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Evaluating the beneficial and detrimental effects of bile pigments in early and later life.

Frontiers in pharmacology

Dennery PA.
PMID: 22737125
Front Pharmacol. 2012 Jun 22;3:115. doi: 10.3389/fphar.2012.00115. eCollection 2012.

The heme degradation pathway has been conserved throughout phylogeny and allows for the removal of a pro-oxidant and the generation of unique molecules including bile pigments with important cellular functions. The impact of bile pigments on health and disease...

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Dennery PA. Evaluating the beneficial and detrimental effects of bile pigments in early and later life. Front Pharmacol. 2012;3:115doi: 10.3389/fphar.2012.00115.
Dennery, P. A. (2012). Evaluating the beneficial and detrimental effects of bile pigments in early and later life. Frontiers in pharmacology, 3115. https://doi.org/10.3389/fphar.2012.00115
Dennery, Phyllis A. "Evaluating the beneficial and detrimental effects of bile pigments in early and later life." Frontiers in pharmacology vol. 3 (2012): 115. doi: https://doi.org/10.3389/fphar.2012.00115
Dennery PA. Evaluating the beneficial and detrimental effects of bile pigments in early and later life. Front Pharmacol. 2012 Jun 22;3:115. doi: 10.3389/fphar.2012.00115. eCollection 2012. PMID: 22737125; PMCID: PMC3381237.
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Biopyrrin Pigments: From Heme Metabolites to Redox-Active Ligands and Luminescent Radicals.

Accounts of chemical research

Tomat E, Curtis CJ.
PMID: 34870973
Acc Chem Res. 2021 Dec 06; doi: 10.1021/acs.accounts.1c00613. Epub 2021 Dec 06.

ConspectusRedox-active ligands in coordination chemistry not only modulate the reactivity of the bound metal center but also serve as electron reservoirs to store redox equivalents. Among many applications in contemporary chemistry, the scope of redox-active ligands in biology is...

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Tomat E, Curtis CJ. Biopyrrin Pigments: From Heme Metabolites to Redox-Active Ligands and Luminescent Radicals. Acc Chem Res. 2021;doi: 10.1021/acs.accounts.1c00613.
Tomat, E., & Curtis, C. J. (2021). Biopyrrin Pigments: From Heme Metabolites to Redox-Active Ligands and Luminescent Radicals. Accounts of chemical research, . https://doi.org/10.1021/acs.accounts.1c00613
Tomat, Elisa, and Curtis, Clayton J. "Biopyrrin Pigments: From Heme Metabolites to Redox-Active Ligands and Luminescent Radicals." Accounts of chemical research vol. (2021). doi: https://doi.org/10.1021/acs.accounts.1c00613
Tomat E, Curtis CJ. Biopyrrin Pigments: From Heme Metabolites to Redox-Active Ligands and Luminescent Radicals. Acc Chem Res. 2021 Dec 06; doi: 10.1021/acs.accounts.1c00613. Epub 2021 Dec 06. PMID: 34870973.
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Bile pigments in pulmonary and vascular disease.

Frontiers in pharmacology

Ryter SW.
PMID: 22408625
Front Pharmacol. 2012 Mar 08;3:39. doi: 10.3389/fphar.2012.00039. eCollection 2012.

The bile pigments, biliverdin, and bilirubin, are endogenously derived substances generated during enzymatic heme degradation. These compounds have been shown to act as chemical antioxidants in vitro. Bilirubin formed in tissues circulates in the serum, prior to undergoing hepatic...

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Ryter SW. Bile pigments in pulmonary and vascular disease. Front Pharmacol. 2012;3:39doi: 10.3389/fphar.2012.00039.
Ryter, S. W. (2012). Bile pigments in pulmonary and vascular disease. Frontiers in pharmacology, 339. https://doi.org/10.3389/fphar.2012.00039
Ryter, Stefan W. "Bile pigments in pulmonary and vascular disease." Frontiers in pharmacology vol. 3 (2012): 39. doi: https://doi.org/10.3389/fphar.2012.00039
Ryter SW. Bile pigments in pulmonary and vascular disease. Front Pharmacol. 2012 Mar 08;3:39. doi: 10.3389/fphar.2012.00039. eCollection 2012. PMID: 22408625; PMCID: PMC3296960.
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Choledochus angulation by T-tube.

Revista medica del Instituto Mexicano del Seguro Social

Castaños-Guadarrama M, Alvarado-Padilla AM, Sánchez-Fernández P.
PMID: 34520150
Rev Med Inst Mex Seguro Soc. 2020 Sep 01;58(5):622-627. doi: 10.24875/RMIMSS.M20000092.

BACKGROUND: The presence of bile stasis is a frequent mechanism for presenting choledocholithiasis and recurrence of this one. The bile duct angulation, also known as "elbow sign," could be a risk factor for reducing the flow of bile and...

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Castaños-Guadarrama M, Alvarado-Padilla AM, Sánchez-Fernández P. Angulación de colédoco por sonda en T. Choledochus angulation by T-tube. Rev Med Inst Mex Seguro Soc. 2020;58(5):622-627doi: 10.24875/RMIMSS.M20000092.
Castaños-Guadarrama, M., Alvarado-Padilla, A. M., & Sánchez-Fernández, P. (2020). Angulación de colédoco por sonda en T. Choledochus angulation by T-tube. Revista medica del Instituto Mexicano del Seguro Social, 58(5), 622-627. https://doi.org/10.24875/RMIMSS.M20000092
Castaños-Guadarrama, Marisol, et al. "Angulación de colédoco por sonda en T." Choledochus angulation by T-tube. Revista medica del Instituto Mexicano del Seguro Social vol. 58,5 (2020): 622-627. doi: https://doi.org/10.24875/RMIMSS.M20000092
Castaños-Guadarrama M, Alvarado-Padilla AM, Sánchez-Fernández P. Angulación de colédoco por sonda en T. Choledochus angulation by T-tube. Rev Med Inst Mex Seguro Soc. 2020 Sep 01;58(5):622-627. doi: 10.24875/RMIMSS.M20000092. Spanish. PMID: 34520150.
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Biopyrrin Pigments: From Heme Metabolites to Redox-Active Ligands and Luminescent Radicals.

Accounts of chemical research

Tomat E, Curtis CJ.
PMID: 34870973
Acc Chem Res. 2021 Dec 21;54(24):4584-4594. doi: 10.1021/acs.accounts.1c00613. Epub 2021 Dec 06.

ConspectusRedox-active ligands in coordination chemistry not only modulate the reactivity of the bound metal center but also serve as electron reservoirs to store redox equivalents. Among many applications in contemporary chemistry, the scope of redox-active ligands in biology is...

Cite
Tomat E, Curtis CJ. Biopyrrin Pigments: From Heme Metabolites to Redox-Active Ligands and Luminescent Radicals. Acc Chem Res. 2021;54(24):4584-4594doi: 10.1021/acs.accounts.1c00613.
Tomat, E., & Curtis, C. J. (2021). Biopyrrin Pigments: From Heme Metabolites to Redox-Active Ligands and Luminescent Radicals. Accounts of chemical research, 54(24), 4584-4594. https://doi.org/10.1021/acs.accounts.1c00613
Tomat, Elisa, and Curtis, Clayton J. "Biopyrrin Pigments: From Heme Metabolites to Redox-Active Ligands and Luminescent Radicals." Accounts of chemical research vol. 54,24 (2021): 4584-4594. doi: https://doi.org/10.1021/acs.accounts.1c00613
Tomat E, Curtis CJ. Biopyrrin Pigments: From Heme Metabolites to Redox-Active Ligands and Luminescent Radicals. Acc Chem Res. 2021 Dec 21;54(24):4584-4594. doi: 10.1021/acs.accounts.1c00613. Epub 2021 Dec 06. PMID: 34870973.
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THE PATHOGENESIS OF ICTERUS.

The Journal of experimental medicine

Whipple GH, King JH.
PMID: 19867390
J Exp Med. 1911 Jan 05;13(1):115-35. doi: 10.1084/jem.13.1.115.

These experiments indicate that, in obstructive jaundice, the bile which escapes from the liver is absorbed by the hepatic capillaries and carried by the blood to the kidneys. The presence of a thoracic duct fistula influences in no way...

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Whipple GH, King JH. THE PATHOGENESIS OF ICTERUS. J Exp Med. 1911;13(1):115-35doi: 10.1084/jem.13.1.115.
Whipple, G. H., & King, J. H. (1911). THE PATHOGENESIS OF ICTERUS. The Journal of experimental medicine, 13(1), 115-35. https://doi.org/10.1084/jem.13.1.115
Whipple, G H, and King, J H. "THE PATHOGENESIS OF ICTERUS." The Journal of experimental medicine vol. 13,1 (1911): 115-35. doi: https://doi.org/10.1084/jem.13.1.115
Whipple GH, King JH. THE PATHOGENESIS OF ICTERUS. J Exp Med. 1911 Jan 05;13(1):115-35. doi: 10.1084/jem.13.1.115. PMID: 19867390; PMCID: PMC2124859.
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MALARIAL PIGMENT (SO-CALLED MELANIN): ITS NATURE AND MODE OF PRODUCTION.

The Journal of experimental medicine

Brown WH.
PMID: 19867409
J Exp Med. 1911 Feb 01;13(2):290-9. doi: 10.1084/jem.13.2.290.

1. Two important methods for the study of malarial pigment are described. (a) A method for obtaining a solution of malarial pigment from fixed tissues without the removal of a trace of hemoglobin from the red blood corpuscles. (b)...

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Brown WH. MALARIAL PIGMENT (SO-CALLED MELANIN): ITS NATURE AND MODE OF PRODUCTION. J Exp Med. 1911;13(2):290-9doi: 10.1084/jem.13.2.290.
Brown, W. H. (1911). MALARIAL PIGMENT (SO-CALLED MELANIN): ITS NATURE AND MODE OF PRODUCTION. The Journal of experimental medicine, 13(2), 290-9. https://doi.org/10.1084/jem.13.2.290
Brown, W H. "MALARIAL PIGMENT (SO-CALLED MELANIN): ITS NATURE AND MODE OF PRODUCTION." The Journal of experimental medicine vol. 13,2 (1911): 290-9. doi: https://doi.org/10.1084/jem.13.2.290
Brown WH. MALARIAL PIGMENT (SO-CALLED MELANIN): ITS NATURE AND MODE OF PRODUCTION. J Exp Med. 1911 Feb 01;13(2):290-9. doi: 10.1084/jem.13.2.290. PMID: 19867409; PMCID: PMC2124860.
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Familial Hepatitis and Chronic Jaundice: (Section for the Study of Disease in Children).

Proceedings of the Royal Society of Medicine

Debré R.
PMID: 19992037
Proc R Soc Med. 1939 Jul;32(9):1173-84.

The author reports the history of a family of six children, of whom two, the eldest and the fifth, are normal; three died, a boy when 6 months old and two girls when 9 and 10 years old, from...

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Debré R. Familial Hepatitis and Chronic Jaundice: (Section for the Study of Disease in Children). Proc R Soc Med. 1939;32(9):1173-84
Debré, R. (1939). Familial Hepatitis and Chronic Jaundice: (Section for the Study of Disease in Children). Proceedings of the Royal Society of Medicine, 32(9), 1173-84.
Debré, R. "Familial Hepatitis and Chronic Jaundice: (Section for the Study of Disease in Children)." Proceedings of the Royal Society of Medicine vol. 32,9 (1939): 1173-84.
Debré R. Familial Hepatitis and Chronic Jaundice: (Section for the Study of Disease in Children). Proc R Soc Med. 1939 Jul;32(9):1173-84. PMID: 19992037; PMCID: PMC1997899.
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Bile pigments. VI. Biliverdin, uteroverdin and oocyan.

The Biochemical journal

Lemberg R.
PMID: 16745490
Biochem J. 1934;28(3):978-87. doi: 10.1042/bj0280978.

No abstract available.

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Lemberg R. Bile pigments. VI. Biliverdin, uteroverdin and oocyan. Biochem J. 1934;28(3):978-87doi: 10.1042/bj0280978.
Lemberg, R. (1934). Bile pigments. VI. Biliverdin, uteroverdin and oocyan. The Biochemical journal, 28(3), 978-87. https://doi.org/10.1042/bj0280978
Lemberg, R. "Bile pigments. VI. Biliverdin, uteroverdin and oocyan." The Biochemical journal vol. 28,3 (1934): 978-87. doi: https://doi.org/10.1042/bj0280978
Lemberg R. Bile pigments. VI. Biliverdin, uteroverdin and oocyan. Biochem J. 1934;28(3):978-87. doi: 10.1042/bj0280978. PMID: 16745490; PMCID: PMC1253290.
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Studies on bile pigments: A new test for bilirubin in the urine and its use for detection of bilirubin in normal urine.

The Biochemical journal

Naumann HN.
PMID: 16746083
Biochem J. 1936 May;30(5):762-4. doi: 10.1042/bj0300762.

No abstract available.

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Naumann HN. Studies on bile pigments: A new test for bilirubin in the urine and its use for detection of bilirubin in normal urine. Biochem J. 1936;30(5):762-4doi: 10.1042/bj0300762.
Naumann, H. N. (1936). Studies on bile pigments: A new test for bilirubin in the urine and its use for detection of bilirubin in normal urine. The Biochemical journal, 30(5), 762-4. https://doi.org/10.1042/bj0300762
Naumann, H N. "Studies on bile pigments: A new test for bilirubin in the urine and its use for detection of bilirubin in normal urine." The Biochemical journal vol. 30,5 (1936): 762-4. doi: https://doi.org/10.1042/bj0300762
Naumann HN. Studies on bile pigments: A new test for bilirubin in the urine and its use for detection of bilirubin in normal urine. Biochem J. 1936 May;30(5):762-4. doi: 10.1042/bj0300762. PMID: 16746083; PMCID: PMC1263093.
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Biladienones from the photooxidation of a meso-gem-disubstituted phlorin: crystal and molecular structures of the 3N + O coordinated nickel(II) and copper(II) complexes.

Inorganic chemistry

Jeandon C, Krattinger B, Ruppert R, Callot HJ.
PMID: 11399186
Inorg Chem. 2001 Jun 18;40(13):3149-53. doi: 10.1021/ic001205b.

The photooxidation of a meso-gem-disubstituted phlorin gave two isomeric biladienones in an equilibrium involving a Z-E double bond photoisomerism. The structures of these bile pigments were elucidated using NMR techniques and show terminal benzoyl and pyrrolone moieties. Complexation with...

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Jeandon C, Krattinger B, Ruppert R, et al. Biladienones from the photooxidation of a meso-gem-disubstituted phlorin: crystal and molecular structures of the 3N + O coordinated nickel(II) and copper(II) complexes. Inorg Chem. 2001;40(13):3149-53doi: 10.1021/ic001205b.
Jeandon, C., Krattinger, B., Ruppert, R., & Callot, H. J. (2001). Biladienones from the photooxidation of a meso-gem-disubstituted phlorin: crystal and molecular structures of the 3N + O coordinated nickel(II) and copper(II) complexes. Inorganic chemistry, 40(13), 3149-53. https://doi.org/10.1021/ic001205b
Jeandon, C, et al. "Biladienones from the photooxidation of a meso-gem-disubstituted phlorin: crystal and molecular structures of the 3N + O coordinated nickel(II) and copper(II) complexes." Inorganic chemistry vol. 40,13 (2001): 3149-53. doi: https://doi.org/10.1021/ic001205b
Jeandon C, Krattinger B, Ruppert R, Callot HJ. Biladienones from the photooxidation of a meso-gem-disubstituted phlorin: crystal and molecular structures of the 3N + O coordinated nickel(II) and copper(II) complexes. Inorg Chem. 2001 Jun 18;40(13):3149-53. doi: 10.1021/ic001205b. PMID: 11399186.
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Metabolic and drug profiling.

Journal of pharmaceutical and biomedical analysis

Honour JW, Lim CK, Mitchell FL.
PMID: 16867811
J Pharm Biomed Anal. 1983;1(2):127-42. doi: 10.1016/0731-7085(83)80020-x.

Over recent years, advances in analytical technology have greatly improved our ability to study the metabolism of compounds from either endogenous or erogenous sources. The application of gas-liquid chromatography, mass spectrometry, high-performance liquid chromatography and immunological approaches are discussed...

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Honour JW, Lim CK, Mitchell FL. Metabolic and drug profiling. J Pharm Biomed Anal. 1983;1(2):127-42doi: 10.1016/0731-7085(83)80020-x.
Honour, J. W., Lim, C. K., & Mitchell, F. L. (1983). Metabolic and drug profiling. Journal of pharmaceutical and biomedical analysis, 1(2), 127-42. https://doi.org/10.1016/0731-7085(83)80020-x
Honour, J W, et al. "Metabolic and drug profiling." Journal of pharmaceutical and biomedical analysis vol. 1,2 (1983): 127-42. doi: https://doi.org/10.1016/0731-7085(83)80020-x
Honour JW, Lim CK, Mitchell FL. Metabolic and drug profiling. J Pharm Biomed Anal. 1983;1(2):127-42. doi: 10.1016/0731-7085(83)80020-x. PMID: 16867811.
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Showing 13 to 24 of 40 entries