Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C28H27NO3 |
| Molecular Weight | 425.5189 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=CC(=C1)C2=CC3=C(C=C2)N(CC4=CC=C(C=C4)C(C)(C)C)C=C3C(=O)C(O)=O
InChI
InChIKey=HSXLMAFNWCSZGP-UHFFFAOYSA-N
InChI=1S/C28H27NO3/c1-18-6-5-7-20(14-18)21-10-13-25-23(15-21)24(26(30)27(31)32)17-29(25)16-19-8-11-22(12-9-19)28(2,3)4/h5-15,17H,16H2,1-4H3,(H,31,32)
| Molecular Formula | C28H27NO3 |
| Molecular Weight | 425.5189 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Wyeth was developing the small molecule plasminogen activator inhibitor-1 (PAI-1) antagonist aleplasinin for the treatment of Alzheimer's disease in the US. PAZ-417 inhibits PAI-I (Plasminogen activator inhibitor-1), thereby increasing the activation of plasminogen to form plasmin. There is some evidence that plasmin can increase the cleavage of amyloid precursor protein at the alpha cleavage site, which could reduce the formation or increase the clearance of amyloid beta, a suspected culprit in Alzheimer's disease. However, it`s development for Alzheimer's disease treatment was discontinued.
Originator
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:06:10 GMT 2023
by
admin
on
Fri Dec 15 16:06:10 GMT 2023
|
| Record UNII |
LL56J87F3X
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C783
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admin on Fri Dec 15 16:06:10 GMT 2023 , Edited by admin on Fri Dec 15 16:06:10 GMT 2023
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10224267
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CHEMBL325424
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TT-15
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481629-87-2
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C76071
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300000034037
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8939
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DB12635
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DTXSID80197447
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LL56J87F3X
Created by
admin on Fri Dec 15 16:06:10 GMT 2023 , Edited by admin on Fri Dec 15 16:06:10 GMT 2023
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PRIMARY |
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