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Sumatriptan Succinate Hemi(Ethanol Solvate)
1-(3-(2-(Dimethylammonio)ethyl)-1H-indol-5-yl)-N-methylmethanesulfonamide succinate (sumatriptan succinate, HSum+·HSucc−) is a serotonin receptor agonist used to treat migraines. By the recrystallization of this substance from ethanol, its hemi(ethanol solvate), HSum+·HSucc−·0.5EtOH, was obtained. T...
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Published in: | MolBank 2024-01, Vol.2024 (1), p.M1766 |
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description | 1-(3-(2-(Dimethylammonio)ethyl)-1H-indol-5-yl)-N-methylmethanesulfonamide succinate (sumatriptan succinate, HSum+·HSucc−) is a serotonin receptor agonist used to treat migraines. By the recrystallization of this substance from ethanol, its hemi(ethanol solvate), HSum+·HSucc−·0.5EtOH, was obtained. The solid was characterized by X-ray diffraction and FT-IR spectroscopy. In HSum+·HSucc−·0.5EtOH, solvent molecules link succinate anions into infinite O–H…O bonded chains, which are further connected by N–H…O interactions with cations into H-bonded layers. |
doi_str_mv | 10.3390/M1766 |
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By the recrystallization of this substance from ethanol, its hemi(ethanol solvate), HSum+·HSucc−·0.5EtOH, was obtained. The solid was characterized by X-ray diffraction and FT-IR spectroscopy. In HSum+·HSucc−·0.5EtOH, solvent molecules link succinate anions into infinite O–H…O bonded chains, which are further connected by N–H…O interactions with cations into H-bonded layers.</description><identifier>ISSN: 1422-8599</identifier><identifier>EISSN: 1422-8599</identifier><identifier>DOI: 10.3390/M1766</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Acetaldehyde ; active pharmaceutical ingredient ; Alcohol ; Alcohol, Denatured ; Analysis ; Chemical synthesis ; Crystals ; Diffraction ; Ethanol ; Fourier transform infrared spectroscopy ; H-bond propensity ; Headaches ; Hydrogen ; Hydrogen bonding ; Identification and classification ; Infrared spectroscopy ; Methods ; Migraine ; Pharmaceutical industry ; Recrystallization ; Serotonin ; single-crystal X-ray diffraction ; Solvents ; Spectrum analysis ; Structure ; Sumatriptan ; X-rays</subject><ispartof>MolBank, 2024-01, Vol.2024 (1), p.M1766</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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By the recrystallization of this substance from ethanol, its hemi(ethanol solvate), HSum+·HSucc−·0.5EtOH, was obtained. The solid was characterized by X-ray diffraction and FT-IR spectroscopy. In HSum+·HSucc−·0.5EtOH, solvent molecules link succinate anions into infinite O–H…O bonded chains, which are further connected by N–H…O interactions with cations into H-bonded layers.</description><subject>Acetaldehyde</subject><subject>active pharmaceutical ingredient</subject><subject>Alcohol</subject><subject>Alcohol, Denatured</subject><subject>Analysis</subject><subject>Chemical synthesis</subject><subject>Crystals</subject><subject>Diffraction</subject><subject>Ethanol</subject><subject>Fourier transform infrared spectroscopy</subject><subject>H-bond propensity</subject><subject>Headaches</subject><subject>Hydrogen</subject><subject>Hydrogen bonding</subject><subject>Identification and classification</subject><subject>Infrared spectroscopy</subject><subject>Methods</subject><subject>Migraine</subject><subject>Pharmaceutical industry</subject><subject>Recrystallization</subject><subject>Serotonin</subject><subject>single-crystal X-ray diffraction</subject><subject>Solvents</subject><subject>Spectrum analysis</subject><subject>Structure</subject><subject>Sumatriptan</subject><subject>X-rays</subject><issn>1422-8599</issn><issn>1422-8599</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkV1LwzAUhoMoOOf-w0AERTqTJmmayzGmG0y8mF6H0zSZGW0z01bw3xs38QPkXJzDy3sezgdCI4InlEp8-0BElh2hAWFpmuRcyuNf9Sk6a9stxoykFA_QzbqvoQtu10EzXvdauwY6M16Y2l3NuxdofDVe--otitfn6MRC1ZrRVx6i57v502yRrB7vl7PpKtFUiC4hlnNhCLNMWpFSKY0kmdCSsqIs0qIwJaOmLG2OOUhpU9CCUQ6WgWaM0JwO0fLALT1s1S64GsK78uDUXvBhoyB0TldGWZxLWwKPCMEkB0gLXRDBucWGZURE1sWBtQv-tTdtp7a-D00cX1GMKWVSYPbj2kCEusb6LoCuXavVVOR5yuP5cHRN_nHFKOO1tG-MdVH_03B5aNDBt20w9nsZgtXnq9T-VfQDt_SBUg</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Buikin, Petr A</creator><creator>Vologzhanina, Anna V</creator><creator>Korlyukov, Alexander A</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>L7M</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-6228-303X</orcidid><orcidid>https://orcid.org/0000-0002-5600-9886</orcidid></search><sort><creationdate>20240101</creationdate><title>Sumatriptan Succinate Hemi(Ethanol Solvate)</title><author>Buikin, Petr A ; Vologzhanina, Anna V ; Korlyukov, Alexander A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-1f557e14f49f72399e9167c934bdb2bbed43eddf805a99f2ac7435af4ac441383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acetaldehyde</topic><topic>active pharmaceutical ingredient</topic><topic>Alcohol</topic><topic>Alcohol, Denatured</topic><topic>Analysis</topic><topic>Chemical synthesis</topic><topic>Crystals</topic><topic>Diffraction</topic><topic>Ethanol</topic><topic>Fourier transform infrared spectroscopy</topic><topic>H-bond propensity</topic><topic>Headaches</topic><topic>Hydrogen</topic><topic>Hydrogen bonding</topic><topic>Identification and classification</topic><topic>Infrared spectroscopy</topic><topic>Methods</topic><topic>Migraine</topic><topic>Pharmaceutical industry</topic><topic>Recrystallization</topic><topic>Serotonin</topic><topic>single-crystal X-ray diffraction</topic><topic>Solvents</topic><topic>Spectrum analysis</topic><topic>Structure</topic><topic>Sumatriptan</topic><topic>X-rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Buikin, Petr A</creatorcontrib><creatorcontrib>Vologzhanina, Anna V</creatorcontrib><creatorcontrib>Korlyukov, Alexander A</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>https://resources.nclive.org/materials</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Materials science collection</collection><collection>ProQuest - Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>MolBank</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Buikin, Petr A</au><au>Vologzhanina, Anna V</au><au>Korlyukov, Alexander A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sumatriptan Succinate Hemi(Ethanol Solvate)</atitle><jtitle>MolBank</jtitle><date>2024-01-01</date><risdate>2024</risdate><volume>2024</volume><issue>1</issue><spage>M1766</spage><pages>M1766-</pages><issn>1422-8599</issn><eissn>1422-8599</eissn><abstract>1-(3-(2-(Dimethylammonio)ethyl)-1H-indol-5-yl)-N-methylmethanesulfonamide succinate (sumatriptan succinate, HSum+·HSucc−) is a serotonin receptor agonist used to treat migraines. By the recrystallization of this substance from ethanol, its hemi(ethanol solvate), HSum+·HSucc−·0.5EtOH, was obtained. The solid was characterized by X-ray diffraction and FT-IR spectroscopy. In HSum+·HSucc−·0.5EtOH, solvent molecules link succinate anions into infinite O–H…O bonded chains, which are further connected by N–H…O interactions with cations into H-bonded layers.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/M1766</doi><orcidid>https://orcid.org/0000-0002-6228-303X</orcidid><orcidid>https://orcid.org/0000-0002-5600-9886</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acetaldehyde active pharmaceutical ingredient Alcohol Alcohol, Denatured Analysis Chemical synthesis Crystals Diffraction Ethanol Fourier transform infrared spectroscopy H-bond propensity Headaches Hydrogen Hydrogen bonding Identification and classification Infrared spectroscopy Methods Migraine Pharmaceutical industry Recrystallization Serotonin single-crystal X-ray diffraction Solvents Spectrum analysis Structure Sumatriptan X-rays |
title | Sumatriptan Succinate Hemi(Ethanol Solvate) |
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