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T8678NaphthazarinNaturally,Apoptosis,Naphthazarin,stress,microtubules,mitochondrial,AIF,Inhibitor,p21,lys
Naphthazarin is effective by various cellular mechanisms including oxidative stress, activation of mitochondrial apoptosis-inducing factor (AIF), depolymerization of microtubules, interference with lysosomal function and p53-dependent p21 activation. It triggers apoptosis and has anti-tumor effects
价 格：￥电议型 号：T8678产 地：中国大陆
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TN11661,3,6-Tri-O-galloyl-beta-D-glucoseinhibit,Inhibitor,1,3,6TriOgalloylbetaDglucose,1,3,6 Tri O galloyl
1,3,6-Tri-O-galloyl-beta-D-glucose is a phenolic compound in Black Walnut Kernels. It shows anti-inflammatory activity.
价 格：￥电议型 号：TN1166产 地：中国大陆
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TN1969N-(p-Coumaroyl) serotoninVSMC,PDGFR,aortic wall,N (p Coumaroyl) serotonin,inhibit,anti-inflammatory,
N-(p-Coumaroyl) Serotonin is a polyphenol isolated from the seeds of safflower. N-(p-Coumaroyl) serotonin has antioxidant, cardioprotective effects after ischemia and antitumor activity, it may be beneficial in improving vascular distensibility and in reducing cardiovascular risk.N-(p-Coumaroyl) Serotonin ameliorates atherosclerosis and distensibility of the aortic wall in vivo and is usually used for the atherosclerosis research
价 格：￥电议型 号：TN1969产 地：中国大陆
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T21818Pregnenolone CarbonitrileCYPs,Cytochrome P450,P4503A,orally,Pregnenolone Carbonitrile,Pregnenolone 1
Pregnenolone Carbonitrile is an activator of rodent-PXR and induces the expression of CYP3A.
价 格：￥电议型 号：T21818产 地：中国大陆
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T7831NitecaponeGSH,Nitecapone,glutathione,OR-462,Inhibitor,ROS,Parkinson,COMT,OR 462,inhibit,OR462,allody
Nitecapone is a reversible inhibitor of S-COMT (IC50 values of 300 nM in rat liver)
价 格：￥电议型 号：T7831产 地：中国大陆
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T9346CVN424penetrant,CVN 424,GPR6,inhibit,orally,CVN424,brain,Inhibitor,Parkinson,CVN-424,disease
CVN424 is a selective and novel GPR6 Inverse agonist effective in models of Parkinson Disease.
价 格：￥电议型 号：T9346产 地：中国大陆
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TP1658LType A Allatostatin I acetateType A Allatostatin I acetate
Type A Allatostatin I acetate is a tridecapeptide. Allatostatins are pleiotropic neuropeptides for inhibition of juvenile hormone synthesis in insects.
价 格：￥电议型 号：TP1658L产 地：中国大陆
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T8961GW280264XGW-280264X,inhibit,GIC,Inhibitor,immunotherapy,metalloproteinases,Matrix metalloproteinases
GW280264X is an inhibitor of ADAM17 .
价 格：￥电议型 号：T8961产 地：中国大陆
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T8497SX-682cells,SX-682,allosteric,SX 682,recruitment,suppressor,Inhibitor,tumor,CXCR,CXC chemokine recep
SX-682 is a potent, selective and orally bioavailable inhibitor of CXCR1/2 ,has the potential to treat castration-resistant prostate cancer.
价 格：￥电议型 号：T8497产 地：中国大陆
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T9214ELOVL6-IN-1ELOVL6IN1,noncompetitive,orally,palmitoyl-CoA,potent,malonyl-CoA,ELOVL-6-IN-1,Inhibitor,s
ELOVL6-IN-1 is a potent, orally active and selective ELOVL6 inhibitor. ELOVL6-IN-1 dose-dependently inhibits mouse ELOVL6 activities, with an IC50 value of 0.350 μM. ELOVL6-IN-1 inhibits ELOVL6 in a noncompetitive manner for malonyl-CoA (Ki=994 nM) and palmitoyl-CoA[1].
价 格：￥电议型 号：T9214产 地：中国大陆
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T7522GI254023XSRI 028594,SRI028594,GI 4023,inhibit,GI-254023X,Matrix metalloproteinases,SRI-028594,Inhibi
GI254023X is a potent MMP9 and ADAM10 inhibitor (IC50s: 2.5 and 5.3 nM) with 100-fold selectivity for the α-secretase ADAM10 over ADAM17 (TACE). GI254023X can remarkably inhibit the proliferation and induce the apoptosis of H929 cells. Its mechanism may be associated with inbihition of Notch1 activation.
价 格：￥电议型 号：T7522产 地：中国大陆
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T21747VU0483605Inhibitor,inhibit,VU0483605,Metabotropic glutamate receptors,allosteric modulator,brain pen
VU0483605 is an effective and selective positive allosteric modulator of mGluR1 with EC50s of 390 and 356 nM for human and rat, respectively.
价 格：￥电议型 号：T21747产 地：中国大陆
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T8310MMP-9-IN-1PEX,anti-metastatic,metastasis,MMP,Matrix metalloproteinases,tumor,MMP 9 IN 1,inhibit,MMP9
MMP-9-IN-1 is an inhibitor of specific matrix metalloproteinase-9 (MMP-9).
价 格：￥电议型 号：T8310产 地：中国大陆
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T8235L-732138cytotoxicity,vagally-induced,NK receptor,Neurokinin Receptor,Inhibitor,ntravenously,lipopoly
L-732138 is a potent and competitive antagonist of neurokinin-1 (NK-1) receptor(IC50 : 2.3 nM)
价 格：￥电议型 号：T8235产 地：中国大陆
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T6710Troxipidefactor,Inhibitor,gastritis,Troxipide,inhibit,orally,defensive,ulcer,antiulcer,gastric
Troxipide, a new-type systemic non-antisecretory gastric cytoprotective agent, which is mucus-secreting, anti-ulcer, and anti-inflammatory properties irrespective of pH of stomach or duodenum.
价 格：￥电议型 号：T6710产 地：中国大陆
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T6636RefametinibMEK1,allosteric,RDEA 119,BAY-869766,inhibit,Inhibitor,MAP2K,MEK2,orally,MAPKK,RDEA-119,Mi
Refametinib (RDEA119, Bay 86-9766) is an effective, ATP non-competitive and specific inhibitor of MEK1/2 (IC50: 19/47 nM).
价 格：￥电议型 号：T6636产 地：中国大陆
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T8348Phentolamineerectile dysfunction,inhibit,Adrenergic Receptor,orally active,insulin secretion,Phentol
Phentolamine mesylate is an alpha-1 and alpha-2 selective adrenergic receptor antagonist
价 格：￥电议型 号：T8348产 地：中国大陆
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T6595Moexipril hydrochlorideorally active,Apoptosis,Ischemic brain injury,inhibit,hepatic disease,RS10085
Moexipril HCl is a potent orally active nonsulfhydrylangiotensin converting enzyme (ACE)inhibitor, used for the treatment of hypertension and congestive heart failure.
价 格：￥电议型 号：T6595产 地：中国大陆
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T8581Flecainide hydrochlorideNa channels,fetal tachycardias,Potassium Channel,orally active,Inhibitor,Sod
Flecainide is a medication used to prevent and treat abnormally fast heart rates. This includes ventricular and supraventricular tachycardias.
价 格：￥电议型 号：T8581产 地：中国大陆
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T6376Allopurinol Sodiumanti-nociception,HIF-2α,inhibit,anti-leishmanial,gout,hyperuricemia,HIF-1α,HUVEC c
Allopurinol Sodium is a xanthine oxidase inhibitor with an IC50 of 7.82±0.12 μM.
价 格：￥电议型 号：T6376产 地：中国大陆
