Description |
InvivoChem Cat #:V4241CAS #:618913-30-7 Purity >=98%Description: AZD5904 is a novel, potent, orally bioavailable, irreversible inhibitor of human MPO (Myeloperoxidase) with an IC50 of 140 nM and with similar potency in mouse and rat. It is 10 to 19-fold selective compared to the closely related lactoperoxidase and thyroid peroxidase; it shows > 70-fold selectivity over a broad panel of other enzymes, ion channels, and receptors. In isolated human neutrophils, 1 uM inhibited PMA stimulated HOCl by > 90%. In rats, a plasma concentration of ca.5 uM decreased the in vivo formation of glutathione sulphonamide (a product of the reaction of HOCl with glutathione) from in situ zymosan activated peritoneum neutrophils. Description:References: Myeloperoxidase (MPO) inhibitor. References:
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![AZD-5904](/Private/g3/M00/03/D8/CgAH5122qUSASM1JAAAiT5pO3V0576.png) |
Name: AZD-5904 CAS#: 618913-30-7 Chemical Formula: C10H12N4O2S Exact Mass: 252.0681 Molecular Weight: 252.292 Elemental Analysis: C, 47.61; H, 4.79; N, 22.21; O, 12.68; S, 12.71 |
Technical Information |
Synonym: AZD-5904; AZD 5904; AZD5904; AZ1, AZ 1 AZ-1; TX4; TX-4; TX 4; IUPAC/Chemical Name: (S)-3-((tetrahydrofuran-2-yl)methyl)-2-thioxo-1, 2, 3, 7-tetrahydro-6H-purin-6-one InChi Key: RSPDBEVKURKEII-LURJTMIESA-N InChi Code: InChI=1S/C10H12N4O2S/c15-9-7-8(12-5-11-7)14(10(17)13-9)4-6-2-1-3-16-6/h5-6H, 1-4H2, (H, 11, 12)(H, 13, 15, 17)/t6-/m0/s1 SMILES Code: O=C1NC(N(C[CH]2OCCC2)C3=C1NC=N3)=S |