- PRX-08066
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- $55.00 / 1mg
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2024-11-19
- CAS:866206-54-4
- Min. Order:
- Purity: 98.07%
- Supply Ability: 10g
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| | PRX-08066 Basic information |
| Product Name: | PRX-08066 | | Synonyms: | PRX-08066;PRX-8066;5-[[4-[(6-Chlorothieno[2,3-d]pyrimidin-4-yl)amino]-1-piperidinyl]methyl]-2-fluorobenzonitrile;PRX08066;PRX 08066;Benzonitrile, 5-[[4-[(6-chlorothieno[2,3-d]pyrimidin-4-yl)amino]-1-piperidinyl]methyl]-2-fluoro-;5-HT Receptor,5-hydroxytryptamine Receptor,Serotonin Receptor,PRX-08066,PRX 08066,PRX08066,inhibit,Inhibitor;5-((4-((6-Chlorothieno[2,3-d]pyrimidin-4-yl)amino)piperidin-1-yl)methyl)-2-fluorobenzonitrile;PRX-08066, 10 mM in DMSO | | CAS: | 866206-54-4 | | MF: | C19H17ClFN5S | | MW: | 401.89 | | EINECS: | | | Product Categories: | | | Mol File: | 866206-54-4.mol |  |
| | PRX-08066 Chemical Properties |
| density | 1.44 | | storage temp. | Store at -20°C | | solubility | ≥20.1 mg/mL in DMSO with ultrasonic; insoluble in H2O; ≥2.85 mg/mL in EtOH with gentle warming | | form | solid | | color | White to off-white |
| | PRX-08066 Usage And Synthesis |
| Uses | PRX 08066 is a class 2 receptor antagonist which may be used in the treatment of pulmonary diseases. | | Biological Activity | prx-08066 is a selective antagonist of 5-hydroxytryptamine receptor 2b (5-ht2br) with ki value of 3.4nm [1].prx-08066 is found to causes selective vasodilation of pulmonary arteries and is developed to treat for pulmonary arterial hypertension (pah). in the in vitro studies, prx-08066 shows effects on the vascular muscularization induced by 5-ht. it inhibits 5-ht induced mitogen-activated protein kinase activation with ic50 value of 12nm. in addition, it significantly reduces thymidine incorporation in cho cells expressing human 5-ht2br with ic50 value of 3nm. in both mice and rat models, prx-08066 reverses the hypoxia-dependent increase in right ventricular systolic pressure. besides that, prx-08066 is also found to have anti-proliferative and anti-fibrotic effects. it inhibits the secretion of 5-ht, the phosphorylation of erk1/2 and synthesis of profibrotic growth factor. moreover, prx-08066 inhibits the proliferation of the small intestinal neuroendocrine tumor cell line krj-i with ic50 value of 4.6nm [1, 2]. | | references | [1] porvasnik s l, germain s, embury j, et al. prx-08066, a novel 5-hydroxytryptamine receptor 2b antagonist, reduces monocrotaline-induced pulmonary arterial hypertension and right ventricular hypertrophy in rats. journal of pharmacology and experimental therapeutics, 2010, 334(2): 364-372.
[2] svejda b, kidd m, giovinazzo f, et al. the 5-ht2b receptor plays a key regulatory role in both neuroendocrine tumor cell proliferation and the modulation of the fibroblast component of the neoplastic microenvironment. cancer, 2010, 116(12): 2902-2912. |
| | PRX-08066 Preparation Products And Raw materials |
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