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31

抑制剂 & 化合物

1

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T19947	EDC hydrochloride EDC-HCl Crosslinker,1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride	Others	Others
	EDC hydrochloride (EDC-HCl Crosslinker) 是一种零长度交联剂。 EDC hydrochloride 非常适合将蛋白质或肽共价结合到含羧基的珠子、树脂或其他纳米颗粒上。
T31716L	Etidocaine	Others	Others
	Etidocaine 是一种氨基酸酰胺，用作局部麻醉剂，具有快速起效和长效特性。
T31716	Etidocaine Hydrochloride W-19053,Duranest,W19053,W 19053	Sodium Channel	Membrane transporter/Ion channel
	Etidocaine Hydrochloride (W19053) 是一种长效麻醉剂和电压门控钠通道阻滞剂。
T22502	2-TEDC	Lipoxygenase	Metabolism
	2-TEDC 是一种有效的脂氧合酶（LOX）抑制剂，对 5-LOX、12-LOX 和 15-LOX 具有抑制作用，IC50 值分别为 0.09 μM、0.013 μM 和 0.5 μM。2-TEDC 可用于研究动脉粥样硬化。
TNU1520	5’-O-DMTr-5-MedC(Ac)-methyl phosphonamidite
	5’-O-DMTr-5-MedC(Ac)-methyl phosphonamidite 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 TNU1520。
T75201	5’-O-DMTr-5-MedC (Ac)-methyl phosphonamidite
	5’-O-DMTr-5-MedC (Ac)-methyl phosphonamidite 是一种嘌呤核苷类似物，主要具有抗肿瘤活性，并且能够针对惰性淋巴系统中的恶性肿瘤。其抗癌机制包括抑制 DNA 合成以及诱导细胞凋亡 (apoptosis)。
T69315	5-TAMRA Cadaverine
	5-TAMRA cadaverine can used to modify carboxylic acid group in the presence of activators (e.g. EDC, or DCC) or activated esters (e.g. NHS esters) through a stable amide bond.
T70146	10-Oxononadecanedioic acid
	10-Oxononadecanedioic acid is a long alkane linker with two terminal carboxylic acid groups. The terminal carboxylic acid groups can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
T69729	Benzyloxy carbonyl-PEG4-Acid
	Benzyloxy carbonyl-PEG4-acid is a linker with a benzyl protecting group and a carboxylic acid. The carboxylic acid can undergo reactions with primary amines with the help of activators (EDC or HATU). The benzyl protecting group can be removed via hydrogenolysis.
T20899	m-PEG1-acid
	M-PEG1-acid is a PEG derivative containing a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. In the presence of activators (e.g. EDC, DCC), the terminal carboxylic acid can be reacted with primary amine groups t
T69280	7-methyl-8-oxononanoic acid
	7-methyl-8-oxononanoic acid is an intermidate for synthesis of conjugated molecules. The acid group can derivatize amine-containing molecules in the presence of activators such as EDC or HATU.
T71872	Boc-8-aoc-oh
	Boc-8-aoc-oh can be used as a PROTAC linker in the synthesis of PROTACs. Boc-8-aoc-oh is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
T70303	N-Boc-15-aminopentadecanoic acid
	N-Boc-15-aminopentadecanoic acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
T71976	Fmoc-5-aminopentanoic acid
	Fmoc-5-aminopentanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
T70057	14-(Fmoc-amino)-tetradecanoic acid
	14-(Fmoc-amino)-tetradecanoic acid can be used as a PROTAC linker in the synthesis of PROTACs. 14-(Fmoc-amino)-tetradecanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
T69887	Fmoc-9-aminononanoic acid
	Fmoc-9-aminononanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs and and other conjugation applications. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
T71731	Fmoc-11-aminoundecanoic acid
	Fmoc-11-aminoundecanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applicaitons. Fmoc-11-aminoundecanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bo...
T71920	9-(Boc-amino)nonanoic Acid
	9-(Boc-amino)nonanoic Acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
T71919	Boc-10-Aminodecanoic acid
	Boc-10-Aminodecanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. Boc-10-Aminodecanoic acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
T71972	N-Fmoc-8-aminooctanoic acid
	N-Fmoc-8-aminooctanoic acid can be used as a PROTAC linker in the synthesis of PROTACs. N-Fmoc-8-aminooctanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
T71732	Fmoc-ε-Acp-OH
	Fmoc-ε-Acp-OH can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. Fmoc-ε-Acp-OH is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
T71986	Fmoc-4-aminobutanoic acid
	Fmoc-4-aminobutanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. Fmoc-4-aminobutanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
T71953	Thiol-PEG2-acid
	Thiol-PEG2-acid is a PEG derivative containing a thiol group and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The thiol group reacts with maleimide, OPSS, vinylsulfone and transition metal surfaces including gold, silver, etc. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond.
T71906	Boc-12-Ado-OH
	Boc-12-Ado-OH can be used as a PROTAC linker in the synthesis of PROTACs. Boc-12-Ado-OH is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
TD0067	5(6)-ROX [5-(and 6)-Carboxy-X-rhodamine] Mixed isomers
	ROX dyes have a strong red fluorescence.Their excitation and emission wavelengths are longer than those of traditional rhodamine dyes.They are used as labels for peptides, proteins, and other biological ligands.5-ROX, 6-ROx, and their mixture of 5(6) -RoX
T71789	Boc-7-Aminoheptanoic acid
	Boc-7-Aminoheptanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applicaitons. Boc-7-Aminoheptanoic acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
T71967	Fmoc-12-aminododecanoic acid
	Fmoc-12-aminododecanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
T71970	Fmoc-7-amino-heptanoic acid
	Fmoc-7-amino-heptanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
T69901	WUN 73823
	WUN 73823, also known as N,N'-bis-(acid-PEG3)-Benzothiazole Cy5 is a PEG derivative containing a cyanine dye with excitation/emission maximum 649/667 nm and a free terminal carboxyl acid. Terminal carboxylic acid can react with primary amine groups in the presence of of activators (e.g. EDC, or DCC) to form a stable amide bond. The hydophilic PEG spacer increases solubility in aqueous media. This product has no formal name at the moment. For the convenience of communication, a temporary code nam...
T69902	VUN 00829
	VUN 00829, also known as N-(m-PEG4)-N'-(PEG4-acid)-Cy5 is a near infrared (NIR) fluorescent Cy 5 labeled PEG derivative containing free terminal carboxyl acid. Terminal carboxylic acid can react with primary amine groups in the presence of of activators (e.g. EDC, or DCC) to form a stable amide bond. The hydophilic PEG spacer increases solubility in aqueous media. Cy5 labeled PEG derivative can be easily traced from its blue color and strong fluorescence. This product has no formal name at the ...
T69900	GUN 00775
	GUN 00775, also known as N-(m-PEG4)-3,3-Dimethyl-3H-indole-N'-(acid-PEG3)-Benzothiazole Cy5, is a PEG derivative containing a cyanine dye with excitation/emission maximum 649/667 nm and a free terminal carboxyl acid. Terminal carboxylic acid can react with primary amine groups in the presence of of activators (e.g. EDC, or DCC) to form a stable amide bond. The hydophilic PEG spacer increases solubility in aqueous media. This product has no formal name at the moment. For the convenience of commu...

化合物

EDC hydrochloride

Cat.No: T19947

Synonym: EDC-HCl Crosslinker,1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride

Target: Others

Cat.No: T31716L

Target: Others

Etidocaine Hydrochloride

Cat.No: T31716

Synonym: W-19053,Duranest,W19053,W 19053

Target: Sodium Channel

Cat.No: T22502

Target: Lipoxygenase

5’-O-DMTr-5-MedC(Ac)-methyl phosphonamidite

Cat.No: TNU1520

5’-O-DMTr-5-MedC (Ac)-methyl phosphonamidite

Cat.No: T75201

5-TAMRA Cadaverine

Cat.No: T69315

10-Oxononadecanedioic acid

Cat.No: T70146

Benzyloxy carbonyl-PEG4-Acid

Cat.No: T69729

Cat.No: T20899

7-methyl-8-oxononanoic acid

Cat.No: T69280

Cat.No: T71872

N-Boc-15-aminopentadecanoic acid

Cat.No: T70303

Fmoc-5-aminopentanoic acid

Cat.No: T71976

14-(Fmoc-amino)-tetradecanoic acid

Cat.No: T70057

Fmoc-9-aminononanoic acid

Cat.No: T69887

Fmoc-11-aminoundecanoic acid

Cat.No: T71731

9-(Boc-amino)nonanoic Acid

Cat.No: T71920

Boc-10-Aminodecanoic acid

Cat.No: T71919

N-Fmoc-8-aminooctanoic acid

Cat.No: T71972

Cat.No: T71732

Fmoc-4-aminobutanoic acid

Cat.No: T71986

Thiol-PEG2-acid

Cat.No: T71953

Cat.No: T71906

5(6)-ROX [5-(and 6)-Carboxy-X-rhodamine] *Mixed isomers*

Cat.No: TD0067

Boc-7-Aminoheptanoic acid

Cat.No: T71789

Fmoc-12-aminododecanoic acid

Cat.No: T71967

Fmoc-7-amino-heptanoic acid

Cat.No: T71970

Cat.No: T69901

Cat.No: T69902

Cat.No: T69900

Cat. No.	Product Name	Target	Signaling Pathways
T5623	Bisphenol A	Others; Endogenous Metabolite	Metabolism; Others
	Bisphenol A 是酚类内源性代谢合成物，广泛用于环氧树脂和聚碳酸酯塑料的生产。它是生殖、发育和全身毒性物质，常被归类为内分泌干扰物。它与许多疾病有关，包括呼吸系统疾病、心血管疾病、糖尿病、肾脏疾病、肥胖和生殖障碍。

天然产物

Cat.No: T5623

Target: Others, Endogenous Metabolite

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