23141-25-5

Basic information

• Product Name: 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
• Synonyms: (15β)-19,20-Didehydro-16α-ethenyl-17β-(β-D-glucopyranosyloxy)-18-oxayohimban-21-one;(1R)-1β-Ethenyl-2α-(β-D-glucopyranosyloxy)-1,2,7,8,13,13bβ,14,14aα-octahydro-5H-indolo[2,3-a]pyrano[3,4-g]quinolizine-5-one;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;Strictosamide
• CAS NO: 23141-25-5
• Molecular Formula: C₂₆H₃₀N₂O₈
• Molecular Weight: 498.525
• Mol File: 23141-25-5.mol
• Article Data: 3

Chemical Properties

• Melting Point: 176-177 °C(Solv: methanol (67-56-1))
• Boiling Point: 816.181°C at 760 mmHg
• Flash Point: 447.41°C
• Appearance: /
• Density: 1.531g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.716
• PKA: 12.79±0.70(Predicted)
• CAS DataBase Reference: 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(CAS DataBase Reference)
• NIST Chemistry Reference: 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(23141-25-5)
• EPA Substance Registry System: 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(23141-25-5)

Safety Data

• Hazardous Substances Data: 23141-25-5(Hazardous Substances Data)

Usage

General Description

The chemical "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 a complex molecule with a fused polycyclic structure. It contains a vinyl group and a glucopyranosyloxy group attached to a 5H-indoloquinolizine core, resulting in a highly intricate and unique chemical structure. 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 has the potential to exhibit a range of biological activities due to its complex arrangement of atoms, and further research may reveal its potential applications in medicinal chemistry and pharmacology.

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

Upstream product

• 19351-63-4 secologanin 
• 343-94-2 tryptamine hydochloride 
• 84638-29-9 Rhynchophine 

Downstream Products

• 77513-45-2 naucleidinal 
• 23141-26-6 O',O',O',O'-tetraacetylstrictosamide 

Relevant articles and documents

Two chromone-secoiridoid glycosides and three indole alkaloid glycosides from Neonauclea sessilifolia

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.

Studies on plants containing indole alkaloids. VIII. Indole alkaloid glycosides and other constituents of the leaves of Uncaria rhynchophylla Miq

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