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Cat. No.	Product Name	Target	Signaling Pathways
T7318	Elimusertib BAY-1895344	ATM/ATR	DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
	Elimusertib (BAY-1895344) 是一种可口服的选择性ATR 抑制剂，IC50值为 7 nM。它具有抗肿瘤活性，可研究实体瘤和淋巴瘤。
T72024	ZIM
	ZIM，一种从4-Aminoantipyrine衍生的降冰片烯，有效诱导DNA损伤，造成基因组及染色体损害，进而引发细胞死亡和激活吞噬。其化疗潜力适用于癌症研究。
T3710	XMD16-5	Tyrosinase; PPAR	DNA Damage/DNA Repair; Metabolism; Proteases/Proteasome
	XMD16-5 是TNK2抑制剂，对D163E 和R806Q 突变体的IC50值分别为16和77nM。
T3353	Niraparib hydrochloride 尼拉帕利盐酸盐,MK-4827 hydrochloride,MK-4827 (hydrochloride)	Apoptosis; Others; PARP	Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Others
	Niraparib hydrochloride (MK-4827 hydrochloride) 是一种具有口服活性的PARP1和PARP2抑制剂，IC50值分别为 3.8 nM 和 2.1 nM。它抑制 DNA 损伤修复，诱导凋亡并具有抗肿瘤活性。
T35363	HM-cytosine 5hmC,5-Hydroxymethylcytosine,5-羟甲基胞嘧啶	Others	Others
	HM-cytosine (5hmC) (5hmC) 是哺乳动物基因组 DNA 中天然存在的成分，被认为是 DNA 的第六个碱基。HM-cytosine 是活性 DNA 去甲基化的中间代谢物。HM-cytosine 是已知会影响哺乳动物全局基因表达的表观遗传标记。
T9497	Niraparib tosylate monohyrate	PARP	Chromatin/Epigenetic; DNA Damage/DNA Repair
	Niraparib tosylate monohyrate 也称为 MK-4827，是一种聚 (ADP-核糖) 聚合酶 (PARP) 抑制剂，具有潜在的抗肿瘤活性。 MK4827 抑制 PARP 活性，增强 DNA 链断裂的积累，促进基因组不稳定性和细胞凋亡。 PARP 蛋白家族通过碱基切除修复 (BER) 途径检测和修复单链 DNA 断裂。
T11409	GLP-26	HBV	Microbiology/Virology
	GLP-26 是一种HBV 衣壳组装调节剂，抑制 Hep AD38 系统中的 HBV DNA 复制，IC50值为3 nM。在 1 μM 时，使 cccDNA 降低> 90％。它破坏前基因组 RNA 的衣壳化，导致核衣壳解体，并减少 cccDNA 库。
T17031	TEI-9647	Others	Others
	TEI-9647 is a 1α,25-dihydroxy vitamin D3-26,23-lactone (1α,25-lactone) analog and is an effective VDR/vitamin D-responsive element (DRE)-mediated genomic actions antagonist.
T70115	Pamiparib hydrate
	Pamiparib, also known as BGB-290, is a highly potent and selective PARP inhibitor with favorable drug metabolism and pharmacokinetic properties. BGB-290 selectively binds to PARP and prevents PARP-mediated repair of single-strand DNA breaks via the base-excision repair (BER) pathway. This enhances the accumulation of DNA strand breaks, promotes genomic instability, and eventually leads to apoptosis. BGB-290 may both potentiate the cytotoxicity of DNA-damaging agents and reverse tumor cell chemo...
T36593	TEI-9648
	TEI-9648, a Vitamin D3 Lactone analogue, is a potent and specific vitamin D receptor (VDR) antagonist. TEI-9648 inhibits VDR/VDRE-mediated genomic actions of 1α,25(OH)2D3. TEI-9648 also inhibits HL-60 cell differentiation induced by of 1α,25(OH)2D3. TEI-9648 has the potential for bone metabolism research[1][2]. TEI-9648 (10-1000 nM) dose-dependently blocks the reciprocal changes of CD11b and CD71 expression associated with HL-60 cell differentiation induced by 1α,25(OH)2D3[1]. TEI-9648 has cons...
T28293	Pamiparib maleate BGB290,BGB 290,BGB-29 maleat 0
	Pamiparib is a highly potent and selective PARP inhibitor. BGB-290 selectively binds to PARP and prevents PARP-mediated repair of single-strand DNA breaks via the base-excision repair (BER) pathway. This enhances the accumulation of DNA strand breaks, pro
T73500	AB-506
	AB-506 是一种具有口服活性的，靶向病毒核心蛋白 HBV 复制的抑制剂。AB-506 可以与 HBV 核心蛋白结合，加速衣壳组装并抑制 HBV pgRNA 包壳。AB-506 可用于慢性乙型肝炎 (CHB)研究。
T63741	SGK1-IN-3
	SGK1-IN-3 是有效的、口服具有活力的 SGK1 抑制剂。其中丝氨酸/苏氨酸激酶 SGK1 是 β-连环蛋白途径的激活剂，也是强大的软骨降解刺激剂，在患病的骨关节炎软骨中被发现在基因组控制下被上调。SGK1-IN-3 对骨关节炎表现出研究潜力。
T35567	BIX01294 (hydrochloride hydrate)
	The methylation of lysine residues on histones plays a central role in determining euchromatin structure and gene expression. The histone methyltransferase (HMTase) G9a can mono- or dimethylate lysine 9 on histone 3 (H3), contributing to early embryogenesis, genomic imprinting, and lymphocyte development. BIX01294 (hydrochloride hydrate) is a selective inhibitor of G9a HMTase (IC50 = 1.7 μM). It less effectively inhibits the HMTase G9a-like protein (GLP; IC50 = 38 μM) and has no effect on other ...
T63632	Anti-MRSA agent 3
	Anti-MRSA agent 3 能够明显的抑制耐甲氧西林金黄色葡萄球菌 (MRSA) 的活性 (MIC: 0.098 μg/ml)，并且对正常细胞毒性较低。Anti-MRSA agent 3 对细菌基因组 DNA 具有较高的结合亲和力，对细菌细胞壁和细胞膜具有较强的破坏能力。
T62383	Anti-MRSA agent 2
	Anti-MRSA agent 2 (compound 14) 能够较好的抑制耐甲氧西林金黄色葡萄球菌 (MRSA) (MIC: 0.098 μg/ml)，对正常细胞的毒性相对较低。Anti-MRSA agent 2 能够较强的破坏细菌膜，并具有较好的与细菌基因组DNA 结合的能力。
T82842	BODIPY FL EDA free base
	ODIPY FL EDA free base为绿色荧光胺类探针，能通过R-NH2与醛或酮反应形成可逆的席夫碱产物。使用如硼氢化钠或氰硼氢化钠等还原剂，ODIPY FL EDA free base可转化成稳定的胺衍生物，适用于检测修饰或未修饰脱氧核苷酸，以及评估DNA损伤和基因组DNA甲基化情况。
T38309	LL-37 amide (trifluoroacetate salt)
	LL-37 is a cationic and α-helical antimicrobial peptide expressed in human bone marrow, testis, granulocytes, and gingival epithelium and is upregulated in psoriatic lesions. It inhibits growth of Gram-positive E. coli D21 and Gram-negative B. megatarium in a concentration-dependent manner and LL-37 expression is induced in A549 epithelial cells, alveolar macrophages, neutrophils, and monocyte-derived macrophages following M. tuberculosis infection. LL-37 binds sheep erythrocytes coated with S. ...

化合物

Cat.No: T7318

Synonym: BAY-1895344

Target: ATM/ATR

Cat.No: T72024

Cat.No: T3710

Target: Tyrosinase, PPAR

Niraparib hydrochloride

Cat.No: T3353

Synonym: 尼拉帕利盐酸盐,MK-4827 hydrochloride,MK-4827 (hydrochloride)

Target: Apoptosis, Others, PARP

Cat.No: T35363

Synonym: 5hmC,5-Hydroxymethylcytosine,5-羟甲基胞嘧啶

Target: Others

Niraparib tosylate monohyrate

Cat.No: T9497

Target: PARP

Cat.No: T11409

Target: HBV

Cat.No: T17031

Target: Others

Pamiparib hydrate

Cat.No: T70115

Cat.No: T36593

Pamiparib maleate

Cat.No: T28293

Synonym: BGB290,BGB 290,BGB-29 maleat 0

Cat.No: T73500

Cat.No: T63741

BIX01294 (hydrochloride hydrate)

Cat.No: T35567

Anti-MRSA agent 3

Cat.No: T63632

Anti-MRSA agent 2

Cat.No: T62383

BODIPY FL EDA free base

Cat.No: T82842

LL-37 amide (trifluoroacetate salt)

Cat.No: T38309

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