General Information of This Linker
Linker ID
LIN0QQCIX
Linker Name
Phenoxy silyl linker 37
Linker Type
Reduction sensitive linker
Antibody-Linker Relation
Cleavable
Structure
Formula
C38H58N6O13S2Si
Isosmiles
CC([Si](OC1=CC=C(CO)C=C1OC)(OCCOCC(N=N2)=CN2CCOCCOCCOCCNC(C3=CC(NS(C=C)(=O)=O)=CC(NS(C=C)(=O)=O)=C3)=O)C(C)C)C
InChI
InChI=1S/C38H58N6O13S2Si/c1-8-58(47,48)41-33-23-32(24-34(25-33)42-59(49,50)9-2)38(46)39-12-14-52-16-18-54-19-17-53-15-13-44-26-35(40-43-44)28-55-20-21-56-60(29(3)4,30(5)6)57-36-11-10-31(27-45)22-37(36)51-7/h8-11,22-26,29-30,41-42,45H,1-2,12-21,27-28H2,3-7H3,(H,39,46)
InChIKey
MLLZNPNQAYACGH-UHFFFAOYSA-N
Pharmaceutical Properties
Molecule Weight
899.131
Polar area
236.99
Complexity
1893.690216
xlogp Value
3.9036
Heavy Count
60
Rot Bonds
31
Hbond acc
16
Hbond Donor
4
Each Antibody-drug Conjugate Related to This Linker
Full Information of The Activity Data of The ADC(s) Related to This Linker
39914224 Ate-37 [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)
4.27 nM
Positive PD-L1 expression (PD-L1+++/++)
Method Description
The starting point of the small molecule drug was 500 nM, and the drug was diluted 5 times sequentially, for a total of eight concentration points. Cells were laid on 96-well plate at 4000 cells/well, cultured overnight and were added with diluted drugs, in the incubator for 72 h. All cells incubated with the drug were tested for cell viability using Cell Counting Kit-8 (CCK-8) kit (Meilunbio, Dalian, China).

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In Vitro Model Glioblastoma U87 cells CVCL_0022
References
Ref 1 Fine-tuning phenoxy silyl scaffolds for the development of glutathione-responsive prodrugs and antibody-drug conjugates