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Cabazitaxel Microtubule Associated Remmer

Cat.nr.: S3022

Cabazitaxel is een semi-synthetisch derivaat van een natuurlijke taxoïde dat kankercellen doodt door celdeling en -groei te remmen. Deze verbinding oefent zijn effecten uit door de groei en assemblage van microtubule te remmen, processen die essentieel zijn voor cellen om te delen. Het induceert autophagy via de PI3K/Akt/mTOR-route.
Cabazitaxel Microtubule Associated Remmer Chemical Structure

Chemische structuur

Molecuulgewicht: 835.93

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Kwaliteitscontrole (Quality Control)

Batch: Zuiverheid: 99.99%
99.99

Celkweek, behandeling & werkzame concentratie
(Cell Culture, Treatment & Working Concentration)

Cellijnen Assaytype Concentratie Incubatietijd Formulering Activiteitsbeschrijving PMID
SGC7901 Growth inhibition assay Growth inhibition of human SGC7901 cells by MTT assay, GI50=0.0003553μM 24405702
U937 Growth inhibition assay Growth inhibition of human U937 cells by MTT assay, GI50=0.0005391μM 24405702
MCF7 Growth inhibition assay Growth inhibition of human MCF7 cells by MTT assay, GI50=0.001187μM 24405702
PANC1 Growth inhibition assay Growth inhibition of human PANC1 cells by MTT assay, GI50=0.001283μM 24405702
HT1080 Growth inhibition assay Growth inhibition of human HT1080 cells by MTT assay, GI50=0.001406μM 24405702
DU145 Growth inhibition assay Growth inhibition of human DU145 cells by MTT assay, GI50=0.001429μM 24405702
A549 Growth inhibition assay Growth inhibition of human A549 cells by MTT assay, GI50=0.001483μM 24405702
A431 Growth inhibition assay Growth inhibition of human A431 cells by MTT assay, GI50=0.001483μM 24405702
HeLa Growth inhibition assay Growth inhibition of human HeLa cells by MTT assay, GI50=0.001799μM 24405702
K562 Growth inhibition assay Growth inhibition of human K562 cells by MTT assay, GI50=0.004186μM 24405702
HL60 Growth inhibition assay Growth inhibition of human HL60 cells by MTT assay, GI50=0.004736μM 24405702
BGC823 Growth inhibition assay Growth inhibition of human BGC823 cells by MTT assay, GI50=0.4672μM 24405702
A549 Cytotoxicity assay Cytotoxicity against human A549 cells, IC50=0.00148μM 28850227
MES-SA/Dx5 Growth inhibition assay 72 hrs Growth inhibition of human MES-SA/Dx5 cells after 72 hrs by SRB assay, IC50=0.015μM 29251920
TC32 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for TC32 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
Saos-2 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Saos-2 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
OHS-50 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for OHS-50 cells 29435139
Rh41 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh41 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
TC32 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for TC32 cells 29435139
MG 63 (6-TG R) qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for MG 63 (6-TG R) 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
Saos-2 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Saos-2 cells 29435139
OHS-50 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for OHS-50 cells 29435139
NCI-H524 Cytotoxicity assay 2 hrs Cytotoxicity in human NCI-H524 cells pre-incubated for 2 hrs followed by compound wash out and subsequently incubated for 70 hrs by Cell Titer Glo assay, IC50=0.00026μM 30735385
Klik om meer experimentele gegevens over cellijnen te bekijken

Chemische informatie, opslag en stabiliteit (Chemical Information, Storage & Stability)

Molecuulgewicht 835.93 Formule

C45H57NO14

Opslag (vanaf de datum van ontvangst)
CAS-nr. 183133-96-2 SDF downloaden Opslag van stamoplossingen

Synoniemen XRP6258, RPR-116258A, TXD 258, Taxoid XRP6258 Smiles CC1=C2C(C(=O)C3(C(CC4C(C3C(C(C2(C)C)(CC1OC(=O)C(C(C5=CC=CC=C5)NC(=O)OC(C)(C)C)O)O)OC(=O)C6=CC=CC=C6)(CO4)OC(=O)C)OC)C)OC

Oplosbaarheid (Solubility)

In vitro
Batch:

DMSO : 167 mg/mL (199.77 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 (Mechanism of Action)

Kenmerken
A semi-synthetic derivative of a natural taxoid.
Targets/IC50/Ki
Microtubule
(Cell-free assay)
In vitro

Cabazitaxel increases CYP3A enzyme activities in rat hepatocytes. The mean ex-vivo human plasma protein binding of this compound is 91.6%. It is rapidly and extensively metabolised in numerous metabolites. This compound demonstrates activity in several murine and human resistant cell lines.

With a 4-day exposure to this chemical, cytotoxicity is noted with relatively low cabazitaxel concentrations. It shows high antitumor activity in 3 human colorectal cell lines (HCT-116, HCT-8, and HT-29).

In vivo

In accompanying models, Cabazitaxel is noted to have significant antitumor activity. In murine tumor xenografts (colon C38 and pancreas P03), this compound elicites complete tumor regressions. Using SF-295 and U251 human glioblastoma cell lines, both orthotopic and subcutaneous murine xenografts are generated. This chemical treatment leads to complete regression in the majority of subcutaneously implanted tumors. Furthermore, in orthotopic models, it leads to complete tumor regression in 4 out of 10 U251 tumors.

Referenties
  • [4] https://pubmed.ncbi.nlm.nih.gov/27608834/

Informatie over klinische proeven (Clinical Trial Information)

(gegevens van https://clinicaltrials.gov, bijgewerkt op 2024-05-22)

NCT-nummer Werving Aandoeningen Sponsor/medewerkers Startdatum Fasen
NCT04622761 Not yet recruiting
Prostate Cancer
The Clatterbridge Cancer Centre NHS Foundation Trust|University of Liverpool
January 15 2021 Phase 2
NCT04495179 Completed
Progressive Metastatic Castrate-Resistant Prostate Cancer
AstraZeneca|Parexel
August 4 2020 Phase 2
NCT03257891 Unknown status
Adrenocortical Carcinoma
Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia|San Luigi Gonzaga Hospital
January 25 2018 Phase 2
NCT03043989 Terminated
Prostate Cancer
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins|Maryland Technology Development Corporation
March 21 2017 Phase 1

Veelgestelde vragen (Frequently Asked Questions)

Vraag 1:
What is the elimination half-life of this compound?

Antwoord:
According to the paper report, its elimination half-life is 95h.