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Showing 25 to 33 of 33 entries
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Design, synthesis, and preliminary biological evaluation of catalpol propionates as antiaging drugs.

BMC chemistry

Dong C, Liu S, Cheng X, Wang Q, Jiang S, Wang G.
PMID: 31453572
BMC Chem. 2019 Aug 21;13(1):109. doi: 10.1186/s13065-019-0626-3. eCollection 2019 Dec.

In this paper, catalpol propionylated analogs (CPs) were designed as drug ligands of glutathione peroxidase (GSH-Px) based on molecular docking (MD) using Surflex-Docking method. The calculated total scores (Total_score) and C log

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Dong C, Liu S, Cheng X, et al. Design, synthesis, and preliminary biological evaluation of catalpol propionates as antiaging drugs. BMC Chem. 2019;13(1):109doi: 10.1186/s13065-019-0626-3.
Dong, C., Liu, S., Cheng, X., Wang, Q., Jiang, S., & Wang, G. (2019). Design, synthesis, and preliminary biological evaluation of catalpol propionates as antiaging drugs. BMC chemistry, 13(1), 109. https://doi.org/10.1186/s13065-019-0626-3
Dong, Chunhong, et al. "Design, synthesis, and preliminary biological evaluation of catalpol propionates as antiaging drugs." BMC chemistry vol. 13,1 (2019): 109. doi: https://doi.org/10.1186/s13065-019-0626-3
Dong C, Liu S, Cheng X, Wang Q, Jiang S, Wang G. Design, synthesis, and preliminary biological evaluation of catalpol propionates as antiaging drugs. BMC Chem. 2019 Aug 21;13(1):109. doi: 10.1186/s13065-019-0626-3. eCollection 2019 Dec. PMID: 31453572; PMCID: PMC6702743.
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Preventing Growth of Potentially Toxic Molds Using Antifungal Agents .

Journal of food protection

Ray LL, Bullerman LB.
PMID: 30866272
J Food Prot. 1982 Aug;45(10):953-963. doi: 10.4315/0362-028X-45.10.953.

Mold inhibitors such as sorbates, propionates and benzoates have been used commercially for some time. Recently these and other potential inhibitors have been studied from the standpoint of their effects on growth of potentially toxic molds and mycotoxin production....

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Ray LL, Bullerman LB. Preventing Growth of Potentially Toxic Molds Using Antifungal Agents . J Food Prot. 1982;45(10):953-963doi: 10.4315/0362-028X-45.10.953.
Ray, L. L., & Bullerman, L. B. (1982). Preventing Growth of Potentially Toxic Molds Using Antifungal Agents . Journal of food protection, 45(10), 953-963. https://doi.org/10.4315/0362-028X-45.10.953
Ray, Lisa L, and Bullerman, Lloyd B. "Preventing Growth of Potentially Toxic Molds Using Antifungal Agents ." Journal of food protection vol. 45,10 (1982): 953-963. doi: https://doi.org/10.4315/0362-028X-45.10.953
Ray LL, Bullerman LB. Preventing Growth of Potentially Toxic Molds Using Antifungal Agents . J Food Prot. 1982 Aug;45(10):953-963. doi: 10.4315/0362-028X-45.10.953. PMID: 30866272.
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Regioselectively substituted cellulose benzoate propionates for compensation film in optical displays.

Carbohydrate polymers

Buchanan C, Guzman-Morales E, Wang B.
PMID: 33183604
Carbohydr Polym. 2021 Jan 15;252:117146. doi: 10.1016/j.carbpol.2020.117146. Epub 2020 Sep 28.

Cellulose benzoate propionates (CBzP) were prepared via a staged addition of Pr

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Buchanan C, Guzman-Morales E, Wang B. Regioselectively substituted cellulose benzoate propionates for compensation film in optical displays. Carbohydr Polym. 2020;252:117146doi: 10.1016/j.carbpol.2020.117146.
Buchanan, C., Guzman-Morales, E., & Wang, B. (2021). Regioselectively substituted cellulose benzoate propionates for compensation film in optical displays. Carbohydrate polymers, 252117146. https://doi.org/10.1016/j.carbpol.2020.117146
Buchanan, Charles, et al. "Regioselectively substituted cellulose benzoate propionates for compensation film in optical displays." Carbohydrate polymers vol. 252 (2021): 117146. doi: https://doi.org/10.1016/j.carbpol.2020.117146
Buchanan C, Guzman-Morales E, Wang B. Regioselectively substituted cellulose benzoate propionates for compensation film in optical displays. Carbohydr Polym. 2021 Jan 15;252:117146. doi: 10.1016/j.carbpol.2020.117146. Epub 2020 Sep 28. PMID: 33183604.
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Dynamics of the Degradation of Acetyl-CoA Carboxylase Herbicides in Vegetables.

Foods (Basel, Switzerland)

Jursík M, Hamouzová K, Hajšlová J.
PMID: 33673116
Foods. 2021 Feb 12;10(2). doi: 10.3390/foods10020405.

(1) Background: Aryloxyphenoxy-propionates and cyclohexanediones are herbicides most widely used in dicot crops worldwide. The main objective of the study was to determine the dynamics of herbicide residues in carrot, lettuce, cauliflower, and onion in order to suggest a...

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Jursík M, Hamouzová K, Hajšlová J. Dynamics of the Degradation of Acetyl-CoA Carboxylase Herbicides in Vegetables. Foods. 2021;10(2)doi: 10.3390/foods10020405.
Jursík, M., Hamouzová, K., & Hajšlová, J. (2021). Dynamics of the Degradation of Acetyl-CoA Carboxylase Herbicides in Vegetables. Foods (Basel, Switzerland), 10(2), . https://doi.org/10.3390/foods10020405
Jursík, Miroslav, et al. "Dynamics of the Degradation of Acetyl-CoA Carboxylase Herbicides in Vegetables." Foods (Basel, Switzerland) vol. 10,2 (2021). doi: https://doi.org/10.3390/foods10020405
Jursík M, Hamouzová K, Hajšlová J. Dynamics of the Degradation of Acetyl-CoA Carboxylase Herbicides in Vegetables. Foods. 2021 Feb 12;10(2). doi: 10.3390/foods10020405. PMID: 33673116; PMCID: PMC7918062.
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Synthesis, Spectroscopic, Thermal, and Catalytic Properties of Eight New Complexes of Metal(II) Formates or Propionates with Imidazole; Relationship between the Carbon Chain Length and Catalytic Activity.

Materials (Basel, Switzerland)

Rogalewicz B, Maniecki T, Ciesielski R, Czylkowska A.
PMID: 35009285
Materials (Basel). 2021 Dec 25;15(1). doi: 10.3390/ma15010142.

In one of our previously published articles, we reported the synthesis, spectroscopic, thermal, and catalytic properties of four new M(II) acetate (where M = Co, Ni, Cu, Zn) complexes with imidazole. Presented compounds exhibited activity in the reaction on...

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Rogalewicz B, Maniecki T, Ciesielski R, et al. Synthesis, Spectroscopic, Thermal, and Catalytic Properties of Eight New Complexes of Metal(II) Formates or Propionates with Imidazole; Relationship between the Carbon Chain Length and Catalytic Activity. Materials (Basel). 2021;15(1)doi: 10.3390/ma15010142.
Rogalewicz, B., Maniecki, T., Ciesielski, R., & Czylkowska, A. (2021). Synthesis, Spectroscopic, Thermal, and Catalytic Properties of Eight New Complexes of Metal(II) Formates or Propionates with Imidazole; Relationship between the Carbon Chain Length and Catalytic Activity. Materials (Basel, Switzerland), 15(1), . https://doi.org/10.3390/ma15010142
Rogalewicz, Bartłomiej, et al. "Synthesis, Spectroscopic, Thermal, and Catalytic Properties of Eight New Complexes of Metal(II) Formates or Propionates with Imidazole; Relationship between the Carbon Chain Length and Catalytic Activity." Materials (Basel, Switzerland) vol. 15,1 (2021). doi: https://doi.org/10.3390/ma15010142
Rogalewicz B, Maniecki T, Ciesielski R, Czylkowska A. Synthesis, Spectroscopic, Thermal, and Catalytic Properties of Eight New Complexes of Metal(II) Formates or Propionates with Imidazole; Relationship between the Carbon Chain Length and Catalytic Activity. Materials (Basel). 2021 Dec 25;15(1). doi: 10.3390/ma15010142. PMID: 35009285.
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Tetranuclear copper(I) carboxylates: the effect of a stepwise increase in Lewis acidity on solid-state structures and photoluminescence.

Dalton transactions (Cambridge, England : 2003)

Hietsoi O, Filatov AS, Dubceac C, Petrukhina MA.
PMID: 21805000
Dalton Trans. 2011 Sep 14;40(34):8598-603. doi: 10.1039/c1dt10848d. Epub 2011 Aug 01.

X-Ray diffraction studies of three aliphatic copper(I) carboxylates revealed a tetranuclear core structure for [Cu(4)(O(2)CCH(2)CH(3))(4)] (1), [Cu(4)(O(2)CCF(3))(O(2)CCH(2)CH(3))(3)] (2), and [Cu(4)(O(2)CCF(2)CF(3))(4)] (3). The effect of a stepwise increase in electrophilicity on solid-state interactions of copper(I) tetramers as well as the...

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Hietsoi O, Filatov AS, Dubceac C, et al. Tetranuclear copper(I) carboxylates: the effect of a stepwise increase in Lewis acidity on solid-state structures and photoluminescence. Dalton Trans. 2011;40(34):8598-603doi: 10.1039/c1dt10848d.
Hietsoi, O., Filatov, A. S., Dubceac, C., & Petrukhina, M. A. (2011). Tetranuclear copper(I) carboxylates: the effect of a stepwise increase in Lewis acidity on solid-state structures and photoluminescence. Dalton transactions (Cambridge, England : 2003), 40(34), 8598-603. https://doi.org/10.1039/c1dt10848d
Hietsoi, Oleksandr, et al. "Tetranuclear copper(I) carboxylates: the effect of a stepwise increase in Lewis acidity on solid-state structures and photoluminescence." Dalton transactions (Cambridge, England : 2003) vol. 40,34 (2011): 8598-603. doi: https://doi.org/10.1039/c1dt10848d
Hietsoi O, Filatov AS, Dubceac C, Petrukhina MA. Tetranuclear copper(I) carboxylates: the effect of a stepwise increase in Lewis acidity on solid-state structures and photoluminescence. Dalton Trans. 2011 Sep 14;40(34):8598-603. doi: 10.1039/c1dt10848d. Epub 2011 Aug 01. PMID: 21805000.
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Gut Microbiota Analysis in Rats with Methamphetamine-Induced Conditioned Place Preference.

Frontiers in microbiology

Ning T, Gong X, Xie L, Ma B.
PMID: 28890714
Front Microbiol. 2017 Aug 25;8:1620. doi: 10.3389/fmicb.2017.01620. eCollection 2017.

Methamphetamine abuse is a major public health crisis. Because accumulating evidence supports the hypothesis that the gut microbiota plays an important role in central nervous system (CNS) function, and research on the roles of the microbiome in CNS disorders...

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Ning T, Gong X, Xie L, et al. Gut Microbiota Analysis in Rats with Methamphetamine-Induced Conditioned Place Preference. Front Microbiol. 2017;8:1620doi: 10.3389/fmicb.2017.01620.
Ning, T., Gong, X., Xie, L., & Ma, B. (2017). Gut Microbiota Analysis in Rats with Methamphetamine-Induced Conditioned Place Preference. Frontiers in microbiology, 81620. https://doi.org/10.3389/fmicb.2017.01620
Ning, Tingting, et al. "Gut Microbiota Analysis in Rats with Methamphetamine-Induced Conditioned Place Preference." Frontiers in microbiology vol. 8 (2017): 1620. doi: https://doi.org/10.3389/fmicb.2017.01620
Ning T, Gong X, Xie L, Ma B. Gut Microbiota Analysis in Rats with Methamphetamine-Induced Conditioned Place Preference. Front Microbiol. 2017 Aug 25;8:1620. doi: 10.3389/fmicb.2017.01620. eCollection 2017. PMID: 28890714; PMCID: PMC5575146.
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Growth of Highly Epitaxial YBa2Cu3O(7-δ) Films from a Simple Propionate-Based Solution.

Inorganic chemistry

Zhao Y, Torres P, Tang X, Norby P, Grivel JC.
PMID: 26473556
Inorg Chem. 2015 Nov 02;54(21):10232-8. doi: 10.1021/acs.inorgchem.5b01486. Epub 2015 Oct 16.

Intensive investigations have been conducted to develop epitaxial oxide thin films with superior electromagnetic performance by low-cost chemical solution deposition routes. In this paper, a novel propionate-based precursor solution without involving any other additive was proposed and employed to...

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Zhao Y, Torres P, Tang X, et al. Growth of Highly Epitaxial YBa2Cu3O(7-δ) Films from a Simple Propionate-Based Solution. Inorg Chem. 2015;54(21):10232-8doi: 10.1021/acs.inorgchem.5b01486.
Zhao, Y., Torres, P., Tang, X., Norby, P., & Grivel, J. C. (2015). Growth of Highly Epitaxial YBa2Cu3O(7-δ) Films from a Simple Propionate-Based Solution. Inorganic chemistry, 54(21), 10232-8. https://doi.org/10.1021/acs.inorgchem.5b01486
Zhao, Yue, et al. "Growth of Highly Epitaxial YBa2Cu3O(7-δ) Films from a Simple Propionate-Based Solution." Inorganic chemistry vol. 54,21 (2015): 10232-8. doi: https://doi.org/10.1021/acs.inorgchem.5b01486
Zhao Y, Torres P, Tang X, Norby P, Grivel JC. Growth of Highly Epitaxial YBa2Cu3O(7-δ) Films from a Simple Propionate-Based Solution. Inorg Chem. 2015 Nov 02;54(21):10232-8. doi: 10.1021/acs.inorgchem.5b01486. Epub 2015 Oct 16. PMID: 26473556.
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Influence of heme propionates on the nitrite reductase activity of myoglobin.

Journal of inorganic biochemistry

Galinato MGI, Trail AM, Steinbeck OR, Si Z, Rodland AM, Gowen J.
PMID: 34688205
J Inorg Biochem. 2022 Jan;226:111630. doi: 10.1016/j.jinorgbio.2021.111630. Epub 2021 Oct 16.

The heme propionates in myoglobin (Mb) form a H-bonding network among several residues within its second-sphere coordination, providing a key structural role towards Mb's functional properties. Our work aims to understand the role of the heme propionates on the...

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Galinato MGI, Trail AM, Steinbeck OR, et al. Influence of heme propionates on the nitrite reductase activity of myoglobin. J Inorg Biochem. 2021;226:111630doi: 10.1016/j.jinorgbio.2021.111630.
Galinato, M. G. I., Trail, A. M., Steinbeck, O. R., Si, Z., Rodland, A. M., & Gowen, J. (2022). Influence of heme propionates on the nitrite reductase activity of myoglobin. Journal of inorganic biochemistry, 226111630. https://doi.org/10.1016/j.jinorgbio.2021.111630
Galinato, Mary Grace I, et al. "Influence of heme propionates on the nitrite reductase activity of myoglobin." Journal of inorganic biochemistry vol. 226 (2022): 111630. doi: https://doi.org/10.1016/j.jinorgbio.2021.111630
Galinato MGI, Trail AM, Steinbeck OR, Si Z, Rodland AM, Gowen J. Influence of heme propionates on the nitrite reductase activity of myoglobin. J Inorg Biochem. 2022 Jan;226:111630. doi: 10.1016/j.jinorgbio.2021.111630. Epub 2021 Oct 16. PMID: 34688205.
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Showing 25 to 33 of 33 entries