Details
Stereochemistry | ACHIRAL |
Molecular Formula | C16H16N2S |
Molecular Weight | 268.377 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=C(C=C1)C2=CN3C(SC4=C3CCCC4)=N2
InChI
InChIKey=IMUKUMUNZJILCG-UHFFFAOYSA-N
InChI=1S/C16H16N2S/c1-11-6-8-12(9-7-11)13-10-18-14-4-2-3-5-15(14)19-16(18)17-13/h6-10H,2-5H2,1H3
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/24646317Curator's Comment: Description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/21362431 | https://www.ncbi.nlm.nih.gov/pubmed/21324703
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24646317
Curator's Comment: Description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/21362431 | https://www.ncbi.nlm.nih.gov/pubmed/21324703
Pifithrin-alpha is a small molecule p53 functional inhibitor reported to behave like an antiapoptotic agent in neurodegenerative models. Pifithrin-alpha is a prodrug that under physiological conditions
spontaneously undergoes ring closure to yield pifithrin-beta. Pifithrin-beta demonstrated antiproliferative and neuroprotective effects in vitro. Pifithrin-beta is able to activate the aryl hydrocarbon receptor (AhR) in a complete independent way of the p53 inhibition.
Originator
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10481009 | http://adisinsight.springer.com/drugs/800012866
Curator's Comment: Pifithrin-beta is cyclic Pifithrin-alpha, Pifithrin-alpha first described by Komarov et al
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL3201 Sources: https://www.ncbi.nlm.nih.gov/pubmed/21362431 |
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Target ID: CHEMBL4164 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24646317
10 μM pifithrin-β prevented apoptosis induced by the fibrillar non-β-amyloid component in human neuroblastoma SH-SY5Y cells
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SUBSTANCE RECORD