Chemical Structure : Rupintrivir
CAS No.: 223537-30-2
货号: PC-63345Not For Human Use, Lab Use Only.
Rupintrivir (AG-7088, AG7088) is a potent, irreversible inhibitor of human rhinovirus 3C protease, inhibits the replication of all HRV serotypes with EC50 of 23 nM and EC90 of 82 nM.
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---|---|---|---|
5 mg | ¥2580 | In stock | |
10 mg | ¥3880 | In stock | |
25 mg | Get quote | ||
50 mg | Get quote | ||
100 mg | Get quote |
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Rupintrivir (AG-7088, AG7088) is a potent, irreversible inhibitor of human rhinovirus 3C protease, inhibits the replication of all HRV serotypes with EC50 of 23 nM and EC90 of 82 nM.
Rupintrivir (AG-7088) potently and irreversibly inhibits HRV 3C protease with an inactivation rate constant (kobs/[I]) of 1,470,000 ± 440,000 M-1 s-1 for HRV 14.
Rupintrivir (AG-7088) also potently inhibits related picornaviruses including coxsackieviruses A21 and B3, enterovirus 70, and echovirus 11.
分子量 | 598.672 | |
分子式 | C31H39FN4O7 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
Ethyl (2E,4S)-4-[[(2R,5S)-2-[(4-fluorophenyl)methyl]-6-methyl-5-[[(5-methyl-3-isoxazolyl)carbonyl]amino]-1,4-dioxoheptyl]amino]-5-[(3S)-2-oxo-3-pyrrolidinyl]-2-pentenoate |
1. Patick AK, et al. Antimicrob Agents Chemother. 1999 Oct;43(10):2444-50.
2. Dragovich PS, et al. J Med Chem. 1999 Apr 8;42(7):1213-24.
3. Matthews DA, et al. Proc Natl Acad Sci U S A. 1999 Sep 28;96(20):11000-7.
4. Zalman LS, et al. Antimicrob Agents Chemother. 2000 May;44(5):1236-41.
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