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T1766Empagliflozin恩格列净BI 10773|||恩格列净
Empagliflozin (BI 10773) is an SGLT-2 inhibitor (IC50=3.1 nM) that is potent and selective, with more than 300-fold selectivity for SGLT-1/4/5/6. Empagliflozin is used for the treatment of type 2 diabetes.
价 格：￥电议型 号：T1766产 地：中国大陆
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T17577Biotin-PEG36-acid；化合物 T17577Biotin-PEG36-acid
Biotin-PEG36-acid 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：T17577产 地：中国大陆
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T1750Pirodavir；吡罗达韦R77975；R77975|||吡罗达韦
Pirodavir (R77975) (R 77975), the prototype of broad-spectrum anti-picornavirus compounds, is a potent human rhinovirus (HRV) capsid-binding inhibitor.
价 格：￥电议型 号：T1750产 地：中国大陆
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T17477Azido-PEG1-CH2COO-Cl；化合物 T17477Azido-PEG1-CH2COO-Cl
Azido-PEG1-CH2COO-Cl (compound 43a) is an alkyl/ether-based PROTAC linker, commonly employed in the synthesis of PROTAC BRD4 Degrader-1[1].
价 格：￥电议型 号：T17477产 地：中国大陆
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T17377Ald-Ph-PEG5-Boc；化合物 T17377Ald-Ph-PEG5-Boc
Ald-Ph-PEG5-Boc 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：T17377产 地：中国大陆
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T17313(+)-SJ733；化合物n(+)-SJ733SJ000557733；SJ000557733
(+)-SJ733 (SJ000557733) is a potent Na+-ATPase PfATP4 inhibitor with antimalarial activity for the study of malaria.
价 格：￥电议型 号：T17313产 地：中国大陆
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T17286Zaurategrast；化合物 T17286CT7758；CT7758
Zaurategrast is an effective and oral-effective inhibitor of the α4-integrin.
价 格：￥电议型 号：T17286产 地：中国大陆
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T17285Zatosetron maleate；扎托司琼马来酸盐LY 277359 maleate；LY 277359 maleate
Zatosetron maleate（LY 277359 maleate） is a potent and selective serotonin 5HT3 receptor antagonist for the study of acute migraine.
价 格：￥电议型 号：T17285产 地：中国大陆
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T17277YS-201；化合物 T17277YS-201
YS-201 is an antagonist of dihydropyridine-type calcium channel.
价 格：￥电议型 号：T17277产 地：中国大陆
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T17197UCL 2077；化合物UCL 2077UCL 2077
UCL 2077 is a subtype-selective blocker of the epilepsy-associated KCNQ channels and it also is a selective slow-afterhyperpolarization channel blocker，with IC50 of 500 nM in hippocampal neurons in culture, having minimal effects on Ca2+ channels, action potentials, input resistance, and the medium afterhyperpolarization.
价 格：￥电议型 号：T17197产 地：中国大陆
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T17177TUG-424；化合物TUG-424TUG424；TUG424
TUG-424 significantly enhances glucose-stimulated insulin secretion at 100 nM. TUG-424 is a potent and selective free fatty acid receptor 1 agonist (EC50: 32 nM).
价 格：￥电议型 号：T17177产 地：中国大陆
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T17157TRAF-STOP inhibitor 6877002；化合物TRAF-STOP抑制剂6877002CD40-TRAF6 inhibitor；CD40-TRAF6 inhibitor
TRAF-STOP inhibitor 6877002 (CD40-TRAF6 inhibitor), is a selective inhibitor of CD40-TRAF6 interaction. TRAF-STOP 6877002 reduces leukocyte recruitment, and reduces macrophage activation; reduces macrophage proliferation in atherosclerotic plaques.
价 格：￥电议型 号：T17157产 地：中国大陆
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T17114Tolrestat；托瑞司他AY-27773；托瑞司他|||AY-27773
Tolrestat (AY-27773) is a potent inhibitor of aldose reductase (IC50 = 35 nM).
价 格：￥电议型 号：T17114产 地：中国大陆
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T17102Tipifarnib (S enantiomer)；化合物Tipifarnib S entiomerTipifarnib S enantiomer|||(S)-(-)-R-115777|||(S)-T
Tipifarnib S enantiomer ((S)-(-)-R-115777) is the S-enantiomer of Tipifarnib. Tipifarnib is a potent and specific farnesyltransferase inhibitor (IC50: 0.6 nM).
价 格：￥电议型 号：T17102产 地：中国大陆
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T17077Thiol-PEG4-acid；化合物 T17077Thiol-PEG4-acid
Thiol-PEG4-acid 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：T17077产 地：中国大陆
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T17034Temarotene；替马罗汀Ro 15-0778；Ro 15-0778
Temarotene (Ro 15-0778) is an orally active and potent small molecule compound that modulates human immune function in vitro.Temarotene may be used in the study of lichen planus.
价 格：￥电议型 号：T17034产 地：中国大陆
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T16990Tarafenacin；化合物 T16990SVT-40776；SVT-40776
Tarafenacin is a highly selective M3 muscarinic receptor antagonist (Ki= 0.19 nM), ~200 fold selectivity over the M2 receptor.
价 格：￥电议型 号：T16990产 地：中国大陆
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T16989Tarafenacin D-tartrate；Tarafenacin D-酒石酸盐SVT-40776 D-tartrate；SVT-40776 D-tartrate
Tarafenacin D-tartrate (SVT-40776 D-tartrate) is a selective and potent muscarinic acetylcholine M3 receptor antagonist used in the study of overactive bladder and bronchial disorders.
价 格：￥电议型 号：T16989产 地：中国大陆
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T16977Talampanel；化合物TalampanelGYKI-53773|||LY-300164；GYKI-53773|||LY-300164
Talampanel (LY-300164) is an orally and selective α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptor antagonist with anti-seizure activity. Talampanel (IVAX) has neuroprotective effects in rodent stroke models.
价 格：￥电议型 号：T16977产 地：中国大陆
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T16877SHP394；化合物 T16877SHP394
SHP394 is an orally efficacious inhibitor of protein tyrosine phosphatase SHP2 (IC50: 23 nM).
价 格：￥电议型 号：T16877产 地：中国大陆
