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K777 

Cat. No. M29515

All AbMole products are for research use only, cannot be used for human consumption.

K777  Structure
Size Price Availability Quantity
5mg USD 190 In stock
10mg USD 300 In stock
25mg USD 500 In stock
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Quality Control & Documentation
Biological Activity

K777 is a potent, orally active and irreversible cysteine protease inhibitor. K777 is also a potent CYP3A4 inhibitor with an IC50 of 60 nM and a selective CCR4 antagonist featuring the potent chemotaxis inhibition. K777 irreversibly inhibits Cruzain, the major cysteine protease of Trypansoma cruzi, and cathepsins B and L. K777 is a broad-spectrum antiviral by targeting cathepsin-mediated cell entry. K777 inhibits SARS-CoV and EBOV pseudovirus entry with IC50 values of 0.68 nM and 0.87 nM, respectively.

Chemical Information
Molecular Weight 574.73
Formula C32H38N4O4S
CAS Number 233277-99-1
Form Solid
Solubility (25°C) DMSO 100 mg/mL (ultrasonic)
Storage Powder -20°C
References

[1] Drake M Mellott, et al. ACS Chem Biol. A Clinical-Stage Cysteine Protease Inhibitor blocks SARS-CoV-2 Infection of Human and Monkey Cells

[2] Drake M Mellott, et al. bioRxiv. A cysteine protease inhibitor blocks SARS-CoV-2 infection of human and monkey cells

[3] Dayane Andriotti Otta, et al. Antimicrob Agents Chemother. Identification of Anti-Trypanosoma cruzi Lead Compounds with Putative Immunomodulatory Activity

[4] Erica R Kiemele, et al. Org Lett. Total Synthesis of K777: Successful Application of Transition-Metal-Catalyzed Alkyne Hydrothiolation toward the Modular Synthesis of a Potent Cysteine Protease Inhibitor

[5] Takashi Sato, et al. Pharmacology. Internalization of CCR4 and inhibition of chemotaxis by K777, a potent and selective CCR4 antagonist

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  Catalog
Abmole Inhibitor Catalog




Keywords: K777  supplier, Cathepsin, inhibitors, activators

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