当前位置:易推广 > 上海陶术生物科技有限公司 > 产品展示
企业档案
会员类型:会员
已获得易推广信誉 等级评定
(0 -40)基础信誉积累,可浏览访问
(41-90)良好信誉积累,可接洽商谈
(91+ )优质信誉积累,可持续信赖
易推广会员:5年
最后认证时间:
注册号: 【已认证】
法人代表: 【已认证】
企业类型:生产商 【已认证】
注册资金:人民币万 【已认证】
产品数:86101
参观次数:3314724
已选条件
-
T80657SARS-CoV-2 3CLpro-IN-15;化合物 SARS-CoV-2 3CLpro-IN-15SARS-CoV-2 3CLpro-IN-15
SARS-CoV-2 3CLpro-IN-15 (compound a), a beta-nitrostyrene derivative, acts as an inhibitor of the SARS-CoV-2 3CL protease (3CLpro), effectively inhibiting viral replication and transcription. It is instrumental in the identification of potential anti-COVID-19 lead compounds [1].
价 格:¥电议型 号:T80657产 地:中国大陆
-
T79661SARS-CoV-2 3CLpro-IN-18;化合物 SARS-CoV-2 3CLpro-IN-18SARS-CoV-2 3CLpro-IN-18
SARS-CoV-2 3CLpro-IN-18 (Compound 3C) is a covalent inhibitor of SARS-CoV-2 3CLpro with an IC50 of 0.478 μM. It demonstrates inhibition of SARS-CoV-2 in Vero E6 cells, with an EC50 of 2.499 μM, and exhibits low cytotoxicity (CC50 > 200 μM) [1].
价 格:¥电议型 号:T79661产 地:中国大陆
-
T79660SARS-CoV-2 3CLpro-IN-17;化合物 SARS-CoV-2 3CLpro-IN-17SARS-CoV-2 3CLpro-IN-17
Compound 3h, also known as SARS-CoV-2 3CLpro-IN-17, is a selective inhibitor of the SARS-CoV-2 3CL protease, demonstrating an IC50 of 0.322 μM [1].
价 格:¥电议型 号:T79660产 地:中国大陆
-
T79659SARS-CoV-2 3CLpro-IN-16;SARS-CoV-2 3CLpro 抑制剂16SARS-CoV-2 3CLpro-IN-16
SARS-CoV-2 3CLpro-IN-16 is a covalent SARS-CoV-2 3CLpro inhibitor that inhibits 3CLpro activity and achieves its inhibitory effect by forming a covalent bond with Cys145.
价 格:¥电议型 号:T79659产 地:中国大陆
-
T79462SARS-CoV-2 3CLpro-IN-14;化合物 SARS-CoV-2 3CLpro-IN-14SARS-CoV-2 3CLpro-IN-14
SARS-CoV-2 3CLpro-IN-14 (compound 11j) is an orally active inhibitor of SARS-CoV-2 3CLpro, demonstrating potent anti-SARS-CoV-2 properties with an EC50 of 0.18 μM and exhibits minimal cytotoxicity, having a CC50 greater than 50 μM, in Vero E6 cells [1].
价 格:¥电议型 号:T79462产 地:中国大陆
-
T79376SARS-CoV-2 3CLpro-IN-19;化合物 SARS-CoV-2 3CLpro-IN-19SARS-CoV-2 3CLpro-IN-19
SARS-CoV-2 3CLpro-IN-19 (Compound C5a), a non-covalent, non-peptide inhibitor of the SARS-CoV-2 3CLpro enzyme, exhibits potent in vitro activity with an IC50 of 0.7 μM. It demonstrates broad-spectrum efficacy against infection by Omicron subvariants (BA.5, BQ.1.1, and XBB.1.5) in human cells, with EC50 values ranging from 30-69 nM [1].
价 格:¥电议型 号:T79376产 地:中国大陆
-
T74807SARS-CoV-2 3CLpro-IN-13;化合物 SARS-CoV-2 3CLpro-IN-13SARS-CoV-2 3CLpro-IN-13
SARS-CoV-2 3CLpro-IN-13 is a potent inhibitor of the SARS-CoV-2 3CL protease, demonstrating significant anti-coronavirus activity with an IC50 value of 21 nM [1].
价 格:¥电议型 号:T74807产 地:中国大陆
-
T72313SARS-CoV-2 3CLpro-IN-11;化合物 SARS-CoV-2 3CLpro-IN-11SARS-CoV-2 3CLpro-IN-11
SARS-CoV-2 3CLpro-IN-11(11d) is a broad-spectrum antiviral compound that effectively inhibits the SARS-CoV-2 3CL protease, achieving an IC50 of 140 nM. Additionally, it exhibits inhibitory activity against SARS-CoV-1 and MERS-CoV with IC50 values of 240 nM and 70 nM, respectively.
价 格:¥电议型 号:T72313产 地:中国大陆
-
T72312SARS-CoV-2 3CLpro-IN-10;化合物 SARS-CoV-2 3CLpro-IN-10SARS-CoV-2 3CLpro-IN-10
SARS-CoV-2 3CLpro-IN-10(5d) is a potent inhibitor of the SARS-CoV-2 3CL protease, exhibiting an IC50 value of 190 nM, and demonstrates varied efficiency against other coronaviruses with IC50 values of 790 nM for SARS-CoV-1 and 70 nM for MERS-CoV, indicating broad-spectrum antiviral activity.
价 格:¥电议型 号:T72312产 地:中国大陆
-
T63537SARS-CoV-2 3CLpro-IN-1;化合物 SARS-CoV-2 3CLpro-IN-1SARS-CoV-2 3CLpro-IN-1
SARS-CoV-2 3CLpro-IN-1 (Compound 14c) is a highly potent inhibitor specifically designed to target and inhibit the activity of SARS-CoV-2 3CL pro, which is a cysteine-protease found in the main coronaviruses. This particular enzyme has been recognized as a highly promising target for the development of effective antiviral drugs. Therefore, SARS-CoV-2 3CLpro-IN-1 holds significant potential for advancing research and development in the field of infectious diseases [1].
价 格:¥电议型 号:T63537产 地:中国大陆
-
T61774SARS 3CLpro-IN-1;化合物 SARS 3CLpro-IN-1SARS 3CLpro-IN-1
SARS 3CLpro-IN-1 (Compound 3b) is a stereo-specific SARS 3CL protease inhibitor that belongs to the octahydroisochromene scaffold. It demonstrates inhibition against the P1 site imidazole, with an IC50 value of 95 μM [1].
价 格:¥电议型 号:T61774产 地:中国大陆