P021
P021 (Peptide 021) is an orally active, blood-brain barrier penetrant neurotrophic/neurogenic pentapeptide derived from the most active region of ciliary neurotrophic factor (CNTF). P021 competitively inhibits leukemia inhibitory factor (LIF) and promotes BDNF transcription. P021 targets neurogenesis and synaptic plasticity. P021 prevents neurodegeneration, Amyloid-β pathology, tau protein pathology and cognitive deficits, rescues episodic memory impairment and reduces mortality in 3xTg-AD mice. P021 is applicable to the research of Alzheimer's disease.
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: 1246751-68-7
- 分子式: C27H42N6O8
- 分子量:578.66
-
保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
製品説明
Parmacokinetics
| Species | Dose | Route | T1/2 |
|---|---|---|---|
| Mice[1] | 162 nM | p.o. | >3 h |
体内実験
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Animal Model:3xTg-AD (female, 3 months old at study initiation, hybrid 129/Sv x C57BL/6 genetic background, Alzheimer's disease transgenic model harboring APP_Swe, tau P301L, and PS1 M146V knock-in mutations)[1]
-
Dosage:60 nM P021/g feed (equivalent to ~162 nM P021/mouse/day)
-
Administration:p.o.; continuously; 18 months
-
Result:Prevented neurodegeneration (measured by Fluorojade C staining percent area) in CA3, dentate gyrus, parietal cortex, and frontal cortex at 9 months post-treatment relative to vehicle-treated mice.
Prevented neurodegeneration in CA1, CA3, DG, and parietal cortex at 18 months post-treatment relative to vehicle-treated mice.
Reduced Aβ plaque load (percent area occupied by 4G8 staining) in the subiculum at 9 months post-treatment relative to vehicle-treated mice, with no significant effect in CA1.
Reduced Aβ load in the subiculum at 15 months post-treatment relative to vehicle-treated mice, with no effect in CA1.
Reduced Aβ load in both CA1 and subiculum at 18 months post-treatment relative to vehicle-treated mice.
Slowed Aβ load increase over time in the subiculum via regression analysis.
Reduced tau hyperphosphorylation (PHF1 staining percent area) in CA1 and subiculum, with a trend toward reduction in AT8 staining in CA1 at 9 months post-treatment relative to vehicle-treated mice.
Reduced AT8 staining in CA1 and subiculum, and reduced PHF1 staining in CA1 and subiculum at 15 months post-treatment relative to vehicle-treated mice.
Reduced AT8 staining in CA1 and subiculum, reduced PHF1 staining in CA1 and subiculum, and reduced hippocampal PHF1-positive tau on western blot at 18 months post-treatment relative to vehicle-treated mice.
Slowed the increase in AT8 and PHF1 staining over time in CA1 and subiculum via regression analysis.
Rescued episodic memory impairment in the Novel Object Recognition task at 16-17 months post-treatment, with treated mice showing a significantly higher discrimination index relative to vehicle-treated mice.
Increased survival rate from 41% (vehicle) to 87% by week 71 of treatment, and reduced hindlimb paralysis incidence (1/32 vs 5/34 vehicle-treated mice).
化学情報
-
CAS 番号 1246751-68-7
-
分子量 578.66
-
分子式 C27H42N6O8
-
SMILES
OC(C[C@H](NC(C)=O)C(NCC(NCC(N[C@@H](CC(C)C)C(NC12CC3(CC(CC(C3)C2)C1)C(N)=O)=O)=O)=O)=O)=O
-
別名
Peptide 021
-
配列
Ac-Asp-Gly-Gly-Leu-{Gly(adamantane)}
-
シーケンスの短縮
Ac-DGGL-{Gly(adamantane)}
-
輸送条件
Room temperature in continental US; may vary elsewhere.
-
保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)