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Chemical Structure| 26305-03-3 Chemical Structure| 26305-03-3

Structure of Pepstatin A
CAS No.: 26305-03-3

Chemical Structure| 26305-03-3

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CAS No.: 26305-03-3

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Pepstatin (Pepstatin A) is a specific, orally active aspartic protease inhibitor produced by actinomycetes, with IC50 values of 4.5 nM for hemoglobin-pepsin, 6.2 nM for hemoglobin-proctase, 150 nM for casein-pepsin, 290 nM for casein-proctase, 520 nM for casein-acid protease, and 260 nM for hemoglobin-acid protease. Pepstatin also inhibits HIV protease.

Synonyms: Pepstatin; NSC 272671; Pepstatinum

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Product Details of Pepstatin A

CAS No. :26305-03-3
Formula : C34H63N5O9
M.W : 685.89
SMILES Code : CC(C)CC(N[C@@H](C(C)C)C(N[C@@H](C(C)C)C(N[C@@H](CC(C)C)[C@@H](O)CC(N[C@@H](C)C(N[C@@H](CC(C)C)[C@@H](O)CC(O)=O)=O)=O)=O)=O)=O
Synonyms :
Pepstatin; NSC 272671; Pepstatinum
MDL No. :MFCD00060740
InChI Key :FAXGPCHRFPCXOO-LXTPJMTPSA-N
Pubchem ID :5478883

Safety of Pepstatin A

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
HSG cells 10 μM 8 hours Inhibited LAMP1 protein degradation PMC9298453
HSG cells 5 μM 14 hours Reduced apoptosis PMC9298453
H9c2 cells 10 μg/ml 6 or 12 hours Inhibition of lysosomal cathepsins, increasing the number of cells with red-only dots and the abundance of red-only dots per cell PMC10472865
HCT116 cells 10 μM To investigate the effect of CASP9 KD and cathepsin inhibitors on LAMP2 distribution, results showed that CASP9 KD and E64D/pepA co-treatment had an additive effect on the juxtanuclear accumulation of LAMP2-positive vesicles. PMC8204962
HeLa cells 4 μM 4 hours To investigate whether ADRB2 accumulates in lysosomes following MTOR inhibition, results showed that ADRB2 moderately accumulates in lysosomes after MTOR inhibition. PMC11062367
Synovial Fibroblasts (SFs) 10 μM 24 hours Inhibit lysosomal function, promote autophagy and citrullination of intracellular VIM PMC7144877
rabbit IVD cells 20 μM 60 minutes Inhibition of cathepsin D significantly attenuated bupivacaine-induced cell death PMC6037912

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Zebrafish Transgenic zebrafish model Aqueous solution 25 or 50 mg/kg Once daily for five days Inhibited degradation of autophagosomes, increased the number of autophagosomes PMC6613892

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.46mL

0.29mL

0.15mL

7.29mL

1.46mL

0.73mL

14.58mL

2.92mL

1.46mL

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