Zobrazeno 1 - 10
of 107
pro vyhledávání: '"Systematic name"'
Autor:
Oriakhi, Christopher O., author
Publikováno v:
Chemistry in Quantitative Language : Fundamentals of General Chemistry Calculations, 2021.
Externí odkaz:
https://doi.org/10.1093/oso/9780198867784.003.0005
Autor:
Mayer Matthias, Keller Markus A., Watschinger Katrin, Werner-Felmayer Gabriele, Werner Ernst R., Golderer Georg
Publikováno v:
Pteridines, Vol 24, Iss 1, Pp 111-115 (2013)
Alkylglycerol monooxygenase (AGMO; EC 1.14.16.5) is the only enzyme known to cleave the O-alkyl ether bond of alkylglycerols in humans. It is an integral membrane protein with nine predicted transmembrane domains. We attempted to express and purify f
Externí odkaz:
https://doaj.org/article/21f6cb85669b46c89368416e87bdf714
Autor:
Cheorl-Ho Kim
Publikováno v:
Ganglioside Biochemistry ISBN: 9789811558146
SAs as a group of nine carbon saccharides are named nonulosonates (NulOs) or nonoses and they are mainly appeared in the animal tissues including invertebrates and vertebrates. They are located and distributed on the surfaces of eukaryotic cells, mai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acfa40410a9fbd27d2fc25adad14b9bb
https://doi.org/10.1007/978-981-15-5815-3_6
https://doi.org/10.1007/978-981-15-5815-3_6
Publikováno v:
IUCrdata
IUCrData, Vol 4, Iss 5, p x190662 (2019)
IUCrData, Vol 4, Iss 5, p x190662 (2019)
The title compound [systematic name: 4-(2,3-Dichlorophenyl)benzene-1,2-diol], C12H8Cl2O2, is a putative dihydroxylated metabolite of 2,3-dichlorobiphenyl (PCB 5). The title structure displays intramolecular O—H...O hydrogen bonding, and the π–π
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4421e178e5df8919ce3a984d48861b0
https://doi.org/10.1107/s241431461900662x
https://doi.org/10.1107/s241431461900662x
Publikováno v:
Zeitschrift für Kristallographie-New Crystal Structures, Vol 232, Iss 4, Pp 685-687 (2017)
C4H10N4O2, orthorhombic, P212121 (no. 19), a = 5.4922(3) Å, b = 7.4024(5) Å, c = 17.5083(10) Å, V = 711.81(7) Å3, Z = 4, R gt(F) = 0.0395, wR ref(F 2) = 0.0923, T = 150(2) K.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a7097c09b3332c94829c63a6cc60f01
https://doi.org/10.1515/ncrs-2017-0003
https://doi.org/10.1515/ncrs-2017-0003
Publikováno v:
IUCrData, Vol 3, Iss 10, p x181444 (2018)
The asymmetric unit of the title compound (systematic name: 2-benzoyl-4-chloroaniline), C13H10ClNO, contains four independent molecules with similar dihedral angles between the benzene rings [ranging from 53.7 (2) to 59.8 (2)°]. In the crystal, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85e7e3308b4c82700c6e28d348fb13fb
https://doi.org/10.1107/s241431461801444x
https://doi.org/10.1107/s241431461801444x
Publikováno v:
Molecular Crystals and Liquid Crystals. 607:192-199
The title compound with systematic name: (S)-5-secbutyl-2-thiohydantoin, is synthesized through a solvent-free reaction, crystallizes in the non-centrosymmetric space group P212121. In the crystal structure, the molecules are joined by N‒H···O a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfbfd3e8b65c176d9e42b0ded64453f1
https://doi.org/10.1080/15421406.2014.928433
https://doi.org/10.1080/15421406.2014.928433
Publikováno v:
Acta Crystallographica Section C Structural Chemistry. 71:32-38
The name `bath salts', for an emerging class of synthetic cathinones, is derived from an attempt to evade prosecution and law enforcement. These are truly illicit drugs that have psychoactive CNS (central nervous system) stimulant effects and they ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a4543be2c1a02e8a37926f207c0ad23
https://doi.org/10.1107/s2053229614025637
https://doi.org/10.1107/s2053229614025637
Autor:
Georg Golderer, Ernst R. Werner, Katrin Watschinger, Gabriele Werner-Felmayer, Markus A. Keller, Matthias Mayer
Publikováno v:
Pteridines, Vol 24, Iss 1, Pp 111-115 (2013)
Alkylglycerol monooxygenase (AGMO; EC 1.14.16.5) is the only enzyme known to cleave the O-alkyl ether bond of alkylglycerols in humans. It is an integral membrane protein with nine predicted transmembrane domains. We attempted to express and purify f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f00adb55fac19ddf1153089699163e7
https://doi.org/10.1515/pterid-2013-0014
https://doi.org/10.1515/pterid-2013-0014
Autor:
David J. Watkin, Robert J. Nash, Christopher R. Newton, George W. J. Fleet, Jeroen van Ameijde
The title compound [systematic name: (1R,2R,3S,6S,7S,7aR)-3-hydroxymethyl-1,2,6,7-tetrahydroxypyrrolizidine monohydrate or (2S,3R,4R,5R,6S,7S)-2-hydroxymethyl-1-azabicyclo[3.3.0]octan-3,4,6,7-tetraol monohydrate], C8H15NO5·H2O, was forme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30fe48010f39aadf502bd2a7e9c84464
https://doi.org/10.1107/s1600536804018665
https://doi.org/10.1107/s1600536804018665