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Results: 1-9 |
Results: 9
Spongistatins as tubulin targeting agents
Authors: Uckun, FM Mao, C Jan, ST Huang, H Vassilev, AO Navara, CS Narla, RK
Citation: Fm. Uckun et al., Spongistatins as tubulin targeting agents, CUR PHARM D, 7(13), 2001, pp. 1291-1296
Structure-based design of a novel synthetic spiroketal pyran as a pharmacophore for the marine natural product Spongistatin 1
Authors: Uckun, FM Mao, C Vassilev, AO Huang, H Jan, ST
Citation: Fm. Uckun et al., Structure-based design of a novel synthetic spiroketal pyran as a pharmacophore for the marine natural product Spongistatin 1, BIOORG MED, 10(6), 2000, pp. 541-545
COBRA-1, a rationally-designed epoxy-THF containing compound with potent tubulin depolymerizing activity as a novel anticancer agent
Authors: Jan, ST Mao, C Vassilev, AO Navara, CS Uckun, FM
Citation: St. Jan et al., COBRA-1, a rationally-designed epoxy-THF containing compound with potent tubulin depolymerizing activity as a novel anticancer agent, BIOORG MED, 10(11), 2000, pp. 1193-1197
A rationally designed anticancer drug targeting a unique binding cavity oftubulin
Authors: Uckun, FM Mao, C Vassilev, AO Navara, CS Narla, RKS Jan, ST
Citation: Fm. Uckun et al., A rationally designed anticancer drug targeting a unique binding cavity oftubulin, BIOORG MED, 10(10), 2000, pp. 1015-1018
Stereocontrolled synthesis of a novel pharmacophore of the tubulin-depolymerizing marine natural product spongistatin
Authors: Huang, H Mao, C Jan, ST Uckun, FM
Citation: H. Huang et al., Stereocontrolled synthesis of a novel pharmacophore of the tubulin-depolymerizing marine natural product spongistatin, TETRAHEDR L, 41(11), 2000, pp. 1699-1702
Synthesis of dual function (5R,6R)- and (5S,6S)-5-bromo-6-methoxy-5,6-dihydro-AZT-5 '-(para-bromophenyl methoxyalaninyl phosphate) as novel spermicidal and anti-HIV agents
Authors: Jan, ST Shih, MJ Venkatachalam, TK D'Cruz, OJ Chen, CL Uckun, FM
Citation: St. Jan et al., Synthesis of dual function (5R,6R)- and (5S,6S)-5-bromo-6-methoxy-5,6-dihydro-AZT-5 '-(para-bromophenyl methoxyalaninyl phosphate) as novel spermicidal and anti-HIV agents, ANTIVIR CHE, 10(1), 1999, pp. 39-46
AZT-5 '-(p-bromophenyl methoxyalaninyl phosphate) as a potent and non-toxic anti-human immunodeficiency virus agent
Authors: Jan, ST Zhu, Z Tai, HL Shih, MJ Venkatachalam, TK Uckun, FM
Citation: St. Jan et al., AZT-5 '-(p-bromophenyl methoxyalaninyl phosphate) as a potent and non-toxic anti-human immunodeficiency virus agent, ANTIVIR CHE, 10(1), 1999, pp. 47-52
Stereoselective synthesis of a versatile intermediate for the total synthesis of mono- and bis-THF containing annonaceous acetogenins
Authors: Jan, ST Li, KQ Vig, S Rudolph, A Uckun, FM
Citation: St. Jan et al., Stereoselective synthesis of a versatile intermediate for the total synthesis of mono- and bis-THF containing annonaceous acetogenins, TETRAHEDR L, 40(2), 1999, pp. 193-196
Enhancing effects of a mono-bromo substitution at the para position of thephenyl moiety on the metabolism and anti-HIV activity of D4T-phenyl methoxyalaninyl phosphate derivatives
Authors: Venkatachalam, TK Tai, HL Vig, R Chen, CL Jan, ST Uckun, FM
Citation: Tk. Venkatachalam et al., Enhancing effects of a mono-bromo substitution at the para position of thephenyl moiety on the metabolism and anti-HIV activity of D4T-phenyl methoxyalaninyl phosphate derivatives, BIOORG MED, 8(22), 1998, pp. 3121-3126
Risultati: 1-9 |