G9512
Gly-Phe β-naphthylamide
crystalline
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关于此项目
经验公式（希尔记法）:
C21H21N3O2
化学文摘社编号:
分子量:
347.41
UNSPSC Code:
12352204
PubChem Substance ID:
MDL number:
form
crystalline
storage temp.
−20°C
SMILES string
NCC(N[C@@H](CC1=CC=CC=C1)C(NC2=CC3=CC=CC=C3C=C2)=O)=O
InChI
1S/C21H21N3O2/c22-14-20(25)24-19(12-15-6-2-1-3-7-15)21(26)23-18-11-10-16-8-4-5-9-17(16)13-18/h1-11,13,19H,12,14,22H2,(H,23,26)(H,24,25)
InChI key
YABDXPBHLDPMOA-UHFFFAOYSA-N
General description
Substrate for cathepsin C
Other Notes
Similar to G 4255, but produced by Sigma.
Yu Liu et al.
PloS one, 7(9), e45910-e45910 (2012-10-03)
Cancer cells invade by secreting enzymes that degrade the extracellular matrix and these are sequestered in lysosomal vesicles. In this study, the effects of the selective lysosome lysing drug GPN and the lysosome exocytosis inhibitor vacuolin-1 on lysosome exocytosis were
T O Berg et al.
The Biochemical journal, 300 ( Pt 1), 229-236 (1994-05-15)
Lysosome-disrupting enzyme substrates have been used to distinguish between lysosomal and prelysosomal compartments along the endocytic pathway in isolated rat hepatocytes. The cells were incubated for various periods of time with 125I-labelled tyramine cellobiose (125I-TC) covalently coupled to asialoorosomucoid (AOM)
T O Berg et al.
European journal of biochemistry, 221(1), 595-602 (1994-04-01)
In density-gradient analyses of autophagic vacuoles from isolated rat hepatocytes, autophagosomes could be recognized by the presence of an autophagically sequestered cytosolic enzyme, lactate dehydrogenase (LDH). Lysosomes were identified by marker enzymes such as acid phosphatase, or by degradation products
Gao-Feng Qiu et al.
Journal of biomedicine & biotechnology, 2009, 746289-746289 (2009-08-27)
Cathepsin C (CTSC) is a lysosomal cysteine protease belonging to the papain superfamily. Our previous study showed that CTSC precursor (zymogen) is localized exclusively in cortical rods (CRs) of mature oocyte in the kuruma prawn Marsupenaeus japonicus, suggesting that CTSC
A C de Vries et al.
Biochimica et biophysica acta, 922(3), 259-269 (1987-12-14)
We have recently shown that lamellar body fractions purified from human lung contain a distinct acid alpha-glucosidase distinguishable from lysosomal acid alpha-glucosidase in that it does not cross-react with antibodies raised against the lysosomal enzyme and does not bind to
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