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GMX1778 NAMPT remmer

Cat.nr.S8117

GMX1778 is een potente en specifieke remmer van nicotinamide fosforibosyltransferase (NAMPT) met een IC50 en Kd van respectievelijk < 25 nM en 120 nM. Deze verbinding induceert geprogrammeerde celdood met apoptotische kenmerken. Fase 1.
GMX1778 NAMPT remmer Chemical Structure

Chemische structuur

Molecuulgewicht: 371.86

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Kwaliteitscontrole

Batch: S811701 DMSO]74 mg/mL]false]Water]Insoluble]false]Ethanol]Insoluble]false Zuiverheid: 99.82%
  • Geciteerd in Nature Medicine vanwege de topkwaliteit
  • COA
  • NMR
  • HPLC
  • SDS
  • Datasheet
99.82

Celkweek, behandeling & werkzame concentratie

Cellijnen Assaytype Concentratie Incubatietijd Formulering Activiteitsbeschrijving PMID
A2780 Cytotoxicity assay 72 hrs Cytotoxicity against human A2780 cells after 72 hrs by SRB assay, IC50=0.005μM 23617784
NYH Cytotoxicity assay 3 weeks Cytotoxicity against human NYH cells after 3 weeks by clonogenic survival assay, LD50=0.0017μM 23679915
A2780 Antiproliferative assay 72 hrs Antiproliferative activity against human A2780 cells assessed as growth inhibition after 72 hrs by SRB-based microplate reader analysis, IC50=0.005μM 23859118
A2780 Cytotoxicity assay 72 hrs Cytotoxicity against human A2780 cells assessed as growth inhibition after 72 hrs by WST-1 assay, IC50=0.00056μM 24164086
MCF-7 Cytotoxicity assay 72 hrs Cytotoxicity against human MCF-7 cells assessed as growth inhibition after 72 hrs by WST-1 assay, IC50=0.0016μM 24164086
HepG2 Function assay 1 hr Inhibition of NAMPT in human HepG2 cells using [14C]-nicotinamide/PRPP as substrate assessed as formation of [14C]-nicotinamide mononucleotide after 1 hr by liquid scintillation counting analysis, IC50=0.0183μM 24164086
A2780 Antiproliferative assay 72 hrs Antiproliferative activity against human A2780 cells after 72 hrs by sulforhodamine B assay, IC50=0.005μM 24405419
HONE1 Cytotoxicity assay 24 hrs Cytotoxicity against human HONE1 cells after 24 hrs by SRB assay, IC50=0.015μM 25147148
MCF Cytotoxicity assay 24 hrs Cytotoxicity against human MCF cells after 24 hrs by SRB assay, IC50=0.018μM 25147148
NUGC Cytotoxicity assay 24 hrs Cytotoxicity against human NUGC cells after 24 hrs by SRB assay, IC50=0.025μM 25147148
HepG2 Cytotoxicity assay 24 hrs Cytotoxicity against human HepG2 cells after 24 hrs by SRB assay, IC50=1.245μM 25147148
HA22T Cytotoxicity assay 24 hrs Cytotoxicity against human HA22T cells after 24 hrs by SRB assay, IC50=2.067μM 25147148
DLD1 Cytotoxicity assay 24 hrs Cytotoxicity against human DLD1 cells after 24 hrs by SRB assay, IC50=2.315μM 25147148
A2780 Function assay 72 hrs Inhibition of NAMPT in human A2780 cells assessed as decrease in cell viability after 72 hrs by SRB assay, IC50=0.001μM 27541271
Rosetta (DE3) Function assay 15 mins Inhibition of human full length C-terminal His6-tagged NAMPT expressed in Escherichia coli Rosetta (DE3) cells using nicotinamide as substrate incubated for 15 mins prior to substrate addition measured after 30 mins in presence of PRPP, IC50=0.002μM 27541271
PC3 Antiproliferative assay 5 days Antiproliferative activity against human PC3 cells assessed as reduction in cell viability incubated for 5 days by Cell-titer Glo reagent based assay, IC50=0.0044μM 28610984
TC32 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for TC32 cells 29435139
DAOY qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for DAOY cells 29435139
SJ-GBM2 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SJ-GBM2 cells 29435139
A673 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for A673 cells 29435139
SK-N-MC qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-MC cells 29435139
BT-37 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-37 cells 29435139
NB-EBc1 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB-EBc1 cells 29435139
U-2 OS qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for U-2 OS cells 29435139
SK-N-SH qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-SH cells 29435139
NB1643 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB1643 cells 29435139
LAN-5 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for LAN-5 cells 29435139
BT-12 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-12 cells 29435139
Rh18 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh18 cells 29435139
OHS-50 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for OHS-50 cells 29435139
RD qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for RD cells 29435139
MG 63 (6-TG R) qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for MG 63 (6-TG R) cells 29435139
Rh30 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh30 cells 29435139
Rh41 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh41 cells 29435139
NB1643 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for NB1643 cells 29435139
A673 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for A673 cells) 29435139
SK-N-MC qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SK-N-MC cells 29435139
LAN-5 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for LAN-5 cells 29435139
DAOY qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for DAOY cells 29435139
NB-EBc1 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for NB-EBc1 cells 29435139
SJ-GBM2 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SJ-GBM2 cells 29435139
BT-37 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for BT-37 cells 29435139
TC32 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for TC32 cells 29435139
U-2 OS qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for U-2 OS cells 29435139
Rh41 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh41 cells 29435139
RD qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for RD cells 29435139
Rh18 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh18 cells 29435139
Rh30 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh30 cells 29435139
Saos-2 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Saos-2 cells 29435139
4T1 Antitumor assay 10 mg/kg 12 days Antitumor activity against mouse 4T1 cells implanted in BALB/c mouse assessed as reduction in tumour volume at 10 mg/kg, ip bid for 12 days by vernier caliper method 31400709
4T1 Antitumor assay 10 mg/kg 12 days Antitumor activity against mouse 4T1 cells implanted in BALB/c mouse assessed as reduction in tumor weight at 10 mg/kg, ip bid for 12 days 31400709
4T1 Antitumor assay 10 mg/kg 12 days Antitumor activity against mouse 4T1 cells implanted in Balb/c mouse mouse assessed as inhibition of tumor metastasis at 10 mg/kg, ip bid for 12 days measured post last dose by crystal violet staining based thioguanine clonogenic assay 31400709
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Chemische informatie, opslag en stabiliteit

Molecuulgewicht 371.86 Formule

C19H22ClN5O

Opslag (vanaf de datum van ontvangst)
CAS-nr. 200484-11-3 SDF downloaden Opslag van stamoplossingen

Synoniemen CHS828 Smiles C1=CC(=CC=C1OCCCCCCN=C(NC#N)NC2=CC=NC=C2)Cl

Oplosbaarheid

In vitro
Batch:

DMSO : 74 mg/mL (198.99 mM)
(Met vocht verontreinigd DMSO kan de oplosbaarheid verminderen. Gebruik verse, watervrije DMSO.)

Water : Insoluble

Ethanol : Insoluble

Molariteitscalculator

Massa Concentratie Volume Molecuulgewicht
Verdunningscalculator Molecuulgewichtcalculator

In vivo
Batch:

In vivo formulatiecalculator (heldere oplossing)

Stap 1: Voer onderstaande informatie in (Aanbevolen: een extra dier om rekening te houden met verlies tijdens het experiment)

mg/kg g μL

Stap 2: Voer de in vivo formulering in (Dit is alleen de calculator, geen formulering. Neem eerst contact met ons op als er geen in vivo formulering is in de sectie oplosbaarheid.)

% DMSO % % Tween 80 % ddH2O
%DMSO %

Berekeningsresultaten:

Werkconcentratie: mg/ml;

Methode voor het bereiden van DMSO-moedervloeistof: mg geneesmiddel vooropgelost in μL DMSO ( Concentratie moedervloeistof mg/mL, Neem eerst contact met ons op als de concentratie de DMSO-oplosbaarheid van de batch van het geneesmiddel overschrijdt. )

Methode voor het bereiden van in vivo formulering: Neem μL DMSO moedervloeistof, voeg daarna toeμL PEG300, mengen en verhelderen, daarna toevoegenμL Tween 80, mengen en verhelderen, daarna toevoegen μL ddH2O, mengen en verhelderen.

Methode voor het bereiden van in vivo formulering: Neem μL DMSO moedervloeistof, voeg daarna toe μL Maïsolie, mengen en verhelderen.

Opmerking: 1. Zorg ervoor dat de vloeistof helder is voordat u het volgende oplosmiddel toevoegt.
2. Zorg ervoor dat u het/de oplosmiddel(en) in de juiste volgorde toevoegt. U moet ervoor zorgen dat de verkregen oplossing, bij de vorige toevoeging, een heldere oplossing is voordat u verdergaat met het toevoegen van het volgende oplosmiddel. Fysieke methoden zoals vortexen, ultrasoon of een warmwaterbad kunnen worden gebruikt om het oplossen te bevorderen.

Werkingsmechanisme

Targets/IC50/Ki
NAMPT
<25 nM
NAMPT
120 nM(Kd)
In vitro

GMX1778 induceert NAD+-depletie door remming van de NAD+-biosynthese, gevolgd door ATP-depletie en resulteerde uiteindelijk in celdood. Deze verbinding induceert geprogrammeerde celdood met apoptotische kenmerken. Het onderdrukt de nucleaire factor-kappa B-activiteit in kankercellen door downregulatie van de IKK-activiteit (IC50=8 nM).

Kinase Assay
In vitro gekoppelde-enzym NAMPT-analyse
Recombinante NAMPT-activiteit wordt beoordeeld met behulp van een gekoppelde-enzymanalyse gebaseerd op de kwantificering van NAD+. Reacties worden uitgevoerd bij kamertemperatuur gedurende 180 min met mengsels bestaande uit 50 mM HEPES (pH 7,4), 50 mM KCl, 5 mM MgCl2, 0,5 mM β-mercapto-ethanol, 0,005% bovine serumalbumine, 1% DMSO, 2,0 U/ml lactaatdehydrogenase, 4 mM natrium-L-lactaat, 0,4 U/ml diaforase, 6 μM resazurine-natriumzout, 0,4 mM PRPP, 3,0 nM NMNAT1, 125 μM ATP, 50 μM NM en 2 tot 5 μM recombinante NAMPT. Fluorescentie wordt gemeten met een Tecan Safire plaatlezer (excitatiegolflengte, 560 nm; emissiegolflengte, 590 nm). Ki-waarden worden berekend met Graphpad Prism 4.0 software en de Cheng-Prusoff-vergelijking.
In vivo

GMX1778 (250 mg/kg, p.o.) vertoont een uitgesproken antitumorale activiteit tegen drie verschillende menselijke neuro-endocriene tumoren, middendarmcarcinoïd (GOT1), pancreatisch carcinoïd (BON) en medullair schildkliercarcinoom (GOT2), getransplanteerd in naaktmuizen.

Referenties
  • [4] https://pubmed.ncbi.nlm.nih.gov/16508338/

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Veelgestelde vragen

Vraag 1:
Could you please suggest me the suitable formulation of it for in vivo study?

Antwoord:
It can be dissolved in 1%CMC-Na (suspension) for oral administration.