![(6aR,11aR)-6a,11a-Dihydro-2,10-bis(3-methyl-2-buten-1-yl)-6H-benzofuro[3,2-c][1]benzopyran-3,9-diol](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F155013-6ar-11ar-6a-11a-dihydro-210-bis-3-methyl-2-buten-1-yl-6h-benzofuro-32-c-1-benzopyran-39-diol.webp&w=3840&q=75)
CAS 77263-06-0: (6aR,11aR)-6a,11a-Diidro-2,10-bis(3-metil-2-buten-1-il)-6H-benzofuro[3,2-c][1]benzopirano-3,9-diolo
Descrizione:
La sostanza chimica nota come (6aR,11aR)-6a,11a-Diidro-2,10-bis(3-metil-2-buten-1-il)-6H-benzofuro[3,2-c][1]benzopirano-3,9-diolo, con il numero CAS 77263-06-0, è un composto organico complesso caratterizzato dalla sua struttura policiclica, che include unità di benzofurano e benzopirano fuse. Questo composto presenta più gruppi funzionali, inclusi gruppi idrossilici (-OH), che contribuiscono alla sua potenziale attività biologica e alle proprietà di solubilità. La presenza di catene laterali isopreniliche aumenta la sua lipofilia e può influenzare la sua interazione con le membrane biologiche. La stereochimica indicata dalla configurazione (6aR,11aR) suggerisce disposizioni spaziali specifiche che possono influenzare la reattività del composto e la sua interazione con bersagli biologici. Composti di questo tipo sono spesso studiati per le loro potenziali proprietà farmacologiche, comprese le attività antiossidanti e anti-infiammatorie. Tuttavia, sarebbero necessari studi dettagliati sui suoi effetti biologici specifici, tossicità e applicazioni in chimica medicinale per comprendere appieno i suoi potenziali usi.
Formula:C25H28O4
InChI:InChI=1S/C25H28O4/c1-14(2)5-7-16-11-19-23(12-22(16)27)28-13-20-17-9-10-21(26)18(8-6-15(3)4)24(17)29-25(19)20/h5-6,9-12,20,25-27H,7-8,13H2,1-4H3/t20-,25-/m0/s1
InChI key:InChIKey=LDKAMVCGTURXMH-CPJSRVTESA-N
SMILES:C(C=C(C)C)C=1C=C2[C@]3([C@](C=4C(O3)=C(CC=C(C)C)C(O)=CC4)(COC2=CC1O)[H])[H]
Sinonimi:- (6aR,11aR)-6a,11a-Dihydro-2,10-bis(3-methyl-2-buten-1-yl)-6H-benzofuro[3,2-c][1]benzopyran-3,9-diol
- 6H-Benzofuro[3,2-c][1]benzopyran-3,9-diol, 6a,11a-dihydro-2,10-bis(3-methyl-2-butenyl)-, (6aR,11aR)-
- 6H-Benzofuro[3,2-c][1]benzopyran-3,9-diol,6a,11a-dihydro-2,10-bis(3-methyl-2-butenyl)-, (6aR,11aR)- (9CI)
- 6H-Benzofuro[3,2-c][1]benzopyran-3,9-diol,6a,11a-dihydro-2,10-bis(3-methyl-2-butenyl)-, (6aR-cis)-
- Erythrabyssin II
- 6H-Benzofuro[3,2-c][1]benzopyran-3,9-diol, 6a,11a-dihydro-2,10-bis(3-methyl-2-buten-1-yl)-, (6aR,11aR)-
Ordinare per
4 prodotti.
Erythrabyssin II
CAS:Formula:C25H28O4Purezza:98.0%Colore e forma:SolidPeso molecolare:392.48741999999993Erythrabyssin II
CAS:Erythrabyssin II is a biflavonoid compound, which is a type of secondary metabolite primarily sourced from specific plant species within the genus *Erythrina*. This compound is known for its unique and complex chemical structure, which contributes to its notable biological activities. It functions through a multifaceted mode of action that involves modulation of immune responses, inhibition of certain enzyme activities, and potential antioxidant properties. These features make Erythrabyssin II of significant interest in pharmacological research and applications. The main uses and applications of Erythrabyssin II include its exploration as a potential therapeutic agent in immunology and cancer research. By modulating immune cell activity and influencing inflammatory pathways, it holds promise in the development of treatments for autoimmune diseases and cancer. Additionally, its antioxidant properties suggest a role in combating oxidative stress-related conditions. As a compound derived from natural plant sources, Erythrabyssin II also draws interest in studies aimed at discovering novel, naturally-derived therapeutic agents. Further research is ongoing to fully elucidate its mechanism of action and therapeutic potential.Formula:C25H28O4Purezza:Min. 95%Peso molecolare:392.49 g/molErythrabyssin II
CAS:Erythrabyssin II combats Staph/Strep (MIC 0.78-1.56 μg/ml) and inhibits bacterial neuraminidase (IC50 0.09-3.25 μM).Formula:C25H28O4Purezza:98%Colore e forma:SolidPeso molecolare:392.495
