GLPBio

PHCCC

Catalog No.: GC17383Purity:>98.00%
PHCCC ist ein mGluR-Antagonist der Gruppe I mit einem IC50 von 3 μM. PHCCC ist ein selektiver positiver Modulator des mGlu4-Rezeptors. Antiparkinson-Effekt.

Die Produkte sind ausschließlich für Forschungszwecke bestimmt. Nicht zur Anwendung am Menschen. Wir verkaufen nicht an Patienten.


PHCCC
Cas No.: 179068-02-1
10mM (in 1mL DMSO)In Stock
$53.00
1
5mgIn Stock
$48.00
1
10mgIn Stock
$80.00
1
25mgIn Stock
$144.00
1
50mgIn Stock
$230.00
1
100mgIn Stock
$368.00
1

Zitate (Citations)

Für dieses Produkt sind derzeit keine Zitate verfügbar. Nachfolgend finden Sie ausgewählte Publikationen, die GlpBio-Produkte zitieren.
  • Nature cover
    Nature
    641, 529–536 (2025)
  • Nature cover
    Nature
    628, 630–638 (2024)
  • Nature cover
    Nature
    632, 686–694 (2024)
  • Nature cover
    Nature
    618, 1017–1023 (2023)
  • Nature cover
    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
  • Science cover
    Science
    388(6745) (2025)
  • Science cover
    Science
    387(6739) (2025)
  • Science cover
    Science
    387(6734) (2025)
  • Cell Research cover
    Cell Research
    35, 97–116 (2025)
  • Cell Research cover
    Cell Research
    34, 683–706 (2024)
  • Cell Research cover
    Cell Research
    33, 273–287 (2023)
  • Cell Research cover
    Cell Research
    33, 546–561 (2023)
  • Cell Research cover
    Cell Research
    33, 904–922 (2023)
  • Cell Research cover
    Cell Research
    31, 1291–1307 (2021)

Beschreibung (Description)

PHCCC is a group I mGluR antagonist with an IC50 value of 3μM [1]. PHCCC acts as the small molecule glutamate receptor enhancer, altering the functions of dendritic cells to metabolize glutamate, skewing cytokine secretion to bias T cell function [2]. PHCCC has been widely used to activate the mGlu6 receptor and regulate the natural calcium current in the sympathetic neurons isolated from the superior cervical ganglia of rats[3].

In vitro, PHCCC treatment (30µM) for 5 minutes significantly reduced the activity of the PI-3-K pathway in D283med cells and DAOY cells, and inhibited cAMP production[4]. In the presence of 1μM retinoic acid (RA), treatment with PHCCC (30µM) for 4 days enhanced the differentiation of mouse embryonic stem cells into neuronal lineage cells, resulting in increased expression of early neural markers Dlx-2 and Nestin[5].

In vivo, PHCCC treatment via a single intracerebroventricular injection (75nmol/2.5μl) for 30 minutes significantly reversed the movement disorders induced by reserpine in rats [6]. Intraperitoneal injection of PHCCC at a dose of 10mg/kg every other day for 20 days significantly inhibited tumor growth in the OS18 xenograft mouse model without affecting the body weight of the mice[7]. Subcutaneous injection of PHCCC at a dose of 3mg/kg every three days for 18 days significantly delayed disease progression and alleviated disease severity in mice with experimental autoimmune encephalomyelitis[8].

References:
[1] Recasens M, Guiramand J, Aimar R, et al. Metabotropic glutamate receptors as drug targets[J]. Current Drug Targets, 2007, 8(5): 651-681.
[2] Fallarino F, Volpi C, Fazio F, et al. Metabotropic glutamate receptor-4 modulates adaptive immunity and restrains neuroinflammation[J]. Nature medicine, 2010, 16(8): 897-902.
[3] Beqollari D, Kammermeier P J. The mGlu4 receptor allosteric modulator N-phenyl-7-(hydroxyimino) cyclopropa [b] chromen-1a-carboxamide acts as a direct agonist at mGlu6 receptors[J]. European journal of pharmacology, 2008, 589(1-3): 49-52.
[4] Iacovelli L, Arcella A, Battaglia G, et al. Pharmacological activation of mGlu4 metabotropic glutamate receptors inhibits the growth of medulloblastomas[J]. Journal of Neuroscience, 2006, 26(32): 8388-8397.
[5] Sarichelou I, Cappuccio I, Ferranti F, et al. Metabotropic glutamate receptors regulate differentiation of embryonic stem cells into GABAergic neurons[J]. Cell Death & Differentiation, 2008, 15(4): 700-707.
[6] Marino M J, Williams Jr D L, O'Brien J A, et al. Allosteric modulation of group III metabotropic glutamate receptor 4: a potential approach to Parkinson's disease treatment[J]. Proceedings of the National Academy of Sciences, 2003, 100(23): 13668-13673.
[7] Kansara M, Thomson K, Pang P, et al. Infiltrating myeloid cells drive osteosarcoma progression via GRM4 regulation of IL23[J]. Cancer discovery, 2019, 9(11): 1511-1519.
[8] Gammon J M, Tostanoski L H, Adapa A R, et al. Controlled delivery of a metabolic modulator promotes regulatory T cells and restrains autoimmunity[J]. Journal of Controlled Release, 2015, 210: 169-178.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

D283med cells

Preparation Method

D283med cells were cultured in Dulbecco’s modified Eagle’s medium/Nutrient Mix F12 supplemented with 10% fetal bovine serum, 100U/ml penicillin, and 100μg/ml streptomycin at 37°C with 5% CO2 and 95% saturated atmospheric humidity. Cells were seeded into 96-well microplates at a density of 3×104 cells/well. After 24h, cells were serum starved for 16-18h and challenged with different concentrations of PHCCC (0, 0.3, 3, 10, and 30µM) for 24h. [3H]Thymidine (1μCi/well) was added for the last 16-18h. The DNA synthesis in D283med cells was analyzed.

Reaction Conditions

0, 0.3, 3, 10, and 30µM; 24h

Applications

PHCCC treatment significantly reduced DNA synthesis in D283med cells in a dose-dependent manner.
Animal experiment [2]:

Animal models

C57B6/J mice

Preparation Method

C57B6/J mice, 7 weeks old, were maintained under a 12-h light and 12-h dark cycle at a temperature of 25°C and humidity of 50%±10%, free with water and diet. OS18 cells were mixed with 1:1 Matrigel: Minimum Essential medium, and a total volume of 100μl (106 cells) was injected subcutaneously in the flank. Mice were monitored for tumor growth relative to the adjacent non-tumor cell-injected leg. One week later, a 10mg/kg dose of PHCCC was intraperitoneally injected every other day for 20 days. The tumor growth and body weight of the mice were analyzed.

Dosage form

10mg/kg; every other day for 20 days; i.p.

Applications

PHCCC significantly inhibited tumor growth in the OS18 xenograft mouse model without affecting the body weight.

References:
[1] Iacovelli L, Arcella A, Battaglia G, et al. Pharmacological activation of mGlu4 metabotropic glutamate receptors inhibits the growth of medulloblastomas[J]. Journal of Neuroscience, 2006, 26(32): 8388-8397.
[2] Kansara M, Thomson K, Pang P, et al. Infiltrating myeloid cells drive osteosarcoma progression via GRM4 regulation of IL23[J]. Cancer discovery, 2019, 9(11): 1511-1519.

Produktdokumente (Product Documents)

Purity:>98.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
179068-02-1
Chemischer Name
(1aS,7aS,Z)-7-(hydroxyimino)-N-phenyl-1,1a,7,7a-tetrahydrocyclopropa[b]chromene-1a-carboxamide
SMILES
O=C([C@]1([C@H]/2C1)OC3=CC=CC=C3C2=N/O)NC4=CC=CC=C4
Summenformel
C17H14N2O3
Molekulargewicht
294.31
Löslichkeit
Soluble in DMSO
Lagerung
Store at -20°C
Allgemeine Hinweise
Wählen Sie anhand der Löslichkeitsdaten des Produkts ein geeignetes Lösungsmittel. Aliquotieren Sie die Stammlösung nach der Herstellung, um wiederholte Gefrier-Auftau-Zyklen zu vermeiden.
Verwenden Sie Stammlösungen bei Lagerung bei -80°C innerhalb von 6 Monaten bzw. bei -20°C innerhalb von 1 Monat.
Zur Verbesserung der Löslichkeit das Röhrchen auf 37°C erwärmen und für eine angemessene Dauer beschallen.
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

Reviews

Review for PHCCC

Rating: 5
  • 5 Star100%
  • 4 Star0%
  • 3 Star0%
  • 2 Star0%
  • 1 Star0%