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PDP-EA

Cat. No. M8449
PDP-EA Structure
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Biological Activity

3-N-Pentadecylphenolethanolamide (PDP-EA) is an activator of fatty acid amide hydrolase (FAAH) from plant and mammalian species. PDP-EA appears to enhance FAAH activity by reduction of negative feedback from free ethanoloamine.

Chemical Information
Molecular Weight 405.61
Formula C25H43NO3
CAS Number 861891-72-7
Solubility (25°C) DMSO: 5 mg/mL (warmed)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Jaikumar Duraiswamy, et al. Myeloid antigen-presenting cell niches sustain antitumor T cells and license PD-1 blockade via CD28 costimulation

[2] Deborah Blythe Doroshow, et al. PD-L1 as a biomarker of response to immune-checkpoint inhibitors

[3] Rajasekharan Somasundaram, et al. Tumor-infiltrating mast cells are associated with resistance to anti-PD-1 therapy

[4] Alexander C Huang, et al. A single dose of neoadjuvant PD-1 blockade predicts clinical outcomes in resectable melanoma

[5] Gang Chen, et al. Exosomal PD-L1 contributes to immunosuppression and is associated with anti-PD-1 response

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Keywords: PDP-EA supplier, inhibitors, activators


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