CAS: 4066-39-1; 2-Amino-3-(Furan-2-yl)Propanoic Acid

该化合物是一种氨酸衍生物,其特征是配有松树结构碳的松果环,该化合物具有松果味,它由五人组成,含有氧气,有助于其独特的化学特性;呋喃环的存在可以影响化合物的抗反应和相互作用,使其对各种生物化学和制药应用感兴趣;作为氨酸,3-furan-2-yaline含有氨基化合物组(-NH2)和氨基酸组(-COOH),允许其参与联结的形成和蛋白质合成;其结构特性还可能带来具体的生物活动,有可能使其成为药物开发研究的候选方,或作为生物化学探测器.

结构式图片

相似化合物

159611-02-6 220497-85-8 110772-46-8

欧盟法规

C&L通报

上下游产品

CAS号4066-14-2 (2Z)-3-(2-furyl... | CAS号121786-31-0 3-(2-呋喃基)-L-丙氨酸 | CAS号4066-17-5 9-(4-methoxyphe... | CAS号98-00-0 糠醇 | CAS号617-88-9 2-氯甲基呋喃 | CAS号4437-18-7 2-溴甲基呋喃 | CAS号110772-46-8 H-β-(2-呋喃基)-D-丙氨酸 | CAS号539-47-9 2-呋喃丙烯酸 | CAS号73495-08-6 (R)-3-Amino-3-(...

合成工艺路线路线简述

  • 合成目标产物 Dl-2-Furylalanine 主要起始原料 Furfuryl Alcohol
  • (文献来源)合成步骤主要原料 Furfuryl Alcohol
📜糠基氯置于lithium Hydroxide,Sodium Hydroxide,Sodium Hydride体系中,用 甲醇,N,N-二甲基甲酰胺,甲苯 作为反应溶剂,化学反应 32.0H,反应生成 2-呋喃丙氨酸
参考文献:杂芳基丙烯酸酯和丙氨酸与欧芹中的苯丙氨酸氨裂解酶的相互作用.
标题:杂芳基丙烯酸酯和丙氨酸与欧芹中的苯丙氨酸氨裂解酶的相互作用.
摘要:合成了在β位置被杂芳基取代的丙烯酸和丙氨酸,并进行了光谱表征(uv,Hrms,(1)h NMR和(13)c NMR光谱).杂芳基基团是呋喃基,噻吩基,苯并呋喃基和苯并噻吩基,并且在2-或3-位含有丙酰基侧链.前者是苯丙氨酸解氨酶(pal)的非常好底物,而后者是抑制剂.例外的是噻吩-3-基丙氨酸(一种中等的底物)和呋喃-3-基丙氨酸(惰性).讨论了这些例外的可能原因.从外消旋杂芳基-2-丙氨酸开始,它们的d-对映异构体通过立体破坏方法制备.由杂芳基-2-丙烯酸酯以高氨浓度制备杂芳基-2-丙氨酸的l-对映异构体.
DOI:10.1002/chem.200501034

海关参考信息

专利信息


专利号:US-9475837-B2
优先权日:2011-12-23
标题 :Process for the synthesis of therapeutic peptides
发明人:HURLEY FIONN; WEGNER KATARZYNA; FOLEY PATRICK
权利人:IPSEN MFG IRELAND LTD
摘要:The present invention relates to a process for the large-scale synthesis of therapeutic peptides using a Sieber Amide resin, which comprises solid-phase Fmoc-chemistry.

专利号:US-2009069334-A1
优先权日:2007-08-18
标题:Pyridazine based alpha-helix mimetics
发明人:REBEK JR JULIUS; BIROS SHANNON; MOISAN LIONEL; VOLONTERIO ALESSANDRO; MANN ENRIQUE; DALE TREVOR
权利人:SCRIPPS RESEARCH INST
摘要:The synthesis of new α-helix scaffolds mimicking i, i+3 or i+4, i+7 residues, was accomplished. The common pyridazine heterocycle originates from the easily available building block, 6. These scaffolds may be thought of as synthetic counterparts of amphiphilic α-helices having a “wet faceâ€? along one side and a hydrophobic face along the other side of the helix.

专利号:US-2010022549-A1
优先权日:2008-07-23
标题 :Alpha-helix mimetic with functionalized pyridazine
发明人:REBEK JR JULIUS; MOISAN LIONEL; CARELLA ALEXANDRE; MANN ENRIQUE
权利人:SCRIPPS RESEARCH INST
摘要:The synthesis of new α-helix scaffolds mimicking i, i+3 or i+4, i+7 residues, was accomplished. The common pyridazine heterocycle originates from the easily available dimethyl pyridazine-3,6-dicarboxylate building block. These scaffolds may be thought of as synthetic counterparts of amphiphilic α-helices having a hydrophilic face along one side and a hydrophobic face along the other side of the helix.

专利号:US-2015045534-A1
优先权日:2011-12-23
标题:Process for the Synthesis of Therapeutic Peptides

专利号:EP-2794634-A1
优先权日:2011-12-23
标题 :Process for the synthesis of therapeutic peptides

专利号:EP-2794634-B1
优先权日:2011-12-23
标 题:Process for the synthesis of ghrelin analogues

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

合成参考文献


参考文献:10.1248/cpb.51.994
摘要:Kitagawa T, Nakamura M, Masai K. Synthesis and root growth-inhibitory activity of 2- and 3-(haloacetylamino)-3-(2-furyl)propanoic acids. Chem Pharm Bull (Tokyo). 2003 Aug;51(8):994–8. doi: 10.1248/cpb.51.994.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知