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:3242458
已选条件
-
T63429SMO-IN-2;SMO抑制剂2SMO-IN-2
SMO-IN-2 is a potent smoothened (SMO) inhibitor of hedgehog (Hh) signaling.SMO-IN-2 shows antiproliferative activity and anticancer activity against human medulloblastoma cell lines.SMO-IN-2 can be used in the study of cancer.
价 格:¥电议型 号:T63429产 地:中国大陆
-
T63385SARS-CoV-2 3CLpro-IN-2;化合物 SARS-CoV-2 3CLpro-IN-2SARS-CoV-2 3CLpro-IN-2
SARS-CoV-2 3CLpro-IN-2 is a potent inhibitor of the 3CL protease pair and has shown research potential for SARS-CoV-2 disease.
价 格:¥电议型 号:T63385产 地:中国大陆
-
T63288SCP1-IN-2;化合物 SCP1-IN-2SCP1-IN-2
SCP1-IN-2 is a potent, selective, and metric inhibitor of SCP1. SCP1-IN-2 is able to induce REST degradation and inhibit its transcriptional activity. High levels of REST protein induce tumor growth in some glioblastoma cells. sCP1-IN-2 has the potential to perform studies of glioblastomas in which REST transcriptional activity drives growth.
价 格:¥电议型 号:T63288产 地:中国大陆
-
T63181SARS-CoV-2-IN-32;化合物 SARS-CoV-2-IN-32SARS-CoV-2-IN-32
SARS-CoV-2-IN-32 is a COVID-19 inhibitor. SARS-CoV-2-IN-32 exhibits good binding affinity (-8.8 Kcal/mole) for the COVID-19 major protease (Mpro) (PDB ID: 6LU7) and has anti-proliferative effects on cancer cells. IN-32 can be used to study cancer and COVID-19.
价 格:¥电议型 号:T63181产 地:中国大陆
-
T63098SARS-CoV-2 Mpro-IN-2;SARS-CoV-2 Mpro 抑制剂 2SARS-CoV-2 Mpro-IN-2
SARS-CoV-2 Mpro-IN-2 is a selective SARS-CoV-2M pro inhibitor with an IC50 value of 0.40 μM.SARS-CoV-2 Mpro-IN-2 has good antiviral activity and can be used to study COVID-19.
价 格:¥电议型 号:T63098产 地:中国大陆
-
T6305SNX2112;化合物SNX2112SNX-2112|||PF 04928473|||SNX 2112;SNX-2112|||PF 04928473|||SNX 2112
SNX2112 (PF 04928473) is an orally active Hsp90 inhibitor, with a Kd of 16 nM.
价 格:¥电议型 号:T6305产 地:中国大陆
-
T63017SphK2-IN-2;化合物 SphK2-IN-2SphK2-IN-2
SphK2-IN-2 (21g) is a potent and selective inhibitor of SphK2 (IC50: 0.23 μM).
价 格:¥电议型 号:T63017产 地:中国大陆
-
T62909SGC agonist 2;化合物 SGC agonist 2SGC agonist 2
SGC agonist 2 is a potent soluble guanylate cyclase (SGC) agonist. SGC agonist 2 has potential for cardiovascular disease (heart failure, angina, pulmonary hypertension, myocardial infarction) and fibrotic disease (renal fibrosis, systemic sclerosis).
价 格:¥电议型 号:T62909产 地:中国大陆
-
T62886S1PR1 agonist 2;化合物 S1PR1 agonist 2S1PR1 agonist 2
S1PR1 agonist 2 is a potent agonist of S1PR1. S1PR1 agonist 2 has potential for studies of autoimmune diseases.
价 格:¥电议型 号:T62886产 地:中国大陆
-
T62834SARS-CoV-2-IN-22;化合物 SARS-CoV-2-IN-22SARS-CoV-2-IN-22
SARS-CoV-2-IN-22 is a SARS-CoV-2 pseudovirus inhibitor (IC50: 16.96 μM).
价 格:¥电议型 号:T62834产 地:中国大陆
-
T62819SARS-CoV-2 nsp14-IN-2;化合物 SARS-CoV-2 nsp14-IN-2SARS-CoV-2 nsp14-IN-2
SARS-CoV-2 nsp14-IN-2 is a potent inhibitor of SARS-CoV-2 Nsp14 methyltransferase (IC50: 0.093 μM). SARS-CoV-2 nsp14-IN-2 has the potential to be used in COVID-19 studies.
价 格:¥电议型 号:T62819产 地:中国大陆
-
T62803STAT3-IN-12;化合物 STAT3-IN-12STAT3-IN-12
STAT3-IN-12 is a potent inhibitor of STAT3 signalling and inhibits IL-6-induced activation of the JAK/STAT3 signalling pathway. STAT3-IN-12 inhibits the growth and migration of cancer cells, blocks the cell cycle and induces apoptosis. HCC), oesophageal cancer.)
价 格:¥电议型 号:T62803产 地:中国大陆
-
T62600RYL-552S;化合物 RYL-552SRYL-552S
RYL-552S is a drug-resistant strain of Plasmodium falciparum that effectively kills the asexual blood stage of the parasite in vitro.
价 格:¥电议型 号:T62600产 地:中国大陆
-
T62519SW02;化合物 SW02SW02
SW02 is a potent ATPase activator of Hsp70 (EC50: 150 μM). SW02 is able to accumulate total tau and phosphorylated tau (pTau).
价 格:¥电议型 号:T62519产 地:中国大陆
-
T62517S1p receptor agonist 2;化合物 S1p receptor agonist 2S1p receptor agonist 2
S1p receptor agonist 2 (compound 1) is an agonist of the S1P5 receptor with a higher selectivity than S1P1 and/or S1P3 receptors.S1p receptor agonist 2 can be used in the endogenous SIP signaling system and in the mitigation/prevention of central nervous system (CNS) diseases such as neurodegenerative diseases. .
价 格:¥电议型 号:T62517产 地:中国大陆
-
T62404SHMT-IN-2;化合物SHMT-IN-2SHMT-IN-2
SHMT-IN-2 (compound 2) is a specific human SHMT1/2 small molecule inhibitor that acts on SHMT1 (IC50: 13 nM) and SHMT2 (IC50: 66 nM). SHMT-IN-2 inhibits the growth of many human cancer cells and is sensitive to B-cell lymphoma.
价 格:¥电议型 号:T62404产 地:中国大陆
-
T62371SOS1-IN-12;化合物 SOS1-IN-12SOS1-IN-12
SOS1-IN-12 is a potent inhibitor of SOS1, acting on SOS1 (Ki: 0.11 nM) and on pERK (IC50: 47 nM).
价 格:¥电议型 号:T62371产 地:中国大陆
-
T62264SARS-CoV-2 nsp13-IN-2;化合物 SARS-CoV-2 nsp13-IN-2SARS-CoV-2 nsp13-IN-2
SARS-CoV-2 nsp13-IN-2 (Compound C2) is a small molecule inhibitor of SARS-CoV-2 non-structural protein 13 (nsp13) that acts on nsp13 ssDNA+ATPase (IC50: 42 μM).
价 格:¥电议型 号:T62264产 地:中国大陆
-
T62032SIRT5 inhibitor 2;化合物 SIRT5 inhibitor 2SIRT5 inhibitor 2
SIRT5 inhibitor 2 (compound 49) is a potent SIRT5 inhibitor (IC 50= 2.3 μM). SIRT5 inhibitor 2 shows inhibitory activity against the SIRT5-dependent desuccinylation. SIRT5 inhibitor 2 has research value in cancer and neurodegenerative diseases.
价 格:¥电议型 号:T62032产 地:中国大陆
-
T61894sEH inhibitor-2;化合物 sEH inhibitor-2sEH inhibitor-2
SEH inhibitor-2 (compound 5l) is a soluble epoxide hydrolase (sEH) inhibitor with oral activity (IC50=0.9 nM), and the predicted oral absorption percentage is 71.2-88.4%. SEH inhibitor-2 can maintain a high concentration of eicosanoic acid (EETs) in serum. SEH inhibitor-2 has research value in cardiovascular protection.
价 格:¥电议型 号:T61894产 地:中国大陆