Novel mustard functionalized sophoridine derivatives were synthesized and evaluated for their cytotoxicity against of a panel of various cancer cell lines. They were shown to be more sensitive to S180 and H22 tumor cells with IC50 values ranging from 1.01–3.65 μM, and distinctly were more cytotoxic to cancer cells than normal cell L929. In addition, compounds 7a, 7c, and 7e displayed moderate tumor suppression without apparent organ toxicity in vivo against mice bearing H22 liver tumors. Furthermore, they arrested tumor cells in the G1 phase and induced cellular apoptosis. Their potential binding modes with DNA-Top I complex have also been investigated
International audienceA new series of sulfonylcycloureas derivatives have been synthesized and evalu...
The design, synthesis, in vitro and in vivo activity against L1210 murine leukaemia of the dibromo n...
The design, synthesis, in vitro and in vivo activity against L1210 murine leukaemia of the dibromo n...
Novel mustard functionalized sophoridine derivatives were synthesized and evaluated for their cytoto...
AbstractTaking 12-N-p-chlorobenzyl sophoridinol 2 as a lead, a series of novel sophoridinic derivati...
Using sophoridine 1 and chalcone 3 as the lead compounds, a series of novel α, β-unsaturated sophori...
A series of nitroarylmethyl phosphoramide mustards was designed, synthesized and evaluated as nitror...
A series of achiral hypoxia-activated prodrugs were synthesized on the basis of the DNA cross-linkin...
A series of N-mustards, which was conjugated to mono- or bis-naphthalimides with a flexible amine li...
Advanced cancers after metastasis need to be treated systemically using chemotherapy or radiation, w...
A series of sulfonyl-group containing analogues of aldophosphamide (Aldo) were synthesized as potent...
A series of N-mustards, which was conjugated to mono-or bis-naphthalimides with a flexible amine lin...
A series of nitroarylmethyl phosphoramide mustards was designed, synthesized and evaluated as nitror...
A series of 12<i>N</i>-substituted sophoridinamine derivatives were synthesized and evaluated for th...
International audienceThe synthesis and biological activity of a novel DNA cross-linking antitumor a...
International audienceA new series of sulfonylcycloureas derivatives have been synthesized and evalu...
The design, synthesis, in vitro and in vivo activity against L1210 murine leukaemia of the dibromo n...
The design, synthesis, in vitro and in vivo activity against L1210 murine leukaemia of the dibromo n...
Novel mustard functionalized sophoridine derivatives were synthesized and evaluated for their cytoto...
AbstractTaking 12-N-p-chlorobenzyl sophoridinol 2 as a lead, a series of novel sophoridinic derivati...
Using sophoridine 1 and chalcone 3 as the lead compounds, a series of novel α, β-unsaturated sophori...
A series of nitroarylmethyl phosphoramide mustards was designed, synthesized and evaluated as nitror...
A series of achiral hypoxia-activated prodrugs were synthesized on the basis of the DNA cross-linkin...
A series of N-mustards, which was conjugated to mono- or bis-naphthalimides with a flexible amine li...
Advanced cancers after metastasis need to be treated systemically using chemotherapy or radiation, w...
A series of sulfonyl-group containing analogues of aldophosphamide (Aldo) were synthesized as potent...
A series of N-mustards, which was conjugated to mono-or bis-naphthalimides with a flexible amine lin...
A series of nitroarylmethyl phosphoramide mustards was designed, synthesized and evaluated as nitror...
A series of 12<i>N</i>-substituted sophoridinamine derivatives were synthesized and evaluated for th...
International audienceThe synthesis and biological activity of a novel DNA cross-linking antitumor a...
International audienceA new series of sulfonylcycloureas derivatives have been synthesized and evalu...
The design, synthesis, in vitro and in vivo activity against L1210 murine leukaemia of the dibromo n...
The design, synthesis, in vitro and in vivo activity against L1210 murine leukaemia of the dibromo n...