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T11755KF 13218；化合物 T11755KF 13218
KF 13218 is a selective, potent and long lasting thromboxane B2 (TXB2) synthase inhibitor with an IC50 value of 5.3±1.3 nM.
价 格：￥电议型 号：T11755产 地：中国大陆
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T1175217-BFC；7-苄氧基-4-三氟甲基香豆素7-Benzyloxy-4-(trifluoromethyl)coumarin|||Y040-0031；7-Benzyloxy-4-(trifluoromet
7-BFC (7-Benzyloxy-4-(trifluoromethyl)coumarin) is a coumarin-like fluorescent substrate that serves as a biomarker for cytochrome P 450 and can be used to study CYP isoforms and cytochrome P 450 metabolism.
价 格：￥电议型 号：T117521产 地：中国大陆
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T11721LJDTic dihydrochloride；化合物 T11721LJDTic dihydrochloride
JDTic is a powerful antagonist of kappa-opioid receptors (KOR), effectively inhibiting the antinociceptive effects induced by the κ-agonist U50, 488.
价 格：￥电议型 号：T11721L产 地：中国大陆
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T11700J-2156；化合物 T11700J-2156
The ED50 of J-2156 in rats for the relief of mechanical allodynia and mechanical hyperalgesia in the ipsilateral hindpaws was 3.7 and 8.0 mg/kg, respectively. J-2156 is a high potent, selective somatostatin receptor type 4 (SST4 receptor) agonist with IC50s of 0.05 nM and 0.07 nM for human and rat SST4 receptors, respectively.
价 格：￥电议型 号：T11700产 地：中国大陆
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T1169Moguisteine莫吉司坦莫吉司坦|||BBR-2173
Moguisteine (BBR-2173) is a new-type peripheral non-narcotic antitussive drug.
价 格：￥电议型 号：T1169产 地：中国大陆
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T11689ITI-214；化合物ITI214ITI214；ITI214
ITI-214 is a picomolar PDE1 inhibitor with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters, and ion channels, exhibits potent PDE1 inhibitory activity (Ki = 58 pM).
价 格：￥电议型 号：T11689产 地：中国大陆
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T11688ITI-214 free base；化合物 T11688ITI214 free base；ITI214 free base
ITI-214 free base is a picomolar PDE1 inhibitor with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters, and ion channels, exhibits potent PDE1 inhibitory activity (Ki = 58 pM).
价 格：￥电议型 号：T11688产 地：中国大陆
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T11677Irindalone；化合物 T11677Lu 21-?098；Lu 21-?098
IrindaloneIrindalone is a potent serotonin (5-HT2) antagonist.
价 格：￥电议型 号：T11677产 地：中国大陆
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T11621IDO-IN-8；化合物 T11621NLG-1487；NLG-1487
IDO-IN-8 is an indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 1-10 μM).
价 格：￥电议型 号：T11621产 地：中国大陆
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T1162Acipimox；阿昔莫司Olbemox|||K-9321；Olbemox|||K-9321|||阿西莫司|||阿昔莫司
Acipimox (K-9321) is a niacin derivative and nicotinic acid analog with activity as a hypolipidemic agent. Acipimox has special application for the treatment of hyperlipidemia in non-insulin-dependent diabetic patients.
价 格：￥电议型 号：T1162产 地：中国大陆
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T1161Prothionamide；丙硫异烟胺1321-TH|||Protionamide；1321-TH|||Protionamide|||丙硫异烟胺
Prothionamide (1321-TH)is a thioamide derivative with antitubercular activity.
价 格：￥电议型 号：T1161产 地：中国大陆
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T1159Leflunomide来氟米特SU101|||RS-34821|||HWA486|||来氟米特
Leflunomide (HWA486) is an immunomodulatory agent used in the therapy of rheumatoid arthritis and psoriatic arthritis.
价 格：￥电议型 号：T1159产 地：中国大陆
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T11553LHeptamidine；化合物 T11553LSBi4211；SBi4211
Heptamidine is an effective Pentamidine-related inhibitor of the calcium-binding protein S100B (Kd: 6.9 μM). It selectively kills melanoma cells with S100B over those without S100B. It is a useful tool for the investigation of Myotonic dystrophy.
价 格：￥电议型 号：T11553L产 地：中国大陆
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T11553Heptamidine dimethanesulfonate；化合物Heptamidine dimethanesulfonateSBi4211 dimethanesulfonate；SBi4211 d
Heptamidine dimethanesulfonate (SBi4211 dimethanesulfonate) serves as a potent inhibitor related to Pentamidine, targeting the calcium-binding protein S100B with a dissociation constant (Kd) of 6.9 ?M. It demonstrates specificity by preferentially killing melanoma cells overexpressing S100B compared to cells lacking this protein. Additionally, Heptamidine is employed as a valuable research tool in the study of Myotonic dystrophy (DM).
价 格：￥电议型 号：T11553产 地：中国大陆
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T11521GW 766994；化合物 T11521GW 994；GW 994
GW 766994 is a specific and oral chemokine receptor-3 (CCR3) antagonist. It has the potential for asthma and eosinophilic bronchitis treatment.
价 格：￥电议型 号：T11521产 地：中国大陆
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T11487LFiboflapon sodium；化合物 T11487LGSK2190915 sodium salt|||AM-803 sodium；GSK2190915 sodium salt|||AM-803
Fiboflapon sodium (GSK2190915) is an orally bioavailable 5-lipoxygenase-activating protein (FLAP) inhibitor with a potency of 2.9 nM in FLAP binding, an IC50 of 76 nM for inhibition of LTB4 in human blood.
价 格：￥电议型 号：T11487L产 地：中国大陆
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T11487Fiboflapon；化合物FiboflaponGSK2190915|||AM-803；GSK2190915|||AM-803
Fiboflapon (GSK2190915) is an orally available and effective 5-lipoxygenase-activating protein (FLAP) inhibitor that binds FLAP with a titer of 2.9 nM and inhibition of LTB4 in human blood with an IC50 of 76 nM.
价 格：￥电议型 号：T11487产 地：中国大陆
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T11479GSK1521498；化合物 T11479GSK1521498
GSK1521498 is a selective antagonist of the μ-opioid receptor (MOR). It is being used for the treatment of disorders of compulsive consumption of food, alcohol, and drugs.
价 格：￥电议型 号：T11479产 地：中国大陆
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T11478LGSK1521498 free base；化合物 T11478LGSK1521498 free base
GSK1521498 free base is a potent and selective antagonist of the μ-opioid receptor. GSK1521498 free base also has the potential for disorders of compulsive consumption of food, alcohol, and drugs.
价 格：￥电议型 号：T11478L产 地：中国大陆
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T11478GSK1521498 free base (hydrochloride)；化合物 T11478GSK1521498 free base (hydrochloride)
GSK1521498 free base (hydrochloride) is a selective antagonist of the μ-opioid receptor (MOR). It is being used for the treatment of disorders of compulsive consumption of food, alcohol, and drugs.
价 格：￥电议型 号：T11478产 地：中国大陆
