(+)-Bulbocapnine

CAS: 298-45-3

Ref. 3D-FB65594

Produktinformation

• Name: (+)-Bulbocapnine
• Synonyme: (7aS)-11-methoxy-7-methyl-6,7,7a,8-tetrahydro-5H-[1,3]benzodioxolo[6,5,4-de]benzo[g]quinolin-12-ol, (7aS)-6,7,7a,8-Tetrahydro-11-methoxy-7-methyl-5H-benzo[g]-1,3-benzodioxolo[6,5,4-de]quinolin-12-ol, (S)-(+)-Bulbocapnine, 10-Methoxy-1,2-(methylenedioxy)-6aα-aporphin-11-ol, 11-methoxy-7-methyl-6,7,7a,8-tetrahydro-5H-[1,3]benzodioxolo[6,5,4-de]benzo[g]quinolin-12-ol, 4-Hydroxy-3-methoxy-5,6-methylenedioxy-aporphin, 5H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-12-ol, 6,7,7a,8-tetrahydro-11-methoxy-7-methyl-, (S)-, 5H-Benzo[g]-1,3-benzodioxolo[6,5,4-de]quinolin-12-ol, 6,7,7a,8-tetrahydro-11-methoxy-7-methyl-, (7aS)-, 6a-alpha-Aporphin-11-ol, 10-methoxy-1,2-(methylenedioxy)-, 6aα-Aporphin-11-ol, 10-methoxy-1,2-(methylenedioxy)-, Bulbokapnin, Bulbokaprin, d-Bulbocapnine

Beschreibung

(+)-Bulbocapnine is an alkaloid that has been studied for its various characteristics. It has been found to induce catalepsy, a state of immobility and rigidity, in animal models. (+)-Bulbocapnine has also shown potential as an acetylcholinesterase inhibitor, which means it can inhibit the breakdown of acetylcholine, a neurotransmitter involved in muscle movement and cognition. Additionally, (+)-Bulbocapnine has been investigated for its antimicrobial properties, particularly against metronidazole-resistant strains of bacteria. This alkaloid is derived from plants such as corydalis and dicentra and belongs to the class of natural products known as ingenol mebutate derivatives. Overall, (+)-Bulbocapnine exhibits diverse biological activities and holds promise for further research in various fields.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 325.36 g/mol
• Formel: C₁₉H₁₉NO₄
• Reinheit: Min. 95%
• InChl: InChI=1S/C19H19NO4/c1-20-6-5-11-8-14-19(24-9-23-14)17-15(11)12(20)7-10-3-4-13(22-2)18(21)16(10)17/h3-4,8,12,21H,5-7,9H2,1-2H3/t12-/m0/s1
• InChI Key: InChIKey=LODGIKWNLDQZBM-LBPRGKRZSA-N
• SMILES: COc1ccc2c(c1O)-c1c3c(cc4c1[C@H](C2)N(C)CC4)OCO3