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
工商认证 【已认证】
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：3872578
自主品牌
已选条件
-
T81101ST8154AA1；化合物 ST8154AA1ST8154AA1
ST8154AA1, an antibody-drug conjugate (ADC) component coupled with an HDAC inhibitor via a linker, exhibits antitumor activity [1].
价 格：￥电议型 号：T81101产 地：中国大陆
-
T81100ST8155AA1；化合物 ST8155AA1ST8155AA1
ST8155AA1, a component of antibody-drug conjugates (ADCs), is tethered to an HDAC inhibitor via a linker and exhibits antitumor activity [1].
价 格：￥电议型 号：T81100产 地：中国大陆
-
T8110(+)-Longifolene；长叶烯(+)-Longifolene
(+)-Longifolene is a naturally occurring.
价 格：￥电议型 号：T8110产 地：中国大陆
-
T80819WAY-325811；化合物 WAY-325811WAY-325811
WAY-325811 is an active pharmaceutical compound.
价 格：￥电议型 号：T80819产 地：中国大陆
-
T80811WAY-359473；化合物 WAY-359473WAY-359473
WAY-359473 is an active compound.
价 格：￥电议型 号：T80811产 地：中国大陆
-
T80802WAY-608119；化合物 WAY-608119WAY-608119
WAY-608119 is an active molecule.
价 格：￥电议型 号：T80802产 地：中国大陆
-
T79811DDR1/2 inhibitor-2；化合物 DDR1/2 inhibitor-2DDR1/2 inhibitor-2
DDR1/2 Inhibitor-2 (Example 31) serves as an inhibitor of DDR1/DDR2, exhibiting IC50 values below 100 nM. It is applicable in cancer and fibrotic disease research [1].
价 格：￥电议型 号：T79811产 地：中国大陆
-
T78811PROTAC AR-NTD degrader 1；化合物 PROTAC AR-NTD degrader 1PROTAC AR-NTD degrader 1
PROTAC AR-NTD antagonist 1 (compound 18) is a small molecule belonging to the protein-targeting chimeras (PROTACs) that selectively targets the N-terminal domain (AR-NTD) of the Androgen Receptor variant AR-V7. By antagonizing AR-NTD, this compound effectively degrades AR-V7 protein and triggers apoptosis in prostate cancer (PC) cells, with degradation efficiencies in VCaP cells recorded at 62.2% (1 μM) and 71.1% (5 μM), as noted in reference [1].
价 格：￥电议型 号：T78811产 地：中国大陆
-
T78218Ilaprazole sodium hydrate；化合物 Ilaprazole sodium hydrateIY-81149 sodium hydrate；IY-81149 sodium hydra
Ilaprazole (IY-81149) sodium hydrate is an orally active proton pump inhibitor that irreversibly inhibits H+/K+-ATPase in rabbit parietal cells with a dose-dependent IC50 of 6 μM. It is employed in gastric ulcer research and acts as a potent inhibitor of T-lymphokine-activated killer cell-originated protein kinase (TOPK) [1] [2].
价 格：￥电议型 号：T78218产 地：中国大陆
-
T78119Z-L(D-Val)G-CHN2；化合物 Z-L(D-Val)G-CHN2Z-L(D-Val)G-CHN2
Z-L(D-Val)G-CHN2, an isoform of Z-LVG-CHN2, serves as a cell-permeable and irreversible inhibitor of cysteine proteinase. This tripeptide derivative emulates a segment of the human cysteine proteinase-binding center and demonstrates selective antiviral activity, inhibiting herpes simplex virus (HSV) yet exhibiting negligible impact on poliovirus replication. Notably, Z-LVG-CHN2 effectively impedes SARS-CoV-2 replication with an EC50 value of 190 nM by targeting the SARS-CoV-2 3CL protease [3].
价 格：￥电议型 号：T78119产 地：中国大陆
-
T78117FN-439 TFA；化合物 FN-439 TFAFN-439 TFA
FN-439 TFA is a selective inhibitor of collagenase-1, exhibiting inhibition with an IC50 of 1 μM, and is utilized in cancer and inflammation research [1] [2].
价 格：￥电议型 号：T78117产 地：中国大陆
-
T78116Antifungal agent 49；化合物 Antifungal agent 49Antifungal agent 49
Antifungal agent 49 (Example 112) exhibits activity against Cryptococcus neoformans, demonstrating a minimum inhibitory concentration (MIC) of 49 μM [1].
价 格：￥电议型 号：T78116产 地：中国大陆
-
T78115Antifungal agent 48；化合物 Antifungal agent 48Antifungal agent 48
Antifungal agent 48 (Example 308), active against Cryptococcus neoformans, exhibits a minimum inhibitory concentration (MIC) value of 11 μM [1].
价 格：￥电议型 号：T78115产 地：中国大陆
-
T78114Phenethicillin sodium；非奈西林钠盐α-Phenoxyethylpenicillin sodium|||Pheneticillin sodium；α-Phenoxyethylpen
Phenethicillin sodium (α-Phenoxyethylpenicillin) is a penicillin-class antibiotic that exhibits antimicrobial activity [1].
价 格：￥电议型 号：T78114产 地：中国大陆
-
T78113Tylvalosin；化合物 TylvalosinAcetylisovaleryltylo?sin；Acetylisovaleryltylo?sin
Tylvalosin (Acetylisovaleryltylosin) is a broad-spectrum macrolide antibiotic with antibacterial and antiviral properties, effective against PRRSV infection. It induces apoptosis and possesses anti-inflammatory activity. Furthermore, Tylvalosin mitigates oxidative stress and acute lung injury through the suppression of NF-κB activation [1] [2].
价 格：￥电议型 号：T78113产 地：中国大陆
-
T78112Voxvoganan trihydrochloride；化合物 Voxvoganan trihydrochlorideLTX-109 trihydrochloride；LTX-109 trihydro
Voxvoganan (LTX-109) trihydrochloride, a topical antimicrobial, demonstrates a high efficacy against S. aureus, exhibiting a MIC range of 2 to 4 μg/mL. It is utilized in research for treating bacterial skin infections, fungal infections, and nasal decolonization of MRSA [1] [2].
价 格：￥电议型 号：T78112产 地：中国大陆
-
T78111NCS-382 sodium；化合物 NCS-382 sodiumNCS-382 sodium
NCS-382 (sodium) is a potent antagonist of the GABA receptor, exhibiting anti-sedative and anti-hypnotic properties, with applications in neurological disease research [1].
价 格：￥电议型 号：T78111产 地：中国大陆
-
T78110DOTA-LM3 TFA；化合物 DOTA-LM3 TFADOTA-LM3 TFA
DOTA-LM3 TFA is a somatostatin receptor (SSTR) antagonist with the molecular structure p-Cl-Phe-cyclo(D-Cys-Tyr-D-4-amino-Phe(carbamoyl)-Lys-Thr-Cys)D-Tyr-NH2. It is effectively used in tracing tumors in vivo through isotopic labeling, examples being 177Lu-DOTA-LM3 TFA and 68Ga-DOTA-LM3 TFA. The 68Ga-labeled compound demonstrates favorable biodistribution, high tumor uptake, good tumor retention, and minimal safety concerns. Meanwhile, the 177Lu-labeled variant is utilized in research targeting
价 格：￥电议型 号：T78110产 地：中国大陆
-
T7811Pilsicainide HCl盐酸吡西卡呢SUN 1165|||盐酸吡西卡呢
Pilsicainide HCl (SUN 1165) is a pure sodium channel blocker
价 格：￥电议型 号：T7811产 地：中国大陆
-
T7708DL-Buthionine-(S,R)-sulfoximine丁基硫Butionine sulfoximine|||丁基硫|||NSC 381100|||D,L-Buthionine-(S,R)-su
DL-Buthionine-(S,R)-sulfoximine (Butionine sulfoximine) is an inhibitor of γ-glutamylcysteine synthetase for the treatment of solid tumors.
价 格：￥电议型 号：T7708产 地：中国大陆
