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Search Results for " h9c2 "

7

抑制剂 & 化合物

7

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T22795	Gadolinium chloride	CaSR	GPCR/G Protein
	Gadolinium chloride 是特殊的钙敏感受体激动剂，可用于研究心血管疾病。
T0143	Bisoprolol hemifumarate 富马酸比索洛尔,(±)-Bisoprolol hemifumarate,Bisoprolol fumarate,Bisoprolol hemifumarate salt,EMD33512,(±)-Bisoprolol (hemifumarate)	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Bisoprolol hemifumarate 是一种 β1 肾上腺素受体阻断剂。
T6495	EUK-134 EUK 134,乙基双亚氨基甲基愈创木酚锰氯化物	Beta Amyloid	Neuroscience
	EUK-134 是合成的超氧化物歧化酶和过氧化氢酶模拟物，可保护大鼠肾脏免受缺血再灌注引起的损伤。它作用于 H9C2 细胞，降低NF-κB 表达、MDA 水平和蛋白质羰基化。它是具有过氧化氢酶活性的超氧化物歧化酶 (SOD) 模拟物 (SODm)。它是保护有丝分裂的抗氧化剂。
T36490	AZT triphosphate TEA
	AZT triphosphate TFA (3'-Azido-3'-deoxythymidine-5'-triphosphate TFA) is a active triphosphate metabolite of Zidovudine (AZT). AZT triphosphate TFA exhibits antiretroviral activity and inhibits replication of HIV. AZT triphosphate TFA also inhibits the DNA polymerase of HBV. AZT triphosphate TFA activates the mitochondria-mediated apoptosis pathway[1][2][3]. Treatment with 100 μM Zidovudine (AZT) for 48h disrupts the mitochondrial tubular network via accumulation of AZT triphosphate (AZT-TP) in ...
T62112	CDK8-IN-6
	CDK8-IN-6 (compound 9) 是一种细胞周期蛋白依赖性激酶8 (CDK8) 的有效抑制剂 (Kd: 13 nM)。CDK8-IN-6 对 MOLM-13、OCI-AML3、MV4-11、NRK 和 H9c2 细胞表现出细胞毒性，他们 IC50s 分别为 11.2、7.5、8.6、20.5、12.5-25 μM。CDK8-IN-6 对 AML 癌症表现出潜在的研究价值。
T62354	CDK8-IN-7
	CDK8-IN-7 (compound 12) 是一种有效的、选择性的细胞周期蛋白依赖性激酶 8 (CDK8) 抑制剂 (Kd: 3.5 nM)。CDK8-IN-7 对 MOLM-13 细胞 (IC50: 5.9 μM)、OCI-AML3 细胞 (IC50: 4.8 μM)、MV4-11 细胞 (IC50: 5.4 μM)、NRK 细胞 (IC50: 16.2 μM) 和 H9c2 细胞 (IC50: 12.5-25 μM) 具有细胞毒性。CDK8-IN-7 对 AML-癌症表现出研究潜力。
T35712	Debutyldronedarone hydrochloride SR35021 hydrochloride
	N-Desbutyl dronedarone is an active metabolite of the antiarrhythmic agent dronedarone .1,2,3It is formed from dronedarone by cytochrome P450s (CYPs) and monoamine oxidase (MAO) in human hepatocyte preparations.4N-Desbutyl dronedarone inhibits the binding of 3,3’,5-triiodo-L-thyronine to the thyroid hormone receptors TRα1and TRβ1(IC50s = 59 and 280 μM for the chicken and human receptors, respectively).1It inhibits CYP2J2-mediated formation of 14,15-EET from arachidonic acid and soluble epoxide h...

化合物

Gadolinium chloride

Cat.No: T22795

Target: CaSR

Bisoprolol hemifumarate

Cat.No: T0143

Synonym: 富马酸比索洛尔,(±)-Bisoprolol hemifumarate,Bisoprolol fumarate,Bisoprolol hemifumarate salt,EMD33512,(±)-Bisoprolol (hemifumarate)

Target: Adrenergic Receptor

Cat.No: T6495

Synonym: EUK 134,乙基双亚氨基甲基愈创木酚锰氯化物

Target: Beta Amyloid

AZT triphosphate TEA

Cat.No: T36490

Cat.No: T62112

Cat.No: T62354

Debutyldronedarone hydrochloride

Cat.No: T35712

Synonym: SR35021 hydrochloride

Cat. No.	Product Name	Target	Signaling Pathways
TN6490	Regaloside C	Others	Others
	Regaloside C 是一种从百合属的中分离出来的甘油葡糖苷，具有抗炎作用。
T6S1740	Nardosinone 苷松新酮,甘松新酮	Others	Others
	Nardosinone 是一个 dbcAMP 和 staurosporine 的神经生成作用增强剂，分离自Nardostachys chinensis 中。Nardosinone 可能成为一种有用的药理学工具，不仅可用于研究神经生长因子 (NGF) 的作用机理，而且可用于研究神经毒性物质的作用机理。
TN3660	Cinnamyl caffeate	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Cinnamyl caffeate has cardiovascular protective effects, it can increase H9c2 cellular antioxidant potential, decrease intracellular calcium ion ([Ca2+]i) level, and prevent cell apoptosis; it possesses potent antiproliferative activity with the EC(50) value of 0.114 microM, toward colon 26-L5 carcinoma. Cinnamyl caffeate possesses potent NO inhibitory activity with the IC(50) value of 9.53 microM.
T81956	Ladanetin-6-O-β-(6′′-O-acetyl)glucoside
	Ladanetin-6-O-β-(6′′-O-acetyl)glucoside 是一种从甘青青兰 (Dracocephalum tanguticum) 全株中提取的黄酮化合物，具备抗氧化特性。该化合物能够保护H9c2心肌细胞免受Doxorubicin(DOX)引起的细胞毒性。
T81532	Pedaliin 6''-acetate
	Pedaliin 6''-acetate (compound 10) 为甘青青兰中分离得到的天然产物，具有抗氧化活性，并能对抗DOX诱导的H9c2心肌细胞毒性，表现出细胞保护效应，其EC50为19.1 μM。
TN4892	Randialic acid B	Others	Others
	Randialic acid B shows significant cell-protective effects against H2O2-induced H9c2 cardiomyocyte injury.
TN1951	Moracin O 桑辛素 O,桑辛素O	HIF	Angiogenesis; Chromatin/Epigenetic
	Moracin O shows significant neuroprotective, and analgesic activities, it also has a strong protective influence against doxorubicin-induced cardiomyopathy in H9c2 cells with the EC50 value of 4.5 ± 1.3 μM. Moracin O exhibits potent in vitro inhibitory ac

天然产物

Cat.No: TN6490

Target: Others

Cat.No: T6S1740

Synonym: 苷松新酮,甘松新酮

Target: Others

Cinnamyl caffeate

Cat.No: TN3660

Target: Calcium Channel

Ladanetin-6-O-β-(6′′-O-acetyl)glucoside

Cat.No: T81956

Pedaliin 6''-acetate

Cat.No: T81532

Randialic acid B

Cat.No: TN4892

Target: Others

Cat.No: TN1951

Synonym: 桑辛素 O,桑辛素O

Target: HIF

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