Chromatine/Épigénétique
Les inhibiteurs de la chromatine/épigénétique sont des composés qui modulent la structure et la fonction de la chromatine ou interfèrent avec les modifications épigénétiques, telles que la méthylation de l'ADN et la modification des histones. Ces inhibiteurs sont des outils essentiels pour étudier la régulation de l'expression génique et le rôle de l'épigénétique dans des maladies telles que le cancer, les troubles neurologiques et les anomalies du développement. En ciblant les processus épigénétiques, ces inhibiteurs peuvent modifier les schémas d'expression génique et offrir de nouvelles perspectives thérapeutiques. Chez CymitQuimica, nous offrons une large sélection d'inhibiteurs de la chromatine/épigénétique de haute qualité pour soutenir vos recherches en biologie moléculaire, génétique et épigénétique.
Sous-catégories appartenant à la catégorie "Chromatine/Épigénétique"
2613 produits trouvés pour "Chromatine/Épigénétique"
Trier par
Degré de pureté (%)
0
100
|
0
|
50
|
90
|
95
|
100
TMPA
CAS :TMPA is a nuclear receptor Nur77 and LKB1 interaction antagonist.Formule :C21H32O6Degré de pureté :99.21%Couleur et forme :SolidMasse moléculaire :380.48Ref: TM-T13173
1mg75,00€5mg164,00€10mg260,00€25mg440,00€50mg620,00€100mg964,00€1mL*10mM (DMSO)167,00€GSK-1268997
CAS :GSK-1268997 is a bio-active chemical.Formule :C21H23N7O3SDegré de pureté :99.33% - 99.81%Couleur et forme :SolidMasse moléculaire :453.52TAK-285
CAS :TAK-285 is a novel dual HER2 and EGFR(HER1) inhibitor, >10-fold selectivity for HER1/2 than HER4, less potent to MEK1/5, c-Met, Aurora B, Lck, CSK etc.Formule :C26H25ClF3N5O3Degré de pureté :99.73%Couleur et forme :SolidMasse moléculaire :547.96Ref: TM-T6039
1mg38,00€5mg80,00€10mg120,00€25mg216,00€50mg354,00€100mg512,00€200mg727,00€1mL*10mM (DMSO)96,00€GW843682X
CAS :GW843682X (GW843682) is a selective and ATP-competitive inhibitor of PLK1 and PLK3 (IC50s = 2.2 nM and 9.1 nM).Formule :C22H18F3N3O4SDegré de pureté :99.92%Couleur et forme :SolidMasse moléculaire :477.46UNC0224
CAS :UNC0224 is a selective inhibitor of G9a with a Ki of 2.6 nM and IC50 of 15 nM. UNC0224 also potently inhibits GLP with assay-dependent IC50 values of 20-58 nM.Formule :C26H43N7O2Degré de pureté :99.80%Couleur et forme :SolidMasse moléculaire :485.67MY-1B
CAS :MY-1B is a nitrogen-substituted butenamide stereoprobe that blocks stereoselective enrichment of NSUN2, binding selectively to the C271 of NSUN2.Formule :C22H18BrN3O2Degré de pureté :99.81% - >99.99%Couleur et forme :SoildMasse moléculaire :436.3CPI-4203
CAS :CPI-4203 is a selective inhibitor of KDM5 demethylases.Formule :C16H14N4OCouleur et forme :SolidMasse moléculaire :278.31BPTF-IN-1
CAS :BPTF-IN-1 (AU1), a BPTF bromodomain inhibitor with 2.8 μM affinity, shows higher selectivity over BRD4 and possesses antimalarial properties.Formule :C23H23FN6O3Couleur et forme :SolidMasse moléculaire :450.47(Rac)-BAY1238097
CAS :(Rac)-BAY1238097 is a inhibitor of BET(IC50 of 1.02 μM for BRD4),used in cancer research.Formule :C25H33N5O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :451.56NSC-311068
CAS :NSC-311068: A selective TET1 inhibitor, reducing 5hmC and AML cell viability with high TET1.Formule :C10H6N4O4SCouleur et forme :SolidMasse moléculaire :278.24HDAC6-IN-11
CAS :HDAC6-IN-11 (Compound 9) is a cancer cell growth blocker, selectively inhibiting HDAC6 (>300-fold) with an IC50 of 20.7 nM.Formule :C19H16N2O4Couleur et forme :SolidMasse moléculaire :336.34NCD38
CAS :NCD38 is a potent, selective LSD1 inhibitor.Formule :C37H37ClF3N3O4Degré de pureté :98.21% - 98.86%Couleur et forme :SolidMasse moléculaire :680.16JAK-IN-11
CAS :JAK-IN-11 (R-348) is a potent and selective inhibitor of JAK, has the potential for the skin disorders treatment.Formule :C23H22FN5O4SDegré de pureté :99.75%Couleur et forme :SolidMasse moléculaire :483.52Aurora A/PKC-IN-1
CAS :Aurora A/PKC-IN-1 inhibits AurA (IC50: 6.9 nM), PKCα (IC50: 16.9 nM), and hinders breast cancer cell growth and spread.Formule :C16H14N6OSe2Couleur et forme :SolidMasse moléculaire :464.24JNJ-9350
CAS :JNJ-9350: SMOX inhibitor (IC50 0.01 μM), PAO inhibitor (IC50 0.79 μM), for cancer research.Formule :C25H22N6OCouleur et forme :SolidMasse moléculaire :422.48HPB
CAS :HPB is a selective HDAC6 deacetylase inhibitorFormule :C18H20N2O4Couleur et forme :SolidMasse moléculaire :328.36ZIKV-IN-3
CAS :ZIKV-IN-3, an andrographolide derivative, inhibits ZIKV NS5 MTase (IC50: 18.34 μM) and replication. Used for Zika virus research.Formule :C39H41NO4Couleur et forme :SolidMasse moléculaire :587.75NVS-BET-1
CAS :NVS-BET-1 is a BET bromodomain inhibitor. NVS-BET-1 can regulate keratinocyte plasticity.Formule :C22H21ClN4O2Couleur et forme :SolidMasse moléculaire :408.88HIF-1α-IN-3
CAS :HIF-1α-IN-3, also known as Compound (S)-3f, is a hypoxia-selective inhibitor of HIF-1α. It exhibits potent antiestrogenic activity [1].Formule :C19H17N5O2Couleur et forme :SolidMasse moléculaire :347.37PF-739
CAS :PF-739 is an AMPK agonist that has been shown to activate AMPK in hepatocytes and skeletal muscle.Formule :C23H23ClN2O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :442.89HDAC-IN-29
CAS :HDAC-IN-29 (compound 13b) is a potent pan- HDAC inhibitor with antitumor activity.Formule :C20H23N3O4SCouleur et forme :SolidMasse moléculaire :401.48EML741
CAS :EML741 also inhibits DNMT1 (IC50, 3.1 μM), with no effect on DNMT3a or DNMT3b.Formule :C31H49N5O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :523.75HDAC1-IN-4
CAS :HDAC1-IN-4 is a potent inhibitor of Plasmodium falciparum HDAC1 (PfHDAC1) with low cytotoxicity and antimalarial effects (IC50<5 nM).Formule :C21H24BrClN6O2Couleur et forme :SolidMasse moléculaire :507.82YUKA1
CAS :YUKA1, a cell-permeable KDM5A inhibitor with a weak effect on KDM5C, increase H3K4me3 and inhibit the proliferation, prevent drug-resistant.Formule :C13H16N4O2SDegré de pureté :99.85%Couleur et forme :SolidMasse moléculaire :292.36Ref: TM-T17278
1mg105,00€5mg250,00€10mg409,00€25mg802,00€50mg1.224,00€100mg1.783,00€200mg2.457,00€1mL*10mM (DMSO)268,00€Setin-1
CAS :Setin-1 is the most potent Set7 inhibitor that acts by inhibiting the KMTase G9a.Formule :C29H21F3N2O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :486.48GSK 525768A
CAS :GSK 525768A, the inactive enantiomer of GSK525762A, exhibits no activity towards BET.Formule :C22H22ClN5O2Couleur et forme :SolidMasse moléculaire :423.9OXFBD03
CAS :OXFBD03 is the bromodomain and extra terminal domain bromodomain family member BRD4(1) inhibitor.Formule :C20H19NO4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :337.37LY 170198
CAS :LY 170198 is a protein kinase C inhibitor.Formule :C22H25N5O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :439.46DHPCC-9
CAS :DHPCC-9 is an inhibitor of Pim kinase.Formule :C15H10N2OCouleur et forme :SolidMasse moléculaire :234.25DC_501
CAS :DC_501 is a selective non-nucleoside DNA methyltransferase 1 inhibitor.Formule :C25H23Cl2N3ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :452.38DCE_254
CAS :DCE_254 is a novel EZH2 inhibitor, it also displays significant anti-proliferation activity against lymphoma cell lines.Formule :C21H17N9OSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :443.48Langkamide
CAS :Langkamide is a HIF-2 inhibitor with EC₅₀ values of 14.0 uM.Formule :C16H17NO5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :303.31Aurora kinase inhibitor-10
CAS :Aurora kinase inhibitor-10 is an orally active Aurora B inhibitor (IC50: 8 nM) that exhibits antitumour effects.Formule :C21H19F5N6O4SCouleur et forme :SolidMasse moléculaire :546.47BF1
CAS :BF1 is an inhibitor of HAT (histone acetyltransferase) active both in vitro and in vivo.Formule :C12H12ClN3SCouleur et forme :SolidMasse moléculaire :265.76Farnesylthiotriazole
CAS :Farnesylthiotriazole is a persistent PKC activator agent.Formule :C17H27N3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :305.48Tenovin-D3
CAS :Tenovin-D3 is a sirtuin SirT2 inhibitor. It acts by increasing p21 (CDKN1A) expression in a p53-independent manner.Formule :C22H27Cl3N4O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :533.9ML399
CAS :ML399 inhibits menin–MLL interaction, selectively blocking oncogenic MLL signaling in leukemia cells, supporting functional genomics and therapeutic research.Formule :C27H28FN3O2Degré de pureté :97.84% - 98.20%Couleur et forme :SolidMasse moléculaire :445.53HIF-IN-33
CAS :HIF-IN-33 is an inhibitor of HIF pathway.Formule :C21H17F3N4O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :414.38BET-BAY 002
CAS :BET-BAY 002 is an effective BET bromodomain inhibitor demonstrating efficacy in vivo and in vitro against multiple myeloma and leukaemia models.Formule :C22H18ClN5OCouleur et forme :SolidMasse moléculaire :403.86Fagaronine chloride
CAS :Fagaronine chloride is a potent inhibitor of Topoisomerases I.Formule :C21H20ClNO4Couleur et forme :SolidMasse moléculaire :385.84MT477
CAS :MT477 inhibits PKC-α, impairs Ras/ERK1/2 phosphorylation, induces apoptosis, and reduces proliferation in various cancer cells.Formule :C31H30N2O12S3Couleur et forme :SolidMasse moléculaire :718.77Lobelane Hydrochloride
CAS :Lobelane Hydrochloride is a vesicular monoamine transporter-2 (VMAT2) inhibitor.Formule :C22H30ClNCouleur et forme :SolidMasse moléculaire :343.93SirReal-1
CAS :SirReal-1 is an effective and selective inhibitor of Sirt2.Formule :C18H18N4OS2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :370.49Prospasmine
CAS :Prospasmine is an anticholinergic.Formule :C17H28ClNO2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :313.87KF 13218
CAS :KF 13218 is a selective, potent and long lasting thromboxane B2 (TXB2) synthase inhibitor with an IC50 value of 5.3±1.3 nM.Formule :C20H20N2O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :336.38Hns 32
CAS :Hns 32 possesses antiarrhythmic properties in dog and guinea pig hearts. It also has vasodilator action.Formule :C24H29N3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :359.51Rucaparib camsylate
CAS :Rucaparib camsylate, a PARP-1, -2, -3 inhibitor (Ki=1.4 nM for PARP-1) & H6PD blocker, may treat resistant prostate cancer.Formule :C19H18FN3O·xC10H16O4SCouleur et forme :SolidHIF-PHD-IN-2
CAS :HIF-PHD-IN-2 (compound 25) is a highly effective PHD inhibitor, displaying IC50 values below 100 nM for PHD1, PHD2, and PHD3 [1].Formule :C17H15N5O3SCouleur et forme :SolidMasse moléculaire :369.4Y08284
CAS :Y08284: selective CBP bromodomain inhibitor, IC50: 4.21 nM, oral. Halts prostate cancer cell growth; anti-tumor.Formule :C26H25FN4O4Couleur et forme :SolidMasse moléculaire :476.5GSK926
CAS :GSK926 is a selective, SAM-competitive, and cell-active EZH2 inhibitor.Formule :C29H35N7O2Couleur et forme :SolidMasse moléculaire :513.63Y06036
CAS :Y06036, a potent and selective BET inhibitor, can bind to the BRD4(1) bromodomain (Kd: 82 nM).Formule :C16H15BrN2O5SDegré de pureté :99.97%Couleur et forme :SolidMasse moléculaire :427.27CREBBP-IN-9
CAS :CREBBP-IN-9, a CREBBP inhibitor, acts on the bromodomain of the protein.Formule :C16H15N5O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :341.39Bizine
CAS :Bizine, a Phenelzine analogue, selectively inhibits LSD1 (Ki=59 nM), modulates histone methylation in cancer, and may have neuroprotective uses.Formule :C18H23N3OCouleur et forme :SolidMasse moléculaire :297.39M133
CAS :M133 is a selective histone deacetylase HDAC1 and HDAC2 inhibitor and potent antitumor agent.Formule :C23H24N4OS2Couleur et forme :SolidMasse moléculaire :436.59Peficitinib hydrobromide
CAS :Peficitinib hydrobromide is used in the treatment of Psoriasis and Rheumatoid Arthritis.Formule :C18H23BrN4O2Couleur et forme :SolidMasse moléculaire :407.312H8-A5
CAS :H8-A5, a HDAC8 inhibitor, shows antiproliferation activity in MDA-MB-231 cancer cells.Formule :C14H9F3N2O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :326.29Arazine
CAS :Arazine, a cell-permeable G protein modulator, is an isoprenylcysteine methyltransferase substrate.Formule :C20H33NO3SDegré de pureté :90%Couleur et forme :SolidMasse moléculaire :367.55Thi-DPPY
CAS :Thi-DPPY: Potent JAK3/BTK inhibitor (IC50: 1.38/62.4 nM), anti-proliferative, anti-inflammatory, potential in IPF research.Formule :C28H28ClN5O4SCouleur et forme :SolidMasse moléculaire :566.07MS453
CAS :MS453 is a potent and selective SETD8 inhibitor with an IC50 value of 804 nM.Formule :C20H27N5O3Couleur et forme :SolidMasse moléculaire :385.46HIF-1/2α-IN-2
CAS :HIF-1/2α-IN-2 is a potent inhibitor of HIF-1/2α, which effectively reduces the levels of HIF-1/2α.Formule :C16H11FN4O2SCouleur et forme :SolidMasse moléculaire :342.35SIRT2-IN-11
CAS :SIRT2-IN-11 (AEM1), a SIRT2 inhibitor (IC50 18.5μM), induces apoptosis and affects p53, used in cancer research.Formule :C21H22N2OCouleur et forme :SolidMasse moléculaire :318.41Galegine hydrochloride
CAS :Galegine hydrochloride, from G. officinalis, leads to weight loss, activates AMPK in various cells, and has antibacterial properties.Formule :C6H14ClN3Couleur et forme :SolidMasse moléculaire :163.651,2-Didecanoylglycerol
CAS :1,2-Didecanoylglycerol has functions as bioregulator of protein kinase C in human platelets.Formule :C23H44O5Couleur et forme :SolidMasse moléculaire :400.59KDM2B-IN-3
CAS :KDM2B-IN-3, from patent WO2016112284A1 as compound 183c, potently inhibits histone demethylase KDM2B, with cancer research potential.Formule :C25H30N2O2Couleur et forme :SolidMasse moléculaire :390.52JNJ-7925476 free base
CAS :JNJ-7925476 is an TRI antidepressant agent.Formule :C20H19NDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :273.37PRMT5-IN-2
CAS :PRMT5-IN-2 is an inhibitor of protein arginine methyltransferase 5.Formule :C17H16ClFN4O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :394.78J1075
CAS :J1075 is an histone deacetylase 8 (HDAC8) inhibitor.Formule :C9H6ClNO2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :227.67S-Aristeromycinylhomocysteine
CAS :S-Aristeromycinylhomocysteine is an inhibitor of adenosylmethionine decarboxylase.Formule :C15H22N6O4SCouleur et forme :SolidMasse moléculaire :382.44(R)-OR-S1
CAS :(R)-OR-S1 is a SAM-competitive, highly selective, orally bioavailable dual inhibitor of EZH1/2.Formule :C26H34BrN3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :532.47Acefylline piperazine
CAS :Acefylline piperazine, a less toxic theophylline derivative, treats asthma and bronchitis by bronchodilation, stimulating respiration and CNS.Formule :C9H10N4O4·xC4H10N2Couleur et forme :SolidMasse moléculaire :562.54MI-3
CAS :MI-3 (Menin-MLL Inhibitor) (Menin-MLL Inhibitor) is an effective inhibitor of Menin-MLL interaction (IC50: 648 nM).Formule :C18H25N5S2Degré de pureté :98.66% - 99.61%Couleur et forme :SolidMasse moléculaire :375.55ZLD10A
CAS :ZLD10A is a highly potent and selective small molecule inhibitor of EZH2.Formule :C37H48N4O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :612.8WAY-260022
CAS :WAY-260022 is the norepinephrine transporter inhibitor.Formule :C21H31F3N2O2Degré de pureté :97.61% - 99.41%Couleur et forme :SolidMasse moléculaire :400.48BNS
CAS :BNS is a potent, prolyl-hydroxylase 2 (PHD2)-selective inhibitor.Formule :C18H16N2O6S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :420.46NR-160
CAS :NR-160 is a selective HDAC6 inhibitor (IC50=0.03μM), weaker on HDAC1-4,8, toxic to 7 cancer lines, boosts bortezomib and anthracycline effects.Formule :C25H21F3N6O3Couleur et forme :SolidMasse moléculaire :510.47Ro 31-8830
CAS :Ro 31-8830, a derivative of Ro 31-8425, has in vivo anti-inflammatory activity.Formule :C28H28N4O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :452.55S2101
CAS :S2101 is a specific LSD1 histone demethylase inhibitor with an IC50 of 0.99 μM and a Ki of 0.61 μM, suitable for research into cancer and viral infections.Formule :C16H16ClF2NODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :311.75LEM-14-1189
CAS :LEM-14-1189 inhibits NSD1/2/3 (IC50: 418/111/60 μM), targets nuclear receptors, and may treat cancer and blood diseases.Formule :C35H34N6O5S2Degré de pureté :98.06%Couleur et forme :SolidMasse moléculaire :682.81BRD4-BD1-IN-2
CAS :BRD4-BD1-IN-2: Potent, selective BRD4-BD1 inhibitor, IC50=2.51µM; 20x less active on BD2; for cardiovascular/cancer research.
Formule :C20H15Br3N4O2Degré de pureté :99.39%Couleur et forme :SolidMasse moléculaire :583.07NCGC00247743
CAS :NCGC00247743 is an inhibitor of histone lysine demethylase KDM4.Formule :C24H29N3O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :391.51ST7710AA1
CAS :ST7710AA1 inhibits PARP-1, effectively targets in vitro, and overcomes Pgp-associated multidrug resistance.Formule :C20H22N4OCouleur et forme :SolidMasse moléculaire :334.41SIRT5 inhibitor 2
CAS :SIRT5 inhibitor 2 (compound 49) has inhibitory activity through SIRT5-dependent deacetylation and cancer and neurodegenerative diseases.Formule :C18H12Cl2N2O3SDegré de pureté :99.38% - 99.87%Couleur et forme :SolidMasse moléculaire :407.27JAK-IN-18
CAS :"JAK-IN-18: potent JAK inhibitor for eye, skin, respiratory disease research (WO2018204238A1, comp 1)."Formule :C27H28F2N6O3Couleur et forme :SolidMasse moléculaire :522.55INCB054329 Racemate
CAS :INCB054329 Racemate is an inhibitor of BET protein.Formule :C19H16N4O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :348.36AMPK activator 12
CAS :AMPK activator 12 is an AMPK activator and GDF15 inducer that elevates the expression level of GDF15 protein for cancer research.Formule :C23H24BrNO2Degré de pureté :99.55%Couleur et forme :SolidMasse moléculaire :426.35RSC-133
CAS :promotes the reprogramming of human somatic cells to pluripotent stem cellsFormule :C18H15N3O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :305.33BET-IN-2
CAS :BET-IN-2 is a BET inhibitor (IC50: 52 nM for BRD4-BD1).Formule :C23H29N3ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :363.5INO-1001 methanesulfonate
CAS :INO-1001 methanesulfonate is a strong PARP inhibitor with chemosensitization and radiosensitization effects.Formule :C24H29N3O7S2Couleur et forme :SolidMasse moléculaire :535.63UMB-136
CAS :UMB-136 is a bromodomain BRD4 inhibitor that acts by significantly inducing HIV-1 reactivation.Formule :C24H27N5O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :417.5(R)-BAY1238097
CAS :(R)-BAY1238097 is a selective inhibitor against the binding of BET proteins to histones, used in acute myeloid leukemia (AML) and multiple myeloma (MM) studies.Formule :C25H33N5O3Degré de pureté :98.77%Couleur et forme :SolidMasse moléculaire :451.56Ref: TM-T13442
1mg49,00€5mg101,00€10mg172,00€25mg355,00€50mg620,00€100mg1.044,00€200mg1.404,00€1mL*10mM (DMSO)113,00€D 595
CAS :D595 is a phenethylamine-type calcium channel blocker. The most potent phenylethylamine with respect to negative inotropy was D595 (EC50: 794 nmol/l).Formule :C25H32Cl2N2O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :463.44KDM5-C49
CAS :KDM5-C49 is a potent and selective inhibitor of KDM5, which regulates cell proliferation and stem cell self-renewal and differentiation.Formule :C15H24N4O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :308.38RET-IN-19
CAS :RET-IN-19, a potent RET inhibitor, anticancer: IC50 6.8 nM (RET-wt), 13.51 nM (RET V804M); for NSCLC research.Formule :C28H28N6O4SCouleur et forme :SolidMasse moléculaire :544.62AMPK activator 8
CAS :AMPK activator 8 targets rAMPK α1β1γ1/α2β1γ1/α1β2γ1 (EC50: 11/27/4 nM) for type 2 diabetes research.Formule :C25H21ClN2O6Couleur et forme :SolidMasse moléculaire :480.9DFPM
CAS :DFPM activates plant resistance, inhibits root growth, reduces Col-0 root cell viability, and is light-sensitive in water.Formule :C16H15Cl2NOSCouleur et forme :SolidMasse moléculaire :340.27Metformin icosapent
CAS :Metformin icosapent activates AMPK, enhancing insulin sensitivity and reducing glucose absorption for better glycemic control.Formule :C24H41N5O2Couleur et forme :SolidMasse moléculaire :431.62CK2/PIM1-IN-1
CAS :CK2/PIM1-IN-1 inhibits CK2 & PIM1 (IC50s: 3.787 & 4.327 μM), aimed for cancer research.Formule :C15H9NO4S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :331.37EZH2-IN-3
CAS :EZH2-IN-3 is an inhibitor of EZH2 and EZH1 with selective impact on diffuse large B cell lymphoma cell growth.Formule :C27H28ClN5O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :490UL04
CAS :UL04 is an inhibitor of CREBBP bromodomain.Formule :C18H17NO5Couleur et forme :SolidMasse moléculaire :327.33TNKS-IN-41
CAS :TNKS-IN-41 highly potent and selective inhibitor of tankyrase.Formule :C24H22N10O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :482.5
