Chemistry:Oleandrose
From HandWiki
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| IUPAC name
(3S,4S,5S)-4,5-Dihydroxy-3-methoxyhexanal
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| Other names
2,6-Dideoxy-3-O-methyl-L-arabinohexose
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3D model (JSmol)
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PubChem CID
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| Properties | |
| C7H14O4 | |
| Molar mass | 162.185 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Tracking categories (test):
Oleandrose is a type of carbohydrate with the chemical formula C7H14O4. With a six-carbon chain, it is classified as a hexose. With two hydroxyl groups replaced with hydrogen atoms, it is a dideoxy sugar. The hydroxyl group at C3 is methylated.
Occurrence
Oleandrdose is found in the leaves of Nerium oleander and may contribute to the toxicity of the plant.[1][2] Oleandrose is also a component of several naturally-occurring chemical compounds including the avermectins (emamectin, abamectins, ivermectin, and others), the macrolide antibiotic oleandomycin, and the cardiac glycoside oleandrin.
Laboratory syntheses of L-oleandrose[3] and DL-oleandrose[4] have been reported.
See also
- Sarmentose, a diastereomeric dideoxy sugar
References
- ↑ Siddiqui, Bina Shaheen; Khatoon, Nasima; Begum, Sabira; Farooq, Ahsana Dar; Qamar, Kehkashan; Bhatti, Huma Aslam; Ali, Syed Kashif (2012). "Flavonoid and cardenolide glycosides and a pentacyclic triterpene from the leaves of Nerium oleander and evaluation of cytotoxicity". Phytochemistry 77: 238–244. doi:10.1016/j.phytochem.2012.01.001. PMID 22281382. Bibcode: 2012PChem..77..238S.
- ↑ Bakir Çilesizoğlu, Neşe; Yalçin, Emine; Çavuşoğlu, Kültiğin; Sipahi Kuloğlu, Selin (2022). "Qualitative and quantitative phytochemical screening of Nerium oleander L. Extracts associated with toxicity profile". Scientific Reports 12 (1): 21421. doi:10.1038/s41598-022-26087-0. PMID 36504046. Bibcode: 2022NatSR..1221421B.
- ↑ Bredenkamp, Martin W.; Holzapfel, Cedric W.; Toerien, Francois (1992). "Alternative Syntheses of L-(-)-Oleandrose from L-Rhamnose1Preparation of Glycals". Synthetic Communications 22 (17): 2459–2477. doi:10.1080/00397919208021642.
- ↑ Berti, G.; Catelani, G.; Colonna, F.; Monti, L. (1982). "A highly diastereoselective synthesis of dl-oleandrose". Tetrahedron 38 (20): 3067–3072. doi:10.1016/0040-4020(82)80194-4.
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