Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H11F3N2O |
Molecular Weight | 328.2879 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
FC(F)(F)C1=CC2=C(C=CC(\C=C\C(=O)C3=CC=NC=C3)=N2)C=C1
InChI
InChIKey=IAJOMYABKVAZCN-AATRIKPKSA-N
InChI=1S/C18H11F3N2O/c19-18(20,21)14-3-1-12-2-4-15(23-16(12)11-14)5-6-17(24)13-7-9-22-10-8-13/h1-11H/b6-5+
Molecular Formula | C18H11F3N2O |
Molecular Weight | 328.2879 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Optical Activity | NONE |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:55:25 GMT 2023
by
admin
on
Sat Dec 16 10:55:25 GMT 2023
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Record UNII |
2HOK1JQ203
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Record Status |
Validated (UNII)
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Record Version |
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2HOK1JQ203
Created by
admin on Sat Dec 16 10:55:25 GMT 2023 , Edited by admin on Sat Dec 16 10:55:25 GMT 2023
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PFK-158 FREE BASE
Created by
admin on Sat Dec 16 10:55:25 GMT 2023 , Edited by admin on Sat Dec 16 10:55:25 GMT 2023
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PRIMARY | MedKoo CAT NO.: 206166, CAS NO.: 1462249-75-7Description: PFK-158, also known as ACT-PFK-158, is an inhibitor of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatases (PFK-2/FBPase) isoform 3 (PFKFB3) with potential antineoplastic activity. Upon administration, PFKFB3 inhibitor PFK-158 binds to and inhibits the activity of PFKFB3, which leads to the inhibition of both the glycolytic pathway in and glucose uptake by cancer cells. This prevents the production of macromolecules and energy that causes the enhanced cellular proliferation in cancer cells as compared to that of normal, healthy cells. Depriving cancer cells of nutrients and energy leads to the inhibition of cancer cell growth. (Last updated: 3/22/2016)Synonym: PFK158, PFK 158, PFK158, ACTPEK158. | ||
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1462249-75-7
Created by
admin on Sat Dec 16 10:55:25 GMT 2023 , Edited by admin on Sat Dec 16 10:55:25 GMT 2023
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71730058
Created by
admin on Sat Dec 16 10:55:25 GMT 2023 , Edited by admin on Sat Dec 16 10:55:25 GMT 2023
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
Originator: University of Louisville; Developer: Advanced Cancer Therapeutics; Class: Antineoplastic, Small molecule; Mechanism of Action: Glucose modulator, PFKFB3 protein inhibitor
Orphan Drug Status: No; On Fast track: No; New Molecular Entity: Yes; Highest Development Phase: Phase I for Solid tumours; Most Recent Events: 01 Mar 2014 Phase-I clinical trials in Solid tumours in USA (IV) (NCT02044861), 22 Jan 2014 Preclinical trials in Solid tumours in USA (IV), 22 Jan 2014 Advanced Cancer Therapeutics plans a phase I trial for Solid tumours (second-line therapy or greater, late-stage disease) in USA (NCT02044861)
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