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HCID 65663Erstellt: 1. November 2026

Aloxistatin

aloxistatin · E-64D · EST · ep453 · Estate · CS-1622 · oxistatin · NSC694281

https://huagongshe.com/de/chemical/65663

Molekülstruktur von Aloxistatin

Identifikatoren & physikalische Daten

CAS No.88321-09-9
SummenformelC17H30N2O5
Durchschnittliche Molmasse342,4 g/mol
Monoisotopische Masse342,21547206 g/mol
SMILESCCOC(=O)[C@H]1O[C@@H]1C(=O)N[C@@H](CC(C)C)C(=O)NCCC(C)C
InChIKeySRVFFFJZQVENJC-IHRRRGAJSA-N
PubChem CID65663
ChEMBLCHEMBL63440
ChEBICHEBI:101381
EC No.635-831-3
DTXSIDDTXSID00904150

Chemische & physikalische Eigenschaften

XLogP2,3
Polarare Oberfläche (TPSA)97
H-Brücken-Donoren2
H-Brücken-Akzeptoren5
Frei drehbare Bindungen11
Schwere Atome24
Formalladung0
Komplexität450
Schmelzpunkt126.2°C
Siedepunkt477.88°C (rough estimate)
Dichte1.0657 (rough estimate)
Brechungsindex1.5800 (estimate)
Lagerbedingungen-20°C
LöslichkeitSoluble in DMSO, DMF or ethanol
AggregatzustandWhite solid
pKa (Säurekonstante)13.32±0.40(Predicted)
FarbeFine needles from EtOH
Biologische Quellesynthetic (organic)
StabilitätStable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 1 month.
InChI1S/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
InChIKeySRVFFFJZQVENJC-IHRRRGAJSA-N
SMILESN([C@@H](CC(C)C)C(=O)NCCC(C)C)C(=O)[C@H]1O[C@@H]1C(=O)OCC

Sicherheit & Vorschriften

GHS-EinstufungWarningH315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 40 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard Classes and CategoriesSkin Irrit. 2 (100%)
Wassergefährdungsklasse (WGK)2
UN-Transportnummer3077
Zollcode29242990
RTECS-Nr.RR0404300
R-Sätze (R)36/37/38
Toxizitätcyt-ham:lng 200 mg/L IYKEDH 17,815,86
GefahrensymboleXi
Sicherheitshinweise (S)26-36-24/25
Lagerklasse11 - Combustible Solids

Anwendungen & Verwendung

Beschreibung

E-64d is an irreversible, membrane-permeable inhibitor of lysosomal and cytosolic cysteine proteases and has diverse biological activities. It is a synthetic analog of E-64 and prodrug form of E-64c that inhibits calpain and the cysteine proteases cathepsins F, -K, -B, -H, and -L. E-64d (20-200 μM) induces cell cycle arrest at the G2/M phase in A431 human epidermoid carcinoma cells. It inhibits protease-resistant prion protein accumulation in scrapie-infected neuroblastoma cells with an IC50 value of 0.5 μM. E-46d also inhibits entry of vesicular stomatitis virus (VSV) particles pseudotyped with severe acute respiratory syndrome coronavirus (SARS-CoV) or SARS-CoV-2 spike glycoprotein into Vero cells, an effect that is reduced by expression of the serine protease TMPRSS2.