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发现一系列新型胍基苯甲酸酯类化合物,作为胃肠道限制型肠肽酶和胰蛋白酶双重抑制剂,用于治疗代谢综合征。

Discovery of a novel series of guanidinebenzoates as gut-restricted enteropeptidase and trypsin dual inhibitors for the treatment of metabolic syndrome.

机构信息

Discovery Chemistry, Janssen Research and Development, LLC, Spring House, PA, United States.

Discovery Chemistry, Janssen Research and Development, LLC, Spring House, PA, United States.

出版信息

Bioorg Med Chem Lett. 2021 May 15;40:127939. doi: 10.1016/j.bmcl.2021.127939. Epub 2021 Mar 11.

DOI:10.1016/j.bmcl.2021.127939
PMID:33713780
Abstract

A novel series of guanidinebenzoate enteropeptidase and trypsin dual inhibitors has been discovered and SAR studies were conducted. Optimization was focused on improving properties for gut restriction, including increased aqueous solubility, lower cellular permeability, and reduced oral bioavailability. Lead compounds were identified with efficacy in a mouse fecal protein excretion study.

摘要

研究人员发现了一系列新型胍基苯甲酸肠肽酶和胰蛋白酶双重抑制剂,并对其进行了构效关系研究。优化的重点是改善肠道限制的特性,包括提高水溶解度、降低细胞通透性和减少口服生物利用度。在小鼠粪便蛋白排泄研究中,确定了具有疗效的先导化合物。

相似文献

1
Discovery of a novel series of guanidinebenzoates as gut-restricted enteropeptidase and trypsin dual inhibitors for the treatment of metabolic syndrome.发现一系列新型胍基苯甲酸酯类化合物,作为胃肠道限制型肠肽酶和胰蛋白酶双重抑制剂,用于治疗代谢综合征。
Bioorg Med Chem Lett. 2021 May 15;40:127939. doi: 10.1016/j.bmcl.2021.127939. Epub 2021 Mar 11.
2
Enteropeptidase inhibition improves obesity by modulating gut microbiota composition and enterobacterial metabolites in diet-induced obese mice.肠肽酶抑制通过调节饮食诱导肥胖小鼠肠道微生物组成和肠杆菌代谢物改善肥胖。
Pharmacol Res. 2021 Jan;163:105337. doi: 10.1016/j.phrs.2020.105337. Epub 2020 Dec 1.
3
SCO-792, an enteropeptidase inhibitor, improves disease status of diabetes and obesity in mice.SCO-792,一种肠肽酶抑制剂,可改善小鼠的糖尿病和肥胖疾病状况。
Diabetes Obes Metab. 2019 Oct;21(10):2228-2239. doi: 10.1111/dom.13799. Epub 2019 Jul 2.
4
Design, Synthesis, and Biological Evaluation of a Novel Series of 4-Guanidinobenzoate Derivatives as Enteropeptidase Inhibitors with Low Systemic Exposure for the Treatment of Obesity.新型 4-胍基苯甲酸酯衍生物作为肠肽酶抑制剂的设计、合成及生物学评价及其用于肥胖治疗的低全身暴露特性。
J Med Chem. 2022 Jun 23;65(12):8456-8477. doi: 10.1021/acs.jmedchem.2c00463. Epub 2022 Jun 10.
5
Targeting Enteropeptidase with Reversible Covalent Inhibitors To Achieve Metabolic Benefits.用可逆共价抑制剂靶向肠肽酶以实现代谢益处。
J Pharmacol Exp Ther. 2020 Dec;375(3):510-521. doi: 10.1124/jpet.120.000219. Epub 2020 Oct 8.
6
Inhibition of trypsin and urokinase by Cbz-amino(4-guanidinophenyl)methanephosphonate aromatic ester derivatives: the influence of the ester group on their biological activity.Cbz-氨基(4-胍基苯基)甲膦酸芳基酯衍生物对胰蛋白酶和尿激酶的抑制作用:酯基对其生物活性的影响。
Bioorg Med Chem Lett. 2006 Jun 1;16(11):2886-90. doi: 10.1016/j.bmcl.2006.03.002. Epub 2006 Mar 20.
7
Synthesis and structure activity relationship of guanidines as NPY Y5 antagonists.胍类作为神经肽Y Y5拮抗剂的合成及其构效关系
Bioorg Med Chem. 2004 May 15;12(10):2691-708. doi: 10.1016/j.bmc.2004.03.012.
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[An inhibitor of enteropeptidases and trypsin from the bovine duodenum].[来自牛十二指肠的肠肽酶和胰蛋白酶抑制剂]
Vopr Med Khim. 1998 Jul-Aug;44(4):338-46.
9
Trypsin inhibitors: promising candidate satietogenic proteins as complementary treatment for obesity and metabolic disorders?胰蛋白酶抑制剂:作为肥胖和代谢紊乱的辅助治疗有前途的饱腹感蛋白候选物?
J Enzyme Inhib Med Chem. 2019 Dec;34(1):405-419. doi: 10.1080/14756366.2018.1542387.
10
Discovery and characterization of a small-molecule enteropeptidase inhibitor, SCO-792.发现并表征小分子肠肽酶抑制剂 SCO-792。
Pharmacol Res Perspect. 2019 Sep 4;7(5):e00517. doi: 10.1002/prp2.517. eCollection 2019 Oct.

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The Global Status and Trends of Enteropeptidase: A Bibliometric Study.肠肽酶的全球现状与趋势:一项文献计量学研究
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