AN15368
AN15368 is an orally active trypanocidal agent and a prodrug of AN14667. AN15368 selectively targets CPSF3-mediated mRNA maturation in intracellular amastigotes of Trypanosoma cruzi, reducing the mRNA levels of the parasite. As a prodrug, AN15368 can be cleaved into its active carboxylate form by CBP of Trypanosoma cruzi. AN15368 completely clears long-term naturally acquired Trypanosoma cruzi infections in non-human primates. AN15368 can be used in the research of Chagas disease.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
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。
- CAS 番号: 2152662-92-3
- 分子式: C20H28BNO6
- 分子量:389.25
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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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
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生物活性
AN15368 (2-fold serial dilutions; 48-72 h) potently inhibits growth of wild-type intracellular T. cruzi amastigotes with an IC50 of 2.4 nM and wild-type extracellular T. cruzi amastigotes with an IC50 of 5 nM[1].
AN15368 (2-fold serial dilutions; 72 h) has reduced susceptibility in intracellular T. cruzi amastigotes overexpressing CPSF3, with an IC50 of 11.8 nM, confirming CPSF3 as a target of AN15368[1].
AN15368 (2-fold serial dilutions; 72 h) has drastically reduced susceptibility in intracellular T. cruzi amastigotes with the engineered Asn232His mutation in CPSF3, with an IC50 of 0.5 μM, confirming CPSF3 as a target of AN15368[1].
AN15368 (2-fold serial dilutions; 72 h) has drastically reduced susceptibility in intracellular T. cruzi amastigotes with disrupted TcCBP, with an IC50 of 2.5 μM, confirming AN15368 requires activation by parasite serine carboxypeptidase[1].
AN15368 (10 μM; 6 h) for epimastigotes, (50 nM) for amastigotes is converted to its active cleaved product AN14667 in wild-type T. cruzi epimastigotes and amastigotes, but not in TcCBP knockout parasites, confirming TcCBP mediates prodrug activation[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
AN15368 (1-5 mg/kg; p.o.; daily; 21 days) reduces Trypanosoma cruzi parasite load in hairless mice, with the 2.5 and 5 mg/kg doses achieving near-complete parasite suppression[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:C57BL/6J (6-9 weeks old, male and female, intraperitoneally infected with 104 Trypanosoma cruzi Brazil strain trypomastigotes)[1]
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Dosage:2.5 and 10 mg/kg
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Administration:p.o.; daily; 40 days
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Result:Showed no parasite recovery by haemoculture and no parasite DNA detection in skeletal muscle via qPCR, with parasite equivalents per 50 ng DNA at or below the assay cut-off.
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Animal Model:SKH-1 hairless backcrossed to C57BL/6J (6-9 weeks old, male and female, intraperitoneally infected with 5 × 104 luciferase-expressing Trypanosoma cruzi Colombiana strain trypomastigotes)[1]
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Dosage:1 mg/kg; 2.5 mg/kg; 5 mg/kg; 10 mg/kg
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Administration:p.o.; daily; 21 days
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Result:Reduced bioluminescence signals over time.
Reduced signals to near background levels (≤104 photons s-1 cm-2) by 30 dpi at 5 mg/kg dose.
Reduced signals to near background levels by 33 dpi at 2.5 mg/kg dose.
Resulted in a significant reduction in bioluminescence signals compared to untreated controls, with signals reaching ~106 photons s-1 cm-2 by 33 dpi at 1 mg/kg dose.
化学情報
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CAS 番号 2152662-92-3
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分子量 389.25
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分子式 C20H28BNO6
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SMILES
OB1OCC2=C1C(C)=C(C=C2)C(N[C@@H](C(C)C)C(OCC3CCOCC3)=O)=O
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
AN15368 関連分類
HY-153238 関連分類
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