- Oxysophocarpine
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- $39.00 / 1mL
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2026-04-21
- CAS:26904-64-3
- Min. Order:
- Purity: 99.69%
- Supply Ability: 10g
- Oxysophocarpine
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- $0.00 / 20mg
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2023-02-24
- CAS:26904-64-3
- Min. Order: 5mg
- Purity: ≥98%(HPLC)
- Supply Ability: 10 g
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| | OXYSOPHOCARPINE Basic information |
| Product Name: | OXYSOPHOCARPINE | | Synonyms: | N-OXYSOPHOCARPINE;OXYSOPHOCARPINE;Sophocarpine N-oxide;Oxysophocarpine 26904-64-3;ophocarpidine;Sophocarpidin;1H,5H,10H-Dipyrido[2,1-f:3',2',1'-ij][1,6]naphthyridin-10-one, 2,3,6,7,7a,8,13,13a,13b,13c-decahydro-, 4-oxide, (4R,7aS,13aR,13bR,13cS)-;OXYSOPHOCARPINE USP/EP/BP | | CAS: | 26904-64-3 | | MF: | C15H22N2O2 | | MW: | 262.35 | | EINECS: | | | Product Categories: | Miscellaneous Natural Products;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Inhibitors | | Mol File: | 26904-64-3.mol |  |
| | OXYSOPHOCARPINE Chemical Properties |
| Melting point | 73-76 °C | | solubility | Soluble in chloroform and water | | pka | 4.92±0.20(Predicted) | | form | powder | | color | White-pale yellow | | InChI | InChI=1S/C15H22N2O2/c18-14-7-1-6-13-12-5-3-9-17(19)8-2-4-11(15(12)17)10-16(13)14/h1,7,11-13,15H,2-6,8-10H2/t11-,12+,13+,15,17+/m0/s1 | | InChIKey | QMGGMESMCJCABO-RDVIFRKPSA-N | | SMILES | [N@@+]12([O-])CCC[C@]3([H])C1[C@@]([H])([C@@]1([H])CC=CC(=O)N1C3)CCC2 |
| | OXYSOPHOCARPINE Usage And Synthesis |
| Chemical Properties | In water, methanol, ethanol, chloroform, stupid, insoluble in ether. Derived from the bean root acacia plant bitter cucumber (Sophra flavescens Ait.). | | Uses | Oxysophocarpine is an alkaloid extract from Siphocampylus verticillatus it maintains anti-nociceptive effects through systemic and intracerebroventricular administration in rodents. Derivative of Sophocarpine (S676825), an antiviral agent. | | Synthesis | Extraction from wolfsbane flowers:
1) Pretreatment: Soaking with a mushroom filtrate.
2) Extraction: Sequential extraction with organic solvents and dilute acetic acid solution. The extracts are combined.
3) Water precipitation: The extract is diluted with water, pH adjusted to 11, and filtered after standing.
4) Purification: The filtrate is concentrated, then purified via silica column, ether crystallization, and acetone recrystallization. |
| | OXYSOPHOCARPINE Preparation Products And Raw materials |
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