U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C21H25N3O
Molecular Weight 335.4427
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LSD-PIP

SMILES

[H][C@@]12CC3=CNC4=C3C(=CC=C4)C1=C[C@H](CN2C)C(=O)N5CCCCC5

InChI

InChIKey=URDULHYODQAQTM-DNVCBOLYSA-N
InChI=1S/C21H25N3O/c1-23-13-15(21(25)24-8-3-2-4-9-24)10-17-16-6-5-7-18-20(16)14(12-22-18)11-19(17)23/h5-7,10,12,15,19,22H,2-4,8-9,11,13H2,1H3/t15-,19-/m1/s1

HIDE SMILES / InChI

Molecular Formula C21H25N3O
Molecular Weight 335.4427
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:03:38 GMT 2023
Edited
by admin
on Sat Dec 16 17:03:38 GMT 2023
Record UNII
CKN3AJ58H9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LSD-PIP
Common Name English
D-LYSERGIC ACID PIPERIDIDE
Common Name English
(8β)-6-Methyl-8-(piperidin-1-ylcarbonyl)-9,10-didehydroergoline
Systematic Name English
PIPERIDINE, 1-LYSERGOYL-
Common Name English
(7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-yl)-piperidin-1-ylmethanone
Systematic Name English
NSC-210590
Code English
Code System Code Type Description
PUBCHEM
131879845
Created by admin on Sat Dec 16 17:03:38 GMT 2023 , Edited by admin on Sat Dec 16 17:03:38 GMT 2023
PRIMARY
WIKIPEDIA
LSD-Pip
Created by admin on Sat Dec 16 17:03:38 GMT 2023 , Edited by admin on Sat Dec 16 17:03:38 GMT 2023
PRIMARY
FDA UNII
CKN3AJ58H9
Created by admin on Sat Dec 16 17:03:38 GMT 2023 , Edited by admin on Sat Dec 16 17:03:38 GMT 2023
PRIMARY
EPA CompTox
DTXSID20308999
Created by admin on Sat Dec 16 17:03:38 GMT 2023 , Edited by admin on Sat Dec 16 17:03:38 GMT 2023
PRIMARY
NSC
210590
Created by admin on Sat Dec 16 17:03:38 GMT 2023 , Edited by admin on Sat Dec 16 17:03:38 GMT 2023
PRIMARY
CAS
50485-23-9
Created by admin on Sat Dec 16 17:03:38 GMT 2023 , Edited by admin on Sat Dec 16 17:03:38 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST