Chymostatin
SIGMA/C7268 - microbial
Synonym: N-(Nα-Carbonyl-Cpd-X-Phe-al)-Phe (Cpd = capreomycidine) (capreomycidine = [S,S]-α-(2-Iminohexahydro-4-pyrimidyl)glycine)
CAS Number: 9076-44-2
MDL Number: MFCD00071059
Product Type: Chemical
| biological source | microbial |
| form | powder |
| InChI key | MRXDGVXSWIXTQL-HYHFHBMOSA |
| Quality Level | 300 ![]() |
| SMILES string | OC(C(NC(NC(C1NC(NCC1)=N)C |
| solubility | DMSO: 10 mM (Stock solutions stable for months at −20 °C.) |
| storage temp. | −20°C |
| Application: | Chymostatin has been used in a study that determined that molecular calculations are useful for evaluating the interactions between ligands, including inhibitors and homologous enzymes, in docking models. Chymostatin has also been used in a study to investigate the norovirus protease as an attractive target for antiviral drug development. |
| Biochem/physiol Actions: | Chymostatin is a strong inhibitor of many proteases, including chymotrypsin, papain, chymotrypsin-like serine proteinases, chymases, and lysosomal cysteine proteinases such as cathepsins A,B,C, B, H, and L. It weakly inhibits human leucocyte elastase. It is effective at a final concentration of 100 to 200 μg/ml (10 to 100 μM). Chymostatin is often included in protease inhibitor cocktails used with plant extracts. |
| Biochem/physiol Actions: | Inhibits the lysosomal proteinase cathepsin B, and the soluble Ca2+-activated proteinase. Many young plant tissues express a chomostatin-sensitive serine protease. |
| Other Notes: | A mixture of A (major), B and C components. A: X=Leu; B: X=Val; C: X=Ile chymostatin A MW = 607.7 chymostatin B MW = 593.7 chymostatin C MW = 607.7 |
| Packaging: | 1, 5, 25, 50 mg in glass bottle |
| Packaging: | 100 mg in poly bottle |
| Preparation Note: | Solubility testing in glacial acetic acid at 10 mg/ml yields a clear solution, which is usually colorless, but can be yellow in appearance. It is reportedly also soluble in DMSO; only slightly soluble in water and short-chain alcohols; insoluble in ethyl acetate, butyl acetate, ether, hexane, and petroleum ether. Stock solutions (10 mM) can be prepared in DMSO and are stable for months at -20 °C. Stock solutions can also be made in 0.1 M HCl. Dilute solutions (10-100 μM) are only stable for several hours, due to oxidation of the terminal aldehyde. |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Storage Temp. | −20°C |
| UNSPSC | 12352202 |

