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DC-LC3in-D5 Sale

目录号 : GC65191

DC-LC3in-D5 通过减弱 LC3B 脂化作用而作为自噬 (autophagy) 抑制剂。DC-LC3in-D5 与 LC3B 结合。DC-LC3in-D5 破坏 LC3B-LBP2 相互作用,IC50 为 200 nM。DC-LC3in-D5 可能通过抑制自噬有助于抗 HCV 或肿瘤的联合治疗。

DC-LC3in-D5 Chemical Structure

Cas No.:2868312-73-4

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5mg
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Sample solution is provided at 25 µL, 10mM.

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产品描述

DC-LC3in-D5 acts as an autophagy inhibitor by attenuating LC3B lipidation. DC-LC3in-D5 binds with LC3B. DC-LC3in-D5 disrupts the LC3B-LBP2 interaction with an IC50 of 200 nM. DC-LC3in-D5 may contribute to anti-HCV or combination treatments in cancer through inhibiting autophagy[1].

DC-LC3in-D5 demonstrates high selectivity to LC3A/B in the proteome. DC-LC3in-D5 exhibits a potent covalent reactivity and selectivity to LC3A/B in HeLa cells[1].Treatment of HeLa cells with DC-LC3in-D5 (3-30 μM) results in disruption of LC3B lipidation, inhibition of autophagic vesicle formation, and accumulation of p62[1].

[1]. Shijie Fan, et al. Inhibition of Autophagy by a Small Molecule through Covalent Modification of the LC3 Protein. Angew Chem Int Ed Engl. 2021 Dec 6;60(50):26105-26114.

Chemical Properties

Cas No. 2868312-73-4 SDF Download SDF
分子式 C19H22Cl2N2O3 分子量 397.3
溶解度 DMSO : 35.71 mg/mL (89.88 mM; ultrasonic and warming and heat to 60°C) 储存条件 Store at -20°C
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1 mM 2.517 mL 12.5849 mL 25.1699 mL
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10 mM 0.2517 mL 1.2585 mL 2.517 mL
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Research Update

Inhibition of Autophagy by a Small Molecule through Covalent Modification of the LC3 Protein

Angew Chem Int Ed Engl 2021 Dec 6;60(50):26105-26114.PMID:34590387DOI:PMC8845813

The autophagic ubiquitin-like protein LC3 functions through interactions with LC3-interaction regions (LIRs) of other autophagy proteins, including autophagy receptors, which stands out as a promising protein-protein interaction (PPI) target for the intervention of autophagy. Post-translational modifications like acetylation of Lys49 on the LIR-interacting surface could disrupt the interaction, offering an opportunity to design covalent small molecules interfering with the interface. Through screening covalent compounds, we discovered a small molecule modulator of LC3A/B that covalently modifies LC3A/B protein at Lys49. Activity-based protein profiling (ABPP) based evaluations reveal that a derivative molecule DC-LC3in-D5 exhibits a potent covalent reactivity and selectivity to LC3A/B in HeLa cells. DC-LC3in-D5 compromises LC3B lipidation in vitro and in HeLa cells, leading to deficiency in the formation of autophagic structures and autophagic substrate degradation. DC-LC3in-D5 could serve as a powerful tool for autophagy research as well as for therapeutic interventions.