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
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)
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.
CNS Activity
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL254 Sources: https://www.ncbi.nlm.nih.gov/pubmed/24784567 |
8.6 null [pIC50] | ||
Target ID: CHEMBL275 Sources: https://www.ncbi.nlm.nih.gov/pubmed/24784567 |
8.8 null [pIC50] | ||
Target ID: CHEMBL288 Sources: https://www.ncbi.nlm.nih.gov/pubmed/24784567 |
8.7 null [pIC50] |
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT01031186
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
Edited
Sat Dec 16 03:37:34 GMT 2023
by
admin
on
Sat Dec 16 03:37:34 GMT 2023
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Record UNII |
1QTA9P992C
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Record Status |
Validated (UNII)
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Record Version |
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