Inventor

HAGMANN WILLIAM K

US65 patents

⚠️ This page may combine multiple inventors who share the name “HAGMANN WILLIAM K”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.

HAGMANN WILLIAM K

MERCK & CO INC

Hexahydro-5-imino-1,4-1,4-thiazepine derivatives as inhibitors of nitric oxide synthases

Substituted aminoquinolines as modulators of chemokine receptor activity

Substituted azetidinones as anti-inflammatory and antidegenerative agents

Substituted amides

Substituted β-alanine derivatives as cell adhesion inhibitors

Diphenyl cyclopentyl amides as cannabinoid-1 receptor inverse agonists

Substituted pyrimidines

N-arylsulfonyl aryl aza-bicyclic derivatives as potent cell adhesion inhibitors

Biarylalkanoic acids as cell adhesion inhibitors

Sulfonamides as cell adhesion inhibitors

Para-aminomethylaryl carboxamide derivatives

4-substituted-4-piperidine carboxamide derivatives

16-pyrazinyl-substituted-4-aza-androstane 5-α-reductase isozyme 1 inhibitors

16-substituted-4-aza-androstane 5-alpha-reductase isozyme 1 inhibitors

Steroidal glycolipids as host resistance stimulators

Substituted nipecotyl derivatives as inhibitors of cell adhesion

Substituted ureas as cell adhesion inhibitors

Hexahydro-5-imino-1,4-heteroazepine derivatives as inhibitors of nitric oxide synthases

Substituted azetidinones as anti-inflammatory and antidegenerative agents

β-lactams useful in determining the amount of elastase in a clinical sample

Heterocycle amides as cell adhesion inhibitors

Substituted azetidinones as anti-inflammatory and antidegenerative agents

Aralkyl amines as cannabinoid receptor modulators

Cyclic amino acid derivatives as cell adhesion inhibitors

Substituted N-arylsulfonyl-proline derivatives as potent cell adhesion inhibitors

16-substituted-4-aza-3-oxo-androstane as 5-alpha-reductase isozyme 1 inhibitors

Substituted cephalosporin sulfones as anti-inflammatory and antidegenerative agents

Substituted ketone derivatives as inhibitors of interleukin-1β converting enzyme

Steroidal glycolipids as host resistance stimulators against viral infection

Tetrazolyl derivatives of beta-lactams useful as elastase inhibitors

Substituted 1-oxa-dethiacephalosporins as anti-inflammatory and antidegenerative agents

Tetrazolyl derivatives of β-lactams useful as elastase inhibitors

N-arylsulfonyl aza-bicyclic derivatives as potent cell adhesion inhibitors

Substituted cephalosporin sulfones as anti-inflammatory and anti-degenerative agents

Substituted amidine derivatives as inhibitors of cell adhesion

Substituted isonipecotyl derivatives as inhibitors of cell adhesion

Preparation of carboxyalkyl derivatives as inhibitors of matrix metalloproteinases

Substituted 3-phenanthridinone derivatives as 5-alpha-reductase inhibitors

Haptens useful in evaluating inhibition of PNN elastase by N-substituted azetidinones

Steroidal glycolipids as host resistance stimulators against viral infection

Steroidal glycolipids as host resistance stimulators against viral infection

Steroidal glycolipids

Substituted pyrrole derivatives as cell adhesion inhibitors

Substituted phosphinic acid-containing peptidyl derivatives as antidegenerative agents

Chromophore containing compounds and their use in determining interleukin-1β convertase activity

Substituted N-carboxyalkylpeptidyl derivatives as antidegenerative agents

Substituted N-carboxyalkylpeptidyl derivatives as antidegenerative active agents

MERCK SHARP & DOHME

Antidiabetic tricyclic compounds

Antidiabetic tricyclic compounds

Antidiabetic substituted heteroaryl compounds