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IDX-184 is a superior HCV direct-acting antiviral drug: a QSAR study.

Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents

Elfiky AA, Elshemey WM.
PMID: 32214769
Med Chem Res. 2016;25(5):1005-1008. doi: 10.1007/s00044-016-1533-y. Epub 2016 Mar 04.

ABSTRACT: Quantitative structure-activity relationship (QSAR) parameters are good indicators for the reactivity of direct-acting antiviral drugs. Since molecular structure is related to molecular function, careful selection of molecular substitutions will result in more drugs that are potent. In this...

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Elfiky AA, Elshemey WM. IDX-184 is a superior HCV direct-acting antiviral drug: a QSAR study. Med Chem Res. 2016;25(5):1005-1008doi: 10.1007/s00044-016-1533-y.
Elfiky, A. A., & Elshemey, W. M. (2016). IDX-184 is a superior HCV direct-acting antiviral drug: a QSAR study. Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents, 25(5), 1005-1008. https://doi.org/10.1007/s00044-016-1533-y
Elfiky, Abdo A, and Elshemey, Wael M. "IDX-184 is a superior HCV direct-acting antiviral drug: a QSAR study." Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents vol. 25,5 (2016): 1005-1008. doi: https://doi.org/10.1007/s00044-016-1533-y
Elfiky AA, Elshemey WM. IDX-184 is a superior HCV direct-acting antiviral drug: a QSAR study. Med Chem Res. 2016;25(5):1005-1008. doi: 10.1007/s00044-016-1533-y. Epub 2016 Mar 04. PMID: 32214769; PMCID: PMC7080126.
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Social networks and subjective wellbeing of adults in a Housing First program.

Journal of community psychology

Addo R, Yuma P, Barrera I, Layton D, McKay FH, Dunn M.
PMID: 33751632
J Community Psychol. 2021 Mar 22; doi: 10.1002/jcop.22548. Epub 2021 Mar 22.

This study explored the social network properties and the correlates between social networks and subjective wellbeing of adults (N = 80) in a Housing First (HF) program. Using structured interviews, participants' social network properties were assessed. Bivariate correlations and...

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Addo R, Yuma P, Barrera I, et al. Social networks and subjective wellbeing of adults in a Housing First program. J Community Psychol. 2021;doi: 10.1002/jcop.22548.
Addo, R., Yuma, P., Barrera, I., Layton, D., McKay, F. H., & Dunn, M. (2021). Social networks and subjective wellbeing of adults in a Housing First program. Journal of community psychology, . https://doi.org/10.1002/jcop.22548
Addo, Reuben, et al. "Social networks and subjective wellbeing of adults in a Housing First program." Journal of community psychology vol. (2021). doi: https://doi.org/10.1002/jcop.22548
Addo R, Yuma P, Barrera I, Layton D, McKay FH, Dunn M. Social networks and subjective wellbeing of adults in a Housing First program. J Community Psychol. 2021 Mar 22; doi: 10.1002/jcop.22548. Epub 2021 Mar 22. PMID: 33751632.
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Regulation of Tumor Metabolism and Extracellular Acidosis by the TIMP-10-CD63 Axis in Breast Carcinoma.

Cells

Najy AJ, Jung YS, Kim S, Fridman R, Kim HC.
PMID: 34685701
Cells. 2021 Oct 12;10(10). doi: 10.3390/cells10102721.

A hallmark of malignant solid tumor is extracellular acidification coupled with metabolic switch to aerobic glycolysis. Using the human MCF10A progression model of breast cancer, we show that glycolytic switch and extracellular acidosis in aggressive cancer cells correlate with...

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Najy AJ, Jung YS, Kim S, et al. Regulation of Tumor Metabolism and Extracellular Acidosis by the TIMP-10-CD63 Axis in Breast Carcinoma. Cells. 2021;10(10)doi: 10.3390/cells10102721.
Najy, A. J., Jung, Y. S., Kim, S., Fridman, R., & Kim, H. C. (2021). Regulation of Tumor Metabolism and Extracellular Acidosis by the TIMP-10-CD63 Axis in Breast Carcinoma. Cells, 10(10), . https://doi.org/10.3390/cells10102721
Najy, Abdo J, et al. "Regulation of Tumor Metabolism and Extracellular Acidosis by the TIMP-10-CD63 Axis in Breast Carcinoma." Cells vol. 10,10 (2021). doi: https://doi.org/10.3390/cells10102721
Najy AJ, Jung YS, Kim S, Fridman R, Kim HC. Regulation of Tumor Metabolism and Extracellular Acidosis by the TIMP-10-CD63 Axis in Breast Carcinoma. Cells. 2021 Oct 12;10(10). doi: 10.3390/cells10102721. PMID: 34685701; PMCID: PMC8535136.
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Dual Trapping of a Metastable Planarized Triarylborane π-System Based on Folding and Lewis Acid-Base Complexation for Seeded Polymerization.

Journal of the American Chemical Society

Choi H, Ogi S, Ando N, Yamaguchi S.
PMID: 33565863
J Am Chem Soc. 2021 Feb 24;143(7):2953-2961. doi: 10.1021/jacs.0c13353. Epub 2021 Feb 10.

We report the kinetically controlled supramolecular polymerization of boron-containing π-conjugated molecules, which was enabled by a seeding method based on dual trapping of a metastable state by synergistic intramolecular hydrogen bonding and Lewis acid-based complexation. Planarized triarylborane-based

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Choi H, Ogi S, Ando N, et al. Dual Trapping of a Metastable Planarized Triarylborane π-System Based on Folding and Lewis Acid-Base Complexation for Seeded Polymerization. J Am Chem Soc. 2021;143(7):2953-2961doi: 10.1021/jacs.0c13353.
Choi, H., Ogi, S., Ando, N., & Yamaguchi, S. (2021). Dual Trapping of a Metastable Planarized Triarylborane π-System Based on Folding and Lewis Acid-Base Complexation for Seeded Polymerization. Journal of the American Chemical Society, 143(7), 2953-2961. https://doi.org/10.1021/jacs.0c13353
Choi, Heekyoung, et al. "Dual Trapping of a Metastable Planarized Triarylborane π-System Based on Folding and Lewis Acid-Base Complexation for Seeded Polymerization." Journal of the American Chemical Society vol. 143,7 (2021): 2953-2961. doi: https://doi.org/10.1021/jacs.0c13353
Choi H, Ogi S, Ando N, Yamaguchi S. Dual Trapping of a Metastable Planarized Triarylborane π-System Based on Folding and Lewis Acid-Base Complexation for Seeded Polymerization. J Am Chem Soc. 2021 Feb 24;143(7):2953-2961. doi: 10.1021/jacs.0c13353. Epub 2021 Feb 10. PMID: 33565863.
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GRP78: A possible relationship of COVID-19 and the mucormycosis; in silico perspective.

Computers in biology and medicine

Elgohary AM, Elfiky AA, Barakat K.
PMID: 34695683
Comput Biol Med. 2021 Dec;139:104956. doi: 10.1016/j.compbiomed.2021.104956. Epub 2021 Oct 23.

Mucormycosis is a severe fungal infection reported in many cancer survivors, diabetic and immune-suppressed patients during organ transplants. A vast spark in the reported COVID-19 cases is noticed in India during the second wave in May 2021, when Mucormycosis...

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Elgohary AM, Elfiky AA, Barakat K. GRP78: A possible relationship of COVID-19 and the mucormycosis; in silico perspective. Comput Biol Med. 2021;139:104956doi: 10.1016/j.compbiomed.2021.104956.
Elgohary, A. M., Elfiky, A. A., & Barakat, K. (2021). GRP78: A possible relationship of COVID-19 and the mucormycosis; in silico perspective. Computers in biology and medicine, 139104956. https://doi.org/10.1016/j.compbiomed.2021.104956
Elgohary, Alaa M, et al. "GRP78: A possible relationship of COVID-19 and the mucormycosis; in silico perspective." Computers in biology and medicine vol. 139 (2021): 104956. doi: https://doi.org/10.1016/j.compbiomed.2021.104956
Elgohary AM, Elfiky AA, Barakat K. GRP78: A possible relationship of COVID-19 and the mucormycosis; in silico perspective. Comput Biol Med. 2021 Dec;139:104956. doi: 10.1016/j.compbiomed.2021.104956. Epub 2021 Oct 23. PMID: 34695683; PMCID: PMC8536376.
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Maternal and fetal serum leptin levels and their association with maternal and fetal variables and labor: A cross-sectional study.

Annals of medicine and surgery (2012)

Obeidat RA, Abdo N, Sakee B, Alghazo S, Jbarah OF, Hazaimeh EA, Albeitawi S.
PMID: 34815864
Ann Med Surg (Lond). 2021 Nov 14;72:103050. doi: 10.1016/j.amsu.2021.103050. eCollection 2021 Dec.

BACKGROUND: Leptin is a polypeptide hormone that may be implicated in the pathogenesis of various disorders during pregnancy. We sought to determine serum leptin levels among pregnant women and their fetuses and to investigate their association with fetal and...

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Obeidat RA, Abdo N, Sakee B, et al. Maternal and fetal serum leptin levels and their association with maternal and fetal variables and labor: A cross-sectional study. Ann Med Surg (Lond). 2021;72:103050doi: 10.1016/j.amsu.2021.103050.
Obeidat, R. A., Abdo, N., Sakee, B., Alghazo, S., Jbarah, O. F., Hazaimeh, E. A., & Albeitawi, S. (2021). Maternal and fetal serum leptin levels and their association with maternal and fetal variables and labor: A cross-sectional study. Annals of medicine and surgery (2012), 72103050. https://doi.org/10.1016/j.amsu.2021.103050
Obeidat, Rawan A, et al. "Maternal and fetal serum leptin levels and their association with maternal and fetal variables and labor: A cross-sectional study." Annals of medicine and surgery (2012) vol. 72 (2021): 103050. doi: https://doi.org/10.1016/j.amsu.2021.103050
Obeidat RA, Abdo N, Sakee B, Alghazo S, Jbarah OF, Hazaimeh EA, Albeitawi S. Maternal and fetal serum leptin levels and their association with maternal and fetal variables and labor: A cross-sectional study. Ann Med Surg (Lond). 2021 Nov 14;72:103050. doi: 10.1016/j.amsu.2021.103050. eCollection 2021 Dec. PMID: 34815864; PMCID: PMC8591461.
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A phase 3, open-label, randomized study of asciminib, a STAMP inhibitor, vs bosutinib in CML after 2 or more prior TKIs.

Blood

Réa D, Mauro MJ, Boquimpani C, Minami Y, Lomaia E, Voloshin S, Turkina A, Kim DW, Apperley JF, Abdo A, Fogliatto LM, Kim DDH, le Coutre P, Saussele S, Annunziata M, Hughes TP, Chaudhri N, Sasaki K, Chee L, García-Gutiérrez V, Cortes JE, Aimone P, Allepuz A, Quenet S, Bédoucha V, Hochhaus A.
PMID: 34407542
Blood. 2021 Nov 25;138(21):2031-2041. doi: 10.1182/blood.2020009984.

Patients with chronic myeloid leukemia in chronic phase (CML-CP) resistant/intolerant to ≥2 tyrosine kinase inhibitors (TKIs) are at high risk of experiencing poor outcomes because of disease biology and inadequate efficacy and/or safety of current therapies. Asciminib, a first-in-class...

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Réa D, Mauro MJ, Boquimpani C, et al. A phase 3, open-label, randomized study of asciminib, a STAMP inhibitor, vs bosutinib in CML after 2 or more prior TKIs. Blood. 2021;138(21):2031-2041doi: 10.1182/blood.2020009984.
Réa, D., Mauro, M. J., Boquimpani, C., Minami, Y., Lomaia, E., Voloshin, S., Turkina, A., Kim, D. W., Apperley, J. F., Abdo, A., Fogliatto, L. M., Kim, D. D. H., le Coutre, P., Saussele, S., Annunziata, M., Hughes, T. P., Chaudhri, N., Sasaki, K., Chee, L., García-Gutiérrez, V., Cortes, J. E., Aimone, P., Allepuz, A., Quenet, S., Bédoucha, V., & Hochhaus, A. (2021). A phase 3, open-label, randomized study of asciminib, a STAMP inhibitor, vs bosutinib in CML after 2 or more prior TKIs. Blood, 138(21), 2031-2041. https://doi.org/10.1182/blood.2020009984
Réa, Delphine, et al. "A phase 3, open-label, randomized study of asciminib, a STAMP inhibitor, vs bosutinib in CML after 2 or more prior TKIs." Blood vol. 138,21 (2021): 2031-2041. doi: https://doi.org/10.1182/blood.2020009984
Réa D, Mauro MJ, Boquimpani C, Minami Y, Lomaia E, Voloshin S, Turkina A, Kim DW, Apperley JF, Abdo A, Fogliatto LM, Kim DDH, le Coutre P, Saussele S, Annunziata M, Hughes TP, Chaudhri N, Sasaki K, Chee L, García-Gutiérrez V, Cortes JE, Aimone P, Allepuz A, Quenet S, Bédoucha V, Hochhaus A. A phase 3, open-label, randomized study of asciminib, a STAMP inhibitor, vs bosutinib in CML after 2 or more prior TKIs. Blood. 2021 Nov 25;138(21):2031-2041. doi: 10.1182/blood.2020009984. PMID: 34407542.
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Prevalence of Childhood Short Stature, Underweight, Overweight, and Obesity Among Primary School Children.

Cureus

Bouali H, Boujtat K, Ezzerrouqui A, Lazreg Y, Rouf S, Abda N, Latrech H.
PMID: 34956770
Cureus. 2021 Nov 16;13(11):e19651. doi: 10.7759/cureus.19651. eCollection 2021 Nov.

Background This study, the first of its kind in Morocco, was conducted to compare the prevalence of growth disorders among children enrolled in public, private, urban, and rural schools in Oujda-Angad Province. Methods A cross-sectional observational study was conducted...

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Bouali H, Boujtat K, Ezzerrouqui A, et al. Prevalence of Childhood Short Stature, Underweight, Overweight, and Obesity Among Primary School Children. Cureus. 2021;13(11):e19651doi: 10.7759/cureus.19651.
Bouali, H., Boujtat, K., Ezzerrouqui, A., Lazreg, Y., Rouf, S., Abda, N., & Latrech, H. (2021). Prevalence of Childhood Short Stature, Underweight, Overweight, and Obesity Among Primary School Children. Cureus, 13(11), e19651. https://doi.org/10.7759/cureus.19651
Bouali, Houda, et al. "Prevalence of Childhood Short Stature, Underweight, Overweight, and Obesity Among Primary School Children." Cureus vol. 13,11 (2021): e19651. doi: https://doi.org/10.7759/cureus.19651
Bouali H, Boujtat K, Ezzerrouqui A, Lazreg Y, Rouf S, Abda N, Latrech H. Prevalence of Childhood Short Stature, Underweight, Overweight, and Obesity Among Primary School Children. Cureus. 2021 Nov 16;13(11):e19651. doi: 10.7759/cureus.19651. eCollection 2021 Nov. PMID: 34956770; PMCID: PMC8675597.
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Deciphering OPDA Signaling Components in the Momilactone-Producing Moss .

Frontiers in plant science

Inagaki H, Miyamoto K, Ando N, Murakami K, Sugisawa K, Morita S, Yumoto E, Teruya M, Uchida K, Kato N, Kaji T, Takaoka Y, Hojo Y, Shinya T, Galis I, Nozawa A, Sawasaki T, Nojiri H, Ueda M, Okada K.
PMID: 34135933
Front Plant Sci. 2021 May 31;12:688565. doi: 10.3389/fpls.2021.688565. eCollection 2021.

Jasmonic acid (JA) and its biologically active form jasmonoyl-L-isoleucine (JA-Ile) regulate defense responses to various environmental stresses and developmental processes in plants. JA and JA-Ile are synthesized from α-linolenic acids derived from membrane lipids

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Inagaki H, Miyamoto K, Ando N, et al. Deciphering OPDA Signaling Components in the Momilactone-Producing Moss . Front Plant Sci. 2021;12:688565doi: 10.3389/fpls.2021.688565.
Inagaki, H., Miyamoto, K., Ando, N., Murakami, K., Sugisawa, K., Morita, S., Yumoto, E., Teruya, M., Uchida, K., Kato, N., Kaji, T., Takaoka, Y., Hojo, Y., Shinya, T., Galis, I., Nozawa, A., Sawasaki, T., Nojiri, H., Ueda, M., & Okada, K. (2021). Deciphering OPDA Signaling Components in the Momilactone-Producing Moss . Frontiers in plant science, 12688565. https://doi.org/10.3389/fpls.2021.688565
Inagaki, Hideo, et al. "Deciphering OPDA Signaling Components in the Momilactone-Producing Moss ." Frontiers in plant science vol. 12 (2021): 688565. doi: https://doi.org/10.3389/fpls.2021.688565
Inagaki H, Miyamoto K, Ando N, Murakami K, Sugisawa K, Morita S, Yumoto E, Teruya M, Uchida K, Kato N, Kaji T, Takaoka Y, Hojo Y, Shinya T, Galis I, Nozawa A, Sawasaki T, Nojiri H, Ueda M, Okada K. Deciphering OPDA Signaling Components in the Momilactone-Producing Moss . Front Plant Sci. 2021 May 31;12:688565. doi: 10.3389/fpls.2021.688565. eCollection 2021. PMID: 34135933; PMCID: PMC8201998.
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EDP-305 in patients with NASH: A phase II double-blind placebo-controlled dose-ranging study.

Journal of hepatology

Ratziu V, Rinella ME, Neuschwander-Tetri BA, Lawitz E, Denham D, Kayali Z, Sheikh A, Kowdley KV, Desta T, Elkhashab M, DeGrauw J, Goodwin B, Ahmad A, Adda N.
PMID: 34740705
J Hepatol. 2021 Nov 02; doi: 10.1016/j.jhep.2021.10.018. Epub 2021 Nov 02.

BACKGROUND & AIMS: EDP-305 is an oral farnesoid X receptor (FXR) agonist under development for treating nonalcoholic steatohepatitis (NASH). The efficacy, safety, and tolerability of EDP-305 was evaluated in a Phase 2, randomized, double-blind, placebo-controlled study.METHODS: Non-cirrhotic patients with...

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Ratziu V, Rinella ME, Neuschwander-Tetri BA, et al. EDP-305 in patients with NASH: A phase II double-blind placebo-controlled dose-ranging study. J Hepatol. 2021;doi: 10.1016/j.jhep.2021.10.018.
Ratziu, V., Rinella, M. E., Neuschwander-Tetri, B. A., Lawitz, E., Denham, D., Kayali, Z., Sheikh, A., Kowdley, K. V., Desta, T., Elkhashab, M., DeGrauw, J., Goodwin, B., Ahmad, A., & Adda, N. (2021). EDP-305 in patients with NASH: A phase II double-blind placebo-controlled dose-ranging study. Journal of hepatology, . https://doi.org/10.1016/j.jhep.2021.10.018
Ratziu, Vlad, et al. "EDP-305 in patients with NASH: A phase II double-blind placebo-controlled dose-ranging study." Journal of hepatology vol. (2021). doi: https://doi.org/10.1016/j.jhep.2021.10.018
Ratziu V, Rinella ME, Neuschwander-Tetri BA, Lawitz E, Denham D, Kayali Z, Sheikh A, Kowdley KV, Desta T, Elkhashab M, DeGrauw J, Goodwin B, Ahmad A, Adda N. EDP-305 in patients with NASH: A phase II double-blind placebo-controlled dose-ranging study. J Hepatol. 2021 Nov 02; doi: 10.1016/j.jhep.2021.10.018. Epub 2021 Nov 02. PMID: 34740705.
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Boron-Doped Polycyclic π-Electron Systems with an Antiaromatic Borole Substructure That Forms Photoresponsive B-P Lewis Adducts.

Journal of the American Chemical Society

Ando N, Yamada T, Narita H, Oehlmann NN, Wagner M, Yamaguchi S.
PMID: 34109785
J Am Chem Soc. 2021 Jul 07;143(26):9944-9951. doi: 10.1021/jacs.1c04251. Epub 2021 Jun 10.

Heteroatom doping is a powerful strategy to alter the electronic structure of polycyclic aromatic hydrocarbons (PAHs). Especially boron doping endows PAH scaffolds with electron-accepting character and Lewis acidic centers. Herein, we report that embedding a five-membered borole ring into...

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Ando N, Yamada T, Narita H, et al. Boron-Doped Polycyclic π-Electron Systems with an Antiaromatic Borole Substructure That Forms Photoresponsive B-P Lewis Adducts. J Am Chem Soc. 2021;143(26):9944-9951doi: 10.1021/jacs.1c04251.
Ando, N., Yamada, T., Narita, H., Oehlmann, N. N., Wagner, M., & Yamaguchi, S. (2021). Boron-Doped Polycyclic π-Electron Systems with an Antiaromatic Borole Substructure That Forms Photoresponsive B-P Lewis Adducts. Journal of the American Chemical Society, 143(26), 9944-9951. https://doi.org/10.1021/jacs.1c04251
Ando, Naoki, et al. "Boron-Doped Polycyclic π-Electron Systems with an Antiaromatic Borole Substructure That Forms Photoresponsive B-P Lewis Adducts." Journal of the American Chemical Society vol. 143,26 (2021): 9944-9951. doi: https://doi.org/10.1021/jacs.1c04251
Ando N, Yamada T, Narita H, Oehlmann NN, Wagner M, Yamaguchi S. Boron-Doped Polycyclic π-Electron Systems with an Antiaromatic Borole Substructure That Forms Photoresponsive B-P Lewis Adducts. J Am Chem Soc. 2021 Jul 07;143(26):9944-9951. doi: 10.1021/jacs.1c04251. Epub 2021 Jun 10. PMID: 34109785.
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Corrigendum to "Ribavirin, Remdesivir, Sofosbuvir, Galidesivir, and Tenofovir against SARSCoV-2 RNA dependent RNA polymerase (RdRp): A molecular docking study" [Life Sci. 253 (2020) 117592].

Life sciences

Elfiky AA.
PMID: 32863005
Life Sci. 2020 Oct 01;258:118350. doi: 10.1016/j.lfs.2020.118350. Epub 2020 Aug 28.

No abstract available.

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Elfiky AA. Corrigendum to "Ribavirin, Remdesivir, Sofosbuvir, Galidesivir, and Tenofovir against SARSCoV-2 RNA dependent RNA polymerase (RdRp): A molecular docking study" [Life Sci. 253 (2020) 117592]. Life Sci. 2020;258:118350doi: 10.1016/j.lfs.2020.118350.
Elfiky, A. A. (2020). Corrigendum to "Ribavirin, Remdesivir, Sofosbuvir, Galidesivir, and Tenofovir against SARSCoV-2 RNA dependent RNA polymerase (RdRp): A molecular docking study" [Life Sci. 253 (2020) 117592]. Life sciences, 258118350. https://doi.org/10.1016/j.lfs.2020.118350
Elfiky, Abdo A. "Corrigendum to "Ribavirin, Remdesivir, Sofosbuvir, Galidesivir, and Tenofovir against SARSCoV-2 RNA dependent RNA polymerase (RdRp): A molecular docking study" [Life Sci. 253 (2020) 117592]." Life sciences vol. 258 (2020): 118350. doi: https://doi.org/10.1016/j.lfs.2020.118350
Elfiky AA. Corrigendum to "Ribavirin, Remdesivir, Sofosbuvir, Galidesivir, and Tenofovir against SARSCoV-2 RNA dependent RNA polymerase (RdRp): A molecular docking study" [Life Sci. 253 (2020) 117592]. Life Sci. 2020 Oct 01;258:118350. doi: 10.1016/j.lfs.2020.118350. Epub 2020 Aug 28. PMID: 32863005; PMCID: PMC7957227.
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