000 01426 a2200349 4500
005 20250517145223.0
264 0 _c20190909
008 201909s 0 0 eng d
022 _a1873-5576
024 7 _a10.2174/1568009617666170330145709
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPang, Siu-Kwong
245 0 0 _aRedox Biotransformation and Delivery of Anthracycline Anticancer Antibiotics: How Interpretable Structure-activity Relationships of Lethality Using Electrophilicity and the London Formula for Dispersion Interaction Work.
_h[electronic resource]
260 _bCurrent cancer drug targets
_c2018
300 _a600-607 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAnthracyclines
_xchemistry
650 0 4 _aAntibiotics, Antineoplastic
_xchemistry
650 0 4 _aBiotransformation
650 0 4 _aDrug Delivery Systems
650 0 4 _aDrug Design
650 0 4 _aDrug-Related Side Effects and Adverse Reactions
650 0 4 _aHumans
650 0 4 _aHydrophobic and Hydrophilic Interactions
650 0 4 _aLethal Dose 50
650 0 4 _aNeoplasms
_xdrug therapy
650 0 4 _aOxidation-Reduction
650 0 4 _aQuantitative Structure-Activity Relationship
650 0 4 _aSignal Transduction
773 0 _tCurrent cancer drug targets
_gvol. 18
_gno. 6
_gp. 600-607
856 4 0 _uhttps://doi.org/10.2174/1568009617666170330145709
_zAvailable from publisher's website
999 _c27031923
_d27031923