Cabazitaxel Microtubule Associated 억제제

제품 번호: S3022

Cabazitaxel은 세포 분열과 성장을 억제하여 암세포를 사멸시키는 천연 taxoid의 반합성 유도체입니다. 이 화합물은 세포 분열에 필수적인 과정인 Microtubule의 성장과 조립을 억제함으로써 그 효과를 나타냅니다. 이는 PI3K/Akt/mTOR 경로를 통해 Autophagy를 유도합니다.
Cabazitaxel Microtubule Associated 억제제 Chemical Structure

화학 구조

분자량: 835.93

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품질 관리 (Quality Control)

배치: 순도: 99.99%
99.99

세포 배양, 처리 및 작업 농도
(Cell Culture, Treatment & Working Concentration)

세포주 분석 유형 농도 배양 시간 제형 활성 설명 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
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화학 정보, 보관 및 안정성 (Chemical Information, Storage & Stability)

분자량 835.93 화학식

C45H57NO14

보관 (수령일로부터)
CAS 번호 183133-96-2 SDF 다운로드 원액 보관

동의어 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

용해도 (Solubility)

In vitro
배치:

DMSO : 167 mg/mL (199.77 mM)
(수분으로 오염된 DMSO는 용해도를 감소시킬 수 있습니다. 신선하고 무수 DMSO를 사용하십시오.)

Water : Insoluble

Ethanol : Insoluble

몰농도 계산기

질량 농도 부피 분자량
희석 계산기 분자량 계산기

In vivo
배치:

생체 내 제형 계산기 (투명한 용액)

1단계: 아래 정보 입력 (권장: 실험 중 손실을 고려하여 추가 동물 포함)

mg/kg g μL

2단계: 생체 내 제형 입력 (이것은 계산기일 뿐 제형이 아닙니다. 용해도 섹션에 생체 내 제형이 없는 경우 먼저 당사에 문의하십시오.)

% DMSO % % Tween 80 % ddH2O
%DMSO %

계산 결과:

작업 농도: mg/ml;

DMSO 원액 준비 방법: mg 약물 사전 용해 μL DMSO ( 원액 농도 mg/mL, 농도가 해당 약물 배치의 DMSO 용해도를 초과하는 경우 먼저 당사에 문의하십시오. )

생체 내 제형 준비 방법: 취하다 μL DMSO 원액, 다음 추가μL PEG300, 혼합하고 투명하게 한 다음 추가μL Tween 80, 혼합하고 투명하게 한 다음 추가 μL ddH2O, 혼합하고 투명하게 합니다.

생체 내 제형 준비 방법: 취하다 μL DMSO 원액, 다음 추가 μL 옥수수 기름, 혼합하고 투명하게 합니다.

참고: 1. 다음 용매를 추가하기 전에 액체가 투명한지 확인하십시오.
2. 용매를 순서대로 추가해야 합니다. 다음 용매를 추가하기 전에 이전 추가에서 얻은 용액이 투명한 용액인지 확인해야 합니다. 와동, 초음파 또는 뜨거운 물 중탕과 같은 물리적 방법을 사용하여 용해를 도울 수 있습니다.

작용 메커니즘 (Mechanism of Action)

특징
A semi-synthetic derivative of a natural taxoid.
Targets/IC50/Ki
Microtubule
(Cell-free assay)
시험관 내(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).

생체 내(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.

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

임상시험 정보 (Clinical Trial Information)

(데이터 출처 https://clinicaltrials.gov, 업데이트 날짜 2024-05-22)

NCT 번호 모집 조건 스폰서/협력자 시작일 단계
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

자주 묻는 질문 (Frequently Asked Questions)

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

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