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Details

Stereochemistry ABSOLUTE
Molecular Formula C14H18N2
Molecular Weight 214.3061
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of WAY-163909

SMILES

[H][C@@]12CCC[C@]1([H])C3=CC=CC4=C3N2CCNC4

InChI

InChIKey=XOSKJKGKWRIMGV-DGCLKSJQSA-N
InChI=1S/C14H18N2/c1-3-10-9-15-7-8-16-13-6-2-4-11(13)12(5-1)14(10)16/h1,3,5,11,13,15H,2,4,6-9H2/t11-,13-/m1/s1

HIDE SMILES / InChI

Molecular Formula C14H18N2
Molecular Weight 214.3061
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 18:49:55 UTC 2023
Edited
by admin
on Sat Dec 16 18:49:55 UTC 2023
Record UNII
MN9LW8268N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
WAY-163909
Code English
(7BR,10AR)-2,3,4,7B,8,9,10,10A-OCTAHYDRO-1H-CYCLOPENTA(B)(1,4)DIAZEPINO(6,7,1-HI)INDOLE
Systematic Name English
WAY163909
Code English
WAY-163,909
Code English
8H-CYCLOPENTA(4,5)PYRROLO(3,2,1-JK)(1,4)BENZODIAZEPINE, 1,2,3,4,7A,9,10,10A-OCTAHYDRO-, (7BR,10AR)-
Systematic Name English
(7BR,10AR)-1,2,3,4,7A,9,10,10A-OCTAHYDRO-8H-CYCLOPENTA(4,5)PYRROLO(3,2,1-JK)(1,4)BENZODIAZEPINE
Systematic Name English
Code System Code Type Description
PUBCHEM
10130594
Created by admin on Sat Dec 16 18:49:55 UTC 2023 , Edited by admin on Sat Dec 16 18:49:55 UTC 2023
PRIMARY
EPA CompTox
DTXSID40436021
Created by admin on Sat Dec 16 18:49:55 UTC 2023 , Edited by admin on Sat Dec 16 18:49:55 UTC 2023
PRIMARY
FDA UNII
MN9LW8268N
Created by admin on Sat Dec 16 18:49:55 UTC 2023 , Edited by admin on Sat Dec 16 18:49:55 UTC 2023
PRIMARY
WIKIPEDIA
WAY-163909
Created by admin on Sat Dec 16 18:49:55 UTC 2023 , Edited by admin on Sat Dec 16 18:49:55 UTC 2023
PRIMARY
CAS
428868-32-0
Created by admin on Sat Dec 16 18:49:55 UTC 2023 , Edited by admin on Sat Dec 16 18:49:55 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
20-and 46-fold binding selectivity over 5-HT2A and 5-HT2Breceptors,respectively.
Ki
OFF TARGET->WEAK AGONIST
Emax,40%
TARGET -> AGONIST
Emax, ~90%
EC50
Related Record Type Details
ACTIVE MOIETY