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产品数：86095
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T9890HIF1-IN-3?Hypoxia-inducible factors,HIF1 IN 3?,Inhibitor,HIFs,inhibit,HIF-PH,HIF1IN3?,Anticancer,HIF
HIF1-IN-3 is an effective inhibitor of HIF-1 (EC50 = 0.9 μM) and can be used in anticancer studies.
价 格：￥电议型 号：T9890产 地：中国大陆
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T6603NelarabineHSB-2,Inhibitor,T-ALL,Nucleoside Antimetabolite/Analog,Apoptosis,acute lymphoblastic leuka
Nelarabine is a purine nucleoside analog and DNA synthesis inhibitor with IC50 from 0.067-2.15 μM in tumor cells.
价 格：￥电议型 号：T6603产 地：中国大陆
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T40101(±)-1,2-Dioleinmuscle,Protein kinase C,Inhibitor,PKC α,skeletal,myoblasts,inhibit,PKC,cell,(±) 1,2 D
(±)-1,2-Diolein (1,2-Dioleoyl-rac-glycerol) is a PKC activator. (±)-1,2-Diolein could increases myotubes Ca 2+ influx.
价 格：￥电议型 号：T40101产 地：中国大陆
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T8545FEN1-IN-4flap,colorectal,Inhibitor,endonuclease,FEN1IN4,cells,colon,cancer,inhibit,FEN-1-IN-4,gliobl
FEN1-IN-4 is an inhibitor of human flap endonuclease-1 (hFEN1)
价 格：￥电议型 号：T8545产 地：中国大陆
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T6916OICR-9429OICR9429,pancreatic,Histone Methyltransferase,MLL,inhibit,OICR-9429,colon,prostate cance,bl
OICR-9429 is a potent antagonist of the interaction that WDR5 effect with peptide regions of MLL and Histone 3. It reduces the viability of acute myeloid leukemia cells in vitro.
价 格：￥电议型 号：T6916产 地：中国大陆
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TQ0256FGFR4-IN-1Fibroblast growth factor receptor,FGFR-4-IN-1,FGFR,inhibit,FGFR4IN1,Inhibitor,FGFR4 IN 1
FGFR4-IN-1 is a potent FGFR4 inhibitor (IC50: 0.7 nM).
价 格：￥电议型 号：TQ0256产 地：中国大陆
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T9809E3 ligase Ligand 23inhibit,Inhibitor,Cereblon,Aiolos,ubiquitin proteasome,Ligands for E3 Ligase,Ikar
E3 ligase Ligand 23 is a cereblon binder and degrades Ikaros or Aiolos through ubiquitin proteasome.
价 格：￥电议型 号：T9809产 地：中国大陆
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T8782MitoBloCK-11?(MB-11)MitoBloCK11?(MB11),MitoBloCK 11?(MB 11)
MitoBloCK-11 (MB-11) is a s mall molecule inhibitor of mitochondrial protein import possibly acts through transport protein Seo1, but not Tom70 or Tom20; inhibits precursor proteins that contain hydrophobic segments, confers growth in media lacking uracil in a specific manner and affects zebrafish development.
价 格：￥电议型 号：T8782产 地：中国大陆
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T6892Niraparib tosylatePARP,Niraparib tosylate,Apoptosis,inhibit,bioavailable,MK-4827,MK4827,cancer,damag
MK-4827(Niraparib) tosylate (with IC50 of 3.8 nM/2.1 nM) is a selective PARP1/PARP2 inhibitor.
价 格：￥电议型 号：T6892产 地：中国大陆
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T8388VonoprazanTAK-438,TAK 438,GERD,TAK438,Bacterial,antisecretory,blocker,peptic,Proton Pump,secretion,i
Vonoprazan is an orally active potassium-competitive acid blocker.Vonoprazan can be used for the treatment of gastroduodenal ulcer and reflux esophagitis
价 格：￥电议型 号：T8388产 地：中国大陆
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T6397Atracurium besylateinflammatory,anticancer,Inhibitor,Atracurium besylate,neuromuscular blockade,inhi
Atracurium besylate is a non-depolarizing neuromuscular blocking agent with short duration of action. Its lack of significant cardiovascular effects and its lack of dependence on good kidney function for elimination provide clinical advantage over alternate non-depolarizing neuromuscular blocking agents.
价 格：￥电议型 号：T6397产 地：中国大陆
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T7955EB-3Dlipid,inhibit,lymphoblastic,AMP-activated protein kinase,EB3D,acute,tumorigenesis,Apoptosis,hom
EB-3D is a potent and selective choline kinase alpha 1 (ChoKα1) inhibitor(IC50 : 1 μM).with anti-cancer activity.
价 格：￥电议型 号：T7955产 地：中国大陆
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T8488GMB-475Bcr-Abl,GMB-475,PROTACs,GMB 475,Apoptosis,Inhibitor,inhibit,GMB475
GMB-475 is a BCR-ABL1 tyrosine kinase degrader based on PROTAC, overcoming BCR-ABL1-dependent drug resistance. GMB-475 targets BCR-ABL1 protein and recruits the E3 ligase Von Hippel Lindau (VHL).resulting in ubiquitination and subsequent degradation of the oncogenic fusion protein
价 格：￥电议型 号：T8488产 地：中国大陆
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T60143MitoBloCK-6MitoBloCK6
MitoBloCK-6 is a potent Erv1/ALR inhibitor, with an IC 50 of 900 nM and 700 nM, respectively. MitoBloCK-6 also inhibits Erv2 with IC 50 of 1.4 μM. MitoBloCK-6 can induce apoptosis via cytochrome c release in human embryonic stem cells (hESCs) [1].
价 格：￥电议型 号：T60143产 地：中国大陆
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T77882-Phenyl-2-(1-piperidinyl)propane2 Phenyl 2 (1 piperidinyl)propane,Reversible,inhibit,CYPs,Cytochrom
2-Phenyl-2-(1-piperidinyl)propane (PPP), an analog of phencyclidine
价 格：￥电议型 号：T7788产 地：中国大陆
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T60076Oritinibpharmacodynamics,non-small cell lung cancer,EGFR-T790M,EGFR TKI,SH1028,Irreversible,mutant-s
Oritinib is an inhibitor of EGFR with IC50s of 18, 0.7, 4, 0.1, 1.4 and 0.89 nM for EGFR (wt), EGFR (L858R), EGFR (L861Q), EGFR (L858R/T790M), EGFR (d746-750), EGFR (d746-750/T790M), respectively. Oritinib can be used in studies about the treatment of non-small cell lung cancer.
价 格：￥电议型 号：T60076产 地：中国大陆
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T7780Blarcamesinesyndrome,Inhibitor,Muscarinic acetylcholine receptor,inhibit,mAChR,Rett,anticonvulsant,B
AVex-73 is a muscarinic M1 agonist potentially for the treatment of Alzheimer´s disease.
价 格：￥电议型 号：T7780产 地：中国大陆
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T7753Thalidomide-O-COOHinhibit,Ligands for E3 Ligase,ThalidomideOCOOH,Inhibitor,Thalidomide O COOH,Cerebl
Thalidomide-O-COOH is the Thalidomide-based Cereblon ligand used in the recruitment of CRBN protein. It can be connected to the ligand for protein by a linker to form PROTACs.
价 格：￥电议型 号：T7753产 地：中国大陆
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T60092CHEMBL1276927
CHEMBL1276927 shows antibacterial and antiparasitic activities against Chlamydia pneumoniae and Leishmania donovani.
价 格：￥电议型 号：T60092产 地：中国大陆
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T7022PEG300immunogenic,Polyethylene glycol300,biocompatible,PEG300,PEG 300,marker,PEG-300,gastrointestina
PEG300 is a neutral polymer of molecular weight 300, is a water-soluble, low immunogenic and biocompatible polymer formed by repeating units of ethylene glycol
价 格：￥电议型 号：T7022产 地：中国大陆
