I didnt argue you on that point, i mean the dotted line should point to the carbon not nitrogen, this is the same as what the reference mentioned.
Lemme draw picture:
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I Like to Draw Pictures of Random Molecules
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I didnt argue you on that point, i mean the dotted line should point to the carbon not nitrogen, this is the same as what the reference mentioned.
Lemme draw picture:
Another fanciful attempt to mimic the opioid agonist properties of morphine in a simpler molecule not involving fused ring systems. Not a simple molecule & would require some tinkering to optimize effect. Known compound but found no biological data.
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sekio
Bluelight Crew
hmm, logic sez it might be a ghb-type drug... that's a goodun... and no silly name? has dresden's account been hacked or something?? </s>
but more likely some sort of GABAB stuff happenin...
but more likely some sort of GABAB stuff happenin...
At first glance you are missing the aminomethyl function found in muscimol, which mimics the gamma-amino function in GABA. And I would guess regarding stability that the hydroxymethyl group in your suggestion might want to tautomerize to the aldehyde at certain pH ranges, which wouldn't be active. Nice idea, though.
Interesting acetylenic analog of trans-4-aminocrotonic acid. Interesting that it did not turn up in a Google search though I think it would be an interesting biological tool as well as moderately challenging synthetically.
I screwed this structure & nomenclature before. It is a known compound but the only uses are as pharma raw materials. No bio data found.
I screwed this structure & nomenclature before. It is a known compound but the only uses are as pharma raw materials. No bio data found.
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sekio
Bluelight Crew
Just, uh, cough torrent ChemBioDraw and keygen it.
Bagseed
Bluelighter
chemsketch sucks bigtime ime
Why do you say that? Difficult to earn how to use, etc?
ACD/ChemSketch has 4.5 star reviews on CNet (19 reviewers). Their 'how to use' tutorial video looks very straight-forward: https://www.selectscience.net/Selec...o-use-acd-chemsketch-video-guide?videoID=4285 And at FREE, it beats ChemDraw's $2300 price tag by a lot. (That's a rough price based on my having previously owned ChemDraw 11.0, giving me a 20% discount over their $2945 list for ChemDraw 17).
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Chemsketch is the best free one if you cannot afford chemdraw or obtain it behind a curtain.
It has most of the functionality you would want to use.
However it will feel quite sluggish to (not the performance tho); until you get use to which button do what and where they are.
@JacksinPA
While u still have access to chemdraw, try using its Chem3D program, and use the overlay function.
You will like it very much if you like comparison with the dotted lines like what are posted.
(Draw two molecules, press CtrlE to open model explorer, select target atom, R click the choose overlay, set some 2-3 overlay points, continue to minimize and overlay, can also measure distance differneces after)
It has most of the functionality you would want to use.
However it will feel quite sluggish to (not the performance tho); until you get use to which button do what and where they are.
@JacksinPA
While u still have access to chemdraw, try using its Chem3D program, and use the overlay function.
You will like it very much if you like comparison with the dotted lines like what are posted.
(Draw two molecules, press CtrlE to open model explorer, select target atom, R click the choose overlay, set some 2-3 overlay points, continue to minimize and overlay, can also measure distance differneces after)
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The 2-aminotetralins are known psychoactive compounds, although I don't know of any that are mu opioid agonists. See: 2-AT (and the compounds listed under "Chemical derivatives" on this page).
Thanks for the 'heads up' on this class, which I had ignored until now. Here is a reference: https://www.revolvy.com/page/2%2DAminotetralin. Some of these are stimulants. Lots of liks on various substituents in this class.
sekio
Bluelight Crew
JacksinPA, have you heard of the "morphine rule"? It's a rough SAR predictor for opioid-type activity. Some of these compounds you are drawing do not follow it (no quaternary carbons).
so maybe:
note the underlines are my corrections.
so maybe:
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Thanks for the input, which I am aware of. Feel free to add methyl groups wherever you want to my structures. I am not interested in cluttering up my sketches with all the possible methylated forms. Anyone looking to do creative work based ion my drawings would either have the sense to optimize those structures or waste a lot of time & $$$ in the lab.
As with the 2-aminotetralin strictures, some interesting non-opioid activities derive from simply dissecting the morphine structure into simpler analogs.
As with the 2-aminotetralin strictures, some interesting non-opioid activities derive from simply dissecting the morphine structure into simpler analogs.
Another analog of morphine:
The stereochemistry at the amine may be off. Even though simpler in structure & not involving any fused ring systems, this would not be a simple synthesis project. Not found in Google search.
While R is the correct stereochemistry for potent dopaminergic activity in this series of 2-ATs, I found very little on the 6-hydroxy compound. There is a lot of interest in 6,7-ADTN:
A broad spectrum dopamine receptor agonist. Demonstrates a marked selectivity for the human dopamine D3 receptor. 6,7-ADTN and psychostimulants such as cocaine and amphetamine reduce excitatory synaptic transmission in the nucleus accumbens by activating presynaptic dopamine receptors.
A number of multi-step syntheses of 6,7-ADTN have been published, all low-yielding. The R stereochemistry has to be at least 97%.
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