THPP-1

CAS No. 1257051-63-0

THPP-1( —— )

Catalog No. M22050 CAS No. 1257051-63-0

THPP-1 is a potent and orally bioavailable inhibitor of PDE10A(Ki of 1 nM and 1.3 nM for human and rat PDE10A, respectively).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 42 In Stock
5MG 41 In Stock
10MG 69 In Stock
25MG 150 In Stock
50MG 249 In Stock
100MG 367 In Stock
200MG 524 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    THPP-1
  • Note
    Research use only, not for human use.
  • Brief Description
    THPP-1 is a potent and orally bioavailable inhibitor of PDE10A(Ki of 1 nM and 1.3 nM for human and rat PDE10A, respectively).
  • Description
    THPP-1 is a potent and orally bioavailable inhibitor of PDE10A(Ki of 1 nM and 1.3 nM for human and rat PDE10A, respectively). Consistent with rodent data, both THPP-1 and risperidone significantly attenuated the stimulant effects in SIMA when administered alone, though some differences were noted. Combination therapy with a low dose of risperidone produced significantly more robust effects. THPP-1 and risperidone also produced a marked reduction of wake cycle time and gamma frequency power in EEG. However, THPP-1 differed from risperidone by reducing spectral power of lower frequencies.
  • In Vitro
    ——
  • In Vivo
    THPP-1 (0.1-1.0 mg/kg, p.o.) shows novel object recognition in rats.THPP-1 (p.o., 1-30 mg/kg) dose-dependently increases phosphorylation of GluR1 S845 in the rat striatum whereas the total levels of GluR1 in the striatum are not affected. Administration of THPP-1 also results in an associated increase in the pGluR1/GluR1 ratios at all doses examined in this study.THPP-1 (1, 3, 10 mg/kg, p.o.) significantly attenuated the stimulant effects in stimulant-induced motor activity (SIMA) in monkey. Animal Model:Male Wistar Hannover rats ranging from 200 to 300 g.Dosage:0.1-1.0 mg/kg.Administration:P.O.Result:Showed novel object recognition.Animal Model:Eleven monkeys were surgically implanted with subcutaneous telemetric devices to permit the simultaneous recording of electrocorticogram (ECoG), electrooculogram (EOG), and electromyogram (EMG) activit Dosage:1, 3, 10 mg/kg. Administration:P.O.Result:Significantly attenuated the stimulant effects in SIMA.Animal Model:Male Wistar Hannover rats ranging from 200 to 300 g.Dosage:1-30 mg/kg.Administration:P.O. (10% Tween 80/90% water) 2 h prior to tissue collection (Pharmacokinetic Analysis).Result:Dose-dependently increases phosphorylation of GluR1 S845.
  • Synonyms
    ——
  • Pathway
    Angiogenesis
  • Target
    PDE
  • Recptor
    PDE10A
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1257051-63-0
  • Formula Weight
    464.9
  • Molecular Formula
    C23H21ClN6O3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:31 mg/mL (66.68 mM; Need ultrasonic)
  • SMILES
    COCCOC1=C2CN(CCC2=NC(=N1)C1=CC=C(Cl)N=C1)C(=O)C1=C2C=CC=CN2C=N1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Vardigan JD, et al. Behavioral and qEEG effects of the PDE10A inhibitor THPP-1 in a novel rhesus model of antipsychotic activity. Psychopharmacology (Berl). 2016 Jul;233(13):2441-50.
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