Mao B - Search Results

1

Design, synthesis, and biological evaluation of imidazo[1,2-b]pyridazine derivatives as mTOR inhibitors.

Mao B, Gao S, Weng Y, Zhang L, Zhang L. Mao B, et al. Eur J Med Chem. 2017 Mar 31;129:135-150. doi: 10.1016/j.ejmech.2017.02.015. Epub 2017 Feb 9. Eur J Med Chem. 2017. PMID: 28235701

2

Discovery of 2-(2-aminobenzo[d]thiazol-6-yl) benzo[d]oxazol-5-amine derivatives that regulated HPV relevant cellular pathway and prevented cervical cancer from abnormal proliferation.

Jiao P, Wang Y, Mao B, Wang B, Zhong Y, Jin H, Zhang L, Zhang L, Liu Z. Jiao P, et al. Among authors: mao b. Eur J Med Chem. 2020 Oct 15;204:112556. doi: 10.1016/j.ejmech.2020.112556. Epub 2020 Jul 13. Eur J Med Chem. 2020. PMID: 32739649

3

Discovery of N-(Naphtho[1,2-b]Furan-5-Yl) Benzenesulfonamides as Novel Selective Inhibitors of Triple-Negative Breast Cancer (TNBC).

Chen Y, Tang Y, Mao B, Li W, Jin H, Zhang L, Liu Z. Chen Y, et al. Among authors: mao b. Molecules. 2018 Mar 16;23(3):678. doi: 10.3390/molecules23030678. Molecules. 2018. PMID: 29547591 Free PMC article.

4

Synthesis and biological evaluation of quinazolin-4(3H)-one derivatives bearing dithiocarbamate side chain at C2-position as potential antitumor agents.

Ding PP, Gao M, Mao BB, Cao SL, Liu CH, Yang CR, Li ZF, Liao J, Zhao H, Li Z, Li J, Wang H, Xu X. Ding PP, et al. Eur J Med Chem. 2016 Jan 27;108:364-373. doi: 10.1016/j.ejmech.2015.11.044. Epub 2015 Nov 28. Eur J Med Chem. 2016. PMID: 26703795

5

Synthesis and antiproliferative activity of 4-substituted-piperazine-1-carbodithioate derivatives of 2,4-diaminoquinazoline.

Cao SL, Han Y, Yuan CZ, Wang Y, Xiahou ZK, Liao J, Gao RT, Mao BB, Zhao BL, Li ZF, Xu X. Cao SL, et al. Eur J Med Chem. 2013 Jun;64:401-9. doi: 10.1016/j.ejmech.2013.04.017. Epub 2013 Apr 15. Eur J Med Chem. 2013. PMID: 23665106

6

SIRT1 mediates the protective function of Nkx2.5 during stress in cardiomyocytes.

Zheng W, Lu YB, Liang ST, Zhang QJ, Xu J, She ZG, Zhang ZQ, Yang RF, Mao BB, Xu Z, Li L, Hao DL, Lu J, Wei YS, Chen HZ, Liu DP. Zheng W, et al. Basic Res Cardiol. 2013 Jul;108(4):364. doi: 10.1007/s00395-013-0364-y. Epub 2013 Jun 7. Basic Res Cardiol. 2013. PMID: 23744058

7

SIRT1 deacetylates SATB1 to facilitate MAR HS2-MAR ε interaction and promote ε-globin expression.

Xue Z, Lv X, Song W, Wang X, Zhao GN, Wang WT, Xiong J, Mao BB, Yu W, Yang B, Wu J, Zhou LQ, Hao DL, Dong WJ, Liu DP, Liang CC. Xue Z, et al. Among authors: mao bb. Nucleic Acids Res. 2012 Jun;40(11):4804-15. doi: 10.1093/nar/gks064. Epub 2012 Feb 10. Nucleic Acids Res. 2012. PMID: 22328728 Free PMC article.

8

PML4 facilitates erythroid differentiation by enhancing the transcriptional activity of GATA-1.

Wu J, Zhou LQ, Yu W, Zhao ZG, Xie XM, Wang WT, Xiong J, Li M, Xue Z, Wang X, Zhang P, Mao BB, Hao DL, Lv X, Liu DP. Wu J, et al. Blood. 2014 Jan 9;123(2):261-70. doi: 10.1182/blood-2013-02-483289. Epub 2013 Nov 19. Blood. 2014. PMID: 24255919 Free article.

9

Synthesis and Monoamine Oxidase Inhibitory Activity of Halogenated Flavones.

Castillo-Arellano JI, Stryker Z, Wyatt MD, León F. Castillo-Arellano JI, et al. ACS Med Chem Lett. 2024 Apr 3;15(5):610-618. doi: 10.1021/acsmedchemlett.3c00573. eCollection 2024 May 9. ACS Med Chem Lett. 2024. PMID: 38746894

Small molecule neurotransmitters containing amines are metabolized by monoamine oxidase (MAO) in the nervous system. Monoamine oxidase inhibitors are a valuable class of drugs prescribed for the management of neurological disorders, including depressio …

Small molecule neurotransmitters containing amines are metabolized by monoamine oxidase (MAO) in the nervous system. Monoam …

10

In vitro and in vivo metabolism of psilocybin's active metabolite psilocin.

Thomann J, Kolaczynska KE, Stoeckmann OV, Rudin D, Vizeli P, Hoener MC, Pryce CR, Vollenweider FX, Liechti ME, Duthaler U. Thomann J, et al. Front Pharmacol. 2024 Apr 29;15:1391689. doi: 10.3389/fphar.2024.1391689. eCollection 2024. Front Pharmacol. 2024. PMID: 38741590 Free PMC article.

Metabolism studies were performed using human liver microsomes (HLM), cytochrome P450 (CYP) enzymes, monoamine oxidase (MAO), and UDP-glucuronosyltransferase (UGT). In vivo, metabolism was examined using male C57BL/6J mice and human plasma samples. ...

Metabolism studies were performed using human liver microsomes (HLM), cytochrome P450 (CYP) enzymes, monoamine oxidase (MAO), …

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