GLPBio

MSH Release-Inhibiting Factor (trifluoroacetate salt)

Catalog No.: GC91914Purity:>95.00%Synonyms: Melanocyte-stimulating Hormone Release-Inhibiting Factor; MIF-1; MSH-R-IF
MSH Release-Inhibiting Factor (trifluoroacetate salt) (msh-r-if)は、ラットの条体(kd = 4.69 nm)に結合し、多様な生理活性を持つ視床下部トリペプチドです。

製品は研究用途にのみ使用できます。人体には使用できません。患者への販売は行っておりません。


MSH Release-Inhibiting Factor (trifluoroacetate salt)
10 mgIn Stock
$113.00
1
25 mgIn Stock
$251.00
1
50 mgIn Stock
$444.00
1
100 mgIn Stock
$665.00
1

引用文献 (Citations)

現在、この製品の引用文献はありません。以下はGlpBio製品を引用した代表的な文献です。
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    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    Science
    388(6745) (2025)
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    35, 97–116 (2025)
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    33, 904–922 (2023)
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    31, 1291–1307 (2021)

製品説明 (Description)

MSH release-inhibiting factor (MSH-R-IF) is a hypothalamic tripeptide that binds to rat striatum (Kd = 4.69 nM) and has diverse biological activities.1,2,3,4 In vivo, MSH-R-IF (0.1 mg/kg) decreases immobility of mice in the forced swim test, indicating antidepressant-like activity.2 MSH-R-IF (20 mg/kg) increases striatal concentration of dopamine and the dopamine metabolites DOPAC, 3-methoxy tyramine (3-MT), and homovanillic acid (HVA) in a mouse model of Parkinson's disease induced by MPTP.3 It decreases vacuous chewing movements induced by haloperidol in a rat model of tardive dyskinesia when administered at a dose of 2 mg/kg.4 MSH-R-IF also has anti-opiate effects, reversing analgesia induced by morphine and an enkephalin in mice in a radiant heat tail-flick assay.1

References:
[1]. Pan, W., and Kastin, A.J.From MIF-1 to endomorphin: The Tyr-MIF-1 family of peptidesPeptides28(12)2411-2434(2007).
[2]. Kastin, A.J., Abel, D.A., Ehrensing, R.H., et al.Tyr-MIF-1 and MIF-1 are active in the water wheel test for antidepressant drugsPharmacol. Biochem. Behav.21(5)767-771(1984).
[3]. Marcotte, E.R., Chugh, A., Mishra, R.K., et al.Protection against MPTP treatment by an analog of Pro-Leu-Gly-NH2 (PLG, MIF-1)Peptides19(2)403-406(1998).
[4]. Sharma, S., Paladino, P., Gabriele, J., et al.Pro-Leu-glycinamide and its peptidomimetic, PAOPA, attenuate haloperidol induced vacuous chewing movements in rat: A model of human tardive dyskinesiaPeptides24(2)313-319(2003).

製品資料 (Product Documents)

Purity:>95.00%Appearance:A solid

化学的性質 (Chemical Properties)

同義語
Melanocyte-stimulating Hormone Release-Inhibiting Factor; MIF-1; MSH-R-IF
化学名
L-prolyl-L-leucyl-glycinamide, trifluoroacetate salt
SMILES
O=C([C@@H](NC([C@H]1NCCC1)=O)CC(C)C)NCC(N)=O.FC(F)(C(O)=O)F
分子式
C13H24N4O3 ? XCF3COOH
分子量
284.4
溶解性
Water: 1 mg/ml
保存条件
-20°C
一般的な注意事項
製品の溶解性データに基づいて適切な溶媒を選択してください。調製後は、凍結融解の繰り返しを避けるため、ストック溶液を小分けしてください。
ストック溶液は、-80°Cで保存する場合は6か月以内、-20°Cで保存する場合は1か月以内に使用してください。
溶解性を高めるには、チューブを37°Cに温め、適切な時間超音波処理してください。
配送条件
評価用サンプルは保冷剤とともに発送します。その他の容量は室温で発送し、ご要望に応じて保冷剤を同梱します。

計算ツール (Calculators)モル濃度 / 希釈 / 分子量 / 単位変換 / in vivo製剤 / 溶解度

g/mol

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