P

Inventor

WIERENGA WENDELL

US35 patents
⚠️ This page may combine multiple inventors who share the name “WIERENGA WENDELL”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.

UPJOHN CO

33 patents
US4978757ADec 18, 1990

1,2,8,8a-tetrahydrocyclopropa (C) pyrrolo [3,2-e)]-indol-4(5H)-ones and related compounds

UPJOHN CO61 citations96
US4975537ADec 4, 1990

Δ9(11) -angiostatic steroids

UPJOHN CO60 citations96
US4912227AMar 27, 1990

1,2,8,8A-tetrahydrocyclopropa(c)pyrrolo(3,2-e)-indol-4-(5H)-ones and related compounds

UPJOHN CO73 citations96
US4771042ASep 13, 1988

Inhibition of angiogenesis involving the coadministration of steroids with heparin or heparin fragments

UPJOHN CO87 citations94
US4413132ANov 1, 1983

Antibiotic CC-1065 indoline intermediates

UPJOHN CO20 citations82
US4235887ANov 25, 1980

Process for therapeutic treatment

UPJOHN CO22 citations82
US4140850AFeb 20, 1979

2,2'-Anhydrotriazine nucleosides and process for preparing the same

UPJOHN CO20 citations82
US4086254AApr 25, 1978

Photocleavable steroids

UPJOHN CO22 citations82
US4948533AAug 14, 1990

11a-hydroxy steroid diester

UPJOHN CO20 citations80
US4590211AMay 20, 1986

Process for therapeutic treatment

UPJOHN CO7 citations74
US4460589AJul 17, 1984

Process for treating hypertension

UPJOHN CO8 citations74
US4423229ADec 27, 1983

Composition of matter and process

UPJOHN CO13 citations74
US4423228ADec 27, 1983

Process for preparing N-(methyl-sulfonyl)-1,2,8,8a-cyclopropa[c]benzo[1,2-b:4,3-b']dipyrrol-4(5H)-one

UPJOHN CO8 citations74
US4423230ADec 27, 1983

Preparation of an intermediate for N-(methylsulfonyl)-1,2,8,8a-cyclopropa[c][1,2-b:-4,3-b']dipyrol-4(5H)-one

UPJOHN CO7 citations74
US4400518AAug 23, 1983

Composition of matter and process

UPJOHN CO8 citations74
US4308272ADec 29, 1981

Process for treating hypertension

UPJOHN CO6 citations74
US4302456ANov 24, 1981

Process for therapeutic treatment

UPJOHN CO10 citations74
US4256898AMar 17, 1981

α(substituted) Amino-3-substituted-2-isoxazoline-5-acetic acids (esters)

UPJOHN CO14 citations74
US5434157AJul 18, 1995

6-aryl pyrimidine compounds and method for treating viral infections and inducing interferon production

UPJOHN CO15 citations73
US4507302AMar 26, 1985

Method for treating arthritis with 6-aryl pyrimidine compounds

UPJOHN CO14 citations72
US4593030AJun 3, 1986

Use of 6-aryluracils as antiinflammatory and antiarthritic agents

UPJOHN CO2 citations63
US4521599AJun 4, 1985

Process for the preparation of 1,3-oxazine-4-ones

UPJOHN CO2 citations63
US4496492AJan 29, 1985

Substituted phenylalkyl compounds

UPJOHN CO2 citations63
US4495349AJan 22, 1985

6-Aryluracils

UPJOHN CO4 citations63
US4455430AJun 19, 1984

Process for preparing tricholomic acid and derivatives thereof

UPJOHN CO2 citations63
US4431820AFeb 14, 1984

6-Methoxy indoline acetate and its 5-nitro and 5-amino derivatives

UPJOHN CO5 citations63
US4424365AJan 3, 1984

1,2,8,8a-Cyclopropa c!benzo 1,2,-b:-4,3-b'!dipyrrol-4(5H)-ones

UPJOHN CO5 citations63
US4302457ANov 24, 1981

Process for therapeutic treatment

UPJOHN CO6 citations63
US4298744ANov 3, 1981

Method for preparing (αS,5S)-α-amino-3-chloro-2-isoxazoline-5-acetic acid (AT-125) and analogs thereof

UPJOHN CO3 citations63
US4275214AJun 23, 1981

Substituted alkoxy carbonyl-3-oxo-α-phthalimido-5-isoxozolidineacetic acids

UPJOHN CO4 citations63
US4795812AJan 3, 1989

4-substituted-6-aryl-pyrimidine compounds

UPJOHN CO0 citations52
US4593096AJun 3, 1986

Novel compounds and process for treating hypertension

UPJOHN CO1 citations52
US4578466AMar 25, 1986

Processes for the preparation of 6-aryluracils

UPJOHN CO0 citations42

WARNER LAMBERT CO

2 patents