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Details

Stereochemistry UNKNOWN
Molecular Formula C15H20N2
Molecular Weight 228.3327
Optical Activity ( + )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SDZ SER-082

SMILES

[H][C@]12CCN(C)C[C@@]1([H])C3=CC=CC4=C3N(CC4)C2

InChI

InChIKey=YASBOGFWAMXINH-TZMCWYRMSA-N
InChI=1S/C15H20N2/c1-16-7-5-12-9-17-8-6-11-3-2-4-13(15(11)17)14(12)10-16/h2-4,12,14H,5-10H2,1H3/t12-,14-/m1/s1

HIDE SMILES / InChI

Molecular Formula C15H20N2
Molecular Weight 228.3327
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P41595
Gene ID: 3357.0
Gene Symbol: HTR2B
Target Organism: Homo sapiens (Human)
Target ID: P28335
Gene ID: 3358.0
Gene Symbol: HTR2C
Target Organism: Homo sapiens (Human)
7.8 null [pKd]
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:41:07 GMT 2023
Edited
by admin
on Sat Dec 16 17:41:07 GMT 2023
Record UNII
M7FHF24Q22
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SDZ SER-082
Code English
(+)-CIS 4,5,7A,8,9,10,11,11A-OCTAHYDRO-7H-10-METHYLINDOLO(1,7-BC)(2,6)-NAPHTHYRIDINE
Systematic Name English
7H-INDOLO(1,7-BC)(2,6)NAPHTHYRIDINE, 4,5,7A,8,9,10,11,11A-OCTAHYDRO-10-METHYL-, CIS-(+)-
Systematic Name English
Code System Code Type Description
PUBCHEM
9859407
Created by admin on Sat Dec 16 17:41:08 GMT 2023 , Edited by admin on Sat Dec 16 17:41:08 GMT 2023
PRIMARY
CAS
141474-59-1
Created by admin on Sat Dec 16 17:41:08 GMT 2023 , Edited by admin on Sat Dec 16 17:41:08 GMT 2023
PRIMARY
WIKIPEDIA
SDZ_SER-082
Created by admin on Sat Dec 16 17:41:08 GMT 2023 , Edited by admin on Sat Dec 16 17:41:08 GMT 2023
PRIMARY
IUPHAR
195
Created by admin on Sat Dec 16 17:41:08 GMT 2023 , Edited by admin on Sat Dec 16 17:41:08 GMT 2023
PRIMARY
FDA UNII
M7FHF24Q22
Created by admin on Sat Dec 16 17:41:08 GMT 2023 , Edited by admin on Sat Dec 16 17:41:08 GMT 2023
PRIMARY
EPA CompTox
DTXSID001028477
Created by admin on Sat Dec 16 17:41:08 GMT 2023 , Edited by admin on Sat Dec 16 17:41:08 GMT 2023
PRIMARY
CAS
141474-54-6
Created by admin on Sat Dec 16 17:41:08 GMT 2023 , Edited by admin on Sat Dec 16 17:41:08 GMT 2023
NON-SPECIFIC STEREOCHEMISTRY
Related Record Type Details
TARGET -> INHIBITOR
Acts as a mixed antagonist for the 5-HT2B and 5-HT2C serotonin receptors, with good selectivity over other serotonin receptor subtypes and slight preference for 5-HT2C over 5-HT2B.
ANTAGONIST
TARGET -> INHIBITOR
Acts as a mixed antagonist for the 5-HT2B and 5-HT2C serotonin receptors, with good selectivity over other serotonin receptor subtypes and slight preference for 5-HT2C over 5-HT2B.
ANTAGONIST