Screening and Characterization of Hydrate Forms of T-3256336, a Novel Inhibitor of Apoptosis (IAP) Protein Antagonist
Different crystal packing of hydrates from anhydrate crystals leads to different physical properties, such as solubility and stability. Investigation of the potential of varied hydrate formation, and understanding the stability in an anhydrous/hydrate system, are crucial to prevent an undesired tran...
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Veröffentlicht in: | Chemical & pharmaceutical bulletin 2015/11/01, Vol.63(11), pp.858-865 |
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creator | Takeuchi, Shoko Kojima, Takashi Hashimoto, Kentaro Saito, Bunnai Sumi, Hiroyuki Ishikawa, Tomoyasu Ikeda, Yukihiro |
description | Different crystal packing of hydrates from anhydrate crystals leads to different physical properties, such as solubility and stability. Investigation of the potential of varied hydrate formation, and understanding the stability in an anhydrous/hydrate system, are crucial to prevent an undesired transition during the manufacturing process and storage. Only one anhydrous form of T-3256336, a novel inhibitor of apoptosis (IAP) protein antagonist, was discovered during synthesis, and no hydrate form has been identified. In this study, we conducted hydrate screening such as dynamic water vapor sorption/desorption (DVS), and the slurry experiment, and characterized the solid-state properties of anhydrous/hydrate forms to determine the most desirable crystalline form for development. New hydrate forms, both mono-hydrate and hemi-hydrate forms, were discovered as a result of this hydrate screening. The characterization of two new hydrate forms was conducted, and the anhydrous form was determined to be the most desirable development form of T-3256336 in terms of solid-state stability. In addition, the stability of the anhydrous form was investigated using the water content and temperature controlled slurry experiment to obtain the desirable crystal form in the crystallization process. The water content regions of the stable phase of the desired form, the anhydrous form, were identified for the cooling crystallization process. |
doi_str_mv | 10.1248/cpb.c15-00262 |
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Investigation of the potential of varied hydrate formation, and understanding the stability in an anhydrous/hydrate system, are crucial to prevent an undesired transition during the manufacturing process and storage. Only one anhydrous form of T-3256336, a novel inhibitor of apoptosis (IAP) protein antagonist, was discovered during synthesis, and no hydrate form has been identified. In this study, we conducted hydrate screening such as dynamic water vapor sorption/desorption (DVS), and the slurry experiment, and characterized the solid-state properties of anhydrous/hydrate forms to determine the most desirable crystalline form for development. New hydrate forms, both mono-hydrate and hemi-hydrate forms, were discovered as a result of this hydrate screening. The characterization of two new hydrate forms was conducted, and the anhydrous form was determined to be the most desirable development form of T-3256336 in terms of solid-state stability. In addition, the stability of the anhydrous form was investigated using the water content and temperature controlled slurry experiment to obtain the desirable crystal form in the crystallization process. The water content regions of the stable phase of the desired form, the anhydrous form, were identified for the cooling crystallization process.</description><identifier>ISSN: 0009-2363</identifier><identifier>EISSN: 1347-5223</identifier><identifier>DOI: 10.1248/cpb.c15-00262</identifier><identifier>PMID: 26521850</identifier><language>eng</language><publisher>Japan: The Pharmaceutical Society of Japan</publisher><subject>Calorimetry, Differential Scanning ; Crystallography, X-Ray ; Drug Discovery ; Drug Stability ; Humans ; Humidity ; hydrate ; inhibitor of apoptosis (IAP) protein ; Inhibitor of Apoptosis Proteins - antagonists & inhibitors ; Models, Molecular ; Oligopeptides - chemistry ; Phase Transition ; Pyrazines - chemistry ; Solubility ; T-3256336 ; Water - chemistry ; water activity</subject><ispartof>Chemical and Pharmaceutical Bulletin, 2015/11/01, Vol.63(11), pp.858-865</ispartof><rights>2015 The Pharmaceutical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c443t-91a688d5d5d436c2a964f76b3085ac07ccdcad47eba6421d53c9c0d286fecf733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1881,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26521850$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takeuchi, Shoko</creatorcontrib><creatorcontrib>Kojima, Takashi</creatorcontrib><creatorcontrib>Hashimoto, Kentaro</creatorcontrib><creatorcontrib>Saito, Bunnai</creatorcontrib><creatorcontrib>Sumi, Hiroyuki</creatorcontrib><creatorcontrib>Ishikawa, Tomoyasu</creatorcontrib><creatorcontrib>Ikeda, Yukihiro</creatorcontrib><title>Screening and Characterization of Hydrate Forms of T-3256336, a Novel Inhibitor of Apoptosis (IAP) Protein Antagonist</title><title>Chemical & pharmaceutical bulletin</title><addtitle>Chem. Pharm. Bull.</addtitle><description>Different crystal packing of hydrates from anhydrate crystals leads to different physical properties, such as solubility and stability. Investigation of the potential of varied hydrate formation, and understanding the stability in an anhydrous/hydrate system, are crucial to prevent an undesired transition during the manufacturing process and storage. Only one anhydrous form of T-3256336, a novel inhibitor of apoptosis (IAP) protein antagonist, was discovered during synthesis, and no hydrate form has been identified. In this study, we conducted hydrate screening such as dynamic water vapor sorption/desorption (DVS), and the slurry experiment, and characterized the solid-state properties of anhydrous/hydrate forms to determine the most desirable crystalline form for development. New hydrate forms, both mono-hydrate and hemi-hydrate forms, were discovered as a result of this hydrate screening. The characterization of two new hydrate forms was conducted, and the anhydrous form was determined to be the most desirable development form of T-3256336 in terms of solid-state stability. In addition, the stability of the anhydrous form was investigated using the water content and temperature controlled slurry experiment to obtain the desirable crystal form in the crystallization process. The water content regions of the stable phase of the desired form, the anhydrous form, were identified for the cooling crystallization process.</description><subject>Calorimetry, Differential Scanning</subject><subject>Crystallography, X-Ray</subject><subject>Drug Discovery</subject><subject>Drug Stability</subject><subject>Humans</subject><subject>Humidity</subject><subject>hydrate</subject><subject>inhibitor of apoptosis (IAP) protein</subject><subject>Inhibitor of Apoptosis Proteins - antagonists & inhibitors</subject><subject>Models, Molecular</subject><subject>Oligopeptides - chemistry</subject><subject>Phase Transition</subject><subject>Pyrazines - chemistry</subject><subject>Solubility</subject><subject>T-3256336</subject><subject>Water - chemistry</subject><subject>water activity</subject><issn>0009-2363</issn><issn>1347-5223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkdFLHDEQh4NY6lX76GsJ-GKhq0lmk919PM5aD0SF2ueQzWY1x16yTbKC_vXNeXpCGchA5uPHMB9Cx5ScUVbW53pszzTlBSFMsD00o1BWBWcM9tGMENIUDAQcoC8xrjLCSQWf0QETnNGakxmafutgjLPuASvX4cWjCkonE-yLStY77Ht89dwFlQy-9GEdNx_3BTAuAMQPrPCNfzIDXrpH29rkw2Y-H_2YfLQRny7nd9_xXfDJWIfnLqkH72xMR-hTr4Zovr71Q_Tn8uf94qq4vv21XMyvC12WkIqGKlHXHc9VgtBMNaLsK9ECqbnSpNK606orK9MqUTLacdCNJh2rRW90XwEcotNt7hj838nEJNc2ajMMyhk_RUkr1gAHoE1GT_5DV34KLm-XKQ4Ny_etMlVsKR18jMH0cgx2rcKzpERufMjsQ2Yf8tVH5r-9pU7t2nQ7-l1ABi62wCrm45gdoEKyejCvcQIkpZt3l_sxzr6kcfAPpvucjQ</recordid><startdate>20151101</startdate><enddate>20151101</enddate><creator>Takeuchi, Shoko</creator><creator>Kojima, Takashi</creator><creator>Hashimoto, Kentaro</creator><creator>Saito, Bunnai</creator><creator>Sumi, Hiroyuki</creator><creator>Ishikawa, Tomoyasu</creator><creator>Ikeda, Yukihiro</creator><general>The Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20151101</creationdate><title>Screening and Characterization of Hydrate Forms of T-3256336, a Novel Inhibitor of Apoptosis (IAP) Protein Antagonist</title><author>Takeuchi, Shoko ; Kojima, Takashi ; Hashimoto, Kentaro ; Saito, Bunnai ; Sumi, Hiroyuki ; Ishikawa, Tomoyasu ; Ikeda, Yukihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-91a688d5d5d436c2a964f76b3085ac07ccdcad47eba6421d53c9c0d286fecf733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Calorimetry, Differential Scanning</topic><topic>Crystallography, X-Ray</topic><topic>Drug Discovery</topic><topic>Drug Stability</topic><topic>Humans</topic><topic>Humidity</topic><topic>hydrate</topic><topic>inhibitor of apoptosis (IAP) protein</topic><topic>Inhibitor of Apoptosis Proteins - antagonists & inhibitors</topic><topic>Models, Molecular</topic><topic>Oligopeptides - chemistry</topic><topic>Phase Transition</topic><topic>Pyrazines - chemistry</topic><topic>Solubility</topic><topic>T-3256336</topic><topic>Water - chemistry</topic><topic>water activity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takeuchi, Shoko</creatorcontrib><creatorcontrib>Kojima, Takashi</creatorcontrib><creatorcontrib>Hashimoto, Kentaro</creatorcontrib><creatorcontrib>Saito, Bunnai</creatorcontrib><creatorcontrib>Sumi, Hiroyuki</creatorcontrib><creatorcontrib>Ishikawa, Tomoyasu</creatorcontrib><creatorcontrib>Ikeda, Yukihiro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takeuchi, Shoko</au><au>Kojima, Takashi</au><au>Hashimoto, Kentaro</au><au>Saito, Bunnai</au><au>Sumi, Hiroyuki</au><au>Ishikawa, Tomoyasu</au><au>Ikeda, Yukihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Screening and Characterization of Hydrate Forms of T-3256336, a Novel Inhibitor of Apoptosis (IAP) Protein Antagonist</atitle><jtitle>Chemical & pharmaceutical bulletin</jtitle><addtitle>Chem. Pharm. Bull.</addtitle><date>2015-11-01</date><risdate>2015</risdate><volume>63</volume><issue>11</issue><spage>858</spage><epage>865</epage><pages>858-865</pages><issn>0009-2363</issn><eissn>1347-5223</eissn><abstract>Different crystal packing of hydrates from anhydrate crystals leads to different physical properties, such as solubility and stability. Investigation of the potential of varied hydrate formation, and understanding the stability in an anhydrous/hydrate system, are crucial to prevent an undesired transition during the manufacturing process and storage. Only one anhydrous form of T-3256336, a novel inhibitor of apoptosis (IAP) protein antagonist, was discovered during synthesis, and no hydrate form has been identified. In this study, we conducted hydrate screening such as dynamic water vapor sorption/desorption (DVS), and the slurry experiment, and characterized the solid-state properties of anhydrous/hydrate forms to determine the most desirable crystalline form for development. New hydrate forms, both mono-hydrate and hemi-hydrate forms, were discovered as a result of this hydrate screening. The characterization of two new hydrate forms was conducted, and the anhydrous form was determined to be the most desirable development form of T-3256336 in terms of solid-state stability. In addition, the stability of the anhydrous form was investigated using the water content and temperature controlled slurry experiment to obtain the desirable crystal form in the crystallization process. The water content regions of the stable phase of the desired form, the anhydrous form, were identified for the cooling crystallization process.</abstract><cop>Japan</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>26521850</pmid><doi>10.1248/cpb.c15-00262</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Calorimetry, Differential Scanning Crystallography, X-Ray Drug Discovery Drug Stability Humans Humidity hydrate inhibitor of apoptosis (IAP) protein Inhibitor of Apoptosis Proteins - antagonists & inhibitors Models, Molecular Oligopeptides - chemistry Phase Transition Pyrazines - chemistry Solubility T-3256336 Water - chemistry water activity |
title | Screening and Characterization of Hydrate Forms of T-3256336, a Novel Inhibitor of Apoptosis (IAP) Protein Antagonist |
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