Naamidine J |
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カタログ番号GC27640
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Naamidine J is an imidazole-type alkaloids discovered in a sponge.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 2227550-73-2
Sample solution is provided at 25 µL, 10mM.
Naamidine J is an imidazole-type alkaloids discovered in a sponge. Naamidine J inhibits inflammation by binding to the protein CSE1L (KD = 5.41 μM). Namidine J significantly inhibits the expression of pro-inflammatory factors such as TNF-α, IL-1β, and IL-6, and upregulates anti-inflammatory factors such as CD206 and Arg-1. Namidine J inhibits PD-L1 and shows antitumor activity. Namidine J significantly reduces pulmonary tissue edema, inflammatory cell infiltration and cytokine storm in mice. Namidine J can be used for the research on the immune microenvironment of acute lung injury and tumors[1][2].
Naamidine J (5 μM, 24 h) was cytotoxic to K562 cells with an IC50 of 11.3 μM, but non-toxic to macrophages and RKO cells (IC50 > 40 μM) [1][2].
Naamidine J (10 μM, 24 h) reduced PD-L1 expression in RKO cells and PDAC cells [1][3].
Naamidine J (1-5 μM, 5 h) inhibited LPS-induced inflammatory responses in RAW264.7 macrophages [2].
Naamidine J (5 μM, 5 h) inhibited CSE1L-mediated SP1 nuclear translocation in LPS-induced macrophages [2].
Naamidine J (10 μM, 24 hours) can restore the cytotoxicity of CD8+ T cells and significantly reduce the survival rate of PDAC cells (MIA-PaCa2, BxPC-3)[3].
References:
[1]. Fu PP, et al. Bioactivity-Driven Synthesis of the Marine Natural Product Naamidine J and Its Derivatives as Potential Tumor Immunological Agents by Inhibiting Programmed Death-Ligand 1. J Med Chem. 2023 Apr 27;66(8):5427-5438.
[2]. Gao CL, et al. Chemoproteomics of Marine Natural Product Naamidine J Unveils CSE1L as a Therapeutic Target in Acute Lung Injury. J Am Chem Soc. 2024 Oct 16;146(41):28384-28397.
[3]. Chen E, et al. NAT10 regulates tumor progression and immune microenvironment in pancreatic ductal adenocarcinoma via the N4-acetylated LAMB3-mediated FAK/ERK pathway. Cancer Commun (Lond). 2025 Sep;45(9):1162-1187.
Naamidine J (10-20 mg/kg, intraperitoneal injection, once daily for 3 consecutive days) significantly alleviated LPS-induced acute lung injury and pulmonary edema in mice.
Naamidine J (30 mg/kg, intraperitoneal injection, every three days for 28 days) significantly increased the proportion of CD8+ T cell subsets and decreased the proportion of CD8+ Th cell subsets in tumor-bearing mice with high NAT10 expression.
| Cas No. | 2227550-73-2 | SDF | |
| Formula | C25H27N5O5 | M.Wt | 477.51 |
| 溶解度 | DMSO : 4.55 mg/mL (9.53 mM; ultrasonic and warming and heat to 60°C) | Storage | 4°C, protect from light |
| Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. | ||
| Prepare stock solution | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 2.0942 mL | 10.471 mL | 20.942 mL |
| 5 mM | 418.8 μL | 2.0942 mL | 4.1884 mL |
| 10 mM | 209.4 μL | 1.0471 mL | 2.0942 mL |
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Quality Control & SDS
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- Purity: >98.00% Appearance: A solid
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Average Rating: 5 (Based on Reviews and 30 reference(s) in Google Scholar.)















