85409-38-7
Chemical Structure
Rilmenidine phosphate
- CAS No.: 85409-38-7
- Formula:C10H19N2O5P
- Molecular Weight:278.24
IUPAC Name: N-(dicyclopropylmethyl)-4,5-dihydrooxazol-2-amine phosphate
InChIKey: ZJCOWRFWZOAVFY-UHFFFAOYSA-N
SMILES: O=P(O)(O)O.C1(NC(C2CC2)C3CC3)=NCCO1
Biological Activity: Rilmenidine phosphate, an innovative antihypertensive agent, is an orally active, selective I1 imidazoline receptor agonist. Rilmenidine phosphate is an alpha 2-adrenoceptor agonist. Rilmenidine phosphate induces autophagy. Rilmenidine phosphate acts both centrally by reducing sympathetic overactivity and in the kidney by inhibiting the Na+/H+ antiport. Rilmenidine phosphate modulates proliferation and stimulates the proapoptotic protein Bax thus inducing the perturbation of the mitochondrial pathway and apoptosis in human leukemic K562 cells [1][2][3].
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Rilmenidine phosphate | 99.48% | Rilmenidine phosphate, an innovative antihypertensive agent, is an orally active, selective I1 imidazoline receptor agonist. Rilmenidine phosphate is an alpha 2-adrenoceptor agonist. Rilmenidine phosphate induces autophagy. Rilmenidine phosphate acts both centrally by reducing sympathetic overactivity and in the kidney by inhibiting the Na+/H+ antiport. Rilmenidine phosphate modulates proliferation and stimulates the proapoptotic protein Bax thus inducing the perturbation of the mitochondrial pathway and apoptosis in human leukemic K562 cells . | ||||||||||||||||||||
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Rilmenidine phosphate (Standard) | ≥98% | Rilmenidine (phosphate) (Standard) is the analytical standard of Rilmenidine (phosphate). This product is intended for research and analytical applications. Rilmenidine phosphate, an innovative antihypertensive agent, is an orally active, selective I1 imidazoline receptor agonist. Rilmenidine phosphate is an alpha 2-adrenoceptor agonist. Rilmenidine phosphate induces autophagy. Rilmenidine phosphate acts both centrally by reducing sympathetic overactivity and in the kidney by inhibiting the Na+/H+ antiport. Rilmenidine phosphate modulates proliferation and stimulates the proapoptotic protein Bax thus inducing the perturbation of the mitochondrial pathway and apoptosis in human leukemic K562 cells . | ||||||||||||||||||||
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Similarity Score 0.80
HY-100490ARRilmenidine hemifumarate (Standard) -
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HY-W453851Boc-3,3-DicPr-Ala-OH -
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HY-B1334Perhexiline -
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HY-113128Bsn-Glycerol 3-phosphate biscyclohexylammonium salt -
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HY-187133sEH-IN-26 -
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HY-78609tert-Butyl (trans-4-(2-hydroxyethyl)cyclohexyl)carbamate -
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HY-42374trans-4-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclohexaneacetic acid -
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HY-W0056312-(cis-4-((tert-Butoxycarbonyl)amino)cyclohexyl)acetic acid -
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HY-W2596252-(4-((tert-Butoxycarbonyl)amino)cyclohexyl)acetic acid -
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References
- [1]. Reid JL. Rilmenidine: a clinical overview. Am J Hypertens. 2000;13(6 Pt 2):106S-111S. [Content Brief]
- [2]. Srdic-Rajic T, et al. Rilmenidine suppresses proliferation and promotes apoptosis via the mitochondrial pathway in human leukemic K562 cells. Eur J Pharm Sci. 2016;81:172-180. [Content Brief]
- [3]. Rose C, et al. Rilmenidine attenuates toxicity of polyglutamine expansions in a mouse model of Huntington's disease. Hum Mol Genet. 2010;19(11):2144-2153. [Content Brief]