1013405-49-6 = 931-03-3 反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Acetonitrile,Water; 24 H,Rt 标题:A New Synthetic Route To 3-Polyfluoroalkyl-Containing Pyrroles 作者:Shaitanova,Elena N.; Gerus,Igor I.; Kukhar,Valery P. 参考文献:Tetrahedron Letters 日期:2008 卷标:49(7) 页码:1184-1187]
931-03-3 = 931-03-3 反应条件:1.1 Reagents: Cupric Chloride; 3 H,Rt 标题:Coordinated Molecularly Imprinted-Based Ratiometric Sensor For Electrochemical Sensing Of Hazardous Ciprofloxacin Based On Nitrogen And Sulfur Co-Doped Porous Carbon/silver Nanoparticles Hybrid 作者:Mahmoud,Ashraf M.; Abu-Alrub,Samer S.; Al-Qarni,Ali O.; Alshareef,F. M.; El-Wekil,Mohamed M. 参考文献:Microchemical Journal 日期:2023 卷标:193]
93362-49-3 = 931-03-3 [标题:Reaction Conditions 标题:Product Subclass 14: Aryllithium And Hetaryllithium Compounds 作者:Gribble,Gordon W. 参考文献:Science Of Synthesis 日期:2006 卷标:8 页码:357-426]
87630-35-1 = 931-03-3 [标题:Reaction Conditions 标题:N-(Triisopropylsilyl)Pyrrole. A Progenitor "Par Excellence" Of 3-Substituted Pyrroles 作者:Bray,Brian L.; Mathies,Peter H.; Naef,Reto; Solas,Dennis R.; Tidwell,Thomas T.; Et Al 参考文献:Journal Of Organic Chemistry 日期:1990 卷标:55(26) 页码:6317-28]
= 931-03-3 [标题:Reaction Conditions 标题:Screening Of A Custom-Designed Acid Fragment Library Identifies 1-Phenylpyrroles And 1-Phenylpyrrolidines As Inhibitors Of Notum Carboxylesterase Activity 作者:Mahy,William; Patel,Mikesh; Steadman,David; Woodward,Hannah L.; Atkinson,Benjamin N.; Et Al 参考文献:Journal Of Medicinal Chemistry 日期:2020 卷标:63(17) 页码:9464-9483]
= 931-03-3 [标题:Reaction Conditions 标题:Functionalization Of 2-Trifluoromethyl-1H-Pyrrole: A Convenient Entry Into Advanced Fluorinated Building Blocks Including All Isomeric 2-(Trifluoromethyl)Prolines 作者:Hys,Vasyl Yu.; Shevchuk,Oleksandr I.; Vashchenko,Bohdan V.; Karpenko,Oleksandr V.; Gorlova,Alina O.; Et Al 参考文献:European Journal Of Organic Chemistry 日期:2020 卷标:2020(25) 页码:3896-3905]
= 931-03-3 [标题:Reaction Conditions 标题:Structure Of Batrachotoxin,A Steroidal Alkaloid From The Colombian Arrow Poison Frog,Phyllobates Aurotaenia,And Partial Synthesis Of Batrachotoxin And Its Analogs And Homologs 作者:Tokuyama,Takashi; Daly,J. 参考文献:Journal Of The American Chemical Society 日期:1969 卷标:91(14) 页码:3931-8]
106058-86-0 = 931-03-3 反应条件:1.1 Reagents: Sodium Hydroxide Solvents: Water 标题:A Facile And Efficient Synthesis Of Pyrrole-3-Carboxylic Acid From Pyrrole 作者:Cativiela,Carlos; Garcia,Jose I. 参考文献:Organic Preparations And Procedures International 日期:1986 卷标:18(4) 页码:283-5]
85684-93-1 = 931-03-3 [标题:Reaction Conditions 标题:Product Class 13: 1H-Pyrroles 作者:Black,D. Stc. 参考文献:Science Of Synthesis 日期:2002 卷标:9 页码:441-552]
7126-39-8 = 931-03-3 反应条件:1.1 Reagents: Silver Oxide (Ag2O) 标题:Studies Of The Maillard Reaction. I. Reaction Of Amino Sugars With Malondialdehyde 作者:Gomez-Sanchez,Antonio; Maya,Ines; Hermosin,Isidro 参考文献:Carbohydrate Research 日期:1990 卷标:200 页码:167-80]
85684-93-1 = 931-03-3 反应条件:1.1 Reagents: Ammonia Solvents: Methanol 标题:The Protecting-Directing Role Of The Trityl Group In Syntheses Of Pyrrole Derivatives: Efficient Preparations Of 1H-Pyrrole-3-Carboxylic Acid And 3-Acyl-,3-Amino-,And 3-Bromo-1-Tritylpyrroles 作者:Chadwick,Derek J.; Hodgson,Simon T. 参考文献:Journal Of The Chemical Society 日期:1983 卷标:(1) 页码:93-102]
= 931-03-3 [标题:Reaction Conditions 标题:Preparation Of Novobiocin Analogs Having Modified Glycoside Moieties As Antitumor Agents 参考文献:United States]
= 931-03-3 [标题:Reaction Conditions 标题:3-Lithiopyrroles By Halogen-Metal Interchange Of 3-Bromo-1-(Triisopropylsilyl)Pyrroles. Synthesis Of Verrucarin E And Other 3-Substituted Pyrroles 作者:Muchowski,Joseph M.; Naef,Reto 参考文献:Helvetica Chimica Acta 日期:1984 卷标:67(4) 页码:1168-72]
= 931-03-3 + 634-97-9 反应条件:1.1 Reagents: Chlorodimethylaluminum Solvents: Toluene,Hexane; 3 H,Rt1.2 Reagents: Hydrochloric Acid Solvents: Water; Rt1.3 Reagents: Sodium Carbonate Solvents: Water; Rt1.4 Reagents: Hydrochloric Acid Solvents: Water; Acidified,Rt 标题:Carboxylation Of Indoles And Pyrroles With Co2 In The Presence Of Dialkylaluminum Halides 作者:Nemoto,Koji; Onozawa,Satoru; Egusa,Naoki; Morohashi,Naoya; Hattori,Tetsutaro 参考文献:Tetrahedron Letters 日期:2009 卷标:50(31) 页码:4512-4514
专利号:US-6683189-B1 优先权日:1996-02-26 标 题 :Method for the synthesis of pyrrole and imidazole carboxamides on a solid support 发明人:DERVAN PETER B; BAIRD ELDON 权利人:CALIFORNIA INST OF TECHN 摘要:The present invention describes a novel method for the solid phase synthesis of polyamides containing imidazole and pyrrole carboxamides. The polyamides are prepared on a solid support from aromatic carboxylic acids and aromatic amines with high stepwise coupling yields (>99%), providing milligram quantities of highly pure polyamides. The present invention also describes the synthesis of analogs of the natural products Netropsin and Distamycin A, two antiviral antibiotics. The present invention also describes a novel method for the solid phase synthesis of imidazole and pyrrole carboxamide polyamide-oligonucleotide conjugates. This methodology will greatly increase both the complexity and quantity of minor-groove binding polyamides and minor-groove binding polyamide-oligonucleotide conjugates which can be synthesized and tested.
专利号:WO-2024185775-A1 优先权日:2023-03-06 标 题:Long-chain alkenyloxy–substituted benzoyl derivative and oligonucleotide synthesis method using same 发明人:OKADA YOHEI; INANAGA KAZATO; SHOJI Yukiya; MIZUFUNE HIDEYA; SUDO TATSUYA; ADACHI Sota; HOSOI Kazushi 权利人:SPERA PHARMA INC; TOKYO UNIV OF AGRICULTURE AND TECHNOLOGY 摘要:The purpose of the present invention is to provide a novel pseudo–solid phase protecting group that can be used in liquid-phase oligonucleotide synthesis. The purpose of the present invention is also to provide an oligonucleotide synthesis method that uses a novel pseudo–solid phase protecting group. The present invention provides a compound represented by formula (1) (in which R represents a C14–60 alkenyl group, n represents 2 or 3, m represents 0 or 1, p represents 1 or 2, X represents C, N, O, or S, Y represents a single bond or B(CH 2 ) t * or may form a ring with X, and Z represents a single bond or (CH 2 ) s (s being an integer from 1 to 5)). The present invention also provides an oligonucleotide production method that uses the compound.
专利号:US-2005119332-A1 优先权日:1998-03-12 标 题 :Substituted thiophene compounds as modulators of protein tyrosine phosphatases (PTPases) 发明人:JEPPESEN LONE; ANDERSEN HENRIK S; OLSEN OLE H; JUDGE LUKE M; HOLSWORTH DANIEL D; BAKIR FARID; AXE FRANK U; GE YU 摘要:The present invention provides novel compounds of formula 1a, n nnovel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTPα, LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.
专利号:WO-9946244-A1 优先权日:1998-03-12 标题 :Modulators of protein tyrosine phosphatases (ptpases) 发明人:JEPPESEN LONE; ANDERSEN HENRIK SUNE; OLSEN OLE HVILSTED; JUDGE LUKE MILBURN; HOLSWORTH DANIEL DALE; BAKIR FARID; AXE FRANK URBAN; GE YU 权利人:NOVO NORDISK AS; ONTOGEN CORP 摘要:The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTPα, LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.
专利号:US-2002019412-A1 优先权日:1998-03-12 标题:Modulators of protein tyrosine phosphatases (ptpases) 发明人:ANDERSEN HENRIK SUNE; JONES TODD KEVIN; HOLSWORTH DANIEL DALE 摘要:The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTPα, LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.
专利号:US-7951905-B2 优先权日:2006-09-18 标 题 :Synthesis of carbohydrate-templated amino acids and methods of using same 发明人:SCHWEIZER FRANK; ZHANG KAIDONG; OWENS NEIL; ZHANEL GEORGE 权利人:UNIV MANITOBA 摘要:The present invention generally relates to tetrahydropyranyl-derivatized amino acids, their syntheses and their incorporation into peptides and peptidomimetics. The tetrahydropyran moiety constrains the side chain of an amino acid, thereby providing a molecule that may act as a sugar- or amino acid-mimetic as well as a scaffold for combinatorial synthesis.
摘要:M. Scrocco and R. Nicolaus, Atti accad. naz. Lincei, Rend. Classe sci. fis. mat. e nat. 22, 311 (1957); CA 52, 50i. 摘要:H. Rapoport and C. D. Willson, J. Org. Chem. 26, 1102 (1961). 摘要:M. M. T. Khan and A. E. Martell, J. Am. Chem. Soc. 91, 4668 (1969). 参考文献:10.1021/acs.jmedchem.0c00660 摘要:Mahy W, Patel M, Steadman D, Woodward HL, Atkinson BN, Svensson F, Willis NJ, Flint A, Papatheodorou D, Zhao Y, Vecchia L, Ruza RR, Hillier J, Frew S, Monaghan A, Costa A, Bictash M, Walter MW, Jones EY, Fish PV. Screening of a Custom-Designed Acid Fragment Library Identifies 1-Phenylpyrroles and 1-Phenylpyrrolidines as Inhibitors of Notum Carboxylesterase Activity. J Med Chem. 2020 Sep 10;63(17):9464–83. doi: 10.1021/acs.jmedchem.0c00660.