Photoactivatable prodrugs of highly potent duocarmycin analogues for a selective cancer therapy.
about
Palladium-mediated dealkylation of N-propargyl-floxuridine as a bioorthogonal oxygen-independent prodrug strategyIn Vivo Activation of Duocarmycin-Antibody Conjugates by Near-Infrared LightObservation by NMR of cationic Wheland-like intermediates in the deiodination of protected 1-iodonaphthalene-2,4-diamines in acidic media.The two faces of potent antitumor duocarmycin-based drugs: a structural dissection reveals disparate motifs for DNA versus aldehyde dehydrogenase 1 affinity.
P2860
Photoactivatable prodrugs of highly potent duocarmycin analogues for a selective cancer therapy.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Photoactivatable prodrugs of h ...... or a selective cancer therapy.
@en
Photoactivatable prodrugs of h ...... or a selective cancer therapy.
@nl
type
label
Photoactivatable prodrugs of h ...... or a selective cancer therapy.
@en
Photoactivatable prodrugs of h ...... or a selective cancer therapy.
@nl
prefLabel
Photoactivatable prodrugs of h ...... or a selective cancer therapy.
@en
Photoactivatable prodrugs of h ...... or a selective cancer therapy.
@nl
P2093
P2860
P356
P1476
Photoactivatable prodrugs of h ...... or a selective cancer therapy.
@en
P2093
Ingrid Schuberth
Kianga Schmuck
Lutz F Tietze
Michael Müller
Svenia-C Duefert
P2860
P304
P356
10.1002/CHEM.201202773
P407
P577
2012-12-07T00:00:00Z