Laricitrin
Based on 1 Customer Validation
Laricitrin is a natural product with multiple biological activities. Laricitrin inhibits the phosphorylation and DNA-binding activity of STAT3, and downregulates the expression of IL-10. Laricitrin acts as an immunomodulator to regulate the differentiation, maturation and function of dendritic cells (DCs). Laricitrin inhibits the migration and invasion of lung cancer cells, and ameliorates lung cancer progression. Laricitrin can be used in research related to hypertension and lung cancer.
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研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 純度: 99.36%
- CAS 番号: 53472-37-0
- 分子式: C16H12O8
- 分子量:332.26
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保管条件:
4°C, sealed storage, away from moisture and light
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
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生物活性
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化学情報
- 純度とドキュメンテーション
- 参考文献
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Help & FAQs
生物活性
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STAT3 |
IL-10 |
IL-12 |
Laricitrin binds to regions adjacent to the ACE active site, active site residues of renin, and core active site residues of ATR; it inhibits LPS-induced phosphorylation and DNA-binding activity of STAT3 in human CD14+ monocytes, and downregulates the expression of IL-10[1].
Laricitrin (2 μM; 5 days) restores the differentiation, maturation and cytokine balance (increased IL-12, decreased IL-10) of human CD14+ monocyte-derived dendritic cells impaired by the conditioned medium of A549 or CL1-5 lung cancer cells[1].
Laricitrin (2 μM) restores the T cell activation function of dendritic cells treated with conditioned medium from human A549 or CL1-5 lung cancer cells, promotes the proliferation of naive CD4+ T cells, and shifts the cytokine secretion profile from a Th2-type to a Th1-type pattern[1].
Laricitrin (2 µM; 1 h pretreatment of dendritic cells followed by 24-48 h chemoattractant exposure) inhibits the migration of human lung adenocarcinoma H1395 and HCC2935 cells induced by H1395-TADC-CM, BaP-H1395-TADC-CM, HCC2935-TADC-CM, and BaP-HCC2935-TADC-CM[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:human lung adenocarcinoma H1395 cells, human lung adenocarcinoma HCC2935 cells
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Concentration:2 µM (pretreated on dendritic cells)
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Incubation Time:1 h (dendritic cell pretreatment); 24, 48 h (conditioned media incubation as chemoattractant)
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Result:Inhibited the migration of human lung adenocarcinoma H1395 and HCC2935 cells induced by H1395-TADC-CM, BaP-H1395-TADC-CM, HCC2935-TADC-CM, and BaP-HCC2935-TADC-CM.
Laricitrin (30 mg/kg; i.p.; 3 times over 5 days) potentiates the anticancer activity of Cisplatin (HY-17394) (2.5 mg/kg; i.p.; weekly) in LLC-bearing mice, resulting in fewer lung tumor nodules than Cisplatin treatment alone[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
化学情報
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CAS 番号 53472-37-0
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性状 Solid
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分子量 332.26
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分子式 C16H12O8
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Color Light yellow to yellow
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SMILES
O=C1C(O)=C(C2=CC(OC)=C(O)C(O)=C2)OC3=CC(O)=CC(O)=C13
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Structure Classification
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Initial Source
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
4°C, sealed storage, away from moisture and light
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
純度とドキュメンテーション
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データシート (274 KB)
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SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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取扱説明書 (2659 KB)
参考文献
[1]. Chang WA, et al. Laricitrin ameliorates lung cancer-mediated dendritic cell suppression by inhibiting signal transducer and activator of transcription 3. Oncotarget. 2016 Dec 20;7(51):85220-85234. [Content Brief]
[2]. Chang WA, et al. Laricitrin suppresses increased benzo(a)pyrene-induced lung tumor-associated monocyte-derived dendritic cell cancer progression. Oncology letters. 2016 Mar;11(3):1783-1790. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
Laricitrin 関連分類
HY-N8840 関連分類
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