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T8555Neuraminidase-IN-1virus,Influenza Virus,inhibit,A/WSN/33H1N1,Inhibitor,influenza,neuraminidase,H1N1,
Compound Y-1 is a novel neuraminidase inhibitor.
价 格：￥电议型 号：T8555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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T6605NH125NH 125,Calmodulin-dependent protein kinases,NH-125,Calmodulin-dependent kinases,NH125,Inhibitor
NH125 is a selective eEF-2 kinase inhibitor with IC50 of 60 nM, >125-fold selectivity over PKC, PKA, and CaMKII, and also a potent histidine kinase inhibitor.
价 格：￥电议型 号：T6605产 地：中国大陆
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T6506FPH1inhibit,FPH1,BRD6125,BRD 6125,FPH 1,FPH-1,Inhibitor
FPH1 (BRD-6125) can promote the expansion of iPS-derived hepatocytes.
价 格：￥电议型 号：T6506产 地：中国大陆
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T600385-(5-methyl-1H-1,2,4-triazol-3-yl)-3-[4-(trifluoromethoxy)phenyl]-1,2,4-oxadiazole5(5methyl1H1,2,4tr
5-(5-methyl-1H-1,2,4-triazol-3-yl)-3-[4-(trifluoromethoxy)phenyl]-1,2,4-oxadiazole can be used in the synthesis of heterocyclic compounds to inhibit HIF pathway activity.
价 格：￥电议型 号：T60038产 地：中国大陆
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T10343AOH1160
AOH1160 is an inhibitor of proliferating cell nuclear antigen (PCNA). AOH1160 induces apoptosis and causes cell-cycle arrest by interfering with DNA replication.
价 格：￥电议型 号：T10343产 地：中国大陆
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T7477Antazolinenervous system,Inhibitor,H1 receptor antagonist,inhibit,Phenazoline,Antazoline,Histamine R
Antazoline has antihistamine and anticholinergic effects.It used to treat a variety of arrhythmias.
价 格：￥电议型 号：T7477产 地：中国大陆
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T67864TH1760
TH1760 is an inhibitor of NUDIX-type 15 (NUDT15, IC50= 25 nM). TH1760 can sensitize cells to 6-thioguanine by increasing the accumulation of 6-thio- (d) GTP in nucleic acids. TH1760 can enhance the anti-leukemia effect of thiopurine.
价 格：￥电议型 号：T67864产 地：中国大陆
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T9733PAL-4PAL-4,inhibit,PAL 4,LYPLAL1,Lysophospholipase-like 1,Metabolic disorders,Inhibitor,PAL4,1H1,2,4
PAL-4 stimulates the activity of LYPLAL1, a poorly characterized serine hydrolase with complex genetic links to human metabolic traits.
价 格：￥电议型 号：T9733产 地：中国大陆
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T5209INH14
INH14 is a novel inhibitor of the IKKα/β-dependent TLR inflammatory response (IC50s: 8.97/3.59 μM for IKKα/IKKβ).
价 格：￥电议型 号：T5209产 地：中国大陆
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T4138UCPH-101UCPH 101；UCPH101
UCPH-101 is an inhibitor of excitatory amino acid transporter subtype 1 (EAAT1) with an IC50 of 0.66 μM.
价 格：￥电议型 号：T4138产 地：中国大陆
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T3793(20R)-Ginsenoside Rh120(R)-Ginsenoside Rh1；人参皂苷 R-RH1；人参皂苷R-RH1
20S, 20R ginsenoside-Rh1 can inhibit the thrombin-induced conversion of fibrinogen to fibrin.
价 格：￥电议型 号：T3793产 地：中国大陆
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T3556NIH-12848NIH12848；NIH 12848
NIH-12848 is a putative inhibitor of phosphatidylinositol 5-phosphate 4-kinase γ (PI5P4Kγ) with an IC50 of 1 μM.
价 格：￥电议型 号：T3556产 地：中国大陆
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T2932Ginsenoside Rh1人参皂苷 Rh1；人参皂苷Rh1；Sanchinoside B2；Prosapogenin A2；Sanchinoside Rh1；20(S)-Ginsenoside R
Ginsenoside Rg1, one of the main constituents of Panax ginseng, exhibits anti-inflammatory effect.
价 格：￥电议型 号：T2932产 地：中国大陆
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T2502INH1IBT13131
INH1 is a cell-permeable Hec1 inhibitor that specifically disrupts the Hec1/Nek2 interaction.
价 格：￥电议型 号：T2502产 地：中国大陆
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T2451GlyH-101GlyH 101；GlyH101
GlyH-101 is a cell-permeable glycinyl hydrazone compound that blocks CFTR with Ki of 1.4 uM.
价 格：￥电议型 号：T2451产 地：中国大陆
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T2405Revaprazan hydrochloride盐酸瑞伐拉赞；YH1885
Revaprazan Hydrochloride is the hydrochloride salt form of a lipophilic, weak base with potassium-competitive acid blocking (P-CAB) activity.
价 格：￥电议型 号：T2405产 地：中国大陆
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T2355CFTR(inh)-172CFTR Inhibitor-172；CFTRinh172；CFTRinh-172；CFTRinh 172
CFTRinh-172 is a voltage-independent, selective CFTR inhibitor.
价 格：￥电议型 号：T2355产 地：中国大陆
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T2102FH1BRD-K4477；NSC 12407
FH1 (BRD-K4477), a small molecule, enhances the functions of hepatocytes and promotes differentiation hepatocytes derived by iPS.
价 格：￥电议型 号：T2102产 地：中国大陆
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