E. Chao

发表

Novel selective small molecule agonists for peroxisome proliferator-activated receptor delta (PPARdelta)--synthesis and biological activity.

T. Willson, M. Lambert, H. Xu, 2003, Bioorganic & medicinal chemistry letters.

Structure-guided synthesis of tamoxifen analogs with improved selectivity for the orphan ERRgamma.

T. Willson, W. Zuercher, J. Collins, 2006, Bioorganic & medicinal chemistry letters.

A novel method for the generation of nitrile oxides on solid phase: application to the synthesis of substituted benzopyranoisoxazoles.

J. Collins, D. Sternbach, B. Shearer, 2002, Organic letters.

Synthesis and evaluation of potent and selective beta3 adrenergic receptor agonists containing heterobiaryl carboxylic acids.

K. Brown, C. Cowan, K. Adkison, 2007, Bioorganic & medicinal chemistry letters.

Imidazo[4,5-c]pyridines (3-deazapurines) and their nucleosides as immunosuppressive and antiinflammatory agents.

R. Crouch, E. Chao, N. Cohn, 1986, Journal of medicinal chemistry.

Adenosine kinase from rabbit liver. II. Substrate and inhibitor specificity.

R. Miller, J. Haggerty, L. M. Beacham, 1979, The Journal of biological chemistry.

The preparation and reactions of esters of dichloromethaneboronic acid

M. Rathke, E. Chao, Grace Wu, 1976 .

Imidazo[4,5‐c]pyridines (3‐Deazapurines) and Their Nucleosides as Immunosuppressive and Antiinflammatory Agents.

R. Crouch, E. Chao, N. Cohn, 1986 .

The preparation and reactions of esters of dichloromethaneboronic acid

M. Rathke, E. Chao, Grace Wu, 1976 .

Pyrazolo[3,4-d]pyrimidine ribonucleosides as anticoccidials. 1. Synthesis and activity of some nucleosides of purines and 4-(alkylthio)pyrazolo[3,4-d]pyrimidines.

R. Williams, G. Elion, E. Chao, 1982, Journal of Medicinal Chemistry.

PYRAZOLO(3,4-D)PYRIMIDINE RIBONUCLEOSIDES AS ANTICOCCIDIALS. 1. SYNTHESIS AND D ACTIVITY OF SOME NUCLEOSIDES OF PURINES AND 4-(ALKYLTHIO)PYRAZOLO(3,4-D)PYRIMIDINES

R. Williams, G. Elion, E. Chao, 1982 .

Novel selective small molecule agonists for peroxisome proliferator-activated receptor δ (PPARδ)—synthesis and biological activity

T. Willson, M. Lambert, H. Xu, 2003 .

Crystal structure of the PXR-T1317 complex provides a scaffold to examine the potential for receptor antagonism.

Timothy M Willson, William J Zuercher, T. Willson, 2007, Bioorganic & medicinal chemistry.

Structure-guided design of N-phenyl tertiary amines as transrepression-selective liver X receptor modulators with anti-inflammatory activity.

Angela Smallwood, Ping Wang, Timothy M Willson, 2008, Journal of medicinal chemistry.

Identification and Structure−Activity Relationship of Phenolic Acyl Hydrazones as Selective Agonists for the Estrogen-Related Orphan Nuclear Receptors ERRβ and ERRγ

T. Willson, W. Zuercher, J. Collins, 2005 .

Biarylaniline phenethanolamines as potent and selective beta3 adrenergic receptor agonists.

K. Brown, C. Cowan, N. Cariello, 2006, Journal of medicinal chemistry.

Structure-Guided Synthesis of Tamoxifen Analogues with Improved Selectivity for the Orphan ERRγ.

T. Willson, W. Zuercher, J. Collins, 2006 .