Results 1 to 10 of about 12,602 (203)

Nifedipine–pyrazine (2/1) [PDF]

open access: yesActa Crystallographica Section E, 2010
In the title compound, 2C17H18N2O6·C4H4N2 [systematic name: 3,5-dimethyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate–pyrazine (2/1)], the complete pyrazine molecule is generated by crystallographic inversion ...
Nate Schultheiss   +2 more
doaj   +3 more sources

Dissecting the Relationship between Microbial Community Succession and Pyrazine Metabolite Synthesis in Nongxiangxing Daqu [PDF]

open access: yesShipin Kexue, 2023
The correlation between the stages of pyrazine synthesis and the microbial flora during the making of Nongxiang Daqu was analyzed, and the effect of microbial interactions on the synthesis of pyrazine during Daqu making was explored.
CHEN Yingqi, CHEN Jie, ZHOU Yaojin, LI Zijian, TANG Shichao, ZHAO Yuchuan, LUO Huibo, HUANG Dan
doaj   +1 more source

Pyrazine-2-substituted carboxamide derivatives: synthesis, antimicrobial and Leuconostoc mesenteroides growth inhibition activity [PDF]

open access: yesJournal of the Serbian Chemical Society, 2006
Condensation of pyrazine-2,3-dicarboxylic acid anhydride with aminoacetophenones gave the corresponding N-(acetylphenyl)pyrazine-2-carboxamide. Their reactions with some electrophilic (carbonyl group, bromine) and nucleophilic (malononitrile, hydrazine ...
A. H. F. ABD EL-WAHAB   +5 more
doaj   +3 more sources

Syntheses and Photovoltaic Properties of New Pyrazine-Based Organic Photosensitizers for Dye-Sensitized Solar Cells

open access: yesEnergies, 2022
Three novel pyrazine-based organic photosensitizers denoted as TPP, TPPS, and TPPF were synthesized for dye-sensitized solar cell (DSSC) studies. Chemical structures of the pyrazine-based photosensitizers were designed with pyrazine derivatives as ...
Mi-Ra Kim   +7 more
doaj   +1 more source

Natural Products–Pyrazine Hybrids: A Review of Developments in Medicinal Chemistry

open access: yesMolecules, 2023
Pyrazine is a six-membered heterocyclic ring containing nitrogen, and many of its derivatives are biologically active compounds. References have been downloaded through Web of Science, PubMed, Science Direct, and SciFinder Scholar.
Guo-Qing Chen   +5 more
doaj   +1 more source

Mechanism of Enhancing Pyrazines in Daqu via Inoculating Bacillus licheniformis with Strains Specificity

open access: yesFoods, 2023
Despite the importance of pyrazines in Baijiu flavor, inoculating functional strains to increase the contents of pyrazine in Daqu and how those interact with endogenic communities is not well characterized.
Qiuxiang Tang   +10 more
doaj   +1 more source

Experimental, DFT and QSAR models for the discovery of new pyrazines corrosion inhibitors for steel in oilfield acidizing environment

open access: yesInternational Journal of Electrochemical Science, 2020
Eight (8) pyrazine derivatives were tested as mild steel corrosion inhibitors in a simulated oil field acidizing environment. Immersion tests and DFT calculations were adopted for the study. Immersion tests were carried out at 0.2 wt.
I.B. Obot, S.A. Umoren
doaj   +1 more source

Diethyl pyrazine-2,5-dicarboxylate [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2012
The mol-ecule of the title compound, C(10)H(12)N(2)O(4), is located around an inversion center. The carboxyl-ate groups are twisted slightly with respect to the pyrazine ring, making a dihedral angle of 2.76 (19)°. In the crystal, mol-ecules are stacked along the c axis via weak C-H⋯O hydrogen bonds.
Chuan-Hui Li, Wen-Shi Wu, Yu-Min Huang
openaire   +3 more sources

Methyl pyrazine-2-carboxylate [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2009
The title compound, C(6)H(6)N(2)O(2), is approximately planar [r.m.s. deviation = 0.0488 (3) Å]. In the crystal, weak inter-molecular C-H⋯O and C-H⋯N inter-actions join the mol-ecules into an infinite three-dimensional network.
Chang-Hua Zhang   +2 more
openaire   +3 more sources

Novel Triterpenoid Alkaloids With Their Potential Cytotoxic Activity From the Roots of Siraitia grosvenorii

open access: yesFrontiers in Chemistry, 2022
Four novel triterpenoid alkaloids, siragrosvenins A–D (1–4), and two new cucurbitane-type triterpenoids, siragrosvenins E–F (5, 6), together with eight known analogs (7−14), were isolated from the roots of Siraitia grosvenorii.
Huijuan Wang   +8 more
doaj   +1 more source

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