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Details

Stereochemistry ACHIRAL
Molecular Formula C21H25N7O2S
Molecular Weight 439.534
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GSK-356278

SMILES

CCN1N=CC2=C(NC3CCOCC3)C(=CN=C12)C4=NN=C(CC5=C(C)N=C(C)S5)O4

InChI

InChIKey=AWDJJMXJUOHGLC-UHFFFAOYSA-N
InChI=1S/C21H25N7O2S/c1-4-28-20-15(11-23-28)19(25-14-5-7-29-8-6-14)16(10-22-20)21-27-26-18(30-21)9-17-12(2)24-13(3)31-17/h10-11,14H,4-9H2,1-3H3,(H,22,25)

HIDE SMILES / InChI

Molecular Formula C21H25N7O2S
Molecular Weight 439.534
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

GlaxoSmithKline is developing GSK-356278 as a selective, brain-penetrant phosphodiesterase 4 (PDE4) inhibitor that demonstrates anxiolytic and cognition-enhancing effects. Small molecule phosphodiesterase (PDE) 4 inhibitors have long been known to show therapeutic benefit in various preclinical models of psychiatric and neurologic diseases because of their ability to elevate cAMP in various cell types of the central nervous system. The drug was studied for the treatment of Huntington's disease, depressive and anxiety disorders. GSK-356278 has completed phase I clinical trials for evaluation of the safety, tolerability, and pharmacokinetics in male volunteers with the therapeutic dose for future clinical development.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
8.6 null [pIC50]
8.8 null [pIC50]
8.7 null [pIC50]
PubMed

PubMed

TitleDatePubMed
Quantification of human brain PDE4 occupancy by GSK356278: A [(11)C](R)-rolipram PET study.
2018 Nov
Patents

Patents

Sample Use Guides

In Dosing Session 1, the subjects will be administered 0.5 mg GSK356278 and placebo in a fasted state. In Dosing Session 2, the subjects will be administered GSK356278 (0.5 mg and 1.5 mg) and placebo in a fasted state. In Dosing Session 3, the subjects will be administered GSK356278 (1.5 mg and 4 mg) and placebo in a fasted state.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 03:37:34 GMT 2023
Edited
by admin
on Sat Dec 16 03:37:34 GMT 2023
Record UNII
1QTA9P992C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GSK-356278
Common Name English
1H-PYRAZOLO(3,4-B)PYRIDIN-4-AMINE, 5-(5-((2,4-DIMETHYL-5-THIAZOLYL)METHYL)-1,3,4-OXADIAZOL-2-YL)-1-ETHYL-N-(TETRAHYDRO-2H-PYRAN-4-YL)-
Systematic Name English
GSK356278
Code English
Code System Code Type Description
EPA CompTox
DTXSID40222401
Created by admin on Sat Dec 16 03:37:34 GMT 2023 , Edited by admin on Sat Dec 16 03:37:34 GMT 2023
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FDA UNII
1QTA9P992C
Created by admin on Sat Dec 16 03:37:34 GMT 2023 , Edited by admin on Sat Dec 16 03:37:34 GMT 2023
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CAS
720704-34-7
Created by admin on Sat Dec 16 03:37:34 GMT 2023 , Edited by admin on Sat Dec 16 03:37:34 GMT 2023
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PUBCHEM
10252640
Created by admin on Sat Dec 16 03:37:34 GMT 2023 , Edited by admin on Sat Dec 16 03:37:34 GMT 2023
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DRUG BANK
DB12542
Created by admin on Sat Dec 16 03:37:34 GMT 2023 , Edited by admin on Sat Dec 16 03:37:34 GMT 2023
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