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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H14Cl2N2O
Molecular Weight 273.158
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GSK-2849446

SMILES

C[C@H](NC1=CC=C(C#N)C(Cl)=C1Cl)C(C)(C)O

InChI

InChIKey=KYBPRVBQMUAOFG-ZETCQYMHSA-N
InChI=1S/C12H14Cl2N2O/c1-7(12(2,3)17)16-9-5-4-8(6-15)10(13)11(9)14/h4-5,7,16-17H,1-3H3/t7-/m0/s1

HIDE SMILES / InChI

Molecular Formula C12H14Cl2N2O
Molecular Weight 273.158
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 07:57:15 GMT 2023
Edited
by admin
on Sat Dec 16 07:57:15 GMT 2023
Record UNII
G6UPC5EU71
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GSK-2849446
Common Name English
2,3-DICHLORO-4-(((1S)-2-HYDROXY-1,2-DIMETHYL-PROPYL)AMINO)BENZONITRILE
Systematic Name English
GSK-2849466A
Code English
GSK2849446
Common Name English
Code System Code Type Description
PUBCHEM
162623750
Created by admin on Sat Dec 16 07:57:15 GMT 2023 , Edited by admin on Sat Dec 16 07:57:15 GMT 2023
PRIMARY
FDA UNII
G6UPC5EU71
Created by admin on Sat Dec 16 07:57:15 GMT 2023 , Edited by admin on Sat Dec 16 07:57:15 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY
Official Title: A Single-center, Randomized, Blinded, Placebo-controlled Two-part Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of the Selective Androgen Receptor Modulator (SARM), GSK2849466, in Single and Repeat Doses, With and Without Food, in Healthy Male Subjects Purpose: This study is the first administration of GSK2849466 in humans. This will be a single centre, randomized, double-blind, placebo-controlled study, to investigate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of GSK2849466, given as single and repeat oral doses up to 14 days to healthy male subjects. Part A will be a randomized placebo controlled and 4-way crossover study. It will include two cohorts of 8 subjects each. In each cohort there will be 4 study periods each approximately of 1 week including 6 days of washout.
ACTIVE MOIETY
Originator: GlaxoSmithKline; Mechanism of Action: Selective androgen receptor modulator; Orphan Drug Status: No; On Fast track: No; New Molecular Entity: Yes; Highest Development Phases: Discontinued for Cachexia, Heart failure; Most Recent Events: 23 Jun 2014 Adverse events and pharmacokinetics data from a phase I trial in Healthy volunteers presented at the Joint Meeting of the 16th International Congress of Endocrinology and the 96th Annual Meeting of the Endocrine Society (ICE/ENDO-2014), 01 Feb 2014 Discontinued - Phase-I for Cachexia (In volunteers) in USA (PO) (GlaxoSmithKline pipeline, February 2014), 01 Feb 2014 Discontinued - Phase-I for Heart failure in USA (PO) (GlaxoSmithKline pipeline, February 2014)