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🌟🌟 Social 🌟🌟 Rectify's molecular poetry thread

BOUNCE: It's Legal! Let The Good Times Roll.

1-phenyl-1-carbomethoxy-2-methylaminopropane.png


1-phenyl-1-carbomethoxy-2-methylaminopropane
 
The Saoshyant's 3rd Major Discovery After 1. EVELYN For Longer Life 2. BOUNCE For Pure Hedonistic Imperative And Now 3. HYDROXYCILLIN As An Antibacterial Physical Rejuvenator.
 
This Just In.

HYDROXYCILLIN

Very Nice, But I Don't Think It's Going To Save The World Or Anything.
 
Not Entirely Sure If These Exist.

N-ethynyl-1-phenyl-2-aminopropane.png


TOM
N-ethynyl-1-phenyl-2-aminopropane

N-ethynyl-1-(4-methoxyphenyl)-2-aminopropane.png


RICHARD
N-ethynyl-1-(4-methoxyphenyl)-2-aminopropane

N-ethynyl-1-(3,4-methylenedioxyphenyl)-2-aminopropane.png


HARRY
N-ethynyl-1-(3,4-methylenedioxyphenyl)-2-aminopropane
 
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en.wikipedia.org

Desmethylselegiline - Wikipedia

en.wikipedia.org en.wikipedia.org

Fair to say it's in the public domain Well, the (R) enantiomer anyway.

Now it opens up some interesting questions. Does it blockade the tetrabenzapine (TBZ) and/or the reserpine site? Is the action of selegine partly mediated by desmethylsegeline with the medicine itself acting on the reserpine site but it's active metabolite action ad the TBZ site?

I'm sure the data is out there somewhere but I got to see the fallout 4MTA caused from close quarters so I'm extremely cautious when a design might possess significant MAOI activity. The (S) enatiomer may actually be more active BUT would also have 'side effects' like CNS stimulation. I don't know the answer to that either but the fact that from day one the medicine wasn't the raecemate does rather suggest that for whatever reasons, it was cosidered inferior... but who knows why?
 
Smyth2 said:
No it exists all right. https://pubchem.ncbi.nlm.nih.gov/compound/14475299

Are you batting for MAOI's like selegiline?
Click to expand...

Not really. I took selegiline 1x and didn't feel much. More like looking for "barely legal" meth, pma, and mda. Each one of each I have had before but, for a variety of reasons, don't have now; mainly, penury and Schedule I status. (Schedule II in the case of meth, but although I did well on the MCAT, I am no medical doctor.)
 
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"And, If It All Turned Out The Way We Knew It Wouldn't, I'd Know." - The Connells, "Ring."
 
1-(indole-3-yl)-N,N-diethynyl-2-aminoethane.png


FLOTSAM
1-(indole-3-yl)-N,N-diethynyl-2-aminoethane

N,N-diethynyl-lysergamide.png


JETSAM
N,N-diethynyl-lysergamide
 
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1-(5-methoxyindole-3-yl)-N,N-diethynyl-2-aminoethane.png


JAMES
1-(5-methoxyindole-3-yl)-N,N-diethynyl-2-aminoethane

1-(4-hydroxyindole-3-yl)-N,N-diethynyl-2-aminoethane.png


LEE
1-(4-hydroxyindole-3-yl)-N,N-diethynyl-2-aminoethane
 
1-(4-ethynyl-2,5-dimethoxyphenyl)-2-aminoethane.png


ALLEN
1-(4-ethynyl-2,5-dimethoxyphenyl)-2-aminoethane

1-(4-ethynyl-2,5-dimethoxyphenyl)-2-aminopropane.png


DARRELL
1-(4-ethynyl-2,5-dimethoxyphenyl)-2-aminopropane
 
4DQSAR said:
en.wikipedia.org

Desmethylselegiline - Wikipedia

en.wikipedia.org en.wikipedia.org

The (S) enatiomer may actually be more active BUT would also have 'side effects' like CNS stimulation. I don't know the answer to that either but the fact that from day one the medicine wasn't the raecemate does rather suggest that for whatever reasons, it was cosidered inferior... but who knows why?
Click to expand...

Because

N-methyl-N-(prop-2-ynyl)-1-phenyl-2-(2S)-methyl-2-aminoethane.png


(S)-SELEGILINE
N-methyl-N-(prop-2-ynyl)-1-phenyl-2-(2S)-methyl-2-aminoethane

Would Be Too Stimulating, Probably. Which Is Pretty Much What You Are Saying, I Think.
 
These 2 May Not Be All That Active, But Imma Share Anyway. Maybe As Antidepressants?

N-(prop-2-ynyl)-1-phenyl-2-aminopropane.png


TRICKY
N-(prop-2-ynyl)-1-phenyl-2-aminopropane

N-(prop-2-ynyl)-1-(3,4-methylenedioxyphenyl)-2-aminopropane.png


BOY_GEORGE
N-(prop-2-ynyl)-1-(3,4-methylenedioxyphenyl)-2-aminopropane
 
1-(3,4,5-trimethoxyphenyl)-2-aminoethyne.png


STR8
1-(3,4,5-trimethoxyphenyl)-2-aminoethyne

But

1-(indole-3-yl)-2-dimethylaminoethyne.png


GR8
1-(indole-3-yl)-2-dimethylaminoethyne

And

1-(5-methoxyindole-3-yl)-2-dimethylaminoethyne.png


GR8ER
.1-(5-methoxyindole-3-yl)-2-dimethylaminoethyne
 
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