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产品数：86101
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T14087ABT-239ABT-239
ABT-239 is a novel, highly efficacious, non-imidazole?class of H3R antagonist. Its a transient receptor potential vanilloid type 1 (TRPV1) antagonist.?
价 格：￥电议型 号：T14087产 地：美洲
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T14090AC-55649AC-55649
AC-55649 is a highly isoform-selective agonist of human RARβ2 receptor (pEC50: 6.9).
价 格：￥电议型 号：T14090产 地：美洲
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T14148AH 6809AH 6809
AH 6809 is an EP and DP receptor antagonist with nearly equal affinity for the cloned human EP1, EP2, EP3-III, and DP1 receptors. IC50 Value: ~3 nM (EC50 for calcium mobilization by PGE2) [1] Oral administration of the EP1 receptor antagonist, AH6809 (10
价 格：￥电议型 号：T14148产 地：美洲
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T14201AM-2099AM-2099
AM-2099 is a voltage-gated sodium channel Nav1.7 inhibitor (IC50: 0.16 μM).
价 格：￥电议型 号：T14201产 地：美洲
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T14205AM679AM679
AM679 is a potent and selective FLAP inhibitor with IC50s of 2.2 nM/0.6 nM/154 nM for FLAP binding/hLA/hWB respectively. IC50 value: 2.2 nM/0.6 nM/154 nM(FLAP binding/hLA/hWB) [1] AM679 showed an improved CYP inhibition profile (IC50 3A4 = 16.7 lM, 2C9 =
价 格：￥电议型 号：T14205产 地：美洲
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T14217AMG 579AMG 579
AMG 579 is a phosphodiesterase 10A (PDE10A) inhibitor (IC50: 0.1 nM).
价 格：￥电议型 号：T14217产 地：美洲
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T14383AZD8329AZD8329
AZD8329 is a potent 11β-Hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitor with an IC50 of 9 nM for human 11β-HSD1. Which displays excellent selectivity versus 11β-HSD2, 17β-HSD1 and 17β-HSD3[1].
价 格：￥电议型 号：T14383产 地：美洲
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T15303FMK 9aFMK 9a
FMK 9a is an inhibitor of autophagin-1 (IC50: 80 and 73 μM in FRET and LRA assay).
价 格：￥电议型 号：T15303产 地：美洲
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T2119ABT-199ABT-199,ABT199,ABT 199
ABT-199 is a selective inhibitor of Bcl-2 (Ki < 0.010 nM), binding over 3 orders of magnitude less avidly to Bcl-xL, and Bcl-W (Kis = 48 and 245 nM, respectively).
价 格：￥电议型 号：T2119产 地：美洲
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T4997Umeclidinium bromideUmeclidinium bromide,GSK573719A,
Umeclidinium bromide is a novel mAChR antagonist.
价 格：￥电议型 号：T4997产 地：美洲
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T5155AG 99AG 99,(E)-Tyrphostin AG 99,(E)-Tyrphostin 46
AG-99 is an inhibitor of EGFR kinase (IC50: 10 μM in the human epidermoid carcinoma cell line A431).
价 格：￥电议型 号：T5155产 地：美洲
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T5409AZD3229AZD3229
AZD3229 is a potent pan-KIT mutant inhibitor for the treatment of gastrointestinal stromal tumors. It demonstrates potent single-digit nM growth inhibition across a broad cell panel.
价 格：￥电议型 号：T5409产 地：美洲
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T6003GSK1904529AGSK1904529A,GSK 4529,
GSK1904529A is a specific inhibitor of IGF-1R (IC50=27 nM) and IR(IC50=25 nM) .
价 格：￥电议型 号：T6003产 地：美洲
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T6205AT7519AT7519
AT7519 is a CDK1/2/4/6/9 inhibitor (IC50: 10-210 nM). It is less effective to CDK3 and little active to CDK7.
价 格：￥电议型 号：T6205产 地：美洲
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T8472ERK1/2 inhibitor 2；化合物ASTX029ASTX-029|||ASTX029；ASTX-029|||ASTX029
ERK1/2 inhibitor 2 (ASTX029) is a selective and orally bioavailable extracellular signal-regulated kinases 1 and 2 (ERK 1/2) inhibitor, with potential antineoplastic activity.
价 格：￥电议型 号：T8472产 地：中国大陆
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T8378AS2863619；化合物AS2863619AS2863619
AS2863619 is an orally active inhibitor of cyclin-dependent kinase 8 (CDK8) and CDK19 (IC50s of 0.61 nM and 4.28 nM, respectively).
价 格：￥电议型 号：T8378产 地：中国大陆
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T83213AC-099；化合物 AC-099AC-099
AC-099 (compound 3) serves as a selective full agonist at NPFF2R (EC50 = 1189 nM) and a partial agonist at NPFF1R (EC50 = 2370 nM). It has been shown to mitigate hypersensitivity induced by spinal nerve ligation in rats [1] [2].
价 格：￥电议型 号：T83213产 地：中国大陆
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T83119Androgen receptor antagonist 9；化合物 Androgen receptor antagonist 9Androgen receptor antagonist 9
Androgen Receptor Antagonist 9 (compound 28) serves as an antagonist to the androgen receptor [1].
价 格：￥电议型 号：T83119产 地：中国大陆
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T83089Anticancer agent 149；化合物 Anticancer agent 149Anticancer agent 149
Anticancer Agent 149 (compound 3), isolated from the rhizome of Dioscorea dioscorea (DM), demonstrates selective cytotoxicity against MCF-7 cells with an IC50 of 31.41 μM [1].
价 格：￥电议型 号：T83089产 地：中国大陆
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T83061Anti-inflammatory agent 29；化合物 Anti-inflammatory agent 29Anti-inflammatory agent 29
Compound 29 (Compound 7) is an anti-inflammatory agent that exhibits hepatoprotective activity [1].
价 格：￥电议型 号：T83061产 地：中国大陆
