購(gòu)物車(chē) 
-
(4bS,8aS,9R)-11-(cyclopropylmethyl)-5,6,7,8,9,10-hexahydro-8aH-9,4b-(epiminoethano)phenanthrene-3,8a-diol
- names：
(4bS,8aS,9R)-11-(cyclopropylmethyl)-5,6,7,8,9,10-hexahydro-8aH-9,4b-(epiminoethano)phenanthrene-3,8a-diol
- CAS號(hào)：
42281-59-4
MDL Number： - MF(分子式)： C20H27NO2 MW(分子量)： 313.44
- EINECS: Reaxys Number:
- Pubchem ID: Brand:BIOFOUNT
| 貨品編碼 | 規(guī)格 | 純度 | 價(jià)格 (￥) | 現(xiàn)價(jià)(￥) | 特價(jià)(￥) | 庫(kù)存描述 | 數(shù)量 | 總計(jì) (￥) |
|---|---|---|---|---|---|---|---|---|
| FMK23590-500mg | 500mg | >98% | ￥ 0.00 | ￥ 0.00 | Get quote | ￥ 0.00 | ||
| FMK23590-100mg | 100mg | >98% | ￥ 0.00 | ￥ 0.00 | Get quote | ￥ 0.00 |
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| 中文別名 | |
| 英文別名 | Oxilorphan |
| CAS號(hào) | 42281-59-4 |
| Inchi | |
| InchiKey | |
| 分子式 Formula | C20H27NO2 |
| 分子量 Molecular Weight | 313.44 |
| 溶解度Solubility | |
| 性狀 | |
| 儲(chǔ)藏條件 Storage conditions | Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years). |
| 產(chǎn)品說(shuō)明 | (4bS,8aS,9R)-11-(cyclopropylmethyl)-5,6,7,8,9,10-hexahydro-8aH-9,4b-(epiminoethano)phenanthrene-3,8a-diol(CAS:42281-59-4):僅限應(yīng)用于工業(yè)或者科學(xué)研究過(guò)程中非醫(yī)療目的，不應(yīng)用于人類(lèi)或動(dòng)物的臨床診斷以及治過(guò)程療，該產(chǎn)品非藥用，非食用。 |
| Introduction | Oxilorphan is discotninued (DEA controlled substance). Oxilorphan is an opioid antagonist of the morphinan family that was never marketed. It acts as a μ-opioid receptor (MOR) antagonist but a κ-opioid receptor (KOR) partial agonist, and has similar effects to naloxone and around the same potency as an MOR antagonist. Oxilorphan has some weak partial agonist actions at the MOR (with miosis, nausea, dizziness, and some euphoria observed) and can produce hallucinogenic/dissociative effects at sufficient doses, indicative of KOR activation. It was trialed for the treatment of opioid addiction, but was not developed commercially. The KOR agonist effects of oxilorphan are associated with dysphoria, which combined with its hallucinogenic effects, serve to limit its clinical usefulness; indeed, many patients who experienced these side effects refused to take additional doses in clinical trials. |
| Application1 | |
| Application2 | |
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