23141-25-5 Usage
Uses
Used in Medicinal Chemistry:
1,2,7,8,13,13bβ,14,14aα-Octahydro-1β-vinyl-2α-(β-D-glucopyranosyloxy)-5H-indolo[2,3-a]pyrano[3,4-g]quinolizine-5-one is used as a potential therapeutic agent for its potential biological activities. Its complex structure may allow it to interact with various biological targets, offering opportunities for the development of new drugs and treatments.
Used in Pharmacology Research:
In the field of pharmacology, 1,2,7,8,13,13bβ,14,14aα-Octahydro-1β-vinyl-2α-(β-D-glucopyranosyloxy)-5H-indolo[2,3-a]pyrano[3,4-g]quinolizine-5-one serves as a subject of study to explore its potential effects on biological systems. Understanding its interactions with cellular components and its pharmacological profile can lead to insights into new mechanisms of action and therapeutic applications.
Used in Drug Discovery:
1,2,7,8,13,13bβ,14,14aα-Octahydro-1β-vinyl-2α-(β-D-glucopyranosyloxy)-5H-indolo[2,3-a]pyrano[3,4-g]quinolizine-5-one is utilized in drug discovery processes to identify its potential as a lead compound. Its unique structure may provide a foundation for the design of new pharmaceuticals with specific therapeutic properties.
Used in Chemical Synthesis:
In the chemical synthesis industry, 1,2,7,8,13,13bβ,14,14aα-Octahydro-1β-vinyl-2α-(β-D-glucopyranosyloxy)-5H-indolo[2,3-a]pyrano[3,4-g]quinolizine-5-one may be used as a starting material or intermediate in the synthesis of other complex organic compounds, potentially leading to the development of novel chemical entities with various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 23141-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,4 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23141-25:
(7*2)+(6*3)+(5*1)+(4*4)+(3*1)+(2*2)+(1*5)=65
65 % 10 = 5
So 23141-25-5 is a valid CAS Registry Number.
InChI:InChI=1/C26H30N2O8/c1-2-12-15-9-18-20-14(13-5-3-4-6-17(13)27-20)7-8-28(18)24(33)16(15)11-34-25(12)36-26-23(32)22(31)21(30)19(10-29)35-26/h2-6,11-12,15,18-19,21-23,25-27,29-32H,1,7-10H2/t12-,15+,18+,19-,21-,22+,23-,25+,26+/m1/s1
23141-25-5Relevant academic research and scientific papers
Two chromone-secoiridoid glycosides and three indole alkaloid glycosides from Neonauclea sessilifolia
Itoh, Atsuko,Tanahashi, Takao,Nagakura, Naotaka,Nishi, Toyoyuki
, p. 359 - 369 (2007/10/03)
From the dried roots of Neonauclea sessilifolia, two new chromone-secoiridoid glycosides, sessilifoside and 7″-O-β-D-glucopyranosylsessilifoside, and three novel indole alkaloid glycosides, neonaucleosides A, B, and C, were isolated along with the main known glycosides, 5-hydroxy-2-methylchromone-7-O-β-D-apiofuranosyl-(1→6)- β-D-glucopyranoside, sweroside, loganin, grandifloroside, and quinovic acid 3β-O-β-D-quinovopyranoside-28-O-β-D-glucopyranoside. The structures of these new glycosides were determined by spectroscopic and chemical means. Neonaucleoside A and its C-3 epimer were prepared from secologanin and tryptamine.
Con figurative correlation and conformational analysis of strictosidine and vincoside derivatives
Patthy-Lukats, Agnes,Kocsis, Akos,Szabo, Laszlo F.,Podanyi
, p. 1492 - 1499 (2007/10/03)
On the basis of the configuration of C-15 of the secologanin unit, using detailed NMR analysis, the configuration of C-3, the solution conformation around C-14, and the glucosidic bridge, as well as those of the dihydropyran and tetrahydropyridine rings, were determined in the vincosamide and strictosamide derivatives 4b and 5b. The stereochemical analysis was extended by chemical correlation to the 4-benzylated strictosidine and vincoside derivatives 3c and 3d. Experimental proof was presented for the interpretation of the 'anomalous' chemical shift of acetylated strictosamide derivatives.
