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Daclatasvir (BMS-790052) HCV Protease 억제제

제품 번호S1482

Daclatasvir (BMS-790052, EBP883)는 광범위한 HCV 복제 유전자형 및 세포 배양에서 JFH-1 유전자형 2a 감염성 바이러스에 대해 EC50이 9-50 pM인 HCV NS5A의 고도로 선택적인 억제제입니다. 3상.
Daclatasvir (BMS-790052) HCV Protease 억제제 Chemical Structure

화학 구조

분자량: 738.88

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품질 관리

배치: 순도: 99.70%
99.70

세포 배양, 처리 및 작업 농도

세포주 분석 유형 농도 배양 시간 제형 활성 설명 PMID
human CEM cells Cytotoxicity assay 3 days Cytotoxicity against human CEM cells after 3 days, CC50=9.6 μM 25154714
Huh7 Antiviral assay 3 days Antiviral activity against HCV genotype 1b infected in human Huh7 cells after 3 days by cell-based replicon assay, EC50=0.000003μM 25148100
Huh-luc/neo-ET replicon Antiviral assay 48 hrs Antiviral activity against Hepatitis C virus genotype 1b harboring NS5A L28V mutant gene in Huh-luc/neo-ET replicon cells after 48 hrs by transient replicon mutant-based luciferase assay, EC50=0.000004μM 24568313
HuH7 Antiviral assay Antiviral activity against HCV genotype 1b infected in human HuH7 cells assessed as reduction in viral RNA replication, EC50=0.000004μM 26099532
HuH7 Antiviral assay Antiviral activity against HCV1b infected in human HuH7 cells assessed as inhibition of viral replication by RT-PCR analysis, EC50=0.0000066μM 22507961
HuH-Lcu-Neo Function assay 48 hrs Inhibition of NS5A in HCV genotype 1b infected in HuH-Lcu-Neo cells assessed as reduction in viral replication incubated for 48 hrs by luciferase reporter gene assay, EC50=0.0000081μM 32202782
Huh-5.2 Antiviral assay 4 days Antiviral activity against Hepatitis C virus genotype 1b infected in human Huh-5.2 cells assessed as decrease in HCV replicon RNA replication after 4 days by luciferase assay, EC50=0.000009μM 24900811
HuH7 Antiviral assay 3 days Antiviral activity against HCV genotype 1b Con1 infected in human HuH7 cells assessed as inhibition of viral RNA replication after 3 days by renilla luciferase reporter gene assay, EC50=0.000009μM 24320933
HuH7 Antiviral assay 72 hrs Antiviral activity against HCV1b infected in human HuH7 cells assessed as inhibition of viral replication after 72 hrs by FRET assay, EC50=0.000009μM 24521299
HuH7 Antiviral assay Antiviral activity against HCV genotype 1b Con1 infected in human HuH7 cells assessed as inhibition of viral replication, EC50=0.000009μM 26077493
Huh7.5/J6/JFH1/EMCVIRES/hRlucNeo Function assay 72 hrs Inhibition of NS5A in HCV genotype 2a infected in human Huh7.5/J6/JFH1/EMCVIRES/hRlucNeo cells assessed as inhibition of replicon levels incubated for 72 hrs by luciferase reporter gene assay, IC50=0.000009μM 31710479
HuH7 replicon Function assay 2 days Inhibition of NS5A in HCV genotype 1b infected in human HuH7 replicon cells assessed as reduction in subgenomic viral RNA replication treated for 2 days followed by compound washout and subsequent compound dosing measured after 1 day by SEAP reporter gene, EC50=0.000009μM 30772607
HuH7 Antiviral assay Antiviral activity against HCV 1b infected in human HuH7 cells by in vitro replicon assay, EC50=0.00001μM 23466233
Huh-luc/neo-ET replicon Antiviral assay 48 hrs Antiviral activity against Hepatitis C virus genotype 1b in Huh-luc/neo-ET replicon cells after 48 hrs by replicon-based luciferase assay, EC50=0.00001μM 24568313
HuH7 Function assay Inhibition of NS5A in HCV genotype-1b infected in human HuH7 cells by luciferase reporter gene assay, EC50=0.000023μM 25453810
HuH7.5/Con1/SG-Neo(I)-hRluc2aUb Function assay 72 hrs Inhibition of NS5A in HCV genotype 1b infected in human HuH7.5/Con1/SG-Neo(I)-hRluc2aUb cells assessed as inhibition of replicon levels incubated for 72 hrs by luciferase reporter gene assay, IC50=0.000023μM 31710479
HuH7 Antiviral assay Antiviral activity against HCV genotype 1b JFH-1 infected in human HuH7 cells assessed as inhibition of viral replication, EC50=0.000028μM 26077493
HuH7 Antiviral assay Antiviral activity against HCV 1b infected in human HuH7 cells by in vitro replicon assay, EC90=0.00003μM 23466233
HuH-Lcu-Neo Function assay 48 hrs Inhibition of NS5A in HCV genotype 1a infected in HuH-Lcu-Neo cells assessed as reduction in viral replication incubated for 48 hrs by luciferase reporter gene assay, EC50=0.0000324μM 32202782
HuH7 Antiviral assay Antiviral activity against HCV genotype 1b expressing NS5A L31V mutant infected in human HuH7 cells assessed as reduction in viral RNA replication, EC50=0.000035μM 26099532
Huh-luc/neo-ET replicon Antiviral assay 48 hrs Antiviral activity against Hepatitis C virus genotype 1a in Huh-luc/neo-ET replicon cells after 48 hrs by replicon-based luciferase assay, EC50=0.0000398μM 24568313
HuH7 Antiviral assay Antiviral activity against wild type HCV genotype 1b infected in human HuH7 cells assessed as reduction in viral RNA replication, EC50=0.000048μM 26099532
W11.8 Antiviral assay 4 days Antiviral activity against Hepatitis C virus genotype 1a infected in W11.8 cells assessed as decrease in NS5A expression in replicon cell after 4 days by luminescence based ELISA, EC50=0.00005μM 24900811
HuH7 Antiviral assay 3 days Antiviral activity against HCV genotype 1a H77 infected in human HuH7 cells assessed as inhibition of viral RNA replication after 3 days by renilla luciferase reporter gene assay, EC50=0.00005μM 24320933
HuH7 Antiviral assay 72 hrs Antiviral activity against HCV1a infected in human HuH7 cells assessed as inhibition of viral replication after 72 hrs by FRET assay, EC50=0.00005μM 24521299
HuH7 Antiviral assay Antiviral activity against HCV genotype 5a infected in human HuH7 cells by luciferase reporter gene assay, EC50=0.000051μM 25453811
HuH7 Antiviral assay Antiviral activity against HCV genotype 1b infected in human HuH7 cells by luciferase reporter gene assay, EC50=0.000073μM 25453811
HuH-Lcu-Neo Function assay 48 hrs Inhibition of NS5A in patient-derived HCV genotype 3a infected in HuH-Lcu-Neo cells assessed as reduction in viral replication incubated for 48 hrs by luciferase reporter gene assay, EC50=0.0001145μM 32202782
Huh-luc/neo-ET replicon Antiviral assay 48 hrs Antiviral activity against Hepatitis C virus genotype 1b harboring NS5A L31V mutant gene in Huh-luc/neo-ET replicon cells after 48 hrs by transient replicon mutant-based luciferase assay, EC50=0.0001259μM 24568313
HuH7 Function assay Inhibition of NS5A in HCV genotype-1a infected in human HuH7 cells by luciferase reporter gene assay, EC50=0.00014μM 25453810
HuH7 Antiviral assay Antiviral activity against HCV genotype 1a infected in human HuH7 cells by luciferase reporter gene assay, EC50=0.00014μM 25453811
HuH7 Antiviral assay Antiviral activity against HCV genotype 1b expressing NS5A Y93H mutant infected in human HuH7 cells assessed as reduction in viral RNA replication, EC50=0.00018μM 26099532
Huh-luc/neo-ET replicon Antiviral assay 48 hrs Antiviral activity against Hepatitis C virus genotype 1b harboring NS5A Y93H mutant gene in Huh-luc/neo-ET replicon cells after 48 hrs by transient replicon mutant-based luciferase assay, EC50=0.0003162μM 24568313
HuH7 Antiviral assay 72 hrs Antiviral activity against HCV1a infected in human HuH7 cells assessed as inhibition of viral replication after 72 hrs by FRET assay, EC90=0.00038μM 24521299
HuH7 Antiviral assay Antiviral activity against HCV genotype 4a infected in human HuH7 cells by luciferase reporter gene assay, EC50=0.00041μM 25453811
HuH-Lcu-Neo Function assay 48 hrs Inhibition of NS5A in HCV genotype 3a con infected in HuH-Lcu-Neo cells assessed as reduction in viral replication incubated for 48 hrs by luciferase reporter gene assay, EC50=0.0004115μM 32202782
HuH7 Antiviral assay Antiviral activity against HCV genotype 6a infected in human HuH7 cells by luciferase reporter gene assay, EC50=0.00045μM 25453811
HuH7 Antiviral assay Antiviral activity against HCV genotype 3a infected in human HuH7 cells by luciferase reporter gene assay, EC50=0.00067μM 25453811
HuH7 Antiviral assay Antiviral activity against HCV genotype 2a infected in human HuH7 cells by luciferase reporter gene assay, EC50=0.00067μM 25453811
HuH-Lcu-Neo Function assay 48 hrs Inhibition of NS5A in patient-derived HCV genotype 2a infected in HuH-Lcu-Neo cells assessed as reduction in viral replication incubated for 48 hrs by luciferase reporter gene assay, EC50=0.0494μM 32202782
HuH-Lcu-Neo Function assay 48 hrs Inhibition of NS5A in HCV genotype 2a con infected in HuH-Lcu-Neo cells assessed as reduction in viral replication incubated for 48 hrs by luciferase reporter gene assay, EC50=0.05285μM 32202782
CEM Cytotoxicity assay 3 days Cytotoxicity against human CEM cells after 3 days, CC50=9.6μM 22507961
CEM Cytotoxicity assay Cytotoxicity against human CEM cells, CC50=9.6μM 22704887
Vero Cytotoxicity assay Cytotoxicity against african green monkey Vero cells, CC50=9.6μM 23466233
CEM Cytotoxicity assay Cytotoxicity against human CEM cells, CC50=10μM 26099532
PBMC Cytotoxicity assay Cytotoxicity against human PBMC cells, CC50=19μM 22704887
Vero Cytotoxicity assay 3 days Cytotoxicity against african green monkey Vero cells after 3 days, CC50=21μM 22507961
Vero Cytotoxicity assay Cytotoxicity against african green monkey Vero cells, CC50=21μM 22704887
CEM Cytotoxicity assay Cytotoxicity against human CEM cells, CC50=21μM 23466233
Vero Cytotoxicity assay Cytotoxicity against african green monkey Vero cells, CC50=21μM 26099532
Huh7.5.1 Antiviral assay 100 pM to 1 uM Antiviral activity against HCV genotype 1b NK/R2AN infected in human Huh7.5.1 cells expressing NS5A L31V mutant assessed as reduction in virus replication at 100 pM to 1 uM by luciferase reporter gene assay 26134551
Huh7.5.1 Antiviral assay 100 pM to 1 uM Antiviral activity against HCV genotype 1b NK/R2AN infected in human Huh7.5.1 cells expressing NS5A Y93H mutant assessed as reduction in virus replication at 100 pM to 1 uM by luciferase reporter gene assay 26134551
GS4.3 Antiviral assay 0.15 uM 6 days Antiviral activity against HCV infected in human GS4.3 cells assessed as inhibition of NS3/4A levels at 0.15 uM treated with fresh media containing compound every 2 days measured after 6 days by Western blot method 29232582
GS4.3 Antiviral assay 0.15 uM 6 days Antiviral activity against HCV infected in human GS4.3 cells assessed as inhibition of viral core protein levels at 0.15 uM treated with fresh media containing compound every 2 days measured after 6 days by Western blot method 29232582
HuH7 Antiviral assay 3 days Antiviral activity against HCV genotype 1b infected in human HuH7 cells at >= 10 times antiviral EC50 after 3 days by luciferase reporter assay 28430437
HuH7 Antiviral assay 3 days Antiviral activity against HCV genotype 1b infected in human HuH7 cells co-treated with asunaprevir after 3 days by luciferase reporter assay 28430437
클릭하여 더 많은 세포주 실험 데이터 보기

화학 정보, 보관 및 안정성

분자량 738.88 화학식

C40H50N8O6

보관 (수령일로부터)
CAS 번호 1009119-64-5 SDF 다운로드 원액 보관

동의어 EBP883 Smiles CC(C)C(C(=O)N1CCCC1C2=NC=C(N2)C3=CC=C(C=C3)C4=CC=C(C=C4)C5=CN=C(N5)C6CCCN6C(=O)C(C(C)C)NC(=O)OC)NC(=O)OC

용해도

In vitro
배치:

DMSO : 148 mg/mL (200.3 mM)
(수분으로 오염된 DMSO는 용해도를 감소시킬 수 있습니다. 신선하고 무수 DMSO를 사용하십시오.)

Ethanol : 148 mg/mL

Water : 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

특징
First-in-class, highly selective inhibitor of hepatitis C virus (HCV) NS5A with picomolar EC50 values.
Targets/IC50/Ki
HCV NS5A
9 pM-50 pM(EC50)
시험관 내(In vitro)
Daclatasvir (BMS-790052)는 지금까지 보고된 HCV 복제에 대한 가장 강력한 억제제 중 하나입니다. 이 화합물의 평균 EC50 값은 HCV 유전자형 1a 및 1b 복제체에 대해 각각 50 및 9 pM입니다. 이는 최소 105의 치료 지수 (CC50/EC50)를 나타내며, 10 μM보다 높은 EC50을 갖는 10가지 RNA 및 DNA 바이러스 패널에 대해 비활성입니다. 이는 HCV에 대한 특이성을 확인합니다. HCV 유전자형 1b 복제체를 보유한 Huh7 세포에서, 이 화합물은 EC50 값이 1-15 pM 범위로 일시적 및 안정적인 HCV 게놈 복제를 모두 차단합니다. 100 pM 또는 1 nM 농도에서 NS5A의 세포 내 위치 및 생화학적 분획을 변경하는 것으로 나타났습니다. 이 화합물은 EC50이 7-13 pM인 HCV 유전자형-4 NS5A 유전자를 포함하는 하이브리드 복제체를 억제합니다. NS5A의 잔기 30은 하이브리드 복제체에서 BMS-790052 매개 저항성의 중요한 부위입니다.
키나아제 분석
HCV NS5A 억제제에 대한 FRET 분석
이 펩타이드 (Ac-Asp-Glu-Asp [EDANS]-Glu-Glu-Abu-[COO] Ala-Ser-Lys [DABCYL]-NH2)는 한쪽 끝 근처에 형광 공여체 {EDANS, 5-[(2-아미노에틸)아미노]나프탈렌-1-술폰산}를, 다른 쪽 끝 근처에 수용체 {DABCYL, 4-[(4-디메틸아미노)페닐]아조}벤조산}를 포함합니다. 공여체와 수용체 사이의 분자간 공명 에너지 전달은 펩타이드의 형광을 억제하지만, NS3 Protease가 펩타이드를 절단함에 따라 생성물은 공명 에너지 전달 억제로부터 해제됩니다. NS3 Protease에 의해 더 많은 기질이 절단될수록 공여체의 형광은 시간에 따라 증가합니다. 검출 시약은 다음과 같습니다: 5배 루시페라제 세포 배양 용해 시약을 dH2O로 1배 희석하고, NaCl (150 mM)과 FRET 펩타이드 (20 μM)를 첨가합니다. HCV-Huh-7 세포를 96웰 플레이트에 넣고 밤새 부착시켰습니다 (웰당 1×104 세포). 다음 날 Daclatasvir (BMS-790052)를 웰에 첨가하고 플레이트를 72시간 동안 배양했습니다. 그 다음 플레이트를 PBS로 헹구고, 앞서 언급된 FRET 펩타이드 검출 시약 30 μL를 각 웰에 첨가하여 FRET 분석을 수행했습니다. 신호는 Cytofluor 4000 장비를 사용하여 340 nm (여기)/490 nm (방출) 자동 모드로 설정하고 20주기 이하로 실행하며 운동 모드에서 플레이트를 판독하여 얻었습니다. FRET 분석 후, 각 웰에 루시페라제 기질 40 μL를 첨가하고 루시페라제 활성을 측정했습니다.
참조
  • [4] https://pubmed.ncbi.nlm.nih.gov/15793110/

임상시험 정보

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

NCT 번호 모집 조건 스폰서/협력자 시작일 단계
NCT05992077 Recruiting
HCV Infection
ANRS Emerging Infectious Diseases
August 7 2023 Not Applicable
NCT04852614 Recruiting
Hepatitis C Virus Infection
Ain Shams University
December 1 2020 --
NCT04773756 Completed
Covid19
Alexandria University
November 1 2020 Phase 4
NCT03208322 Withdrawn
Hepatitis C
Bristol-Myers Squibb
November 30 2018 --

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