General Information of This Linker
Linker ID
LIN0GLUHA
Linker Name
Ser-Gln linker
Linker Type
Cathepsin-cleavable linker
Antibody-Linker Relation
Cleavable
Structure
Formula
C10H16BrN3O6
Isosmiles
OC([C@H](CCC(N)=O)NC([C@H](CO)NC(CBr)=O)=O)=O
InChI
InChI=1S/C10H16BrN3O6/c11-3-8(17)13-6(4-15)9(18)14-5(10(19)20)1-2-7(12)16/h5-6,15H,1-4H2,(H2,12,16)(H,13,17)(H,14,18)(H,19,20)/t5-,6-/m0/s1
InChIKey
NNFHXSYOQPTRIH-WDSKDSINSA-N
Pharmaceutical Properties
Molecule Weight
354.157
Polar area
158.82
Complexity
356.2346001
xlogp Value
-2.3067
Heavy Count
20
Rot Bonds
9
Hbond acc
5
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
38283215 ADC 17 [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 Effective Concentration (EC50)
1.08 ug/mL
High TNF expression (TNF +++)
Method Description
ADC1-ADC27 with a DAR value of ~4 were screened in a GRE luciferase reporter assay in K562 cells over expressing mTNF and wild-type K562 cells to assess potency resulting from targeted delivery vs. nonspecific uptake. All the ADCs were inactive in the wild-type cells, suggesting the activity seen in mTNF over expressed cells was through targeted ADC uptake followed by intracellular release of compound C1.

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In Vitro Model Blast phase chronic myelogenous leukemia, BCR-ABL1 positive, Chronic myeloid leukemia K562 cells (TNF) CVCL_0004
Experiment 2 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal Effective Concentration (EC50) > 50 ug/mL Negative TNF expression (TNF-)
Method Description
ADC1-ADC27 with a DAR value of ~4 were screened in a GRE luciferase reporter assay in K562 cells over expressing mTNF and wild-type K562 cells to assess potency resulting from targeted delivery vs. nonspecific uptake. All the ADCs were inactive in the wild-type cells, suggesting the activity seen in mTNF over expressed cells was through targeted ADC uptake followed by intracellular release of compound C1.

   Click to Show/Hide
In Vitro Model Blast phase chronic myelogenous leukemia, BCR-ABL1 positive, Chronic myeloid leukemia K562 cells (wt) CVCL_0004
References
Ref 1 Impact of dipeptide on ADC physicochemical properties and efficacy identifies Ala-Ala as the optimal dipeptide