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:3236067
已选条件
-
T80620Anti-Mouse CD19 Antibody (1D3);化合物 Anti-Mouse CD19 Antibody (1D3)Anti-Mouse CD19 Antibody (1D3)
Anti-Mouse CD19 Antibody (1D3) is an IgG2a isotype inhibitor targeting mouse CD19.
价 格:¥电议型 号:T80620产 地:中国大陆
-
T80501Myr-TAT-CBD3;化合物 Myr-TAT-CBD3Myr-TAT-CBD3
Myr-TAT-CBD3, a CRMP2-CaV2.2 interaction inhibitor, has been shown to significantly attenuate carrageenan-induced thermal hypersensitivity and reverse thermal hypersensitivity in a rat model of postoperative pain, making it a useful compound for studying inflammation and postoperative pain [1].
价 格:¥电议型 号:T80501产 地:中国大陆
-
T79732CD38 inhibitor 3;化合物 CD38 inhibitor 3CD38 inhibitor 3
CD38 Inhibitor 3 (compound 1), with an IC50 of 11 nM, is a potent agent that enhances mitochondrial biogenesis, diminishes lactate levels, and augments both NAD+ content and Nrf2 expression. In a Pus1 -/- mouse model of mitochondrial myopathy, it also elevates muscle function and bolstering exercise capacity [1].
价 格:¥电议型 号:T79732产 地:中国大陆
-
T79713JMJD3/HDAC-IN-1;化合物 JMJD3/HDAC-IN-1JMJD3/HDAC-IN-1
Compound A5b, also known as JMJD3/HDAC-IN-1, is a dual inhibitor that targets both JMJD3 (Jumonji domain-containing protein demethylase 3) and HADC1 (histone deacetylase, IC50 = 16 nM). It induces hypermethylation of histone H3K27 and hyperacetylation of H3K9, while also promoting apoptosis through the cleavage of caspase-7 and PARP. This compound has demonstrated the ability to effectively inhibit cancer cell cloning, migration, and invasion [1].
价 格:¥电议型 号:T79713产 地:中国大陆
-
T78956PROTAC BRD3/BRD4-L degrader-2;化合物 PROTAC BRD3/BRD4-L degrader-2PROTAC BRD3/BRD4-L degrader-2
PROTAC BRD3/BRD4-L degrader-2, a PROTAC molecule, selectively degrades cellular BRD3 and BRD4-L with K i values of 16.91 and 2.8 nM, respectively, and exhibits robust antitumor activity in mouse xenograft models, serving as a research tool for cancer [1].
价 格:¥电议型 号:T78956产 地:中国大陆
-
T78779D3R/MOR antagonist 2;化合物 D3R/MOR antagonist 2D3R/MOR antagonist 2
Compound 121, a D3R/MOR antagonist with K i values of 361 nM and 85.2 nM for D3R and MOR respectively, has the potential for analgesic effects through MOR partial agonism and may reduce opioid-misuse liability through D3R antagonism [1].
价 格:¥电议型 号:T78779产 地:中国大陆
-
T78778D3R/MOR antagonist 1;化合物 D3R/MOR antagonist 1D3R/MOR antagonist 1
Compound 114 (D3R/MOR antagonist 1) exhibits dual antagonistic activity at dopamine D3 receptors (D3R) and mu-opioid receptors (MOR), with K i values of 46.5 nM and 691 nM, respectively. It offers analgesic benefits through partial agonism at MOR and may decrease the risk of opioid misuse through its D3R antagonistic properties [1].
价 格:¥电议型 号:T78778产 地:中国大陆
-
T78736D3R ligand 1;化合物 D3R ligand 1D3R ligand 1
D3R Ligand 1 (compound 23b) is a potent, selective antagonist of the dopamine D3 receptor (Ki=66 nM), incorporating a THPB template. It inhibits both G-protein- and β-arrestin-mediated signaling pathways [1].
价 格:¥电议型 号:T78736产 地:中国大陆
-
T78584Prostaglandin D3;化合物 Prostaglandin D3PGD3;PGD3
Prostaglandin D3 (PGD3) functions as an inhibitor of platelet aggregation and modulates autonomic neurotransmission in humans [1].
价 格:¥电议型 号:T78584产 地:中国大陆
-
T78577NCD38 TFA;化合物 NCD38 TFANCD38 TFA
NCD38 TFA serves as a selective inhibitor of LSD1 [1] [2].
价 格:¥电议型 号:T78577产 地:中国大陆
-
T78495Nordeoxycholic acid;化合物 Nordeoxycholic acid3α,12α-Dihydroxynorcholanic acid;3α,12α-Dihydroxynorchola
Nordeoxycholic acid, a 23-carbon bile acid, functions as a metabolite of norcholic acid and a steroid metabolite in humans [1].
价 格:¥电议型 号:T78495产 地:中国大陆
-
T784413-(Dansylamino)phenylboronic acid;化合物 3-(Dansylamino)phenylboronic acid3-(Dansylamino)phenylboronic
3-(Dansylamino)phenylboronic acid, a derivative of phenylboronic acid, serves as a probe for glucose detection [1].
价 格:¥电议型 号:T78441产 地:中国大陆
-
T78257Anti-Mouse CD32/CD16 Antibody (2.4G2);化合物 Anti-Mouse CD32/CD16 Antibody (2.4G2)Anti-Mouse CD32/CD16
Anti-Mouse CD32/CD16 Antibody is a rat-derived IgG2b inhibitor targeting the mouse CD32/CD16 antigens.
价 格:¥电议型 号:T78257产 地:中国大陆
-
T78256Anti-Mouse CD3 Antibody (17A2);化合物 Anti-Mouse CD3 Antibody (17A2)Anti-Mouse CD3 Antibody (17A2)
Anti-Mouse CD3 Antibody is a Rat-derived IgG2b isotype inhibitor targeting the mouse CD3 complex.
价 格:¥电议型 号:T78256产 地:中国大陆
-
T776543-Bromo-6-chloro-2-pyridinecarboxylic acid3-溴-6-氯-2-吡啶甲酸3Bromo6chloro2pyridinecarboxylicacid|||3-Bro
产品可用于生物细胞实验
价 格:¥电议型 号:T77654产 地:中国大陆
-
T76254LCD31 TFA;化合物 CD31 TFACD31 TFA
CD31 TFA, also known as platelet endothelial cell adhesion molecule-1 (PECAM-1), functions as the specific receptor for Clostridium perfringens beta-Toxin (CPB) in endothelial cells. It is recognized as an ER-MP12 antigen and plays a pivotal role in connecting mechanical stress, metabolism, and inflammation. Additionally, the CD31 TFA peptide facilitates the phosphorylation of CD31 ITIM 686 and SHP2, further inhibiting TCR-induced T-cell activation [1]-[5].
价 格:¥电议型 号:T76254L产 地:中国大陆
-
T76254CD31;化合物 CD31CD31
CD31, also known as platelet endothelial cell adhesion molecule-1 (PECAM-1), is a receptor on endothelial cells for clostridium perfringens beta-Toxin (CPB). It also functions as an ER-MP12 antigen and connects mechanical stress, metabolism, and inflammation. The CD31 peptide promotes phosphorylation of CD31 ITIM 686 and SHP2, thereby inhibiting TCR-induced T-cell activation [1]-[5].
价 格:¥电议型 号:T76254产 地:中国大陆
-
T756653-O-Methylellagic acid;化合物 3-O-Methylellagic acid3-O-Methylellagic acid
3-O-Methylellagic acid, a natural product isolated from Myrciaria cauliflora, exhibits anti-inflammatory and antibacterial activities. This compound not only inhibits glucose transport but also demonstrates a minimum inhibitory concentration (MIC) of 32 μg/mL against Staphylococcus aureus ATCC 25923 [1] [2] [3].
价 格:¥电议型 号:T75665产 地:中国大陆
-
T74500FSDD3I;化合物 FSDD3IFSDD3I
FSDD3I, an albumin-binding fibroblast activation protein (FAP) ligand, can be tagged with isotopes 68Ga and 177Lu for use in single photon emission computed tomography (SPECT) imaging [1].
价 格:¥电议型 号:T74500产 地:中国大陆
-
T74373-(3-Hydroxyphenyl)propionic Acid3-(3-羟基苯基)丙酸m-Hydroxyphenylpropionic acid|||3-Hydroxyhydrocinnamic
3-(3-Hydroxyphenyl)propionic Acid (m-Hydroxyphenylpropionic acid) is one of the major metabolites of ingested caffeic acid.it inhibited osteoclastogenesis and bone osteoclastic resorptive activity.
价 格:¥电议型 号:T7437产 地:中国大陆