tuberostemonine
tuberostemonine Basic information
- Product Name:
- tuberostemonine
- Synonyms:
-
- tuberostemonine
- (7aR,8aβ,11aβ,11bα,11cβ)-2β-[(2S,4S)-Tetrahydro-4-methyl-5-oxofuran-2-yl]-8β-ethyltetradecahydro-11β-methylfuro[2,3-h]pyrrolo[3,2,1-jk][1]benzoazepine-10-one
- 2β-[(2S,4S)-Tetrahydro-4-methyl-5-oxofuran-2-yl]stenine
- Nsc366235
- TUBERSTEMONINE(P)
- TuberosteMonin
- Tuberostemonine, 98%, from Stemona tuberosa L.
- Parathymine
- CAS:
- 6879-01-2
- MF:
- C22H33NO4
- MW:
- 375.5
- Product Categories:
-
- chemical reagent
- pharmaceutical intermediate
- phytochemical
- reference standards from Chinese medicinal herbs (TCM).
- standardized herbal extract
- Mol File:
- 6879-01-2.mol
tuberostemonine Chemical Properties
- Melting point:
- 86~88℃
- Boiling point:
- 554.2±50.0 °C(Predicted)
- Density
- 1.19±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C(protect from light)
- solubility
- DMF:10.0(Max Conc. mg/mL);26.63(Max Conc. mM)
DMF:PBS (pH 7.2) (1:2):0.33(Max Conc. mg/mL);0.88(Max Conc. mM)
DMSO:1.0(Max Conc. mg/mL);2.66(Max Conc. mM) - form
- A solid
- pka
- 8.90±0.70(Predicted)
- color
- White to off-white
tuberostemonine Usage And Synthesis
Description
This novel alkaloid has been isolated from Sternona sessilifolia and S. tuberosa and was first given the formula C19H29O4N, subsequently altered to that given above. It crystallizes in colourless needles from MeOH with 1 mole of solvent, m.p. 65-88°C (dec.) and has [α]D - 25.4° (Me2CO). It is a non-phenolic, tertiary base and yields a hydrobromide, m.p. 120°C (dec.) and a perchlorate, m.p. 242°C (dec.). The methiodide monohydrate has m.p. 236-8°C (dec.) and the methochloride, dihydrate, m.p. 172°C. A methosulphate has also been prepared, m.p. 253°C (dec.). The base is not hydrolyzed by acids but in the presence of excess PtO2 it gives the dihydro derivative, m.p. 133°C, furnishing a hydrochloride, m.p. 281 ° C. Oxidation with KMnO4 gives a C17 compound, whereas oxidation with silver oxide forms a neutral substance, C22H29O4N, m.p. 178°C which still contains the lactone groups and gives a positive Ehrlich pyrrole reaction.
Uses
Tuberostemonine is elucidated as one of the major components of Radix Stemonae and has been shown to display therapeutic effects against cigarette smoke-induced acute lung inflammation.
Definition
ChEBI: A natural product found in Stemona phyllantha and Stemona tuberosa.
References
Kondo, Suzuki, Satomi.,J. Pharrn. Soc., Japan, 54,96 (1934)
Kondo, Suzuki, Satomi., ibid, 59, 177 (1939)
Kondo, Suzuki, Satomi., ibid, 60, 149 (1940)
Kondo, Suzuki, Satomi., ibid, 61, 111 (1941)
Kaneko., Ann. Rep. ITSUU Lab. (Tokyo), 11,45 (1960)
Gotz, Bogri, Gray., Tetrahedron Lett., 707 (1961)
Edwards, Feniak, Handa., Can. J. Chern., 40,455,2416 (1962)
Crystal structure:
Harada et ai., Chern. Cornrnun., 460 (1967)
tuberostemonineSupplier
- Tel
- +86-21-20908456
- sales@BioChemBest.com
- Tel
- 400-1166-196 18981987031
- cdhxsj@163.com
- Tel
- +86-0755-89668383
- sales@sungening.com
- Tel
- 4008-755-333 18080918076
- 800078821@qq.com
- Tel
- +86-028-82633397 18982077548
- cwb1@biopurify.cn
tuberostemonine(6879-01-2)Related Product Information
- Peimine
- Praeruptorin A
- Oridonin
- Praeruptorin B
- Bilobalide
- Mangostin
- Curcumol
- BAVACHIN
- Tuberstemonine
- CASTICIN
- (-)-Huperzine A
- epiberberine
- HEXABROMOBENZENE
- (3S,5S)-5-[(1S,2Z,3aβ,10aα,10bα)-Decahydro-2-(2,5-dihydro-3-methoxy-4-methyl-5-oxofuran-2-ylidene)-1α-methyl-2H-furo[3,2-c]pyrrolo[1,2-a]azepin-8α-yl]-4,5-dihydro-3-methylfuran-2(3H)-one
- Tetradecanedioic acid
- tuberostemonine
- ETHYL 3-(PYRROLIDIN-3-YL)PROPANOATE
- 3-(TETRAHYDRO-FURAN-3-YL)-PROPYLAMINE