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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4274 |
Melitracen hydrochloride
盐酸美利曲辛,盐酸美力他欣,Thymeol hydrochloride,Melixeran |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Melitracen hydrochloride (Thymeol hydrochloride) 是一种可口服的双相抗抑郁药和抗焦虑药。它可以通过突触前膜抑制去甲肾上腺素和5-羟色胺(5-HT)的吸收,从而诱导突触空间中单胺递质的增加。 | |||
T23283 |
2-Methoxyidazoxan monohydrochloride
RX 821002 hydrochloride |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
L-Albizziin (2-Methoxyidazoxan monohydrochloride) 是高效的 alpha 2r 肾上腺素受体选择性拮抗剂,对 imidazoline 拮抗作用很小或没有。它对 (豚鼠) alpha 2D 肾上腺素受体 (pKd9.7) 的亲和力明显高于 (兔子) alpha 2A 肾上腺素受体 (pKd8.2)。 | |||
T23479L |
TT-232 TFA(147159-51-1 free base)
|
Others | Others |
TT-232 TFA(147159-51-1 free base)诱导人结肠肿瘤细胞系 SW620 中磷酸酪氨酸磷酸酶活性的双相激活。 | |||
T68765 |
Spirorenone
|
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Spirorenone is an androstadienone derivative as a highly effective aldosterone antagonist. Spirorenone is 8.6 times as potent as spironolactone, but showed a lower affinity for the mineralocorticoid receptors. In phase I clinical trials Spirorenone was absorbed with a half-life of 20-30 min, achieving maximum concentrations of about 100 ng/ml (10 mg) and 260 ng/ml (40 mg) after 1-2 h. Disposition of the parent drug was biphasic with half-lives of 50-60 min (distribution) and 5-6 h (elimination).... | |||
T37297 | Ru360 | ||
Ru360, an oxygen-bridged dinuclear ruthenium amine complex, is a selective mitochondrial calcium uptake inhibitor. Ru360 potently inhibits Ca2+ uptake into mitochondria with an IC50 of 0.184 nM. Ru360 binds to mitochondria with high affinity (Kd of 0.34 nM). Ru360 has antiarrhythmic and cardioprotective effects[1][2]. Ru360 permeates slowly into the cell, and specifically inhibits mitochondrial calcium uptake in intact cardiomyocytes and in isolated heart. 1 μm Ru360 is taken up by myocardial ce... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7033 |
Rosmanol
|
Antioxidant; COX | Immunology/Inflammation; Neuroscience; oxidation-reduction |
Rosmanol 能够显著抑制脂多糖诱导的 INOS、COX-2 的表达,抑制低密度脂蛋白的氧化,并具有抗炎作用。 | |||
TN3973 |
Epinodosin
|
Others | Others |
Epinodosin induces significant DNA damage to HepG2 cells in a time- and dose-dependent manner.Epinodosin has a biphasic, dose-dependent effect on root growth and a strong inhibitory effect on root hair development in Lactuca sativa L. seedlings. |