Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H21NO3 |
| Molecular Weight | 239.3107 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(CCN)=CC(OC)=C1OC(C)C
InChI
InChIKey=UBNHYNYMUORHAM-UHFFFAOYSA-N
InChI=1S/C13H21NO3/c1-9(2)17-13-11(15-3)7-10(5-6-14)8-12(13)16-4/h7-9H,5-6,14H2,1-4H3
| Molecular Formula | C13H21NO3 |
| Molecular Weight | 239.3107 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:08:26 GMT 2025
by
admin
on
Mon Mar 31 23:08:26 GMT 2025
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| Record UNII |
7W67II88GC
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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WIKIPEDIA |
PiHKAL
Created by
admin on Mon Mar 31 23:08:26 GMT 2025 , Edited by admin on Mon Mar 31 23:08:26 GMT 2025
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WIKIPEDIA |
Designer-drugs-Isoproscaline
Created by
admin on Mon Mar 31 23:08:26 GMT 2025 , Edited by admin on Mon Mar 31 23:08:26 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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7W67II88GC
Created by
admin on Mon Mar 31 23:08:26 GMT 2025 , Edited by admin on Mon Mar 31 23:08:26 GMT 2025
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PRIMARY | |||
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15102787
Created by
admin on Mon Mar 31 23:08:26 GMT 2025 , Edited by admin on Mon Mar 31 23:08:26 GMT 2025
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PRIMARY | |||
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DTXSID70215088
Created by
admin on Mon Mar 31 23:08:26 GMT 2025 , Edited by admin on Mon Mar 31 23:08:26 GMT 2025
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PRIMARY | |||
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64778-72-9
Created by
admin on Mon Mar 31 23:08:26 GMT 2025 , Edited by admin on Mon Mar 31 23:08:26 GMT 2025
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PRIMARY | |||
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ISOPROSCALINE
Created by
admin on Mon Mar 31 23:08:26 GMT 2025 , Edited by admin on Mon Mar 31 23:08:26 GMT 2025
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PRIMARY | Isoproscaline or 4-(i)-propoxy-3,5-dimethoxyphenethylamine is an analogue of mescaline. It is closely related to proscaline and was first synthesized by David E. Nichols. It produces hallucinogenic, psychedelic, and entheogenic effects. Little is known about the psychopharmacological effects of isoproscaline. Alexander Shulgin lists a psychedelic dosage as being 40?80 mg, with effects lasting 12?18 hours. The mechanism that produces the hallucinogenic and entheogenic effects of isoproscaline is most likely to result from action as a 5-HT2A serotonin receptor agonist in the brain, a mechanism of action shared by all of the hallucinogenic tryptamines and phenethylamines. |
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TARGET -> AGONIST |
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |
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