HSP
Les inhibiteurs des protéines de choc thermique (HSP) ciblent les HSP, une famille de chaperons moléculaires qui aident au repliement des protéines, à leur stabilité et à leur protection contre les dommages induits par le stress. Les HSP sont souvent surexprimées dans les cellules cancéreuses, les aidant à survivre dans des conditions stressantes telles que l'hypoxie et la chimiothérapie. Inhiber les HSP peut perturber ces mécanismes de protection, entraînant la mort cellulaire. Les inhibiteurs des HSP sont donc précieux dans la thérapie contre le cancer et la recherche sur les réponses au stress. Chez CymitQuimica, nous offrons une gamme complète d'inhibiteurs de HSP de haute qualité pour soutenir vos recherches sur l'homéostasie des protéines, les réponses au stress et l'oncologie.
169 produits trouvés pour "HSP"
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GRP78-IN-3
CAS :<p>GRP78-IN-3: Potent Hsp70 blocker, selective Grp78 (HSPA5) inhib., IC50 0.59 μM, 7x more vs HspA9, 20x vs HspA2.</p>Formule :C17H18N4O2SDegré de pureté :99.11%Couleur et forme :SoildMasse moléculaire :342.42CC-99677
CAS :<p>CC-99677 (Gamcemetinib) is a MK2 inhibitor targeting autoimmune diseases; potent in rat assays with IC50=156.3 nM & EC50=89 nM.</p>Formule :C22H20ClN5O3SDegré de pureté :99.59%Couleur et forme :SolidMasse moléculaire :469.94Novobiocin Sodium
CAS :<p>Novobiocin Sodium (Albamycinsodium) binds to DNA gyrase and blocks adenosine triphosphatase (ATPase) activity. Novobiocin sodium is an antibiotic compound.</p>Formule :C31H35N2NaO11Degré de pureté :99% - 99.28%Couleur et forme :SolidMasse moléculaire :634.61IPI-493
CAS :<p>IPI-493 is a bioactive chemical.</p>Formule :C28H39N3O8Degré de pureté :>99.99%Couleur et forme :SolidMasse moléculaire :545.62Ethoxyquin
CAS :<p>Ethoxyquin (Santoflex) is an antioxidant used in animal feeds.</p>Formule :C14H19NODegré de pureté :97.15% - 98.73%Couleur et forme :Yellow Liquid Mercaptan-Like Odor (Ntp 1992)Masse moléculaire :217.31Arimoclomol maleate
CAS :<p>Arimoclomol maleate (BRX-220) (BRX-220) is a heat shock protein (HSP) co-inducer.</p>Formule :C18H24ClN3O7Degré de pureté :99.44% - 99.98%Couleur et forme :SolidMasse moléculaire :429.85Rifabutin
CAS :<p>Rifabutin (LM-427), a semisynthetic ansamycin, blocks bacterial RNA synthesis by inhibiting RNA polymerase.</p>Formule :C46H62N4O11Degré de pureté :98.87% - 99.7%Couleur et forme :Red-Violet Crystalline PowderMasse moléculaire :847Col003
CAS :<p>Col003 is a selective and potent inhibitor of Hsp47 and competitively binds to the collagen-binding site on Hsp47 (IC50: 1.8 μM).</p>Formule :C14H11NO4Degré de pureté :98.67% - 99.03%Couleur et forme :SolidMasse moléculaire :257.24PU-H71 HCl
CAS :<p>PU-H71 HCl (Zelavespib HCl) is a novel Hsp90 inhibitor, a novel purine-based analog, and a radiosensitizer that may be a promising agent for CIRT.</p>Formule :C18H22ClIN6O2SDegré de pureté :98.95%Couleur et forme :SoildMasse moléculaire :548.83Gamitrinib TPP
CAS :<p>Gamitrinib TPP targets mitochondrial HSP90, inhibiting cancer, and blocks mitochondrial matrix.</p>Formule :C52H65N3O8PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :891.078NMS-E973
CAS :<p>NMS-E973 is a potent and selective Hsp90 inhibitor with DC50 of <10 nM for Hsp90 binding, no activiy against a panel of 52 diverse protein kinases.</p>Formule :C22H22N4O7Degré de pureté :99.84%Couleur et forme :SolidMasse moléculaire :454.43HEMTAC WEE1 degrader-1
CAS :<p>HEMTACWEE1degrader-1 is a WEE1-targeting heterobifunctional chimeric degrader (HEMTAC) facilitated by HSP90, exhibiting an HSP90 enzyme inhibitory activity with an IC50 of 16.76 nM. It enhances the ubiquitination and subsequent degradation of WEE1, effectively blocking the G2/M cell cycle transition. This compound shows anticancer properties in patient-derived xenograft (PDX) models of acute myeloid leukemia (AML). HEMTACWEE1degrader-1 is utilized in AML research.</p>Formule :C57H71N15O6Couleur et forme :SolidMasse moléculaire :1062.273-Phenyltoxoflavin
CAS :<p>3-Phenyltoxoflavin (Phenyltoxoflavin) is an inhibitor of HSP90 (Kd = 585 nM) with anti-cancer activity.</p>Formule :C13H11N5O2Degré de pureté :99.88%Couleur et forme :SolidMasse moléculaire :269.266BrCaQ-C10-TPP
<p>6BrCaQ-C10-TPP inhibits TRAP1, halts cancer cell growth (IC50=0.008-0.30µM), disrupts mitochondrial membrane.</p>Formule :C45H47Br2N2O3PCouleur et forme :SolidMasse moléculaire :854.65Shepherdin (79-87)
CAS :<p>Shepherdin 79-87: Amino acid fragment 79-87 of Hsp90/Survivin antagonist with anticancer properties.</p>Formule :C41H64N12O12SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :949.09JG-258
CAS :<p>JG-258 is an inactive negative control for Hsp70 inhibitors [1] .</p>Formule :C20H22ClN3OS3Couleur et forme :SolidMasse moléculaire :452.06trans-Dehydrocurvularin
CAS :<p>trans-Dehydrocurvularin is a useful organic compound for research related to life sciences. The catalog number is T125357 and the CAS number is 21178-57-4.</p>Formule :C16H18O5Couleur et forme :SolidMasse moléculaire :290.315HSP70/SIRT2-IN-1
<p>HSP70/SIRT2-IN-1 (Compound 2a) serves as a dual inhibitor targeting both SIRT2 and HSP70, exhibiting an IC50 of 17.3±2.0 μM against SIRT2.</p>Degré de pureté :98%Couleur et forme :Odour SolidAlvespimycin TFA
<p>Alvespimycin (17-DMAG) TFA is a potent inhibitor of Hsp90, binding with an EC50 of 62 ± 29 nM.</p>Formule :C34H49F3N4O10Couleur et forme :SolidMasse moléculaire :730.34008Myrtucommulone
CAS :<p>Myrtucommulone is an inhibitor of the chaperonin activity of HSP60, correlating to LRP130 and LONP aggregation.</p>Formule :C38H52O10Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :668.81p5 Ligand for Dnak and DnaJ
CAS :<p>P5 is a nonapeptide ligand for DnaK/DnaJ, mimicking the key sites of mitochondrial aspartate aminotransferase presequence.</p>Formule :C44H81N15O11SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :1028.27PROTAC HSP90 degrader BP3
CAS :<p>PROTAC BP3 selectively degrades HSP90, inhibits breast cancer growth (DC50=0.99µM), CRBN-dependent.</p>Formule :C32H29ClN8O5Couleur et forme :SolidMasse moléculaire :641.08MAL3-101
CAS :<p>MAL3-101 is a molecular chaperone inhibitor of heat shock protein 70 (Hsp 70).</p>Formule :C54H66N4O10Couleur et forme :SolidMasse moléculaire :931.12HA15-Biotin
CAS :<p>HA15-Biotin, a synthetic HA15-biotin conjugate, shows similar activity and may aid in proteomics.</p>Formule :C37H45N7O5S3Couleur et forme :SolidMasse moléculaire :763.99MPC-0767
CAS :<p>MPC-0767, a potent, selective, and orally active hsp90 inhibitor, is the L-alanine ester prodrug of MPC-3100, exhibiting enhanced chemical stability.</p>Formule :C26H36BrN7O9S2Couleur et forme :SolidMasse moléculaire :734.64Hsp70-derived octapeptide
CAS :<p>TPR proteins including CHIP, TPR1, and hSGT affect luciferase refolding by DnaJ and hsc70.</p>Formule :C36H58N8O16Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :858.89Arimoclomol citrate
CAS :<p>Arimoclomol citrate boosts Hsp expression, aiding protein aggregation and neuron protection.</p>Formule :C20H28ClN3O10Couleur et forme :SolidMasse moléculaire :505.9117-DMAP-GA
CAS :<p>17-DMAP-GA, a Geldanamycin analogue, acts as an HSP90 inhibitor, leading to cell cycle abnormalities.</p>Formule :C33H50N4O8Couleur et forme :SolidMasse moléculaire :630.783Chetomin
CAS :<p>Chetomin (BRN0077366) is an inhibitor of HIF-1 by weaken transcription of HIF-1, disrupting the binding of HIF-1α and HIF-2α to p300 at low nanomolar</p>Formule :C31H30N6O6S4Degré de pureté :98%Couleur et forme :Off-White To Fawn SolidMasse moléculaire :710.87TRAP1-IN-1
CAS :<p>TRAP1-IN-1 is a selective TRAP1 inhibitor, induces degradation of TRAP1 downstream proteins, inhibits OXPHOS, and disrupts mitochondrial membrane potential.</p>Formule :C45H39F7N2O4P2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :866.74Grp94 Inhibitor-3
<p>Grp94 Inhibitor-3 (Compound C6) is a selective inhibitor of glucose-regulated protein 94 (Grp94), with an affinity of 5.52 μM. It shows potential for research in primary open-angle glaucoma and metastatic cancer.</p>Formule :C24H20ClNO4Couleur et forme :SolidMasse moléculaire :421.87Hsp90-IN-36
<p>Hsp90-IN-36 (compound 5) is an Hsp90 inhibitor with anticancer properties and exhibits an IC50 value of 14.74 μM against MCF-7 cells.</p>Formule :C20H13F4N3O4Couleur et forme :SolidMasse moléculaire :435.328HS-27
CAS :<p>HS-27 is a fluorescently-tethered inhibitor of Hsp90 with SNX-5422 tethered via a PEG linker to a fluorescein isothiocyanate or FITC.</p>Formule :C52H60N6O12SDegré de pureté :97.09%Couleur et forme :SolidMasse moléculaire :993.13Hsp110-STAT3 interaction-IN-2
<p>Hsp110-STAT3 interaction-IN-2 (compound 10b) is an inhibitor of the Hsp110-STAT3 interaction. It is utilized in research related to pulmonary arterial hypertension (PAH).</p>Formule :C24H18F3N5O3Couleur et forme :SolidMasse moléculaire :481.43NPX800
CAS :<p>NPX800 is an inhibitor of heat shock factor 1 (HSF1) and can be used in studies about the treatment of cancer.</p>Formule :C32H32FN5O4Degré de pureté :99.29%Couleur et forme :SolidMasse moléculaire :569.63HSP90-IN-35
CAS :<p>HSP90-IN-35 is an inhibitor targeting Hsp90, exhibiting anticancer activity. It demonstrates an IC50 ranging from 0.05 to 0.5 μM against Her2. Additionally, HSP90-IN-35 can be utilized in the synthesis of PROTAC.</p>Formule :C27H33N5O5Couleur et forme :SolidMasse moléculaire :507.58DN401
CAS :<p>DN401 is a potent TRAP1 and Hsp90 Inhibitor( IC50 = 79 nM for TRAP1, IC50 = 698 nM for Hsp90) with potent anticancer activity.</p>Formule :C13H9BrClN5O2Degré de pureté :99.63%Couleur et forme :SolidMasse moléculaire :382.6Zelavespib hydrochloride
<p>Zelavespib (PU-H71) hydrochloride is a potent inhibitor of Hsp90, exhibiting an IC50 value of 51 nM in MDA-MB-468 cells.</p>Degré de pureté :98%Couleur et forme :Odour SolidNDNA4
<p>NDNA4 (compound 17) is a selective Hsp90α inhibitor (IC50: 0.34 μM), characterized by its permanent charge and low membrane permeability.</p>Formule :C31H35F3N2O5SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :604.68TRAP1-IN-2
CAS :<p>TRAP1-IN-2, also known as compound 36, is a selective degrader of the TRAP1 client protein that does not affect Hsp90-cytosolic clients.</p>Formule :C46H42F6N2O5P2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :878.77HSP90-IN-25
<p>HSP90-IN-25 (compound 4a) is an inhibitor targeting HSP90, specifically impeding its ATPase function [1].</p>Formule :C29H48O10Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :556.69PROTAC Hsp90α degrader 1
<p>Compound X10g (PROTAC Hsp90α degrader 1) is a selective agent targeting Hsp90α for degradation and is utilized in breast cancer research.</p>Formule :C43H50N6O7Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :762.89NDNA3
<p>NDNA3 (compound 14) selectively inhibits Hsp90α with an IC50 of 0.51 μM, demonstrating low membrane permeability and minimal toxicity to Ovcar-8 and MCF-10A</p>Formule :C28H32N2O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :476.63HSP90-IN-23
<p>HSP90-IN-23 (Comp 12-1), a heat shock protein 90 (HSP90) inhibitor, exhibits potent activity with an IC50 of 9nM.</p>Formule :C22H24N2O6SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :444.5Palmitic acid-1-13C
CAS :<p>Palmitic acid-13C, a 16-C saturated fatty acid internal standard for GC/LC-MS, is prevalent in plasma lipids and influences protein acylation and COX-2 levels.</p>Formule :C16H32O2Couleur et forme :SolidMasse moléculaire :257.422CCT245232
CAS :<p>CCT245232 is a potent HSF1 inhibitor, possibly used for researching cancer.</p>Formule :C27H23N3O4Couleur et forme :SolidMasse moléculaire :453.49PU-H71
CAS :<p>PU-H71 is an effective selective HSP90 inhibitor with an IC50 of 51 nM.</p>Formule :C18H21IN6O2SDegré de pureté :98.31% - 99.937%Couleur et forme :SolidMasse moléculaire :512.37Debio 0932
CAS :<p>Debio 0932 (CUDC-305) is a Hsp9 inhibitor, apoptosis, and has the advantage of being orally available and cross the BBB for cancers NSCLC and neuroblastoma.</p>Formule :C22H30N6O2SDegré de pureté :98.98%Couleur et forme :SolidMasse moléculaire :442.58Dihydroberberine
CAS :<p>Dihydroberberine has anti-atherosclerotic, anti-inflammatory, hypolipidemic and antitumor activities.</p>Formule :C20H19NO4Degré de pureté :93.77%Couleur et forme :SolidMasse moléculaire :337.37Pifithrin-μ
CAS :<p>Pifithrin-μ (NSC-303580) is an inhibitor of p53 and HSP70, with neuroprotective and antitumor activity.</p>Formule :C8H7NO2SDegré de pureté :99.33% - 99.79%Couleur et forme :SolidMasse moléculaire :181.21MK2-IN-1 hydrochloride
CAS :<p>MK2-IN-1 hydrochloride (MK 25) selectively inhibits MK2 with IC50 of 0.11 μM, non-ATP competitive.</p>Formule :C27H26Cl2N4O2Degré de pureté :97.32%Couleur et forme :SolidMasse moléculaire :509.43XL888
CAS :<p>XL888 is an orally bioavailable Hsp90 inhibitor, blocking cell proliferation and inducing tumor regression with an IC50 of 24 nM.</p>Formule :C29H37N5O3Degré de pureté :99.18%Couleur et forme :SolidMasse moléculaire :503.64HM03 trihydrochloride
CAS :<p>HM03 trihydrochloride is a potent and selective inhibitor of HSPA5, also known as Bip or Grp78. It exhibits anticancer activity.</p>Formule :C26H30Cl4N4O2Couleur et forme :SolidMasse moléculaire :572.35Tanespimycin
CAS :<p>Tanespimycin (KOS 953) is an Hsp90 inhibitor (IC50=5 nM) and is selective. Tanespimycin depletes intracellular STK38/NDR1. High-Quality, Low-Cost!</p>Formule :C31H43N3O8Degré de pureté :99.07% - 99.83%Couleur et forme :Dark Purple SolidMasse moléculaire :585.69VER49009
CAS :<p>VER49009 (CCT0129397) is an effective HSP90 inhibitor(IC50 =25 nM, Kd=78 nM).</p>Formule :C19H18ClN3O4Degré de pureté :98.95% - >99.99%Couleur et forme :SolidMasse moléculaire :387.82MitoBloCK-10
CAS :<p>MitoBloCK-10 inhibits Tim44-Hsp70 binding; first to reduce PAM complex activity.</p>Formule :C12H8FN3O3SDegré de pureté :99.51%Couleur et forme :SolidMasse moléculaire :293.27HSP70-IN-1
CAS :<p>HSP70-IN-1 is a heat shock protein (HSP) inhibitor and inhibits the growth of Kasumi-1 cells (IC50: 2.3 μM).</p>Formule :C24H28N6O2SDegré de pureté :99.91%Couleur et forme :SolidMasse moléculaire :464.58HM03
CAS :<p>HM03 is a potent and selective inhibitor of HSPA5, and has anticancer activity.</p>Formule :C26H27ClN4O2Degré de pureté :97.15%Couleur et forme :SolidMasse moléculaire :462.97VER-50589
CAS :<p>VER-50589 is a potent HSP90 inhibitor.</p>Formule :C19H17ClN2O5Degré de pureté :99.96% - >99.99%Couleur et forme :SolidMasse moléculaire :388.8MK2-IN-1
CAS :<p>MK2-IN-1 is a potent and selecitve MAPKAPK2(MK2) inhibitor(IC50=0.11 uM) with a non-ATP competitive binding mode.</p>Formule :C27H25ClN4O2Couleur et forme :SolidMasse moléculaire :472.97MKT-077
CAS :<p>MKT-077 (FJ-776) is a cationic rhodacyanine dye that demonstrates antiproliferative activity against cancer cell lines.</p>Formule :C21H22ClN3OS2Degré de pureté :98.2%Couleur et forme :SolidMasse moléculaire :432HSP27 inhibitor J2
CAS :<p>HSP27 inhibitor J2 (J2) (J2) is a HSP27 inhibitor, inhibits a production of HSP27 giant polymers, thereby having an effect of inhibiting a chaperone function of</p>Formule :C13H12O4SDegré de pureté :99.51%Couleur et forme :SolidMasse moléculaire :264.3ML346
CAS :<p>ML346 is a novel activator of Hsp70.</p>Formule :C14H12N2O4Degré de pureté :97.32% - 99.36%Couleur et forme :SolidMasse moléculaire :272.262-hexyl-4-Pentynoic Acid
CAS :<p>2-hexyl-4-Pentynoic Acid, a valproic acid (VPA) derivatives, is a potent and robust HDACs inhibitor with IC50 value of 13 μM.</p>Formule :C11H18O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :182.26Luminespib
CAS :<p>Luminespib (VER-52296) is an HSP90 inhibitor that inhibits HSP90α and HSP90β. Luminespib has antitumor activity. Cost-effective and quality-assured.</p>Formule :C26H31N3O5Degré de pureté :98% - 99.25%Couleur et forme :SolidMasse moléculaire :465.54Onalespib
CAS :<p>Onalespib (AT13387) is an oral Hsp90 inhibitor with anticancer potential, disrupting tumor cell growth and survival.</p>Formule :C24H31N3O3Degré de pureté :98.05% - 99.66%Couleur et forme :SolidMasse moléculaire :409.52Rocaglamide
CAS :<p>Rocaglamide (Roc-A) from Aglaia treats coughs, injuries, asthma, skin issues, and inhibits NF-κB in T-cells.</p>Formule :C29H31NO7Degré de pureté :95.32% - 99.67%Couleur et forme :SolidMasse moléculaire :505.56Alvespimycin hydrochloride
CAS :<p>Alvespimycin hydrochloride (BMS 826476) is a potent HSP90 inhibitor with IC50 of 62 nM. Phase 2.</p>Formule :C32H48N4O8·HClDegré de pureté :99.94%Couleur et forme :SolidMasse moléculaire :653.21PF-04929113 Mesylate
CAS :<p>PF-04929113 Mesylate (SNX-5422 Mesylate), a prodrug of SNX-2112, is an orally available Hsp90 inhibitor (Kd: 41 nM) and also induces Her-2 degradation (IC50: 37</p>Formule :C26H34F3N5O7SDegré de pureté :99% - 99.46%Couleur et forme :SolidMasse moléculaire :617.63JG-98
CAS :<p>JG-98 is an allosteric Hsp70 inhibitor, displays high active against the breast cancer cell lines MDA-MB-231 and MCF-7 (EC50s: 0.4/0.7 μM).</p>Formule :C24H21Cl2N3OS3Degré de pureté :99.13%Couleur et forme :SolidMasse moléculaire :534.53Teprenone
CAS :<p>Teprenone (Geranylgeranylacetone) is a anti-ulcer drug, and works as an inducer of heat shock proteins (HSPs).</p>Formule :C23H38ODegré de pureté :99.1% - 99.96%Couleur et forme :SolidMasse moléculaire :330.55DDO-5936
CAS :<p>DDO-5936 is a potent and specific HSP90-Cdc37 PPI inhibitor.</p>Formule :C25H29N5O4SDegré de pureté :99.81%Couleur et forme :SolidMasse moléculaire :495.59NVP-HSP990
CAS :<p>NVP-HSP990 (HSP990) is an effective and specific HSP90α/β inhibitor (IC50: 0.6 /0.8 nM).</p>Formule :C20H18FN5O2Degré de pureté :98.03% - 99.32%Couleur et forme :SolidMasse moléculaire :379.39L-Alanyl-L-glutamine
CAS :<p>L-Alanyl-L-glutamine (Ala-Gln), a dipeptide composed of alanine and Gln, is an alternative supplement to L-glutamine in the production of biopharmaceuticals.</p>Formule :C8H15N3O4Degré de pureté :99.71% - 99.97%Couleur et forme :SolidMasse moléculaire :217.22PF04929113
CAS :<p>PF04929113 (SNX-5422), a synthetic small molecule Hsp90 inhibitor, offers potent efficacy orally for various cancers.</p>Formule :C25H30F3N5O4Degré de pureté :99.04%Couleur et forme :SolidMasse moléculaire :521.53Eupalinolide A
CAS :<p>Eupalinolide B is a natural product ,and demonstrates potent cytotoxicity against A-549, BGC-823, SMMC-7721, and HL-60 tumour cell lines.</p>Formule :C24H30O9Degré de pureté :98.82% - 99.22%Couleur et forme :SolidMasse moléculaire :462.49Grp94 Inhibitor-1
CAS :<p>Grp94 Inhibitor-1 is a potent, selective Grp94 inhibitor (IC50 : 2 nM).</p>Formule :C22H28N2O2Degré de pureté :97.02%Couleur et forme :SolidMasse moléculaire :352.47Paeoniflorin
CAS :<p>Paeoniflorin (Peoniflorin) is a herbal constituent extracted from the root of Paeonia albiflora Pall.</p>Formule :C23H28O11Degré de pureté :96.9% - 97.43%Couleur et forme :White Fine PowderMasse moléculaire :480.46Gedunin
CAS :<p>Gedunin, a Meliaceae seed limonoid, inhibits Hsp90 and ovarian cancer growth.</p>Formule :C28H34O7Degré de pureté :99.64% - 99.68%Couleur et forme :SolidMasse moléculaire :482.57Ganetespib
CAS :<p>Ganetespib (STA-9090) is a synthetic small-molecule inhibitor of heat shock protein 90 (Hsp90) with potential antineoplastic activity.</p>Formule :C20H20N4O3Degré de pureté :98% - 99.95%Couleur et forme :SolidMasse moléculaire :364.4TRC051384
CAS :<p>TRC051384 is a HSP70 inducer that reduces stroke-associated neuronal damage and increases survival in a rat model of transient ischemic stroke.</p>Formule :C25H31N5O4Degré de pureté :98.79%Couleur et forme :SolidMasse moléculaire :465.54KRIBB11
CAS :<p>KRIBB11 is an inhibitor of Heat shock factor (HSF) inhibitor.</p>Formule :C13H12N6O2Degré de pureté :97.25% - 99.91%Couleur et forme :SolidMasse moléculaire :284.27Pimitespib
CAS :<p>Pimitespib (TAS-116) is an ATP-competitive and highly specific HSP90α/HSP90β inhibitor (Kis: 34.7 nM and 21.3 nM, respectively).</p>Formule :C25H26N8ODegré de pureté :99.22% - 99.49%Couleur et forme :SolidMasse moléculaire :454.53VER-49009
CAS :<p>VER-49009 (CCT 129397) is a potent Hsp90 inhibitor(IC50 of 25 nM and Kd of 78 nM).</p>Formule :C19H18ClN3O4Degré de pureté :99.36% - 99.99%Couleur et forme :SolidMasse moléculaire :387.82TRC051384 HCl
CAS :<p>TRC051384 is an inducer of heat shock protein Hsp70, activating heat shock factor-1 and enhancing Hsp72 expression in neurons and glial cells.</p>Formule :C25H32ClN5O4Degré de pureté :97.55%Couleur et forme :SolidMasse moléculaire :502.01BIIB021
CAS :<p>BIIB021 (CNF2024) is an orally-available, fully synthetic inhibitor of HSP90(Ki=1.7 nM, EC50=38 nM).</p>Formule :C14H15ClN6ODegré de pureté :98% - 99.82%Couleur et forme :SolidMasse moléculaire :318.76Geldanamycin
CAS :<p>Geldanamycin, an HSP90 inhibitor (Kd: 1.2 μM), specifically disrupts glucocorticoid receptor (GR)/HSP association.</p>Formule :C29H40N2O9Degré de pureté :97.59% - 99.27%Couleur et forme :Yellow To Orange PowderMasse moléculaire :560.64Feretoside
CAS :<p>Feretoside is a natural product extracted from the barks of E. ulmoides. Feretoside shows inducible activity on the heat shock factor 1 (HSF1).</p>Formule :C17H24O11Degré de pureté :99.85%Couleur et forme :SolidMasse moléculaire :404.37HA15
CAS :<p>HA15 targets BiP/GRP78/HSPA5, showing anti-cancer effects on all tested melanoma cells, resistant or patient-derived.</p>Formule :C23H22N4O3S2Degré de pureté :99.77% - 99.86%Couleur et forme :SolidMasse moléculaire :466.58Palmitic acid
CAS :<p>Palmitic acid (Cetylic acid) is a natural product, a common saturated fatty acid found in animals, plants and microorganisms.</p>Formule :C16H32O2Degré de pureté :99.17% - 99.67%Couleur et forme :White Crystalline Scales SolidMasse moléculaire :256.42KNK437
CAS :<p>KNK437 (Heat Shock Protein Inhibitor I), a pan-HSP inhibitor, suppresses the synthesis of inducible HSPs(HSP105, HSP72, and HSP40).</p>Formule :C13H11NO4Degré de pureté :98.90%Couleur et forme :SolidMasse moléculaire :245.23DTHIB
CAS :<p>DTHIB robustly inhibits the HSF1 cancer gene signature and prostate cancer cell proliferation.</p>Formule :C13H9ClFN3O3Degré de pureté :98.86% - 99.29%Couleur et forme :SolidMasse moléculaire :309.68Apoptozole
CAS :<p>Apoptozole (Apoptosis Activator VII) is an inhibitor of the ATPase domain of Hsc70 and Hsp70, and can induce apoptosis.</p>Formule :C33H25F6N3O3Degré de pureté :99.75%Couleur et forme :SolidMasse moléculaire :625.56Azadiradione
CAS :<p>Azadiradione (AZD) (AZD) from the methanolic extract of seeds of Azadirachta indica</p>Formule :C28H34O5Degré de pureté :99.52%Couleur et forme :SolidMasse moléculaire :450.57HSF1A
CAS :<p>HSF1A is a cell-permeable activator of HSF1 that protects mammalian cells against stress-induced apoptosis.</p>Formule :C21H19N3O2S2Degré de pureté :98.89%Couleur et forme :SolidMasse moléculaire :409.52YUM70
CAS :<p>YUM70 inhibits GRP78 (IC50: 1.5μM), inducing ER stress and apoptosis in pancreatic cancer.</p>Formule :C21H19ClN2O4Degré de pureté :97.25%Couleur et forme :SolidMasse moléculaire :398.84KBU2046
CAS :<p>KBU2046: oral anti-metastasis compound, enhances survival, targets chaperone complexes, not a typical HSP90 inhibitor.</p>Formule :C15H11FO2Degré de pureté :99.89%Couleur et forme :SolidMasse moléculaire :242.24VER-82576
CAS :<p>VER-82576 (NVP-BEP800), a synthetic HSP90β inhibitor (IC50: 58 nM), exhibits >70-fold selectivity against Hsp90 family members Trap-1 and Grp94.</p>Formule :C21H23Cl2N5O2SDegré de pureté :97.31% - 99.85%Couleur et forme :SolidMasse moléculaire :480.41VER-155008
CAS :<p>VER-155008 is a potent Hsp70 family inhibitor with IC50 of 0.5 μM, 2.6 μM, and 2.6 μM in cell-free assays for HSP70, HSC70, and GRP78, respectively.</p>Formule :C25H23Cl2N7O4Degré de pureté :97.03% - 99.55%Couleur et forme :SolidMasse moléculaire :556.4PU-H54
CAS :<p>PU-H54 is a purine-derived Grp94 inhibitor targeting the S2 subpocket's unique binding region.</p>Formule :C18H19N5SDegré de pureté :99.13%Couleur et forme :SolidMasse moléculaire :337.44
