CAS 24697-74-3
:Leonurina
Descrição:
Leonurina, com o número CAS 24697-74-3, é um alcaloide que ocorre naturalmente, derivado principalmente da planta Leonurus cardiaca, comumente conhecida como erva-mãe. Este composto é caracterizado por suas características estruturais, que incluem um anel de piridina e um grupo hidroxila fenólico, contribuindo para sua atividade biológica. Leonurina é conhecido por suas potenciais propriedades farmacológicas, incluindo efeitos anti-inflamatórios, antioxidantes e neuroprotetores. Tem sido estudado por suas possíveis aplicações na medicina tradicional, particularmente no tratamento de distúrbios cardiovasculares e neurológicos. Além disso, Leonurina exibe efeitos sedativos leves, que podem ser benéficos para a ansiedade e alívio do estresse. Sua solubilidade em água é limitada, o que pode afetar sua biodisponibilidade e eficácia terapêutica. À medida que a pesquisa avança, todo o espectro de seus efeitos e mecanismos de ação está sendo explorado, destacando a importância dos compostos naturais no desenvolvimento de medicamentos e aplicações terapêuticas.
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)
Chave 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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9 produtos.
Benzoic acid, 4-hydroxy-3,5-dimethoxy-, 4-[(aminoiminomethyl)amino]butyl ester
CAS:Fórmula:C14H21N3O5Pureza:%Cor e Forma: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:Leonurine (SCM-198) is an alkaloid that has been found in H. leonuri and with anti-oxidative and anti-inflammatory.Fórmula:C14H21N3O5Pureza:98.55%Cor e Forma:White Crystalline PowderPeso molecular:311.33Leonurine
CAS:Produto ControladoApplications 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. 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)Fórmula:C14H21N3O5Cor e Forma:NeatPeso molecular:311.33Leonurine
CAS: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.Pureza:Min. 95%
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