Dr. Timothy Winston Doyle D.O.
Family Practitioner
310 N Hammes Ave Suite 101 Joliet IL, 60435About
Dr. Timothy Doyle is a family practitioner practicing in Joliet, IL. Dr. Doyle specializes in comprehensive health care for people of all ages. In addition to diagnosing and treating illnesses, family practitioners also put focus on preventative care with routine checkups, tests and personalized coaching on how to maintain a healthy lifestyle. Dr. Doyle possesses immense general knowledge on maintaining health and today, family practitioners provide more care for the underserved and rural populations than any other medical specialty.
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Expert Publications
Data provided by the National Library of Medicine- Isolation and identification of metabolites of porfiromycin formed in the presence of a rat liver preparation.
- Isolation and identification of urinary metabolites of porfiromycin in dogs and humans.
- Syntheses and antitumor activities of potent inhibitors of ribonucleotide reductase: 3-amino-4-methylpyridine-2-carboxaldehyde-thiosemicarba-zone (3-AMP), 3-amino-pyridine-2-carboxaldehyde-thiosemicarbazone (3-AP) and its water-soluble prodrugs.
- Production, isolation and structure determination of novel fluoroindolocarbazoles from Saccharothrix aerocolonigenes ATCC 39243.
- 10'-Desmethoxystreptonigrin, a novel analog of streptonigrin.
- Determination of DNA cleavage specificity by esperamicins.
- Activity of C-7 substituted cyclic acetal derivatives of mitomycin C and
- Second generation analogs of etoposide and mitomycin C.
- Cyclic acetal derivatives of mitomycin C.
- AT2433-A1, AT2433-A2, AT2433-B1, and AT2433-B2 novel antitumor antibiotic compounds produced by Actinomadura melliaura. Taxonomy, fermentation, isolation and biological properties.
- AT2433-A1, AT2433-A2, AT2433-B1 and AT2433-B2 novel antitumor compounds produced by Actinomadura melliaura. II. Structure determination.
- Esperamicins, a class of potent antitumor antibiotics: mechanism of action.
- Synthesis and in vivo antitumor activity of novel mitomycin A disulfide analogs.
- Antitumor activity of chrysomycins M and V.
- Nucleotide-specific cleavage and minor-groove interaction of DNA with esperamicin antitumor antibiotics.
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