Zelkovamycin
CAS: 221197-33-7
Ref. 3D-WIA19733
| 5mg | 1,950.00 € | ||
| 10mg | 3,120.00 € | ||
| 25mg | 5,851.00 € | ||
| 50mg | 9,361.00 € |
Product Information
- Cyclo[2-aminobutanoyl-(2Z)-2-amino-2-butenoyl-N-methylglycyl-2-(1-aminoethyl)-4-thiazolecarbonyl-7-methoxytryptophyl-3-oxoisovalylglycyl]
Zelkovamycin is a potent inhibitor of the ubiquitin-proteasome system. It has been shown to inhibit the replication of human T-cell leukemia virus (HTLV) and the herpes simplex virus in vitro. Zelkovamycin has been found to have potent inhibitory activity against a variety of proteases including papain, cathepsin B, and chymotrypsin. This drug also inhibits the synthesis of proteins required for cell replication and is effective as a control agent for human papillomavirus, herpes simplex virus, and other viruses. Structural studies show that this compound binds to the catalytic site of ubiquitin-proteasome system enzymes. The molecular weight of zelkovamycin is 593.5 Da, which corresponds to an empirical formula C40H50N6O8S2.
Chemical properties
Technical inquiry about: 3D-WIA19733 Zelkovamycin
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