Details
Stereochemistry | ACHIRAL |
Molecular Formula | C16H13ClN2OS |
Molecular Weight | 316.805 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(Cl)C=C2N=C(NC(=O)CC3=CC=CC=C3)SC2=C1
InChI
InChIKey=DYHAMRNAHTWYKY-UHFFFAOYSA-N
InChI=1S/C16H13ClN2OS/c1-10-7-14-13(9-12(10)17)18-16(21-14)19-15(20)8-11-5-3-2-4-6-11/h2-7,9H,8H2,1H3,(H,18,19,20)
Molecular Formula | C16H13ClN2OS |
Molecular Weight | 316.805 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/21954091
Sources: https://www.ncbi.nlm.nih.gov/pubmed/21954091
LH846 targets casein kinase 1δ activity. It is able to regulate circadian rhythms.
Originator
Sources: https://www.ncbi.nlm.nih.gov/pubmed/21954091
Curator's Comment: 2011
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2828 Sources: https://www.ncbi.nlm.nih.gov/pubmed/21954091 |
290.0 nM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/21954091
The benzothiazole derivative LH846 (8 μM) lengthened the period (10 h) with minimal effect on the amplitude of both Per2-dLuc and Bmal1-dLuc rhythms in U2OS cells
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:38:12 GMT 2023
by
admin
on
Fri Dec 15 16:38:12 GMT 2023
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Record UNII |
RW5ZBU2L6P
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Record Status |
Validated (UNII)
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Record Version |
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