GLPBio

DC661

Catalog No.: GC19485Purity:>98.00%
DC661 هو مثبط قوي لبروتين بالميتويل ثيويستيراز 1 (PPT1) ، يثبط الالتهام الذاتي ، ويعمل كعامل مضاد للجسيمات الليزوزومية. نشاط مضاد للسرطان.

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


DC661
Cas No.: 1872387-43-3
10mM (in 1mL DMSO)In Stock
$145.00
1
2mgIn Stock
$77.00
1
5mgIn Stock
$119.00
1
10mgIn Stock
$189.00
1
25mgIn Stock
$378.00
1

المراجع (Citations)

1 publicationsمنشورات الباحثين الذين استخدموا هذا المنتج

الوصف (Description)

DC661 is a small-molecule compound capable of inhibiting palmitoyl-protein thioesterase 1 (PPT1) and effectively suppressing cellular autophagy, serving as an antilysosomal agent[1-2]. DC661 is primarily utilized in cancer-related research[3-4].

In vitro, pretreatment of human umbilical vein endothelial cells (HUVECs) with DC661 (1.5–3μM) for 30 minutes, followed by 5.5 hours of hypoxia exposure, significantly inhibited PPT1 expression and reduced angiogenic responses[5]. Pretreatment of hepatocellular carcinoma cells Hep 3B and Hep 1-6 with DC661 (0.5–3μM) for 6–24 hours, followed by stimulation with sorafenib (1.5–10μM) for 24–48 hours, significantly suppressed PPT1 expression and autophagic activity while enhancing sensitivity to sorafenib[6].

In vivo, intraperitoneal injection of DC661 (3mg/kg/day) for 21 days in melanoma tumor-bearing mice (Ppt1 conditional knockout mice) showed no effect on melanoma tumor initiation or growth[7]. In a lead-exposed (200mg/kg/day for 6 weeks) Wistar rat model, hippocampal stereotactic administration of DC661 (10mM, 5μl/day for 6 weeks) significantly inhibited autophagy levels in hippocampal neurons and upregulated IGF-1 signaling pathway activity. DC661 treatment markedly activated the IGF-1/PI3K/Akt/mTOR pathway, reversed lead-induced excessive autophagy, and improved hippocampal neuronal function[8].

References:
[1] Weng J, Liu S, Zhou Q, et al. Intratumoral PPT1-positive macrophages determine immunosuppressive contexture and immunotherapy response in hepatocellular carcinoma. J Immunother Cancer. 2023 Jun;11(6):e006655.
[2] Jain V, Harper SL, Versace AM, et al. Amaravadi RK. Targeting UGCG Overcomes Resistance to Lysosomal Autophagy Inhibition. Cancer Discov. 2023 Feb 6;13(2):454-473.
[3] Bildik G, Gray JP, Mao W, et al. DIRAS3 induces autophagy and enhances sensitivity to anti-autophagic therapy in KRAS-driven pancreatic and ovarian carcinomas. Autophagy. 2024 Mar;20(3):675-691.
[4] Ferret L, Pol JG, Sauvat A, et al. Lysosomal membrane permeabilization enhances the anticancer effects of POLR1 (RNA polymerase I) transcription inhibitors. Autophagy. 2025 Oct;21(10):2246-2265.
[5] Ma Y, Yuan X, Wei A, et al. Enhancing Gpx1 palmitoylation to inhibit angiogenesis by targeting PPT1. Redox Biol. 2024 Nov;77:103376.
[6] Xu J, Su Z, Cheng X, et al. High PPT1 expression predicts poor clinical outcome and PPT1 inhibitor DC661 enhances sorafenib sensitivity in hepatocellular carcinoma. Cancer Cell Int. 2022 Mar 11;22(1):115.
[7] Crissey MAS, Versace A, Bhardwaj M, et al. Divergent effects of acute and chronic PPT1 inhibition in melanoma. Autophagy. 2025 Feb;21(2):394-406.
[8] Zhang B, Li H, Wang Y, et al. Mechanism of autophagy mediated by IGF-1 signaling pathway in the neurotoxicity of lead in pubertal rats. Ecotoxicol Environ Saf. 2023 Feb;251:114557.

البروتوكول (Protocol)

Cell experiment [1]:

Cell lines

HUVECs (human umbilical vein endothelial cells), HRECs (human retinal endothelial cells), and HEK293T cells

Preparation Method

Cells were maintained in DMEM (HUVECs, HEK293T) or ECM medium (HRECs) supplemented with 10% fetal bovine serum (FBS) and antibiotics at 37°C, 5% CO₂. Cells were treated with DC661 at concentrations of 1.5–3μM for 6–24 hours.

Reaction Conditions

1.5–3μM; 6-24h

Applications

DC661 significantly enhanced Gpx1 palmitoylation levels by inhibiting PPT1, leading to suppressed angiogenesis and cell migration in HUVECs and HRECs. DC661 reduced VEGF and HIF-1α expression under hypoxic conditions and decreased reactive oxygen species (ROS) by stabilizing Gpx1 activity. DC661 also inhibited cell proliferation and induced lysosomal deacidification, impairing autophagic flux.

Animal experiment [2]:

Animal models

Wistar rats (pubertal)

Preparation Method

Rats were exposed to lead Acetate (200mg/kg/day) for 6 weeks. DC661 (10mM) was administered via stereotactic hippocampal injection (5μL/day) until the end of lead exposure. Hippocampal tissues and serum were collected for analysis.

Dosage form

10mM; 5μl/day; Hippocampal microinjection for 6 weeks.

Applications

DC661 significantly inhibited lead-induced autophagy in hippocampal neurons, reduced LC3B and Beclin1 protein levels, and upregulated IGF-1, IGF-1R, p-Akt, and p-mTOR expression. DC661 attenuated lead-impaired learning and memory by modulating the IGF-1/PI3K/Akt/mTOR pathway, demonstrating neuroprotective effects against lead neurotoxicity.

References:
[1] Ma Y, Yuan X, Wei A, et al. Enhancing Gpx1 palmitoylation to inhibit angiogenesis by targeting PPT1. Redox Biol. 2024 Nov;77:103376.
[2] Zhang B, Li H, Wang Y, et al. Mechanism of autophagy mediated by IGF-1 signaling pathway in the neurotoxicity of lead in pubertal rats. Ecotoxicol Environ Saf. 2023 Feb;251:114557.

وثائق المنتج (Product Documents)

Purity:>98.00%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
1872387-43-3
SMILES
CN(CCCCCCNC1=CC=NC2=CC(Cl)=CC=C12)CCCCCCNC3=CC=NC4=CC(Cl)=CC=C34
الصيغة الجزيئية
C₃₁H₃₉Cl₂N₅
الوزن الجزيئي
552.58
الذوبانية
Soluble 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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