amine

BI-1467335 HCl(BI 1467335) 是口服具有活性的、选择性的氨基脲敏感性胺氧化酶(SSAO) 抑制剂。PXS-4728A (BI 1467335) 能够改善小鼠的慢性阻塞性肺疾病。

3-([2,2':5',2'':5'',2'''-quaterthiophen]-5-yl)propan-1-amine FA 是一种有用的有机化合物，可用于生命科学领域的相关研究，其产品编号为 T67824L。

6-Chloropyridazin-3-amine是一个片段分子，CAS号为5469-69-2，可作为分子拼接、扩展和修饰的重要骨架，为新型候选药物的设计与筛选提供结构基础与研究工具，常用于药物发现、药物合成等相关研究。

N-METHYL-N-(4-PYRIMIDIN-5-YLBENZYL)AMINE是一个片段分子，CAS号为859850-85-4，可作为分子拼接、扩展和修饰的重要骨架，为新型候选药物的设计与筛选提供结构基础与研究工具，常用于药物发现、药物合成等相关研究。

2-methyl-2-phenylpropan-1-amine hydrochloride是一个片段分子，CAS号为21404-94-4，可作为分子拼接、扩展和修饰的重要骨架，为新型候选药物的设计与筛选提供结构基础与研究工具，常用于药物发现、药物合成等相关研究。

m-PEG12-amine是一种基于PEG的PROTAC连接器，同时也是一种在PROTACs[1]和抗体药物偶联物(ADCs)[2]的合成中使用的不可切割的12单位PEG ADC连接器。

Xanthine amine congener trihydrochloride 是一种有效的腺苷拮抗剂，可逆转由腺苷激动剂 N6-环己基腺苷产生的尿流量、钠排泄和心率的减少。

7-benzyl-5,6-dimethyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine 是丙型肝炎病毒 (HCV) 的抑制剂。

2-(5,7-dichloro-1H-indol-3-yl)ethan-1-amine 是一种吲哚胺类化合物，在结构上与血清素相似。它是5-HT2A 受体的选择性激动剂，在神经科学领域具有潜在的应用。

[2-(2,6-dimethylphenoxy)ethyl]amine hydrochloride是一个片段分子，CAS号为313527-92-3，可作为分子拼接、扩展和修饰的重要骨架，为新型候选药物的设计与筛选提供结构基础与研究工具，常用于药物发现、药物合成等相关研究。

N-(2-thienylmethyl)pyridin-2-amine是一个片段分子，CAS号为140-19-2，可作为分子拼接、扩展和修饰的重要骨架，为新型候选药物的设计与筛选提供结构基础与研究工具，常用于药物发现、药物合成等相关研究。

5-METHYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDIN-7-AMINE是一个片段分子，CAS号为33376-96-4，可作为分子拼接、扩展和修饰的重要骨架，为新型候选药物的设计与筛选提供结构基础与研究工具，常用于药物发现、药物合成等相关研究。

ABZ-amine (Amino albendazole) is an impurity of Albendazole, a drug indicated for treating various worm infestations.

111-Trifluoroethyl-PEG4-amine is a polyethylene glycol (PEG)-based linker suitable for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

Amino-PEG10-amine is a PEG-based PROTAC linker employed for the conjugation of two mono diethylstilbestrol (DES)-based ligands. This compound offers an alternative approach to the synthesis of highly selective and active ER antagonists, which are crucial for the advancement of endocrine therapy in breast cancer treatment[1].

Amino-PEG4-C2-amine, a PEG-based linker (4 units) for PROTAC development, facilitates the synthesis of PROTACs.

Amino-PEG5-amine, a PEG-based linker containing 5 units, is utilized in PROTAC synthesis.

Amino-PEG7-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Amino-PEG6-amine, a polyethylene glycol-based (PEG-based) linker with six units, is utilized for the synthesis of PROTACs.

Azido-PEG11-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Azido-PEG2-C2-amine (N3-PEG2-CH2CH2NH2) is a PEG-based PROTAC linker employed for the synthesis of PROTACs[1]. It is also a non-cleavable 2 unit PEG ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs)[2].

Azido-PEG5-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Azido-PEG6-amine is a polyethylene glycol (PEG)-based linker compound commonly employed in the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1]. Additionally, it serves as a non-cleavable 6-unit PEG linker in the synthesis of antibody-drug conjugates (ADCs)[2].

Azido-PEG8-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.