Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C17H30N2O5 |
Molecular Weight | 342.4305 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)[C@H]1O[C@@H]1C(=O)N[C@@H](CC(C)C)C(=O)NCCC(C)C
InChI
InChIKey=SRVFFFJZQVENJC-IHRRRGAJSA-N
InChI=1S/C17H30N2O5/c1-6-23-17(22)14-13(24-14)16(21)19-12(9-11(4)5)15(20)18-8-7-10(2)3/h10-14H,6-9H2,1-5H3,(H,18,20)(H,19,21)/t12-,13-,14-/m0/s1
Molecular Formula | C17H30N2O5 |
Molecular Weight | 342.4305 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/26388830Curator's Comment: Description was created based on several sources, including
http://www.selleckchem.com/products/Aloxistatin.html
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26388830
Curator's Comment: Description was created based on several sources, including
http://www.selleckchem.com/products/Aloxistatin.html
Aloxistatin (E64d) is an irreversible and membrane-permeable cysteine protease inhibitor. Aloxistatin was developed for treating muscular dystrophy. Open trials on 73 Duchene’s muscular dystrophy patients were conducted for 3 years at four Japanese national sanatoriums and resulted in some muscle strength improvement but the results were inconclusive and final double-blind studies did not confirm the results. Taisho has discontinued development of aloxistatin for the potential treatment of muscular dystrophy. The trials completed through Phase 3. In animal models Aloxistatin (100 mg/kg, p.o.) strongly inhibits the cathepsin B&L activities in the skeletal muscle, heart and liver of hamsters. In spinal cord injury (SCI) rats, Aloxistatin provides neuroprotection in SCI lesion and penumbra.Aloxistatin reduces brain amyloid-β and improves memory deficits in Alzheimer's disease animal models by inhibiting cathepsin B activity.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL4072 Sources: https://www.ncbi.nlm.nih.gov/pubmed/21613740 |
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Target ID: CHEMBL3891 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26388830 |
4.0 µM [IC50] | ||
Target ID: CHEMBL4143 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26388830 |
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Target ID: CHEMBL3837 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26388830 |
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Target ID: CHEMBL4071 |
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Target ID: CHEMBL2334 Sources: https://www.ncbi.nlm.nih.gov/pubmed/11306462 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
Sample Use Guides
In the first stage, 100mg was administered 3 times a day after meals for 1 day, and in the next stage, 100 mg was administered 3 times a day after meals for 7 consecutive days .
Route of Administration:
Unknown
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/11306462
Pretreatment of P39 cells with 50uM of E-64d (ALOXISTATIN) suppressed etoposide-induced activation of caspase-3 by 52% as compared with no pretreatment
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:34:37 GMT 2023
by
admin
on
Fri Dec 15 16:34:37 GMT 2023
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Record UNII |
L5W337AOUR
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Record Status |
Validated (UNII)
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Record Version |
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Systematic Name | English |
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NCI_THESAURUS |
C783
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FDA ORPHAN DRUG |
874322
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65663
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C108192
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DTXSID00904150
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CHEMBL63440
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6138
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L5W337AOUR
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SUB05360MIG
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C76907
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Aloxistatin
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694281
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100000087467
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88321-09-9
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Related Record | Type | Details | ||
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ACTIVE MOIETY |