JP2008538586A5 - - Google Patents
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- JP2008538586A5 JP2008538586A5 JP2008507992A JP2008507992A JP2008538586A5 JP 2008538586 A5 JP2008538586 A5 JP 2008538586A5 JP 2008507992 A JP2008507992 A JP 2008507992A JP 2008507992 A JP2008507992 A JP 2008507992A JP 2008538586 A5 JP2008538586 A5 JP 2008538586A5
- Authority
- JP
- Japan
- Prior art keywords
- mixture
- compound
- composition
- nac amide
- isomers
- 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.)
- Pending
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- 239000000203 mixture Substances 0.000 claims 94
- 150000001875 compounds Chemical class 0.000 claims 48
- UJCHIZDEQZMODR-BYPYZUCNSA-N (2r)-2-acetamido-3-sulfanylpropanamide Chemical compound CC(=O)N[C@@H](CS)C(N)=O UJCHIZDEQZMODR-BYPYZUCNSA-N 0.000 claims 38
- 238000000034 method Methods 0.000 claims 30
- 230000008569 process Effects 0.000 claims 30
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 20
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 18
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 17
- 238000001914 filtration Methods 0.000 claims 16
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims 15
- 238000001035 drying Methods 0.000 claims 14
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 12
- 210000004027 cell Anatomy 0.000 claims 11
- 239000003446 ligand Substances 0.000 claims 11
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims 10
- 238000002156 mixing Methods 0.000 claims 10
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 9
- 229910001868 water Inorganic materials 0.000 claims 9
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims 8
- 150000008064 anhydrides Chemical class 0.000 claims 8
- 239000002105 nanoparticle Substances 0.000 claims 8
- QAEDZJGFFMLHHQ-UHFFFAOYSA-N trifluoroacetic anhydride Chemical compound FC(F)(F)C(=O)OC(=O)C(F)(F)F QAEDZJGFFMLHHQ-UHFFFAOYSA-N 0.000 claims 8
- 201000010099 disease Diseases 0.000 claims 7
- 210000001519 tissue Anatomy 0.000 claims 7
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims 6
- 239000003963 antioxidant agent Substances 0.000 claims 6
- RWSXRVCMGQZWBV-WDSKDSINSA-N glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 claims 6
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims 5
- 229910021529 ammonia Inorganic materials 0.000 claims 5
- 235000019270 ammonium chloride Nutrition 0.000 claims 5
- 230000003078 antioxidant effect Effects 0.000 claims 5
- -1 lithium aluminum hydride Chemical compound 0.000 claims 5
- 235000017281 sodium acetate Nutrition 0.000 claims 5
- 239000001632 sodium acetate Substances 0.000 claims 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 4
- 159000000021 acetate salts Chemical class 0.000 claims 4
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims 4
- 230000008859 change Effects 0.000 claims 4
- 230000000694 effects Effects 0.000 claims 4
- 230000014509 gene expression Effects 0.000 claims 4
- 230000003902 lesion Effects 0.000 claims 4
- 239000012280 lithium aluminium hydride Substances 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 4
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims 4
- UYCAUPASBSROMS-AWQJXPNKSA-M sodium;2,2,2-trifluoroacetate Chemical compound [Na+].[O-][13C](=O)[13C](F)(F)F UYCAUPASBSROMS-AWQJXPNKSA-M 0.000 claims 4
- 150000003573 thiols Chemical class 0.000 claims 4
- 108010024636 Glutathione Proteins 0.000 claims 3
- 229960003180 glutathione Drugs 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 208000019838 Blood disease Diseases 0.000 claims 2
- 206010040047 Sepsis Diseases 0.000 claims 2
- 238000006731 degradation reaction Methods 0.000 claims 2
- 208000035475 disorder Diseases 0.000 claims 2
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 claims 2
- 238000010438 heat treatment Methods 0.000 claims 2
- 208000014951 hematologic disease Diseases 0.000 claims 2
- 208000018706 hematopoietic system disease Diseases 0.000 claims 2
- 230000008520 organization Effects 0.000 claims 2
- 238000012261 overproduction Methods 0.000 claims 2
- 239000007800 oxidant agent Substances 0.000 claims 2
- 230000001590 oxidative effect Effects 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 230000001376 precipitating effect Effects 0.000 claims 2
- 230000005855 radiation Effects 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 230000000451 tissue damage Effects 0.000 claims 2
- 231100000827 tissue damage Toxicity 0.000 claims 2
- 230000008354 tissue degradation Effects 0.000 claims 2
- 238000005406 washing Methods 0.000 claims 2
- OYPOYMPGFACTLO-RGVONZFCSA-N (2r)-2-amino-3-[[(2r)-2,3-diamino-3-oxopropyl]disulfanyl]propanamide;dihydrochloride Chemical compound Cl.Cl.NC(=O)[C@@H](N)CSSC[C@H](N)C(N)=O OYPOYMPGFACTLO-RGVONZFCSA-N 0.000 claims 1
- PFRXZICTHLYYGK-UHFFFAOYSA-N 2,5,7-trimethoxynaphthalene-1,4-dione Chemical compound C1=C(OC)C=C2C(=O)C(OC)=CC(=O)C2=C1OC PFRXZICTHLYYGK-UHFFFAOYSA-N 0.000 claims 1
- VKUYLANQOAKALN-UHFFFAOYSA-N 2-[benzyl-(4-methoxyphenyl)sulfonylamino]-n-hydroxy-4-methylpentanamide Chemical compound C1=CC(OC)=CC=C1S(=O)(=O)N(C(CC(C)C)C(=O)NO)CC1=CC=CC=C1 VKUYLANQOAKALN-UHFFFAOYSA-N 0.000 claims 1
- 208000030507 AIDS Diseases 0.000 claims 1
- 200000000007 Arterial disease Diseases 0.000 claims 1
- 241000894006 Bacteria Species 0.000 claims 1
- 208000020084 Bone disease Diseases 0.000 claims 1
- 206010007559 Cardiac failure congestive Diseases 0.000 claims 1
- 208000024172 Cardiovascular disease Diseases 0.000 claims 1
- OYPOYMPGFACTLO-XWJKVJTJSA-N Cl.Cl.NC(=O)[C@H](N)CSSC[C@@H](N)C(N)=O Chemical compound Cl.Cl.NC(=O)[C@H](N)CSSC[C@@H](N)C(N)=O OYPOYMPGFACTLO-XWJKVJTJSA-N 0.000 claims 1
- 201000000054 Coronary Restenosis Diseases 0.000 claims 1
- 206010056489 Coronary artery restenosis Diseases 0.000 claims 1
- 108090000695 Cytokines Proteins 0.000 claims 1
- 102000004127 Cytokines Human genes 0.000 claims 1
- 208000004449 DNA Virus Infections Diseases 0.000 claims 1
- 206010019280 Heart failures Diseases 0.000 claims 1
- 102100032742 Histone-lysine N-methyltransferase SETD2 Human genes 0.000 claims 1
- 101000654725 Homo sapiens Histone-lysine N-methyltransferase SETD2 Proteins 0.000 claims 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 claims 1
- 208000019693 Lung disease Diseases 0.000 claims 1
- 102000000422 Matrix Metalloproteinase 3 Human genes 0.000 claims 1
- 108010016160 Matrix Metalloproteinase 3 Proteins 0.000 claims 1
- 102000005741 Metalloproteases Human genes 0.000 claims 1
- 108010006035 Metalloproteases Proteins 0.000 claims 1
- 208000029578 Muscle disease Diseases 0.000 claims 1
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 claims 1
- 208000012902 Nervous system disease Diseases 0.000 claims 1
- 238000000636 Northern blotting Methods 0.000 claims 1
- 208000001132 Osteoporosis Diseases 0.000 claims 1
- 208000024777 Prion disease Diseases 0.000 claims 1
- 208000009341 RNA Virus Infections Diseases 0.000 claims 1
- 102100030416 Stromelysin-1 Human genes 0.000 claims 1
- 101710108790 Stromelysin-1 Proteins 0.000 claims 1
- 230000021736 acetylation Effects 0.000 claims 1
- 238000006640 acetylation reaction Methods 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 208000006673 asthma Diseases 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 210000000601 blood cell Anatomy 0.000 claims 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 claims 1
- 235000018417 cysteine Nutrition 0.000 claims 1
- 239000000412 dendrimer Substances 0.000 claims 1
- 229920000736 dendritic polymer Polymers 0.000 claims 1
- 206010012601 diabetes mellitus Diseases 0.000 claims 1
- 210000002889 endothelial cell Anatomy 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 229960000304 folic acid Drugs 0.000 claims 1
- 235000019152 folic acid Nutrition 0.000 claims 1
- 239000011724 folic acid Substances 0.000 claims 1
- 235000013373 food additive Nutrition 0.000 claims 1
- 239000002778 food additive Substances 0.000 claims 1
- 230000003394 haemopoietic effect Effects 0.000 claims 1
- 238000003018 immunoassay Methods 0.000 claims 1
- 238000003119 immunoblot Methods 0.000 claims 1
- 238000010166 immunofluorescence Methods 0.000 claims 1
- 208000015181 infectious disease Diseases 0.000 claims 1
- 208000027866 inflammatory disease Diseases 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 210000000265 leukocyte Anatomy 0.000 claims 1
- 210000004185 liver Anatomy 0.000 claims 1
- 208000002780 macular degeneration Diseases 0.000 claims 1
- 201000004792 malaria Diseases 0.000 claims 1
- UDHSAWHYRXHQJP-HNCPQSOCSA-N methyl (2R)-2-amino-3-phenylmethoxypropanoate hydrochloride Chemical compound Cl.COC(=O)[C@H](N)COCC1=CC=CC=C1 UDHSAWHYRXHQJP-HNCPQSOCSA-N 0.000 claims 1
- QVJDVOZRQMIIHP-PPHPATTJSA-N methyl (2r)-2-amino-3-benzylsulfanylpropanoate;hydrochloride Chemical compound Cl.COC(=O)[C@@H](N)CSCC1=CC=CC=C1 QVJDVOZRQMIIHP-PPHPATTJSA-N 0.000 claims 1
- QVJDVOZRQMIIHP-HNCPQSOCSA-N methyl (2s)-2-amino-3-benzylsulfanylpropanoate;hydrochloride Chemical compound Cl.COC(=O)[C@H](N)CSCC1=CC=CC=C1 QVJDVOZRQMIIHP-HNCPQSOCSA-N 0.000 claims 1
- 238000010208 microarray analysis Methods 0.000 claims 1
- 230000000813 microbial effect Effects 0.000 claims 1
- 244000005700 microbiome Species 0.000 claims 1
- 230000036542 oxidative stress Effects 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 230000007170 pathology Effects 0.000 claims 1
- 230000037361 pathway Effects 0.000 claims 1
- 229920000962 poly(amidoamine) Polymers 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 238000001556 precipitation Methods 0.000 claims 1
- 230000004044 response Effects 0.000 claims 1
- 238000003757 reverse transcription PCR Methods 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 208000007056 sickle cell anemia Diseases 0.000 claims 1
- NGDIAZZSCVVCEW-UHFFFAOYSA-M sodium;butyl sulfate Chemical compound [Na+].CCCCOS([O-])(=O)=O NGDIAZZSCVVCEW-UHFFFAOYSA-M 0.000 claims 1
- 230000004936 stimulating effect Effects 0.000 claims 1
- 230000008685 targeting Effects 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
- 231100000133 toxic exposure Toxicity 0.000 claims 1
- 201000008827 tuberculosis Diseases 0.000 claims 1
- 230000002792 vascular Effects 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US67356105P | 2005-04-21 | 2005-04-21 | |
| US70596705P | 2005-08-05 | 2005-08-05 | |
| PCT/US2006/015548 WO2006116353A2 (en) | 2005-04-21 | 2006-04-21 | N-acetylcysteine amide (nac amide) for the treatment of diseases and conditions associated with oxidative stress |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008538586A JP2008538586A (ja) | 2008-10-30 |
| JP2008538586A5 true JP2008538586A5 (enExample) | 2009-07-09 |
Family
ID=37215387
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008507992A Pending JP2008538586A (ja) | 2005-04-21 | 2006-04-21 | 酸化ストレスに関連する疾患および病気の処置のためのn−アセチルシステインアミド(nacアミド) |
Country Status (9)
| Country | Link |
|---|---|
| US (3) | US20090234011A1 (enExample) |
| EP (1) | EP1877044A4 (enExample) |
| JP (1) | JP2008538586A (enExample) |
| KR (1) | KR20080028357A (enExample) |
| AU (1) | AU2006238888A1 (enExample) |
| CA (1) | CA2606053A1 (enExample) |
| IL (1) | IL186684A0 (enExample) |
| RU (1) | RU2007143040A (enExample) |
| WO (1) | WO2006116353A2 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12458608B2 (en) | 2019-01-11 | 2025-11-04 | Nacuity Pharmaceuticals, Inc. | N-Acetylcysteine Amide (NACA) and (2R,2R′)-3,3′ disulfanediyl BIS(2-acetamidopropanamide) (DINACA) for the prevention and treatment of radiation dermatitis and skin lightening, skin whitening and skin improvement |
Families Citing this family (61)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE552260T1 (de) | 1999-01-25 | 2012-04-15 | Nat Jewish Health | Substituierte porphyrine und deren therapeutische verwendung |
| US8993627B2 (en) | 2005-04-21 | 2015-03-31 | Sentient Lifesciences, Inc. | N-acetylcysteine amide (NAC amide) for the treatment of diseases and conditions associated with oxidative stress |
| KR20080028357A (ko) | 2005-04-21 | 2008-03-31 | 글렌 에이. 골드스타인 | 산화성 스트레스에 관련된 질병 및 증상 치료용n-아세틸시스테인 아미드(nac 아미드) |
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| WO2013138744A1 (en) * | 2012-03-16 | 2013-09-19 | M. Alphabet 1, Llc | Compositions for the treatment of skin disorders |
| WO2013152076A1 (en) * | 2012-04-04 | 2013-10-10 | The Brigham And Women's Hospital, Inc. | Compositions and methods for treating hypertension |
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| US20170049727A1 (en) * | 2014-02-12 | 2017-02-23 | Glenn A. Goldstein | Use of N-Acetylcysteine Amide in the Treatment of Acquired Immune Deficiency Syndrome and HIV Infection |
| WO2016044314A1 (en) * | 2014-09-15 | 2016-03-24 | Sound Pharmaceuticals Incorporated | Methods and compositions for treating psychotic disorders |
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| US11268964B2 (en) | 2014-11-11 | 2022-03-08 | The Johns Hopkins University | Biomarkers useful in the treatment of subjects having diseases of the eye |
| EP3250196A4 (en) | 2015-01-27 | 2018-09-26 | Florengale, LLC | Healing topical composition |
| WO2016197089A1 (en) * | 2015-06-05 | 2016-12-08 | Goldstein Glenn A | Use of n-acetylcysteine amide in the treatment of acetaminophen overdose |
| WO2017122120A1 (en) | 2016-01-11 | 2017-07-20 | Pledpharma Ab | Methods and formulations for treatment of and/or protection against acute liver failure and other hepatotoxic conditions |
| EP3448378B1 (en) * | 2016-04-29 | 2024-04-17 | Ophirex, Inc. | Pla2 and hmg-coa inhibitors for treatment of pathological conditions causing hemolysis, cerebral edema, and acute kidney injury |
| US11548851B2 (en) | 2017-09-20 | 2023-01-10 | Nacuity Pharmaceuticals, Inc. | Method for preparation of n-acetyl cysteine amide and derivatives thereof |
| CN111386255B (zh) | 2017-09-20 | 2021-11-23 | 纳崔泰制药有限公司 | 用于制备n-乙酰基半胱氨酸酰胺及其衍生物的方法 |
| US20240368072A1 (en) * | 2017-09-20 | 2024-11-07 | Nacuity Pharmaceuticals, Inc. | Method for preparation of n-acetyl cysteine amide or di- n-acetyl cysteine amide and derivatives |
| US20240342118A1 (en) * | 2017-09-20 | 2024-10-17 | Nacuity Pharmaceuticals, Inc. | Method for preparation of n-acetyl cysteine amide or di- n-acetyl cysteine amide and derivatives |
| US11091433B2 (en) | 2017-09-20 | 2021-08-17 | Nacuity Pharmaceutials, Inc. | Method for preparation of N-acetyl cysteine amide and derivatives thereof |
| US20240217927A1 (en) * | 2017-11-09 | 2024-07-04 | Nacuity Pharmaceuticals, Inc. | Methods of Making Deuterium-Enriched N-Acetylcysteine Amide (D-NACA) and (2R,2R)-3,3-Disulfanediyl BIS(2-Acetamidopropanamide) (DINACA) and Using D-NACA and DINACA to Treat Diseases Involving Oxidative Stress |
| US20190135741A1 (en) * | 2017-11-09 | 2019-05-09 | Nacuity Pharmaceuticals, Inc. | Methods of Making Deuterium-Enriched N-acetylcysteine Amide (D-NACA) and (2R, 2R')-3,3'-Disulfanediyl BIS(2-Acetamidopropanamide) (DINACA) and Using D-NACA and DINACA to Treat Diseases Involving Oxidative Stress |
| US20190151271A1 (en) * | 2017-11-21 | 2019-05-23 | The Johns Hopkins University | Compositions and methods for treatment of eye diseases |
| KR102145929B1 (ko) * | 2017-11-28 | 2020-08-20 | 주식회사 셀투인 | 실시간 글루타치온 측정을 통한 치료용 세포의 품질 측정 방법 |
| CU20200106A7 (es) | 2018-06-20 | 2021-08-06 | Axcella Health Inc | Composiciones y métodos para el tratamiento de hemoglobinopatías y talasemias |
| US11497758B2 (en) | 2018-11-15 | 2022-11-15 | Samuel L. Shepherd | Method of treating oxidative stress due to radiation exposure |
| US11766413B2 (en) | 2019-01-11 | 2023-09-26 | Nacuity Pharmaceuticals, Inc. | Treatment of age-related macular degeneration, glaucoma, and diabetic retinopathy with n-acetylcysteine amide (NACA) or (2R,2R′)-3,3′-disulfanediyl BIS(2-acetamidopropanamide)(DiNACA) |
| US12245998B2 (en) * | 2019-01-11 | 2025-03-11 | Nacuity Pharmaceuticals, Inc. | N-acetylcysteine amide (NACA) and (2R,2R′)-3,3′ disulfanediyl bis(2-acetamidopropanamide) (diNACA) for the prevention and treatment of radiation pneumonitis and treatment of pulmonary function in Cystic Fibrosis |
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| US5733535A (en) * | 1995-10-25 | 1998-03-31 | The Procter & Gamble Co. | Topical compositions containing N-acetylcysteine and odor masking materials |
| US5962421A (en) * | 1996-05-16 | 1999-10-05 | Zambon, S.A. | Pharmacological association between N-acetylcysteine and levulose for preventing cellular death and related diseases |
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-
2006
- 2006-04-21 KR KR1020077027031A patent/KR20080028357A/ko not_active Withdrawn
- 2006-04-21 US US11/912,293 patent/US20090234011A1/en not_active Abandoned
- 2006-04-21 RU RU2007143040/15A patent/RU2007143040A/ru unknown
- 2006-04-21 CA CA002606053A patent/CA2606053A1/en not_active Abandoned
- 2006-04-21 EP EP06751310A patent/EP1877044A4/en not_active Withdrawn
- 2006-04-21 JP JP2008507992A patent/JP2008538586A/ja active Pending
- 2006-04-21 AU AU2006238888A patent/AU2006238888A1/en not_active Abandoned
- 2006-04-21 WO PCT/US2006/015548 patent/WO2006116353A2/en not_active Ceased
-
2007
- 2007-10-16 IL IL186684A patent/IL186684A0/en unknown
-
2010
- 2010-01-12 US US12/686,106 patent/US8354449B2/en not_active Expired - Fee Related
- 2010-02-17 US US12/707,092 patent/US8937099B2/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12458608B2 (en) | 2019-01-11 | 2025-11-04 | Nacuity Pharmaceuticals, Inc. | N-Acetylcysteine Amide (NACA) and (2R,2R′)-3,3′ disulfanediyl BIS(2-acetamidopropanamide) (DINACA) for the prevention and treatment of radiation dermatitis and skin lightening, skin whitening and skin improvement |
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