GLPBio

CA 074

Catalog No.: GC16317Purity:>98.00%Synonyms: CA-074,CA074
CA 074 is a selective inhibitor of cathepsin B with a Ki value of 2-5 nM. CA 074 is 10000-30000 times more potent against purified rat cathepsin B than against cathepsin H and L.

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CA 074
Cas No.: 134448-10-5
10mM (in 1mL DMSO)In Stock
$160.00
1
1mgIn Stock
$63.00
1
5mgIn Stock
$190.00
1
10mgIn Stock
$294.00
1

Citations

1 publicationsPublications from researchers using this product

Description

CA 074 is a selective inhibitor of cathepsin B with a Ki value of 2-5 nM. CA 074 is 10000-30000 times more potent against purified rat cathepsin B than against cathepsin H and L[1]. CA 074 is a synthetic analog of E-64, a natural peptidyl epoxide that irreversibly inhibits most lysosomal cysteine​proteases[2]. CA 074 cannot cross cell membranes, but its methyl ester form, CA-074 Me (GC15917), can cross cell membranes[3].

In vitro, CA 074 (10 μM) treatment of HT29, DLD1, and SW480 cells for 2-3 weeks significantly inhibited cell invasion through Matrigel by approximately 45-60% [4].

In vivo, CA 074 (10 mg/kg) treated intravenously in mice inoculated with human melanoma cells significantly inhibited tumor growth and the number of lung metastases [5]. CA 074 (50 mg/kg) was injected intraperitoneally into 4T1.2 tumor-bearing mice, which significantly inhibited tumor growth, reduced tumor cathepsin B activity, and inhibited lung and bone metastasis[6]. CA 074 (4 mg/kg) was injected intravenously into rats with focal cerebral ischemia, which significantly reduced the levels of cathepsin B and L and increased the number of eosinophilic (necrotic) and apoptotic neurons in brain tissue[7].

References:
[1] Towatari T, Nikawa T, Murata M, et al. Novel epoxysuccinyl peptides A selective inhibitor of cathepsin B, in vivo[J]. FEBS letters, 1991, 280(2): 311-315.
[2] Matsumoto K, Mizoue K, Kitamura K, et al. Structural basis of inhibition of cysteine proteases by E‐64 and its derivatives[J]. Peptide Science, 1999, 51(1): 99-107.
[3] Patel N, Nizami S, Song L, et al. CA‐074Me compound inhibits osteoclastogenesis via suppression of the NFATc1 and c‐FOS signaling pathways[J]. Journal of Orthopaedic Research, 2015, 33(10): 1474-1486.
[4] Bian B, Mongrain S, Cagnol S, et al. Cathepsin B promotes colorectal tumorigenesis, cell invasion, and metastasis[J]. Molecular carcinogenesis, 2016, 55(5): 671-687.
[5] Matarrese P, Ascione B, Ciarlo L, et al. Cathepsin B inhibition interferes with metastatic potential of human melanoma: an in vitro and in vivo study[J]. Molecular cancer, 2010, 9: 1-14.
[6] Withana N P, Blum G, Sameni M, et al. Cathepsin B inhibition limits bone metastasis in breast cancer[J]. Cancer research, 2012, 72(5): 1199-1209.
[7] Özkara E, Durmaz R, Özbek Z, et al. The Effect of Ca-074 (Cathepsın B Inhibitor) on Necrotic and Apoptotic Neuronal Cell Death in Model of Cerebral Ischemia[J]. Osmangazi Tıp Dergisi, 2023, 45(5): 781-790.

Protocol

Cell experiment [1]:

Cell lines

HT29, DLD1, SW480 cells 

Preparation Method

HT29, DLD1, and SW480 cells were cultured in soft agarose in the presence or absence of 10 μM CA 074 for 2–3 week.

Reaction Conditions

10μM; 2–3 week

Applications

CA 074 significantly inhibited cell invasion through Matrigel by approximately 45–60%.
Animal experiment [2]:

Animal models

CD-1 male nude (nu/nu) mice

Preparation Method

MM4 cells were injected into the hind leg muscle of mice. Beginning on day 6 after tumor implantation (tumor mass approximately 250mg), mice were treated with CA 074 at 10 mg/kg intravenously for eight consecutive days.

Dosage form

10mg/kg; i.v.

Applications

CA 074 significantly inhibited tumor growth and suppressed the number of metastases in artificial lungs.

References:
[1]Bian B, Mongrain S, Cagnol S, et al. Cathepsin B promotes colorectal tumorigenesis, cell invasion, and metastasis[J]. Molecular carcinogenesis, 2016, 55(5): 671-687.
[2]Matarrese P, Ascione B, Ciarlo L, et al. Cathepsin B inhibition interferes with metastatic potential of human melanoma: an in vitro and in vivo study[J]. Molecular cancer, 2010, 9: 1-14.

Product Documents

Purity:>98.00%Appearance:A solid

Chemical Properties

CAS No.
134448-10-5
Synonyms
CA-074,CA074
Chemical Name
(2S)-1-[(2S,3S)-3-methyl-2-[[(3S)-3-(propylcarbamoyl)oxirane-2-carbonyl]amino]pentanoyl]pyrrolidine-2-carboxylic acid
SMILES
CCCNC(=O)C1C(O1)C(=O)NC(C(C)CC)C(=O)N2CCCC2C(=O)O
Molecular Formula
C18H29N3O6
Molecular Weight
383.44
Solubility
≥ 19.17mg/mL in DMSO
Storage
Store at -20°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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