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产品数：86101
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T6853GSK591GSK 591,EPZ-015866,GSK591,Inhibitor,GSK 3203591,EPZ 015866,inhibit,GSK-3203591,GSK-591,Histone
GSK591, Alternative Names are EPZ015866, GSK3203591, is a potent selective inhibitor of the arginine methyltransferase PRMT5 (IC50=11 nM).
价 格：￥电议型 号：T6853产 地：中国大陆
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T7089SGC2085SGC2085,SGC 2085,Inhibitor,inhibit,SGC-2085,Histone Methyltransferase
SGC2085 is an effective and selective coactivator-associated arginine methyltransferase 1 (CARM1) inhibitor (IC50: 50 nM).
价 格：￥电议型 号：T7089产 地：中国大陆
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T7064Valproic AcidHistone deacetylases,Mitochondrial Autophagy,bipolar disorder,epilepsy,Autophagy,Apopto
Valproic Acid is a branched chain fatty acid which potentially enhances central GABAergic neurotransmission and inhibits Na+ channels. Currently, the various molecular mechanisms of action of Valproic Acid have not been completely elucidated. Valproic Acid has been reported to be a potent inhibitor of histone deacetylases (HDACs) in vitro. Valproic Acid is also noted to relieve HDAC-dependent transcriptional repression and causes the hyperacetylation of histones in cultured cells. Additionally,
价 格：￥电议型 号：T7064产 地：中国大陆
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TN1150Procyanidin B3Histone Acetyltransferase,Procyanidin B-3,Procyanidin B 3,HAT,HATs,inhibit,Inhibitor,P
Procyanidin B3(B3) is a procyanidin dimer that is widely studied due to its high abundance in the human diet and antioxidant activity.
价 格：￥电议型 号：TN1150产 地：中国大陆
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T8201Gambogenic acidGambogenic acid,Histone Methyltransferase,inhibit,Inhibitor
Gambogenic acid is a natural product,is an effective inhibitor of EZH2,with anticancer activity.
价 格：￥电议型 号：T8201产 地：中国大陆
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T2430HPOBHDAC,Apoptosis,cells,anticancer,Histone deacetylases,HPOB,tumor,A549,U87,Inhibitor,inhibit,LNCaP
HPOB is an effective and specific HDAC6 inhibitor (IC50: 56 nM), >30-fold selectivity over other HDACs.
价 格：￥电议型 号：T2430产 地：中国大陆
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T6678SplitomicinInhibitor,Histone deacetylases,Splitomycin,HDAC,inhibit,Splitomicin
Splitomicin (IC50 of 60 μM), a specific inhibitor of NAD(+)-dependent histone deacetylase Sir2p, displays a high activity in a cell-based assay.
价 格：￥电议型 号：T6678产 地：中国大陆
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TQ0074ACY-775ACY-775,Histone deacetylases,inhibit,Inhibitor,ACY 775,HDAC,ACY775
ACY-775 is an effective and specific inhibitor of HDAC6 (IC50: 7.5 nM).
价 格：￥电议型 号：TQ0074产 地：中国大陆
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T9745ElevenostatHistone deacetylases,Elevenostat,JB3-22,multiple myeloma,inhibit,HDAC11,Inhibitor,HDAC
Elevenostat is an HDAC11-selective inhibitor with an IC50 value of 0.235??M.
价 格：￥电议型 号：T9745产 地：中国大陆
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T7082HDAC8-IN-1HDAC-8-IN-1,HDAC8IN1,Histone deacetylases,Inhibitor,inhibit,HDAC,HDAC8 IN 1
MDK-7933 (HDAC8-IN-1) is a HDAC8 inhibitor with an IC50 of 27.2 nM in cancer cell lines. MDK-7933 shows antiproliferative effects toward several human lung cancer cell lines (A549, H1299, and CL1-5). HDAC8-IN-1 exhibits cytotoxicity against human lung CL1-5 cells without significant cytotoxicity for normal IMR-90 cells[1].
价 格：￥电议型 号：T7082产 地：中国大陆
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T8768MM-102 TFAMM102,HMTase Inhibitor IX,MM-102,MM 102 TFA,MM 102,inhibit,MM102 TFA,Histone Methyltransfe
MM-102 TFA is a potent WDR5/MLL interaction inhibitor, achieves IC50 = 2.4 nM. MM-102 compound prevents the interaction between mixed lineage leukemia 1 (MLL1) and WD Trp-Asp repeat domain 5 (WDR5) and results in the inhibition of MLL1 H3K4 histone methyltransferase (HMT) activity. Down-Regulation of H3K4me3 by MM-102 Facilitates Epigenetic Reprogramming of Porcine Somatic Cell Nuclear Transfer Embry
价 格：￥电议型 号：T8768产 地：中国大陆
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T8381AmodiaquineCCL2,Nurr1,IL-1β,Histone Methyltransferase,Amodiaquine,Amodiaquin,inhibit,Inhibitor,anti-
Amodiaquine is a synthetic aminoquinoline, used to treat malaria.
价 格：￥电议型 号：T8381产 地：中国大陆
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T6474Divalproex SodiumMitophagy,Notch,Apoptosis,Histone deacetylases,Autophagy,hepatic fat accumulation,H
Divalproex Sodium binds to and inhibits gamma-aminobutyric acid (GABA) transaminase and its anticonvulsant activity may be exerted by increasing brain concentration of GABA and by inhibiting enzymes that catabolize GABA or block the reuptake of GABA into glia and nerve endings. It also is an HDAC inhibitor. Divalproex Sodium is a stable coordination compound comprised of sodium valproate and valproic acid with anticonvulsant and antiepileptic activities. Divalproex may also work by suppressing r
价 格：￥电议型 号：T6474产 地：中国大陆
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TQ0100AZ505Histone Methyltransferase,AZ 505,inhibit,AZ505,Inhibitor,AZ-505
AZ505 is an effective and specific SMYD2 inhibitor (IC50: 0.12 μM).
价 格：￥电议型 号：TQ0100产 地：中国大陆
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T7403BAY-598BAY-598,Inhibitor,BAY598,inhibit,Histone Methyltransferase,BAY 598
BAY-598 is a selective inhibitor of SMYD2 with IC50 values of 27 nM.
价 格：￥电议型 号：T7403产 地：中国大陆
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T6900MS023Inhibitor,MS 023,MS-023,MS023,inhibit,Histone Methyltransferase
MS023 is a potent, selective, and cell-active Type I PRMT inhibitor with IC50 of 30 nM, 119 nM, 83 nM, 4 nM, and 5 nM for PRMT1, PRMT3, PRMT4, PRMT6 and PRMT8, respectively.
价 格：￥电议型 号：T6900产 地：中国大陆
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T8879MR837PWWP1,nuclear,MR837,SET,NSD2,Histone Methyltransferase,MR 837,domain,inhibit,Inhibitor,MR-837
ZINC30303842 is a NSD2-PWWP1 antagonist.
价 格：￥电议型 号：T8879产 地：中国大陆
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T60002Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylateHistone Methyltransferase,
Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate is a selective inhibitor of histone methyltransferase SETD7 (IC50 = 4.59 μM) with anticancer activity.
价 格：￥电议型 号：T60002产 地：中国大陆
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T38766LHistone H3 (1-35) acetate
Histone H3 (1-35) acetate is a 35-residue peptide of histone H3. Histone H3 is an important protein that plays a role in the dynamic and long term regulation of genes.
价 格：￥电议型 号：T38766L产 地：中国大陆
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T3206NKL 22PAOA；Histone Deacetylase Inhibitor IV
An effective Histone Deacetylase Inhibitor.
价 格：￥电议型 号：T3206产 地：中国大陆
