General Information of This Linker
Linker ID
LIN0UPIHT
Linker Name
H1H21234N-N297Q- LP6 lINKER
Linker Type
Cathepsin-cleavable linker
Antibody-Linker Relation
Cleavable
Structure
Formula
C58H85N11O15
Isosmiles
CC([C@@H](NC(O)CCOCCOCCOCCOCCNC(CCC(N1C2=C(C=CC=C2)C3=C(N(N=N3)CCCCCOCCOCCN)C4=C(C1)C=CC=C4)=O)=O)C(N[C@@H](CCCNC(N)=O)C(NC5=CC=C(C=C5)COC(O)=O)=O)=O)C
InChI
InChI=1S/C58H85N11O15/c1-41(2)52(56(74)64-47(14-10-24-62-57(60)75)55(73)63-44-18-16-42(17-19-44)40-84-58(76)77)65-50(71)22-28-79-32-35-82-37-38-83-36-34-81-30-25-61-49(70)20-21-51(72)68-39-43-11-4-5-12-45(43)54-53(46-13-6-7-15-48(46)68)66-67-69(54)26-8-3-9-27-78-31-33-80-29-23-59/h4-7,11-13,15-19,41,47,50,52,65,71H,3,8-10,14,20-40,59H2,1-2H3,(H,61,70)(H,63,73)(H,64,74)(H,76,77)(H3,60,62,75)/t47-,50?,52+/m0/s1
InChIKey
AUSUXLSNPVWJGD-URRGKQONSA-N
Pharmaceutical Properties
Molecule Weight
1176.38
Polar area
353.63
Complexity
2525.014769
xlogp Value
3.673
Heavy Count
84
Rot Bonds
42
Hbond acc
19
Hbond Donor
9
Each Antibody-drug Conjugate Related to This Linker
Full Information of The Activity Data of The ADC(s) Related to This Linker
H1H21234N-N297Q-LP6 [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 Effective Concentration (EC50)
0.685 nM
Positive MSR1 expression (MSR1+++/++)
Method Description
Anti-MSR1-LXR Agonist Conjugate Activity in Differentiated THP-4/LXR-Luc cells
In Vitro Model Acute monoblastic/monocytic leukemia, Childhood acute monocytic leukemia THP-1/LXR-Luc cells CVCL_5115
References
Ref 1 Bis-octahydrophenanthrene carboxamide derivatives and protein conjugates thereof for use as LXR agonists