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PD-1/PD-L1 Inhibitor 3 PD-1/PD-L1 inhibitor

Cat.No.S8158

PD-1/PD-L1 Inhibitor 3(Programmed Death-1/Programmed Death-Ligand 1 Inhibitor 3)is a Macrocyclic inhibitor of PD-1/PD-L1 interaction with IC50 of 5.6 nM
PD-1/PD-L1 Inhibitor 3 PD-1/PD-L1 inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 1852.17

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 1852.17 Formula

C89H126N24O18S

Storage (From the date of receipt)
CAS No. 1629654-95-0 Download SDF Storage of Stock Solutions

Synonyms N/A Smiles CCCCC1C(=O)NC(C(=O)NC(CSCC(=O)NC(C(=O)N(C(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)N(CC(=O)NC(C(=O)NC(C(=O)NC(C(=O)N(C(C(=O)N1C)CCCC)C)CC3=CNC4=CC=CC=C43)CO)CC5=CNC6=CC=CC=C65)C)CC(C)C)CC7=CN=CN7)CC(=O)N)C)C)CC8=CC=CC=C8)C(=O)NCC(=O)N)CCCNC(=N)N

Solubility

In vitro
Batch:

Water : 100 mg/mL

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Mechanism of Action

Targets/IC50/Ki
PD-1/PD-L1 interaction [1]
(Cell-free assay)
5.6 nM
In vitro

PD-1/PD-L1 Inhibitor 3 is capable of inhibiting the interaction of PD-L1 with PD-1 and with CD80. It has highly efficacious binding to PD-L1 and promotes enhanced T cell functional activity[1].

References

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Handling Instructions

Tel: +1-832-582-8158 Ext:3

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Frequently Asked Questions

Question 1:
Could you tell me what the difference is between these products (S7911, S7912, S8158), and do you have any recommendations about which one to select?

Answer:
They are of high purity and can be used for both cell culture and mouse study. S7911 and S7912 are small-molecule inhibitors that have different IC50s, while S8158 is a macrocyclic inhibitor.