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Stanley Kolis

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Chemicals & Drugs

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Publications

TOP 3
Michael G Bell; Douglas Gernert; Timothy Grese; Matthew D Belvo; Peter S Borromeo; Sally A Kelley; joseph kennedy; Stanley P Kolis; Peter A Lander; Rachel Richey; V Scott Sharp; Gregory A Stephenson; Jeffrey D Williams; Hannah Yu; Karen M Zimmerman; Mitchell I Steinberg; Prabhakar K Jadhav
(S)-N-{3-[1-cyclopropyl-1-(2,4-difluoro-phenyl)-ethyl]-1H-indol-7-yl}-methanesulfonamide: a potent, nonsteroidal, functional antagonist of the mineralocorticoid receptor.
Rima S Al-Awar; James E Ray; Kyle A Hecker; Sajan Joseph; Jianping Huang; Chuan Shih; Harold B Brooks; Charles D Spencer; Scott A Watkins; Richard M Schultz; Eileen L Considine; Margaret M Faul; Kevin A Sullivan; Stanley P Kolis; Michael A Carr; Faming Zhang
Preparation of novel aza-1,7-annulated indoles and their conversion to potent indolocarbazole kinase inhibitors.
Rima S Al-Awar; James E Ray; Kyle A Hecker; Jianping Huang; Philip P Waid; Chuan Shih; Harold B Brooks; Charles D Spencer; Scott A Watkins; Bharvin R Patel; Nancy B Stamm; Catherine A Ogg; Richard M Schultz; Eileen L Considine; Margaret M Faul; Kevin A Sullivan; Stanley P Kolis; John L Grutsch; Sajan Joseph
1,7-annulated indolocarbazoles as cyclin-dependent kinase inhibitors.

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All Publications

2007: Michael G Bell; Douglas Gernert; Timothy Grese; Matthew D Belvo; Peter S Borromeo; Sally A Kelley; joseph kennedy; Stanley P Kolis; Peter A Lander; Rachel Richey; V Scott Sharp; Gregory A Stephenson; Jeffrey D Williams; Hannah Yu; Karen M Zimmerman; Mitchell I Steinberg; Prabhakar K Jadhav
(S)-N-{3-[1-cyclopropyl-1-(2,4-difluoro-phenyl)-ethyl]-1H-indol-7-yl}-methanesulfonamide: a potent, nonsteroidal, functional antagonist of the mineralocorticoid receptor.
Journal of medicinal chemistry 2007;50(26):6443-5.
2004: Rima S Al-Awar; James E Ray; Kyle A Hecker; Sajan Joseph; Jianping Huang; Chuan Shih; Harold B Brooks; Charles D Spencer; Scott A Watkins; Richard M Schultz; Eileen L Considine; Margaret M Faul; Kevin A Sullivan; Stanley P Kolis; Michael A Carr; Faming Zhang
Preparation of novel aza-1,7-annulated indoles and their conversion to potent indolocarbazole kinase inhibitors.
Bioorganic & medicinal chemistry letters 2004;14(15):3925-8.
2004: Rima S Al-Awar; James E Ray; Kyle A Hecker; Jianping Huang; Philip P Waid; Chuan Shih; Harold B Brooks; Charles D Spencer; Scott A Watkins; Bharvin R Patel; Nancy B Stamm; Catherine A Ogg; Richard M Schultz; Eileen L Considine; Margaret M Faul; Kevin A Sullivan; Stanley P Kolis; John L Grutsch; Sajan Joseph
1,7-annulated indolocarbazoles as cyclin-dependent kinase inhibitors.
Bioorganic & medicinal chemistry letters 2004;14(12):3217-20.
2004: Margaret M Faul; Thomas A Engler; Kevin A Sullivan; John L Grutsch; Marcella T Clayton; Michael J Martinelli; Joseph M Pawlak; Michael LeTourneau; D Scott Coffey; Steven W Pedersen; Stanley P Kolis; Kelly Furness; Sushant Malhotra; Rima S Al-Awar; James E Ray
Synthetic approaches to indolo[6,7-a]pyrrolo[3,4-c]carbazoles: potent cyclin D1/CDK4 inhibitors.
The Journal of organic chemistry 2004;69(9):2967-75.
2003: Concha Sanchez-Martinez; Margaret M Faul; Chuan Shih; Kevin A Sullivan; John L Grutsch; Jeremy T Cooper; Stanley P Kolis
Synthesis of aryl- and heteroaryl[a]pyrrolo[3,4-c]carbazoles.
The Journal of organic chemistry 2003;68(21):8008-14.
2003: Thomas A Engler; Kelly Furness; Sushant Malhotra; Concha Sanchez-Martinez; Chuan Shih; Walter Xie; Guoxin Zhu; Xun Zhou; Scott E Conner; Margaret M Faul; Kevin A Sullivan; Stanley P Kolis; Harold B Brooks; Bharvin Patel; Richard M Schultz; Tammy B DeHahn; Kashif Kirmani; Charles D Spencer; Scott A Watkins; Eileen L Considine; Jack A Dempsey; Catherine A Ogg; Nancy B Stamm; Bryan D Anderson; Robert M Campbell; Vasu Vasudevan; Michelle L Lytle
Novel, potent and selective cyclin D1/CDK4 inhibitors: indolo[6,7-a]pyrrolo[3,4-c]carbazoles.
Bioorganic & medicinal chemistry letters 2003;13(14):2261-7.