levels.Formula:C25H36O4Colore e forma:SolidPeso molecolare:400.55YM-01 Tosylate
CAS:YM-01 Tosylate, a potent antitumor agent, selectively targets cancer cells and overcoming tamoxifen resistance.Formula:C27H27N3O4S3Colore e forma:SolidPeso molecolare:553.72Displurigen
CAS:Displurigen is an inhibitor of ATPase activity of HSP70.Formula:C15H10O4SPurezza:98%Colore e forma:SolidPeso molecolare:286.36BrCaQ
CAS:6BrCaQ inhibits TRAP1, has antiproliferative effects, and is used in 6BrCaQ-TPP synthesis.Formula:C18H15BrN2O3Colore e forma:SolidPeso molecolare:387.23PU3
CAS:PU3 is an inhibitor of Hsp90.Formula:C19H25N5O3Purezza:98%Colore e forma:SolidPeso molecolare:371.43SEW84
CAS:SEW84, an Aha1-stimulated Hsp90 inhibitor, has an IC50 of 0.3 μM, aiding protein deposition disease research.Formula:C19H14F4N4OSColore e forma:SolidPeso molecolare:422.4HSP90-IN-14
CAS:HSP90-IN-14 inhibits Hsp90 (Kd=0.26 μM) and fights influenza A/H3N2, A/H1N1, B with EC50 of 2.6, 3.9, 17 μM in MDCK cells.Formula:C14H8Cl2N4O4SColore e forma:SolidPeso molecolare:399.21CH5164840
CAS:CH5164840 is an HSP90 inhibitor; IC50=4.1 nM; oral active; degrades client proteins; cancer research tool.Formula:C19H23N5O2SPurezza:99.80%Colore e forma:White SolidPeso molecolare:385.48Hsp90-Cdc37-IN-1
CAS:Hsp90-Cdc37-IN-1 is an Hsp90-Cdc37 interaction disruptor (IC50: 140 nM) that inhibit cell migration and reverse drug resistance.Formula:C43H57FN2O6SPurezza:98%Colore e forma:SolidPeso molecolare:748.99Vibsanin A
CAS:Vibsanin A, an activator of protein kinase C (PKC) and an inhibitor of HSP90, demonstrates anti-proliferative effects on human cancer cell lines.Formula:C25H38O4Colore e forma:SolidPeso molecolare:402.57YM-1
CAS:YM-1 is an HSP70 inhibitor; promotes client protein degradation; disrupts protein folding; cancer research tool.Formula:C20H20ClN3OS2Purezza:99.58%Colore e forma:Red SolidPeso molecolare:417.98BIIB028
CAS:BIIB028: Hsp90 inhibitor, may degrade oncogenic proteins, potentially hindering tumor growth.Formula:C19H21ClN5O5PColore e forma:SolidPeso molecolare:465.83Retaspimycin
CAS:Retaspimycin is a potent and water-soluble Hsp90 inhibitor(EC50s of 119 nM for both Hsp90 and Grp9).Formula:C31H45N3O8Purezza:98%Colore e forma:SolidPeso molecolare:587.7KUNB31
CAS:KUNB31 is a potent and selective inhibitor of Hsp90β.Formula:C19H18N2O3Colore e forma:SolidPeso molecolare:322.36Hsp90-IN-17
CAS:Hsp90-IN-17 (Example 5) is an inhibitor of HSP90, applicable in researching proliferative diseases, including cancer and neurodegenerative conditions.Formula:C21H20N4O7Colore e forma:SolidPeso molecolare:440.41Heat Shock Protein Inhibitor II
CAS:Hsp inhibitor II, an active benzylidene lactam, blocks inducible Hsp synthesis, reduces tumor thermotolerance, and enhances AmB effects on A. fumigatus.Formula:C12H11NO3Colore e forma:SolidPeso molecolare:217.22SW02
CAS:SW02 is a potent ATPase activator of Hsp70 (EC50: 150 μM). SW02 is able to accumulate total tau and phosphorylated tau (pTau).Formula:C19H23BrN2O5Colore e forma:SolidPeso molecolare:439.3PU24FCl
CAS:PU24FCl is a specific inhibitor of tumor Hsp90.Formula:C20H21ClFN5O3Colore e forma:SolidPeso molecolare:433.86BMS-358233
CAS:BMS-358233 is an effective LCK inhibitor with excellent cell activity against T cell proliferation.Formula:C25H25ClN6O2SColore e forma:SolidPeso molecolare:509.02CH5138303
CAS:CH5138303 is an orally available Hsp90 inhibitor with Kd of 0.48 nM.Formula:C19H18ClN5O2SPurezza:98%Colore e forma:SolidPeso molecolare:415.9JG-48
CAS:JG-48 is an inhibitor of Hsp70. JG-48 suppresses phosphorylated and total Tau in cells, endogenous Tau in neuroblastoma cells.Formula:C20H16F3N3OS2Colore e forma:SolidPeso molecolare:435.49CCT251236
CAS:CCT251236 is an orally available Pirin ligand obtained from a heat shock transcription factor 1 (hsf1) phenotypic screen.Formula:C32H32N4O5Purezza:98.82% - 99.89%Colore e forma:White SolidPeso molecolare:552.62Ref: TM-T14905
1mg34,00€5mg105,00€1mL*10mM (DMSO)130,00€10mg200,00€25mg414,00€50mg662,00€100mg1.054,00€Icapamespib HCl
CAS:Icapamespib (PU-HZ151) is an HSP90 inhibitor; EC50 of 5 nM, logD of 2.37; targets epichaperomes, effective in cells, mice, and humans.Formula:C19H25Cl2IN6O2SColore e forma:SolidPeso molecolare:599.31CH5015765
CAS:CH5015765: potent, selective HSP90 inhibitor with high affinity and antitumor effects in human cancer mouse models.Formula:C16H13ClN4OSColore e forma:SolidPeso molecolare:344.82Grp94-IN-2
CAS:Grp94-IN-2 is a inhibitor of Grp94.Formula:C22H23ClN2O5Colore e forma:SolidPeso molecolare:430.88BF844
CAS:BF844 chemical counters USH3-induced hearing loss by transporting mutated CLRN1 to cell membranes, effectively preserving hearing in vivo.Formula:C21H19ClN4OColore e forma:SolidPeso molecolare:378.85STA-2842
CAS:STA-2842 is an inhibitor of heat shock protein 90 (HSP90).Formula:C29H38N6O5Colore e forma:SolidPeso molecolare:550.65EC 144
CAS:EC 144, a second-generation selective inhibitor of Hsp90 , inhibits tumor growth for Hsp90α and degradation of Her-2 in MCF-7 cells.Formula:C21H24ClN5O2Colore e forma:SolidPeso molecolare:413.9Retaspimycin Hydrochloride
CAS:Retaspimycin Hydrochloride is a potent and water-soluble Hsp90 inhibitor(Hsp90 and Grp9 with EC50s of 119 nM).Formula:C31H46ClN3O8Purezza:98%Colore e forma:SolidPeso molecolare:624.17MPC-3100
CAS:MPC-3100 is an orally bioavailable, synthetic, second-generation small-molecule inhibitor of Hsp90 with significant antitumor activity [1].Formula:C22H25BrN6O4SColore e forma:SolidPeso molecolare:549.44HSP90-IN-22
CAS:HSP90-IN-22 is a potent HSP90 inhibitor; client protein degrader; blocks oncogenic signaling; cancer research tool.Formula:C25H30N4O3Purezza:99.90%Colore e forma:White SolidPeso molecolare:434.53Bimoclomol
CAS:Bimoclomol is a heat shock protein co-inducer used for the research of cardiovascular diseases.Formula:C14H20ClN3O2Colore e forma:SolidPeso molecolare:297.78Hsp90-IN-15
CAS:Hsp90-IN-15: Hsp90 blocker with anticancer properties; halts S phase, triggers apoptosis, cuts Hsp90 in Hela cells.Formula:C23H27F3N4Colore e forma:SolidPeso molecolare:416.48SNX0723
CAS:SNX0723 is a potent Hsp90 Inhibitor with anti-Plasmodium activity.Formula:C22H26FN3O3Purezza:99.85%Colore e forma:White SolidPeso molecolare:399.46Ref: TM-T28824
500mgPrezzo su richiesta1mg85,00€5mg178,00€1mL*10mM (DMSO)195,00€10mg299,00€25mg485,00€50mg665,00€100mg892,00€Arimoclomol
CAS:Arimoclomol (BRX-220 free base) is a co-inducer of heat shock proteins (HSP) and can be used in studies about the treatment of amyotrophic lateral sclerosis (Formula:C14H20ClN3O3Purezza:99.15%Colore e forma:SolidPeso molecolare:313.78Iroxanadine
CAS:Iroxanadine (BRX-005) is a Novel small molecule MAPK p38 inhibitor that induces phosphorylation of p38 SAPK and induces concentration-dependent relaxation inFormula:C14H20N4OPurezza:98.04% - 99.04%Colore e forma:SolidPeso molecolare:260.33Colletofragarone A2
CAS:Colletofragarone A2 from Colletotrichum sp. blocks mutant p53 and HSP90, aiding cancer treatment.Formula:C22H26O6Colore e forma:SolidPeso molecolare:386.44MAO A/HSP90-IN-2
CAS:MAO A/HSP90-IN-2 (compound 4-C), a dual inhibitor of HSP90 and MAO A, exhibits IC50 values of 0.016 μM for MAO A and 4.58 μM for HSP90.Formula:C25H31ClN2O4Purezza:98%Colore e forma:SolidPeso molecolare:458.98KU-177
CAS:KU-177 is an Aha1 inhibitor that disrupts the interaction between Hsp90 and Aha1, eliminating cell proliferation and PI resistance induced by elevated AHSA1.Formula:C27H23NO8Purezza:96.92% - 98.54%Colore e forma:SolidPeso molecolare:489.47YM-08
CAS:YM-08 (Compound 7a), a brain-penetrant SIRT2 inhibitor, exhibits an IC50 of 19.9 μM. Additionally, it acts as an inhibitor of Hsp70 [1].Formula:C19H17N3OS2Purezza:98%Colore e forma:SolidPeso molecolare:367.49HSP90-IN-19
CAS:HSP90-IN-19: potent Hsp90 inhibitor, IC50 = 0.27 μM, used in research on viral diseases, neurodegeneration, inflammation.Formula:C29H38O7Purezza:98%Colore e forma:SolidPeso molecolare:498.61MAO A/HSP90-IN-1
CAS:MAO A/HSP90-IN-1 (4-b) is a dual inhibitor of MAO A and HSP90, exhibiting IC50 values of 1.77 μM in glioblastoma (GBM) GL26 cells and 0.019 μM against HSP90α.Formula:C24H29ClN2O4Purezza:98%Colore e forma:SolidPeso molecolare:444.95
