Academic literature on the topic 'Pyrazines/pharmacology'

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Journal articles on the topic "Pyrazines/pharmacology"

1

OHTA, Akihiro, and Yutaka AOYAGI. "Reactions and Syntheses of Pyrazines." YAKUGAKU ZASSHI 117, no. 1 (1997): 1–17. http://dx.doi.org/10.1248/yakushi1947.117.1_1.

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2

Tong, Wenhua, Shuqin Wang, Haoran Xu, Zongwei Qiao, Liming Zhao, and Ying Yang. "Interaction and Binding Kinetics of Different Substituted Pyrazines with HSA: Based on Multispectral, Physiological Activity, and Molecular Dynamics Simulations." Journal of Food Biochemistry 2024 (March 25, 2024): 1–20. http://dx.doi.org/10.1155/2024/4373558.

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Abstract:
Pyrazine is a kind of compound containing pyrazine ring structure, which has attracted the attention of researchers because of its special aroma and healthcare function. It is currently used in spices, pharmaceuticals, food additives, and other industries. Human serum albumin (HSA) is a transport and storage protein in the human circulatory system. Previous research reported that pyrazine can interact with albumin, but the interaction between pyrazine and HSA has not been reported. Consequently, this study is based on the multispectral method and molecular dynamics (MD) simulation, exploring t
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3

Hou, Wen, Wei Dai, Hao Huang, et al. "Pharmacological activity and mechanism of pyrazines." European Journal of Medicinal Chemistry 258 (October 2023): 115544. http://dx.doi.org/10.1016/j.ejmech.2023.115544.

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4

Bohman, Bjorn, Ryan D. Phillips, Gavin Flematti, Rod Peakall, and Russell A. Barrow. "Sharing of Pyrazine Semiochemicals between Genera of Sexually Deceptive Orchids." Natural Product Communications 8, no. 6 (2013): 1934578X1300800. http://dx.doi.org/10.1177/1934578x1300800605.

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It has recently been discovered that novel di-, tri- and tetra- substituted pyrazines are semiochemicals in Drakaea, an orchid genus that secures pollination by the sexual deception of male thynnine wasps. We examined if similar pyrazines were also present in the distantly related Caladenia barbarossa, a sexually deceptive orchid that is also pollinated by a thynnine wasp. Here we report for the first time the occurrence of two pyrazines, (3,5,6-trimethylpyrazin-2-yl)methyl 3-methylbutanoate (1) and 3-(3-methylbutyl)-2,5-dimethylpyrazine (2) in the orchid genus Caladenia. The former is known a
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5

Mitsuhashi, Keiryo, Toshinobu Suzuki, and Yasushi Nagae. "Synthesis of Condenced Polycyclic Pyrazines from Diaminomaleonitrule." HETEROCYCLES 24, no. 1 (1986): 231. http://dx.doi.org/10.3987/r-1986-01-0231.

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6

OHTA, Akihiro, Hiromitsu TAKAHASHI, Naoomi MIYATA, et al. "Anti-Platelet Aggregation Activity of Some Pyrazines." Biological & Pharmaceutical Bulletin 20, no. 10 (1997): 1076–81. http://dx.doi.org/10.1248/bpb.20.1076.

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7

Ohta, Akihiro, Tokuhiro Watanabe, Kazuhiro Hayashi, et al. "Alkylation and Arylation of Pyrazines by Organotin Compounds." HETEROCYCLES 29, no. 1 (1989): 123. http://dx.doi.org/10.3987/com-88-4728.

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8

Ohta, Akihiro, Ryoichi Itoh, Yasunobu Kaneko, Haruo Koike, and Kayo Yuasa. "Alkylation and Arylation of Pyrazines by Organoboron Compounds." HETEROCYCLES 29, no. 5 (1989): 939. http://dx.doi.org/10.3987/com-89-4904.

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9

Likhosherstov, A. M., V. P. Peresada, and A. P. Skoldinov. "New route to the synthesis of octahydropyrrolo[1,2-a]pyrazines." Pharmaceutical Chemistry Journal 27, no. 10 (1993): 716–18. http://dx.doi.org/10.1007/bf00780552.

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10

Quirion, Jean-Charles, Olivier Froelich, Françoise Cossart, Martine Bonin, and Henri-Philippe Husson. "Asymmetric Synthesis of Octahydro-2H-pyrido[1,2-a]pyrazines." HETEROCYCLES 51, no. 9 (1999): 2065. http://dx.doi.org/10.3987/com-99-8544.

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