CAS: 156973-09-0; 5-(Aminomethyl)Pyridin-2-Amine

该化合物是一种双功能性丙烯衍生物,其成分既有原矿,也有氨基甲基组,使其成为有机合成和制药应用的多用途中间体.其结构允许选择性功能化,形成异环化合物,离心体或生物活性分子. 化合物的双重性能增强了其在交叉反应,Schiff基底形成以及作为复杂分子结构的构件的效用. 它在标准条件下的稳定性和与普通试剂的兼容性进一步有助于其在药用化学和材料科学方面的广泛适用性. 这一化合物对于开发定向治疗或功能材料的研究人员特别有用.

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187237-37-2 329-89-5 260794-33-0

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CAS号4214-73-7 2-氨基-5-氰基吡啶 | CAS号329-89-5 6-氨基烟酰胺

合成工艺路线路线简述

    📜6-氨基烟酰胺置于盐酸,硼烷体系中,化学反应生成6-氨基-(9Ci)-3-吡啶甲胺
    参考文献:Discovery Of A Novel,Selective,And Orally Bioavailable Class Of Thrombin Inhibitors Incorporating Aminopyridyl Moieties At The P1 Position
    标题:Discovery Of A Novel,Selective,And Orally Bioavailable Class Of Thrombin Inhibitors Incorporating Aminopyridyl Moieties At The P1 Position
    摘要:A Novel Class Of Thrombin Inhibitors Incorporating Aminopyridyl Moieties At The P1 Position Has Been Discovered. Four Of These Thrombin Inhibitors (13B,C,E And 14D) Showed Nanomolar Potency (K-I 0.8-12 Nm),300-1500-Fold Selectivity For Thrombin Compared With Trypsin,And Good Oral Bioavailability (F = 40-76%) In Rats Or Dogs. The Neutral Fl Was Expected To Increase Metabolic Stability And Oral Absorption. Identification Of This Novel Aminopyridyl Group At Fl Was A Key Step In Our Search For A Clinical Candidate.
    Doi:10.1021/jm970493R

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    专利信息


    专利号:US-2025129021-A1
    优先权日:2023-09-19
    标 题:Small molecule protein synthesis modulators
    发明人:GYGI DAVID; BAHMANYAR SOGOLE SAMI; HAMANN LAWRENCE
    权利人:INTERDICT BIO INC
    摘要:The present disclosure provides compounds of the formulae herein (e.g., Formula (I), Formula (V)), and pharmaceutically acceptable salts thereof, which are useful for modulating protein synthesis (e.g., modulating synthesis of BCL-2, MYC, CCND1, MCL-1, ALK, KRAS-G12D). The present disclosure also provides pharmaceutical compositions and kits comprising the compounds, or pharmaceutically acceptable salts thereof, and methods of treating or preventing diseases or disorders (e.g., diseases or disorders associated with BCL-2, MYC, CCND1, MCL-1, ALK, KRAS-G12D) by administering to a subject in need thereof the compounds, or pharmaceutically acceptable salts thereof, or pharmaceutical compositions thereof.

    专利号:US-10308615-B2
    优先权日:2015-05-29
    标 题:Heterocyclic compounds as inhibitors of Vanin-1 enzyme
    发明人:CASIMIRO-GARCIA AGUSTIN; CONDON JEFFREY SCOTT; FLICK ANDREW CHRISTOPHER; GOPALSAMY ARIAMALA; KIRINCICH STEVEN J; MATHIAS JOHN PAUL; STROBACH JOSEPH WALTER; XIANG JASON SHAOYUN; XING LI HUANG; WANG XIAOLUN
    权利人:PFIZER
    摘要:Compounds, pharmaceutically acceptable salts thereof, are disclosed wherein the compounds have the structure of n nas defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

    专利号:CN-117510471-A
    优先权日:2022-07-29
    标题 :A kind of synthesis method of abeciclib

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