RU2014136339A - Замещенные пролины/пиперидины как антагонисты орексиновых рецепторов - Google Patents
Замещенные пролины/пиперидины как антагонисты орексиновых рецепторов Download PDFInfo
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- RU2014136339A RU2014136339A RU2014136339A RU2014136339A RU2014136339A RU 2014136339 A RU2014136339 A RU 2014136339A RU 2014136339 A RU2014136339 A RU 2014136339A RU 2014136339 A RU2014136339 A RU 2014136339A RU 2014136339 A RU2014136339 A RU 2014136339A
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- alkyl
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- 150000003053 piperidines Chemical class 0.000 title 1
- 150000003148 prolines Chemical class 0.000 title 1
- 239000002464 receptor antagonist Substances 0.000 title 1
- 229940044551 receptor antagonist Drugs 0.000 title 1
- -1 (C) acylamido Chemical group 0.000 claims abstract 26
- 150000001875 compounds Chemical class 0.000 claims abstract 26
- 125000000217 alkyl group Chemical group 0.000 claims abstract 13
- 125000003118 aryl group Chemical group 0.000 claims abstract 12
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract 10
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 9
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 9
- 125000002252 acyl group Chemical group 0.000 claims abstract 7
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract 6
- 125000004122 cyclic group Chemical group 0.000 claims abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 6
- 229910052717 sulfur Inorganic materials 0.000 claims abstract 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract 4
- 229910052736 halogen Inorganic materials 0.000 claims abstract 4
- 125000005544 phthalimido group Chemical group 0.000 claims abstract 4
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 3
- 150000002367 halogens Chemical class 0.000 claims abstract 3
- 125000004043 oxo group Chemical group O=* 0.000 claims abstract 3
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 3
- 125000004423 acyloxy group Chemical group 0.000 claims abstract 2
- 125000003435 aroyl group Chemical group 0.000 claims abstract 2
- 125000004104 aryloxy group Chemical group 0.000 claims abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 2
- 125000004438 haloalkoxy group Chemical group 0.000 claims abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract 2
- 125000005553 heteroaryloxy group Chemical group 0.000 claims abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 2
- 125000002950 monocyclic group Chemical group 0.000 claims 11
- 150000003839 salts Chemical class 0.000 claims 11
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims 10
- 125000006711 (C2-C12) alkynyl group Chemical group 0.000 claims 10
- 108050000742 Orexin Receptor Proteins 0.000 claims 10
- 102000008834 Orexin receptor Human genes 0.000 claims 10
- 238000000034 method Methods 0.000 claims 10
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims 9
- 206010013663 drug dependence Diseases 0.000 claims 6
- 125000004076 pyridyl group Chemical group 0.000 claims 6
- 208000011117 substance-related disease Diseases 0.000 claims 6
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims 5
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 5
- 125000006717 (C3-C10) cycloalkenyl group Chemical group 0.000 claims 4
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 claims 4
- 230000001575 pathological effect Effects 0.000 claims 4
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 4
- 125000005493 quinolyl group Chemical group 0.000 claims 4
- 230000008485 antagonism Effects 0.000 claims 3
- 125000002619 bicyclic group Chemical group 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000003226 pyrazolyl group Chemical group 0.000 claims 3
- 208000017194 Affective disease Diseases 0.000 claims 2
- 208000007848 Alcoholism Diseases 0.000 claims 2
- 208000024827 Alzheimer disease Diseases 0.000 claims 2
- 208000019901 Anxiety disease Diseases 0.000 claims 2
- 208000020925 Bipolar disease Diseases 0.000 claims 2
- 206010012289 Dementia Diseases 0.000 claims 2
- 208000030814 Eating disease Diseases 0.000 claims 2
- 208000019454 Feeding and Eating disease Diseases 0.000 claims 2
- 208000018522 Gastrointestinal disease Diseases 0.000 claims 2
- 206010019233 Headaches Diseases 0.000 claims 2
- 208000023105 Huntington disease Diseases 0.000 claims 2
- 206010020772 Hypertension Diseases 0.000 claims 2
- 206010061218 Inflammation Diseases 0.000 claims 2
- 208000019695 Migraine disease Diseases 0.000 claims 2
- 208000019022 Mood disease Diseases 0.000 claims 2
- 208000012902 Nervous system disease Diseases 0.000 claims 2
- 208000025966 Neurological disease Diseases 0.000 claims 2
- 206010057852 Nicotine dependence Diseases 0.000 claims 2
- 208000008589 Obesity Diseases 0.000 claims 2
- 208000002193 Pain Diseases 0.000 claims 2
- 208000018737 Parkinson disease Diseases 0.000 claims 2
- 208000006262 Psychological Sexual Dysfunctions Diseases 0.000 claims 2
- 208000025569 Tobacco Use disease Diseases 0.000 claims 2
- 201000007930 alcohol dependence Diseases 0.000 claims 2
- 208000028505 alcohol-related disease Diseases 0.000 claims 2
- 230000036506 anxiety Effects 0.000 claims 2
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims 2
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims 2
- 208000028683 bipolar I disease Diseases 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 229960003920 cocaine Drugs 0.000 claims 2
- 208000010877 cognitive disease Diseases 0.000 claims 2
- 235000014632 disordered eating Nutrition 0.000 claims 2
- 206010015037 epilepsy Diseases 0.000 claims 2
- 231100000869 headache Toxicity 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000002883 imidazolyl group Chemical group 0.000 claims 2
- 208000026278 immune system disease Diseases 0.000 claims 2
- 230000004054 inflammatory process Effects 0.000 claims 2
- 208000017169 kidney disease Diseases 0.000 claims 2
- 206010027599 migraine Diseases 0.000 claims 2
- 235000020824 obesity Nutrition 0.000 claims 2
- 229940127240 opiate Drugs 0.000 claims 2
- 125000002971 oxazolyl group Chemical group 0.000 claims 2
- 208000020016 psychiatric disease Diseases 0.000 claims 2
- 208000026961 psychosexual disease Diseases 0.000 claims 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 201000000980 schizophrenia Diseases 0.000 claims 2
- 208000012201 sexual and gender identity disease Diseases 0.000 claims 2
- 208000015891 sexual disease Diseases 0.000 claims 2
- 208000019116 sleep disease Diseases 0.000 claims 2
- 208000022925 sleep disturbance Diseases 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 238000006467 substitution reaction Methods 0.000 claims 2
- 208000011580 syndromic disease Diseases 0.000 claims 2
- 125000000335 thiazolyl group Chemical group 0.000 claims 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 208000027691 Conduct disease Diseases 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 230000006399 behavior Effects 0.000 claims 1
- 230000009286 beneficial effect Effects 0.000 claims 1
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 claims 1
- 125000001164 benzothiazolyl group Chemical class S1C(=NC2=C1C=CC=C2)* 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 230000002124 endocrine Effects 0.000 claims 1
- 208000030172 endocrine system disease Diseases 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 230000001771 impaired effect Effects 0.000 claims 1
- 238000001727 in vivo Methods 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000002098 pyridazinyl group Chemical group 0.000 claims 1
- 102000005962 receptors Human genes 0.000 claims 1
- 108020003175 receptors Proteins 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 0 C*(CC1C(C)(C)C(C)(C)N(*)O)CC(C)(CCC=*=C)C*1C(NC(F)(F)F)=O Chemical compound C*(CC1C(C)(C)C(C)(C)N(*)O)CC(C)(CCC=*=C)C*1C(NC(F)(F)F)=O 0.000 description 4
- HZFKREMTPLGHNZ-UHFFFAOYSA-N CC(CCC1)C(CNc2nccc(OC)n2)N1C(c1c(C2C=CC(F)=CC2)[s]c(C)n1)=O Chemical compound CC(CCC1)C(CNc2nccc(OC)n2)N1C(c1c(C2C=CC(F)=CC2)[s]c(C)n1)=O HZFKREMTPLGHNZ-UHFFFAOYSA-N 0.000 description 1
- AVEJAGBNNFGESW-ITXXBFQVSA-N CC(CCC1)[C@@H](CNC(N=C2)=CCC2Cl)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O Chemical compound CC(CCC1)[C@@H](CNC(N=C2)=CCC2Cl)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O AVEJAGBNNFGESW-ITXXBFQVSA-N 0.000 description 1
- XFEYGGDAAUEMDY-LRHAYUFXSA-N CC(CCC1)[C@@H](CNc2ccnc(Cl)n2)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O Chemical compound CC(CCC1)[C@@H](CNc2ccnc(Cl)n2)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O XFEYGGDAAUEMDY-LRHAYUFXSA-N 0.000 description 1
- JAUIDCOPUGAEFY-UHFFFAOYSA-N CC(CCCC1CNC(c2c(cc(C)[o]3)c3ccc2)=O)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O Chemical compound CC(CCCC1CNC(c2c(cc(C)[o]3)c3ccc2)=O)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O JAUIDCOPUGAEFY-UHFFFAOYSA-N 0.000 description 1
- OZQQWERPXKWLAA-UHFFFAOYSA-N CC(CCCC1CNC(c2c(cc[o]3)c3ccc2)=O)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O Chemical compound CC(CCCC1CNC(c2c(cc[o]3)c3ccc2)=O)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O OZQQWERPXKWLAA-UHFFFAOYSA-N 0.000 description 1
- BJMYJAPKIHPIPW-UHFFFAOYSA-N CC(CCCC1CNC(c2cccc(F)c2OC)=O)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O Chemical compound CC(CCCC1CNC(c2cccc(F)c2OC)=O)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O BJMYJAPKIHPIPW-UHFFFAOYSA-N 0.000 description 1
- HZPZSGOEBWBFRK-UHFFFAOYSA-N CC1N(COCc2c(-c(cc3)ccc3F)[s]c(C)n2)C(CNC(c2c3ncccc3ccc2)=O)CCC1 Chemical compound CC1N(COCc2c(-c(cc3)ccc3F)[s]c(C)n2)C(CNC(c2c3ncccc3ccc2)=O)CCC1 HZPZSGOEBWBFRK-UHFFFAOYSA-N 0.000 description 1
- PQHANPYFHWQTGR-UHFFFAOYSA-N CN(C)C(CCC1CNC(c2c3ncccc3ccc2)=O)CN1C(c(cccc1)c1-c1ccccc1)=O Chemical compound CN(C)C(CCC1CNC(c2c3ncccc3ccc2)=O)CN1C(c(cccc1)c1-c1ccccc1)=O PQHANPYFHWQTGR-UHFFFAOYSA-N 0.000 description 1
- SOLQCEFCASWIBL-JRBCQKTISA-N C[C@H](CCC1)[C@@H](CNC(N2)=NC=CC2(C)Cl)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O Chemical compound C[C@H](CCC1)[C@@H](CNC(N2)=NC=CC2(C)Cl)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O SOLQCEFCASWIBL-JRBCQKTISA-N 0.000 description 1
- VEPJQJFBXDGTGY-UHFFFAOYSA-N Cc([o]c1ccc2)cc1c2C(NCC(CCC(C1)(F)F)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O)=O Chemical compound Cc([o]c1ccc2)cc1c2C(NCC(CCC(C1)(F)F)N1C(c1c(-c(cc2)ccc2F)[s]c(C)n1)=O)=O VEPJQJFBXDGTGY-UHFFFAOYSA-N 0.000 description 1
- WGLJHTQZRNCVHT-UHFFFAOYSA-N Cc1nc(-c2ccccc2)c(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2N)=O)[s]1 Chemical compound Cc1nc(-c2ccccc2)c(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2N)=O)[s]1 WGLJHTQZRNCVHT-UHFFFAOYSA-N 0.000 description 1
- MOXXGRCLAOBXLS-UHFFFAOYSA-N Cc1nc(C(N(C2)C(CNC(c3c(cc[o]4)c4ccc3)=O)CCC2F)=O)c(-c2ccccc2)[s]1 Chemical compound Cc1nc(C(N(C2)C(CNC(c3c(cc[o]4)c4ccc3)=O)CCC2F)=O)c(-c2ccccc2)[s]1 MOXXGRCLAOBXLS-UHFFFAOYSA-N 0.000 description 1
- YCPDCUAUNGQDQS-UHFFFAOYSA-N Cc1nc(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2(F)F)=O)c(-c2cc(F)ccc2)[s]1 Chemical compound Cc1nc(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2(F)F)=O)c(-c2cc(F)ccc2)[s]1 YCPDCUAUNGQDQS-UHFFFAOYSA-N 0.000 description 1
- DDOYCBFXVKQWOL-UHFFFAOYSA-N Cc1nc(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2(F)F)=O)c(-c2ccccc2)[s]1 Chemical compound Cc1nc(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2(F)F)=O)c(-c2ccccc2)[s]1 DDOYCBFXVKQWOL-UHFFFAOYSA-N 0.000 description 1
- BSPIQLLFYKKPND-UHFFFAOYSA-N Cc1nc(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2F)=O)c(-c2ccccc2)[s]1 Chemical compound Cc1nc(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2F)=O)c(-c2ccccc2)[s]1 BSPIQLLFYKKPND-UHFFFAOYSA-N 0.000 description 1
- DGIIYCMWCFSJQG-UHFFFAOYSA-N Cc1nc(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2N)=O)c(-c2cccc(F)c2)[s]1 Chemical compound Cc1nc(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2N)=O)c(-c2cccc(F)c2)[s]1 DGIIYCMWCFSJQG-UHFFFAOYSA-N 0.000 description 1
- CMEYWYAGTUKFKO-UHFFFAOYSA-N Cc1nc(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2N)=O)c(-c2ccccc2)[s]1 Chemical compound Cc1nc(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2N)=O)c(-c2ccccc2)[s]1 CMEYWYAGTUKFKO-UHFFFAOYSA-N 0.000 description 1
- FFMNWZBNGKPLLR-UHFFFAOYSA-N Cc1nc(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2NCCO)O)c(-c2cc(F)ccc2)[s]1 Chemical compound Cc1nc(C(N(C2)C(CNC(c3c4ncccc4ccc3)=O)CCC2NCCO)O)c(-c2cc(F)ccc2)[s]1 FFMNWZBNGKPLLR-UHFFFAOYSA-N 0.000 description 1
- GJDYBOVHDFWUGD-UHFFFAOYSA-N Cc1nc(C(N(C2)C(CNc3ccc(C(F)(F)F)cn3)CCC2F)=O)c(-c2ccccc2)[s]1 Chemical compound Cc1nc(C(N(C2)C(CNc3ccc(C(F)(F)F)cn3)CCC2F)=O)c(-c2ccccc2)[s]1 GJDYBOVHDFWUGD-UHFFFAOYSA-N 0.000 description 1
- JUWKISUHBYETOZ-JNDMISCYSA-N O[C@H](C[C@H]1/C=N/C(c2cccc3c2nccc3)=O)CN1C(c1ccccc1-c1ccccc1)=O Chemical compound O[C@H](C[C@H]1/C=N/C(c2cccc3c2nccc3)=O)CN1C(c1ccccc1-c1ccccc1)=O JUWKISUHBYETOZ-JNDMISCYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
-
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
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| CA2863413A1 (en) | 2012-02-07 | 2013-08-15 | Eolas Therapeutics, Inc. | Substituted prolines / piperidines as orexin receptor antagonists |
| ITMI20120322A1 (it) * | 2012-03-01 | 2013-09-02 | Rottapharm Spa | Composti di 4,4-difluoro piperidina |
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| JP2017001954A (ja) * | 2013-11-08 | 2017-01-05 | 石原産業株式会社 | 含窒素飽和複素環化合物 |
| JP2017024990A (ja) * | 2013-12-13 | 2017-02-02 | 大正製薬株式会社 | オキサゾリジン及びオキサジナン誘導体 |
| TW201613891A (en) * | 2014-02-12 | 2016-04-16 | Eolas Therapeutics Inc | Substituted prolines / piperidines as orexin receptor antagonists |
| EP3180332B1 (en) * | 2014-08-13 | 2021-10-27 | Eolas Therapeutics Inc. | Difluoropyrrolidines as orexin receptor modulators |
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| UA125873C2 (uk) | 2016-03-10 | 2022-06-29 | Янссен Фармацевтика Нв | Спосіб лікування депресії з використанням антагоністів рецептора орексин-2 |
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-
2013
- 2013-02-06 CA CA2863413A patent/CA2863413A1/en not_active Abandoned
- 2013-02-06 EP EP13746989.6A patent/EP2811997B1/en active Active
- 2013-02-06 WO PCT/US2013/024903 patent/WO2013119639A1/en not_active Ceased
- 2013-02-06 NZ NZ628491A patent/NZ628491A/en not_active IP Right Cessation
- 2013-02-06 MX MX2014009281A patent/MX2014009281A/es unknown
- 2013-02-06 SG SG11201404738QA patent/SG11201404738QA/en unknown
- 2013-02-06 KR KR1020147025072A patent/KR20140124398A/ko not_active Withdrawn
- 2013-02-06 ES ES13746989.6T patent/ES2672732T3/es active Active
- 2013-02-06 CN CN201380018420.6A patent/CN104220065A/zh active Pending
- 2013-02-06 JP JP2014556628A patent/JP6346862B2/ja active Active
- 2013-02-06 AU AU2013217323A patent/AU2013217323A1/en not_active Abandoned
- 2013-02-06 BR BR112014019426A patent/BR112014019426A8/pt not_active IP Right Cessation
- 2013-02-06 RU RU2014136339A patent/RU2014136339A/ru not_active Application Discontinuation
- 2013-02-06 HK HK15105691.4A patent/HK1204955A1/xx unknown
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2014
- 2014-02-12 US US14/179,432 patent/US9499517B2/en active Active
- 2014-08-07 PH PH12014501784A patent/PH12014501784A1/en unknown
- 2014-08-07 IL IL234025A patent/IL234025A0/en unknown
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2015
- 2015-02-11 AR ARP150100403A patent/AR099466A1/es unknown
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- 2016-10-20 US US15/299,230 patent/US9896452B2/en active Active
Also Published As
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|---|---|
| CN104220065A (zh) | 2014-12-17 |
| IL234025A0 (en) | 2014-09-30 |
| BR112014019426A2 (cg-RX-API-DMAC7.html) | 2017-06-20 |
| KR20140124398A (ko) | 2014-10-24 |
| US20140364432A1 (en) | 2014-12-11 |
| BR112014019426A8 (pt) | 2017-07-11 |
| US9896452B2 (en) | 2018-02-20 |
| EP2811997B1 (en) | 2018-04-11 |
| JP2015506382A (ja) | 2015-03-02 |
| NZ628491A (en) | 2016-06-24 |
| US9499517B2 (en) | 2016-11-22 |
| AR099466A1 (es) | 2016-07-27 |
| EP2811997A1 (en) | 2014-12-17 |
| WO2013119639A1 (en) | 2013-08-15 |
| US20170101410A1 (en) | 2017-04-13 |
| ES2672732T3 (es) | 2018-06-15 |
| SG11201404738QA (en) | 2014-10-30 |
| MX2014009281A (es) | 2015-01-12 |
| PH12014501784A1 (en) | 2014-11-10 |
| JP6346862B2 (ja) | 2018-06-20 |
| AU2013217323A1 (en) | 2014-08-28 |
| CA2863413A1 (en) | 2013-08-15 |
| HK1204955A1 (zh) | 2015-12-11 |
| EP2811997A4 (en) | 2015-07-22 |
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