Ma Y - Search Results

1

Actinomycetes-derived imine reductases with a preference towards bulky amine substrates.

Zhang J, Li X, Chen R, Tan X, Liu X, Ma Y, Zhu F, An C, Wei G, Yao Y, Yang L, Zhang P, Wu Q, Sun Z, Wang BG, Gao SS, Cui C. Zhang J, et al. Among authors: ma y. Commun Chem. 2022 Oct 8;5(1):123. doi: 10.1038/s42004-022-00743-y. Commun Chem. 2022. PMID: 36697820 Free PMC article.

2

Tuning an Imine Reductase for the Asymmetric Synthesis of Azacycloalkylamines by Concise Structure-Guided Engineering.

Zhang J, Liao D, Chen R, Zhu F, Ma Y, Gao L, Qu G, Cui C, Sun Z, Lei X, Gao SS. Zhang J, et al. Among authors: ma y. Angew Chem Int Ed Engl. 2022 Jun 13;61(24):e202201908. doi: 10.1002/anie.202201908. Epub 2022 Apr 7. Angew Chem Int Ed Engl. 2022. PMID: 35322515

3

A hybrid system for the overproduction of complex ergot alkaloid chanoclavine.

Ma Y, Yan J, Yang L, Yao Y, Wang L, Gao SS, Cui C. Ma Y, et al. Front Bioeng Biotechnol. 2022 Dec 21;10:1095464. doi: 10.3389/fbioe.2022.1095464. eCollection 2022. Front Bioeng Biotechnol. 2022. PMID: 36619381 Free PMC article.

4

Structure-guided semi-rational design of an imine reductase for enantio-complementary synthesis of pyrrolidinamine.

Zhang J, Ma Y, Zhu F, Bao J, Wu Q, Gao SS, Cui C. Zhang J, et al. Among authors: ma y. Chem Sci. 2023 Mar 23;14(16):4265-4272. doi: 10.1039/d2sc07014f. eCollection 2023 Apr 26. Chem Sci. 2023. PMID: 37123194 Free PMC article.

5

Semi-rational design of an imine reductase for asymmetric synthesis of alkylated S-4-azepanamines.

Zhu F, Zhang J, Ma Y, Yang L, Gao Q, Gao S, Cui C. Zhu F, et al. Among authors: ma y. Org Biomol Chem. 2023 May 24;21(20):4181-4184. doi: 10.1039/d3ob00442b. Org Biomol Chem. 2023. PMID: 37129863

6

Chemoenzymatic total synthesis of rotigotine via IRED-catalyzed reductive amination.

Tang D, Ma Y, Bao J, Gao S, Man S, Cui C. Tang D, et al. Among authors: ma y. Org Biomol Chem. 2024 May 15;22(19):3843-3847. doi: 10.1039/d4ob00072b. Org Biomol Chem. 2024. PMID: 38618942

7

Synthetic Nicotinamide Cofactors as Alternatives to NADPH in Imine Reductase-Catalyzed Reactions.

Kang W, Gao S, Bao J, Yang L, Ma Y, Wang P, Wang CY, Cui C. Kang W, et al. Among authors: ma y. Org Lett. 2024 Sep 20;26(37):7817-7821. doi: 10.1021/acs.orglett.4c02560. Epub 2024 Aug 23. Org Lett. 2024. PMID: 39178052

8

Engineered Imine Reductase Catalyzed Enantiodivergent Synthesis of Alkylated Amphetamines.

Ma Y, Gao SS, Li X, Wu J, Bao J, Wang L, Cui C. Ma Y, et al. Org Lett. 2024 Sep 13;26(36):7565-7570. doi: 10.1021/acs.orglett.4c02600. Epub 2024 Sep 4. Org Lett. 2024. PMID: 39230034

9

Correction to "Synthetic Nicotinamide Cofactors as Alternatives to NADPH in Imine Reductase-Catalyzed Reactions".

Kang W, Gao S, Bao J, Yang L, Ma Y, Wang P, Wang CY, Cui C. Kang W, et al. Among authors: ma y. Org Lett. 2025 Jan 10;27(1):539. doi: 10.1021/acs.orglett.4c04624. Epub 2024 Dec 20. Org Lett. 2025. PMID: 39704656 No abstract available.

10

Chanoclavine synthase operates by an NADPH-independent superoxide mechanism.

Chen CC, Yu ZP, Liu Z, Yao Y, Hagedoorn PL, Schmitz RA, Yang L, Yu L, Liu A, Sheng X, Su H, Ma Y, Wang T, Huang JW, Zhang L, Yan J, Bao J, Cui C, Li X, Shen P, Zhang W, Min J, Wang CY, Guo RT, Gao SS. Chen CC, et al. Among authors: ma y. Nature. 2025 Apr;640(8059):840-846. doi: 10.1038/s41586-025-08670-3. Epub 2025 Mar 5. Nature. 2025. PMID: 40044871 Free PMC article.

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