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
SMILES
COC1=CC=CC(\C=N\N(C(=O)C(F)(F)F)C2=C(C)C=C(C)C=C2)=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+
Approval Year
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Code | English | ||
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Systematic Name | English | ||
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Code | English |
Code System | Code | Type | Description | ||
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1807913-16-1
Created by
admin on Sat Dec 16 01:30:19 GMT 2023 , Edited by admin on Sat Dec 16 01:30:19 GMT 2023
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PRIMARY | |||
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1146963-51-0
Created by
admin on Sat Dec 16 01:30:19 GMT 2023 , Edited by admin on Sat Dec 16 01:30:19 GMT 2023
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NON-SPECIFIC STEREOCHEMISTRY | |||
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DB13957
Created by
admin on Sat Dec 16 01:30:19 GMT 2023 , Edited by admin on Sat Dec 16 01:30:19 GMT 2023
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PRIMARY | |||
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25229652
Created by
admin on Sat Dec 16 01:30:19 GMT 2023 , Edited by admin on Sat Dec 16 01:30:19 GMT 2023
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PRIMARY | |||
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J147
Created by
admin on Sat Dec 16 01:30:19 GMT 2023 , Edited by admin on Sat Dec 16 01:30:19 GMT 2023
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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. | ||
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J147
Created by
admin on Sat Dec 16 01:30:19 GMT 2023 , Edited by admin on Sat Dec 16 01:30:19 GMT 2023
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PRIMARY | |||
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J147
Created by
admin on Sat Dec 16 01:30:19 GMT 2023 , Edited by admin on Sat Dec 16 01:30:19 GMT 2023
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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. | ||
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Z41H3C5BT9
Created by
admin on Sat Dec 16 01:30:19 GMT 2023 , Edited by admin on Sat Dec 16 01:30:19 GMT 2023
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PRIMARY |
ACTIVE MOIETY