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产品数：86101
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T677383-pyridine toxoflavin3pyridinetoxoflavin
3-pyridine toxoflavin is a potent KDM4C inhibitor, IC50=19nM.
价 格：￥电议型 号：T67738产 地：中国大陆
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T7323BCI-215specificity,Phosphatase,DUSP-MKP,inhibit,Inhibitor,MAPK,BCI-215,BCI215,BCI 215,dual
BCI-215 causes selective cancer cell cytotoxicity in part through non-redox-mediated activation of MAPK signaling
价 格：￥电议型 号：T7323产 地：中国大陆
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T7787BMS817378BMS817378,BMS-817378
BMS817378 is a potent and selective inhibitor of MET(IC50 : 1.7 nM).
价 格：￥电议型 号：T7787产 地：中国大陆
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T7673ATH686ATH686,inhibit,CD135,Inhibitor,Apoptosis,ATH-686,ATP-competitive,FLT3,antileukemic,Fms like ty
ATH 686 is an potent and selective Inhibitor of FLT3.
价 格：￥电议型 号：T7673产 地：中国大陆
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T9580SB-734117SB 734117,SB734117
SB-734117 inhibits productive replication of several HCMV strains. SB-734117 exhibited polypharmacology and was an inhibitor of several proteins from the AGC and CMCG kinase groups.
价 格：￥电议型 号：T9580产 地：中国大陆
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T6738Z-FA-FMKSARS coronavirus,SARS-CoV,RRMs,DNA fragmentation,DEVDase,Caspase,Cathepsin,Inhibitor,externa
Z-FA-FMK can irreversibly inhibit cysteine protease and also inhibit effector caspases.
价 格：￥电议型 号：T6738产 地：中国大陆
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T8773MID-1MID-1,inhibit,Inhibitor,MG53,ubiquitination,Insulin Receptor,insulin,association,glucose,MID1,I
MID-1 is an inhibitor of MG53-IRS-1 (Mitsugumin 53-Insulin Receptor Substrate-1) interaction. It disrupts molecular association of MG53 with IRS-1 and abolishes MG53-induced IRS-1 ubiquitination and degradation in skeletal muscle, leading to elevated IRS-1 expression level and increased insulin signaling and glucose uptake
价 格：￥电议型 号：T8773产 地：中国大陆
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TP2322Lbeta-Neoendorphin acetate(77739-21-0 free base)betaNeoendorphin acetate(77739210 free base),beta Neo
beta-Neoendorphin acetate is an agonist of κ-opioid receptor
价 格：￥电议型 号：TP2322L产 地：中国大陆
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T9008NPD8733Inhibitor,inhibit,ATPase,p97,fibroblast,cancer,NPD 8733,NPD8733,VCP,migration,NPD-8733
NPD8733 is an inhibitor of cancer cell-enhanced fibroblast migration. It specifically binds to valosin-containing protein (VCP)/p97.
价 格：￥电议型 号：T9008产 地：中国大陆
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T67735Auristatin23Auristatin23
Auristatin23 is an Antitumor agent. Auristatin23 exhibits antiproliferative activity on tumor cell lines.
价 格：￥电议型 号：T67735产 地：中国大陆
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T8738LUN42518 HCl 47142-51-8(free base)LUN-42518 HCl 47142-51-8(free base),LUN42518 HCl 47142 51 8(fre
LUN42518 HCl is an analogue of phentolamine. Phentolamine is a nonselective alpha-adrenergic antagonist.
价 格：￥电议型 号：T8738产 地：中国大陆
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T6440CGP 57380CGP-57380,CGP 57380,Mitogen activated protein kinase interacting kinase,Inhibitor,MAPK inte
CGP 57380 is a potent MNK1 inhibitor with IC50 of 2.2 μM, exhibiting no inhibitory activity on p38, JNK1, ERK1 and -2, PKC, or c-Src-like kinases.
价 格：￥电议型 号：T6440产 地：中国大陆
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T13173TMPAinhibit,hepatic LO2,AMPKα,TMPA,type II diabetes,AMPK,T cells,Inhibitor,AMP-activated protein kin
TMPA is a nuclear receptor Nur77 and LKB1 interaction antagonist.
价 格：￥电议型 号：T13173产 地：中国大陆
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T37376PHY34PHY-34,PHY34
PHY34 is a late stage autophagy inhibitor with nanomolar level inhibitory effect and anti-tumor activity against high-grade serous ovarian cancer (HGSOC) in vivo.
价 格：￥电议型 号：T37376产 地：中国大陆
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T7973BENZOFURAN-3-CARBALDEHYDEBENZOFURAN 3 CARBALDEHYDE,BENZOFURAN3CARBALDEHYDE
BENZOFURAN-3-CARBALDEHYDE is a natural product.
价 格：￥电议型 号：T7973产 地：中国大陆
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T7373CDN1163Inhibitor,CDN 1163,Calcium Channel,Ca channels,Ca2+ channels,CDN-1163,CDN1163,inhibit
CDN1163 is a small molecule activator of sarco/endoplasmic reticulum Ca2+-ATPase (SERCA).
价 格：￥电议型 号：T7373产 地：中国大陆
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TN5073StrophanthidinSodium potassium pump,Na+/K+ ATPase,cardiac,naturally,available,systolic,glycoside,dia
Strophanthidin can induce calcium overload in vivo.
价 格：￥电议型 号：TN5073产 地：中国大陆
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T73457-Hydroxy-4H-chromen-4-oneSrc,7Hydroxy4Hchromen4one,inhibit,7 Hydroxy 4H chromen 4 one,Inhibitor
7-Hydroxychromone is a Src kinase inhibitor (IC50 of <300 μM).
价 格：￥电议型 号：T7345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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T7318Elimusertibresponse,damage,ATM/ATR,stress,Inhibitor,BAY1895344,tumors,DNA,instability,lymphomas,inhi
BAY 1895344 is a potent, highly selective and orally available ATR inhibitor with an IC50 of 7 nM.BAY 1895344 shows potent anti-tumor efficacy in monotherapy and strong combination potential with the targeted alpha therapy Radium-223 dichloride.
价 格：￥电议型 号：T7318产 地：中国大陆
