General Information of This Peptide-drug Conjugate (PDC)
PDC ID
PDC_00261
PDC Name
P4-Chlor-PEG-AuNP
PDC Status
Investigative
Indication
In total 1 Indication(s)
Tumor
Structure
Peptide Name
p4
 Peptide Info 
Drug Name
Chlorambucil
 Drug Info 
Therapeutic Target
DNA topoisomerase 2-alpha (TOP2A)
 Target Info 
Linker Name
Gamma-Aminobutyric Acid
 Linker Info 
Peptide Modified Type
The modification of binding with chemical macromolecules
Modified Segment
PEG-AuNP
Formula
C47H69Cl2N11O14
#Ro5 Violations (Lipinski): 5 Molecular Weight 1083.038
Lipid-water partition coefficient (xlogp) -2.9962
Hydrogen Bond Donor Count (hbonddonor) 12
Hydrogen Bond Acceptor Count (hbondacc) 15
Rotatable Bond Count (rotbonds) 35
Full List of Activity Data of This Peptide-drug Conjugate
Revealed Based on the Cell Line Data
Click To Hide/Show 3 Activity Data Related to This Level
Experiment 1 Reporting the Activity Data of This PDC [1]
Indication Tumor
Efficacy Data A20 growth inhibition
40.00%
Administration Time 72 h
Administration Dosage 50 µM
Evaluation Method XTT assay
Description
All three P4-PDC-coated gold nanoparticles pre-incubated for 24 or 48 h induced statistically similar cytotoxicity in A20 to that induced by freshly prepared PDC4 and to coated particles without pre-incubation (the latter data not shown).
In Vitro Model Mouse reticulum cell sarcoma A20 cell CVCL_1940
Experiment 2 Reporting the Activity Data of This PDC [1]
Indication Tumor
Efficacy Data A20 growth inhibition
72.00%
Administration Time 48 h
Administration Dosage 50 µM
Evaluation Method XTT assay
MOA of PDC
In biological systems, antioxidants such as catalase, superoxide dismutase, glutathione peroxidase, and glutathione reductase are responsible for the elimination or reduction of the adverse effects of ROS, that is, they prevent or reduce ROS generation. Dietary antioxidants, such as vitamins E, A, and C, and anthocyanins and polyphenols have a role in the protection of cells against ROS damage.

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Description
All three P4-PDC-coated gold nanoparticles pre-incubated for 24 or 48 h induced statistically similar cytotoxicity in A20 to that induced by freshly prepared PDC4 and to coated particles without pre-incubation (the latter data not shown).
In Vitro Model Mouse reticulum cell sarcoma A20 cell CVCL_1940
Experiment 3 Reporting the Activity Data of This PDC [1]
Indication Tumor
Efficacy Data A20 growth inhibition
80.00%
Administration Time 24 h
Administration Dosage 50 µM
Evaluation Method XTT assay
Description
All three P4-PDC-coated gold nanoparticles pre-incubated for 24 or 48 h induced statistically similar cytotoxicity in A20 to that induced by freshly prepared PDC4 and to coated particles without pre-incubation (the latter data not shown).
In Vitro Model Mouse reticulum cell sarcoma A20 cell CVCL_1940
References
Ref 1 Gold nanoparticles stabilize peptide-drug-conjugates for sustained targeted drug delivery to cancer cells. J Nanobiotechnology. 2018 Mar 30;16(1):34. doi: 10.1186/s12951-018-0362-1.