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T17487Azido-PEG15-azide；化合物 T17487Azido-PEG15-azide
Azido-PEG15-azide 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：T17487产 地：中国大陆
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T16506PF-4878691；化合物PF-48786913M-852A；3M-852A
PF-4878691 (3M-852A) is an effective and selective Toll-like receptor 7 agonists modelled. It is used to dissociate its antiviral and inflammatory activities.
价 格：￥电议型 号：T16506产 地：中国大陆
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T16487PF-05241328；化合物 T16487PF-05241328
PF-05241328 is an effective and selective inhibitor of human Nav1.7 voltage-dependent sodium channels (IC50: 31 nM).
价 格：￥电议型 号：T16487产 地：中国大陆
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T15487HMR 1556化合物 T15487HMR1556|||HMR 1556|||HMR-1556
HMR 1556 is a chromanol derivative and is an IKs blocker (IC50s of 10.5 nM and 34 nM in canine and guinea pig left ventricular myocytes, respectively).
价 格：￥电议型 号：T15487产 地：中国大陆
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T14879CB 300919；化合物 T14879CB 300919
CB 300919 is a quinazoline-based antitumor agent with high activity in the CH1 human ovarian tumor xenograft and has continuous exposure (96 h) growth inhibition (IC50: 2 nM).
价 格：￥电议型 号：T14879产 地：中国大陆
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T14878CAY10566；化合物CAY10566CAY10566
CAY10566 shows excellent cellular activity in blocking the conversion of saturated long-chain fatty acid-CoAs (LCFA-CoAs) to monounsaturated LCFA-CoAs in HepG2 cells (IC50=7.9 nM or 6.8 nM). CAY10566 is a potent, orally bioavailable and selective stearoyl-CoA desaturase1 (SCD1) inhibitor with IC50s of 4.5 and 26 nM in mouse and human enzymatic assays, respectively..
价 格：￥电议型 号：T14878产 地：中国大陆
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T14877Cauloside C；葳岩仙皂苷 CCauloside C
Cauloside C, a triterpene glycoside isolated from Caulophyllum robustum Max, exerts anti-inflammatory effects through the inhibition of expression of iNOS and proinflammatory cytokines.
价 格：￥电议型 号：T14877产 地：中国大陆
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T14876Carotegrast化合物 T14876Carotegrast
Carotegrast, an orally available α4 integrin receptor inhibitor, has anti-inflammatories activities.
价 格：￥电议型 号：T14876产 地：中国大陆
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T14875Indocyanine green吲哚菁绿Cardiogreen|||IC Green|||Foxgreen|||吲哚菁绿
Indocyanine green (Cardiogreen) is a low toxicic fluorescent agent, is a tricarbocyanine dye,has been widely used in medical diagnostics, such as determining cardiac output, hepatic function, and liver blood flow, and for ophthalmic angiography.
价 格：￥电议型 号：T14875产 地：中国大陆
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T14874Carboxyrhodamine 110-PEG4-alkyne；化合物 T14874Carboxyrhodamine 110-PEG4-alkyne
Carboxyrhodamine 110-PEG4-alkyne is a polyethylene glycol (PEG) derived linker used for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T14874产 地：中国大陆
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T14873Carboxyrhodamine 110-PEG3-Azide；化合物 T14873Carboxyrhodamine 110-PEG3-Azide
Carboxyrhodamine 110-PEG3-Azide is a polyethylene glycol (PEG)-based linker used for the synthesis of Proteolysis Targeting Chimeras (PROTACs) [1].
价 格：￥电议型 号：T14873产 地：中国大陆
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T14872Carboxyamidotriazole；化合物 T14872CAI|||L-651582；CAI|||L-651582
Carboxyamidotriazole is a cytostatic inhibitor of non-voltage-operated calcium channels and calcium channel-mediated signaling pathways. It shows anti-inflammatory, anti-tumor, and antiangiogenic effects.
价 格：￥电议型 号：T14872产 地：中国大陆
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T14871Carboxyamidotriazole Orotate；化合物Carboxyamidotriazole OrotateL-651582 Orotate|||CAI Orotate；L-651582
Carboxyamidotriazole Orotate (L-651582 Orotate) is a cytostatic inhibitor of non-voltage-operated calcium channels and calcium channel-mediated signaling pathways. Carboxyamidotriazole Orotate (L-651582 Orotate) is the orotate salt form of Carboxyamidotriazole (CAI), an orally bioavailable signal transduction inhibitor that in vitro has been shown to possess antileukaemic activities. Carboxyamidotriazole Orotate shows anti-tumor, anti-inflammatory, and antiangiogenic effects.
价 格：￥电议型 号：T14871产 地：中国大陆
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T14870Carboxy-PEG5-sulfonic acid；化合物 T14870Carboxy-PEG5-sulfonic acid
Carboxy-PEG5-sulfonic acid, a PEG-based PROTAC linker, is utilized for the synthesis of PROTACs[1].
价 格：￥电议型 号：T14870产 地：中国大陆
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T1487Fluvastatin sodium；氟伐他汀钠XU 62320 sodium|||XU-62-320|||Fluvastatin sodium salt；XU 62320 sodium|||XU-6
Fluvastatin sodium (Fluvastatin sodium salt), a competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase (HMGCR), is a commonly used cholesterol lowering agent.
价 格：￥电议型 号：T1487产 地：中国大陆
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T14487AZM475271；化合物 T14487M475271；M475271
AZM475271 is a potent and selective inhibitor of Src kinase(IC50 : 5 nM)
价 格：￥电议型 号：T14487产 地：中国大陆
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T134871-Methylhistamine；化合物 T134872-(1-Methyl-1H-imidazol-4-yl)ethan-1-amine；2-(1-Methyl-1H-imidazol-4-yl)
2-(1-Methyl-1H-imidazol-4-yl)ethan-1-amine is a histamine metabolite.
价 格：￥电议型 号：T13487产 地：中国大陆
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T12690Rapacuronium bromide；化合物 T12690Org 9487；Org 9487
Rapacuronium bromide is an allosteric muscarinic acetylcholine receptor (mAChR) modulator.
价 格：￥电议型 号：T12690产 地：中国大陆
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T126487Alpinoid D；化合物 Alpinoid DAlpinoid D
Alpinoid D is a useful organic compound for research related to life sciences and the catalog number is T126487.
价 格：￥电议型 号：T126487产 地：中国大陆
