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Details

Stereochemistry ACHIRAL
Molecular Formula C24H27FN2O2.ClH
Molecular Weight 430.943
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LY-310762

SMILES

Cl.CC1(C)C(=O)N(CCN2CCC(CC2)C(=O)C3=CC=C(F)C=C3)C4=CC=CC=C14

InChI

InChIKey=BOCLFQZPFYNVFD-UHFFFAOYSA-N
InChI=1S/C24H27FN2O2.ClH/c1-24(2)20-5-3-4-6-21(20)27(23(24)29)16-15-26-13-11-18(12-14-26)22(28)17-7-9-19(25)10-8-17;/h3-10,18H,11-16H2,1-2H3;1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C24H27FN2O2
Molecular Weight 394.4818
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
249.0 nM [Ki]
Substance Class Chemical
Created
by admin
on Sat Dec 16 18:58:29 GMT 2023
Edited
by admin
on Sat Dec 16 18:58:29 GMT 2023
Record UNII
BUX78WM9U2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LY-310762
Code English
2H-INDOL-2-ONE, 1-(2-(4-(4-FLUOROBENZOYL)-1-PIPERIDINYL)ETHYL)-1,3-DIHYDRO-3,3-DIMETHYL-, MONOHYDROCHLORIDE
Systematic Name English
LY 310762 HYDROCHLORIDE
Common Name English
2H-INDOL-2-ONE, 1-(2-(4-(4-FLUOROBENZOYL)-1-PIPERIDINYL)ETHYL)-1,3-DIHYDRO-3,3-DIMETHYL-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID80474689
Created by admin on Sat Dec 16 18:58:29 GMT 2023 , Edited by admin on Sat Dec 16 18:58:29 GMT 2023
PRIMARY
PUBCHEM
11957576
Created by admin on Sat Dec 16 18:58:29 GMT 2023 , Edited by admin on Sat Dec 16 18:58:29 GMT 2023
PRIMARY
FDA UNII
BUX78WM9U2
Created by admin on Sat Dec 16 18:58:29 GMT 2023 , Edited by admin on Sat Dec 16 18:58:29 GMT 2023
PRIMARY
CAS
192927-92-7
Created by admin on Sat Dec 16 18:58:29 GMT 2023 , Edited by admin on Sat Dec 16 18:58:29 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
ANTAGONIST