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{{Drugbox | ||
| verifiedrevid = 414055854 | | verifiedrevid = 414055854 | ||
| IUPAC_name |
| IUPAC_name = 1-(4,8-dimethoxyfuroquinolin-7-yl)oxy-3-methylbutane-2,3-diol | ||
| image |
| image = Evoxine.png | ||
| width |
| width = 200 | ||
⚫ | | CAS_number |
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<!--Clinical data--> | |||
⚫ | | ATC_prefix |
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| |
| tradename = | ||
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| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X --> | ||
| |
| pregnancy_US = <!-- A / B / C / D / X --> | ||
| pregnancy_category = | |||
⚫ | | C=11|H=12|O=2 | ||
⚫ | | legal_AU = <!-- Unscheduled / S2 / S3 / S4 / S5 / S6 / S7 / S8 / S9 --> | ||
⚫ | | molecular_weight |
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⚫ | | legal_CA = <!-- / Schedule I, II, III, IV, V, VI, VII, VIII --> | ||
⚫ | | smiles |
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⚫ | | legal_UK = <!-- GSL / P / POM / CD / Class A, B, C --> | ||
⚫ | | bioavailability |
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⚫ | | legal_US = <!-- OTC / Rx-only / Schedule I, II, III, IV, V --> | ||
| protein_bound = | |||
⚫ | | legal_status = Legal | ||
⚫ | | metabolism |
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⚫ | | routes_of_administration = | ||
⚫ | | elimination_half-life = | ||
⚫ | | excretion |
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<!--Pharmacokinetic data--> | |||
| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X --> | |||
⚫ | | bioavailability = | ||
| pregnancy_US = <!-- A / B / C / D / X --> | |||
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| protein_bound = | ||
⚫ | | metabolism = | ||
⚫ | | legal_AU |
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⚫ | | elimination_half-life = | ||
⚫ | | legal_CA |
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⚫ | | excretion = | ||
⚫ | | legal_UK |
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⚫ | | legal_US |
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<!--Identifiers--> | |||
⚫ | | legal_status |
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⚫ | | CAS_number = 522-11-2 | ||
⚫ | | routes_of_administration = | ||
⚫ | | ATC_prefix = none | ||
| ATC_suffix = | |||
| PubChem = 73416 | |||
| DrugBank = | |||
<!--Chemical data--> | |||
⚫ | | C=11 | H=12 | O=2 | ||
⚫ | | molecular_weight = 347.362 g/mol | ||
⚫ | | smiles = CC(C)(C(COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)O)O | ||
}} | }} | ||
Revision as of 11:10, 3 September 2011
Pharmaceutical compoundClinical data | |
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IUPAC name
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CompTox Dashboard (EPA) | |
Chemical and physical data | |
Formula | C11H12O2 |
Molar mass | 347.362 g/mol g·mol |
3D model (JSmol) | |
SMILES
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(verify) |
Evoxine (Haploperine) is an alkaloid with hypnotic and sedative effects. It is found naturally in a variety of Australian and African plants including Evodia xanthoxyloides and Teclea gerrardii.
References
- Eastwood, FW; Hughes, GK; Ritchie, E. (1954). "Alkaloids of the Australian Rutaceae: Evodia xanthoxyloides F.Muell. IV. The structures of Evoxine and Evoxoidine". Australian Journal of Chemistry. 7 (1): 87–98. doi:10.1071/CH9540087.
- Waffo, AF; Coombes, PH; Crouch, NR; Mulholland, DA; El Amin, SM; Smith, PJ (2007). "Acridone and furoquinoline alkaloids from Teclea gerrardii (Rutaceae: Toddalioideae) of southern Africa". Phytochemistry. 68 (5): 663–7. doi:10.1016/j.phytochem.2006.10.011. PMID 17174364.
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