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  1. Anti-infection
  2. Enterovirus
  3. Pleconaril

Pleconaril  (Synonyms: 普可那利; VP 63843; Win 63843)

目錄號: HY-19952 純度: 99.48%
COA 產(chǎn)品使用指南 技術(shù)支持

Pleconaril 是一種小核糖核酸病毒衣殼結(jié)合抑制劑,可防止病毒附著和/或脫殼。Pleconaril 具有用于研究鼻病毒和腸道病毒的潛力。

MCE 的所有產(chǎn)品僅用作科學(xué)研究或藥證申報,我們不為任何個人用途提供產(chǎn)品和服務(wù)

Pleconaril Chemical Structure

Pleconaril Chemical Structure

CAS No. : 153168-05-9

1.  客戶無需承擔(dān)相應(yīng)的運輸費用。

2.  同一機構(gòu)(單位)同一產(chǎn)品試用裝僅限申領(lǐng)一次,同一機構(gòu)(單位)一年內(nèi)

     可免費申領(lǐng)三個不同產(chǎn)品的試用裝。

3.  試用裝只面向終端客戶。

規(guī)格 價格 是否有貨 數(shù)量
10 mM * 1 mL in DMSO ¥968
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5 mg ¥880
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10 mg ¥1300
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50 mg ¥4500
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Customer Review

Other Forms of Pleconaril:

  • 生物活性

  • 純度 & 產(chǎn)品資料

  • 參考文獻

生物活性

Pleconaril is a picornavirus capsid binding inhibitor that prevents attachment and/or virus uncoating. Pleconaril has potential for use in rhinoviruses and enteroviruses research[1][2].

細(xì)胞效力
(Cellular Effect)
Cell Line Type Value Description References
H1-HeLa CC50
19.7 μM
Compound: Pleconaril
Cytotoxicity against human H1HeLa cells assessed as reduction in cell viability after 3 days by MTT assay
Cytotoxicity against human H1HeLa cells assessed as reduction in cell viability after 3 days by MTT assay
[PMID: 30034598]
H1-HeLa CC50
19.7 μM
Compound: 1
Cytotoxicity against human H1HeLa cells assessed as decrease in cell viability after 3 days by MTT assay
Cytotoxicity against human H1HeLa cells assessed as decrease in cell viability after 3 days by MTT assay
[PMID: 28581749]
H1-HeLa CC50
20.8 μM
Compound: Pleconaril
Cytotoxicity against human H1-HeLa cells assessed as reduction in cell viability by MTT assay
Cytotoxicity against human H1-HeLa cells assessed as reduction in cell viability by MTT assay
[PMID: 35292344]
H1-HeLa CC50
53.5 μM
Compound: Pleconaril
Cytotoxicity in human H1HeLa cells assessed as reduction in cell viability incubated for 3 days by MTT assay
Cytotoxicity in human H1HeLa cells assessed as reduction in cell viability incubated for 3 days by MTT assay
[PMID: 28587824]
HeLa EC50
> 42.8 μM
Compound: Pleconaril
Antiviral activity against human coxsackievirus B3 infected in human HeLa cells assessed as reduction in virus-induced cytopathicity incubated for 3 days by MTT assay
Antiviral activity against human coxsackievirus B3 infected in human HeLa cells assessed as reduction in virus-induced cytopathicity incubated for 3 days by MTT assay
[PMID: 28587824]
HeLa IC50
≤ 0.18 μM
Compound: 55; WIN63843
Cytotoxicity against human HeLa cells after 3 days by MTT assay
Cytotoxicity against human HeLa cells after 3 days by MTT assay
[PMID: 31226653]
HeLa EC50
0.13 μM
Compound: Pleconaril
Antiviral activity against human coxsackievirus B1 infected in human HeLa cells assessed as reduction in virus-induced cytopathicity incubated for 3 days by MTT assay
Antiviral activity against human coxsackievirus B1 infected in human HeLa cells assessed as reduction in virus-induced cytopathicity incubated for 3 days by MTT assay
[PMID: 28587824]
HeLa EC50
0.51 μM
Compound: Pleconaril
Antiviral activity against human poliovirus 3 infected in human HeLa cells assessed as reduction in virus-induced cytopathicity incubated for 3 days by MTT assay
Antiviral activity against human poliovirus 3 infected in human HeLa cells assessed as reduction in virus-induced cytopathicity incubated for 3 days by MTT assay
[PMID: 28587824]
HeLa EC50
1.4 μM
Compound: 1
Antiviral activity against Human poliovirus 3 infected in human HeLa cells assessed as protection against virus induced cytopathic effect after 2 days by MTT assay
Antiviral activity against Human poliovirus 3 infected in human HeLa cells assessed as protection against virus induced cytopathic effect after 2 days by MTT assay
[PMID: 28581749]
HeLa CC50
12.6 μg/mL
Compound: pleconaril
Cytotoxicity against human HeLa cells after 72 hrs
Cytotoxicity against human HeLa cells after 72 hrs
[PMID: 18247552]
HeLa CC50
131 μM
Compound: Pleconaril
Cytotoxicity against human HeLa cells assessed as decrease in cell viability after 72 hrs by MTT assay
Cytotoxicity against human HeLa cells assessed as decrease in cell viability after 72 hrs by MTT assay
[PMID: 29039946]
HeLa EC50
177 nM
Compound: Pleconaril
Antienteroviral activity against Human rhinovirus 14 infected in human HeLa cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
Antienteroviral activity against Human rhinovirus 14 infected in human HeLa cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
[PMID: 24900715]
HeLa EC50
224.1 ng/mL
Compound: 1
Antirhinoviral activity against Human rhinovirus B infected in human HeLa cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antirhinoviral activity against Human rhinovirus B infected in human HeLa cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 24900468]
HeLa EC50
23.2 ng/mL
Compound: 1
Antirhinoviral activity against minor receptor-resistant Human rhinovirus infected in human HeLa cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antirhinoviral activity against minor receptor-resistant Human rhinovirus infected in human HeLa cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 24900468]
HeLa CC50
25.9 μM
Compound: 1
Cytotoxicity aganist human HeLa cells assessed as decrease in cell viability after 2 days by MTT assay
Cytotoxicity aganist human HeLa cells assessed as decrease in cell viability after 2 days by MTT assay
[PMID: 28581749]
HeLa CC50
26.25 μM
Compound: Pleconaril
Cytotoxicity against human HeLa cells assessed as reduction in cell viability incubated for 72 hrs measured by crystal violet based micro plate reader method
Cytotoxicity against human HeLa cells assessed as reduction in cell viability incubated for 72 hrs measured by crystal violet based micro plate reader method
[PMID: 31881489]
HeLa EC50
33.8 ng/mL
Compound: 1
Antirhinoviral activity against antiviral-resistant Human rhinovirus B infected in human HeLa cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antirhinoviral activity against antiviral-resistant Human rhinovirus B infected in human HeLa cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 24900468]
HeLa EC50
37.4 ng/mL
Compound: 1
Antirhinoviral activity against Human rhinovirus A infected in human HeLa cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antirhinoviral activity against Human rhinovirus A infected in human HeLa cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 24900468]
HeLa EC50
387.6 ng/mL
Compound: 1
Antirhinoviral activity against antiviral-resistant Human rhinovirus A infected in human HeLa cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antirhinoviral activity against antiviral-resistant Human rhinovirus A infected in human HeLa cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 24900468]
HeLa CC50
42.8 μM
Compound: Pleconaril
Cytotoxicity in human HeLa cells assessed as reduction in cell viability incubated for 3 days by MTT assay
Cytotoxicity in human HeLa cells assessed as reduction in cell viability incubated for 3 days by MTT assay
[PMID: 28587824]
HeLa EC50
49.2 ng/mL
Compound: 1
Antirhinoviral activity against major receptor-resistant Human rhinovirus infected in human HeLa cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
Antirhinoviral activity against major receptor-resistant Human rhinovirus infected in human HeLa cells assessed as inhibition of virus-induced cytopathic effect after 5 days by MTT assay
[PMID: 24900468]
RD CC50
> 200 μM
Compound: 1
Cytotoxicity against human RD cells assessed as inhibition of cell viability by measuring ATP level incubated for 72 hrs by cell titer-glo luminescent cell viability assay
Cytotoxicity against human RD cells assessed as inhibition of cell viability by measuring ATP level incubated for 72 hrs by cell titer-glo luminescent cell viability assay
[PMID: 36254462]
RD EC50
13400 nM
Compound: Pleconaril
Antienteroviral activity against Enterovirus 71 infected in human RD cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
Antienteroviral activity against Enterovirus 71 infected in human RD cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
[PMID: 24900715]
Vero EC50
0.002 μM
Compound: Pleconaril
Antiviral activity against Coxsackievirus B3 infected in Vero cells assessed as reduction in virus-induced cytopathic effect incubated for 48 hrs by Reed-Muench method
Antiviral activity against Coxsackievirus B3 infected in Vero cells assessed as reduction in virus-induced cytopathic effect incubated for 48 hrs by Reed-Muench method
[PMID: 32378892]
Vero EC50
0.005 μM
Compound: Pleconaril
Antiviral activity against Coxsackievirus B5 infected in African green monkey Vero 76 cells after 3 days by plaque reduction assay
Antiviral activity against Coxsackievirus B5 infected in African green monkey Vero 76 cells after 3 days by plaque reduction assay
[PMID: 25913116]
Vero EC50
1084 nM
Compound: Pleconaril
Antienteroviral activity against poliovirus 2 infected in african green monkey Vero cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
Antienteroviral activity against poliovirus 2 infected in african green monkey Vero cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
[PMID: 24900715]
Vero EC50
13000 nM
Compound: Pleconaril
Antienteroviral activity against Coxsackievirus B3 infected in african green monkey Vero cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
Antienteroviral activity against Coxsackievirus B3 infected in african green monkey Vero cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
[PMID: 24900715]
Vero EC50
2.2 μM
Compound: Pleconaril
Antiviral activity against Poliovirus Sb-1 infected in African green monkey Vero 76 cells after 2 days by plaque reduction assay
Antiviral activity against Poliovirus Sb-1 infected in African green monkey Vero 76 cells after 2 days by plaque reduction assay
[PMID: 25913116]
Vero EC50
24200 nM
Compound: Pleconaril
Antienteroviral activity against poliovirus 1 infected in african green monkey Vero cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
Antienteroviral activity against poliovirus 1 infected in african green monkey Vero cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
[PMID: 24900715]
Vero EC50
33 nM
Compound: Pleconaril
Antienteroviral activity against Coxsackievirus A9 infected in african green monkey Vero cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
Antienteroviral activity against Coxsackievirus A9 infected in african green monkey Vero cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
[PMID: 24900715]
Vero EC50
84 nM
Compound: Pleconaril
Antienteroviral activity against poliovirus 3 infected in african green monkey Vero cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
Antienteroviral activity against poliovirus 3 infected in african green monkey Vero cells assessed as protection against virus-induced cytopathic effect after 2 to 3 days by MTS assay
[PMID: 24900715]
Vero 76 CC50
> 100 μM
Compound: Pleconaril
Cytotoxicity against African green monkey Vero 76 cells assessed as reduction in cell viability after 48 to 96 hrs by MTT assay
Cytotoxicity against African green monkey Vero 76 cells assessed as reduction in cell viability after 48 to 96 hrs by MTT assay
[PMID: 29339251]
Vero 76 EC50
0.008 μM
Compound: Pleconaril
Antiviral activity against human CVB5 infected in african green monkey Vero76 cells assessed as inhibition of virus-induced cytopathogenicity after 3 days by plaque reduction assay
Antiviral activity against human CVB5 infected in african green monkey Vero76 cells assessed as inhibition of virus-induced cytopathogenicity after 3 days by plaque reduction assay
[PMID: 26443549]
Vero 76 EC50
2 μM
Compound: Pleconaril
Antiviral activity against Human poliovirus 1 Sabin infected in african green monkey Vero76 cells assessed as inhibition of virus-induced cytopathogenicity by plaque reduction assay
Antiviral activity against Human poliovirus 1 Sabin infected in african green monkey Vero76 cells assessed as inhibition of virus-induced cytopathogenicity by plaque reduction assay
[PMID: 26443549]
Vero 76 CC50
70 μM
Compound: Pleconaril
Cytotoxicity against african green monkey Vero 76 cells assessed as cell viability after 48 to 96 hrs by crystal violet staining method
Cytotoxicity against african green monkey Vero 76 cells assessed as cell viability after 48 to 96 hrs by crystal violet staining method
[PMID: 26443549]
Vero 76 CC50
80 μM
Compound: Pleconaril
Cytotoxicity against African green monkey Vero 76 cells assessed as cell viability after 48 to 96 hrs by MTT method
Cytotoxicity against African green monkey Vero 76 cells assessed as cell viability after 48 to 96 hrs by MTT method
[PMID: 25913116]
Vero 76 CC50
83 μM
Compound: Pleconaril
Cytotoxicity against African green monkey Vero 76 cells assessed as decrease in cell viability after 48 to 96 hrs by MTT assay
Cytotoxicity against African green monkey Vero 76 cells assessed as decrease in cell viability after 48 to 96 hrs by MTT assay
[PMID: 29028528]
體外研究
(In Vitro)

Pleconaril (0.4-50 μM,2 天) 在 RD 細(xì)胞中在 50 μM 濃度下產(chǎn)生顯著的細(xì)胞毒性[2]
Pleconaril (0.001-4 μg/mL, 24 小時) 可提高感染 EV71 的 RD 細(xì)胞的細(xì)胞活力[3]。

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

體內(nèi)研究
(In Vivo)

Pleconaril (2-200 mg/kg,腹腔注射,每日一次,5 天) 可增加感染 EV71 的小鼠的存活數(shù)量[3]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Clinical Trial
分子量

381.35

Formula

C18H18F3N3O3

CAS 號
性狀

固體

顏色

White to off-white

中文名稱

普可那利

運輸條件

Room temperature in continental US; may vary elsewhere.

儲存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 2 years
-20°C 1 year
溶解性數(shù)據(jù)
細(xì)胞實驗: 

DMSO 中的溶解度 : 100 mg/mL (262.23 mM; 超聲助溶; 吸濕的 DMSO 對產(chǎn)品的溶解度有顯著影響,請使用新開封的 DMSO)

配制儲備液
濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg
1 mM 2.6223 mL 13.1113 mL 26.2226 mL
5 mM 0.5245 mL 2.6223 mL 5.2445 mL
查看完整儲備液配制表

* 請根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲備液;一旦配成溶液,請分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效。
儲備液的保存方式和期限:-80°C, 2 years; -20°C, 1 year。-80°C儲存時,請在2年內(nèi)使用, -20°C儲存時,請在1年內(nèi)使用。

  • 摩爾計算器

  • 稀釋計算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

質(zhì)量
=
濃度
×
體積
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

濃度 (start)

C1

×
體積 (start)

V1

=
濃度 (final)

C2

×
體積 (final)

V2

動物實驗:

請根據(jù)您的 實驗動物和給藥方式 選擇適當(dāng)?shù)娜芙夥桨浮?

以下溶解方案都請先按照 In Vitro 方式配制澄清的儲備液,再依次添加助溶劑:
——為保證實驗結(jié)果的可靠性,澄清的儲備液可以根據(jù)儲存條件,適當(dāng)保存;體內(nèi)實驗的工作液,建議您現(xiàn)用現(xiàn)配,當(dāng)天使用
以下溶劑前顯示的百分比是指該溶劑在您配制終溶液中的體積占比;如在配制過程中出現(xiàn)沉淀、析出現(xiàn)象,可以通過加熱和/或超聲的方式助溶

  • 方案 一

    請依序添加每種溶劑: 10% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: ≥ 2.5 mg/mL (6.56 mM); 澄清溶液

    此方案可獲得 ≥ 2.5 mg/mL(飽和度未知)的澄清溶液。

    1 mL 工作液為例,取 100 μL 25.0 mg/mL 的澄清 DMSO 儲備液加到 400 μL PEG300 中,混合均勻;再向上述體系中加入 50 μL Tween-80,混合均勻;然后再繼續(xù)加入 450 μL 生理鹽水 定容至 1 mL

    生理鹽水的配制:將 0.9 g 氯化鈉,溶解于 ddH?O 并定容至 100 mL,可以得到澄清透明的生理鹽水溶液。
  • 方案 二

    請依序添加每種溶劑: 10% DMSO    90% Corn Oil

    Solubility: ≥ 2.5 mg/mL (6.56 mM); 澄清溶液

    此方案可獲得 ≥ 2.5 mg/mL(飽和度未知)的澄清溶液,此方案實驗周期在半個月以上的動物實驗酌情使用。

    1 mL 工作液為例,取 100 μL 25.0 mg/mL 的澄清 DMSO 儲備液加到 900 μL玉米油中,混合均勻。

動物溶解方案計算器
請輸入動物實驗的基本信息:

給藥劑量

mg/kg

動物的平均體重

g

每只動物的給藥體積

μL

動物數(shù)量

由于實驗過程有損耗,建議您多配一只動物的量
請輸入您的動物體內(nèi)配方組成:
%
DMSO +
+
%
Tween-80 +
%
Saline
如果您的動物是免疫缺陷鼠或者體弱鼠,建議 DMSO 中的在最后工作液體系中的占比盡量不超過 2%。
方案所需 助溶劑 包括:DMSO, ,均可在 MCE 網(wǎng)站選購。 ,Tween 80,均可在 MCE 網(wǎng)站選購。
計算結(jié)果
工作液所需濃度 : mg/mL
儲備液配制方法 : mg 藥物溶于 μL  DMSO(母液濃度為 mg/mL)。
您所需的儲備液濃度超過該產(chǎn)品的實測溶解度,以下方案僅供參考,如有需要,請與 MCE 中國技術(shù)支持聯(lián)系。
動物實驗體內(nèi)工作液的配制方法 : 取 μL DMSO 儲備液,加入 μL 。 μL ,混合均勻至澄清,再加 μL Tween 80,混合均勻至澄清,再加 μL 生理鹽水。
連續(xù)給藥周期超過半月以上,請謹(jǐn)慎選擇該方案。
請確保第一步儲備液溶解至澄清狀態(tài),從左到右依次添加助溶劑。您可采用超聲加熱 (超聲清洗儀,建議頻次 20-40 kHz),渦旋吹打等方式輔助溶解。
純度 & 產(chǎn)品資料

純度: 99.48%

參考文獻

Pleconaril 相關(guān)分類

完整儲備液配制表

* 請根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲備液;一旦配成溶液,請分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效
儲備液的保存方式和期限:-80°C, 2 years; -20°C, 1 year。-80°C儲存時,請在2年內(nèi)使用, -20°C儲存時,請在1年內(nèi)使用。

可選溶劑 濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.6223 mL 13.1113 mL 26.2226 mL 65.5566 mL
5 mM 0.5245 mL 2.6223 mL 5.2445 mL 13.1113 mL
10 mM 0.2622 mL 1.3111 mL 2.6223 mL 6.5557 mL
15 mM 0.1748 mL 0.8741 mL 1.7482 mL 4.3704 mL
20 mM 0.1311 mL 0.6556 mL 1.3111 mL 3.2778 mL
25 mM 0.1049 mL 0.5245 mL 1.0489 mL 2.6223 mL
30 mM 0.0874 mL 0.4370 mL 0.8741 mL 2.1852 mL
40 mM 0.0656 mL 0.3278 mL 0.6556 mL 1.6389 mL
50 mM 0.0524 mL 0.2622 mL 0.5245 mL 1.3111 mL
60 mM 0.0437 mL 0.2185 mL 0.4370 mL 1.0926 mL
80 mM 0.0328 mL 0.1639 mL 0.3278 mL 0.8195 mL
100 mM 0.0262 mL 0.1311 mL 0.2622 mL 0.6556 mL
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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產(chǎn)品名稱:
Pleconaril
目錄號:
HY-19952
需求量: