Synthetic Inhibitors of Cytochrome P-450 2A6:  Inhibitory Activity, Difference Spectra, Mechanism of Inhibition, and Protein Cocrystallization

• Published in: Journal of medicinal chemistry 2006-11, Vol.49 (24), p.6987-7001
• Main Authors: Yano, Jason K, Denton, Travis T, Cerny, Matthew A, Zhang, Xiaodong, Johnson, Eric F, Cashman, John R
• Format: Article
• Language: English
• Subjects: Acetylene - analogs & derivatives; Acetylene - chemical synthesis; Acetylene - chemistry; Acetylene - metabolism; Animals; Aryl Hydrocarbon Hydroxylases - antagonists & inhibitors; Aryl Hydrocarbon Hydroxylases - chemistry; Aryl Hydrocarbon Hydroxylases - metabolism; Biological and medical sciences; Crystallography, X-Ray; Cytochrome P-450 CYP2A6; Enzyme Inhibitors - chemical synthesis; Enzyme Inhibitors - chemistry; Enzyme Inhibitors - metabolism; Furans - chemical synthesis; Furans - chemistry; Furans - metabolism; Humans; Imidazoles - chemical synthesis; Imidazoles - chemistry; Imidazoles - metabolism; In Vitro Techniques; Isoxazoles - chemical synthesis; Isoxazoles - chemistry; Isoxazoles - metabolism; Medical sciences; Mice; Microsomes, Liver - metabolism; Mixed Function Oxygenases - antagonists & inhibitors; Mixed Function Oxygenases - chemistry; Mixed Function Oxygenases - metabolism; Models, Molecular; Molecular Structure; Nicotine - chemistry; Pyrazoles - chemical synthesis; Pyrazoles - chemistry; Pyrazoles - metabolism; Pyridines - chemical synthesis; Pyridines - chemistry; Pyridines - metabolism; Structure-Activity Relationship; Thiazoles - chemical synthesis; Thiazoles - chemistry; Thiazoles - metabolism; Thiophenes - chemical synthesis; Thiophenes - chemistry; Thiophenes - metabolism; Time Factors; Tobacco, tobacco smoking; Toxicology
• ISSN: 0022-2623; 1520-4804
• DOI: 10.1021/jm060519r

A series of 3-heteroaromatic analogues of nicotine were synthesized to delineate structural and mechanistic requirements for selectively inhibiting human cytochrome P450 (CYP) 2A6. Thiophene, substituted thiophene, furan, substituted furan, acetylene, imidazole, substituted imidazole, thiazole, pyrazole, substituted pyrazole, and aliphatic and isoxazol moieties were used to replace the N-methylpyrrolidine ring of nicotine. A number of potent inhibitors were identified, and several exhibited high selectivity for CYP2A6 relative to CYP2E1, -3A4, -2B6, -2C9, -2C19, and -2D6. The majority of these inhibitors elicited type II difference spectra indicating the formation of a coordinate covalent bond to the heme iron. The majority of inhibitors were reversible inhibitors although several mechanism-based inactivators were identified. Most of the inhibitors were also relatively metabolically stable. X-ray crystal structures of CYP2A6 cocrystallized with three furan analogues bearing methanamino side chains indicated that the amine side chain coordinated to the heme iron. The pyridyl moiety was positioned to accept a hydrogen bond from Asn297, and all three inhibitors exhibited orthogonal aromatic−aromatic interactions with protein side chains. For comparison, the cocrystal structure of 4,4‘-dipyridyl disulfide was also obtained and showed that the pyridine moiety could assume a different orientation than that observed for the 3-heteroaromatic pyridines examined. For the 3-heteroromatic pyridines, N-methyl and N,N-dimethyl amino groups increased the apparent K i and distorted helix I of the protein. Substitution of a phenyl ring for the pyridyl ring also increased the apparent K i, which is likely to reflect the loss of the hydrogen bonding interaction with Asn297. In contrast, inhibitory potency for other P450s was increased, and the selectivity of the phenyl analogues for CYP2A6 was decreased relative to the pyridyl compounds. The results suggest that inhibitors that compliment the active site features of CYP2A6 can exhibit significant selectivity for CYP2A6 relative to other human liver drug-metabolizing P450s.