Linker Information
General Information of This Linker
Linker ID |
LIN0JLFQA
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Linker Name |
Mal-PEG4-Val-Cit-PABC
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Linker Type |
Thiol-sensitive linker
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Antibody-Linker Relation |
Cleavable
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Structure | ||||||
Formula |
C36H55N7O12
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Isosmiles |
CC(C)[C@@H](C(=O)N[C@@H](CCCNC(=O)N)C(=O)NC1=CC=C(C=C1)CO)NC(=O)CCOCCOCCOCCOCCNC(=O)CCN2C(=O)C=CC2=O
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PubChem CID | ||||||
InChI |
InChI=1S/C36H55N7O12/c1-25(2)33(35(50)41-28(4-3-13-39-36(37)51)34(49)40-27-7-5-26(24-44)6-8-27)42-30(46)12-16-52-18-20-54-22-23-55-21-19-53-17-14-38-29(45)11-15-43-31(47)9-10-32(43)48/h5-10,25,28,33,44H,3-4,11-24H2,1-2H3,(H,38,45)(H,40,49)(H,41,50)(H,42,46)(H3,37,39,51)/t28-,33-/m0/s1
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InChIKey |
PEGLOOGTSQEDBL-UVMMSNCQSA-N
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IUPAC Name |
(2S)-5-(carbamoylamino)-2-[[(2S)-2-[3-[2-[2-[2-[2-[3-(2,5-dioxopyrrol-1-yl)propanoylamino]ethoxy]ethoxy]ethoxy]ethoxy]propanoylamino]-3-methylbutanoyl]amino]-N-[4-(hydroxymethyl)phenyl]pentanamide
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Pharmaceutical Properties |
Molecule Weight
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777.9
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Polar area
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266
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Complexity
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1240
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xlogp Value
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-2.4
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Heavy Count
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55
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Rot Bonds
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29
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Hbond acc
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12
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Hbond Donor
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7
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Each Antibody-drug Conjugate Related to This Linker
Full Information of The Activity Data of The ADC(s) Related to This Linker
DAB4-DuoDM [Investigative]
Discovered Using Cell Line-derived Xenograft Model
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 71.40% (Day 8) | Positive La/SSB expression (La/SSB +++/++) | ||
Method Description |
A549 tumor-bearing mice were treated intraperitoneally with 150 mg/kg gemcitabine and 3 mg/kg cisplatin on Day 1. The day after chemotherapy, mice were treated with an intravenous injection of ADC.
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In Vivo Model | A549 CDX model | ||||
In Vitro Model | Lung adenocarcinoma | A-549 cells | CVCL_0023 |
References
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