Thalistyline
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Grundinformationen
- CAS
62251-53-0- Standard-SMILES
COc1ccc(C[C@H]2c3cc(OC)c(OC)c(OC)c3CC[N+]2(C)C)cc1Oc1ccc(C[C@H]2c3cc(OC)c4c(c3CCN2C)OCO4)cc1- InChIKey
UNLANLZLFACELM-LQJZCPKCSA-N- Summenformel
- C41H49N2O8+
- Durchschnittliche Molmasse
- 697,849 g/mol
- Monoisotopische Masse
- 697,34834295
Namen und Bezeichner
- Bevorzugter Name
- Thalistyline
- IUPAC
- (1S)-5,6,7-Trimethoxy-1-{[4-methoxy-3-(4-{[(6S)-4-methoxy-7-methyl-6,7,8,9-tetrahydro-2H-[1,3]dioxolo[4,5-f]isoquinolin-6-yl]methyl}phenoxy)phenyl]methyl}-2,2-dimethyl-1,2,3,4-tetrahydroisoquinolin-2-ium
- Englischer Name
- thalistyline
- Summenformel
- C41H49N2O8
- Molmasse
- 0
Namen und Synonyme
thalistyline(1S)-1,2,3,4-Tetrahydro-5,6,7-trimethoxy-1-[[4-methoxy-3-[4-[[(5S)-5,6,7,8-tetrahydro-9-methoxy-6-methyl-1,3-dioxolo[4,5-g]isoquinolin-5-yl]methyl]phenoxy]phenyl]methyl]-2,2-dimethylisoquinolin-2-ium
Datenbank-Bezeichner
- CAS
62251-53-0- PubChem CID
- 162971
- DTXSID
DTXSID20211313- ChEMBL
CHEMBL1187403、CHEMBL501762
Chemie und Industrie
Anwendungen
BeschreibungA quaternary bisbenzylisoquinoline alkaloid, thalistyline has been isolated from Thalictrum longistylum DC and T. podocarpum Hunb. grown in Columbia, South America. The base has been isolated as the chloride which forms needles from H20 with m.p. ISO-3°C and a specific rotation of [α]20D + 146° (c 0.1, MeOH). The ultraviolet spectrum of this salt has absorption maxima at 276 and 283 nm. The base has also been characterized as the crystalline iodide, m.p. 220-3°C (dec.) and methiodide, m.p. 266-8°C (dec.). Sodium-liquid ammonia cleavage gives an optically inactive phenolic base, C22H31NO4 as an oil and a phenolic base C18H21NO3 as colourless crystals, m.p. 221-2°C.
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