Potency and safety analysis of hemp-derived delta-9 products: The hemp vs. cannabis demarcation problem
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Names | |
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IUPAC name
(1S,4aS,6S,7R,7aS)-1-(β-D-Glucopyranosyloxy)-6-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid
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Systematic IUPAC name
(1S,4aS,6S,7R,7aS)-6-Hydroxy-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid | |
Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.040.781 |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C16H24O10 | |
Molar mass | 376.358 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Loganic acid is an iridoid. Loganic acid is synthesized from 7-deoxyloganic acid by the enzyme 7-deoxyloganic acid hydroxylase (7-DLH).[1][2] It is a substrate for the enzyme loganate O-methyltransferase for the production of loganin.[3]
References
- ^ Salim, Yu, Altarejos and De Luca (2013) Virus-induced gene silencing identifies Catharanthus roseus 7-deoxyloganic acid-7-hydroxylase, a step in iridoid and monoterpene indole alkaloid biosynthesis. The Plant Journal. 76(5). 754-765
- ^ Miettinen, Dong, Navrot, Schneider, Burlat, et al. (2014) The seco-iridoid pathway from Catharanthus roseus. Nat Commun. 5(
- ^ Dewick (2009) Medicinal Natural Products: A Biosynthetic Approach.