RORγt Inverse agonist 6
CAS No. 1887161-80-9
RORγt Inverse agonist 6 ( —— )
产品货号. M26419 CAS No. 1887161-80-9
RORγt Inverse agonist 6 是 RORγt inverse 的激动剂。 RORγt 反向激动剂 6 可用于 Th17 驱动的自身免疫性疾病的研究。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1349 | 有现货 |
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| 10MG | ¥1929 | 有现货 |
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| 25MG | ¥2911 | 有现货 |
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| 50MG | ¥3832 | 有现货 |
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| 100MG | ¥5112 | 有现货 |
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| 200MG | ¥6903 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥1691 | 有现货 |
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生物学信息
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产品名称RORγt Inverse agonist 6
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述RORγt Inverse agonist 6 是 RORγt inverse 的激动剂。 RORγt 反向激动剂 6 可用于 Th17 驱动的自身免疫性疾病的研究。
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产品描述RORγt Inverse agonist 6 is an agonist of RORγt inverse. RORγt Inverse agonist 6 can be used in research on Th17-driven autoimmune diseases.(In Vivo):RORγt Inverse agonist 6 (30 mg/kg; p.o.) inhibits the expression level of IL-17A by 59% compared to the vehicle after the oral administration at the tested dose. RORγt Inverse agonist 6 suppresses IL-17A gene expression by IL-23 stimulation in a mouse pharmacodynamics model. RORγt Inverse agonist 6 (1 mg/kg; p.o.) exhibits improved drug exposure with AUC of 1289 ng h/mL.
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体外实验——
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体内实验RORγt Inverse agonist 6 (compound 43) suppresses IL-17A gene expression by IL-23 stimulation in a mouse pharmacodynamics model.RORγt Inverse agonist 6 (compound 43) exhibits improved drug exposure (mouse AUC: 1289 ng?h/mL at 1 mg/kg, po).RORγt Inverse agonist 6 (compound 43, 30 mg/kg, po, b.i.d) inhibits the expression level of IL-17A by 59% compared to the vehicle after the oral administration at the tested dose. Animal Model:Mice.Dosage:30 mg/kg.Administration:Orally twice: at 30 min before and 8 h after IL-23 administration.Result:Inhibited the expression level of IL-17A by 59% compared to the vehicle after the oral administration at the tested dose.
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同义词——
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通路Nuclear Receptor/Transcription Factor
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靶点ROR
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受体ADC Linker
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研究领域——
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适应症——
化学信息
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CAS Number1887161-80-9
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分子量565.03
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分子式C28H29ClN6O5
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 50 mg/mL (88.49 mM)
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SMILESCC(C)n1c2ccc(NC(=O)N3CCO[C@H](C3)C(=O)Nc3ccc(C#N)c(Cl)c3)cc2c(=O)n(CC2CC2)c1=O
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Bene?ová M, et al. Preclinical Evaluation of a Tailor-Made DOTA-Conjugated PSMA Inhibitor with Optimized Linker Moiety for Imaging and Endoradiotherapy of Prostate Cancer. J Nucl Med. 2015 Jun;56(6):914-20.
产品手册
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