A PPT1 inhibitor
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DC661

Item No. 34899

Technical Information
Formal Name
N6-(7-chloro-4-quinolinyl)-N1-[6-[(7-chloro-4-quinolinyl)amino]hexyl]-N1-methyl-1,6-hexanediamine
CAS Number
1872387-43-3
Molecular Formula
C31H39Cl2N5
Formula Weight
Purity
≥95%
Formulation
A solid
DMF: 30 mg/mlDMF:PBS (pH 7.2) (1:4): 0.20 mg/mlDMSO: 25 mg/mlEthanol: 15 mg/ml
λmax
218, 255, 331 nm
SMILES
ClC1=CC(N=CC=C2NCCCCCCN(CCCCCCNC3=C4C=CC(Cl)=CC4=NC=C3)C)=C2C=C1
InChi Code
InChI=1S/C31H39Cl2N5/c1-38(20-8-4-2-6-16-34-28-14-18-36-30-22-24(32)10-12-26(28)30)21-9-5-3-7-17-35-29-15-19-37-31-23-25(33)11-13-27(29)31/h10-15,18-19,22-23H,2-9,16-17,20-21H2,1H3,(H,34,36)(H,35,37)
InChi Key
VJKCWFZTSDXOBS-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    DC661 is an inhibitor of palmitoyl-protein thioesterase 1 (PPT1) and a dimeric form of hydroxychloroquine (Item No. 17911).1 It binds to PPT1 and inhibits PPT1 enzyme activity in A375 cells when used at concentrations of 5, 10, and 100 µM. DC661 (10 µM) inhibits autophagic flux and induces apoptosis in B-RAF mutant melanoma cell lines. It also induces stimulator of interferon genes (STING) activation and enhances antigen-primed T cell-mediated killing of B16/F10 murine melanoma cells in mouse splenocyte co-cultures.2 In vivo, DC661 (10 mg/kg) reduces intratumor autophagy and suppresses tumor growth in an HT-29 mouse xenograft model.1

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Rebecca, V.W., Nicastri, M.C., Fennelly, C., et alPPT1 promotes tumor growth and is the molecular target of chloroquine derivatives in cancer. Cancer Discov. 9(2), 220-229 (2019).

    2. Sharma, G., Ojha, R., Noguera-Ortega, E., et alPPT1 inhibition enhances the antitumor activity of anti-PD-1 antibody in melanoma. JCI Insight 5(17), e133225 (2020).