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1
Building Chemical Probes Based on the Natural Products YM-254890 and FR900359: Advances toward Scalability.
Synthesis (Stuttg). 2023 Jan;55(1):90-106. doi: 10.1055/a-1873-6891. Epub 2022 Oct 6.
2
A Building Block Approach for the Total Synthesis of YM-385781.
European J Org Chem. 2023 May 22;26(20). doi: 10.1002/ejoc.202300365. Epub 2023 Apr 25.
3
Delineation of molecular determinants for FR900359 inhibition of G unlocks inhibition of Gα.
J Biol Chem. 2020 Oct 2;295(40):13850-13861. doi: 10.1074/jbc.RA120.013002. Epub 2020 Aug 4.
4
Structure-activity relationship and conformational studies of the natural product cyclic depsipeptides YM-254890 and FR900359.
Eur J Med Chem. 2018 Aug 5;156:847-860. doi: 10.1016/j.ejmech.2018.07.023. Epub 2018 Jul 12.
5
Recommended Tool Compounds: Application of YM-254890 and FR900359 to Interrogate Gα-Mediated Signaling Pathways.
ACS Pharmacol Transl Sci. 2023 Nov 10;6(12):1790-1800. doi: 10.1021/acsptsci.3c00214. eCollection 2023 Dec 8.
6
Macrocyclic Gq Protein Inhibitors FR900359 and/or YM-254890-Fit for Translation?
ACS Pharmacol Transl Sci. 2021 Feb 19;4(2):888-897. doi: 10.1021/acsptsci.1c00021. eCollection 2021 Apr 9.
7
Structure-Activity Relationship Studies of the Natural Product G Protein Inhibitor YM-254890.
ChemMedChem. 2019 Apr 17;14(8):865-870. doi: 10.1002/cmdc.201900018. Epub 2019 Mar 21.
8
Structural and Dynamical Basis of G Protein Inhibition by YM-254890 and FR900359: An Inhibitor in Action.
J Chem Inf Model. 2019 Oct 28;59(10):4361-4373. doi: 10.1021/acs.jcim.9b00433. Epub 2019 Sep 26.
9
Rational design of a heterotrimeric G protein α subunit with artificial inhibitor sensitivity.
J Biol Chem. 2019 Apr 12;294(15):5747-5758. doi: 10.1074/jbc.RA118.007250. Epub 2019 Feb 11.
10
Total synthesis and structure-activity relationship studies of a series of selective G protein inhibitors.
Nat Chem. 2016 Nov;8(11):1035-1041. doi: 10.1038/nchem.2577. Epub 2016 Jul 25.

引用本文的文献

1
A Building Block Approach for the Total Synthesis of YM-385781.
European J Org Chem. 2023 May 22;26(20). doi: 10.1002/ejoc.202300365. Epub 2023 Apr 25.

本文引用的文献

1
Promoter-Driven Overexpression in Chromobacterium vaccinii Facilitates Access to FR900359 and Yields Novel Low Abundance Analogs.
Chemistry. 2022 Feb 7;28(8):e202103888. doi: 10.1002/chem.202103888. Epub 2021 Dec 28.
3
Anti-hypertensive mechanisms of cyclic depsipeptide inhibitor ligands for G class G proteins.
Pharmacol Res. 2019 Mar;141:264-275. doi: 10.1016/j.phrs.2019.01.012. Epub 2019 Jan 10.
4
Targeting nucleotide exchange to inhibit constitutively active G protein α subunits in cancer cells.
Sci Signal. 2018 Sep 4;11(546):eaao6852. doi: 10.1126/scisignal.aao6852.
5
Structure-activity relationship and conformational studies of the natural product cyclic depsipeptides YM-254890 and FR900359.
Eur J Med Chem. 2018 Aug 5;156:847-860. doi: 10.1016/j.ejmech.2018.07.023. Epub 2018 Jul 12.
6
Deciphering Specificity Determinants for FR900359-Derived G α Inhibitors Based on Computational and Structure-Activity Studies.
ChemMedChem. 2018 Aug 20;13(16):1634-1643. doi: 10.1002/cmdc.201800304. Epub 2018 Jul 3.
7
Proteolytic degradation of regulator of G protein signaling 2 facilitates temporal regulation of G signaling and vascular contraction.
J Biol Chem. 2017 Nov 24;292(47):19266-19278. doi: 10.1074/jbc.M117.797134. Epub 2017 Oct 3.
8
Structure-Activity Relationship Studies of the Cyclic Depsipeptide Natural Product YM-254890, Targeting the G Protein.
ChemMedChem. 2017 Jun 7;12(11):830-834. doi: 10.1002/cmdc.201700155. Epub 2017 May 16.
9
Total synthesis and structure-activity relationship studies of a series of selective G protein inhibitors.
Nat Chem. 2016 Nov;8(11):1035-1041. doi: 10.1038/nchem.2577. Epub 2016 Jul 25.

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