GLPBio

Disitertide TFA

Catalog No.: GC60782Purity:>96.00%Synonyms: P144 TFA
Disitertide (P144) TFA هو مثبط عامل النمو المحول بيتا 1 (TGF-β1) المصمم خصيصًا لمنع التفاعل مع مستقبلهDisitertide (P144) TFA هو أيضًا مثبط PI3K ومحفز موت الخلايا المبرمج

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


Disitertide TFA
1mgIn Stock
$67.00
1
5mgIn Stock
$203.00
1
10mgIn Stock
$354.00
1

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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    Nature
    641, 529–536 (2025)
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    628, 630–638 (2024)
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    Nature
    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
  • Science cover
    Science
    388(6745) (2025)
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    387(6739) (2025)
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    33, 904–922 (2023)
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    31, 1291–1307 (2021)

الوصف (Description)

Disitertide TFA is a specific inhibitor of transforming growth factor β1 (TGF-β1) receptor type I [1]. Disitertide binds to the TGF-β1 receptor, blocking the TGF-β1 signaling pathway and inhibiting extracellular matrix deposition and fibrotic responses, thereby slowing or reversing the progression of fibrosis [2-3]. Disitertide is primarily used to treat fibrotic diseases of various organs [4].

In LINC00941-overexpressing HCT-116 cells, Disitertide (10μM; 12h) treated cell showed increased mRNA and protein levels of ZO-1 and E-cadherin [5]. In LN229 cells, after Disitertide (100µg/mL; 10d) stimulation, SKI gene expression was significantly inhibited [6]. In MGC803 cells, Disitertide (20μM; 48h) blocks TGFβ1 signaling and effectively rescues the inhibitory effect of MFSD2A deficiency on CD8+ T cells [7].

In fibrosis rabbit mode, the macroscopic and microscopic morphology of muscles in the Disitertide (3.5mg/kg; iv; 72h) treated group was preserved, and extracellular matrix fibrosis was reduced [8].

References:
[1]. Neuzillet C, Tijeras-Raballand A, Cohen R, et al. Targeting the TGFβ pathway for cancer therapy[J]. Pharmacology & therapeutics, 2015, 147: 22-31.
[2]. Yang J, Zhuang Y, Liu J. Upregulation of microRNA‑590 in rheumatoid arthritis promotes apoptosis of bone cells through transforming growth factor‑β1/phosphoinositide 3‑kinase/Akt signaling[J]. International Journal of Molecular Medicine, 2019, 43(5): 2212-2220.
[3]. He W, Liang B, Wang C, et al. MSC-regulated lncRNA MACC1-AS1 promotes stemness and chemoresistance through fatty acid oxidation in gastric cancer[J]. Oncogene, 2019, 38(23): 4637-4654.
[4]. Miwa S, Yokota M, Ueyama Y, et al. Discovery of selective transforming growth factor β type II receptor inhibitors as antifibrosis agents[J]. ACS Medicinal Chemistry Letters, 2021, 12(5): 745-751.
[5]. Wu N, Jiang M, Liu H, et al. LINC00941 promotes CRC metastasis through preventing SMAD4 protein degradation and activating the TGF-β/SMAD2/3 signaling pathway[J]. Cell Death & Differentiation, 2021, 28(1): 219-232.
[6]. Kubelt C, Hellmold D, Esser D, et al. Insights into gene regulation under temozolomide-promoted cellular dormancy and its connection to stemness in human glioblastoma[J]. Cells, 2023, 12(11): 1491.
[7]. Zhang B, Wang C M, Wu H X, et al. MFSD2A potentiates gastric cancer response to anti‐PD‐1 immunotherapy by reprogramming the tumor microenvironment to activate T cell response[J]. Cancer Communications, 2023, 43(10): 1097-1116.
[8]. Cruz-Morande S, Dotor J, San-Julian M. P144 a transforming growth factor beta inhibitor peptide, generates antifibrogenic effects in a radiotherapy induced fibrosis model[J]. Current Oncology, 2022, 29(4): 2650-2661.

البروتوكول (Protocol)

Cell experiment [1]:

Cell lines

LINC00941-overexpressing HCT-116 cells

Preparation Method

Before TGF-β1 or Disitertide treatment, the cells were incubated with DMEM medium containing 10% FBS and 1% penicillin/streptomycin to achieve 80% cell fusion. Next, the cells were treated with TGF-β1 (0.2ng/mL) or Disitertide (10μM) for 12h.

Reaction Conditions

10μM; 12h

Applications

Disitertide-treated LINC00941-overexpressing HCT-116 cells showed increased mRNA and protein levels of ZO-1 and E-cadherin.
Animal experiment [2]:

Animal models

Fibrosis rabbit model

Preparation Method

Disitertide was stored at −80℃ before the manipulation peptide vial was tempered to room temperature and then weighed, resuspended in buffer diazonium salt of carbonic acid 0.1M pH 9.5, and sonicated until a homogeneous solution was obtained. Disitertide was IV in the marginal ear veins of the rabbits at doses 10mg per administration diluted in 10mL of buffer (approximately 3.5mg/kg).

Dosage form

3.5mg/kg; iv; 72h

Applications

The macroscopic and microscopic morphology of muscles in the Disitertide treated group was preserved, and extracellular matrix fibrosis was reduced.

References:
[1]. Wu N, Jiang M, Liu H, et al. LINC00941 promotes CRC metastasis through preventing SMAD4 protein degradation and activating the TGF-β/SMAD2/3 signaling pathway[J]. Cell Death & Differentiation, 2021, 28(1): 219-232.
[2]. Cruz-Morande S, Dotor J, San-Julian M. P144 a transforming growth factor beta inhibitor peptide, generates antifibrogenic effects in a radiotherapy induced fibrosis model[J]. Current Oncology, 2022, 29(4): 2650-2661.

وثائق المنتج (Product Documents)

Purity:>96.00%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

المرادفات
P144 TFA
الصيغة الجزيئية
C70H110N17O24S2F3
الوزن الجزيئي
1694.84
التخزين
-20°C, protect from light
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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