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Fórmula empírica (notación de Hill):
C22H26N2O5
Número CAS:
Peso molecular:
398.45
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
Servicio técnico
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Permítanos ayudarlestorage temp.
−20°C
SMILES string
O=C(N[C@@H](C(C)C)C(N[C@H](C(O)=O)CC1=CC=CC=C1)=O)OCC2=CC=CC=C2
InChI
1S/C22H26N2O5/c1-15(2)19(24-22(28)29-14-17-11-7-4-8-12-17)20(25)23-18(21(26)27)13-16-9-5-3-6-10-16/h3-12,15,18-19H,13-14H2,1-2H3,(H,23,25)(H,24,28)(H,26,27)
InChI key
XINBRUNUJFZFGH-UHFFFAOYSA-N
Clase de almacenamiento
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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D Sindram et al.
Transplantation, 68(1), 136-140 (1999-07-31)
Cold preservation of the liver followed by reperfusion results in sinusoidal endothelial cell (SEC) apoptosis. Calpain-like activity is dramatically increased during reperfusion and inhibition of calpains results in lower graft injury and longer survival. Recently, calpains have been implicated in
V Kohli et al.
Gastroenterology, 116(1), 168-178 (1998-12-31)
Calpain proteases have been implicated in cell death by necrosis and more recently by apoptosis. Experiments were designed to determine the role of calpain proteases in ischemic rat liver injury by measurement of cytosolic calpain activity after different periods of
Heike Weber et al.
International journal of experimental pathology, 90(4), 387-399 (2009-08-08)
The cytosolic cysteine protease calpain is implicated in a multitude of cellular functions but also plays a role in cell damage. Our previous results suggest that an activation of calpain accompanied by a decrease in its endogenous inhibitor calpastatin may