MK-212
MK-212 (CPP) is an orally active, blood-brain barrier permeable agonist of 5-HT1C, 5-HT2 and 5-HT1A receptors. MK-212 induces hyperthermia, nausea, arousal, irritability and restlessness, inhibits the elevation of plasma cortisol and prolactin, and reduces feelings of calmness and overall positive affect. MK-212 mediates anxiety-like behaviors and motor inhibition. MK-212 is applicable to research related to schizophrenia and anxiety disorders.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 64022-27-1
- 分子式: C8H11ClN4
- 分子量:198.65
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保管条件:Powder -20°C, 3 years ; In solvent -80°C, 6 months , -20°C, 1 month
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生物活性
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化学情報
- 純度とドキュメンテーション
- 参考文献
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Help & FAQs
5-HT Receptor アイソフォーム固有の製品をすべて表示
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生物活性
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5-HT1C Receptor |
5-HT2 Receptor |
5-HT1A Receptor |
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| HEK293 | EC50 |
0.028 μM
Compound: MK-212
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Agonist activity at human 5HT2C receptor expressed in HEK293 cells assessed as induction of intracellular calcium release measured for 90 secs by fluorescence assay
Agonist activity at human 5HT2C receptor expressed in HEK293 cells assessed as induction of intracellular calcium release measured for 90 secs by fluorescence assay
|
[PMID: 23301527] |
| HEK293 | EC50 |
0.16 μM
Compound: MK-212
|
Agonist activity at human 5HT2C receptor expressed in HEK293 cells assessed as accumulation of IP1 incubated for 1 hr at 37 degC followed by 15 mins at RT by TR-FRET assay
Agonist activity at human 5HT2C receptor expressed in HEK293 cells assessed as accumulation of IP1 incubated for 1 hr at 37 degC followed by 15 mins at RT by TR-FRET assay
|
[PMID: 23301527] |
| HEK293 | EC50 |
0.42 μM
Compound: MK-212
|
Agonist activity at human 5HT2A receptor expressed in HEK293 cells assessed as induction of intracellular calcium release measured for 90 secs by fluorescence assay
Agonist activity at human 5HT2A receptor expressed in HEK293 cells assessed as induction of intracellular calcium release measured for 90 secs by fluorescence assay
|
[PMID: 23301527] |
| HEK293 | EC50 |
1.2 μM
Compound: MK-212
|
Agonist activity at human 5HT2A receptor expressed in HEK293 cells assessed as accumulation of IP1 incubated for 1 hr at 37 degC followed by 15 mins at RT by TR-FRET assay
Agonist activity at human 5HT2A receptor expressed in HEK293 cells assessed as accumulation of IP1 incubated for 1 hr at 37 degC followed by 15 mins at RT by TR-FRET assay
|
[PMID: 23301527] |
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Wistar (male, 200-290 g)[2]
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Dosage:1.0 mg/kg; 2.0 mg/kg; 4.0 mg/kg
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Administration:i.p.; single injection
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Result:Decreased the percentage of open-arm entries and the percentage of time spent in open arms at 2.0 mg/kg and 4.0 mg/kg doses compared to saline controls.
Decreased the absolute number of closed-arm entries at 4.0 mg/kg dose compared to saline controls.
Showed no significant effect on any measured parameter at 1.0 mg/kg dose.
Confirmed anxiogenic effects of 2.0 mg/kg and 4.0 mg/kg doses remained significant when controlling for closed-arm entries via ANCOVA.
Decreased the number of floor crossings from 78 in saline controls to 17 at 4.0 mg/kg dose compared to saline controls.
Decreased rearings from 18 in saline controls to 9 at 4.0 mg/kg dose compared to saline controls.
Showed no significant effect on either locomotor measure at 1.0 mg/kg and 2.0 mg/kg doses.
Decreased the percentage of open-arm entries and the percentage of time spent in open arms compared to saline-pretreated controls when paired with vehicle or 0.5 μg ritanserin microinfusions into the basolateral amygdala.
Had anxiogenic effect dose-dependently prevented by ritanserin microinfusions at doses of 1.25 μg, 2.5 μg, and 5.0 μg into the basolateral amygdala, with no significant differences between MK-212-pretreated and saline-pretreated groups at these higher ritanserin doses.
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
化学情報
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CAS 番号 64022-27-1
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性状 Solid
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分子量 198.65
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分子式 C8H11ClN4
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SMILES
ClC1=NC(N2CCNCC2)=CN=C1
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別名
CPP
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Powder -20°C 3 years In solvent -80°C 6 months -20°C 1 month
純度とドキュメンテーション
参考文献
[1]. Lee HS, et al. Effect of the serotonin agonist, MK-212, on body temperature in schizophrenia. Biol Psychiatry. 1992 Mar 1;31(5):460-70. [Content Brief]
[2]. de Mello Cruz AP, et al. Behavioral effects of systemically administered MK-212 are prevented by ritanserin microinfusion into the basolateral amygdala of rats exposed to the elevated plus-maze. Psychopharmacology. 2005 Nov;182(3):345-54. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
MK-212 関連分類
HY-101324 関連分類
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