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	1.	Recent advances in JAK3 kinase inhibitors. [electronic resource] by Sudbeck, E A Uckun, F M Producer: 20051013 In: IDrugs : the investigational drugs journal vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	2.	Synthesis, X-ray structure, and anti-leukemic activity of oxovanadium(IV) complexes. [electronic resource] by Dong, Y Narla, R K Sudbeck, E Uckun, F M Producer: 20001109 In: Journal of inorganic biochemistry vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Stereochemistry of halopyridyl and thiazolyl thiourea compounds is a major determinant of their potency as nonnucleoside inhibitors of HIV-1 reverse transcriptase. [electronic resource] by Venkatachalam, T K Sudbeck, E A Mao, C Uckun, F M Producer: 20010329 In: Bioorganic & medicinal chemistry letters vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Structure-based design of non-nucleoside reverse transcriptase inhibitors of drug-resistant human immunodeficiency virus. [electronic resource] by Mao, C Sudbeck, E A Venkatachalam, T K Uckun, F M Producer: 19991209 In: Antiviral chemistry & chemotherapy vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Structure-based drug design of non-nucleoside inhibitors for wild-type and drug-resistant HIV reverse transcriptase. [electronic resource] by Mao, C Sudbeck, E A Venkatachalam, T K Uckun, F M Producer: 20001107 In: Biochemical pharmacology vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Anti-HIV activity of aromatic and heterocyclic thiazolyl thiourea compounds. [electronic resource] by Venkatachalam, T K Sudbeck, E A Mao, C Uckun, F M Producer: 20010510 In: Bioorganic & medicinal chemistry letters vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Rational design of N-[2-(2,5-dimethoxyphenylethyl)]-N'-[2-(5-bromopyridyl)]-thiourea (HI-236) as a potent non-nucleoside inhibitor of drug-resistant human immunodeficiency virus. [electronic resource] by Mao, C Sudbeck, E A Venkatachalam, T K Uckun, F M Producer: 19990923 In: Bioorganic & medicinal chemistry letters vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	An inhibitor of Janus kinase 3:4-(4-hydroxyphenylamino)-6, 7-dimethoxyquinazolin-1-ium chloride methanol solvate. [electronic resource] by Sudbeck, E A Jennissen, J D Liu, X P Uckun, F M Producer: 20010105 In: Acta crystallographica. Section C, Crystal structure communications vol. 56 ( Pt 10) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Inhibitor of HIV-1 reverse transcriptase: N'-(5-bromo-2-pyridyl)-N-[2-(2,5-dimethoxyphenyl)ethyl]thiourea. [electronic resource] by Sudbeck, E A Jennissen, J D Venkatachalam, T K Uckun, F M Producer: 20000228 In: Acta crystallographica. Section C, Crystal structure communications vol. 55 ( Pt 12) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Structure-based design of N-[2-(1-piperidinylethyl)]-N'-[2-(5-bromopyridyl)]-thiourea and N-[2-(1-piperazinylethyl)]-N'-[2-(5-bromopyridyl)]-thiourea as potent non-nucleoside inhibitors of HIV-1 reverse transcriptase. [electronic resource] by Mao, C Vig, R Venkatachalam, T K Sudbeck, E A Uckun, F M Producer: 19990128 In: Bioorganic & medicinal chemistry letters vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Tyrosine kinase inhibitors against EGF receptor-positive malignancies. [electronic resource] by Sudbeck, E A Ghosh, S Liu, X P Zheng, Y Myers, D E Uckun, F M Producer: 20010521 In: Methods in molecular biology (Clifton, N.J.) vol. 166 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Structure-based design of novel dihydroalkoxybenzyloxopyrimidine derivatives as potent nonnucleoside inhibitors of the human immunodeficiency virus reverse transcriptase. [electronic resource] by Sudbeck, E A Mao, C Vig, R Venkatachalam, T K Tuel-Ahlgren, L Uckun, F M Producer: 19990222 In: Antimicrobial agents and chemotherapy vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Rational design and synthesis of phenethyl-5-bromopyridyl thiourea derivatives as potent non-nucleoside inhibitors of HIV reserve transcriptase. [electronic resource] by Vig, R Mao, C Venkatachalam, T K Tuel-Ahlgren, L Sudbeck, E A Uckun, F M Producer: 19990122 In: Bioorganic & medicinal chemistry vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Rational design and synthesis of a novel anti-leukemic agent targeting Bruton's tyrosine kinase (BTK), LFM-A13 [alpha-cyano-beta-hydroxy-beta-methyl-N-(2, 5-dibromophenyl)propenamide]. [electronic resource] by Mahajan, S Ghosh, S Sudbeck, E A Zheng, Y Downs, S Hupke, M Uckun, F M Producer: 19990427 In: The Journal of biological chemistry vol. 274 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Specificity of alpha-cyano-beta-hydroxy-beta-methyl-n-[4-(trifluoromethoxy)phe nyl]-propenamide as an inhibitor of the epidermal growth factor receptor tyrosine kinase. [electronic resource] by Ghosh, S Zheng, Y Jun, X Mahajan, S Mao, C Sudbeck, E A Uckun, F M Producer: 20000214 In: Clinical cancer research : an official journal of the American Association for Cancer Research vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	16.	5-Alkyl-2-[(methylthiomethyl)thio]-6-(benzyl)-pyrimidin-4-(1H)-ones as potent non-nucleoside reverse transcriptase inhibitors of S-DABO series. [electronic resource] by Vig, R Mao, C Venkatachalam, T K Tuel-Ahlgren, L Sudbeck, E A Uckun, F M Producer: 19990201 In: Bioorganic & medicinal chemistry letters vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Antioxidant function of phenethyl-5-bromo-pyridyl thiourea compounds with potent anti-HIV activity. [electronic resource] by Dong, Y Venkatachalam, T K Narla, R K Trieu, V N Sudbeck, E A Uckun, F M Producer: 20000228 In: Bioorganic & medicinal chemistry letters vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Structure-based design of specific inhibitors of Janus kinase 3 as apoptosis-inducing antileukemic agents. [electronic resource] by Sudbeck, E A Liu, X P Narla, R K Mahajan, S Ghosh, S Mao, C Uckun, F M Producer: 19990930 In: Clinical cancer research : an official journal of the American Association for Cancer Research vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	19.	Structure-based design of potent inhibitors of EGF-receptor tyrosine kinase as anti-cancer agents. [electronic resource] by Ghosh, S Narla, R K Zheng, Y Liu, X P Jun, X Mao, C Sudbeck, E A Uckun, F M Producer: 20000427 In: Anti-cancer drug design vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	20.	Alpha-cyano-beta-hydroxy-beta-methyl-N-[4-(trifluoromethoxy)phenyl] propenamide: an inhibitor of the epidermal growth factor receptor tyrosine kinase with potent cytotoxic activity against breast cancer cells. [electronic resource] by Ghosh, S Zheng, Y Jun, X Narla, R K Mahajan, S Navara, C Mao, C Sudbeck, E A Uckun, F M Producer: 19990223 In: Clinical cancer research : an official journal of the American Association for Cancer Research vol. 4 Availability: No items available. Save to lists Add to cart (remove)

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