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产品数：86101
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T6939PFI-3Inhibitor,Epigenetic Reader Domain,PFI3,PFI-3,inhibit
PFI-3 is a selective chemical inhibitor for SMARCA (2/4) (Kd = 89 nM)and PBI (5) bromodomains which may result in the delay and prevention of breast cancer.
价 格：￥电议型 号：T6939产 地：中国大陆
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T6829EPI-001Androgen,amino-terminal,anti-tumor,domain,PPAR,inhibit,EPI-001,Peroxisome proliferator-activa
EPI-001 is an androgen receptor N-terminal domain antagonist with IC50 of ～6 μM and a selective PPAR-gamma modulator.
价 格：￥电议型 号：T6829产 地：中国大陆
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TN2269Tetramethylcurcuminpancreatic,FLLL-31,domain,FLLL 31,Apoptosis,Inhibitor,STAT,Tetramethylcurcumin,ca
Tetramethylcurcumin is a novel curcumin analog, is an effective inhibitors of STAT3 phosphorylation, DNA binding activity, and transactivation in vitro.it also inhibits colony formation in soft agar, cell invasion, and exhibit synergy with the anti-cancer drug doxorubicin against breast cancer cells.
价 格：￥电议型 号：TN2269产 地：中国大陆
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T9194UMB298UMB-298,UMB298,inhibit,MOLM13,Inhibitor,bromodomain,UMB 298,selective,potent,Epigenetic Reader
UMB298 is a potent and selective CBP/P300 bromodomain inhibitor. UMB298 inhibits BRD4 with IC50 of 5193nM.
价 格：￥电议型 号：T9194产 地：中国大陆
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T9629WAY-309060Inhibitor,WAY309060,MCF7,BRD4 Inhibitor-24,antitumor,Epigenetic Reader Domain,inhibit,brea
WAY-309060 is a BRD4 small molecule inhibitor with antitumor activity.
价 格：￥电议型 号：T9629产 地：中国大陆
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T9339Stafia-1Stafia1,domain,Inhibitor,STAT,selectivity,leukemia,inhibit,cells,Stafia 1,Stafia-1,SH2
Stafia-1 is a potent STAT5a inhibitor ( IC50=22.2 μM). Stafia-1 displays high selectivity over STAT5b and other STAT family members.
价 格：￥电议型 号：T9339产 地：中国大陆
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T7856Naphthol AS-EHAT,KIX-KID,MCF-7,cancer,Inhibitor,Naphthol AS-E,inhibit,Epigenetic Reader Domain,CREB,
nAS-E is an the KIX-KID interaction and CREB-mediated gene transcription inhibitor.
价 格：￥电议型 号：T7856产 地：中国大陆
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T6783BI-7273inhibit,Inhibitor,Epigenetic Reader Domain,BI7273,BI-7273,BI 7273
BI-7273 is an effective, specific, BRD9 BD Inhibitor, which can infiltrate cell.
价 格：￥电议型 号：T6783产 地：中国大陆
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T9399Menin-MLL inhibitor 20Epigenetic Reader Domain,mixed-lineage,MeninMLL inhibitor 20,irreversible,leuk
Menin-MLL inhibitor 20 is an irreversible inhibitor of menin-MLL interaction with antitumor activities (WO2020142557A1, compound 6).
价 格：￥电议型 号：T9399产 地：中国大陆
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T6859I-BRD9cancer,inhibit,Epigenetic Reader Domain,bromodomain-containing protein 7(BRD7),bromodomain and
I-BRD9 is the first selective cellular inhibitor for BRD9 with pIC50 of 7.3.
价 格：￥电议型 号：T6859产 地：中国大陆
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T8495AlobresibInhibitor,GS5829,Alobresib,GS 5829,Epigenetic Reader Domain,inhibit
Alobresib is an inhibitor of BET bromodomain,is an antineoplastic drug candidate.
价 格：￥电议型 号：T8495产 地：中国大陆
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T9552BAZ1A-IN-1leukemia,breast cancer,Epigenetic Reader Domain,BAZ1A IN 1,cancer,ZR-75–30,BAZ1A,BAZ1AIN1,
BAZ1A-IN-1 is a potent BAZ1A inhibitor with the KD value of 0.52 μM for the BAZ1A bromodomain. BAZ1A-IN-1 shows good anti-survival activity against cancer cell lines with high BAZ1A expression, but weak or no activity against cancer cells with low BAZ1A expression.
价 格：￥电议型 号：T9552产 地：中国大陆
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T22345INCB054329Inhibitor,inhibit,INCB 054329,Epigenetic Reader Domain
INCB054329, a structurally distinct bromodomain and extraterminal domain (BET) inhibitor, inhibits BRD2-BD1, BRD2-BD2, BRD3-BD1, BRD3-BD2, BRD4-BD1, BRD4-BD2, BRDT-BD1 and BRDT-BD2 with IC50 values of 44 nM, 5 nM, 9 nM, 1 nM, 28 nM, 3 nM, 119 nM and 63 nM respectively.
价 格：￥电议型 号：T22345产 地：中国大陆
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T8932GSK046GSK046,Epigenetic Reader Domain,BRDT,BRD2,inhibit,immuno-inflammation,GSK 046,GSK-046,BRD4,Inh
GSK046 is a potent, selective and orally active BD2 bromodomain inhibitor of the BET proteins(IC50s of 264 nM (BRD2 BD2), 98 nM (BRD3 BD2), 49 nM (BRD4 BD2) and 214 nM (BRDT BD2), respectively). It has immunomodulatory activity.
价 格：￥电议型 号：T8932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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TQ0058MI-463MI463,Epigenetic Reader Domain,MI-463,MI 463,Inhibitor,inhibit
MI-463 is a potent and orally bioavailable inhibitor of the menin-mLL interaction (IC50: 15.3 nM).
价 格：￥电议型 号：TQ0058产 地：中国大陆
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T2072BET bromodomain inhibitor
BET bromodomain inhibitor is a potent BET inhibitor.
价 格：￥电议型 号：T2072产 地：中国大陆
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T2072BET bromodomain inhibitorBET bromodomain inhibitor
BET bromodomain inhibitor is a potent BET inhibitor.
价 格：￥电议型 号：T2072产 地：美洲
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T83739Myr-Tat-CBD3 TFA；化合物 Myr-Tat-CBD3 TFAMyr-Tat-Calcium Channel-binding Domain 3|||N-myristate-Tat-CBD3
Myr-Tat-CBD3 is a chemical compound that serves as an inhibitor of the protein-protein interaction between the N-type voltage-gated calcium channel Cav2.2 and collapsin response mediator protein 2 (CRMP2). This compound effectively disrupts the Cav2.2-CRMP2 interaction by about 81% at a 10 ?M concentration and demonstrates an inhibitory concentration 50 (IC50) value of approximately 2.8 ?M against potassium-induced calcium influx in primary rat dorsal root ganglion (DRG) neurons. Furthermore, at
价 格：￥电议型 号：T83739产 地：中国大陆
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T82261Grb2 SH2 domain inhibitor 1；化合物 Grb2 SH2 domain inhibitor 1Grb2 SH2 domain inhibitor 1
Grb2 SH2 Domain Inhibitor 1 is a cyclic cell-penetrating peptide (CPP) featuring a conformationally restricted d-pro-l-pro motif ring (AF Φ Rpprrfq), where Φ represents L-naphthylalanine, R denotes D-arginine, and P indicates D-proline. This compound primarily functions as a cyclic peptide inhibitor.
价 格：￥电议型 号：T82261产 地：中国大陆
