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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H24BrN3O
Molecular Weight 402.328
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BROMOLYSERGIDE

SMILES

CCN(CC)C(=O)[C@H]1CN(C)[C@@H]2CC3=C(Br)NC4=C3C(=CC=C4)C2=C1

InChI

InChIKey=VKRAXSZEDRWLAG-SJKOYZFVSA-N
InChI=1S/C20H24BrN3O/c1-4-24(5-2)20(25)12-9-14-13-7-6-8-16-18(13)15(19(21)22-16)10-17(14)23(3)11-12/h6-9,12,17,22H,4-5,10-11H2,1-3H3/t12-,17-/m1/s1

HIDE SMILES / InChI

Molecular Formula C20H24BrN3O
Molecular Weight 402.328
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
The non-hallucinogen 2-bromo-lysergic acid diethylamide as preventative treatment for cluster headache: an open, non-randomized case series.
2010-09
Acquisition session length modulates consolidation effects produced by 5-HT2C ligands in a mouse autoshaping-operant procedure.
2010-03
The time-course for up- and down-regulation of the cortical 5-hydroxytryptamine (5-HT)2A receptor density predicts 5-HT2A receptor-mediated behavior in the rabbit.
2007-10
Selective and nonselective serotonin antagonists block the aversive stimulus properties of MK212 and m-chlorophenylpiperazine (mCPP) in mice.
2005-12
Selective remodeling of rabbit frontal cortex: relationship between 5-HT2A receptor density and associative learning.
2004-04
Serotonergic and dopaminergic influence of the duration of embryogenesis and intracapsular locomotion of Lymnaea stagnalis L.
2004
Role of the serotonin 5-HT(2A) receptor in learning.
2003-10-15
5-HT2A receptor-stimulated phosphoinositide hydrolysis in the stimulus effects of hallucinogens.
2002-05
Selective and divergent regulation of cortical 5-HT(2A) receptors in rabbit.
2001-12
Cloning of a novel human serotonin receptor (5-HT7) positively linked to adenylate cyclase.
1993-11-05
Molecular cloning of a mammalian serotonin receptor that activates adenylate cyclase.
1993-08
Cloning and expression of a novel serotonin receptor with high affinity for tricyclic psychotropic drugs.
1993-03
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:54:11 GMT 2025
Edited
by admin
on Mon Mar 31 17:54:11 GMT 2025
Record UNII
JUA77QEU32
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BOL-148
Preferred Name English
BROMOLYSERGIDE
MI  
Common Name English
2-BROMO-LSD
Common Name English
2-BROMO-N,N-DIETHYL-D-LYSERGAMIDE
Common Name English
BROMO-LSD
Common Name English
BROMOLYSERGIDE [MI]
Common Name English
BOL148
Code English
Code System Code Type Description
CAS
478-84-2
Created by admin on Mon Mar 31 17:54:11 GMT 2025 , Edited by admin on Mon Mar 31 17:54:11 GMT 2025
PRIMARY
FDA UNII
JUA77QEU32
Created by admin on Mon Mar 31 17:54:11 GMT 2025 , Edited by admin on Mon Mar 31 17:54:11 GMT 2025
PRIMARY
WIKIPEDIA
2-BROMO-LSD
Created by admin on Mon Mar 31 17:54:11 GMT 2025 , Edited by admin on Mon Mar 31 17:54:11 GMT 2025
PRIMARY
PUBCHEM
10171
Created by admin on Mon Mar 31 17:54:11 GMT 2025 , Edited by admin on Mon Mar 31 17:54:11 GMT 2025
PRIMARY
MERCK INDEX
m2703
Created by admin on Mon Mar 31 17:54:11 GMT 2025 , Edited by admin on Mon Mar 31 17:54:11 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID30878496
Created by admin on Mon Mar 31 17:54:11 GMT 2025 , Edited by admin on Mon Mar 31 17:54:11 GMT 2025
PRIMARY
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SALT/SOLVATE -> PARENT
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ACTIVE MOIETY