General Information of This Linker
Linker ID
LIN0ZJHUI
Linker Name
Tuneable thiol exchange linker 1
Linker Type
Reduction sensitive linker
Antibody-Linker Relation
Cleavable
Structure
Formula
C14H16N4O3S
Isosmiles
OCCS/C=C/C(C(C=C1)=CC=C1C(NCCN=[N+]=[N-])=O)=O
InChI
InChI=1S/C14H16N4O3S/c15-18-17-7-6-16-14(21)12-3-1-11(2-4-12)13(20)5-9-22-10-8-19/h1-5,9,19H,6-8,10H2,(H,16,21)/b9-5+
InChIKey
JTDMMBWOXVYGIE-WEVVVXLNSA-N
Pharmaceutical Properties
Molecule Weight
320.374
Polar area
115.16
Complexity
548.2060363
xlogp Value
2.1486
Heavy Count
22
Rot Bonds
9
Hbond acc
5
Hbond Donor
2
Each Antibody-drug Conjugate Related to This Linker
Full Information of The Activity Data of The ADC(s) Related to This Linker
38888299 ADC 1 [Investigative]
Revealed Based on the Cell Line Data
Click To Hide/Show 1 Activity Data Related to This Level
Experiment 1 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal inhibitory Concentration (lC50)
1 nM
Positive HER2 expression (HER2+++/++)
Method Description
To investigate the cytotoxicity of the unconjugated small-molecule TOP1 inhibitors and ADCs, respective cells were incubated for 4 days (small molecules) and 7 days (ADCs) with increasing concentrations of small molecules (0.015-1,000 nmol/L) and ADCs (0.05-3 ug/mL) to generate a dose-response curve. Killing was analyzed using resazurin cell viability dye at a final concentration of 55 umol/L (Merck) by dividing the fluorescence from control cells in medium by the fluorescence of ADC-treated cells. Fluorescence emission at 590 nmol/L was measured on a microplate reader Infinite 200 Pro (Tecan Group Ltd.).

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In Vitro Model Breast adenocarcinoma SK-BR-3 cells CVCL_0033
References
Ref 1 Tuneable thiol exchange linkers for traceless drug release applications in prodrugs and ADCs