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Effects of electron transport inhibitors on iron reduction in Aeromonas hydrophila strain KB1.

Anaerobe

Woźnica A, Dzirba J, Mańka D, Łabuzek S.
PMID: 16887699
Anaerobe. 2003 Jun;9(3):125-30. doi: 10.1016/S1075-9964(03)00059-3.

The aim of this study was to determine the influence of respiratory chain inhibitors upon iron (III) reduction in Aeromonas hydrophila strain KB1. Optimal conditions of the reduction process were established by determining the amount of biomass, optimal pH,...

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Woźnica A, Dzirba J, Mańka D, et al. Effects of electron transport inhibitors on iron reduction in Aeromonas hydrophila strain KB1. Anaerobe. 2003;9(3):125-30doi: 10.1016/S1075-9964(03)00059-3.
Woźnica, A., Dzirba, J., Mańka, D., & Łabuzek, S. (2003). Effects of electron transport inhibitors on iron reduction in Aeromonas hydrophila strain KB1. Anaerobe, 9(3), 125-30. https://doi.org/10.1016/S1075-9964(03)00059-3
Woźnica, A, et al. "Effects of electron transport inhibitors on iron reduction in Aeromonas hydrophila strain KB1." Anaerobe vol. 9,3 (2003): 125-30. doi: https://doi.org/10.1016/S1075-9964(03)00059-3
Woźnica A, Dzirba J, Mańka D, Łabuzek S. Effects of electron transport inhibitors on iron reduction in Aeromonas hydrophila strain KB1. Anaerobe. 2003 Jun;9(3):125-30. doi: 10.1016/S1075-9964(03)00059-3. PMID: 16887699.
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USE OF THE ANTI-COAGULANTS, HEPARIN AND DICUMAROL.

California medicine

Lucia SP.
PMID: 18731057
Calif Med. 1946 Jul;65(1):5-8.

No abstract available.

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Lucia SP. USE OF THE ANTI-COAGULANTS, HEPARIN AND DICUMAROL. Calif Med. 1946;65(1):5-8
Lucia, S. P. (1946). USE OF THE ANTI-COAGULANTS, HEPARIN AND DICUMAROL. California medicine, 65(1), 5-8.
Lucia, S P. "USE OF THE ANTI-COAGULANTS, HEPARIN AND DICUMAROL." California medicine vol. 65,1 (1946): 5-8.
Lucia SP. USE OF THE ANTI-COAGULANTS, HEPARIN AND DICUMAROL. Calif Med. 1946 Jul;65(1):5-8. PMID: 18731057; PMCID: PMC1642563.
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MEDICAL PROGRESS: DICUMAROL.

California medicine

Petit DW, Berne CJ.
PMID: 18731257
Calif Med. 1947 Jul;67(1):40-4.

No abstract available.

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Petit DW, Berne CJ. MEDICAL PROGRESS: DICUMAROL. Calif Med. 1947;67(1):40-4
Petit, D. W., & Berne, C. J. (1947). MEDICAL PROGRESS: DICUMAROL. California medicine, 67(1), 40-4.
Petit, D W, and Berne, C J. "MEDICAL PROGRESS: DICUMAROL." California medicine vol. 67,1 (1947): 40-4.
Petit DW, Berne CJ. MEDICAL PROGRESS: DICUMAROL. Calif Med. 1947 Jul;67(1):40-4. PMID: 18731257; PMCID: PMC1642890.
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Metabolism, tissue distribution, and pharmacokinetics of N-methyl-N-2,4,6-tetranitroaniline (tetryl).

Environmental toxicology and pharmacology

Myers SR, Spinnato JA.
PMID: 21783812
Environ Toxicol Pharmacol. 2007 Nov;24(3):206-11. doi: 10.1016/j.etap.2007.05.005. Epub 2007 May 24.

Tetryl (N-methyl-N,2,4,6-tetranitroaniline) is a booster explosive that was used in the production of detonators and blasting caps. It is an environmental contaminant that is found in detectable levels in areas associated with its production, use, storage, and disposal. Preliminary...

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Myers SR, Spinnato JA. Metabolism, tissue distribution, and pharmacokinetics of N-methyl-N-2,4,6-tetranitroaniline (tetryl). Environ Toxicol Pharmacol. 2007;24(3):206-11doi: 10.1016/j.etap.2007.05.005.
Myers, S. R., & Spinnato, J. A. (2007). Metabolism, tissue distribution, and pharmacokinetics of N-methyl-N-2,4,6-tetranitroaniline (tetryl). Environmental toxicology and pharmacology, 24(3), 206-11. https://doi.org/10.1016/j.etap.2007.05.005
Myers, Steven R, and Spinnato, Joseph A. "Metabolism, tissue distribution, and pharmacokinetics of N-methyl-N-2,4,6-tetranitroaniline (tetryl)." Environmental toxicology and pharmacology vol. 24,3 (2007): 206-11. doi: https://doi.org/10.1016/j.etap.2007.05.005
Myers SR, Spinnato JA. Metabolism, tissue distribution, and pharmacokinetics of N-methyl-N-2,4,6-tetranitroaniline (tetryl). Environ Toxicol Pharmacol. 2007 Nov;24(3):206-11. doi: 10.1016/j.etap.2007.05.005. Epub 2007 May 24. PMID: 21783812.
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Photovoltaic and electrocatalytic properties of novel ball-type phthalocyanines bridged with four dicumarol.

Dalton transactions (Cambridge, England : 2003)

Salan Ü, Altındal A, Özkaya AR, Salih B, Bekaroğlu Ö.
PMID: 22430033
Dalton Trans. 2012 May 07;41(17):5177-87. doi: 10.1039/c2dt12510b. Epub 2012 Mar 19.

The new ball-type metallo bisphthalocyanines (Co(2)Pc(2) and Zn(2)Pc(2)) were synthesized from the corresponding [4,4'-bis(dicoumaroylphthalonitrile)] which can be obtained from the reaction of 3,3'-methylenebis(4-hydroxy-2H-chromen-2-one) and 4-nitrophthalonitrile. The structures of the newly synthesized compounds have been confirmed and characterized by elemental...

Cite
Salan Ü, Altındal A, Özkaya AR, et al. Photovoltaic and electrocatalytic properties of novel ball-type phthalocyanines bridged with four dicumarol. Dalton Trans. 2012;41(17):5177-87doi: 10.1039/c2dt12510b.
Salan, �. �., Altındal, A., Özkaya, A. R., Salih, B., & Bekaroğlu, �. �. (2012). Photovoltaic and electrocatalytic properties of novel ball-type phthalocyanines bridged with four dicumarol. Dalton transactions (Cambridge, England : 2003), 41(17), 5177-87. https://doi.org/10.1039/c2dt12510b
Salan, Ümit, et al. "Photovoltaic and electrocatalytic properties of novel ball-type phthalocyanines bridged with four dicumarol." Dalton transactions (Cambridge, England : 2003) vol. 41,17 (2012): 5177-87. doi: https://doi.org/10.1039/c2dt12510b
Salan Ü, Altındal A, Özkaya AR, Salih B, Bekaroğlu Ö. Photovoltaic and electrocatalytic properties of novel ball-type phthalocyanines bridged with four dicumarol. Dalton Trans. 2012 May 07;41(17):5177-87. doi: 10.1039/c2dt12510b. Epub 2012 Mar 19. PMID: 22430033.
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Natural products for infectious microbes and diseases: an overview of sources, compounds, and chemical diversities.

Science China. Life sciences

Luo L, Yang J, Wang C, Wu J, Li Y, Zhang X, Li H, Zhang H, Zhou Y, Lu A, Chen S.
PMID: 34705221
Sci China Life Sci. 2021 Oct 21; doi: 10.1007/s11427-020-1959-5. Epub 2021 Oct 21.

As coronavirus disease 2019 (COVID-19) threatens human health globally, infectious disorders have become one of the most challenging problem for the medical community. Natural products (NP) have been a prolific source of antimicrobial agents with widely divergent structures and...

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Luo L, Yang J, Wang C, et al. Natural products for infectious microbes and diseases: an overview of sources, compounds, and chemical diversities. Sci China Life Sci. 2021;doi: 10.1007/s11427-020-1959-5.
Luo, L., Yang, J., Wang, C., Wu, J., Li, Y., Zhang, X., Li, H., Zhang, H., Zhou, Y., Lu, A., & Chen, S. (2021). Natural products for infectious microbes and diseases: an overview of sources, compounds, and chemical diversities. Science China. Life sciences, . https://doi.org/10.1007/s11427-020-1959-5
Luo, Lu, et al. "Natural products for infectious microbes and diseases: an overview of sources, compounds, and chemical diversities." Science China. Life sciences vol. (2021). doi: https://doi.org/10.1007/s11427-020-1959-5
Luo L, Yang J, Wang C, Wu J, Li Y, Zhang X, Li H, Zhang H, Zhou Y, Lu A, Chen S. Natural products for infectious microbes and diseases: an overview of sources, compounds, and chemical diversities. Sci China Life Sci. 2021 Oct 21; doi: 10.1007/s11427-020-1959-5. Epub 2021 Oct 21. PMID: 34705221; PMCID: PMC8548270.
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Virtual Screening for Potential Phytobioactives as Therapeutic Leads to Inhibit NQO1 for Selective Anticancer Therapy.

Molecules (Basel, Switzerland)

Shreevatsa B, Dharmashekara C, Swamy VH, Gowda MV, Achar RR, Kameshwar VH, Thimmulappa RK, Syed A, Elgorban AM, Al-Rejaie SS, Ortega-Castro J, Frau J, Flores-Holguín N, Shivamallu C, Kollur SP, Glossman-Mitnik D.
PMID: 34833955
Molecules. 2021 Nov 14;26(22). doi: 10.3390/molecules26226863.

NAD(P)H:quinone acceptor oxidoreductase-1 (NQO1) is a ubiquitous flavin adenine dinucleotide-dependent flavoprotein that promotes obligatory two-electron reductions of quinones, quinonimines, nitroaromatics, and azo dyes. NQO1 is a multifunctional antioxidant enzyme whose expression and deletion are linked to reduced and increased...

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Shreevatsa B, Dharmashekara C, Swamy VH, et al. Virtual Screening for Potential Phytobioactives as Therapeutic Leads to Inhibit NQO1 for Selective Anticancer Therapy. Molecules. 2021;26(22)doi: 10.3390/molecules26226863.
Shreevatsa, B., Dharmashekara, C., Swamy, V. H., Gowda, M. V., Achar, R. R., Kameshwar, V. H., Thimmulappa, R. K., Syed, A., Elgorban, A. M., Al-Rejaie, S. S., Ortega-Castro, J., Frau, J., Flores-Holguín, N., Shivamallu, C., Kollur, S. P., & Glossman-Mitnik, D. (2021). Virtual Screening for Potential Phytobioactives as Therapeutic Leads to Inhibit NQO1 for Selective Anticancer Therapy. Molecules (Basel, Switzerland), 26(22), . https://doi.org/10.3390/molecules26226863
Shreevatsa, Bhargav, et al. "Virtual Screening for Potential Phytobioactives as Therapeutic Leads to Inhibit NQO1 for Selective Anticancer Therapy." Molecules (Basel, Switzerland) vol. 26,22 (2021). doi: https://doi.org/10.3390/molecules26226863
Shreevatsa B, Dharmashekara C, Swamy VH, Gowda MV, Achar RR, Kameshwar VH, Thimmulappa RK, Syed A, Elgorban AM, Al-Rejaie SS, Ortega-Castro J, Frau J, Flores-Holguín N, Shivamallu C, Kollur SP, Glossman-Mitnik D. Virtual Screening for Potential Phytobioactives as Therapeutic Leads to Inhibit NQO1 for Selective Anticancer Therapy. Molecules. 2021 Nov 14;26(22). doi: 10.3390/molecules26226863. PMID: 34833955; PMCID: PMC8622762.
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Purification, Characterization, and Submitochondrial Localization of the 32-Kilodalton NADH Dehydrogenase from Maize.

Plant physiology

Knudten AF, Thelen JJ, Luethy MH, Elthon TE.
PMID: 12232393
Plant Physiol. 1994 Nov;106(3):1115-1122. doi: 10.1104/pp.106.3.1115.

Plant mitochondria have the unique ability to directly oxidize exogenous NAD(P)H. We recently separated two NAD(P)H dehydrogenase activities from maize (Zea mays L.) mitochondria using anion-exchange (Mono Q) chromatography. The first peak of activity oxidized only NADH, whereas the...

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Knudten AF, Thelen JJ, Luethy MH, et al. Purification, Characterization, and Submitochondrial Localization of the 32-Kilodalton NADH Dehydrogenase from Maize. Plant Physiol. 1994;106(3):1115-1122doi: 10.1104/pp.106.3.1115.
Knudten, A. F., Thelen, J. J., Luethy, M. H., & Elthon, T. E. (1994). Purification, Characterization, and Submitochondrial Localization of the 32-Kilodalton NADH Dehydrogenase from Maize. Plant physiology, 106(3), 1115-1122. https://doi.org/10.1104/pp.106.3.1115
Knudten, A. F., et al. "Purification, Characterization, and Submitochondrial Localization of the 32-Kilodalton NADH Dehydrogenase from Maize." Plant physiology vol. 106,3 (1994): 1115-1122. doi: https://doi.org/10.1104/pp.106.3.1115
Knudten AF, Thelen JJ, Luethy MH, Elthon TE. Purification, Characterization, and Submitochondrial Localization of the 32-Kilodalton NADH Dehydrogenase from Maize. Plant Physiol. 1994 Nov;106(3):1115-1122. doi: 10.1104/pp.106.3.1115. PMID: 12232393; PMCID: PMC159638.
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Purification and Characterization of Two Distinct NAD(P)H Dehydrogenases from Onion (Allium cepa L.) Root Plasma Membrane.

Plant physiology

Serrano A, Cordoba F, Gonzalez-Reyes JA, Navas P, Villalba JM.
PMID: 12232306
Plant Physiol. 1994 Sep;106(1):87-96. doi: 10.1104/pp.106.1.87.

Highly purified plasma membrane fractions were obtained from onion (Allium cepa L.) roots and used as a source for purification of redox proteins. Plasma membranes solubilized with Triton X-100 contained two distinct polypeptides showing NAD(P)H-dependent dehydrogenase activities. Dehydrogenase I...

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Serrano A, Cordoba F, Gonzalez-Reyes JA, et al. Purification and Characterization of Two Distinct NAD(P)H Dehydrogenases from Onion (Allium cepa L.) Root Plasma Membrane. Plant Physiol. 1994;106(1):87-96doi: 10.1104/pp.106.1.87.
Serrano, A., Cordoba, F., Gonzalez-Reyes, J. A., Navas, P., & Villalba, J. M. (1994). Purification and Characterization of Two Distinct NAD(P)H Dehydrogenases from Onion (Allium cepa L.) Root Plasma Membrane. Plant physiology, 106(1), 87-96. https://doi.org/10.1104/pp.106.1.87
Serrano, A., et al. "Purification and Characterization of Two Distinct NAD(P)H Dehydrogenases from Onion (Allium cepa L.) Root Plasma Membrane." Plant physiology vol. 106,1 (1994): 87-96. doi: https://doi.org/10.1104/pp.106.1.87
Serrano A, Cordoba F, Gonzalez-Reyes JA, Navas P, Villalba JM. Purification and Characterization of Two Distinct NAD(P)H Dehydrogenases from Onion (Allium cepa L.) Root Plasma Membrane. Plant Physiol. 1994 Sep;106(1):87-96. doi: 10.1104/pp.106.1.87. PMID: 12232306; PMCID: PMC159502.
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Action of Dicumarol on Glucosamine-1-Phosphate Acetyltransferase of GlmU and .

Frontiers in microbiology

Han X, Chen C, Yan Q, Jia L, Taj A, Ma Y.
PMID: 31481936
Front Microbiol. 2019 Aug 20;10:1799. doi: 10.3389/fmicb.2019.01799. eCollection 2019.

No abstract available.

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Han X, Chen C, Yan Q, et al. Action of Dicumarol on Glucosamine-1-Phosphate Acetyltransferase of GlmU and . Front Microbiol. 2019;10:1799doi: 10.3389/fmicb.2019.01799.
Han, X., Chen, C., Yan, Q., Jia, L., Taj, A., & Ma, Y. (2019). Action of Dicumarol on Glucosamine-1-Phosphate Acetyltransferase of GlmU and . Frontiers in microbiology, 101799. https://doi.org/10.3389/fmicb.2019.01799
Han, Xiuyan, et al. "Action of Dicumarol on Glucosamine-1-Phosphate Acetyltransferase of GlmU and ." Frontiers in microbiology vol. 10 (2019): 1799. doi: https://doi.org/10.3389/fmicb.2019.01799
Han X, Chen C, Yan Q, Jia L, Taj A, Ma Y. Action of Dicumarol on Glucosamine-1-Phosphate Acetyltransferase of GlmU and . Front Microbiol. 2019 Aug 20;10:1799. doi: 10.3389/fmicb.2019.01799. eCollection 2019. PMID: 31481936; PMCID: PMC6710349.
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Photovoltaic and electrocatalytic properties of novel ball-type phthalocyanines bridged with four dicumarol.

Dalton transactions (Cambridge, England : 2003)

Salan Ü, Altındal A, Özkaya AR, Salih B, Bekaroğlu Ö.
PMID: 22430033
Dalton Trans. 2012 May 07;41(17):5177-87. doi: 10.1039/c2dt12510b. Epub 2012 Mar 19.

The new ball-type metallo bisphthalocyanines (Co(2)Pc(2) and Zn(2)Pc(2)) were synthesized from the corresponding [4,4'-bis(dicoumaroylphthalonitrile)] which can be obtained from the reaction of 3,3'-methylenebis(4-hydroxy-2H-chromen-2-one) and 4-nitrophthalonitrile. The structures of the newly synthesized compounds have been confirmed and characterized by elemental...

Cite
Salan Ü, Altındal A, Özkaya AR, et al. Photovoltaic and electrocatalytic properties of novel ball-type phthalocyanines bridged with four dicumarol. Dalton Trans. 2012;41(17):5177-87doi: 10.1039/c2dt12510b.
Salan, �. �., Altındal, A., Özkaya, A. R., Salih, B., & Bekaroğlu, �. �. (2012). Photovoltaic and electrocatalytic properties of novel ball-type phthalocyanines bridged with four dicumarol. Dalton transactions (Cambridge, England : 2003), 41(17), 5177-87. https://doi.org/10.1039/c2dt12510b
Salan, Ümit, et al. "Photovoltaic and electrocatalytic properties of novel ball-type phthalocyanines bridged with four dicumarol." Dalton transactions (Cambridge, England : 2003) vol. 41,17 (2012): 5177-87. doi: https://doi.org/10.1039/c2dt12510b
Salan Ü, Altındal A, Özkaya AR, Salih B, Bekaroğlu Ö. Photovoltaic and electrocatalytic properties of novel ball-type phthalocyanines bridged with four dicumarol. Dalton Trans. 2012 May 07;41(17):5177-87. doi: 10.1039/c2dt12510b. Epub 2012 Mar 19. PMID: 22430033.
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Ethoxyresorufin O-deethylase activity in intact human cells.

Toxicology in vitro : an international journal published in association with BIBRA

Hammond DK, Strobel HW.
PMID: 20732090
Toxicol In Vitro. 1992 Jan;6(1):41-6. doi: 10.1016/0887-2333(92)90083-4.

The cytochrome P450IA (P-450) family can be induced in both primary and continuous cell culture, as well as in lymphocytes, by polycyclic aromatic and halogenated hydrocarbons. Ethoxyresorufin O-deethylase (EROD) activity has been correlated with both cytochrome P450IA1 and arylhydrocarbon...

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Hammond DK, Strobel HW. Ethoxyresorufin O-deethylase activity in intact human cells. Toxicol In Vitro. 1992;6(1):41-6doi: 10.1016/0887-2333(92)90083-4.
Hammond, D. K., & Strobel, H. W. (1992). Ethoxyresorufin O-deethylase activity in intact human cells. Toxicology in vitro : an international journal published in association with BIBRA, 6(1), 41-6. https://doi.org/10.1016/0887-2333(92)90083-4
Hammond, D K, and Strobel, H W. "Ethoxyresorufin O-deethylase activity in intact human cells." Toxicology in vitro : an international journal published in association with BIBRA vol. 6,1 (1992): 41-6. doi: https://doi.org/10.1016/0887-2333(92)90083-4
Hammond DK, Strobel HW. Ethoxyresorufin O-deethylase activity in intact human cells. Toxicol In Vitro. 1992 Jan;6(1):41-6. doi: 10.1016/0887-2333(92)90083-4. PMID: 20732090.
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Showing 1 to 12 of 33 entries