Details
Stereochemistry | ACHIRAL |
Molecular Formula | C14H16ClN3O4S2 |
Molecular Weight | 389.878 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)NC1=NC(C)=C(S1)C2=CC=C(Cl)C(=C2)S(=O)(=O)NCCO
InChI
InChIKey=JFVNFXCESCXMBC-UHFFFAOYSA-N
InChI=1S/C14H16ClN3O4S2/c1-8-13(23-14(17-8)18-9(2)20)10-3-4-11(15)12(7-10)24(21,22)16-5-6-19/h3-4,7,16,19H,5-6H2,1-2H3,(H,17,18,20)
Molecular Formula | C14H16ClN3O4S2 |
Molecular Weight | 389.878 |
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/16647110Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/20510927
Sources: https://www.ncbi.nlm.nih.gov/pubmed/16647110
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/20510927
PIK-93 is the two most potent and multitargeted synthetic PI3-K inhibitors that have been reported. PIK-93 inhibits PI3Kγ and PI4KIIIβ, with IC50 values of 16 nM and 19 nM, respectively. PIK-93 also inhibits other members of PI3Ks, including PI3Kα, β, and δ, with IC50 values of 39 nM, 0.59 uM, and 0.12 uM, respectively. PIK-93 shows no obvious inhibitory effect against a panel of other kinases, even at a concentration of 10 uM. PIK-93 was identified as a potent anti-enterovirus compound. PIK-93 targeted PI4Kβ to inhibit interaction of viral 3D polymerase and phosphatidylinositol 4-phosphate on the reorganized membrane vesicle for viral replication complex formation. PIK-93 may provide a basis for the design of new classes of therapeutics against viral RNA replication.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL4005 Sources: https://www.ncbi.nlm.nih.gov/pubmed/16647110 |
39.0 nM [IC50] | ||
Target ID: CHEMBL3267 |
16.0 nM [IC50] | ||
Target ID: CHEMBL3142 |
64.0 nM [IC50] | ||
Target ID: CHEMBL3130 Sources: https://www.ncbi.nlm.nih.gov/pubmed/16647110 |
120.0 nM [IC50] | ||
Target ID: CHEMBL3268 Sources: https://www.ncbi.nlm.nih.gov/pubmed/16647110 |
19.0 nM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
A pharmacological map of the PI3-K family defines a role for p110alpha in insulin signaling. | 2006 May 19 |
|
Viral reorganization of the secretory pathway generates distinct organelles for RNA replication. | 2010 May 28 |
|
Involvement of phosphoinositide 3-kinase and PTEN protein in mechanism of activation of TRPC6 protein in vascular smooth muscle cells. | 2012 May 18 |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/22493444
In T6.11 cells, PIK-93 (300 nM) reduces carbachol-induced translocation of TRPC6 to the plasma membrane and net Ca2+ entry.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 15:30:13 GMT 2023
by
admin
on
Sat Dec 16 15:30:13 GMT 2023
|
Record UNII |
QS3XFL5JRX
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
DTXSID30425868
Created by
admin on Sat Dec 16 15:30:13 GMT 2023 , Edited by admin on Sat Dec 16 15:30:13 GMT 2023
|
PRIMARY | |||
|
593960-11-3
Created by
admin on Sat Dec 16 15:30:13 GMT 2023 , Edited by admin on Sat Dec 16 15:30:13 GMT 2023
|
PRIMARY | |||
|
6852167
Created by
admin on Sat Dec 16 15:30:13 GMT 2023 , Edited by admin on Sat Dec 16 15:30:13 GMT 2023
|
PRIMARY | |||
|
QS3XFL5JRX
Created by
admin on Sat Dec 16 15:30:13 GMT 2023 , Edited by admin on Sat Dec 16 15:30:13 GMT 2023
|
PRIMARY |