LIT-001
CAS No. 2245072-21-1
LIT-001 ( —— )
产品货号. M22581 CAS No. 2245072-21-1
LIT-001 改善自闭症小鼠模型的社交互动。它是第一个非肽催产素受体激动剂,EC50 为 55 nM,Ki 为 226 nM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1256 | 有现货 |
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| 10MG | ¥2325 | 有现货 |
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| 25MG | ¥3686 | 有现货 |
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| 50MG | ¥5443 | 有现货 |
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| 100MG | ¥7744 | 有现货 |
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| 500MG | ¥15552 | 有现货 |
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| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称LIT-001
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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LIT-001 改善自闭症小鼠模型的社交互动。它是第一个非肽催产素受体激动剂,EC50 为 55 nM,Ki 为 226 nM。
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产品描述LIT-001 improves social interaction in a mouse model of autism.It is the first nonpeptide oxytocin receptor agonist with EC50 of 55 nM and Ki of 226 nM.In the in vitro signal transduction experiment, LITL-001 is an unbiased OT-R agonist, acting on the two main signal transduction pathways of this receptor, with slight antagonistic effect on V1a and agonist effect on V1b receptor, only observed at high concentration.LIT-001 (10-20 mg/kg; i.p.) alleviates core symptoms in the context of autism spectrum disorders (ASD).
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体外实验In vitro signaling experiments, LIT-001 is a nonbiased OT-R agonist on the two main signaling pathways of this receptor, with minor antagonist effect on V1a and agonist effect on V1b receptors, observed at high concentrations only.
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体内实验LIT-001 (10-20 mg/kg; i.p.) alleviates core symptoms in the context of autism spectrum disorders (ASD ). Animal Model:Oprm1–/– mice (bred in house on a 50% 129SVPas–50% C57BL/6J hybrid background) Dosage:10, 20 mg/kg Administration:i.p.Result:Alleviated core symptoms in the context of ASD.
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同义词——
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通路Others
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靶点Other Targets
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受体oxytocin receptor
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研究领域——
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适应症——
化学信息
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CAS Number2245072-21-1
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分子量645.7
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分子式C30H34F3N7O4S
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纯度>98% (HPLC)
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溶解度DMSO:247 mg/mL (382.53mM; Need ultrasonic)
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SMILESOC(=O)C(F)(F)F.CN(C)C(=S)[C@@H]1CCCN1C(=O)NCc1ccc(cc1C)C(=O)N1Cc2cnn(C)c2Nc2ccccc12
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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.Frantz MC, et al. LIT-001, the First Nonpeptide Oxytocin Receptor Agonist that Improves Social Interaction in a Mouse Model of Autism. J Med Chem. 2018 Oct 11;61(19):8670-8692.
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