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T1542Pirenzepine dihydrochloridePirenzepine dihydrochloride,LS519,Tabe
Pirenzepine dihydrochloride is a selective M1 muscarinic receptor antagonist, inhibiting gastric secretion.
价 格：￥电议型 号：T1542产 地：美洲
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T15422GSK-626616GSK-626616
GSK-626616 is a potent and orally bioavailable DYRK3 inhibitor (IC50=0.7 nM). GSK-626616 inhibits other members of the DYRK family with similar potency. It is a potential therapy for the treatment of anemia.
价 格：￥电议型 号：T15422产 地：美洲
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T15424GSK1379725AGSK1379725A
GSK1379725A is a selective BPTF ligand (Kd: 2.8 uM). It also showing no binding activity for Brd4.
价 格：￥电议型 号：T15424产 地：美洲
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T15425GSK1702934AGSK1702934A
GSK1702934A modulates cardiac contractility and f arrhythmogenesis by activation of TRPC3. GSK1702934A is a selective agonist of TRPC3.
价 格：￥电议型 号：T15425产 地：美洲
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T15427GSK2033GSK2033
GSK2033 is an antagonist of LXR (pIC50s: 7 and 7.4 for LXRα or LXRβ, respectively).
价 格：￥电议型 号：T15427产 地：美洲
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T15429GSK2194069GSK2194069
GSK2194069 is a potent and specific inhibitor of the β-ketoacyl reductase (KR) activity of hFAS (IC50: 7.7 ± 4.1 nM in an assay detecting released CoA). It is also hFAS inhibitor.
价 格：￥电议型 号：T15429产 地：美洲
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T1543Naftifine hydrochlorideNaftifine hydrochloride,Naftifine HCl,Naftin
Naftifine Hydrochloride is the hydrochloride salt form of naftifine, an allylamine derivate with synthetic broad-spectrum antifungal activity. Although the exact mechanism through which naftifine hydrochloride exerts its effect is unknown, it appears to s
价 格：￥电议型 号：T1543产 地：美洲
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T15430GSK2256294AGSK2256294A,GSK 2256294,
GSK2256294A is a potent, reversible, tight binding inhibitor of isolated recombinant human sEH (soluble epoxide hydrolase) (IC50 = 27 pM; t1/2 = 121 min) and displays potent inhibition against the rat (IC50 = 61 pM) and murine (IC50 = 189 pM) orthologs of
价 格：￥电议型 号：T15430产 地：美洲
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T15431NemiralisibNemiralisib,GSK2269557 (free base),
Nemiralisib is a potent and highly selective inhibitor of PI3Kδ (pKi: 9.9).
价 格：￥电议型 号：T15431产 地：美洲
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T15433GSK2795039GSK2795039
GSK2795039 inhibits reactive oxygen species (ROS) production and NADPH consumption. GSK2795039 decreases apoptosis. GSK2795039 is an inhibitor of NADPH oxidase 2 (NOX2) (a mean pIC50: 6 in different cell-free assays).
价 格：￥电议型 号：T15433产 地：美洲
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T15434GSK2798745GSK2798745
GSK2798745 is used in research for the treatment of pulmonary edema associated with congestive heart failure. GSK2798745 is a selective and orally active transient receptor potential vanilloid 4 (TRPV4) ion channel blocker (IC50s of 1.8 and 1.6 nM for hTR
价 格：￥电议型 号：T15434产 地：美洲
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T15435GSK2837808AGSK2837808A
GSK2837808A is a potent and selective inhibitor of lactate dehydrogenase A (LDHA) (IC50s: 1.9 and 14 nM for LDHA and LDHB, respectively).
价 格：￥电议型 号：T15435产 地：美洲
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T15436GSK2838232GSK2838232
GSK2838232 inhibits HIV reverse transcriptase activity that a broad panel of HIV-1 isolates.
价 格：￥电议型 号：T15436产 地：美洲
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T15437GSK3145095GSK3145095
GSK3145095 is an inhibitor of RIP1 kinase (IC50: 6.3 nM).
价 格：￥电议型 号：T15437产 地：美洲
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T1546NitazoxanideNitazoxanide,NSC 697855,
Nitazoxanide is a synthetic benzamide with antiprotozoal activity. Nitazoxanide exerts its antiprotozoal activity by interfering with the pyruvate ferredoxin/flavodoxin oxidoreductase dependent electron transfer reaction.
价 格：￥电议型 号：T1546产 地：美洲
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T15460Halofantrine hydrochlorideHalofantrine hydrochloride,SKF-102886,WR-171669
Halofantrine hydrochloride is a blocker of delayed rectifier potassium current. Halofantrine hydrochloride also via the inhibition of the human-ether-a-go-go-related gene (HERG) channel and a potent antimalarial agent.
价 格：￥电议型 号：T15460产 地：美洲
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T15461HalopemideHalopemide
Halopemid is a dopamine receptors antagonist. Halopemide is an effective inhibitor of phospholipase D (PLD) (IC50s: 220 and 310 nM for human PLD1 and PLD2, respectively). It acts as a psychotropic agent.
价 格：￥电议型 号：T15461产 地：美洲
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T15462HaloxonHaloxon
Haloxon is an organophosphorus anthelmintic. Haloxon is used against nematodes of the abomasum and small intestine in ruminants..
价 格：￥电议型 号：T15462产 地：美洲
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T15464HBX 19818HBX 19818
HBX 19818 is a specific ubiquitin-specific protease 7 (USP7) inhibitor (IC50: 28.1 μM).
价 格：￥电议型 号：T15464产 地：美洲
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T15465HC-070HC-070
HC-070 is a TRPC4/TRPC5 antagonist (IC50s of 9.3 nM and 46 nM for hTRPC5 and hTRPC4 in cells, respectively).
价 格：￥电议型 号：T15465产 地：美洲
