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：3854668
自主品牌
已选条件
-
T11662INT-777 R-enantiomer；化合物 T11662S-EMCA R enantiomer；S-EMCA R enantiomer
INT-777 is the R-enantiomer of INT-777, less potent than INT-777,EC50 of 4.79 μM for TGR5.
价 格：￥电议型 号：T11662产 地：中国大陆
-
T11661INT-767；化合物 INT-767INT-767
INT-767 is a potent farnesoid X receptor (FXR)/TGR5 dual agonist that prevents NASH and promotes visceral adipose brown lipogenesis and mitochondrial function for the study of non-alcoholic steatohepatitis.
价 格：￥电议型 号：T11661产 地：中国大陆
-
T11660Insulin levels modulator；化合物 T11660Insulin levels modulator
Insulin level regulators can be used to treat diabetes.
价 格：￥电议型 号：T11660产 地：中国大陆
-
T1166Ellipticine；玫瑰树碱NSC 71795|||Elliptisine；玫瑰树碱|||NSC 71795|||Elliptisine
Ellipticine (Elliptisine) is a potent antineoplastic agent exhibiting multiple mechanisms of action, IC50 of 0.67±0.06, 1.25±0.13, 1.25±0.13, 0.67±0.06, 0.27±0.02, 0.49±0.04, 0.44±0.03, and 1.48±0.62 μM for Leukemia HL-60, Breast adenocarcinoma MCF-7, Breast adenocarcinoma MCF-7, Leukemia HL-60, Neuroblastoma IMR-32, Neuroblastoma UKF-NB-4, Neuroblastoma UKF-NB-3, and Glioblastoma U87 mg cell, respectively.
价 格：￥电议型 号：T1166产 地：中国大陆
-
T11659Inogatran；伊诺加群H-314-27；伊诺加群|||H-314-27
Inogatran is a synthetic thrombin inhibitor, developed for the possible treatment and prophylaxis of venous and arterial thrombotic diseases.
价 格：￥电议型 号：T11659产 地：中国大陆
-
-
T11657INH154；化合物INH154INH154
INH154 is a potent Nek2 and Hec1 binding (INH) inhibitor with IC50s of 120 nM in MB468 cells and 200 nM in Hela cells for INH.
价 格：￥电议型 号：T11657产 地：中国大陆
-
T11655Indomethacin-D4；吲哚美辛-D4Indomethacin-D-4|||Indometacin-D4|||Indometacin-D4|||吲哚美辛-D4|||Indomethacin D
Indomethacin-D4 is a deuterium labeled Indomethacin. Indomethacin is a potent and nonselective inhibitor of COX1 and COX2, with IC50s of 18 nM and 26 nM for human COX-1 and COX-2, respectively, in CHO cells.
价 格：￥电议型 号：T11655产 地：中国大陆
-
T11654Indirubin Derivative E804；化合物 T11654Indirubin Derivative E804
Indirubin Derivative E804 is an effective inhibitor of IGF1R, which has an IC50 value of 0.65.
价 格：￥电议型 号：T11654产 地：中国大陆
-
T11653Indirubin-5-sulfonate；化合物 T11653Indirubin-5-sulfonate
Indirubin-5-sulfonate shows inhibitory activity against GSK-3β. Indirubin-5-sulfonate is a cyclin-dependent kinase (CDK) inhibitor, with IC50 values of 55 nM, 35 nM, 150 nM, 300 nM and 65 nM for CDK1/cyclin B, CDK2/cyclin A, CDK2/cyclin E, CDK4/cyclin D1, and CDK5/p35, respectively.
价 格：￥电议型 号：T11653产 地：中国大陆
-
T11651Indanidine；吲达尼定Indanidine
Indanidine is a highly selective and potent α-adrenergic agonist with antihypertensive activity.Indanidine is an α-adrenergic antagonist that can be used in the study of neurological disorders.
价 格：￥电议型 号：T11651产 地：中国大陆
-
T11650INCB3344 R-isomer；化合物 T11650INCB3344 R-isomer
INCB3344 is a potent CCR2 antagonist. INCB3344 R-isomer is the R-isomer of INCB3344.
价 格：￥电议型 号：T11650产 地：中国大陆
-
T1165Ethionamide乙硫异烟胺Bayer 5312|||乙硫异烟胺|||2-ethylthioisonicotinamide|||Ethinamide
Ethionamide (2-ethylthioisonicotinamide) is a nicotinamide derivative, with antibacterial activity, used to treat tuberculosis. Although the exact mechanism of action of ethionamide is unknown, it may inhibit the synthesis of mycolic acid, a saturated fatty acid found in the bacterial cell wall, thereby inhibiting bacterial cell wall synthesis. This eventually leads to bacterial cell wall disruption and cell lysis. Ethionamide may be bacteriostatic or bactericidal in action, depending on the con
价 格：￥电议型 号：T1165产 地：中国大陆
-
T11649INCB054329 Racemate；化合物 T11649INCB054329 Racemate
INCB054329 Racemate is an inhibitor of BET protein.
价 格：￥电议型 号：T11649产 地：中国大陆
-
T11648INCB 3284；化合物 T11648INCB 3284
INCB 3284, a potent and selective human CCR2 antagonist with an oral bioavailability, is utilized in the study of acute liver failure. It effectively inhibits the binding of monocyte chemoattractant protein-1 (MCP-1) to hCCR2, demonstrating an IC50 of 3.7 nM.
价 格：￥电议型 号：T11648产 地：中国大陆
-
T11647INCB 3284 dimesylate；化合物 T11647INCB 3284 dimesylate
INCB 3284 dimesylate is a selective and orally bioavailable human CCR2 antagonist, inhibiting monocyte chemoattractant protein-1 binding to hCCR2 (IC50: 3.7 nM). It can be used in the research of acute liver failure.
价 格：￥电议型 号：T11647产 地：中国大陆
-
T11646Impurity F of Calcipotriol；化合物 T11646Impurity F of Calcipotriol
Impurity F of Calcipotriol is a impurity of Calcipotriol. Calcipotriol (MC 903; Calcipotriene) is a ligand of VDR-like receptors.
价 格：￥电议型 号：T11646产 地：中国大陆
-
T11645Impurity C of Calcitriol；PRE-骨化三醇PTAD加合物Impurity C of Calcitriol
Impurity C of Calcitriol is an impurity of Calcitriol.Impurity C of Calcitriol is used in the synthesis of vitamin D3.
价 格：￥电议型 号：T11645产 地：中国大陆
-
T11644Impurity C of Alfacalcidol；阿法骨化醇杂质 CImpurity C of Alfacalcidol
Impurity of Alfacalcidol is an impurity of Alfacalcidol. Alfacalcidol is a non-selective VDR activator medication.
价 格：￥电议型 号：T11644产 地：中国大陆
-
T11643Impurity B of Calcitriol；化合物 T116431β,25-Dihydroxyvitamin-D3|||1-Epicalcitriol；1β,25-Dihydroxyvitami
Impurity B of Calcitriol is an impurity of Calcitriol. Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
价 格：￥电议型 号：T11643产 地：中国大陆
