Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H12Cl2N2O |
Molecular Weight | 271.142 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)CC1=NC2=C(O)C(Cl)=CC(Cl)=C2C=C1
InChI
InChIKey=YZPOQCQXOSEMAZ-UHFFFAOYSA-N
InChI=1S/C12H12Cl2N2O/c1-16(2)6-7-3-4-8-9(13)5-10(14)12(17)11(8)15-7/h3-5,17H,6H2,1-2H3
Molecular Formula | C12H12Cl2N2O |
Molecular Weight | 271.142 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
PBT-1033, also known as PBT-2, is a neural protective agent potentially for the treatment of Alzheimer's disease and Huntington's Disease. PBT-1033 is a moderate-affinity 8-hydroxyquinoline transition metal-ligand that acts as a synthetic chaperone, re distributing copper, zinc, and iron from locations where they are abundant to subcellular locations where they might be deficient. Delivery of copper and zinc by PBT-1033 into the cytoplasm deactivates the kinase glycogen synthase kinase 3β and the phosphatase calcineurin, both potential targets for Huntington’s disease. In aged wild-type mice, PBT-1033 improves cognitive ability and markers of neuronal plasticity and function. In Alzheimer’s disease mouse models, PBT-1033 inhibits the accumulation of amyloid β, attenuates neuropathological effects of amyloid β, including amyloid-β-induced hyperphosphorylation of tau, and improves cognition. In a 12-week, phase 2a, randomized, double-blind, placebo-controlled trial in 78 individuals with mild Alzheimer’s dementia, PBT-1033 was safe and well tolerated and significantly reduced concentrations of amyloid β42 in CSF.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25467848
once daily 250 mg
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:32:32 GMT 2023
by
admin
on
Sat Dec 16 11:32:32 GMT 2023
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Record UNII |
Q7K6GJQ4O4
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Record Status |
Validated (UNII)
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PBT2
Created by
admin on Sat Dec 16 11:32:32 GMT 2023 , Edited by admin on Sat Dec 16 11:32:32 GMT 2023
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PRIMARY | PBT2 is an experimental drug candidate. It is a second-generation 8-hydroxyquinoline analog intended to be a successor to clioquinol and a potential treatment of Alzheimer's disease.Clinical trials: PBT2 was the subject of phase II clinical trials for Alzheimer's disease and Huntington's disease. The results for Alzheimer's disease failed to meet its goals, and there is no evidence that PBT2 is of any benefit in Alzheimer's dementia. The drug also missed efficacy goals for Huntington's disease. | ||
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Q7K6GJQ4O4
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admin on Sat Dec 16 11:32:32 GMT 2023 , Edited by admin on Sat Dec 16 11:32:32 GMT 2023
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ACTIVE MOIETY |
Class: Antidementia, Dimethylamine, Hydroxyquinoline, Ionophore, Small molecule; Mechanism of Action: Chelating agent; Orphan Drug Status: Yes for Huntington's disease; Available For Licensing: Yes for Alzheimer's disease; Highest Development Phases: Phase II Alzheimer's disease, Huntington's disease; Most Recent Events: 30 Jun 2015 Adverse events data from the IMAGINE Extension trial in Alzheimer's disease released by Prana Biotechnology, 15 Jun 2015 Phase-II development is ongoing for the treatment of Alzheimer's disease and Huntington's disease, 01 Jun 2015 PBT 2 receives Orphan Drug status for Huntington's disease in European Union
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ACTIVE MOIETY |
Drug Name: PBT-1033; Research Code: PBT-1033, PBT-2; MOA: Neural protective agent; Indication: Alzheimer's disease (AD), Huntington's disease; Status: Phase II (Active); Company: Prana (Originator)
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