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：3761382
自主品牌
已选条件
-
T81105SREBP/SCAP-IN-1；化合物 SREBP/SCAP-IN-1SREBP/SCAP-IN-1
SREBP/SCAP-IN-1 (compound 10b) serves as a selective inhibitor of SREBP/SCAP [1].
价 格：￥电议型 号：T81105产 地：中国大陆
-
T7785T-1105；3-羟基吡嗪-2-酰胺T-1105
T-1105 is a broad-spectrum antiviral inhibitor.
价 格：￥电议型 号：T7785产 地：中国大陆
-
T71105AZD2353；化合物 AZD2353AZD2353
AZD2353 is a potent inhibitor of diacylglycerol acetyl transferase 1 (DGAT1).
价 格：￥电议型 号：T71105产 地：中国大陆
-
T63056Dovramilast；化合物 DovramilastCC-11050；CC-11050
Dovramilast (CC-11050) is an orally active phosphodiesterase 4 (PDE4) inhibitor that reduces the production of pro-inflammatory mediators and cytokines.Dovramilast is used in the study of Mycobacterium tuberculosis infections and lupus erythematosus.
价 格：￥电议型 号：T63056产 地：中国大陆
-
T61105GAT228；化合物 GAT228GAT228
GAT228, an allosteric ligand for the cannabinoid receptor 1 (CB1), functions as the enantiomer of GAT211 [1].
价 格：￥电议型 号：T61105产 地：中国大陆
-
T5514Epibrassinolide表油菜素内酯24-Epibrassinolide|||B1105|||表油菜素内酯|||BP55
Epibrassinolide (BP55) (EBR) is a biologically active compound of the brassinosteroids, is a natural brassinosteroid (BR) derivative, is a plant regulator with a similar structure to mammalian steroids.
价 格：￥电议型 号：T5514产 地：中国大陆
-
T33575N-Acetylsarcolysinylleucine；化合物 T33575NSC261105|||NSC 261105|||NSC-261105；NSC261105|||NSC 261105|||N
N-Acetylsarcolysinylleucine is a bioactive chemical.
价 格：￥电议型 号：T33575产 地：中国大陆
-
T31105CS 722；化合物 T31105CS-722|||CS722；CS-722|||CS722
CS 722 is a centrally acting muscle relaxant. CS-722 exerts its muscle relaxant action by affecting both the supraspinal structure and the spinal cord.
价 格：￥电议型 号：T31105产 地：中国大陆
-
T29038KL8604166；化合物 KL8604166UCB11056|||UCB-11056|||UCB 11056；UCB11056|||UCB-11056|||UCB 11056
KL8604166 (UCB-11056) is a potential puzzle compound.UCB-11056 amplifies the formation of inducible cyclic AMP in rat brain tissue.
价 格：￥电议型 号：T29038产 地：中国大陆
-
T23444TCS 1105；化合物TCS 1105N-(4-fluorobenzyl)-2-(1H-indol-3-yl)-2-oxoacetamide；N-(4-fluorobenzyl)-2-(1H-ind
TCS 1105 is a GABAA benzodiazepine receptor (BZR) ligand. TCS 1105 blocks Sema3A induced axonal growth cones collapse. TCS 1105 reduces anxiety-like behavior and enhances offensive behavior and social dominance in mice.
价 格：￥电议型 号：T23444产 地：中国大陆
-
T22748DQP 1105；化合物DQP 1105DQP 1105
DQP 1105 is an NMDA receptor antagonist inhibiting receptor function more potently with glutamate.
价 格：￥电议型 号：T22748产 地：中国大陆
-
T21105Azlocillin；化合物 T21105Azlocilline|||Azlin；Azlocilline|||Azlin
Azlocillin is a semisynthetic ampicillin-derived penicillin belonging to acylureido.
价 格：￥电议型 号：T21105产 地：中国大陆
-
T15565Imetit dihydrobromide化合物 T15565VUF 8325 dihydrobromide|||SKF 91105 dihydrobromide
Imetit dihydrobromide is a high affinity and effective agonist of histamine H3 and H4 receptors (Ki: 0.3 and 2.7 nM). Imetit mimics the histamine effect in triggering a shape change in eosinophils (EC50: 25 nM).
价 格：￥电议型 号：T15565产 地：中国大陆
-
T11105DS88790512；化合物 T11105DS88790512
DS88790512, IC50 at 11 nM, is an effective, selective, oral bioeffective TRPC6 inhibitor.
价 格：￥电议型 号：T11105产 地：中国大陆
-
T11059DM4-SMe；化合物 T11059DM4-SMe
DM4-SMe is a cytotoxic part of antibody-drug conjugates (ADCs) and a metabolite of antibody-maytansin conjugates (AMCs) and tubulin inhibitors, which can also be stabilized by disulfide bonds or thioether The bond binds to the antibody. The IC50 of DM4-SMe on KB cells was 0.026 nM.
价 格：￥电议型 号：T11059产 地：中国大陆
-
T11058DM3；化合物 T11058Maytansinoid DM3；Maytansinoid DM3
DM3 (Maytansinoid DM3) is a maytansine mimic containing disulfide or thiol groups and a tubulin inhibitor. It is the cytotoxic part of antibody-drug conjugates (ADCs) .
价 格：￥电议型 号：T11058产 地：中国大陆
-
T11057DM3-SMe；化合物 T11057DM3-SMe
DM3-SMe is a maytansine derivative and tubulin inhibitor. It is a cytotoxic part of antibody-drug conjugates (ADCs) and can bind to antibodies via disulfide bonds or stable thioether bonds. DM3-SMe has high cytotoxic activity in vitro with IC50 of 0.0011 nM.
价 格：￥电议型 号：T11057产 地：中国大陆
-
T11056DLK-IN-1；化合物 T11056DLK-IN-1
DLK-IN-1 is a selective oral active inhibitor of bisleucine zipper kinase (DLK, MAP3K12) with Ki of 3 nM. DLK-IN-1 is active in the Alzheimer´s disease model, retains excellent CNS permeability, and after multiple days of administration, its concentration exceeds the concentration required for DLK inhibition in the brain, so it has good tolerance Acceptability.
价 格：￥电议型 号：T11056产 地：中国大陆
-
T11055DL-TBOA化合物 T11055DL TBOA|||DLTBOA
DL-TBOA inhibited [14C] glutamate uptake in COS-1 cells expressing human EAAT1 and EAAT2, with Ki values of 42 μM and 5.7 μM, respectively. DL-TBOA blocks EAAT4 and EAAT5 in a competitive manner, with Ki values of 4.4 μM and 3.2 μM, respectively. DL-TBOA is an effective non-transportable excitatory amino acid transporter inhibitor with IC50 of 70 μM, 6 μM and 6 μM for excitatory amino acid transporter 1 (EAAT1, EAAT2 and EAAT3), respectively.
价 格：￥电议型 号：T11055产 地：中国大陆
-
T11054DL-Norvaline；DL-正缬氨酸2-Aminopentanoic acid；2-Aminopentanoic acid|||DL-正缬氨酸
DL-Norvaline (2-Aminopentanoic acid) is a non-competitive inhibitor of arginase.
价 格：￥电议型 号：T11054产 地：中国大陆
