U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C18H17F3N2O2
Molecular Weight 350.335
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of J-147

SMILES

COC1=CC(\C=N\N(C(=O)C(F)(F)F)C2=CC=C(C)C=C2C)=CC=C1

InChI

InChIKey=HYMZAYGFKNNHDN-SSDVNMTOSA-N
InChI=1S/C18H17F3N2O2/c1-12-7-8-16(13(2)9-12)23(17(24)18(19,20)21)22-11-14-5-4-6-15(10-14)25-3/h4-11H,1-3H3/b22-11+

HIDE SMILES / InChI

Molecular Formula C18H17F3N2O2
Molecular Weight 350.335
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q03265
Gene ID: 11946.0
Gene Symbol: Atp5a1
Target Organism: Mus musculus (Mouse)
20.0 nM [EC50]
PubMed

PubMed

TitleDatePubMed
Deciphering the 'Elixir of Life': Dynamic Perspectives into the Allosteric Modulation of Mitochondrial ATP Synthase by J147, a Novel Drug in the Treatment of Alzheimer's Disease.
2019-06
The mitochondrial ATP synthase is a shared drug target for aging and dementia.
2018-04
A novel neurotrophic drug for cognitive enhancement and Alzheimer's disease.
2011
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:53:01 GMT 2025
Edited
by admin
on Mon Mar 31 20:53:01 GMT 2025
Record UNII
Z41H3C5BT9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
J147
Preferred Name English
J-147
Code English
ACETIC ACID, 2,2,2-TRIFLUORO-, (2E)-1-(2,4-DIMETHYLPHENYL)-2-((3-METHOXYPHENYL)METHYLENE)HYDRAZIDE
Systematic Name English
ACETIC ACID, 2,2,2-TRIFLUORO-, 1-(2,4-DIMETHYLPHENYL)-2-((3-METHOXYPHENYL)METHYLENE)HYDRAZIDE
Systematic Name English
N-(2,4-DIMETHYLPHENYL)-2,2,2-TRIFLUORO-N-((E)-(3-METHOXYPHENYL)METHYLIDENEAMINO)ACETAMIDE
Systematic Name English
Code System Code Type Description
CAS
1807913-16-1
Created by admin on Mon Mar 31 20:53:01 GMT 2025 , Edited by admin on Mon Mar 31 20:53:01 GMT 2025
PRIMARY
CAS
1146963-51-0
Created by admin on Mon Mar 31 20:53:01 GMT 2025 , Edited by admin on Mon Mar 31 20:53:01 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
EPA CompTox
DTXSID501045787
Created by admin on Mon Mar 31 20:53:01 GMT 2025 , Edited by admin on Mon Mar 31 20:53:01 GMT 2025
PRIMARY
DRUG BANK
DB13957
Created by admin on Mon Mar 31 20:53:01 GMT 2025 , Edited by admin on Mon Mar 31 20:53:01 GMT 2025
PRIMARY
PUBCHEM
25229652
Created by admin on Mon Mar 31 20:53:01 GMT 2025 , Edited by admin on Mon Mar 31 20:53:01 GMT 2025
PRIMARY
WIKIPEDIA
J147
Created by admin on Mon Mar 31 20:53:01 GMT 2025 , Edited by admin on Mon Mar 31 20:53:01 GMT 2025
PRIMARY J147 is an experimental drug with reported effects against both Alzheimer's disease and ageing in mouse models of accelerated aging. The approach that lead to development of the J147 drug was to screen candidate molecules for anti-aging effects, instead of targeting the amyloid plaques. It is contrary to the most of other approaches to develop drugs against the Alzheimer's disease that target the plaque deposits in the brain. The J147 drug is also reported to address other biological aging factors, such as preventing the leakage of blood from microvessels in mice brains.
EC SCIENTIFIC COMMITTEE ON CONSUMER SAFETY OPINION
J147
Created by admin on Mon Mar 31 20:53:01 GMT 2025 , Edited by admin on Mon Mar 31 20:53:01 GMT 2025
PRIMARY
MANUFACTURER PRODUCT INFORMATION
J147
Created by admin on Mon Mar 31 20:53:01 GMT 2025 , Edited by admin on Mon Mar 31 20:53:01 GMT 2025
PRIMARY Potent neuroprotective and neurotrophic compound. Protects against neurotoxicity in cortical neurons in vitro (EC50 = 25 - 200 nM). Reduces soluble A.BETA.40 and A.BETA.42 levels and increases BDNF levels in the hippocampus in vivo. Enhances memory in wild type rats. Prevents memory deficits and rescues cognitive deficits in young and aged transgenic Alzheimer's disease mice, respectively. Orally active.
FDA UNII
Z41H3C5BT9
Created by admin on Mon Mar 31 20:53:01 GMT 2025 , Edited by admin on Mon Mar 31 20:53:01 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY