연구용
제품 번호S7295
| 세포주 | 분석 유형 | 농도 | 배양 시간 | 제형 | 활성 설명 | PMID |
|---|---|---|---|---|---|---|
| HepG2 | Function assay | ~60 μM | DMSO | induces apoA-I mRNA and de novo synthesis of apoA-I. | 20513599 | |
| U2OS | Function assay | ~5 μM | displaces BET proteins from chromatin | 24248379 | ||
| BL21(DE3)-R3-pRARE2 | Function assay | Inhibition of recombinant human His6-tagged BRD4 bromodomain 2 expressed in Escherichia coli BL21(DE3)-R3-pRARE2 cells preincubated for 30 mins followed by HSGRGK(Ac)GGK(Ac)GLGK(Ac)GGAK(Ac)RHRK(Biotin)-OH peptide substrate addition after 30 mins by alphas, Kd = 0.135 μM. | 28195723 | |||
| BL21(DE3) | Function assay | Binding affinity to human BRD4 bromodomain 2 expressed in Escherichia coli BL21 (DE3) cells by isothermal titration calorimetry, Kd = 0.14 μM. | 26367539 | |||
| BL21(DE3)-R3-pRARE2 | Function assay | Inhibition of recombinant human His6-tagged BRD3 bromodomain 2 expressed in Escherichia coli BL21(DE3)-R3-pRARE2 cells, Kd = 0.195 μM. | 28195723 | |||
| BL21(DE3) | Function assay | Binding affinity to human BRD2 bromodomain 2 expressed in Escherichia coli BL21 (DE3) cells by isothermal titration calorimetry, Kd = 0.25 μM. | 26367539 | |||
| BL21(DE3)-R3-pRARE2 | Function assay | Inhibition of recombinant human His6-tagged BRD2 bromodomain 2 expressed in Escherichia coli BL21(DE3)-R3-pRARE2 cells, Kd = 0.251 μM. | 28195723 | |||
| BL21(DE3) | Function assay | Binding affinity to human BRD4 bromodomain 1 expressed in Escherichia coli BL21 (DE3) cells by isothermal titration calorimetry, Kd = 1.1 μM. | 26367539 | |||
| BL21(DE3)-R3-pRARE2 | Function assay | Inhibition of recombinant human His6-tagged BRD4 bromodomain 1 expressed in Escherichia coli BL21(DE3)-R3-pRARE2 cells preincubated for 30 mins followed by H4K5acK8acK12acK16ac peptide substrate addition after 30 mins by alphascreen assay, Kd = 1.142 μM. | 28195723 | |||
| SAE | Function assay | 24 hrs | Inhibition of BRD4 in human SAE cells assessed as reduction in TLR3 agonist poly(I:C) -induced ISG54 RNA expression preincubated for 24 hrs followed by poly(I:C) addition and measured after 4 hrs by SYBR green dye-based qRT-PCR analysis, IC50 = 2.63 μM. | 29649741 | ||
| SAE | Function assay | 24 hrs | Inhibition of BRD4 in human SAE cells assessed as reduction in TLR3 agonist poly(I:C) -induced ISG56 RNA expression preincubated for 24 hrs followed by poly(I:C) addition and measured after 4 hrs by SYBR green dye-based qRT-PCR analysis, IC50 = 2.74 μM. | 29649741 | ||
| SAE | Function assay | 24 hrs | Inhibition of BRD4 in human SAE cells assessed as reduction in TLR3 agonist poly(I:C) -induced grobeta RNA expression preincubated for 24 hrs followed by poly(I:C) addition and measured after 4 hrs by SYBR green dye-based qRT-PCR analysis, IC50 = 3.73 μM. | 29649741 | ||
| SAE | Function assay | 24 hrs | Inhibition of BRD4 in human SAE cells assessed as reduction in TLR3 agonist poly(I:C) -induced IL-8 RNA expression preincubated for 24 hrs followed by poly(I:C) addition and measured after 4 hrs by SYBR green dye-based qRT-PCR analysis, IC50 = 3.85 μM. | 29649741 | ||
| BL21(DE3)-R3-pRARE2 | Function assay | Inhibition of recombinant human His6-tagged BRD3 bromodomain 1 expressed in Escherichia coli BL21(DE3)-R3-pRARE2 cells, Kd = 4.065 μM. | 28195723 | |||
| MV4-11 | Antiproliferative assay | 72 hrs | Antiproliferative activity against human MV4-11 cells after 72 hrs by MTT assay, IC50 = 4.48 μM. | 28765013 | ||
| BL21(DE3)-R3-pRARE2 | Function assay | Inhibition of recombinant human His6-tagged BRD2 bromodomain 1 expressed in Escherichia coli BL21(DE3)-R3-pRARE2 cells, Kd = 5.78 μM. | 28195723 | |||
| BL21(DE3) | Function assay | Binding affinity to human BRD2 bromodomain 1 expressed in Escherichia coli BL21 (DE3) cells by isothermal titration calorimetry, Kd = 5.8 μM. | 26367539 | |||
| OCI-AML3 | Antiproliferative assay | 72 hrs | Antiproliferative activity against human OCI-AML3 cells after 72 hrs by MTT assay, IC50 = 7.17 μM. | 28765013 | ||
| OCI-AML2 | Antiproliferative assay | 72 hrs | Antiproliferative activity against human OCI-AML2 cells after 72 hrs by MTT assay, IC50 = 8.31 μM. | 28765013 | ||
| MCF7 | Autophagy assay | 150 uM | Induction of autophagy in human MCF7 cells assessed as downregulation of p62/SQSTM1 expression at 150 uM by Western blot analysis | 29172540 | ||
| MDA-MB-231 | Autophagy assay | 150 uM | Induction of autophagy in human MDA-MB-231 cells assessed as downregulation of p62/SQSTM1 expression at 150 uM by Western blot analysis | 29172540 | ||
| 클릭하여 더 많은 세포주 실험 데이터 보기 | ||||||
| 분자량 | 370.4 | 화학식 | C20H22N2O5 |
보관 (수령일로부터) | |
|---|---|---|---|---|---|
| CAS 번호 | 1044870-39-4 | SDF 다운로드 | 원액 보관 |
|
|
| 동의어 | RVX-000222 | Smiles | CC1=CC(=CC(=C1OCCO)C)C2=NC3=C(C(=CC(=C3)OC)OC)C(=O)N2 | ||
|
In vitro |
DMSO
: 74 mg/mL
(199.78 mM)
Water : Insoluble Ethanol : Insoluble |
|
In vivo |
|||||
1단계: 아래 정보 입력 (권장: 실험 중 손실을 고려하여 추가 동물 포함)
2단계: 생체 내 제형 입력 (이것은 계산기일 뿐 제형이 아닙니다. 용해도 섹션에 생체 내 제형이 없는 경우 먼저 당사에 문의하십시오.)
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.
| 특징 |
First-in-class BD2-selective inhibitor of BET bromodomain and has been tested in Phase II clinical trials for treatment of coronary syndromes and atherosclerosis.
|
|---|---|
| Targets/IC50/Ki |
BD2
(Cell-free assay) 0.51 μM
|
| 시험관 내(In vitro) |
BET bromodomain 억제제인 Apabetalone (RVX-208)은 BET 단백질에서 발견되는 두 번째 브로모도메인에 우선적으로 결합합니다. 아포리포단백질(APO) AI 유전자 발현 촉진제로서, 시험관 내에서 apoA-I 및 HDL-C를 증가시킵니다.
|
| 생체 내(In vivo) |
Apabetalone (RVX-208)은 AGM에서 혈청 apoA-I 및 HDL-C를 유의하게 증가시키고, 다른 경로를 통해 콜레스테롤 유출을 강화합니다.
|
참조 |
|
| 방법 | 바이오마커 | 이미지 | PMID |
|---|---|---|---|
| Western blot | p21 / p24 / β-actin cyclin D1 / CDK4 / CDK6 / p24 / β-actin Rb / p-Rb(S780) / p-Rb(S795) / p-Rb(S807/811) / β-actin Cyclin T1 / CDK9-55kDa / CDK9-42kDa / p-CDK9 / CTD / CTD-Ser2P / p24 / β-actin Phospho-RelA / Total-RelA / Actin / BRD2 / α-Tubulin |
|
29789664 |
| Immunofluorescence | monocyte adhesion DNA SARS-CoV-2 CTNT |
|
31300040 |
(데이터 출처 https://clinicaltrials.gov, 업데이트 날짜 2024-05-22)
| NCT 번호 | 모집 | 조건 | 스폰서/협력자 | 시작일 | 단계 |
|---|---|---|---|---|---|
| NCT03160430 | Not yet recruiting | Kidney Failure Chronic |
Resverlogix Corp |
November 22 2024 | Phase 1|Phase 2 |
| NCT03228940 | Withdrawn | Fabry Disease |
Resverlogix Corp |
November 22 2022 | Phase 1|Phase 2 |
| NCT01863225 | Terminated | Dyslipidemia|Coronary Artery Disease |
Resverlogix Corp|South Australian Health and Medical Research Institute |
May 2013 | Phase 2 |
| NCT01728467 | Completed | Diabetes |
Resverlogix Corp|Baker Heart and Diabetes Institute|Nucleus Network Ltd |
November 2012 | Phase 2 |
| NCT01067820 | Completed | Coronary Artery Disease |
Resverlogix Corp|The Cleveland Clinic |
September 2011 | Phase 2 |
| NCT01423188 | Completed | Coronary Artery Disease|Dyslipidemia |
Resverlogix Corp|The Cleveland Clinic |
August 2011 | Phase 2 |