CAS 509-24-0: Songorine
Formula:C22H31NO3
InChI:InChI=1S/C22H31NO3/c1-4-23-10-20(3)6-5-17(25)22-15(20)7-13(18(22)23)21-9-12(11(2)19(21)26)14(24)8-16(21)22/h12-13,15-19,25-26H,2,4-10H2,1,3H3/t12-,13+,15-,16-,17+,18?,19-,20+,21+,22+/m1/s1
InChI key:InChIKey=CBOSLVQFGANWTL-DREQLAFGSA-N
SMILES:O[C@@H]1[C@]23[C@]4([C@@]5([C@@]6(C2(N(CC)C[C@@](C)([C@]3(C6)[H])CC1)[H])[H])C[C@@](C(=O)C4)(C(=C)[C@H]5O)[H])[H]
Synonyms:- (1R,2R,5R,7R,8R,9R,13R,17R)-11-ethyl-7,16-dihydroxy-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.1~5,8~.0~1,10~.0~2,8~.0~13,17~]nonadecan-4-one (non-preferred name)
- (3R,6S,6aR,6bR,9R,11R,11aR,12R,12aR,14R)-1-Ethyldodecahydro-6,11-dihydroxy-3-methyl-10-methylene-12,3,6a-ethanylylidene-9,11a-methanoazuleno[2,1-b]azocin-8(9H)-one
- 11-Ethyl-7,16-Dihydroxy-13-Methyl-6-Methylidene-11-Azahexacyclo[7.7.2.1~5,8~.0~1,10~.0~2,8~.0~13,17~]Nonadecan-4-One (Non-Preferred Name)
- 12,3,6a-Ethanylylidene-9,11a-methanoazuleno[2,1-b]azocin-8(9H)-one, 1-ethyldodecahydro-6,11-dihydroxy-3-methyl-10-methylene-, (3R,6S,6aR,6bR,9R,11R,11aR,12R,12aR,14R)-
- 12,3,6a-Ethanylylidene-9,11a-methanoazuleno[2,1-b]azocin-8(9H)-one, 1-ethyldodecahydro-6,11-dihydroxy-3-methyl-10-methylene-, [3R-(3α,6β,6aα,6bα,9β,11α,11aβ,12α,12aβ,14R*)]-
- 7,20-Cycloveatchan-12-one, 21-ethyl-1,15-dihydroxy-4-methyl-16-methylene-, (1α,15β)-
- Bullatine G
- Napellonin
- Napellonine
- Songorin
- Xuan-Wu 2
- See more synonyms
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Found 7 products.
Songorine
CAS:Controlled ProductApplications Songorine is an extract from the Aconitum flavum root and may act as an inhibitor of JNK and p53 enhancing stimulation of fibroblast colony/cluster formation and proliferative activity of mesosomal precursors. References Zyuz'kov, G.et al.: Bull. Exp. Biol. med., 160, 64 (2015);Formula:C22H31NO3Color and Shape:NeatMolecular weight:357.49Songorine
CAS:Songorine is a diterpenoid alkaloid, which is derived from the natural plant genus Aconitum. It primarily acts by interacting with ion channels and modulating neurotransmitter release in the nervous system. This mode of action makes it a compound of interest in the study of neurological pathways and potential neuroprotective effects. Used chiefly in research settings, Songorine is investigated for its potential therapeutic applications, particularly in the field of neuropharmacology. Studies are exploring its role in protecting neurons, potential analgesic properties, and its effects on ion channel-related disorders. Researchers are also examining its implications in metabolic pathways and its influence on cellular responses. These applications make Songorine a compound of significant interest for scientists seeking novel therapeutic avenues for complex neurological conditions.Formula:C22H31NO3Purity:Min. 95%Color and Shape:White/Off-White SolidMolecular weight:357.49 g/molSongorine
CAS:Songorine (Napellonine) shows anti-tumor activity in preliminary pharmacological verification trials including cell proliferation and molecular docking assays.Formula:C22H31NO3Purity:98% - 99.92%Color and Shape:SolidMolecular weight:357.49
