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T15812LY2979165；化合物LY2979165mGlu2 agonist；mGlu2 agonist
LY2979165 (mGlu2 agonist) is an orthosteric agonist of mGluR2 and can be used in studies about serving as an anti-depressant.
价 格：￥电议型 号：T15812产 地：中国大陆
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T15791LUF6000；化合物 T15791LUF6000
LUF6000 is an allosteric modulator of the human A3 adenosine receptor (AR).
价 格：￥电议型 号：T15791产 地：中国大陆
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T1574LEtoricoxib HCl；化合物 T1574LL-791456 monohydrochloride salt|||L791456 hydrochloride|||L-791456 hydrochl
Etoricoxib HCl is a synthetic, nonsteroidal anti-inflammatory drug. Etoricoxib specifically binds to and inhibits the enzyme cyclooxygenase-2, resulting in inhibition of the conversion of arachidonic acid into prostaglandins.
价 格：￥电议型 号：T1574L产 地：中国大陆
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T1574Etoricoxib；依托考昔Arcoxia|||MK-663|||Tauxib|||L-791456|||Nucoxia|||Desvenlafaxine；Arcoxia|||MK-663|||Ta
Etoricoxib (MK-663) is a synthetic, nonsteroidal anti-inflammatory drug (NSAID) with antipyretic, analgesic, and potential antineoplastic properties. Etoricoxib specifically binds to and inhibits the enzyme cyclooxygenase-2 (COX-2), resulting in inhibition of the conversion of arachidonic acid into prostaglandins. Inhibition of COX-2 may induce apoptosis and inhibit tumor cell proliferation and angiogenesis.
价 格：￥电议型 号：T1574产 地：中国大陆
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T15729LDN-91946；化合物LDN-91946LDN-91946
LDN-91946 is an effective and selective inhibitor of ubiquitin C-terminal hydrolase-L1 (UCH-L1) (Ki = 2.8 μM).
价 格：￥电议型 号：T15729产 地：中国大陆
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T15710Lapaquistat；化合物 T15710T-91485；T-91485
Lapaquistat is a cholesterol biosynthesis inhibitor and is the active metabolite of TAK-475. Lapaquistat can reduce statin-induced myotoxicity in lipid-lowering therapy.
价 格：￥电议型 号：T15710产 地：中国大陆
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T15675Tirbanibulin Mesylate；化合物Tirbanibulin MesylateKX2-391 Mesylate|||KX01 Mesylate；KX2-391 Mesylate|||KX
Tirbanibulin Mesylate (KX01 Mesylate) is an inhibitor of Src that targets the peptide substrate site of Src (GI50: 9-60 nM in cancer cell lines).
价 格：￥电议型 号：T15675产 地：中国大陆
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T15674Tirbanibulin dihydrochloride化合物 T15674KX-01 (dihydrochloride)|||KX2-391 (dihydrochloride)
Tirbanibulin is an inhibitor of Src that targets the peptide substrate site of Src (GI50: 9-60 nM in cancer cell lines).
价 格：￥电议型 号：T15674产 地：中国大陆
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T15654Ketohexokinase inhibitor 1；化合物Ketohexokinase inhibitor 1PF-06835919；PF-06835919
Ketohexokinase inhibitor 1 is a ketohexokinase inhibitor (IC50s: 8.4 nM and 66 nM for KHK-C and KHK-A, respectively).
价 格：￥电议型 号：T15654产 地：中国大陆
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T15624JNJ-64619178；化合物JNJ-64619178JNJ-64619178
JNJ-64619178 is a selective, orally active, and pseudo-irreversible inhibitor of protein arginine methyltransferase 5 (IC50: 0.14 nM). It has effective activity In lung cancer.
价 格：￥电议型 号：T15624产 地：中国大陆
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T15591Ipenoxazone；伊培沙宗NC-1200|||MLV-6976；NC-1200|||MLV-6976|||伊培沙宗
Ipenoxazone is an effective and centrally acting muscle relaxant.
价 格：￥电议型 号：T15591产 地：中国大陆
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T15565Imetit dihydrobromide化合物 T15565VUF 8325 dihydrobromide|||SKF 91105 dihydrobromide
Imetit dihydrobromide is a high affinity and effective agonist of histamine H3 and H4 receptors (Ki: 0.3 and 2.7 nM). Imetit mimics the histamine effect in triggering a shape change in eosinophils (EC50: 25 nM).
价 格：￥电议型 号：T15565产 地：中国大陆
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T1551Tegaserod maleate；马来酸替加色罗HTF-919|||SDZ-HTF-919；HTF-919|||马来酸替加色罗|||SDZ-HTF-919
Tegaserod maleate (SDZ-HTF-919) is a 5-HT4 agonist manufactured by Novartis and used for the management of irritable bowel syndrome and constipation. Its use was the only drug approved by the United States Food and Drug Administration to help relieve the abdominal discomfort, bloating and constipation associated with irritable bowel syndrome. On March 30, 2007, the U.S. Food and Drug Administration requested that Novartis withdraw Zelnorm from shelves. The FDA alleges a relationship between pres
价 格：￥电议型 号：T1551产 地：中国大陆
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T15491HO-PEG17-OH；化合物 T15491HO-PEG17-OH
HO-PEG17-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15491产 地：中国大陆
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T15391Glufosinate ammonium；草铵膦Glufosinate ammonium
Glufosinate ammonium is a phosphinic acid analogue of glutamic acid and is an herbicide. Glufosinate ammonium is converted by plant cells into PT (L-phosphinothricin). Glufosinate ammonium has neurotoxic activity.
价 格：￥电议型 号：T15391产 地：中国大陆
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T15291Fluorescein-PEG3-amine；化合物 T15291Fluorescein-PEG3-amine
Fluorescein-PEG3-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15291产 地：中国大陆
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T15191PROTAC ERRα ligand 1；化合物PROTAC ERRα ligand 1PROTAC ERRα ligand 1
PROTAC ERRα ligand 1 is an α (ERRα) antagonist of estrogen-related receptor (IC50s of 0.04 and 2.8 μM for ERRα and ERRγ, respectively).
价 格：￥电议型 号：T15191产 地：中国大陆
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T15091Decoyinine；德夸菌素Decynylene|||Angustmycin A；Decynylene|||Angustmycin A
Decoyinine (Decynylene), a selective inhibitor of GMP synthase, is a novel potential microbial insecticide, a secondary metabolite produced by Streptomyces hygroscopicus.Decoyinine induces resistance in rice to the small brown ladybug Laodelphax striatellus.
价 格：￥电议型 号：T15091产 地：中国大陆
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T15050Danicamtiv；化合物DanicamtivMYK-491|||SAR 440181；MYK-491|||SAR 440181
Danicamtiv (MYK-491) is an inotropic agent and it also is a selective allosteric activator of cardiac myosin. Danicamtiv increases cardiac systolic function and preserves mechanical efficiency.
价 格：￥电议型 号：T15050产 地：中国大陆
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T15018CUDC-427；化合物CUDC-427GDC-0917；GDC-0917
CUDC-427 (GDC-0917) is an orally bioactive and pan antagonist of inhibitor of apoptosis proteins(IAPs). CUDC-427 can be used in research on cancers.
价 格：￥电议型 号：T15018产 地：中国大陆
