CAS 6879-01-2: Tuberostemonine
Formula:C22H33NO4
InChI:InChI=1S/C22H33NO4/c1-4-13-14-7-5-6-8-23-16(17-9-11(2)21(24)26-17)10-15(19(14)23)18-12(3)22(25)27-20(13)18/h11-20H,4-10H2,1-3H3/t11-,12-,13+,14+,15+,16-,17-,18+,19+,20-/m0/s1
InChI key:InChIKey=GYOGHROCTSEKDY-JJDZUBOLSA-N
SMILES:C(C)[C@@H]1[C@@]2([C@@]3([C@@]([C@@]4([C@]1(OC(=O)[C@H]4C)[H])[H])(C[C@](N3CCCC2)([C@@]5(C[C@H](C)C(=O)O5)[H])[H])[H])[H])[H]
Synonyms:- (2S,7aR,8R,8aS,11S,11aS,11bR,11cR)-8-Ethyldodecahydro-11-methyl-2-[(2S,4S)-tetrahydro-4-methyl-5-oxo-2-furanyl]furo[2,3-h]pyrrolo[3,2,1-jk][1]benzazepin-10(2H)-one
- (2S,7aR,8R,8aS,11S,11aS,11bR,11cR)-8-ethyl-11-methyl-2-[(2S,4S)-4-methyl-5-oxotetrahydrofuran-2-yl]dodecahydroazepino[3,2,1-hi]furo[3,2-e]indol-10(2H)-one
- 8-ethyl-11-methyl-2-(4-methyl-5-oxotetrahydrofuran-2-yl)dodecahydroazepino[3,2,1-hi]furo[3,2-e]indol-10(2H)-one
- Furo[2,3-h]pyrrolo[3,2,1-jk][1]benzazepin-10(2H)-one, 8-ethyldodecahydro-11-methyl-2-(tetrahydro-4-methyl-5-oxo-2-furanyl)-, [2S-[2α(2R*,4R*),7aα,8α,8aα,11α,11aα,11bβ,11cα]]-
- Furo[2,3-h]pyrrolo[3,2,1-jk][1]benzazepin-10(2H)-one, 8-ethyldodecahydro-11-methyl-2-[(2S,4S)-tetrahydro-4-methyl-5-oxo-2-furanyl]-, (2S,7aR,8R,8aS,11S,11aS,11bR,11cR)-
- Furo[2,3-h]pyrrolo[3,2,1-jk][1]benzazepin-10(2H)-one, 8-ethyldodecahydro-11-methyl-2-[(2S,5S)-tetrahydro-4-methyl-5-oxo-2-furanyl]-, (2S,7aR,8R,8aS,11S,11aS,11bR,11cR)-
- Nsc 366235
- Stenine, 2-(tetrahydro-4-methyl-5-oxo-2-furanyl)-, (2beta(2S,4S))-
- Stenine, 2-(tetrahydro-4-methyl-5-oxo-2-furanyl)-, [2β(2S,4S)]-
- Tuberostemonin
- Tuberostemonine
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Found 7 products.
Tuberostemonine
CAS:Tuberostemonine has antitussive activity, acts in part as an open-channel blocker at the crayfish neuromuscular junction; it also exhibits relatively higher intestinal permeabilities.Formula:C22H33NO4Purity:95%~99%Molecular weight:375.509Tuberostemonine
CAS:LactoneFormula:C22H33NO4Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:375.51Tuberstemonine
CAS:Tuberstemonine is a naturally occurring alkaloid, which is derived from the plant genus *Stemona*. This compound is particularly notable for its presence in the roots of these plants. As an alkaloid, tuberstemonine plays a crucial role in the chemical defense mechanisms of the plant, protecting it from herbivores and pathogens. The mode of action of tuberstemonine involves the modulation of neurotransmitter systems. It exhibits antitussive properties, indicating its ability to suppress cough reflexes, potentially through interactions with the central nervous system. This mechanism positions tuberstemonine as a compound of interest for respiratory therapeutic applications. The uses and applications of tuberstemonine are primarily focused on its pharmacological potential. It has been studied for its cough suppressant effects, which could benefit treatments for chronic cough conditions. Additionally, ongoing research is exploring its broader pharmacological profiles, including possible roles in anti-inflammatory and neuroprotective therapies. By understanding its molecular structure and bioactivity, scientists aim to harness its potential in developing novel therapeutic agents.Formula:C22H33NO4Purity:Min. 95%Color and Shape:White PowderMolecular weight:375.5 g/mol
