10 Results for "

cathepsin X

" in MedChemExpress (MCE) Product Catalog:
Products (10)

10 Results for "cathepsin X" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-146985
CAS No.: 2418577-51-0
Purity:  99.62%
Target:  

Cathepsin

Research Areas:  

Neurological Disease Cancer

Cathepsin X-IN-1 (compound 25) is a potent Cathepsin X inhibitor with an IC50 of 7.13 µM. Cathepsin X-IN-1 decreases PC-3 cell migration with low cytotoxic .
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1
1 Cited Publications
Cat. No.: HY-P7758
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CTSZ; cathepsin IV; cathepsin Z; cathepsin B2; cathepsin X; cathepsin Z1; CTSX; cathepsin Y; Cysteine-Type Carboxypeptidase; cathepsin P; Lysosomal Carboxypeptidase B; Preprocathepsin P; Carboxypeptidase LB
Species:  
Human
Source:  
HEK293
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1
1 Cited Publications
Cat. No.: HY-P81163
Synonyms: cathepsin K; Procathepsin K; cathepsin K precursor; cathepsin O; cathepsin O1; cathepsin O2; cathepsin X; cathepsinK; CTS02; CTSK; CTSK protein; CTSO; CTSO1; CTSO2; MGC23107; PKND; PYCD; Pycnodysostosis; cath-K; CK.

Host:  

Rabbit

Application:  

WB, ELISA, IHC-P, IHC-F, ICC/IF

Reactivity:  

Rat

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Cat. No.: HY-W796158
CAS No.: 250584-13-5
Target:  

Cathepsin

Research Areas:  

Inflammation/Immunology

Z-DEVD-CMK is an irreversible inhibitor of most of the cathepsins in vitro .
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Cat. No.: HY-171045
CAS No.: 249618-84-6
Research Areas:  

Others

Abz-FRF(4NO2) is an Abz-tripeptide substrate commonly used for studying the activity of enzymes, especially cysteine proteases such as Cathepsin X .
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Cat. No.: HY-P7758A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CTSZ; cathepsin IV; cathepsin Z; cathepsin B2; cathepsin X; cathepsin Z1; CTSX; cathepsin Y; Cysteine-Type Carboxypeptidase; cathepsin P; Lysosomal Carboxypeptidase B; Preprocathepsin P; Carboxypeptidase LB
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-P75448
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CTSZ; cathepsin IV; cathepsin Z; cathepsin B2; cathepsin X; cathepsin Z1; CTSX; cathepsin Y; Cysteine-Type Carboxypeptidase; cathepsin P; Lysosomal Carboxypeptidase B; Preprocathepsin P; Carboxypeptidase LB
Species:  
Mouse
Source:  
HEK293
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Cat. No.: HY-P72158
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CTSK; cathepsin X; Prev. CTSO2; Mutated cathepsin K; Prev. CTSO; cathepsin O1; Prev. PYCD; CTSK Protein; PKND; CTS02; cathepsin O2; CTSO1; cathepsin O; cathepsin K; cathepsin K (Pycnodysostosis)
Species:  
Rat
Source:  
E. coli
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Cat. No.: HY-P74115
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: GZMH; Cytotoxic T-Lymphocyte Proteinase; Prev. CTSGL2; Granzyme H (cathepsin G-Like 2, Protein H-CCPX); CCP-X; Cytotoxin Serine Protease-C; CSP-C; Cytotoxic Serine Protease C; CGL-2; cathepsin G-Like 2; CTLA1; CGL2; cathepsin G-Like 2, Protein H-CCPX; Gra
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-187367
Research Areas:  

Infection

WJM590 is an orally active antimalarial agent that also exhibits inhibitory activities against renin, cathepsin D, BACE1, and plasmodial aspartic proteases. WJM590 inhibits substrate and protein maturation processing mediated by key proteases of Plasmodium falciparum, arrests asexual blood-stage parasites at the late schizont stage, inhibits merozoite release, and blocks malaria parasite transmission via vectors. WJM590 exerts selective inhibitory activity against multiple Plasmodium species and drug-resistant Plasmodium falciparum strains, and reduces parasitemia in infected mice. WJM590 can be used in malaria-related research .
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