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T6951Pramipexole dihydrochloride hydratetransient,Pramipexole dihydrochloride,Pramipexole dihydrochloride
Pramipexole Dihydrochloride is the hydrochloride salt of pramipexole, a benzothiazole derivative. As a nonergot dopamine agonist, pramipexole binds to D2 and D3 dopamine receptors in the striatum and substantia nigra of the brain.
价 格：￥电议型 号：T6951产 地：中国大陆
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T8471VonafexorNR1H4,HBV,FXR,EYP 001,Inhibitor,Vonafexor,EYP-001,inhibit,Hepatitis B virus
Vonafexor is a farnesoid X receptor (FXR, NR1H4) agonist, with anti-HBV effects
价 格：￥电议型 号：T8471产 地：中国大陆
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T7436CilofexorGS9674,Inhibitor,inhibit,NR1H4,FXR,Cilofexor,PSC,GS 9674,oral,NASH,GS-9674,antifibrotic,non
Cilofexor inhibits binding of a synthetic peptide, Cilofexor is a farnesoid X receptor (FXR) agonist.
价 格：￥电议型 号：T7436产 地：中国大陆
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T9200Exo-1Exo 1,Exo1
Methyl 3-(4-fluorobenzoyl)-6-methyl-2-pyridinecarboxylate is a chemical compound.
价 格：￥电议型 号：T9200产 地：中国大陆
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T6456CRT0044876non-toxic,DNA,Inhibitor,base,exonuclease,inhibit,CRT0044876,endonuclease,DNA/RNA Synthesis
CRT0044876 is a potent and selective APE1 inhibitor with IC50 of ~3 μM.
价 格：￥电议型 号：T6456产 地：中国大陆
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T15826Lometrexol
Lometrexol, an antipurine Antifolate, can inhibit the activity of glycinamide ribonucleotide formyltransferase (GARFT) but do not induce detectable levels of DNA strand breaks. Lometrexol can further inhibit de novo purine synthesis, causing abnormal cell proliferation and Apoptosis, even cell cycle arrest. Lometrexol has anticancer activity. Lometrexol also is a potent human Serine hydroxymethyltransferase1/2 (hSHMT1/2) inhibitor.
价 格：￥电议型 号：T15826产 地：中国大陆
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TQ0055AMG-3969Hexokinase IV,AMG 3969,Hexokinase D,Glucokinase,Inhibitor,AMG3969,AMG-3969,inhibit
AMG-3969 is an effective glucokinase-glucokinase regulatory protein interaction (GK-GKRP) disruptor (IC50: 4 nM).
价 格：￥电议型 号：TQ0055产 地：中国大陆
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T8921M-31850inhibit,M31850,OfHex2,M-31850,β-hexosaminidase,non-carbohydrate,Inhibitor,M 31850
M-31850 is a potent, selective and competitive β-hexosaminidase (Hex) inhibitor(human HexA and human HexB with IC50s of 6.0 μM and 3.1 μM, respectively). IT also competitively inhibits β-N-acetyl-D-hexosaminidase OfHex2 with a Ki of 2.5 μM.
价 格：￥电议型 号：T8921产 地：中国大陆
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T9241o-Cresolphthalein Complexoneo Cresolphthalein Complexone,oCresolphthalein Complexone
o-Cresolphthalein Complexone is a metal complexing indicator and an acid-base indicator.
价 格：￥电议型 号：T9241产 地：中国大陆
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T7886Nidufexorinhibit,Inhibitor,Autophagy,NR1H4,FXR,Nidufexor,LMB-763,LMB763,LMB 763
Nidufexor is an agonist for the farnesoid X receptor (FXR).
价 格：￥电议型 号：T7886产 地：中国大陆
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TP1832Gluten Exorphin Cinhibit,Gluten Exorphin C,Inhibitor,Opioid Receptor
Gluten exorphin C is an opioid peptide derived from wheat gluten. Its IC50 values are 40 μM and 13.5 μM for μ opioid and δ opioid activities in the GPI and MVD assays, respectively.Gluten Exorphin C, isolated from the pepsin-trypsin-chymotrypsin digest of wheat gluten, was considered as a δ-opioid receptor-selective ligand.
价 格：￥电议型 号：TP1832产 地：中国大陆
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T67422-Deoxy-D-glucoseHSV,Hexokinase,Apoptosis,2 Deoxy D glucose,Herpes simplex virus,inhibit,2DeoxyDgluc
2-Deoxy-D-glucose is an analog of glucose, which is a glycolytic inhibitor with antiviral activity.
价 格：￥电议型 号：T6742产 地：中国大陆
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T2S0504Ilexoside DIlexoside D
Ilexoside D has ant-allergic, and anti-coagulant activities, it shows anti-tissue factor activity as well as the antithrombotic activity.
价 格：￥电议型 号：T2S0504产 地：中国大陆
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T6928Pantoprazolerelease,exosome,orally,Doxorubicin,Autophagy,SKF 96022,Inhibitor,A431,BY-1023,H+/K+-ATPa
Pantoprazole is a proton pump inhibitor used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease.
价 格：￥电议型 号：T6928产 地：中国大陆
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T60043DPTIPextracellular,Inhibitor,exosome,DPTIP,Phospholipase,vesicles,inhibit,N-SMase
DPTIP is an effective inhibitor of neutral sphingomyelinase 2 with an IC50 value of 30 nM.
价 格：￥电议型 号：T60043产 地：中国大陆
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T6123VerdinexorKPT-335
Verdinexor (KPT-335), a specific XPO1/CRM1 inhibitor, are orally bioavailable.
价 格：￥电议型 号：T6123产 地：中国大陆
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T6106Selinexor (KPT-330)Selinexor；KPT-330；塞利尼索
Selinexor (KPT-330) is an orally available, small molecule inhibitor of CRM1 (chromosome region maintenance 1 protein, exportin 1 or XPO1), with potential antineoplastic activity.
价 格：￥电议型 号：T6106产 地：中国大陆
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T6053Turofexorate Isopropyl妥芬异丙酯；FXR-450；XL335；WAY-362450
Turofexorate Isopropyl (XL335) is a potent, selective, and orally bioavailable FXR agonist with EC50 of 4 nM
价 格：￥电议型 号：T6053产 地：中国大陆
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T58823-Bromopyruvic acidBromopyruvic acid；Hexokinase II Inhibitor II, 3-BP；3-溴丙酮酸
3-Bromopyruvic acid is a hexokinase II inhibitor with Ki of 2.4 mM for glycolysis/hexokinase inhibition. It is inhibitor of tumour cell energy metabolism and chemopotentiator of platinum drugs.
价 格：￥电议型 号：T5882产 地：中国大陆
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T57901,1,1,1-Kestohexaose1,1,1,1-Kestohexose；蔗果六糖
1,1,1,1-Kestohexose is a natural product isolated from Poa ampla.
价 格：￥电议型 号：T5790产 地：中国大陆
