CAS 24697-74-3
:Leonurina
Descripción:
Leonurina, con el número CAS 24697-74-3, es un alcaloide que se encuentra de forma natural, derivado principalmente de la planta Leonurus cardiaca, comúnmente conocida como hierba madre. Este compuesto se caracteriza por sus características estructurales, que incluyen un anillo de piridina y un grupo hidroxilo fenólico, que contribuyen a su actividad biológica. Leonurina es conocido por sus posibles propiedades farmacológicas, incluyendo efectos antiinflamatorios, antioxidantes y neuroprotectores. Se ha estudiado por sus posibles aplicaciones en la medicina tradicional, particularmente en el tratamiento de trastornos cardiovasculares y neurológicos. Además, Leonurina exhibe efectos sedantes leves, que pueden ser beneficiosos para la ansiedad y el alivio del estrés. Su solubilidad en agua es limitada, lo que puede afectar su biodisponibilidad y eficacia terapéutica. A medida que la investigación continúa, se está explorando todo el espectro de sus efectos y mecanismos de acción, destacando la importancia de los compuestos naturales en el desarrollo de medicamentos y aplicaciones terapéuticas.
Fórmula:C14H21N3O5
InChI:InChI=1S/C14H21N3O5/c1-20-10-7-9(8-11(21-2)12(10)18)13(19)22-6-4-3-5-17-14(15)16/h7-8,18H,3-6H2,1-2H3,(H4,15,16,17)
Clave InChI:InChIKey=WNGSUWLDMZFYNZ-UHFFFAOYSA-N
SMILES:C(OCCCCNC(=N)N)(=O)C1=CC(OC)=C(O)C(OC)=C1
Sinónimos:- 24697-74-3
- 4-Carbamimidamidobutyl 4-Hydroxy-3,5-Dimethoxybenzoate Hydrochloride Hydrate
- 4-Carbamimidamidobutyl-4-hydroxy-3,5-dimethoxybenzolcarboxylat
- 4-Guanidino-1-butanol Syringate
- 4-Hydroxy-3,5-dimethoxybenzoic Acid 4-[(Aminoiminomethyl)amino]butyl Ester
- 4-Hydroxy-3,5-dimethoxybenzoic Acid d-Guanidinobutyl Ester
- 4-[(Diaminomethylidene)Amino]Butyl 4-Hydroxy-3,5-Dimethoxybenzoate
- Benzoic Acid, 4-Hydroxy-3,5-Dimethoxy-, 4-[(Aminoiminomethyl)Amino]Butyl Ester
- Benzoic acid, 4-hydroxy-3,5-dimethoxy-, ester with (4-hydroxybutyl)guanidine
- Guanidine, (4-hydroxybutyl)-, 4-hydroxy-3,5-dimethoxybenzoate
- Guanidine, (4-hydroxybutyl)-, 4-hydroxy-3,5-dimethoxybenzoate (ester)
- Leonurin
- Leonurine
- Scm 198
- Syringic Acid d-Guanidinobutyl Ester
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Encontrado 9 productos.
Benzoic acid, 4-hydroxy-3,5-dimethoxy-, 4-[(aminoiminomethyl)amino]butyl ester
CAS:Fórmula:C14H21N3O5Pureza:%Forma y color:SolidPeso molecular:311.33364-Guanidinobutyl 4-Hydroxy-3,5-Dimethoxybenzoate
CAS:4-Guanidinobutyl 4-Hydroxy-3,5-DimethoxybenzoatePureza:99%Peso molecular:311.33g/molLeonurine
CAS:Leonurine hydrochloride has anti-oxidative, anti-inflammatory, and antitumor activities, it exerts antidiabetic, cardiovascular, and bovine mastitis protection, it has an inhibitory effect on bleeding caused by incomplete abortion. Leonurine hydrochloride increases the expression levels of caspase-3, caspase-9 and Bax/Bcl-2, and it inhibits osteoclastogenesis and prevent osteoporosis associated with estrogen deficiency by inhibiting the NF-κB and PI3K/Akt signaling pathways.Fórmula:C14H21N3O5Pureza:95%~99%Peso molecular:311.338Leonurine
CAS:<p>Leonurine (SCM-198) is an alkaloid that has been found in H. leonuri and with anti-oxidative and anti-inflammatory.</p>Fórmula:C14H21N3O5Pureza:98.55%Forma y color:White Crystalline PowderPeso molecular:311.33Leonurine
CAS:Producto controlado<p>Applications Leonurine is a pseudoalkaloid that has been isolated from Leonotis leonurus. A natural product with antioxidant, anti-inflammatory and cardioprotective properties for the treatment of wild variety of conditions including stroke, cerebral thrombosis and cardiovascular diseases.<br>References He, C., et al.: Zhongguo Linchuang Yaolixue Yu Zhiliaoxue, 18, 1419 (2013); Nsuala, B. N., et al.: J. Ethnopharmacol., 174, 520 (2015); Sun, Y., et al.; Eur. J. Drug Metabo. Pharmacokinet., 41, 423 (2016)<br></p>Fórmula:C14H21N3O5Forma y color:NeatPeso molecular:311.33Leonurine
CAS:<p>Leonurine is a polyphenolic compound that belongs to the group of natural compounds. It has been shown to have neuroprotective effects in vitro by inhibiting neuronal death at low doses. Leonurine also blocks the oxidative injury pathway, which may be related to its ability to inhibit apoptosis and reduce atherosclerotic lesion size in mice. In addition, leonurine inhibits the p-hydroxybenzoic acid (PHBA) oxidation pathway, which may contribute to its anti-inflammatory activities. Leonurine binds with high affinity and specificity to toll-like receptor 4 (TLR4), which may be related to its immunosuppressive properties.</p>Pureza:Min. 95%







