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T17070Thiamethoxam；噻虫嗪Actara 25WG|||Adage 5FS|||(E)-thiamethoxam；噻虫嗪|||Actara 25WG|||Adage 5FS|||(E)-thiam
Thiamethoxam ((E)-thiamethoxam) is an insecticide of broad-spectrum neonicotinoids.
价 格：￥电议型 号：T17070产 地：中国大陆
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T17044Tesaglitazar；替格列扎Tesaglitazar
Tesaglitazar is a potent and selective peroxide PPARα / γ receptor dual agonist with a more potent affinity for PPARγ than PPARα, The EC50 values for rat PPARα and human PPARα were 13.4 μM and 3.6 μM, respectively, and 0.2 μM for rat PPARγ and human PPARγ. Tesaglitazar induced DNA synthesis and fibrosarcoma formation in rat subcutaneous mesenchymal cells.
价 格：￥电议型 号：T17044产 地：中国大陆
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T17005FPR Agonist 43；FPR激动剂43FPR Agonist 43
FPR Agonist 43 is a dual agonist of formyl peptide receptor 1 and formyl peptide receptor 2 (FPR2)/ALX.
价 格：￥电议型 号：T17005产 地：中国大陆
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T16988Taprenepag isopropyl；化合物 T16988PF-04217329；PF-04217329
Taprenepag isopropyl is a highly selective agonist of the EP2 receptor.
价 格：￥电议型 号：T16988产 地：中国大陆
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T16883Sigma-2 receptor antagonist 1；化合物 T16883Sigma-2 receptor antagonist 1
Sigma-2 receptor antagonist 1 is an antagonist of the sigma-2 (σ-2) receptor.
价 格：￥电议型 号：T16883产 地：中国大陆
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T16833S1P1 Agonist III；化合物 T16833S1P1 Agonist III
S1P1 Agonist III is an effective and orally active S1P1 agonist (EC50: 18 nM).
价 格：￥电议型 号：T16833产 地：中国大陆
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T16809Rupintrivir芦平曲韦AG-7088|||AG7088|||Rupintrivirvr
Rupintrivirvr (AG7088) is a selective rhinovirus (HRV) 3C cysteine protease mimetic peptide inhibitor with antiviral and immunomodulatory activities.Rupintrivirvr inhibits the replication of EV71 and EV-D68, and may be useful for the study of viral infections.
价 格：￥电议型 号：T16809产 地：中国大陆
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T1674Nateglinide；那格列奈A4166|||Senaglinide；那格列奈|||A4166|||Senaglinide
Nateglinide (Senaglinide) is an oral hypoglycemic agent and amino acid derivative that stimulates insulin secretion from the pancreas and is used in the therapy of type 2 diabetes. Nateglinide has been linked to rare instances of clinically apparent acute liver injury.
价 格：￥电议型 号：T1674产 地：中国大陆
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T16720Rafigrelide；化合物 T167203,3-Dimethylanagrelide；3,3-Dimethylanagrelide
Rafigrelide is a platelet-lowering agent.
价 格：￥电议型 号：T16720产 地：中国大陆
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T16683Pumosetrag Hydrochloride化合物 T16683MKC-733|||DDP-733
Pumosetrag Hydrochloride is an orally available 5-HT3 partial agonist. It is developed for the treatment of irritable bowel syndrome and gastroesophageal reflux disease.
价 格：￥电议型 号：T16683产 地：中国大陆
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T16522Phenoxodiol脱氢雌马酚脱氢雌马酚|||Dehydroequol|||Idronoxil|||Haginin E
Phenoxodiol (Idronoxil) activates the mitochondrial caspase system, inhibits X-linked inhibitor of apoptosis(XIAP), disrupts FLICE inhibitory protein(FLIP) expression, and sensitizes the cancer cells to Fas-mediated apoptosis. Phenoxodiol induces cell cycle arrest in the G1/S phase of the cell cycle and upregulates p21WAF1 via a p53 independent manner. Phenoxodiol also inhibits DNA topoisomerase II.
价 格：￥电议型 号：T16522产 地：中国大陆
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T16447β-Amino Acid Imagabalin Hydrochloride；化合物 T16447PD-0332334；PD-0332334
β-Amino Acid Imagabalin Hydrochloride is the voltage-dependent calcium channel ligand for the α2δ subunit.
价 格：￥电议型 号：T16447产 地：中国大陆
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T16389Omidenepag；化合物 T16389Omidenepag
Omidenepag is a pharmacologically active form of Omidenepag Isopropyl and is a selective, non-prostanoid EP2 receptor agonist (EC50: 1.1 nM). Omidenepag displays binding affinities (IC50: 10 nM for h-EP2).
价 格：￥电议型 号：T16389产 地：中国大陆
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T16388Omidenepag isopropyl化合物 T16388Omidenepag isopropyl
Omidenepag isopropyl is converted to the active product Omidenepag during corneal penetration. Omidenepag isopropyl is a selective EP2 receptor agonist. Omidenepag isopropyl displays only a weak affinity for EP1, EP2, and FP receptors. Omidenepag isopropyl is under development for the treatment of glaucoma as intraocular pressure (IOP)-lowering drug.
价 格：￥电议型 号：T16388产 地：中国大陆
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T16273Napsagatran hydrate；化合物 T16273Ro 46-6240/010 hydrate|||Ro 46-6240 hydrate；Ro 46-6240/010 hydrate|||R
Napsagatran hydrate is a novel and specific inhibitor of thrombin.
价 格：￥电议型 号：T16273产 地：中国大陆
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T16264Nagilactone B；竹柏内酯 BNagilactone B
Nagilactone B is extracted from the root bark of Podocarpus nagi and it also is a liver X receptor (LXR) agonist.
价 格：￥电议型 号：T16264产 地：中国大陆
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T1626Prostaglandin E1；前列地尔PGE1|||Alprostadil；前列地尔|||PGE1|||列腺素E1|||Alprostadil
Prostaglandin E1 (Alprostadil) is the naturally occurring prostaglandin E1 (PGE1) which displays a variety of pharmacologic actions. Prostaglandin E1 is a potent vasodilator agent that increases peripheral blood flow, inhibits platelet aggregation, and induces bronchodilation. Used in the treatment of erectile dysfunction, this agent produces corporal smooth muscle relaxation by binding to PGE receptors, resulting in the activation of adenylate cyclase and the subsequent accumulation of 3´
价 格：￥电议型 号：T1626产 地：中国大陆
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T16106ML224；化合物ML224NCGC00242364|||ANTAG3；NCGC00242364|||ANTAG3
ML224 (NCGC00242364) is a TSHR antagonist for the treatment of Graves´ orbital disease and Graves´ hyperthyroidism.
价 格：￥电议型 号：T16106产 地：中国大陆
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T16093Telcagepant化合物 T16093MK-0974
Telcagepant is an orally active antagonist of calcitonin gene-related peptide (CGRP) receptor (Kis: 0.77 nM and 1.2 nM for human and rhesus CGRP receptors, respectively).
价 格：￥电议型 号：T16093产 地：中国大陆
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T16083Mizagliflozin；化合物MizagliflozinGSK-1614235 free base|||KGA-3235 free base|||DSP-3235 free base；GSK-16
Mizagliflozin (GSK-1614235 free base) is a sodium-glucose transporter inhibitor( Ki of 27 nM for human SGLT1). Mizagliflozin displays 303-fold selectivity over SGLT2. Mizagliflozin is used as an antidiabetic drug that can modify postprandial blood glucose excursion. Mizagliflozin also exhibits potential in the amelioration of chronic constipation.
价 格：￥电议型 号：T16083产 地：中国大陆
