JP2014527969A5 - - Google Patents
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- Publication number
- JP2014527969A5 JP2014527969A5 JP2014530945A JP2014530945A JP2014527969A5 JP 2014527969 A5 JP2014527969 A5 JP 2014527969A5 JP 2014530945 A JP2014530945 A JP 2014530945A JP 2014530945 A JP2014530945 A JP 2014530945A JP 2014527969 A5 JP2014527969 A5 JP 2014527969A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- pharmaceutically acceptable
- acceptable salt
- hydrogen
- compound
- 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.)
- Ceased
Links
- 125000000217 alkyl group Chemical group 0.000 claims description 94
- 150000001875 compounds Chemical class 0.000 claims description 60
- 229910052739 hydrogen Inorganic materials 0.000 claims description 60
- 239000001257 hydrogen Substances 0.000 claims description 60
- 150000003839 salts Chemical class 0.000 claims description 40
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 34
- 150000002431 hydrogen Chemical class 0.000 claims description 33
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 28
- 125000003118 aryl group Chemical group 0.000 claims description 26
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 21
- 125000000623 heterocyclic group Chemical group 0.000 claims description 18
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 16
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims description 16
- 125000004429 atom Chemical group 0.000 claims description 16
- 125000002091 cationic group Chemical group 0.000 claims description 16
- 229910052757 nitrogen Inorganic materials 0.000 claims description 16
- 239000008194 pharmaceutical composition Substances 0.000 claims description 14
- 125000005496 phosphonium group Chemical group 0.000 claims description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 10
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims description 10
- 230000002438 mitochondrial effect Effects 0.000 claims description 9
- 150000001299 aldehydes Chemical class 0.000 claims description 8
- 125000004948 alkyl aryl alkyl group Chemical group 0.000 claims description 8
- -1 amino, nitro, sulfhydryl Chemical group 0.000 claims description 8
- 150000001450 anions Chemical class 0.000 claims description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 8
- 125000001188 haloalkyl group Chemical group 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 claims description 6
- 150000001408 amides Chemical class 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 230000004898 mitochondrial function Effects 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 5
- 125000004122 cyclic group Chemical group 0.000 claims description 5
- 230000002407 ATP formation Effects 0.000 claims description 4
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000004414 alkyl thio group Chemical group 0.000 claims description 4
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- 125000000539 amino acid group Chemical group 0.000 claims description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 150000001540 azides Chemical class 0.000 claims description 4
- 239000004202 carbamide Substances 0.000 claims description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 4
- 230000002708 enhancing effect Effects 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 125000001475 halogen functional group Chemical group 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- 150000002576 ketones Chemical class 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 210000003470 mitochondria Anatomy 0.000 claims description 4
- 150000002825 nitriles Chemical class 0.000 claims description 4
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 4
- 125000004043 oxo group Chemical group O=* 0.000 claims description 4
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 claims description 4
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims description 4
- 229920001184 polypeptide Polymers 0.000 claims description 4
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 4
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 4
- RJCQMRTZKKPRPL-UHFFFAOYSA-N s-aminosulfanyloxythiohydroxylamine Chemical compound NSOSN RJCQMRTZKKPRPL-UHFFFAOYSA-N 0.000 claims description 4
- 229940124530 sulfonamide Drugs 0.000 claims description 4
- 150000003456 sulfonamides Chemical class 0.000 claims description 4
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical group N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 claims description 3
- 125000001033 ether group Chemical group 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 claims description 2
- 125000000524 functional group Chemical group 0.000 claims description 2
- 125000006850 spacer group Chemical group 0.000 claims description 2
- 208000024891 symptom Diseases 0.000 claims description 2
- 230000008685 targeting Effects 0.000 claims description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
- 125000001841 imino group Chemical group [H]N=* 0.000 claims 1
- 238000000034 method Methods 0.000 description 5
- 0 ****N(*)C(N(*)*)=NI Chemical compound ****N(*)C(N(*)*)=NI 0.000 description 2
- CVSVTCORWBXHQV-UHFFFAOYSA-N creatine Chemical class NC(=[NH2+])N(C)CC([O-])=O CVSVTCORWBXHQV-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000001413 cellular effect Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161536280P | 2011-09-19 | 2011-09-19 | |
| US61/536,280 | 2011-09-19 | ||
| PCT/US2012/055887 WO2013043580A2 (en) | 2011-09-19 | 2012-09-18 | Modified creatine compounds |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017111480A Division JP2017160254A (ja) | 2011-09-19 | 2017-06-06 | 改変クレアチン化合物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2014527969A JP2014527969A (ja) | 2014-10-23 |
| JP2014527969A5 true JP2014527969A5 (enExample) | 2015-11-12 |
Family
ID=46982949
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014530945A Ceased JP2014527969A (ja) | 2011-09-19 | 2012-09-18 | 改変クレアチン化合物 |
| JP2017111480A Pending JP2017160254A (ja) | 2011-09-19 | 2017-06-06 | 改変クレアチン化合物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017111480A Pending JP2017160254A (ja) | 2011-09-19 | 2017-06-06 | 改変クレアチン化合物 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US9434753B2 (enExample) |
| EP (1) | EP2758411A2 (enExample) |
| JP (2) | JP2014527969A (enExample) |
| CN (1) | CN103889993B (enExample) |
| AU (1) | AU2012312654B2 (enExample) |
| CA (1) | CA2849073A1 (enExample) |
| HK (1) | HK1200459A1 (enExample) |
| WO (1) | WO2013043580A2 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ITTO20121098A1 (it) * | 2012-12-18 | 2014-06-19 | Univ Degli Studi Genova | Procedimento per sintetizzare derivati della creatina |
| HK1222323A1 (zh) | 2013-03-15 | 2017-06-30 | 吉奇亚公司 | 用於治疗影响表皮的病状的组合物和方法 |
| US20160289175A1 (en) * | 2013-11-05 | 2016-10-06 | Ultragenyx Pharmaceutical Inc. | Creatine analogs and the use thereof |
| 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 |
| US10883978B2 (en) * | 2017-01-31 | 2021-01-05 | Agilent Technologies, Inc. | Method and device for calibration of biological flux |
| JP6919923B2 (ja) * | 2017-08-04 | 2021-08-18 | 国立大学法人金沢大学 | 微小空間の加温方法及び発熱体 |
| KR102678696B1 (ko) | 2017-12-01 | 2024-06-27 | 울트라제닉스 파마수티컬 인코포레이티드 | 크레아틴 전구약물, 조성물과 이의 사용 방법 |
| KR101920902B1 (ko) * | 2017-12-27 | 2018-11-21 | 전남대학교 산학협력단 | 심혈관 질환 조기진단 pet 조영용 화합물 및 그의 용도 |
| WO2021085906A1 (ko) * | 2019-10-30 | 2021-05-06 | 주식회사 퓨전바이오텍 | 미토콘드리아 표적 화합물 및 이를 포함하는 노화 관련 질환의 치료 또는 예방을 위한 조성물 |
| CN115417898B (zh) * | 2022-08-02 | 2024-03-26 | 浙江工业大学 | 一种三苯基鏻单体化合物及其制备方法与在制备核酸递送纳米载体中的应用 |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL8720442A (nl) | 1986-08-18 | 1989-04-03 | Clinical Technologies Ass | Afgeefsystemen voor farmacologische agentia. |
| US5013556A (en) | 1989-10-20 | 1991-05-07 | Liposome Technology, Inc. | Liposomes with enhanced circulation time |
| EP2327404A1 (en) | 1994-11-08 | 2011-06-01 | Avicena Group, Inc. | Use of creatine or creatine analogs for the treatment of diseases of the nervous system |
| US20060128671A1 (en) | 1998-04-02 | 2006-06-15 | The General Hospital Corporation | Compositions containing a combination of a creatine compound and a second agent |
| AU759467B2 (en) * | 1998-04-02 | 2003-04-17 | Avicena Group, Inc. | Compositions containing a combination of a creatine compound and a second agent |
| JP2002523412A (ja) | 1998-08-25 | 2002-07-30 | ザ ユーエイビー リサーチ ファウンデイション | 細菌ｎａｄシンテターゼ阻害剤 |
| US6472378B2 (en) | 1998-08-31 | 2002-10-29 | Pro-Neuron, Inc. | Compositions and methods for treatment of mitochondrial diseases |
| WO2005019233A1 (en) | 2003-08-22 | 2005-03-03 | Antipodean Pharmaceuticals, Inc. | Mitoquinone derivatives used as mitochondrially targeted antioxidants |
| US20040006242A1 (en) | 1999-02-01 | 2004-01-08 | Hawkins Lynn D. | Immunomodulatory compounds and method of use thereof |
| HU226869B1 (en) | 1999-02-01 | 2010-01-28 | Eisai R & D Man Co | Immunological adjuvant compound and composition containing thereof |
| US6242491B1 (en) | 1999-06-25 | 2001-06-05 | Rima Kaddurah-Daouk | Use of creatine or creatine compounds for skin preservation |
| US6355616B1 (en) | 1999-06-25 | 2002-03-12 | Xoma (Us) Technology Ltd. | Derivative compounds derived from or based on bactericidal/permeability-increasing protein |
| WO2001012600A1 (en) | 1999-08-12 | 2001-02-22 | Cor Therapeutics, Inc. | INHIBITORS OF FACTOR Xa |
| EP1329450A4 (en) | 2000-09-27 | 2005-08-31 | Ajinomoto Kk | BENZODIAZEPINE DERIVATIVE |
| JP2005298343A (ja) | 2002-03-27 | 2005-10-27 | Ajinomoto Co Inc | ベンゾジアゼピン誘導体 |
| JP2003321499A (ja) | 2002-04-30 | 2003-11-11 | Internatl Reagents Corp | ミトコンドリアクレアチンキナーゼ抗体 |
| SI2656854T1 (sl) | 2003-02-04 | 2015-09-30 | Cornell Research Foundation, Inc. | Uporabe aromatsko-kationskega peptida |
| CN1839142B (zh) * | 2003-08-22 | 2010-06-16 | 澳新制药公司 | 用作靶向线粒体的抗氧化剂的线粒体醌衍生物 |
| JP4838722B2 (ja) | 2003-10-24 | 2011-12-14 | ゲンシア コーポレーション | ポリヌクレオチドを送達する方法、及び送達用組成物 |
| CN1997403A (zh) | 2004-07-13 | 2007-07-11 | 奥里迪斯生物医学研究及开发有限责任公司 | 靶向线粒体的抗氧化剂在治疗肝病和上皮癌中的用途 |
| US7915230B2 (en) | 2005-05-17 | 2011-03-29 | Molecular Transfer, Inc. | Reagents for transfection of eukaryotic cells |
| US20070066572A1 (en) | 2005-09-14 | 2007-03-22 | Kalyanaraman Balaraman | Neuroprotection by positively-charged nitroxides |
| FR2896162B1 (fr) | 2006-01-13 | 2008-02-15 | Sanofi Pasteur Sa | Emulsion huile dans eau thermoreversible |
| NZ572564A (en) | 2006-05-05 | 2011-10-28 | Molecular Transfer Inc | Novel reagents for transfection of eukaryotic cells |
| EP2066680B1 (en) * | 2006-09-28 | 2012-08-08 | Medical Research Council | Triphenylphosphonium thionitrite nitric oxide donors |
| AU2008296012A1 (en) * | 2007-09-07 | 2009-03-12 | Gencia Corporation | Mitochondrial compositions and uses thereof |
| CL2009000400A1 (es) | 2008-02-22 | 2010-09-10 | Irm Llc | Compuestos heterociclicos derivados de 3-fenil-1,6- naftiridin-2-ona; moduladores de la actividad cinasa; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como trastornos alergicos, trastornos autoinmunes, neoplasias, rechazo en trasplante de organos, entre otras. |
| US8598145B2 (en) | 2008-03-14 | 2013-12-03 | Stephen John Ralph | Mitochondrially delivered anti-cancer compounds |
| EP2424872B1 (en) * | 2009-04-27 | 2017-05-17 | Medical College of Wisconsin, Inc. | Neuroprotective compounds and their use |
| US20110021362A1 (en) | 2009-07-20 | 2011-01-27 | Constellation Pharmaceuticals | Agents for stimulating activity of methyl modifying enzymes and methods of use thereof |
| US9212177B2 (en) | 2009-08-05 | 2015-12-15 | Versitech Limited | Antiviral compounds and methods of making and using thereof |
| AU2010339414A1 (en) | 2009-12-31 | 2012-07-19 | Stealth Peptides International, Inc. | Methods for performing a coronary artery bypass graft procedure |
| WO2011147199A1 (en) | 2010-05-28 | 2011-12-01 | Versitech Limited | Compounds and methods for treating viral infections |
-
2012
- 2012-09-18 CA CA2849073A patent/CA2849073A1/en not_active Abandoned
- 2012-09-18 EP EP12769555.9A patent/EP2758411A2/en not_active Withdrawn
- 2012-09-18 HK HK15100837.0A patent/HK1200459A1/xx unknown
- 2012-09-18 JP JP2014530945A patent/JP2014527969A/ja not_active Ceased
- 2012-09-18 CN CN201280052878.9A patent/CN103889993B/zh not_active Expired - Fee Related
- 2012-09-18 WO PCT/US2012/055887 patent/WO2013043580A2/en not_active Ceased
- 2012-09-18 US US14/345,503 patent/US9434753B2/en not_active Expired - Fee Related
- 2012-09-18 AU AU2012312654A patent/AU2012312654B2/en not_active Ceased
-
2017
- 2017-06-06 JP JP2017111480A patent/JP2017160254A/ja active Pending
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