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Journal articles on the topic 'Merbromine'

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1

Barrazza, Vincent, and Laurence Ollivaud. "Merbromine-induced pustular contact dermatitis." Contact Dermatitis 40, no. 4 (1999): 219. http://dx.doi.org/10.1111/j.1600-0536.1999.tb06043.x.

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2

&NA;. "Merbromin." Reactions Weekly &NA;, no. 748 (1999): 9–10. http://dx.doi.org/10.2165/00128415-199907480-00028.

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3

&NA;. "Merbromin overdose." Reactions Weekly &NA;, no. 482 (1993): 10. http://dx.doi.org/10.2165/00128415-199304820-00045.

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4

Alkhashrom, Sewar, Jintawee Kicuntod, Sigrun Häge, et al. "Exploring the Human Cytomegalovirus Core Nuclear Egress Complex as a Novel Antiviral Target: A New Type of Small Molecule Inhibitors." Viruses 13, no. 3 (2021): 471. http://dx.doi.org/10.3390/v13030471.

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Nuclear egress is an essential process in the replication of human cytomegalovirus (HCMV), as it enables the migration of newly formed viral capsids from the nucleus into the cytoplasm. Inhibition of the HCMV core nuclear egress complex (core NEC), composed of viral proteins pUL50 and pUL53, has been proposed as a potential new target for the treatment of HCMV infection and disease. Here, we present a new type of small molecule inhibitors of HCMV core NEC formation, which inhibit the pUL50-pUL53 interaction at nanomolar concentrations. These inhibitors, i.e., verteporfin and merbromin, were id
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5

Banerjee, Debashis, Parimal Kumar Das, Haraprasad Singha, and Sanjib Bagchi. "Fluorimetric study of interaction of merbromin with trypsin." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 70, no. 5 (2008): 1109–13. http://dx.doi.org/10.1016/j.saa.2007.10.019.

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6

Gollnick, Klaus, and Stephan Held. "Merbromin (mercurochrome) — a photosensitizer for singlet oxygen reactions." Journal of Photochemistry and Photobiology B: Biology 5, no. 1 (1990): 85–93. http://dx.doi.org/10.1016/1011-1344(90)85007-j.

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7

Iyer, Rema, Albert A. Barrese, Shilpa Parakh, Christian N. Parker, and Brian C. Tripp. "Inhibition Profiling of Human Carbonic Anhydrase II by High-Throughput Screening of Structurally Diverse, Biologically Active Compounds." Journal of Biomolecular Screening 11, no. 7 (2006): 782–91. http://dx.doi.org/10.1177/1087057106289403.

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Human carbonic anhydrase II (CA II), a zinc metalloenzyme, was screened against 960 structurally diverse, biologically active small molecules. The assay monitored CA II esterase activity against the substrate 4-nitrophenyl acetate in a format allowing high-throughput screening. The assay proved to be robust and reproducible with a hit rate of ∼2%. Potential hits were further characterized by determining their IC50 and Kd values and tested for nonspecific, promiscuous inhibition. Three known sulfonamide CA inhibitors were identified: acetazolamide, methazolamide, and celecoxib. Other hits were
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8

Slee, Peter H. Th J., Gerard J. Ottolander, and Frederik A. Wolff. "A Case of Merbromin (Mercurochrome®) Intoxication Possibly Resulting in Aplastic Anemia." Acta Medica Scandinavica 205, no. 1-6 (2009): 463–66. http://dx.doi.org/10.1111/j.0954-6820.1979.tb06085.x.

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9

ADACHI, Kenta, and Nodoka TSURU. "Morphological Analysis of Self-assembled Structures of Merbromin Molecules Adsorbed on Titanium(IV) Oxide Nanoparticles." BUNSEKI KAGAKU 67, no. 12 (2018): 719–26. http://dx.doi.org/10.2116/bunsekikagaku.67.719.

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10

Risher, John F., H. Edward Murray, and George R. Prince. "Organic mercury compounds: human exposure and its relevance to public health." Toxicology and Industrial Health 18, no. 3 (2002): 109–60. http://dx.doi.org/10.1191/0748233702th138oa.

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Humans may be exposed to organic forms of mercury by either inhalation, oral, or dermal routes, and the effects of such exposure depend upon both the type of mercury to which exposed and the magnitude of the exposure. In general, the effects of exposure to organic mercury are primarily neurologic, while a host of other organ systems may also be involved, including gastrointestinal, respiratory, hepatic, immune, dermal, and renal. While the primary source of exposure to organic mercury for most populations is the consumption of methylmercury-contaminated fish and shellfish, there are a number o
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11

Yu, Hua, Yuhai Tang, Guangbin Zhang, Zhongcheng Wang, and Ruixia Gao. "A new chemiluminescence method for determination of dicyandiamide based on the N-bromosuccinimide–merbromin–cetyltrimethylammonium bromide system." Journal of Luminescence 157 (January 2015): 327–32. http://dx.doi.org/10.1016/j.jlumin.2014.08.063.

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12

Korany, Mohamed A., Marwa S. Moneeb, Aya M. Asaad, Nadia A. El-Sebakhy, and Alaa A. El-Banna. "The Use of Merbromin Fluorescence Quenching for the Assay of Silymarin in its Natural Source and Pharmaceutical Preparations." Analytical Chemistry Letters 9, no. 2 (2019): 152–67. http://dx.doi.org/10.1080/22297928.2019.1613927.

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13

Gollnick, Klaus, Theodor Franken, Mohamed F. R. Fouda, Hanns R. Paur, and Stephan Held. "Merbromin (mercurochrome) and other xanthene dyes: Quantum yields of triplet sensitizer generation and singlet oxygen formation in alcoholic solutions." Journal of Photochemistry and Photobiology B: Biology 12, no. 1 (1992): 57–81. http://dx.doi.org/10.1016/1011-1344(92)85018-p.

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14

Almahri, Albandary, and Mohamed A. Abdel‐Lateef. "Applying different spectroscopic techniques for the selective determination of daclatasvir using merbromin as a probe: Applications on pharmaceutical analysis." Luminescence 36, no. 6 (2021): 1544–52. http://dx.doi.org/10.1002/bio.4099.

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15

Martínez, Gabriela, Sonia G. Bertolotti, Oscar E. Zimerman, Daniel O. Mártire, Silvia E. Braslavsky, and Norman A. García. "A kinetic study of the photodynamic properties of the xanthene dye merbromin (mercurochrome) and its aggregates with amino acids in aqueous solutions." Journal of Photochemistry and Photobiology B: Biology 17, no. 3 (1993): 247–55. http://dx.doi.org/10.1016/1011-1344(93)80022-2.

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16

Pahan, Kalipada, Ratan Gachhui, Satyajit Ray, Jayasri Chaudhuri, and Amalendu Mandal. "Bacterial degradation and utilization of merbromine and fluorescein mercuric acetate." Bulletin of Environmental Contamination and Toxicology 48, no. 3 (1992). http://dx.doi.org/10.1007/bf00195642.

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17

"Merbromin." Reactions Weekly 1536, no. 1 (2015): 141. http://dx.doi.org/10.1007/s40278-015-6993-1.

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18

"Merbromin." Reactions Weekly 1456, no. 1 (2013): 23. http://dx.doi.org/10.1007/s40278-013-3788-0.

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