GLPBio

Torin 1

Catalog No.: GC10131Purity:>98.00%Synonyms: Torin1;Torin-1
يعد Torin 1 مثبطًا قويًا لـ mTOR مع IC 50 من 3 نانومترTorin 1 يثبط كلا مجمعي mTORC1 / 2 بقيم IC بين 2 و 10 نانومترTorin 1 هو محفز فعال للالتهام الذاتي

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


Torin 1
Cas No.: 1222998-36-8
5mgIn Stock
$54.00
1
10mgIn Stock
$88.00
1
50mgIn Stock
$280.00
1
100mgIn Stock
$406.00
1

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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    610, 366–372 (2022)
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    187(9):2288-2304 (2024)
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    183(7):1867-1883 (2020)
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الوصف (Description)

Torin 1 is a potent ATP-competitive mammalian target of rapamycin (mTOR) inhibitor with an IC50 value of 3nM[1]. Torin 1 inhibits both mTORC1/2 complexes with IC50 values between 2 and 10nM[2]. Torin 1 is a potent autophagy inducer[3].

In vitro, treatment of glioblastoma (GB) LN-18 cells with Torin 1 (300, 1000nM) for 24h dose-dependently inhibited cell proliferation and migration and significantly inhibited cell entry into the S phase[4]. Treatment of S. pombe cells with Torin 1 (25μM) for 24h inhibited cell growth but did not cause cell death or G1 phase arrest[5].

In vivo, oral treatment of mice with dextran sulfate sodium (DSS)-induced colitis with Torin 1 (10, 20mg/kg) for 6 days significantly reduced pathological damage in the colon tissue and inhibited the production of proinflammatory cytokines in mice[6]. Torin 1 (400nM, 0.5μL) injected bilaterally into the insular cortex (IC) of nerve-injured rats significantly alleviated neuropathic pain and inhibited the increase in phosphorylated p70S6K (p-p70S6K) levels[7].

References:
[1] Thoreen C C, Kang S A, Chang J W, et al. An ATP-competitive mammalian target of rapamycin inhibitor reveals rapamycin-resistant functions of mTORC1[J]. Journal of Biological Chemistry, 2009, 284(12): 8023-8032.
[2] Sun S Y. mTOR kinase inhibitors as potential cancer therapeutic drugs[J]. Cancer letters, 2013, 340(1): 1-8.
[3] Xu S, Li L, Li M, et al. Impact on autophagy and ultraviolet B induced responses of treatment with the MTOR inhibitors rapamycin, everolimus, torin 1, and pp242 in human keratinocytes[J]. Oxidative medicine and cellular longevity, 2017, 2017(1): 5930639.
[4] Amin A G, Jeong S W, Gillick J L, et al. Targeting the mTOR pathway using novel ATP-competitive inhibitors, Torin1, Torin2 and XL388, in the treatment of glioblastoma[J]. International journal of oncology, 2021, 59(4): 83.
[5] Atkin J, Halova L, Ferguson J, et al. Torin1-mediated TOR kinase inhibition reduces Wee1 levels and advances mitotic commitment in fission yeast and HeLa cells[J]. Journal of cell science, 2014, 127(6): 1346-1356.
[6] Liu T, Zheng S, Guo P. Effect of Torin 1 on suppressing inflammation in mice with dextran sodium sulfate-induced colitis[J]. Int J Clin Exp Med, 2017, 10(3): 4723-4731.
[7] Choi S, Kim K, Cha M, et al. mTOR signaling intervention by Torin1 and XL388 in the insular cortex alleviates neuropathic pain[J]. Neuroscience Letters, 2020, 718: 134742.

البروتوكول (Protocol)

Cell experiment [1]:

Cell lines

LN-18 cells

Preparation Method

Cells were treated with two doses (300 and 1000nM) of Torin 1, Torin 2, or XL388 for 24h, and then MTT assay was performed to measure cell proliferation.

Reaction Conditions

300, 1000nM; 24h

Applications

Cell proliferation was significantly inhibited by Torin 1 in a dose-dependent manner.

Animal experiment [2]:

Animal models

C57BL/6 mice

Preparation Method

Mice were given free access to water containing Dextran sulfate sodium (DSS) for 6 days. The mice were randomly assigned to control, Torin 1 (20mg/kg)-treated, DSS-treated, Torin 1 (10mg/kg) +DSS-treated and Torin 1 (20mg/kg)+DSS-treated groups. Torin-1 as a suspension in 20% N-methyl-2-pyrrolidone/40% PEG400/40% water, orvehicle was delivered intragastrically once per day for 6 days from the first day, respectively.

Dosage form

10, 20mg/kg for 6 days; p.o.

Applications

Torin 1 treatment significantly attenuated body weight loss and reduced the mortality induced by DSS. Torin 1 prevented DSS-induced colonic pathological damage, inhibited the production of pro-inflammatory cytokines in colon tissues.

References:
[1]Amin A G, Jeong S W, Gillick J L, et al. Targeting the mTOR pathway using novel ATP-competitive inhibitors, Torin1, Torin2 and XL388, in the treatment of glioblastoma[J]. International journal of oncology, 2021, 59(4): 83.
[2]Liu T, Zheng S, Guo P. Effect of Torin 1 on suppressing inflammation in mice with dextran sodium sulfate-induced colitis[J]. Int J Clin Exp Med, 2017, 10(3): 4723-4731.

وثائق المنتج (Product Documents)

Purity:>98.00%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
1222998-36-8
المرادفات
Torin1;Torin-1
الاسم الكيميائي
1-[4-(4-propanoylpiperazin-1-yl)-3-(trifluoromethyl)phenyl]-9-quinolin-3-ylbenzo[h][1,6]naphthyridin-2-one
SMILES
CCC(=O)N1CCN(CC1)C2=C(C=C(C=C2)N3C(=O)C=CC4=CN=C5C=CC(=CC5=C43)C6=CC7=CC=CC=C7N=C6)C(F)(F)F
الصيغة الجزيئية
C35H28F3N5O2
الوزن الجزيئي
607.64
الذوبانية
<1.22mg/mL in DMSO, ≥ 2.42 mg/mL in EtOH with ultrasonic and warming
التخزين
Desiccate 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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