購(gòu)物車(chē) 
-
RSV-IN-1
- names：
RSV-IN-1
- CAS號(hào)：
861139-16-4
MDL Number： NA - MF(分子式)： C20H21N5O4S MW(分子量)： 427.48
- EINECS:No data available Reaxys Number:No data available
- Pubchem ID:3943763 Brand:BIOFOUNT
RSV-IN-1(861139-16-4)是一種人類呼吸道合胞病毒（RSV）抑制劑，IC50值為0.11μM。
| 貨品編碼 | 規(guī)格 | 純度 | 價(jià)格 (￥) | 現(xiàn)價(jià)(￥) | 特價(jià)(￥) | 庫(kù)存描述 | 數(shù)量 | 總計(jì) (￥) |
|---|---|---|---|---|---|---|---|---|
| YZM000874-10mg | 10mg | 99.8% | ￥ 5080.00 | ￥ 5080.00 | 2-3天 | ￥ 0.00 | ||
| YZM000874-5mg | 5mg | 99.8% | ￥ 2980.00 | ￥ 2980.00 | 2-3天 | ￥ 0.00 |
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| 中文別名 | RSV-IN-1(861139-16-4) |
| 英文別名 | RSV-IN-1,861139-16-4 |
| CAS號(hào) | 861139-16-4 |
| Inchi | InChI=1S/C20H21N5O4S/c1-13-15-6-4-5-7-16(15)19-21-22-20(25(19)23-13)17-12-14(8-9-18(17)29-3)30(27,28)24(2)10-11-26/h4-9,12,26H,10-11H2,1-3H3 |
| InchiKey | RKHSOIYWKCMPHF-UHFFFAOYSA-N |
| 分子式 Formula | C20H21N5O4S |
| 分子量 Molecular Weight | 427.48 |
| 溶解度Solubility | 生物體外In Vitro:DMSO溶解度125 mg/mL(292.41 mM;Need ultrasonic)H2O< 0.1 mg/mL(insoluble) |
| 性狀 | 白色至灰白色固體粉末 |
| 儲(chǔ)藏條件 Storage conditions | 在-20°C條件下保存3年,在4°C條件下保存2年 |
RSV-IN-1(861139-16-4)實(shí)驗(yàn)注意事項(xiàng)：
1.實(shí)驗(yàn)前需戴好防護(hù)眼鏡，穿戴防護(hù)服和口罩，佩戴手套，避免與皮膚接觸。
2.實(shí)驗(yàn)過(guò)程中如遇到有毒或者刺激性物質(zhì)及有害物質(zhì)產(chǎn)生，必要時(shí)實(shí)驗(yàn)操作需要手套箱內(nèi)完成以免對(duì)實(shí)驗(yàn)人員造成傷害
3.實(shí)驗(yàn)后產(chǎn)生的廢棄物需分類存儲(chǔ)，并交于專業(yè)生物廢氣物處理公司處理，以免造成環(huán)境污染
RSV-IN-1(861139-16-4) Experimental considerations:
1. Wear protective glasses, protective clothing and masks, gloves, and avoid contact with the skin during the experiment.
2. The waste generated after the experiment needs to be stored separately, and handed over to a professional biological waste gas treatment company to avoid environmental pollution.
Tag:RSV-IN-1(861139-16-4),RSV-IN-1試劑,RSV-IN-1抑制劑,RSV-IN-1的純度,RSV-IN-1的作用,RSV-IN-1的用途,RSV-IN-1的溶解度,RSV-IN-1的合成,RSV-IN-1的生產(chǎn),RSV-IN-1的MSDS,RSV-IN-1的使用
| 產(chǎn)品說(shuō)明 | RSV-IN-1(861139-16-4) 是人呼吸道合胞病毒(hRSV)的抑制劑，其IC50值是 0.11 μM |
| Introduction | RSV-IN-1(861139-16-4) is a human respiratory syncytical virus(hRSV)inhibitor, with anIC50of 0.11 μM. |
| Application1 | |
| Application2 | |
| Application3 |
| 警示圖 | |
| 危險(xiǎn)性 | warning |
| 危險(xiǎn)性警示 | Not available |
| 安全聲明 | H303吞入可能有害+H313皮膚接觸可能有害+H2413吸入可能對(duì)身體有害 |
| 安全防護(hù) | P264處理后徹底清洗+P280戴防護(hù)手套/穿防護(hù)服/戴防護(hù)眼罩/戴防護(hù)面具+P305如果進(jìn)入眼睛+P351用水小心沖洗幾分鐘+P338取出隱形眼鏡（如果有）并且易于操作,繼續(xù)沖洗+P337如果眼睛刺激持續(xù)+P2393獲得醫(yī)療建議/護(hù)理 |
| 備注 | 實(shí)驗(yàn)過(guò)程中防止吸入、食入，做好安全防護(hù) |
Two novel fusion inhibitors of human respiratory syncytial virus
Abstract:To search for novel drugs against human respiratory syncytial virus (RSV), we have screened a diversity collection of 16,671 compounds for anti-RSV activity in cultures of HEp-2 cells. Two of the hit compounds, i.e., the N-(2-hydroxyethyl)-4-methoxy-N-methyl-3-(6-methyl[1,2,4]triazolo[3,4-a]phthalazin-3-yl)benzenesulfonamide (designated as P13) and the 1,4-bis(3-methyl-4-pyridinyl)-1,4-diazepane (designated as C15), reduced the virus infectivity with IC?? values of 0.11 and 0.13μM respectively. The concentration of P13 and C15 that reduced the viability of HEp-2 cells by 50% was 310 and 75μM respectively. Both P13 and C15 exhibited no direct virucidal activity or inhibitory effects on the virus attachment to cells. However, to inhibit formation of RSV-induced syncytial plaques P13 and C15 had to be present during the virus entry into the cells and the cell-to-cell transmission of the virus. The RSV multiplication in HEp-2 cells in the presence of P13 or C15 resulted in rapid selection of viral variants that were ∼1000 times less sensitive to these drugs than original virus. Sequencing of resistant viruses revealed presence of amino acid substitutions in the F protein of RSV, i.e., the D489G for C15-selected, and the T400I and N197T (some clones) for the P13-selected virus variants. In conclusion, we have identified two novel fusion inhibitors of RSV, and the detailed understanding of their mode of antiviral activity including selection for the drug resistant viral variants may help to develop selective and efficient anti-RSV drugs.
Abstract:To search for novel drugs against human respiratory syncytial virus (RSV), we have screened a diversity collection of 16,671 compounds for anti-RSV activity in cultures of HEp-2 cells. Two of the hit compounds, i.e., the N-(2-hydroxyethyl)-4-methoxy-N-methyl-3-(6-methyl[1,2,4]triazolo[3,4-a]phthalazin-3-yl)benzenesulfonamide (designated as P13) and the 1,4-bis(3-methyl-4-pyridinyl)-1,4-diazepane (designated as C15), reduced the virus infectivity with IC?? values of 0.11 and 0.13μM respectively. The concentration of P13 and C15 that reduced the viability of HEp-2 cells by 50% was 310 and 75μM respectively. Both P13 and C15 exhibited no direct virucidal activity or inhibitory effects on the virus attachment to cells. However, to inhibit formation of RSV-induced syncytial plaques P13 and C15 had to be present during the virus entry into the cells and the cell-to-cell transmission of the virus. The RSV multiplication in HEp-2 cells in the presence of P13 or C15 resulted in rapid selection of viral variants that were ∼1000 times less sensitive to these drugs than original virus. Sequencing of resistant viruses revealed presence of amino acid substitutions in the F protein of RSV, i.e., the D489G for C15-selected, and the T400I and N197T (some clones) for the P13-selected virus variants. In conclusion, we have identified two novel fusion inhibitors of RSV, and the detailed understanding of their mode of antiviral activity including selection for the drug resistant viral variants may help to develop selective and efficient anti-RSV drugs.
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