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Details

Stereochemistry ACHIRAL
Molecular Formula C13H21NO3
Molecular Weight 239.3112
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ISOPROSCALINE

SMILES

CC(C)Oc1c(cc(CCN)cc1OC)OC

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

HIDE SMILES / InChI

Molecular Formula C13H21NO3
Molecular Weight 239.3112
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 Sat Jun 26 02:39:57 UTC 2021
Edited
by admin
on Sat Jun 26 02:39:57 UTC 2021
Record UNII
7W67II88GC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ISOPROSCALINE
Common Name English
4-(I)-PROPOXY-3,5-DIMETHOXYPHENETHYLAMINE
Common Name English
BENZENEETHANAMINE, 3,5-DIMETHOXY-4-(1-METHYLETHOXY)-
Systematic Name English
2-(4-ISOPROPOXY-3,5-DIMETHOXY-PHENYL)-ETHYLAMINE
Systematic Name English
Code System Code Type Description
FDA UNII
7W67II88GC
Created by admin on Sat Jun 26 02:39:58 UTC 2021 , Edited by admin on Sat Jun 26 02:39:58 UTC 2021
PRIMARY
PUBCHEM
15102787
Created by admin on Sat Jun 26 02:39:58 UTC 2021 , Edited by admin on Sat Jun 26 02:39:58 UTC 2021
PRIMARY
EPA CompTox
64778-72-9
Created by admin on Sat Jun 26 02:39:58 UTC 2021 , Edited by admin on Sat Jun 26 02:39:58 UTC 2021
PRIMARY
CAS
64778-72-9
Created by admin on Sat Jun 26 02:39:58 UTC 2021 , Edited by admin on Sat Jun 26 02:39:58 UTC 2021
PRIMARY
WIKIPEDIA
ISOPROSCALINE
Created by admin on Sat Jun 26 02:39:58 UTC 2021 , Edited by admin on Sat Jun 26 02:39:58 UTC 2021
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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ACTIVE MOIETY