14350-67-5
Chemical Structure
Ormosinine
- CAS. Nr.: 14350-67-5
- Formula:C40H66N6
- Molecular Weight:630.99
IUPAC Name: 4-(6-(dodecahydro-2H-6,13-methanodipyrido[1,2-a:3',2'-e]azocin-13(12H)-yl)piperidin-2-yl)tetradecahydro-1H,6H,9H,15H-5a,14a,17-triaza-1,5:10,15a-dimethanodibenzo[b,fg]octalene
InChIKey: AALLVKSRUNOPFP-RPRHKAGISA-N
SMILES: [H][C@@]1(N2)CCC(C3N[C@@H]([C@]45[C@@]6([H])[C@](CCCN6)([H])C[C@](C5)([H])[C@](CCCC7)([H])N7C4)CCC3)[C@@]2([H])N(CCC8)[C@]9([H])[C@]8([H])C[C@]%10([H])[C@](CCCC%11)([H])N%11C[C@]19C%10
Biological Activity: Ormosinine is a natural Ormosia alkaloid dimer consisting of a panamine unit and an ormosanine unit linked via a C21-C22 bond, and it can be converted to panamine by acid treatment or sublimation. Ormosinine serves as a tool molecule for natural product chemistry research[1][2].
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Ormosinine | Ormosinine is a natural Ormosia alkaloid dimer consisting of a panamine unit and an ormosanine unit linked via a C21-C22 bond, and it can be converted to panamine by acid treatment or sublimation. Ormosinine serves as a tool molecule for natural product chemistry research. | |||||||||||||||||||||
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References
- [1]. H. A. et al. Alkaloids of Ormosia panamensis Benth. and Related Species. Journal American Chemical Society 1 March 1958; 80 (6): 1506–1510.
- [2]. P. Deslongchamps. et al. ORMOSIA ALKALOIDS: IV. STEREOCHEMISTRY OF ORMOJANINE; STRUCTURE AND STEREOCHEMISTRY OF PIPTANTHINE, DASYCARPINE, AND ORMOSININE. Canadian Journal of Chemistry. 44(21): 2539-2551.
