CAS 33570-04-6: Bilobalide
Formula:C15H18O8
InChI:InChI=1S/C15H18O8/c1-12(2,3)14(20)4-6-13(5-7(16)21-6)10(19)23-11-15(13,14)8(17)9(18)22-11/h6,8,11,17,20H,4-5H2,1-3H3/t6-,8-,11-,13-,14+,15+/m0/s1
InChI key:InChIKey=MOLPUWBMSBJXER-YDGSQGCISA-N
SMILES:C(C)(C)(C)[C@@]1(O)[C@@]23[C@@]4([C@](C1)(OC(=O)C4)[H])C(=O)O[C@@]2(OC(=O)[C@@H]3O)[H]
Synonyms:- (3aS,5aR,8R,8aS,9R,10aS)-9-(1,1-Dimethylethyl)-10,10a-dihydro-8,9-dihydroxy-4H,5aH,9H-furo[2,3-b]furo[3′,2′:2,3]cyclopenta[1,2-c]furan-2,4,7(3H,8H)-trione
- (3aS,5aS,9R,10aS)-9-tert-butyl-8,9-dihydroxydihydro-9H-furo[2,3-b]furo[3',2':2,3]cyclopenta[1,2-c]furan-2,4,7(3H,8H)-trione
- 4H,5aH,9H-Furo[2,3-b]furo[3′,2′:2,3]cyclopenta[1,2-c]furan-2,4,7(3H,8H)-trione, 9-(1,1-dimethylethyl)-10,10a-dihydro-8,9-dihydroxy-, (3aS,5aR,8R,8aS,9R,10aS)-
- 4H,5aH,9H-Furo[2,3-b]furo[3′,2′:2,3]cyclopenta[1,2-c]furan-2,4,7(3H,8H)-trione, 9-(1,1-dimethylethyl)-10,10a-dihydro-8,9-dihydroxy-, [5aR-(3aS*,5aα,8β,8aS*,9α,10aα)]-
- 4H,5aH,9H-Furo[2,3-b]furo[3′,2′:2,3]cyclopenta[1,2-c]furan-2,4,7(3H,8H)-trione, 9α-tert-butyl-10,10aβ-dihydro-8α,9-dihydroxy-, (-)-
- Bilobalid
- Bilobalide
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Found 12 products.
(-)-bilobalide
CAS:LactoneFormula:C15H18O8Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:326.3Bilobalide
CAS:Bilobalide ((-)-Bilobalide), a bioactive from Gingko Biloba, is active on hypoxia-induced alterations.Formula:C15H18O8Purity:98.27% - 99.91%Color and Shape:White SolidMolecular weight:326.3(-)-Bilobalide
CAS:(-)-Bilobalide analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C15H18O8Purity:(HPLC) ≥99%Color and Shape:PowderMolecular weight:326.3Bilobalide
CAS:Bilobalide is a sesquiterpene trilactone, which is a secondary metabolite isolated from the leaves of the Ginkgo biloba tree. The source of bilobalide, Ginkgo biloba, is one of the oldest tree species, extensively studied for its wide array of bioactive compounds. Bilobalide exerts its mode of action predominantly through modulation of various neurotransmitter systems and protection against neuronal injury. It has demonstrated the ability to antagonize the GABAA receptor and inhibit excitotoxicity related to excessive glutamate release, thereby providing neuroprotective effects. The uses and applications of bilobalide are primarily centered around its potential therapeutic roles in neurodegenerative conditions. It is notably researched for its efficacy in ameliorating symptoms associated with Alzheimer's disease and other forms of cognitive decline. Additionally, bilobalide has shown prospective benefits in enhancing microcirculation and protecting neuronal cells from oxidative stress-induced damage. The compound continues to be a subject of extensive pharmacological investigations to further elucidate its mechanisms and expand its applications in neurological and potentially other systemic diseases.Formula:C15H18O8Purity:Min. 95%Color and Shape:White PowderMolecular weight:326.3 g/molBilobalide
CAS:Formula:C15H18O8Purity:>96.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:326.30Bilobalide
CAS:Controlled ProductStability Hygroscopic Applications Bilobalide provides protection against learning and memory impairment by reducing free radical injury and inhibiting neuronal apoptosis in the brain cortex and hippocampal CA1 region in induced vascular dementia rats. References Li, W., et. al.: Mol. Med. Reports, 8, 935 (2013)Formula:C15H18O8Color and Shape:Off WhiteMolecular weight:326.30
