Talk:Anatoxin-a: Difference between revisions
Wouterstomp (talk | contribs) Assessment: Chemicals: class=Start; Medicine: class=Start (assisted) |
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==Mechanism for toxicity== |
==Mechanism for toxicity== |
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" (+)anatoxin-a, is 150 fold more potent than the synthetic negative enantiomer, (−)anatoxin-a.[8] This is thought to be the case because (+)anatoxin-a, the s-cis enone conformation, has a distance a 6.0 Ao between its nitrogen and carbonyl group, which corresponds well to the 5.9 Ao distance that separate the nitrogen and oxygen in acetylcholine". Well, and now guess what's that distance in the (-)-enantiomer... :D --[[User:FK1954|FK1954]] ([[User talk:FK1954|talk]]) 21:14, 4 September 2013 (UTC) |
" (+)anatoxin-a, is 150 fold more potent than the synthetic negative enantiomer, (−)anatoxin-a.[8] This is thought to be the case because (+)anatoxin-a, the s-cis enone conformation, has a distance a 6.0 Ao between its nitrogen and carbonyl group, which corresponds well to the 5.9 Ao distance that separate the nitrogen and oxygen in acetylcholine". Well, and now guess what's that distance in the (-)-enantiomer... :D --[[User:FK1954|FK1954]] ([[User talk:FK1954|talk]]) 21:14, 4 September 2013 (UTC) |
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== Enantioselective enolization == |
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''This method for anatoxin-a production was one of the first used that does not utilize a chimerically analogous starting substance for anatoxin formation'' |
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What's a chimeric analogue? Sounds like some molecule from hell combined with another molecule from hell. Do they start with a non-chiral (racemic) compound, or an achiral compound here? I am not sure if this is a typo or if it is right, I have not been able to read the reference. |
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[[User:MorbidFlorist|MorbidFlorist]] ([[User talk:MorbidFlorist|talk]]) 21:34, 13 April 2015 (UTC) |
Revision as of 21:34, 13 April 2015
Chemicals Start‑class Low‑importance | ||||||||||
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Medicine: Toxicology Start‑class Low‑importance | |||||||||||||
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Mechanism for toxicity
" (+)anatoxin-a, is 150 fold more potent than the synthetic negative enantiomer, (−)anatoxin-a.[8] This is thought to be the case because (+)anatoxin-a, the s-cis enone conformation, has a distance a 6.0 Ao between its nitrogen and carbonyl group, which corresponds well to the 5.9 Ao distance that separate the nitrogen and oxygen in acetylcholine". Well, and now guess what's that distance in the (-)-enantiomer... :D --FK1954 (talk) 21:14, 4 September 2013 (UTC)
Enantioselective enolization
This method for anatoxin-a production was one of the first used that does not utilize a chimerically analogous starting substance for anatoxin formation
What's a chimeric analogue? Sounds like some molecule from hell combined with another molecule from hell. Do they start with a non-chiral (racemic) compound, or an achiral compound here? I am not sure if this is a typo or if it is right, I have not been able to read the reference.