GLPBio

TPPB (α-Amyloid Precursor Protein Modulator)

Catalog No.: GC10343Purity:>98.00%
α-Amyloid Precursor Protein Modulator ist ein zellgÄngiger, von Benzolactam abgeleiteter Proteinkinase C (PKC)-Aktivator mit einem Ki von 11,9 nM.

Die Produkte sind ausschließlich für Forschungszwecke bestimmt. Nicht zur Anwendung am Menschen. Wir verkaufen nicht an Patienten.


TPPB (α-Amyloid Precursor Protein Modulator)
Cas No.: 497259-23-1
10mM (in 1mL DMSO)In Stock
$368.00
1
1mgIn Stock
$138.00
1
5mgIn Stock
$333.00
1

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Beschreibung (Description)

TPPB (α-Amyloid Precursor Protein Modulator) is a benzolactam-derived, cell-permeable protein kinase C (PKC) activator (Ki = 11.9nM) [1]. TPPB increases α-secretase activity, leading to increased secretion of sAPPα, while simultaneously decreasing β-secretase (BACE1) expression and the release of Aβ40 fragments [2-3]. TPPB is primarily used to treat Alzheimer's disease [4].

In SH-SY5Y cells, TPPB (0.1-100nM; 3h) induces cell secretion of sAPPα [5]. In PC12 cells, TPPB (0-10μM; 3h) promoted the secretion of sAPPα without affecting the expression of full-length APP [6].

In experimental autoimmune encephalomyelitis (EAE) mice model, TPPB (50nmol/kg; ip; 21d; three days a week) can alleviate the neurological deficits [7].

References:
[1]. Kozikowski A P, Nowak I, Petukhov P A, et al. New amide-bearing benzolactam-based protein kinase C modulators induce enhanced secretion of the amyloid precursor protein metabolite sAPPα[J]. Journal of medicinal chemistry, 2003, 46(3): 364-373.
[2]. Yang H Q, Pan J, Ba M W, et al. New protein kinase C activator regulates amyloid precursor protein processing in vitro by increasing α‐secretase activity[J]. European Journal of Neuroscience, 2007, 26(2): 381-391.
[3]. Hong-Qi Y, Zhi-Kun S, Sheng-Di C. Current advances in the treatment of Alzheimer's disease: focused on considerations targeting Aβ and tau[J]. Translational neurodegeneration, 2012, 1(1): 21.
[4]. Yang H Q, Li X, Yang W M, et al. Neuroprotective Effects of New Protein Kinase C Activator TPPB Against Aβ25–35 Induced Neurotoxicity in PC12 Cells[J]. Neurochemical research, 2012, 37(10): 2213-2221.
[5]. Yi P, Schrott L, Castor T P, et al. Bryostatin-1 vs. TPPB: dose-dependent APP processing and PKC-α,-δ, and-ε isoform activation in SH-SY5Y neuronal cells[J]. Journal of Molecular Neuroscience, 2012, 48(1): 234-244.
[6]. Yang H Q, Pan J, Ba M W, et al. New protein kinase C activator regulates amyloid precursor protein processing in vitro by increasing α‐secretase activity[J]. European Journal of Neuroscience, 2007, 26(2): 381-391.
[7]. Shanmukha S, Godfrey W H, Gharibani P, et al. TPPB modulates PKC activity to attenuate neuroinflammation and ameliorate experimental multiple sclerosis[J]. Frontiers in Cellular Neuroscience, 2024, 18: 1373557.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

SH-SY5Y cells

Preparation Method

Cells were grown to confluency in 10 % serum-supplemented medium. Prior to experiments, culture medium was replaced with serum and protein-free (0 %) medium for 2h before drug treatments to remove APP/sAPPα present in FBS and to permit filter concentration of sAPPα. Dilutions of bryostatin-1 or TPPB were added to serum-free culture medium at various concentrations and treatments maintained for 3h, except in time course experiments where several time points up to 24h were taken. Pilot studies showed no change in SH-SY5Y appearance, attachment, or cell density for at least 24h under these conditions.

Reaction Conditions

0.1-100nM; 3h

Applications

TPPB induces cell secretion of sAPPα.
Animal experiment [2]:

Animal models

Experimental autoimmune encephalomyelitis (EAE) mice model

Preparation Method

TPPB was dissolved in DMSO to a 1mM stock solution and then diluted to the desired concentration with sterile PBS for animal experiments. Mice were intraperitoneally injected with TPPB (50nmol/kg) or an equal volume of vehicle control three days a week. Mice were randomized and received their first treatment on the day their clinical score reached 1.0 or higher; thereafter, treatment continued three days a week.

Dosage form

50nmol/kg; ip; 21d; three days a week

Applications

TPPB can alleviate the neurological deficits in EAE.

References:
[1]. Yi P, Schrott L, Castor T P, et al. Bryostatin-1 vs. TPPB: dose-dependent APP processing and PKC-?,-?, and-? isoform activation in SH-SY5Y neuronal cells[J]. Journal of Molecular Neuroscience, 2012, 48(1): 234-244.
[2]. Shanmukha S, Godfrey W H, Gharibani P, et al. TPPB modulates PKC activity to attenuate neuroinflammation and ameliorate experimental multiple sclerosis[J]. Frontiers in Cellular Neuroscience, 2024, 18: 1373557.

Produktdokumente (Product Documents)

Purity:>98.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
497259-23-1
Chemischer Name
(2E,4E)-N-(5-(hydroxymethyl)-2-isopropyl-1-methyl-3-oxo-1,2,3,4,5,6-hexahydrobenzo[e][1,4]diazocin-8-yl)-5-(4-(trifluoromethyl)phenyl)penta-2,4-dienamide
SMILES
CC(C1C(NC(CO)CC2=C(C=CC(NC(/C=C/C=C/C3=CC=C(C(F)(F)F)C=C3)=O)=C2)N1C)=O)C
Summenformel
C27H30F3N3O3
Molekulargewicht
501.54
Löslichkeit
25.08mg/mL in DMSO
Lagerung
Store at -20°C
Allgemeine Hinweise
Wählen Sie anhand der Löslichkeitsdaten des Produkts ein geeignetes Lösungsmittel. Aliquotieren Sie die Stammlösung nach der Herstellung, um wiederholte Gefrier-Auftau-Zyklen zu vermeiden.
Verwenden Sie Stammlösungen bei Lagerung bei -80°C innerhalb von 6 Monaten bzw. bei -20°C innerhalb von 1 Monat.
Zur Verbesserung der Löslichkeit das Röhrchen auf 37°C erwärmen und für eine angemessene Dauer beschallen.
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

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