A PD-1/PD-L1 interaction inhibitor
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Alternative(s)
31441BMS 1166
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BMS 1166 (hydrochloride)

Item No. 27774

Technical Information
Formal Name
(4R)-1-[[5-chloro-2-[(3-cyanophenyl)methoxy]-4-[[3-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-methylphenyl]methoxy]phenyl]methyl]-4-hydroxy-D-proline, monohydrochloride
CAS Number
2113650-05-6
Molecular Formula
C36H33ClN2O7 • HCl
Formula Weight
Purity
≥98%
A solid
SMILES
CC1=C(COC2=CC(OCC3=CC=CC(C#N)=C3)=C(CN4C[C@H](O)C[C@@H]4C(O)=O)C=C2Cl)C=CC=C1C(C=C5)=CC6=C5OCCO6.Cl
InChi Code
InChI=1S/C36H33ClN2O7.ClH/c1-22-26(6-3-7-29(22)25-8-9-32-35(14-25)44-11-10-43-32)21-46-34-16-33(45-20-24-5-2-4-23(12-24)17-38)27(13-30(34)37)18-39-19-28(40)15-31(39)36(41)42;/h2-9,12-14,16,28,31,40H,10-11,15,18-21H2,1H3,(H,41,42);1H/t28-,31-;/m1./s1
InChi Key
HYWQPFPFYSOTHD-UVFMYQNSSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    Product Description

    BMS 1166 is an inhibitor of the protein-protein interaction between programmed cell death 1 (PD-1) and its ligand PD-L1 that has an IC50 value of 1.4 nM in a homologous time-resolved fluorescence (HTRF) assay.1 It increases the activation of Jurkat cells expressing PD-1 in co-culture with CHO cells expressing PD-L1 (EC50 = 276 nM in a reporter assay).2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Guzik, K., Zak, K.M., Grudnik, P., et alSmall-molecule inhibitors of the programmed cell death-1/programmed death-ligand 1 (PD-1/PD-L1) interaction via transiently induced protein states and dimerization of PD-L1. J. Med. Chem. 60(13), 5857-5867 (2017).

    2. Skalniak, L., Zak, K.M., Guzik, K., et alSmall-molecule inhibitors of PD-1/PD-L1 immune checkpoint alleviate the PD-L1-induced exhaustion of T-cells. Oncotarget 8(42), 72167-72181 (2017).