CAS: 830-96-6; 3-Indolepropionic Acid

该化合物是一种生物活性化合物,具有强效抗氧化特性,可凝固自由基以缓解氧化性压力和细胞损伤. 其生物利用率能够有效吸收,使其成为合成药物和诊断剂的宝贵中间体,并有可能用于...

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号120-72-9 吲哚 | CAS号79-10-7 丙烯酸 | CAS号10184-98-2 diethyl 2-(1H-i... | CAS号4361-05-1 Propanedioic ac... | CAS号31529-28-9 3-(2-羧基乙基)-1H-吲... | CAS号109897-76-9 indobinine | CAS号85612-35-7 benzyl 3-indole... | CAS号10075-50-0 5-溴吲哚 | CAS号5457-31-8 1H-indol-3-ylme... | CAS号1050443-69-0 (2R)-3-{[[(叔丁氧基... | CAS号3569-21-9 3-吲哚丙醇 | CAS号141071-79-6 3-(1-Benzyl-1H-... | CAS号20401-90-5 3-(1H-吲哚-3-基)-丙酸 肼 | CAS号219544-69-1 3-[1-[(4-fluoro... | CAS号2387-23-7 N,N’-二环己基脲 | CAS号60586-98-3 1-{[3-(1H-Indol... | CAS号3456-99-3 2,3,4,9-四氢-1H-咔唑-1-酮 | CAS号6245-89-2 3-(1H-吲哚-3-基)丙-1-胺 | CAS号5814-93-7 吲哚-3-丙酰胺

合成工艺路线路线简述

  • 85612-35-7 = 830-96-6
    反应条件:1.1 Reagents: Sodium Hydroxide
    标题:Indobine - A New Alkaloid From Rauwolfia Serpentina Benth
    作者:Siddiqui,Salimuzzaman; Et Al
    参考文献:Zeitschrift Fuer Naturforschung 日期:1987 卷标:42(6) 页码:783-4]

    40641-03-0 = 830-96-6
    反应条件:1.1 Solvents: Water; 24 H,30 °C
    标题:Biocatalytic Hydrolysis Of Various Esters Using Baker'S Yeast Under Neutral Conditions Without Sucrose
    作者:Noguchi,Takuya; Et Al
    参考文献:Tetrahedron Letters 日期:2022 卷标:104]

    72651-98-0 = 830-96-6
    反应条件:1.1 Reagents: Water Solvents: Water
    标题:Two Efficient Syntheses Of Indole-3-Propionic Esters And Acids. Further Applications Of Meldrum'S Acid
    作者:Farlow,Diane S.; Et Al
    参考文献:Organic Preparations And Procedures International 日期:1981 卷标:13(1) 页码:39-48]

    120-72-9 = 830-96-6
    反应条件:1.1 Solvents: Water
    标题:Mechanisms Of Hydrolysis Of Several Atom-Bridged Bicyclic Anhydrides,N-Methylimides,And Lactones
    作者:Hall,H. K. Jr.
    参考文献:Journal Of Organic Chemistry 日期:1963 卷标:28(8) 页码:2027-9]

    29953-71-7 = 830-96-6
    反应条件:1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Ethyl Acetate; 12 H,Rt
    标题:Improved Synthesis Of Natural Ester Sintenin And Its Analogues Via Wittig Reaction
    作者:Sharma,Mukul; Et Al
    参考文献:Journal Of The Indian Chemical Society 日期:2013 卷标:90(10) 页码:1853-1860]

    109897-76-9 = 830-96-6
    反应条件:1.1 Reagents: Sodium Hydroxide
    标题:Isolation Of Indobinine,A New Alkaloid From Roots Of Rauwolfia Serpentina Benth
    作者:Siddiqui,Salimuzzaman; Et Al
    参考文献:Indian Journal Of Chemistry 日期:1987 卷标:(3) 页码:279-80]

    40641-03-0 = 830-96-6
    反应条件:1.1 Reagents: Sodium Hydroxide; 1 H,Reflux
    标题:Beckmann Rearrangement For The Synthesis Of Derivatives Of β- And γ-Carbolinones,Dihydropyrrolopyridinone And Tetrahydroisoquinolinone
    作者:Naik,Prajakta N.; Et Al
    参考文献:Arkivoc (Gainesville 日期:2015 卷标:(7) 页码:362-376]

    72651-98-0 = 830-96-6
    反应条件:1.1 Reagents: Water Solvents: Pyridine; 16 H,Reflux1.2 Reagents: Hydrochloric Acid Solvents: Water; Acidified
    标题:Ethylenation Of Aldehydes To 3-Propanal,Propanol And Propanoic Acid Derivatives
    作者:Payne,Daniel T.; Et Al
    参考文献:Scientific Reports 日期:2017 卷标:7(1) 页码:1-8]

    120-72-9 + 4743-82-2 = 830-96-6
    反应条件:1.1 Catalysts: Acetic Acid,Tetraanhydride With Boric Acid (H4B2O5) Solvents: Acetonitrile; 1 Min,Rt
    标题:B-O-B Catalyzed Cycloadditions Of Acrylic Acids
    作者:Zhang,Peng; Et Al
    参考文献:Acs Sustainable Chemistry & Engineering 日期:2016 卷标:4(12) 页码:6991-6995]

    31529-28-9 = 830-96-6 [标题:Reaction Conditions
    标题:Syntheses Starting From 2-Cyanocyclopentanone. Application Of Arylhydrazones Of 5-Cyano-5-Oxopentanoic Acid To The Preparation Of Indole Derivatives
    作者:Thi Anh Nga Trinh; Et Al
    参考文献:Bulletin De La Societe Chimique De France 日期:1987 卷标:(2) 页码:361-4]

    120-72-9 = 830-96-6
    反应条件:1.1 Reagents: Acetic Anhydride; Rt -> 95 °C; 3.5 H,90 - 95 °C; 95 °C -> Rt1.2 Reagents: Sodium Hydroxide Solvents: Water; Rt; Rt -> 85 °C; 2.5 H,75 - 80 °C; 80 °C -> Rt1.3 Reagents: Hydrochloric Acid Solvents: Water; Rt
    标题:An Improved Synthesis Of 2-Methoxyrutaecarpine
    作者:Wang,Xue-Cheng; Et Al
    参考文献:Zhejiang Huagong 日期:2013 卷标:44(9) 页码:16-17]

    120-72-9 = 830-96-6
    反应条件:1.1 Reagents: Hydrochloric Acid
    标题:3-Indolepropionic Acids
    参考文献:United States]

    160320-11-6 = 830-96-6
    反应条件:1.1 Reagents: Lithium Diisopropylamide Solvents: Tetrahydrofuran; 0 °C; 2 H,40 - 45 °C; Cooled1.2 Reagents: Ammonium Chloride Solvents: Water; Rt
    标题:A Systematic Study Of Two Complementary Protocols Allowing The General,Mild And Efficient Deprotection Of N-Pivaloylindoles
    作者:Ruiz,Miriam; Et Al
    参考文献:Tetrahedron 日期:2012 卷标:68(2) 页码:705-710]

    160320-11-6 = 830-96-6
    反应条件:1.1 Reagents: Lithium Diisopropylamide Solvents: Tetrahydrofuran,Hexane; -78 °C; 2 H,40 - 45 °C; 45 °C -> Rt1.2 Reagents: Ammonium Chloride Solvents: Water; Rt
    标题:An Efficient Procedure For The Deprotection Of N-Pivaloylindoles,Carbazoles And β-Carbolines With Lda
    作者:Avendano,Carmen; Et Al
    参考文献:Synlett 日期:2005 卷标:(1) 页码:107-110]

    160320-11-6 = 830-96-6
    反应条件:1.1 Reagents: Lithium Diisopropylamide Solvents: Tetrahydrofuran; 2 H,40 - 45 °C1.2 Reagents: Water
    标题:Deprotection Of N-Pivaloylindoles,Carbazoles And Beta-Carbolines With A Lithium Base
    作者:Sanchez,J. Domingo; Et Al
    参考文献:International Electronic Conferences On Synthetic Organic Chemistry 日期:2004 卷标:1 页码:1-5]

    6639-06-1 = 830-96-6
    反应条件:1.1 Reagents: Maleic Anhydride,Potassium Hydride
    标题:3-Indolealkanoic Acids
    参考文献:United States]

    52816-02-1 = 830-96-6
    反应条件:1.1 Reagents: Potassium Hydroxide,Hydrazine Hydrate (1:1) Solvents: Ethanol; < 20 °C; 4 H,Reflux
    标题:Synthesis And Antitumor Properties Of Bis-Indole Derivatives
    作者:Song,Binbin; Et Al
    参考文献:Journal Of Chemical And Pharmaceutical Research 日期:2014 卷标:6(10) 页码:239-243
二乙基2-(1H-吲哚-3-基甲基)丙二酸酯置于氢氧化钾体系中,化学反应生成 3-吲哚丙酸
参考文献:Notes: Convenient Syntheses Of 3-Indolesuccinic And 3-Indolepropionic Acids
标题:Notes: Convenient Syntheses Of 3-Indolesuccinic And 3-Indolepropionic Acids
摘要:
DOI:10.1021/jo01090A631

海关参考信息

专利信息


专利号:US-2002055171-A1
优先权日:1998-05-27
标题 :Preparation of biologically active 3-methyleneoxindole and definition of its application in stimulation of plant growth and tissue repair
发明人:TULI VIRENDA KUMAR
摘要:Identification of the true nature and metabolic action of 3 -methyleneoxindole (MO), a naturally occurring catabolite of the plant auxin, indole- 3 -acetic acid (IAA). Description of the two novel methods of synthesis of MO which produce the pure, biologically active auxin compound of MO. Discovery and description of the causes for the erroneous classification of MO as an inert compound with no auxin activity. These findings and methods of synthesis correct the ubiquitous theoretical errors which have driven scientific investigation and plant science research of plant auxins for nearly forty years. n Researchers have failed to observe the auxin activity of MO because of the use of standard but incorrect synthetic techniques which have consistently produced impure forms of 3 -bromooxindole- 3 -acetic acid ( 3 -Brox), the synthetic precursor of MO. In addition, the use of dimethylsulfooxide as a solvent for MO has been identified as a major source of contamination of MO during synthesis. n This invention describes two novel methods for synthesizing (MO). By using purified MO and avoiding the use of dimethylsulfoxide, it was found that the resulting MO product to be 100 to 1,00 fold more effective than IAA in promoting rooting in plant cuttings; supporting tissue differentiation and growth in stage I, stage II and stage III media used for the micropropagation of explants; promoting the formation of callus tissue over wounded plant parts; and, stimulating the production of interstitial tissue between scion and rootstock to increase the success rate for grafting. Therefore, this invention identifies MO as the dominant auxin in shoot acceleration, root development, wound sealing and scion acceptance. n Finally, the correct pathway from IAA to MO is presented.

专利号:US-9574189-B2
优先权日:2005-12-01
标题:Enzymatic encoding methods for efficient synthesis of large libraries
发明人:FRANCH THOMAS; LUNDORF MIKKEL DYBRO; JACOBSEN SØREN NYBOE; OLSEN EVA KAMPMANN; ANDERSEN ANNE LEE; HOLTMANN ANETTE; HANSEN ANDERS HOLM; SØRENSEN ANDERS MALLING; GOLDBECH ANNE; DE LEON DAEN; KALDOR DITTE KIEVSMOSE; SLØK FRANK ABILDGAARD; HUSEMOEN GITTE NYSTRUP; DOLBERG JOHANNES; Jensen Kim Birkebæ; PEDERSEN LENE; NØRREGAARD-MADSEN MADS; GODSKESEN MICHAEL ANDERS; GLAD SANNE SCHRØDER; NEVE SØREN; THISTED THOMAS; KRONBORG TINE TITILOLA AKINLEMINU; SAMS CHRISTIAN KLARNER; FELDING JAKOB; FRESKGÃ…RD PER-OLA; GOULIAEV ALEX HAAHR; PEDERSEN HENRIK
权利人:FRANCH THOMAS; LUNDORF MIKKEL DYBRO; JACOBSEN SØREN NYBOE; OLSEN EVA KAMPMANN; ANDERSEN ANNE LEE; HOLTMANN ANETTE; HANSEN ANDERS HOLM; SØRENSEN ANDERS MALLING; GOLDBECH ANNE; DE LEON DAEN; KALDOR DITTE KIEVSMOSE; SLØK FRANK ABILDGAARD; HUSEMOEN GITTE NYSTRUP; DOLBERG JOHANNES; Jensen Kim Birkebæ; PEDERSEN LENE; NØRREGAARD-MADSEN MADS; GODSKESEN MICHAEL ANDERS; GLAD SANNE SCHRØDER; NEVE SØREN; THISTED THOMAS; KRONBORG TINE TITILOLA AKINLEMINU; SAMS CHRISTIAN KLARNER; FELDING JAKOB; FRESKGÃ…RD PER-OLA; GOULIAEV ALEX HAAHR; PEDERSEN HENRIK; NUEVOLUTION AS
摘要:Disclosed is a method for obtaining a bifunctional complex comprising a molecule linked to a single stranded identifier oligonucleotide, wherein a nascent bifunctional complex comprising a chemical reaction site and a priming site for enzymatic addition of a tag is a) reacted at the chemical reaction site with one or more reactants, and b) reacted enzymatically at the priming site with one or more tag(s) identifying the reactant(s).

专利号:EP-0609638-A1
优先权日:1992-10-27
标 题:Water soluble polymeric systems of phytohormones with slow release: synthesis and application
发明人:TSATSAKIS ARISTIDIS; VLACHAKIS ELEUTERIOS IOANIS; SHTILMAN ISAAK MICHAIL; SHASHKOVA MICHAIL IRINA; ALLAKHVERDIEV SURKHAI RAGIM IN
权利人:TSATSAKIS ARISTIDIS; VLACHAKIS ELEUTERIOS IOANIS; SHTILMAN ISAAK MICHAIL; SHASHKOVA MICHAIL IRINA; ALLAKHVERDIEV SURKHAI RAGIM IN
摘要:Our discovery concerns the method of synthesis and the application of new chemical products for plant growing. These new products are polymeric derivatives of low molecular weight plant growth regulators and are characterized by slow release of the auxin from the polymeric carrier. By copolymerisation of allylic esters of the low molecular weight auxins with the acrylic (or the methylacrylic) acid and the following modification of the synthesized co-polymers of acids to their corresponding ammonium salts, water soluble polymeric auxins possesing optimal molecular weight and desirable (high) content of the low molecular weight auxin in the polymer were prepared. The method of synthesis and the final products fulfill the requirements of the preparation technology and of their application respectively. We suggest the application of the new products in agronomy (i.e. treatment of seeds, rootstocks, plants, scions, cutting etc) either by themselves or by combination of them with other chemicals. The chemical structure of the new products we discover is :n n    R = H-, -CH3, Au = auxin residue

专利号:US-11078526-B2
优先权日:2016-02-11
标 题:Polyphenolic additives in sequencing by synthesis
发明人:OLEJNIK JERZY; Perbost Michel Georges
权利人:ISOPLEXIS CORP
摘要:The invention relates to methods, compositions, devices, systems and kits as described including, without limitation, reagents and mixtures for determining the identity of nucleic acids in nucleotide sequences using, for example, sequencing by synthesis methods. In particular, the present invention contemplates the use of polyphenolic compounds, known as antioxidant additives, to improve the efficiency of Sequencing-By-Synthesis reactions. For example, gallic acid (GA) is shown herein to be one of many exemplary SBS polyphenolic additives.

专利号:US-7390801-B2
优先权日:1996-12-23
标题:Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
发明人:THORSETT EUGENE D; PLEISS MICHAEL A; LATIMER LEE H; JOHN VARGHESE; FREEDMAN STEPHEN; BRITTON THOMAS C; AUDIA JAMES A; REEL JON K; DRESSMAN BRUCE A; DROSTE JAMES J; HENRY STEVEN S; STUCKY RUSSELL D; PORTER WARREN J
权利人:ATHENA NEUROSCIENCES INC; LILLY CO ELI
摘要:Disclosed are compounds which inhibit β-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions comprising a compound which inhibits β-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.

专利号:US-10036011-B2
优先权日:2016-02-11
标 题:Scavenger compounds for improved sequencing-by-synthesis
发明人:ANDRUZZI LUISA
权利人:QIAGEN WALTHAM INC
摘要:The present invention discloses methods of applications of indole-3-propionic acid, L-carnitine and O-acetyl-L-carnitine in one or more different reactive steps of a sequencing-by-synthesis workflow. The reactive steps employing these compounds include, but are not limited to, cleaving, imaging, incorporating bases and washing. The use of these new compounds provides improved sequencing performance including, but not limited to, lower error rates, higher sequence outputs and/or longer read lengths.
天津市光复精细化工研究所
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.guangfu-chem.com
企业联系电话:022-85689619/85689620👤
📞天津市光复精细化工研究所 ⚠️参考联系方式
联系人:光复
电话:022-85689619/85689620

传真:022-85689497
邮箱:tjguangfu@126.com
通信地址: 天津市西青区海泰(环外)大厦F座7-601
邮编: 300000
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:天津市西青区海泰(环外)大厦F座7-601
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
山东西亚化学有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.xiyashiji.com
企业联系电话:400-990-3999👤
📞山东西亚化学有限公司 ⚠️参考联系方式
联系人:徐雪
电话:400-990-3999
手机:13395398332
传真:0539-6365991
邮箱:3007715518@qq.com
通信地址: 临沭经济开发区化工园区(厂址)
邮编: 276000
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:临沭经济开发区化工园区(厂址)
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
安徽省金奥化工有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.ahjachem.com
企业联系电话:0551-63450295;13505511751👤
📞安徽省金奥化工有限公司 ⚠️参考联系方式
联系人:胡刚斌
电话:0551-63450295;13505511751
手机:13505511751
传真:0551-63450295
邮箱:jinao@ahjachem.com
通信地址: 安徽合肥市包河区马鞍山南路760号
邮编: 230001
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:安徽合肥市包河区马鞍山南路760号
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
浙江凯利实业有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.zjklsy.com
电话: 0086 (571) 8524-1926, +86 18758150316👤
📞浙江凯利实业有限公司 ⚠️参考联系方式

销售电话:0086 (571) 8524-1926, +86 18758150316
邮箱:sales@zjklsy.com
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:杭州市拱墅区莫干山路18号蓝天商务中心12层CD座
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别 ✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
上海珅桔化工有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.shsjchem.com
企业联系电话:15921014380,13167128868👤
📞上海珅桔化工有限公司 ⚠️参考联系方式
联系人:蒋经理
电话:15921014380,13167128868
手机:15062602202
传真:13167128868
邮箱:173446357@qq.com
通信地址: 上海市宝山区高逸路112-118号
邮编: 200439
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:上海市宝山区高逸路112-118号
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
上海邦成化工有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.bangchengchem.com
企业联系电话:021-69106990;69106980;13701823733👤
📞上海邦成化工有限公司 ⚠️参考联系方式
联系人:卢小姐
电话:021-69106990;69106980;13701823733
手机:13701823733
传真:QQ:89190072
邮箱:13701823733@163.com
通信地址: 上海市青浦区重固镇赵重公路2278号5号楼3层C57座
邮编: 201803
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:上海市青浦区重固镇赵重公路2278号5号楼3层C57座
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
江西金若实业有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.kingnordchem.com
电话: 0791-86493591👤
📞江西金若实业有限公司 ⚠️参考联系方式

销售电话:0791-86493591
邮箱:sales@kingnord.com
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别 ✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
潍坊市鸣冉化工有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.mingranchem.cn
企业联系电话:0536-2082396;15063661899👤
📞潍坊市鸣冉化工有限公司 ⚠️参考联系方式
联系人:张凡
电话:0536-2082396;15063661899
手机:15063661899
传真:0536-8116865
邮箱:mingranchem@163.com
通信地址: 山东省潍坊市高新技术产业开发区
邮编: 261061
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:山东省潍坊市高新技术产业开发区
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
常州金坛茂盛精细化工厂
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.maoshengchem.com
企业联系电话:0519-82726533👤
📞常州金坛茂盛精细化工厂 ⚠️参考联系方式
联系人:张亮
电话:0519-82726533
手机:13382827140(张亮);13328182214(王兆清)
传真:0519-82726880
邮箱:maoshengchem@126.com
通信地址: 江苏省常州市金坛区洮西工业园
邮编: 213200
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:江苏省常州市金坛区洮西工业园
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
第 1 / 1 页
现货

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献


1: Köse M, Ritter K, Thiemke K, Gillard M, Kostenis E, Müller CE. Development of [(3)H]2-Carboxy-4,6-dichloro-1H-indole-3-propionic Acid ([(3)H]PSB-12150): A Useful Tool for Studying GPR17. ACS Med Chem Lett. 2014 Jan 16;5(4):326-30. doi: 10.1021/ml400399f.
2: Hwang IK, Yoo KY, Li H, Park OK, Lee CH, Choi JH, Jeong YG, Lee YL, Kim YM, Kwon YG, Won MH. Indole-3-propionic acid attenuates neuronal damage and oxidative stress in the ischemic hippocampus. J Neurosci Res. 2009 Jul;87(9):2126-37. doi: 10.1002/jnr.22030. doi: 10.1016/j.phytochem.2015.05.023. Review. doi: 10.1016/j.plaphy.2013.08.003. doi: 10.1038/srep29367.
12: Bosco R, Caser M, Vanara F, Scariot V. Development of a rapid LC-DAD/FLD method for the simultaneous determination of auxins and abscisic acid in plant extracts. J Agric Food Chem. 2013 Nov 20;61(46):10940-7. doi: 10.1021/jf4034305. doi: 10.1016/j.bbamem.2010.07.032.

合成参考文献


摘要:Kelly, C. B.; Matsui, J. K.; Phelan, J. P.; Gutiérrez Bonet, Á.; Lang, S. B.; Molander, G. A., Science of Synthesis: Photocatalysis in Organic Synthesis, (2018) 1, 348.
摘要:Proceedings of the Society for Experimental Biology and Medicine., 34(138), 1936
摘要:HANSCH,C ET AL. (1995)
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知