General Information of This Linker
Linker ID
LIN0MTORH
Linker Name
Acetamide-PEG4-Val-Ala-PABA
Linker Type
Cathepsin-cleavable linker
Antibody-Linker Relation
Cleavable
Structure
Formula
C28H45IN4O9
Isosmiles
CC(NC(=O)C(NC(=O)CCOCCOCCOCCOCCNC(=O)CI)C(C)C)C(=O)Nc1ccc(CO)cc1
InChI
InChI=1S/C28H45IN4O9/c1-20(2)26(28(38)31-21(3)27(37)32-23-6-4-22(19-34)5-7-23)33-24(35)8-10-39-12-14-41-16-17-42-15-13-40-11-9-30-25(36)18-29/h4-7,20-21,26,34H,8-19H2,1-3H3,(H,30,36)(H,31,38)(H,32,37)(H,33,35)
InChIKey
IKPMUMLEBHHRSL-UHFFFAOYSA-N
Pharmaceutical Properties
Molecule Weight
708.591
Polar area
173.55
Complexity
42
xlogp Value
0.7706
Heavy Count
42
Rot Bonds
23
Hbond acc
9
Hbond Donor
5
Each Antibody-drug Conjugate Related to This Linker
Full Information of The Activity Data of The ADC(s) Related to This Linker
Trastuzumab-SG3227 [Investigative]
Revealed Based on the Cell Line Data
Click To Hide/Show 2 Activity Data Related to This Level
Experiment 1 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal Inhibitory Concentration (IC50)
1.48 ng/mL
Low HER2 expression (HER2+)
Method Description
The cytotoxic effect of Trastuzumab-SG3227 was assessed in cell viability assays for a diverse panel of human solid tumor cell lines representing breast and gastric cancers. The potency of Trastuzumab-SG3227 was assessed on the NCI-N87 cell line.
In Vitro Model Gastric tubular adenocarcinoma NCI-N87 cells CVCL_1603
Experiment 2 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal Inhibitory Concentration (IC50)
2130.00 ng/mL
Negative expression (HER2-)
Method Description
The cytotoxic effect of Trastuzumab-SG3227 was assessed in cell viability assays for a diverse panel of human solid tumor cell lines representing breast and gastric cancers. The potency of Trastuzumab-SG3227 was assessed on the MDA-MB-468 cell line.
In Vitro Model Breast adenocarcinoma MDA-MB-468 cells CVCL_0419
Engineered HER-SG3227 [Investigative]
Revealed Based on the Cell Line Data
Click To Hide/Show 2 Activity Data Related to This Level
Experiment 1 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal Inhibitory Concentration (IC50)
4.29 ng/mL
Low HER2 expression (HER2+)
Method Description
The cytotoxic effect of Engineered Her-SG3227 was assessed in cell viability assays for a diverse panel of human solid tumor cell lines representing breast and gastric cancers. The potency of Engineered Her-SG3227 was assessed on the NCI-N87 cell line.
In Vitro Model Gastric tubular adenocarcinoma NCI-N87 cells CVCL_1603
Experiment 2 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal Inhibitory Concentration (IC50)
1220.00 ng/mL
Negative expression (HER2-)
Method Description
The cytotoxic effect of Engineered Her-SG3227 was assessed in cell viability assays for a diverse panel of human solid tumor cell lines representing breast and gastric cancers. The potency of Engineered Her-SG3227 was assessed on the MDA-MB-468 cell line.
In Vitro Model Breast adenocarcinoma MDA-MB-468 cells CVCL_0419
References
Ref 1 Synthesis and in vitro evaluation of SG3227, a pyrrolobenzodiazepine dimer antibody-drug conjugate payload based on sibiromycin. Bioorg Med Chem Lett. 2017 Mar 1;27(5):1154-1158.

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