JP2013528157A5 - - Google Patents
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- Publication number
- JP2013528157A5 JP2013528157A5 JP2012552591A JP2012552591A JP2013528157A5 JP 2013528157 A5 JP2013528157 A5 JP 2013528157A5 JP 2012552591 A JP2012552591 A JP 2012552591A JP 2012552591 A JP2012552591 A JP 2012552591A JP 2013528157 A5 JP2013528157 A5 JP 2013528157A5
- Authority
- JP
- Japan
- Prior art keywords
- pharmaceutical composition
- composition according
- ether
- polyhydric alcohol
- polyoxyethylene
- 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.)
- Granted
Links
- 239000008194 pharmaceutical composition Substances 0.000 claims description 27
- -1 polyoxyethylene Polymers 0.000 claims description 21
- 229920001223 polyethylene glycol Polymers 0.000 claims description 19
- 150000005846 sugar alcohols Polymers 0.000 claims description 19
- 239000002202 Polyethylene glycol Substances 0.000 claims description 15
- 150000005215 alkyl ethers Chemical class 0.000 claims description 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 10
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 10
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 150000004666 short chain fatty acids Chemical class 0.000 claims description 8
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 claims description 8
- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 claims description 8
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims description 7
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical group OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims description 6
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
- 235000011187 glycerol Nutrition 0.000 claims description 5
- 150000004668 long chain fatty acids Chemical class 0.000 claims description 5
- 150000004667 medium chain fatty acids Chemical class 0.000 claims description 5
- 229920001451 polypropylene glycol Polymers 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 claims description 4
- MUHFRORXWCGZGE-KTKRTIGZSA-N 2-hydroxyethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCO MUHFRORXWCGZGE-KTKRTIGZSA-N 0.000 claims description 4
- HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical compound CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 4
- 239000004020 conductor Substances 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 239000001087 glyceryl triacetate Substances 0.000 claims description 4
- 235000013773 glyceryl triacetate Nutrition 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 4
- 150000007984 tetrahydrofuranes Chemical class 0.000 claims description 4
- 229960002622 triacetin Drugs 0.000 claims description 4
- 229940093609 tricaprylin Drugs 0.000 claims description 4
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 4
- QVADRSWDTZDDGR-UHFFFAOYSA-N 5-oxotetrahydrofuran-2-carboxylic acid Chemical compound OC(=O)C1CCC(=O)O1 QVADRSWDTZDDGR-UHFFFAOYSA-N 0.000 claims description 3
- VIHAEDVKXSOUAT-UHFFFAOYSA-N but-2-en-4-olide Chemical compound O=C1OCC=C1 VIHAEDVKXSOUAT-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 claims description 2
- LJVNVNLFZQFJHU-UHFFFAOYSA-N 2-(2-phenylmethoxyethoxy)ethanol Chemical compound OCCOCCOCC1=CC=CC=C1 LJVNVNLFZQFJHU-UHFFFAOYSA-N 0.000 claims description 2
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims description 2
- YTAOBBFIOAEMLL-REQDGWNSSA-N Luliconazole Chemical compound ClC1=CC(Cl)=CC=C1[C@H](CS\1)SC/1=C(\C#N)N1C=NC=C1 YTAOBBFIOAEMLL-REQDGWNSSA-N 0.000 claims description 2
- 150000001266 acyl halides Chemical class 0.000 claims description 2
- 229940061720 alpha hydroxy acid Drugs 0.000 claims description 2
- 150000001280 alpha hydroxy acids Chemical class 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 235000019445 benzyl alcohol Nutrition 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 229940019778 diethylene glycol diethyl ether Drugs 0.000 claims description 2
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical group CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 claims description 2
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 150000002170 ethers Chemical class 0.000 claims description 2
- 229960000570 luliconazole Drugs 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- YFNKIDBQEZZDLK-UHFFFAOYSA-N triglyme Chemical compound COCCOCCOCCOC YFNKIDBQEZZDLK-UHFFFAOYSA-N 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims 4
- 238000006266 etherification reaction Methods 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 claims 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical group CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000004665 fatty acids Chemical group 0.000 description 3
- RNVYQYLELCKWAN-UHFFFAOYSA-N solketal Chemical compound CC1(C)OCC(CO)O1 RNVYQYLELCKWAN-UHFFFAOYSA-N 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 description 2
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 2
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 2
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 0 *c1cc(*)c(C(CS2)SC2=C(C#N)[n]2cncc2)cc1 Chemical compound *c1cc(*)c(C(CS2)SC2=C(C#N)[n]2cncc2)cc1 0.000 description 1
- SIJBDWPVNAYVGY-UHFFFAOYSA-N 2,2-dimethyl-1,3-dioxolane Chemical compound CC1(C)OCCO1 SIJBDWPVNAYVGY-UHFFFAOYSA-N 0.000 description 1
- ZVUNTIMPQCQCAQ-UHFFFAOYSA-N 2-dodecanoyloxyethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCC ZVUNTIMPQCQCAQ-UHFFFAOYSA-N 0.000 description 1
- JWUJQDFVADABEY-UHFFFAOYSA-N 2-methyltetrahydrofuran Chemical compound CC1CCCO1 JWUJQDFVADABEY-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical group 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid ester group Chemical group C(CCCCCCCCCCC)(=O)O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000005473 octanoic acid group Chemical group 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 235000021391 short chain fatty acids Nutrition 0.000 description 1
- UJJLJRQIPMGXEZ-UHFFFAOYSA-N tetrahydro-2-furoic acid Chemical compound OC(=O)C1CCCO1 UJJLJRQIPMGXEZ-UHFFFAOYSA-N 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2012552591A JP5832451B2 (ja) | 2010-06-11 | 2011-06-10 | 抗真菌医薬組成物 |
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010148255 | 2010-06-11 | ||
| JP2010148255 | 2010-06-11 | ||
| JP2010181923 | 2010-07-30 | ||
| JP2010181923 | 2010-07-30 | ||
| PCT/JP2011/063860 WO2011155640A1 (en) | 2010-06-11 | 2011-06-10 | Antimycotic pharmaceutical composition |
| JP2012552591A JP5832451B2 (ja) | 2010-06-11 | 2011-06-10 | 抗真菌医薬組成物 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015123928A Division JP5938497B2 (ja) | 2010-06-11 | 2015-06-19 | 抗真菌医薬組成物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013528157A JP2013528157A (ja) | 2013-07-08 |
| JP2013528157A5 true JP2013528157A5 (https=) | 2014-07-03 |
| JP5832451B2 JP5832451B2 (ja) | 2015-12-16 |
Family
ID=44544289
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012552591A Active JP5832451B2 (ja) | 2010-06-11 | 2011-06-10 | 抗真菌医薬組成物 |
| JP2015123928A Active JP5938497B2 (ja) | 2010-06-11 | 2015-06-19 | 抗真菌医薬組成物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015123928A Active JP5938497B2 (ja) | 2010-06-11 | 2015-06-19 | 抗真菌医薬組成物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8962669B2 (https=) |
| EP (1) | EP2579847A1 (https=) |
| JP (2) | JP5832451B2 (https=) |
| KR (1) | KR101806304B1 (https=) |
| CN (1) | CN102933201B (https=) |
| WO (1) | WO2011155640A1 (https=) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2416757A2 (en) | 2009-04-09 | 2012-02-15 | Pola Pharma Inc. | Antimycotic pharmaceutical composition |
| KR101409792B1 (ko) | 2009-04-09 | 2014-06-19 | 니혼노야쿠가부시키가이샤 | 항진균성 약제학적 조성물 |
| WO2011024620A1 (en) | 2009-08-25 | 2011-03-03 | Pola Pharma Inc. | Antimycotic pharmaceutical composition |
| US10232047B2 (en) | 2011-12-20 | 2019-03-19 | Vyome Biosciences Private Limited | Topical oil composition for the treatment of fungal infections |
| CN103179634A (zh) * | 2011-12-21 | 2013-06-26 | 株式会社Ntt都科摩 | 一种伙伴发现和选择方法、装置及系统 |
| JPWO2014017411A1 (ja) * | 2012-07-23 | 2016-07-11 | マルホ株式会社 | 爪白癬治療用外用剤 |
| JP5589130B1 (ja) | 2012-09-14 | 2014-09-10 | 株式会社ポーラファルマ | 結晶及び該結晶を含有してなる医薬製剤 |
| RU2621615C2 (ru) * | 2012-09-14 | 2017-06-06 | Пола Фарма Инк. | Фармацевтическая композиция, содержащая луликоназол |
| US9068958B1 (en) | 2012-09-14 | 2015-06-30 | Pola Pharma Inc. | Use of surface free energy for differential evaluation of crystal, crystal evaluated on basis of surface free energy as index, and pharmaceutical composition prepared by containing the crystal |
| IN2015DN02376A (https=) | 2012-09-14 | 2015-09-04 | Pola Pharma Inc | |
| JP5460797B1 (ja) * | 2012-09-14 | 2014-04-02 | 株式会社ポーラファルマ | アミド誘導体及び安定性指標としてのその使用 |
| JP5589110B1 (ja) | 2013-03-08 | 2014-09-10 | 株式会社ポーラファルマ | 晶癖を有する結晶及び該結晶を有効成分として含有する医薬組成物 |
| JP2016518306A (ja) * | 2013-05-17 | 2016-06-23 | 株式会社ポーラファルマ | アスペルギルス、カンジダ等を病原体とする疾患用の医薬組成物 |
| JP5680161B1 (ja) | 2013-09-06 | 2015-03-04 | 株式会社ポーラファルマ | 晶癖を有する結晶及び該結晶を有効成分として含有する医薬組成物 |
| JP5587488B1 (ja) | 2013-12-12 | 2014-09-10 | 株式会社ポーラファルマ | ルリコナゾールを含有する製剤の評価方法及び指標物質 |
| CN107865825B (zh) * | 2016-09-28 | 2022-05-20 | 四川海思科制药有限公司 | 一种卢立康唑外用喷雾剂药物组合物及其制备方法 |
| CN108934161A (zh) * | 2017-03-29 | 2018-12-04 | 日本农药株式会社 | 用于治疗感染症的医药组合物 |
| US10898470B1 (en) | 2019-08-13 | 2021-01-26 | Sato Pharmaceutical Co., Ltd. | Pharmaceutical composition containing antifungal agent as active ingredient |
| US12576049B1 (en) | 2019-10-08 | 2026-03-17 | Hallux Inc. | Onychomycosis treatment methods |
| WO2021072027A1 (en) * | 2019-10-08 | 2021-04-15 | Hallux Inc. | Onychomycosis treatment compositions and methods |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4861764A (en) * | 1986-11-17 | 1989-08-29 | Macro Chem. Corp. | Percutaneous absorption enhancers, compositions containing same and method of use |
| JP3081766B2 (ja) | 1994-05-06 | 2000-08-28 | 東興薬品工業株式会社 | 角質貯留型抗真菌外用組成物 |
| JPH08245377A (ja) | 1995-03-15 | 1996-09-24 | Yamanouchi Pharmaceut Co Ltd | 経皮吸収用製剤 |
| GB2317615B (en) | 1995-07-08 | 1998-09-02 | Nihon Nohyaku Co Ltd | Antifungal agent compound therefor process for producing the same |
| JP3278738B2 (ja) | 1995-07-08 | 2002-04-30 | 日本農薬株式会社 | 抗真菌剤 |
| CA2278328C (en) * | 1998-02-09 | 2008-07-22 | Macrochem Corporation | Antifungal nail lacquer and method using same |
| JP2002114680A (ja) | 2000-07-31 | 2002-04-16 | Nippon Nohyaku Co Ltd | 抗真菌剤 |
| JP2002363070A (ja) * | 2001-06-06 | 2002-12-18 | Yuutoku Yakuhin Kogyo Kk | 経皮吸収貼付剤 |
| ES2535045T3 (es) * | 2003-04-10 | 2015-05-04 | Vanderbilt Royalty Sub L.P. | Usos y composiciones para administración de capsaicina |
| JP2007102242A (ja) | 2003-08-05 | 2007-04-19 | Sumitomo Electric Ind Ltd | 液晶パネル |
| CN101137369A (zh) * | 2005-02-09 | 2008-03-05 | 马库赛特公司 | 用于眼治疗的制剂 |
| JP2006306734A (ja) | 2005-04-26 | 2006-11-09 | Tsumura & Co | 尿素配合外用剤 |
| RU2419429C2 (ru) | 2006-03-08 | 2011-05-27 | Нихон Нохияку Ко.,Лтд. | Фармацевтическая композиция для наружного применения |
| CA2645070C (en) * | 2006-03-08 | 2014-02-04 | Nihon Nohyaku Co., Ltd. | Pharmaceutical composition for external use |
| WO2007102243A1 (ja) | 2006-03-08 | 2007-09-13 | Nihon Nohyaku Co., Ltd. | 外用の医薬組成物 |
| JP4476991B2 (ja) | 2006-11-28 | 2010-06-09 | 株式会社半導体エネルギー研究所 | 電気光学装置 |
| PL2191825T3 (pl) * | 2007-08-27 | 2016-11-30 | Środek przeciwko grzybiczemu zapaleniu skóry | |
| CN101808639B (zh) | 2007-09-05 | 2012-12-05 | 宝丽制药股份有限公司 | 抗真菌医药组合物 |
| EP2191827B1 (en) | 2007-09-05 | 2013-10-30 | Pola Pharma Inc. | Antifungal composition |
| JP5529539B2 (ja) | 2007-09-05 | 2014-06-25 | 株式会社ポーラファルマ | 医薬組成物 |
| US8193232B2 (en) | 2009-02-13 | 2012-06-05 | Topica Pharmaceuticals, Inc. | Anti-fungal formulation |
| EP2416757A2 (en) | 2009-04-09 | 2012-02-15 | Pola Pharma Inc. | Antimycotic pharmaceutical composition |
| KR101409792B1 (ko) * | 2009-04-09 | 2014-06-19 | 니혼노야쿠가부시키가이샤 | 항진균성 약제학적 조성물 |
| WO2011024620A1 (en) | 2009-08-25 | 2011-03-03 | Pola Pharma Inc. | Antimycotic pharmaceutical composition |
| JP5460797B1 (ja) | 2012-09-14 | 2014-04-02 | 株式会社ポーラファルマ | アミド誘導体及び安定性指標としてのその使用 |
| JP5589130B1 (ja) | 2012-09-14 | 2014-09-10 | 株式会社ポーラファルマ | 結晶及び該結晶を含有してなる医薬製剤 |
| RU2621615C2 (ru) | 2012-09-14 | 2017-06-06 | Пола Фарма Инк. | Фармацевтическая композиция, содержащая луликоназол |
| IN2015DN02376A (https=) | 2012-09-14 | 2015-09-04 | Pola Pharma Inc | |
| US9068958B1 (en) | 2012-09-14 | 2015-06-30 | Pola Pharma Inc. | Use of surface free energy for differential evaluation of crystal, crystal evaluated on basis of surface free energy as index, and pharmaceutical composition prepared by containing the crystal |
| JP5589110B1 (ja) | 2013-03-08 | 2014-09-10 | 株式会社ポーラファルマ | 晶癖を有する結晶及び該結晶を有効成分として含有する医薬組成物 |
-
2011
- 2011-06-10 EP EP11730088.9A patent/EP2579847A1/en not_active Withdrawn
- 2011-06-10 KR KR1020127033982A patent/KR101806304B1/ko active Active
- 2011-06-10 CN CN201180028753.8A patent/CN102933201B/zh active Active
- 2011-06-10 US US13/703,300 patent/US8962669B2/en active Active
- 2011-06-10 WO PCT/JP2011/063860 patent/WO2011155640A1/en not_active Ceased
- 2011-06-10 JP JP2012552591A patent/JP5832451B2/ja active Active
-
2015
- 2015-06-19 JP JP2015123928A patent/JP5938497B2/ja active Active
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