JP2011529942A5 - - Google Patents

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Publication number
JP2011529942A5
JP2011529942A5 JP2011521561A JP2011521561A JP2011529942A5 JP 2011529942 A5 JP2011529942 A5 JP 2011529942A5 JP 2011521561 A JP2011521561 A JP 2011521561A JP 2011521561 A JP2011521561 A JP 2011521561A JP 2011529942 A5 JP2011529942 A5 JP 2011529942A5
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JP
Japan
Prior art keywords
crystalline form
compound
formula
methylbenzenesulfonate
xrpd
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
JP2011521561A
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English (en)
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JP2011529942A (ja
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Publication date
Priority claimed from GBGB0814340.6A external-priority patent/GB0814340D0/en
Application filed filed Critical
Publication of JP2011529942A publication Critical patent/JP2011529942A/ja
Publication of JP2011529942A5 publication Critical patent/JP2011529942A5/ja
Withdrawn legal-status Critical Current

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Claims (9)

  1. 結晶形態である、式(I)の化合物の4−メチルベンゼンスルホン酸塩またはその溶媒和物。
    Figure 2011529942
  2. 結晶形態が無水型である、結晶形態の式(I)の化合物の4−メチルベンゼンスルホン酸塩。
  3. 結晶形態が水和物である、結晶形態の式(I)の化合物の4−メチルベンゼンスルホン酸塩。
  4. 結晶形態が図1に示す粉末X線回折(XRPD)パターンと実質的に同じパターンを示すことを特徴とする無水結晶形態1である、請求項1または2に記載の結晶形態の式(I)の化合物の4−メチルベンゼンスルホン酸塩。
  5. 結晶形態が図3に示す粉末X線回折(XRPD)パターンと実質的に同じパターンを示すことを特徴とする無水結晶形態2である、請求項1または2に記載の結晶形態の式(I)の化合物の4−メチルベンゼンスルホン酸塩。
  6. 結晶形態が図5に示す粉末X線回折(XRPD)パターンと実質的に同じパターンを示すことを特徴とする水和物1である、請求項1または3に記載の結晶形態の式(I)の化合物の4−メチルベンゼンスルホン酸塩。
  7. 請求項1〜6のいずれか一項に記載の結晶形態の式(I)の化合物の4−メチルベンゼンスルホン酸塩またはその溶媒和物を含んでなる、医薬組成物。
  8. 1種以上の薬学上許容される担体または希釈剤を更に含んでなる、請求項7に記載の医薬組成物。
  9. 精神病性障害、うつ病、気分障害、不安、睡眠障害、および物質関連障害の治療または予防のために用いられる、請求項7または8に記載の医薬組成物
JP2011521561A 2008-08-05 2009-08-04 ピリジン誘導体の結晶体 Withdrawn JP2011529942A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB0814340.6A GB0814340D0 (en) 2008-08-05 2008-08-05 Anhydrous crystol form fo a pyridine derivative
GB0814340.6 2008-08-05
PCT/EP2009/060089 WO2010015626A1 (en) 2008-08-05 2009-08-04 Crystalline forms of a pyridine derivative

Publications (2)

Publication Number Publication Date
JP2011529942A JP2011529942A (ja) 2011-12-15
JP2011529942A5 true JP2011529942A5 (ja) 2012-09-27

Family

ID=39767571

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011521561A Withdrawn JP2011529942A (ja) 2008-08-05 2009-08-04 ピリジン誘導体の結晶体

Country Status (14)

Country Link
US (1) US8093242B2 (ja)
EP (1) EP2321324A1 (ja)
JP (1) JP2011529942A (ja)
KR (1) KR20110052686A (ja)
CN (1) CN102171219A (ja)
AU (1) AU2009279135B2 (ja)
BR (1) BRPI0917224A2 (ja)
CA (1) CA2733235A1 (ja)
EA (1) EA201170300A1 (ja)
GB (1) GB0814340D0 (ja)
IL (1) IL210777A0 (ja)
MX (1) MX2011001414A (ja)
WO (1) WO2010015626A1 (ja)
ZA (1) ZA201100426B (ja)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2012002369A (es) * 2009-08-27 2012-03-29 Glaxosmithkline Llc Formas de anhidrato de un derivado de piridina.
RU2743206C2 (ru) * 2015-05-18 2021-02-16 Кэнди Терапьютикс Лимитед Двойные антагонисты рецептора нейрокинин-1/нейрокинин-3 для лечения заболеваний, зависимых от половых гормонов
MX2020009438A (es) 2018-03-14 2022-05-11 Kandy Therapeutics Ltd Formulacion farmaceutica novedosa que comprende antagonistas del receptor dual nk-1/nk-3.

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69728883T2 (de) 1996-07-17 2005-04-07 Merck & Co., Inc. Änderung des zirkadischen rhythmus mit nicht-peptidischen neurokinin-1 rezeptor antagonisten
PT1394150E (pt) 1999-02-24 2011-02-17 Hoffmann La Roche Derivados de 4-fenilpiridina e a sua utilização como antagonistas dos receptores de nc-1
WO2001030348A1 (en) 1999-10-25 2001-05-03 Janssen Pharmaceutica N.V. Use of substance p antagonists for influencing the circadian timing system
GB0203022D0 (en) 2002-02-08 2002-03-27 Glaxo Group Ltd Chemical compounds
GB0203020D0 (en) 2002-02-08 2002-03-27 Glaxo Group Ltd Chemical compounds
TW200403058A (en) 2002-04-19 2004-03-01 Bristol Myers Squibb Co Heterocyclo inhibitors of potassium channel function
BRPI0412291A (pt) 2003-07-03 2006-09-19 Hoffmann La Roche antagonistas duplos de nka/nk3 para o tratamento de esquizofrenia
SI1928886T1 (sl) * 2005-09-09 2011-08-31 Glaxosmithkline Llc Derivati piridina in njihova uporaba pri zdravljenju psihotiäśnih motenj

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