JP2018502911A5 - - Google Patents
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- Publication number
- JP2018502911A5 JP2018502911A5 JP2017552008A JP2017552008A JP2018502911A5 JP 2018502911 A5 JP2018502911 A5 JP 2018502911A5 JP 2017552008 A JP2017552008 A JP 2017552008A JP 2017552008 A JP2017552008 A JP 2017552008A JP 2018502911 A5 JP2018502911 A5 JP 2018502911A5
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- formula
- compound
- alkyl
- hydrogen
- 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
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- 150000001875 compounds Chemical class 0.000 claims 66
- 125000000217 alkyl group Chemical group 0.000 claims 61
- 229910052739 hydrogen Inorganic materials 0.000 claims 54
- 239000001257 hydrogen Substances 0.000 claims 54
- 150000002431 hydrogen Chemical class 0.000 claims 50
- 125000003118 aryl group Chemical group 0.000 claims 27
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 27
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 27
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 27
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims 26
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 26
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 26
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 25
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 24
- 125000001072 heteroaryl group Chemical group 0.000 claims 24
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 24
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 23
- 125000003710 aryl alkyl group Chemical group 0.000 claims 22
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 claims 21
- 125000004404 heteroalkyl group Chemical group 0.000 claims 21
- 125000005885 heterocycloalkylalkyl group Chemical group 0.000 claims 21
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 20
- 239000008194 pharmaceutical composition Substances 0.000 claims 16
- -1 R 18 Chemical compound 0.000 claims 11
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 7
- 239000012453 solvate Substances 0.000 claims 7
- CVSVTCORWBXHQV-UHFFFAOYSA-N creatine Chemical compound NC(=[NH2+])N(C)CC([O-])=O CVSVTCORWBXHQV-UHFFFAOYSA-N 0.000 claims 6
- 208000035475 disorder Diseases 0.000 claims 6
- 210000000056 organ Anatomy 0.000 claims 6
- 210000001519 tissue Anatomy 0.000 claims 6
- 102000004420 Creatine Kinase Human genes 0.000 claims 5
- 108010042126 Creatine kinase Proteins 0.000 claims 5
- 201000010099 disease Diseases 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 208000026350 Inborn Genetic disease Diseases 0.000 claims 4
- 208000016361 genetic disease Diseases 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- 102100023153 Sodium- and chloride-dependent creatine transporter 1 Human genes 0.000 claims 3
- 230000015572 biosynthetic process Effects 0.000 claims 3
- 229960003624 creatine Drugs 0.000 claims 3
- 239000006046 creatine Substances 0.000 claims 3
- 108010007169 creatine transporter Proteins 0.000 claims 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 3
- 125000003107 substituted aryl group Chemical group 0.000 claims 3
- 238000003786 synthesis reaction Methods 0.000 claims 3
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 2
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 2
- 208000024172 Cardiovascular disease Diseases 0.000 claims 2
- 206010049565 Muscle fatigue Diseases 0.000 claims 2
- 206010063837 Reperfusion injury Diseases 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 230000003833 cell viability Effects 0.000 claims 2
- 230000019439 energy homeostasis Effects 0.000 claims 2
- 208000028867 ischemia Diseases 0.000 claims 2
- 208000012947 ischemia reperfusion injury Diseases 0.000 claims 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 2
- 201000006417 multiple sclerosis Diseases 0.000 claims 2
- 210000003205 muscle Anatomy 0.000 claims 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 230000004770 neurodegeneration Effects 0.000 claims 2
- 208000015122 neurodegenerative disease Diseases 0.000 claims 2
- 230000036542 oxidative stress Effects 0.000 claims 2
- 208000020016 psychiatric disease Diseases 0.000 claims 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 230000035899 viability Effects 0.000 claims 2
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 1
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 230000002068 genetic effect Effects 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 239000006186 oral dosage form Substances 0.000 claims 1
- 125000005504 styryl group Chemical group 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 238000013268 sustained release Methods 0.000 claims 1
- 239000012730 sustained-release form Substances 0.000 claims 1
- 0 CCC(*N(C1)C(N)=NC(*)(N)OC1=O)I Chemical compound CCC(*N(C1)C(N)=NC(*)(N)OC1=O)I 0.000 description 2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462095295P | 2014-12-22 | 2014-12-22 | |
| US62/095,295 | 2014-12-22 | ||
| PCT/US2015/067283 WO2016106284A2 (en) | 2014-12-22 | 2015-12-22 | Creatine prodrugs, compositions and methods of use thereof |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020072408A Division JP7037597B2 (ja) | 2014-12-22 | 2020-04-14 | クレアチンプロドラッグ、その組成物、及びその使用方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018502911A JP2018502911A (ja) | 2018-02-01 |
| JP2018502911A5 true JP2018502911A5 (enExample) | 2018-12-13 |
| JP6692372B2 JP6692372B2 (ja) | 2020-05-13 |
Family
ID=56128653
Family Applications (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017552008A Active JP6692372B2 (ja) | 2014-12-22 | 2015-12-22 | クレアチンプロドラッグ、その組成物、及びその使用方法 |
| JP2020072408A Active JP7037597B2 (ja) | 2014-12-22 | 2020-04-14 | クレアチンプロドラッグ、その組成物、及びその使用方法 |
| JP2022033882A Active JP7676338B2 (ja) | 2014-12-22 | 2022-03-04 | クレアチンプロドラッグ、その組成物、及びその使用方法 |
| JP2025075259A Pending JP2025118733A (ja) | 2014-12-22 | 2025-04-30 | クレアチンプロドラッグ、その組成物、及びその使用方法 |
Family Applications After (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020072408A Active JP7037597B2 (ja) | 2014-12-22 | 2020-04-14 | クレアチンプロドラッグ、その組成物、及びその使用方法 |
| JP2022033882A Active JP7676338B2 (ja) | 2014-12-22 | 2022-03-04 | クレアチンプロドラッグ、その組成物、及びその使用方法 |
| JP2025075259A Pending JP2025118733A (ja) | 2014-12-22 | 2025-04-30 | クレアチンプロドラッグ、その組成物、及びその使用方法 |
Country Status (8)
| Country | Link |
|---|---|
| US (3) | US9617230B2 (enExample) |
| EP (2) | EP3771709B1 (enExample) |
| JP (4) | JP6692372B2 (enExample) |
| AR (2) | AR103254A1 (enExample) |
| CA (1) | CA2971729C (enExample) |
| ES (1) | ES2832333T3 (enExample) |
| TW (3) | TWI832450B (enExample) |
| WO (1) | WO2016106284A2 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9617230B2 (en) | 2014-12-22 | 2017-04-11 | Farmington Pharma Development | Creatine prodrugs, compositions and methods of use thereof |
| US11021501B2 (en) | 2015-03-30 | 2021-06-01 | Farmington Pharma Development | Creatine phosphate analog prodrugs, compositions and methods of use thereof |
| WO2019109067A2 (en) * | 2017-12-01 | 2019-06-06 | Ultragenyx Pharmaceutical Inc. | Creatine prodrugs, compositions and methods of use thereof |
| CN110746325A (zh) * | 2018-07-24 | 2020-02-04 | 上海和辉光电有限公司 | 一种基于胍骨架的n型掺杂化合物及其应用 |
| CN114419050B (zh) * | 2022-03-31 | 2022-06-21 | 武汉大学 | 胃黏膜可视化程度量化方法、装置、终端及可读存储介质 |
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| US11021501B2 (en) | 2015-03-30 | 2021-06-01 | Farmington Pharma Development | Creatine phosphate analog prodrugs, compositions and methods of use thereof |
-
2015
- 2015-12-21 US US14/975,950 patent/US9617230B2/en active Active
- 2015-12-22 JP JP2017552008A patent/JP6692372B2/ja active Active
- 2015-12-22 TW TW111136599A patent/TWI832450B/zh active
- 2015-12-22 ES ES15874283T patent/ES2832333T3/es active Active
- 2015-12-22 EP EP20184803.3A patent/EP3771709B1/en active Active
- 2015-12-22 WO PCT/US2015/067283 patent/WO2016106284A2/en not_active Ceased
- 2015-12-22 CA CA2971729A patent/CA2971729C/en active Active
- 2015-12-22 AR ARP150104265A patent/AR103254A1/es active IP Right Grant
- 2015-12-22 TW TW109123072A patent/TWI779312B/zh active
- 2015-12-22 TW TW104143162A patent/TWI700270B/zh active
- 2015-12-22 EP EP15874283.3A patent/EP3237391B1/en active Active
-
2017
- 2017-04-07 US US15/481,568 patent/US10344007B2/en active Active
-
2019
- 2019-05-22 US US16/419,596 patent/US11407722B2/en active Active
-
2020
- 2020-04-14 JP JP2020072408A patent/JP7037597B2/ja active Active
-
2021
- 2021-05-14 AR ARP210101331A patent/AR122096A2/es unknown
-
2022
- 2022-03-04 JP JP2022033882A patent/JP7676338B2/ja active Active
-
2025
- 2025-04-30 JP JP2025075259A patent/JP2025118733A/ja active Pending
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