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Cat.nr.: S3022
Chemische structuur
| Gerelateerde doelwitten | Akt Wnt/beta-catenin PKC HSP ROCK Integrin Bcr-Abl Actin FAK Kinesin |
|---|---|
| Overig Microtubule Associated Inhibitoren | Nocodazole Patupilone (Epothilone B) CW069 Lexibulin (CYT997) Combretastatin A4 ABT-751 (E7010) Epothilone A Cucurbitacin B TRx0237 (LMTX) mesylate DM1 (Mertansine) |
| 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 | ||||||
| Molecuulgewicht | 835.93 | Formule | C45H57NO14 |
Opslag (vanaf de datum van ontvangst) | |
|---|---|---|---|---|---|
| CAS-nr. | 183133-96-2 | SDF downloaden | Opslag van stamoplossingen |
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| 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 | ||
|
In vitro |
DMSO
: 167 mg/mL
(199.77 mM)
Water : Insoluble Ethanol : Insoluble |
|
In vivo |
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Stap 1: Voer onderstaande informatie in (Aanbevolen: een extra dier om rekening te houden met verlies tijdens het experiment)
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.)
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.
| 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 |
|
(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 |
Vraag 1:
What is the elimination half-life of this compound?
Antwoord:
According to the paper report, its elimination half-life is 95h.