About: isoquinoline

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

any chemical compound having a pyridine ring fused to a benzene ring, the nitrogen atom is in the 2 position

Attributes	Values
rdf:type	Item
description	każdy związek chemiczny zawierający pierścień pirydyny skondensowany z pierścieniem benzenu, przy czym atom azotu znajduje się w pozycji 2 (pl) any chemical compound having a pyridine ring fused to a benzene ring, the nitrogen atom is in the 2 position (en)
rdfs:label	isoquinoline (en) izochinolina (pl) izokinolin (sl) 异喹啉 (zh)
skos:prefLabel	isoquinoline (en) izochinolina (pl) izokinolin (sl) 异喹啉 (zh)
name	isoquinoline (en) izochinolina (pl) izokinolin (sl) 异喹啉 (zh)
instance of	wds:Q61728796-5451245f-4a39-95bd-127f-f886869ff4b7
instance of	structural class of chemical entities
subclass of	wds:Q61728796-313a9688-4a7e-3df9-d4bb-cd9b1c998b3d
subclass of	pyridine
ChEBI ID	wds:Q61728796-4b02121b-40bb-82c9-e811-28f21bbf43b0
ChEBI ID	http://purl.obolibrary.org/obo/CHEBI_24922
ChEBI ID	24922
Commons category	wds:Q61728796-f287d05b-49a4-1203-dc1c-dcaeacf26273
Commons category	Isoquinolines
skos:altLabel	isoquinolines (en) izochinoliny (pl)
NALT ID	wds:Q61728796-5AA19B33-4A1D-4DC3-B07C-603B284DC6DE
JSTOR topic ID	wds:Q61728796-407FCF73-FF19-4CAE-8527-ED924E1D9BB5
MeSH descriptor ID	wds:Q61728796-AB9B2C7C-CB99-4208-B176-C009DA7FB5D8
MeSH tree code	wds:Q61728796-710d60b6-46bc-dda2-ee68-304ef924ff2d
topic's main category	wds:Q61728796-6e39af87-4f17-0737-0fef-022cf7ca39b6
NALT ID	https://lod.nal.usda.gov/nalt/45389
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D007546
MeSH tree code	http://id.nlm.nih.gov/mesh/D03.633.100.531
NALT ID	45389
JSTOR topic ID	isoquinolines
MeSH descriptor ID	D007546
MeSH tree code	D03.633.100.531
topic's main category	Category:Isoquinolines
SMARTS notation	wds:Q61728796-4AB425BE-A86E-4CDD-84F2-0A37AB4A2CA3
SMARTS notation	[$(c1cccc2c1CCNC2),$(C1CC~CC2C1CCNC2)]
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q61728796
is subclass of of	isoquinoline alkaloid 6,7-Dimethoxy-3-(6-methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-2-benzofuran-1(3H)-one tetrahydroisoquinolines Gnoscopine benzylisoquinolines magnoline naphthalimides
is subclass of of	wds:Q978050-92a2eef0-4726-19f8-fa3f-310885699442 wds:Q27107286-6aa44f8c-4bf4-af44-438f-041a3b4745d8 wds:Q73594689-d59f6e7e-4c05-ba42-d697-d51a4b73b20f wds:Q76542978-86d174e5-4c83-2f34-2be0-5aa1ab1d0800 wds:Q73266145-44A5151E-938C-4F42-95BC-B7E0CE9DC3BA wds:Q96631984-61b66e3d-4976-a46c-3094-375bb1ce2ab6 wds:Q72135056-b34a414f-4e1a-4d65-4db0-0616894a6dd2
is main subject of	Synthesis and properties of Praziquantel, a novel broad spectrum anthelmintic with excellent activity against Schistosomes and Cestodes Physiology of Status Epilepticus in Primates Lucifer dyes—highly fluorescent dyes for biological tracing PET visualization of microglia in multiple sclerosis patients using [11C]PK11195 Selective inhibition of T-cell-dependent immune responses by bisbenzylisoquinoline alkaloids in vivo A profile of nomifensine Nomifensine: Diagnostic Test in Hyperprolactinemic States* Nomifensine test for investigation of hyperprolactinaemia Voltage-dependent dye coupling at a rectifying electrotonic synapse of the crayfish Lucifer yellow uptake in developing rat retina: Selective staining of horizontal cells An electron-microscopic study of smooth muscle cell dye coupling in the pig coronary arteries. Role of gap junctions Comparison of three intracellular markers for combined electrophysiological, morphological and immunohistochemical analyses Dopamine receptor model and its application in the design of a new class of rigid pyrrolo[2,3-g]isoquinoline antipsychotics Evaluation of two inhibitory tests (nomifensine and L-dopa + carbidopa) for the diagnosis of hyperprolactinaemic states Density of GABA-receptors in rat cerebral cortex measured with bicuculline-methiodide in the presence of Na+ and other inorganic ions Use of atracurium in caesarean section NMDA receptor antagonists suppress behaviors but not norepinephrine turnover or locus coeruleus unit activity induced by opiate withdrawal Mivacurium infusion during nitrous oxide-isoflurane anesthesia: a comparison with nitrous oxide-opioid anesthesia Configuration and Conformation of Bicuculline, a GABA Antagonist Possible role of tetrahydroisoquinoline alkaloids in postalcohol intoxication states Islets of Langerhans: Dye Coupling Among Immunocytochemically Distinct Cell Types Comparison of vecuronium, atracurium and tubocurarine in normal patients and in patients with no renal function Molecular orbital studies on the conformations of bicuculline and β-hydroxy GABA Acceleromyography as a guide to anesthetic management: a case report Chemical instability of the GABA antagonist bicuculline under physiological conditions Anticancer properties of lamellarins Postnatal development of type I retinal ganglion cells in hamsters: a lucifer yellow study Mivacurium: dose-response relationship and administration by repeated injection or infusion Hydrogenation of Substituted Isoquinolines over Nickel Catalyst I: The Effects of Pressure and Temperature on the Hydrogenation of 5-Nitro-2-alkylisoquinolinium Salts Use of Fluorescent Probes for Describing the Process of Encapsulation by Hypotonic Dialysis Conformation and reactivity of the macrocyclic tumor-inhibitory alkaloid tetrandrine Morphological diversity of displaced retinal ganglion cells in the rat: A lucifer yellow study Mivacurium--a new neuromuscular blocker A NEW SYNTHETIC METHOD OF CYCLIC NITROGENOUS COMPOUNDS. 13. SYNTHESES OF 3-SUBSTITUTED ISOQUINOLINE DERIVATIVES FROM 2-METHYLBENZYLAMINE Studies on the Syntheses of Heterocyclic Compounds. DXVII. Syntheses of Berberine and Related Compounds. II. The Mannich Reaction of 1-Benzylisoquinoline under Various Conditions The enzymatic oxidation of isoquinoline alkaloids Precursors to apomorphine and morphinan analogs. Catalytic reduction of quinoline and isoquinoline Comparison of the Responses in the Nomifensine Test with Hyperprolactinemia due to Prolactin-Secreting Pituitary Tumors and Nonprolactin-Secreting Hypothalamic Tumors* Mass spectrometry of bisbenzylisoquinoline alkaloids. Part I. Alkaloids derived from coclaurine units joined tail-to-tail Mass spectrometry of bisbenzylisoquinoline alkaloids. Part II. Alkaloids derived from one coclaurine and one isococlaurine unit ULTRAVIOLET ABSORPTION SPECTRA PHARMACEUTICAL PREPARATIONS DERIVED FROM ISOQUINOLINE HYPOTENSIVE ACTION OF LIENSININE AND ITS TWO DERIVATIVES SYNTHESIS OF ISOQUINOLINE DERIVATIVES. II. SYNTHESIS OF ACYL DERIVATIVES OF N-METHYLCALYCOTOMINE AND 6,7-DIMETHOXY-3,4-DIHYDRO-1-ISOQUINOLINECARBOXAMIDE DERIVATIVES SYNTHESIS OF PAPAVERINE DERIVATIVES. (12). OXIDATION OF METHYLENE GROUP OF 1-(3,4-DIMETHOXYBENZYL)-6,7-DIMETHOXY-3,4-DIHYDRO(AND 1,2,3,4-TETRAHYDRO)ISOQUINOLINE BY ALUMINA-CHROMATOGRAPHY. (STUDIES ON THE SYNTHESES OF HETEROCYCLIC COMPOUNDS. LXXXVI.)

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