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:3514231
已选条件
-
T72262Antituberculosis agent-6;化合物 Antituberculosis agent-6Antituberculosis agent-6
Antituberculosis agent-6 is a potent antimycobacterial and antifungal compound with significant activity against M. tuberculosis (MIC of 3.49 μM) and A. niger (MIC of 62.50 μM), respectively. It also demonstrates high gastrointestinal (GI) absorption.
价 格:¥电议型 号:T72262产 地:中国大陆
-
T72261Metallo-β-lactamase-IN-9;化合物 Metallo-β-lactamase-IN-9Metallo-β-lactamase-IN-9
Metallo-β-lactamase-IN-9 (Compound 23) serves as a broad-spectrum inhibitor of metallo-beta-lactamases (MBL), exhibiting inhibition constants (IC50) of 35 nM for NDM-1, 269 nM for VIM-1, and 369 nM for IMP-1 [1].
价 格:¥电议型 号:T72261产 地:中国大陆
-
T72260Antileishmanial agent-13;化合物 Antileishmanial agent-13Antileishmanial agent-13
Antileishmanial agent-13, a quinoline-isatin hybrid, functions as an antileishmanial agent targeting the L. Major Leishmania strain through an anti-folate mechanism. This compound exhibits potent inhibition of both the promastigote and amastigote forms, boasting IC50 values of 0.604 μM and 0.508 μM, respectively.
价 格:¥电议型 号:T72260产 地:中国大陆
-
T72226β2AR/M-receptor agonist-2;化合物 β2AR/M-receptor agonist-2β2AR/M-receptor agonist-2
β2AR/M-receptor agonist-2 is a dual-function compound acting as a muscarinic antagonist and β2 adrenoceptor agonist (MABA). It demonstrates significant activity towards the β2 adrenoceptor with an EC50 of 3.7 nM and exhibits affinity for the human cloned M3 receptor with a Ki of 0.73 nM. This potent bronchodilator holds potential for research in chronic obstructive pulmonary disease (COPD) treatment.
价 格:¥电议型 号:T72226产 地:中国大陆
-
T71507PF-4522654;化合物 PF-4522654PF-4522654
PF-4522654 is a potent and selective 5-HT2C receptor agonist.
价 格:¥电议型 号:T71507产 地:中国大陆
-
T71226Opc 15161;化合物 Opc 15161Opc 15161
Opc 15161 is a degradation product of OPC-15160 and superoxide inhibitor.
价 格:¥电议型 号:T71226产 地:中国大陆
-
T70936CGS 22652;化合物 CGS 22652CGS 22652
CGS 22652 has thromboxane receptor antagonism combined with thromboxane synthase inhibition.
价 格:¥电议型 号:T70936产 地:中国大陆
-
T70899Vidofludimus hemicalcium;化合物 Vidofludimus calcium4sc-101 hemicalcium|||SC12267 hemicalcium|||4sc-101
Vidofludimus hemicalcium (4sc-101; SC12267) is an orally active compound that acts as a dihydroorotate dehydrogenase (DHODH) inhibitor and serves as a novel modulator of the farnesoid X receptor (FXR). This immunomodulatory agent is utilized in the research of autoimmune disorders, including inflammatory bowel disease (IBD), and is explored for its potential in fatty liver disease research through FXR targeting.
价 格:¥电议型 号:T70899产 地:中国大陆
-
T70226Amentoflavone hexaacetate;化合物 Amentoflavone hexaacetateAmentoflavone hexaacetate
Amentoflavone hexaacetate is a 3,5-cyclic nucleotide phosphodiesterase inhibitor. It has anti-angiogenic and anti-metastatic effects.
价 格:¥电议型 号:T70226产 地:中国大陆
-
T69402FR-226928;化合物 FR-226928FR-226928
FR-226928 is a potent antagonist of human neuropeptide Y Y5 receptors.
价 格:¥电议型 号:T69402产 地:中国大陆
-
T69226A-688057;化合物 A-688057A-688057
A-688057 is an H3 antagonist/inverse agonist that may play a role in cognition.
价 格:¥电议型 号:T69226产 地:中国大陆
-
T68732FR-226928 free base;化合物 FR-226928 free baseFR-226928 free base
FR-226928 free base is a potent antagonist of human neuropeptide Y Y5 receptors.
价 格:¥电议型 号:T68732产 地:中国大陆
-
T66226Ethyl 1-(4-methoxyphenyl)-6-(4-nitrophenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-ca
Ethyl 1-(4-methoxyphenyl)-6-(4-nitrophenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylate is a useful organic compound for research related to life sciences. The catalog number is T66226 and the CAS number is 536759-91-8.
价 格:¥电议型 号:T66226产 地:中国大陆
-
T6541Ibutilide Fumarate;富马酸伊布利特Corvert Fumarate|||U70226E;Corvert Fumarate|||U70226E|||富马酸伊布利特
Ibutilide Fumarate (U70226E) is the fumarate salt form of ibutilide, a class III antiarrhythmic agent. Ibutilide exerts its effect by activating a slow, inward, predominately sodium current rather than by blocking outward potassium currents. This results in prolongation of atrial and ventricular action potential duration and refractory periods. Ibutilide slightly decreases the sinus rate and atrioventricular (AV) conduction and produces a dose-related prolongation of the QT interval.
价 格:¥电议型 号:T6541产 地:中国大陆
-
T65226H-D-Leu-Gly-OH;化合物 H-D-Leu-Gly-OHH-D-Leu-Gly-OH
H-D-Leu-Gly-OH is a useful organic compound for research related to life sciences. The catalog number is T65226 and the CAS number is 997-05-7.
价 格:¥电议型 号:T65226产 地:中国大陆
-
T64226Tandutinib hydrochloride;化合物 Tandutinib hydrochlorideTandutinib hydrochloride
Tandutinib hydrochloride (MLN518 hydrochloride) is a potent, selective FLT3 inhibitor with an IC50 of 0.22 μM. It also effectively inhibits c-Kit and PDGFR, with IC50 values of 0.17 μM and 0.20 μM, respectively. This compound is clinically applicable for treating acute myelogenous leukemia (AML) and possesses the capability to cross the blood-brain barrier.
价 格:¥电议型 号:T64226产 地:中国大陆
-
T63226Asciminib hydrochloride;化合物 Asciminib hydrochlorideAsciminib hydrochloride
Asciminib (ABL001) hydrochloride is a selective and potent mutant BCR-ABL1 inhibitor that inhibits Ba/F3 cell growth (IC50: 0.25 nM).
价 格:¥电议型 号:T63226产 地:中国大陆
-
T62269F 14679;化合物F 14679F 13714;F 13714
F 14679 is a potent 5-HT1A agonist (pKi=10.23) with a maximum Ca2t response similar to 5-HT.
价 格:¥电议型 号:T62269产 地:中国大陆