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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
Structure of ALOXISTATIN

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

HIDE SMILES / InChI

Description
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.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Studies on myosin light chain phosphorylation in intact platelets, utilizing a cell-penetrating thiol protease inhibitor.
1988 Aug 15
Identification of glutathione conjugate formed from loxistatin in rats.
1989 May
Patents

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
Pretreatment of P39 cells with 50uM of E-64d (ALOXISTATIN) suppressed etoposide-induced activation of caspase-3 by 52% as compared with no pretreatment
Name Type Language
ALOXISTATIN
INN  
INN  
Official Name English
LOXISTATIN [JAN]
Common Name English
aloxistatin [INN]
Common Name English
NSC-694281
Code English
ETHYL (+)-(2S,3S)-2,3-EPOXY-N-((S)-1-(ISOPENTYLCARBAMOYL)-3-METHYLBUTYL)SUCCINAMATE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C783
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
FDA ORPHAN DRUG 874322
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
Code System Code Type Description
PUBCHEM
65663
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
PRIMARY
MESH
C108192
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
PRIMARY
EPA CompTox
DTXSID00904150
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
PRIMARY
ChEMBL
CHEMBL63440
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
PRIMARY
INN
6138
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
PRIMARY
FDA UNII
L5W337AOUR
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
PRIMARY
EVMPD
SUB05360MIG
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
PRIMARY
NCI_THESAURUS
C76907
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
PRIMARY
WIKIPEDIA
Aloxistatin
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
PRIMARY
NSC
694281
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
PRIMARY
SMS_ID
100000087467
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
PRIMARY
CAS
88321-09-9
Created by admin on Fri Dec 15 16:34:37 UTC 2023 , Edited by admin on Fri Dec 15 16:34:37 UTC 2023
PRIMARY