Ogerin
CAS No. 1309198-71-7
Ogerin ( —— )
产品货号. M23467 CAS No. 1309198-71-7
Ogerin 是一种选择性 GPR68 正变构调节剂 (pEC50: 6.83)。奥杰林阻断小鼠恐惧条件反射的回忆。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥356 | 有现货 |
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| 5MG | ¥551 | 有现货 |
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| 10MG | ¥948 | 有现货 |
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| 25MG | ¥1936 | 有现货 |
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| 50MG | ¥3248 | 有现货 |
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| 100MG | ¥4836 | 有现货 |
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| 200MG | 获取报价 | 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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生物学信息
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产品名称Ogerin
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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Ogerin 是一种选择性 GPR68 正变构调节剂 (pEC50: 6.83)。奥杰林阻断小鼠恐惧条件反射的回忆。
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产品描述Ogerin is a selective GPR68 positive allosteric modulator (pEC50: 6.83). Ogerin blocks recall in fear conditioning in mice. Ogerin displays inverse agonist and antagonist activity (Ki, 220 nM) at A2A receptor and weak antagonist activity (Ki, 736 nM) at 5-HT2B receptor.
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体外实验Cell Proliferation Assay Cell Line:Primary human lung fibroblasts (PHLFs) (TGF-β induced)Concentration:50, 100 μMIncubation Time:72 hResult:Inhibited TGF-β stimulated proliferation.Cell Viability Assay Cell Line:HEK293 cells (stably expressing HA-GPR68) Concentration:50 μM Incubation Time:10 min Result:Activated PKA and p42/p44 MAP kinase.RT-PCR Cell Line:Primary human lung fibroblasts (PHLFs) (TGF-β induced)Concentration: 50-150 μM Incubation Time:48 h Result:Suppressed TGF-β induced Col1A1 and Col3A1 mRNA levels in a dose-dependent manner.Western Blot Analysis Cell Line:Primary human lung fibroblasts (PHLFs) (TGF-β induced)Concentration:150 μM Incubation Time:40 min (pre-treat)Result:Induced CREB phosphorylation in both non-fibrotic and fibrotic PHLFs.Western Blot Analysis Cell Line:Primary human lung fibroblasts (PHLFs) (TGF-β induced)Concentration:50-150 μM Incubation Time:72 hResult:Inhibited TGF-β induced αSMA expression in a dose-dependent manner.
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体内实验Animal Model:GPR68 knockout and WT mice.Dosage:10 mg/kg Administration:Single (30 min before the training)Result:Suppressed recall in fear conditioning in wild-type, but not in GPR68 knockout mice.
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同义词——
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通路Endocrinology/Hormones
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靶点5-HT Receptor
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受体5-HT2B|A2A|GPR68
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研究领域——
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适应症——
化学信息
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CAS Number1309198-71-7
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分子量307.35
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分子式C17H17N5O
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纯度>98% (HPLC)
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溶解度DMSO:250 mg/mL (813.40 mM; Need ultrasonic)
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SMILESOCC1=C(C2=NC(N)=NC(NCC3=CC=CC=C3)=N2)C=CC=C1
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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.Huang XP, et al. Allosteric ligands for the pharmacologically dark receptors GPR68 and GPR65. Nature. 2015 Nov 26;527(7579):477-83.
产品手册
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