首页工具

登录

搜索结果

Search Results for " hydroxamic "

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T21505	Suberoyl bis-hydroxamic acid SBHA,软木肟酸,Suberohydroxamic acid	Apoptosis; HDAC	Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair
	Suberoyl bis-hydroxamic acid (SBHA) 是一种竞争性且可透过细胞的HDAC1和HDAC3抑制剂，ID50值分别为 0.25 μM 和 0.30 μM。它使肿瘤细胞易于凋亡并促进线粒体凋亡途径，可研究甲状腺髓样癌。
T1583	Vorinostat MK0683,伏立诺他,suberoylanilide hydroxamic acid,SAHA	Apoptosis; Mitophagy; Virus Protease; HDAC; Autophagy	Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; Microbiology/Virology
	Vorinostat (SAHA) 是一种泛的组蛋白脱乙酰酶 (HDAC) 抑制剂 (IC50=10 nM)，对 HDAC1/2/3/6/7/11 均有抑制活性。 Vorinostat 具有抗肿瘤活性，可以诱导细胞分化，阻滞细胞周期，诱导细胞凋亡。
T36105	coumarin-SAHA coumarin-Suberoylanilide Hydroxamic Acid,coumarin-SAHA
	Suberoylanilide hydroxamic acid (SAHA) is a class I and class II histone deacetylase (HDAC) inhibitor that binds directly to the catalytic site of the enzyme thereby blocking substrate access. [1] coumarin-Suberoylanilide hydroxamic acid (c-SAHA) is a SAHA derivative where the anilino cap" group is replaced by 7-amino-4-methylcoumarin to produce a fluorescent probe that competitively binds HDAC. [2] The fluorescence excitation and emission maxima of free c-SAHA is 325 and 400 nm
T14864	Caracemide NSC-253272,卡醋胺	Others; DNA/RNA Synthesis; Antibacterial	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others
	Caracemide (NSC-253272) 抑制大肠杆菌的核糖核苷酸还原酶。 Caracemide 可用于抗癌研究。
T1592	Acetohydroxamic acid Methylhydroxamic acid,Acetic acid,Lithostat,AHA,oxime,N-Hydroxyacetamide,乙酰氧肟酸	MMP; Antibacterial	Microbiology/Virology; Proteases/Proteasome
	Acetohydroxamic acid (N-Hydroxyacetamide) 是一种不可逆的细菌和植物尿素酶抑制剂，可研究慢性尿路感染。
T13996	1-Naphthohydroxamic acid	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	1-Naphthohydroxamic acid 是一种选择性 HDAC8抑制剂，IC50为 14 μM。它对 HDAC8的选择性高于 I 类 HDAC1 和 II 类 HDAC6，IC50大于100 μM，可诱导微管蛋白乙酰化。
T33614	n-Decanohydroxamic acid N-Hydroxydecanamide,Decanohydroxamic acid,Caprinohydroxamic acid
	n-Decanohydroxamic acid is a biochemical.
T72148	Phosphoglycolohydroxamic acid
	Phosphoglycolohydroxamic acid 是有效抑制醛缩酶(aldolase)和磷酸丙糖异构酶(triose-phosphate isomerase)的化合物，同时在抗菌和抗真菌领域的研究中具有应用潜力。
T14043	4-(tert-Butyl)-benzhydroxamic Acid	Others	Others
	4-(tert-Butyl)-benzhydroxamic Acid is a PqsR antagonist with IC50s of 12.5 μM and 23.6 μM for E. coli and P. aeruginosa, respectively, and it reduces the production of the virulence factor pyocyanin in P. aeruginosa with an IC50 of 87.2 μM[1].
TQ0052	SH5-07	STAT	JAK/STAT signaling; Stem Cells
	SH5-07 是一种基于异羟肟酸的 Stat3 抑制剂，IC50值为 3.9 μM。
T0721	Piroctone olamine Piroctone ethanolamine,羟吡酮,吡罗克酮乙醇胺盐	Antibiotic; Antifungal	Microbiology/Virology
	Piroctone olamine (Piroctone ethanolamine) 是一种吡啶衍生物，可用于治疗真菌感染。
T8517	Belinostat PX105684,PXD101,贝利司他,PXD-101	HDAC; Autophagy	Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair
	Belinostat (PXD101) 是一种异羟肟酸型组蛋白脱乙酰酶抑制剂，具有抗肿瘤活性，在 HeLa 细胞提取物中的IC50为 27 nM。
T16729	Remetinostat SHP-141	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	Remetinostat (SHP-141) 是一种基于异羟肟酸的组蛋白脱乙酰酶抑制剂，可用于治疗皮肤 T 细胞淋巴瘤的研究。
T1852	Rac-Belinostat NSC726630,PXD101,PX-105684	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	Rac-Belinostat (PX-105684) 是一种具有抗肿瘤活性的新型异羟肟酸型组蛋白脱乙酰酶 (HDAC) 抑制剂。 Belinostat 靶向 HDAC 酶，从而抑制肿瘤细胞增殖、诱导细胞凋亡、促进细胞分化和抑制血管生成。这种药物可以使耐药肿瘤细胞对其他抗肿瘤药物敏感，可能是通过一种涉及胸苷酸合酶下调的机制。
T33551	N(alpha)-Acetylfusarinines Nalpha-Acetylfusarinines
	N(alpha)-Acetylfusarinines is a group of naturally occurring hydroxamic acids produced by unidentified species of Penicillium when grown on iron-deficient media.
T68085	Idrapril
	Idrapril 是一种血管紧张素转换酶(ACE)抑制剂，通过将具有重要催化作用的锌离子与羟基肟基团结合而起作用。
T74166	Microtubule destabilizing agent-1
	Microtubule destabilizing agent-1 (Compound 12b)为基于异羟肟酸的微管去稳定剂(MDA)。该化合物表现出良好的代谢稳定性、高生物利用度及有效的抗肿瘤活性。
T35765	SAHA-BPyne
	Suberoylanilide hydroxamic acid (SAHA) is a class I and class II histone deacetylase (HDAC) inhibitor that binds directly to the catalytic site of the enzyme thereby blocking substrate access. SAHA-BPyne is a SAHA derivative with a benzophenone crosslinker and an alkyne tag intended to be used for profiling HDAC activities in proteomes and live cells. Such terminal alkyne groups can be used in linking reactions, known as click chemistry, characterized by high dependability and specificity of azi...
T71110	Nanatinostat TFA
	Nanatinostat, also known as Tractinostat, CHR-3996 and VRx-3996, is an orally bioavailable, second-generation hydroxamic acid-based inhibitor of histone deacetylase (HDAC) with potential antineoplastic activity. HDAC inhibitor CHR-3996 inhibits HDAC, resulting in an accumulation of highly acetylated histones, the induction of chromatin remodeling, and the selective transcription of tumor suppressor genes; these events may result in the inhibition of tumor cell division and the induction of tumor...
T36110	L-Pyrohomoglutamic Acid
	L-Pyrohomoglutamic acid is an amino acid building block.1,2It has been used in the synthesis of ligands for FK506-binding proteins (FKBPs) and histone deacetylase (HDAC) inhibitors. 1.Pomplun, S., Wang, Y., Kirschner, A., et al.Rational design and asymmetric synthesis of potent and neurotrophic ligands for FK506-binding proteins (FKBPs)Angew. Chem. Int. Ed.54(1)345-348(2015) 2.Taddei, M., Cini, E., Giannotti, L., et al.Lactam based 7-amino suberoylamide hydroxamic acids as potent HDAC inhibitors...
T35762	MC1742
	MC1742 is an inhibitor of class I histone deacetylases (HDACs; IC50s = 0.1, 0.11, 0.02, and 0.61 μM for HDAC1, -2, -3, and -8, respectively) and class IIb HDACs (IC50s = 7 and 40 nM for HDAC6 and HDAC10, respectively).1 It is selective for class I and class IIb over class IIa HDACs (IC50s = >50 μM for HDAC4, -5, -7, and -9). MC1742 reduces proliferation of HOS, MG-63, RD, A204, SK-ES-1, and A673 sarcoma cancer stem cells (CSCs). It increases levels of acetylated histone H3 and acetylated tubulin...
T38381	CAY17c
	CAY17c is an inhibitor of bromodomain-containing protein 4 (BRD4; IC50= 0.71 μM), as well as class I histone deacetylases (HDACs; IC50s = 0.046, 0.058, 0.075, and 0.167 μM for HDAC1, -2, -3, and -8, respectively) and class IIb HDACs (IC50s = 0.073 and 0.923 μM for HDAC6 and HDAC10, respectively).1It is selective for these enzymes over BRD2, -3, and -T (IC50s = >20 μM for all), as well as over HDAC4, -5, -7, -9, and -11 (IC50s = >10 μM for all). CAY17c inhibits the proliferation of HCT116, SW620,...

化合物

Suberoyl bis-hydroxamic acid

Cat.No: T21505

Synonym: SBHA,软木肟酸,Suberohydroxamic acid

Target: Apoptosis, HDAC

Cat.No: T1583

Synonym: MK0683,伏立诺他,suberoylanilide hydroxamic acid,SAHA

Target: Apoptosis, Mitophagy, Virus Protease, HDAC, Autophagy

Cat.No: T36105

Synonym: coumarin-Suberoylanilide Hydroxamic Acid,coumarin-SAHA

Cat.No: T14864

Synonym: NSC-253272,卡醋胺

Target: Others, DNA/RNA Synthesis, Antibacterial

Acetohydroxamic acid

Cat.No: T1592

Synonym: Methylhydroxamic acid,Acetic acid,Lithostat,AHA,oxime,N-Hydroxyacetamide,乙酰氧肟酸

Target: MMP, Antibacterial

1-Naphthohydroxamic acid

Cat.No: T13996

Target: HDAC

n-Decanohydroxamic acid

Cat.No: T33614

Synonym: N-Hydroxydecanamide,Decanohydroxamic acid,Caprinohydroxamic acid

Phosphoglycolohydroxamic acid

Cat.No: T72148

4-(tert-Butyl)-benzhydroxamic Acid

Cat.No: T14043

Target: Others

Cat.No: TQ0052

Target: STAT

Piroctone olamine

Cat.No: T0721

Synonym: Piroctone ethanolamine,羟吡酮,吡罗克酮乙醇胺盐

Target: Antibiotic, Antifungal

Cat.No: T8517

Synonym: PX105684,PXD101,贝利司他,PXD-101

Target: HDAC, Autophagy

Cat.No: T16729

Synonym: SHP-141

Target: HDAC

Cat.No: T1852

Synonym: NSC726630,PXD101,PX-105684

Target: HDAC

N(alpha)-Acetylfusarinines

Cat.No: T33551

Synonym: Nalpha-Acetylfusarinines

Cat.No: T68085

Microtubule destabilizing agent-1

Cat.No: T74166

Cat.No: T35765

Nanatinostat TFA

Cat.No: T71110

L-Pyrohomoglutamic Acid

Cat.No: T36110

Cat.No: T35762

Cat.No: T38381

我们的所有产品和服务仅用于科学研究，不能被用于人体，我们也不向个人提供产品和服务。

Copyright © 2015-2024 TargetMol Chemicals Inc. All rights reserved. 沪ICP备20019793号-4

沪公网安备 31010602006700号

沪公网安备 31010602006700号

TargetMol Loading

联系我们

电话：

400-820-0310

邮箱：

service@tsbiochem.com

QQ：

2881945090（终端用户）

2885109491（经销商）

经销：

终端：

地址：

上海市静安区江场三路238号8楼