GLPBio

TPPB (α-Amyloid Precursor Protein Modulator)

Catalog No.: GC10343Purity:>98.00%
α ؛ -Amyloid السلائف مغير البروتين هو منشط بروتين كيناز C (PKC) مشتق من الخلايا من البنزولاكتام مع Ki يبلغ 11.9 نانومتر.

المنتجات مخصصة للاستخدام البحثي فقط، وليست للاستخدام البشري. نحن لا نبيع للمرضى.


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

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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الوصف (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.

البروتوكول (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.

وثائق المنتج (Product Documents)

Purity:>98.00%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
497259-23-1
الاسم الكيميائي
(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
الصيغة الجزيئية
C27H30F3N3O3
الوزن الجزيئي
501.54
الذوبانية
25.08mg/mL in DMSO
التخزين
Store at -20°C
إرشادات عامة
اختر مذيبًا مناسبًا وفقًا لبيانات ذوبانية المنتج. بعد التحضير، قسّم المحلول المخزون إلى أجزاء لتجنب دورات التجميد والذوبان المتكررة.
استخدم المحاليل المخزونة خلال 6 أشهر عند حفظها في -80°C، أو خلال شهر واحد عند حفظها في -20°C.
لتحسين الذوبانية، سخّن الأنبوب إلى 37°C وعرّضه للموجات فوق الصوتية لمدة مناسبة.
شروط الشحن
تُشحن عينات التقييم مع عبوات تبريد. وتُشحن الأحجام الأخرى المتاحة في درجة حرارة الغرفة، أو مع عبوات تبريد عند الطلب.

الحاسبات (Calculators)المولارية / التخفيف / الوزن الجزيئي / تحويل الوحدات / تركيبة داخل الجسم الحي / الذوبانية

g/mol

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