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:3847925
已选条件
-
T11978McN3716;帕莫酸甲酯NSC359682|||Methyl palmoxirate;NSC359682|||Methyl palmoxirate
McN3716 is a carnitine palmitoyltransferase I (CPT-1) inhibitor for the study of metabolic diseases.
价 格:¥电议型 号:T11978产 地:中国大陆
-
T11969MCL-1/BCL-2-IN-2;化合物 T11969MCL-1/BCL-2-IN-2
MCL-1/BCL-2-IN-2 is a potent and selective Bcl-2 and Mcl-1 dual inhibitor.
价 格:¥电议型 号:T11969产 地:中国大陆
-
T11968MCL-1/BCL-2-IN-1化合物 T11968MCL1/BCL2IN1|||MCL 1/BCL 2 IN 1
MCL-1/BCL-2-IN-2 (Compound Nap-1) is a potent and selective dual inhibitor of Mcl-1 and Bcl-2 with IC 50 s of 4.45 and 3.18 μM, respectively [1].
价 格:¥电议型 号:T11968产 地:中国大陆
-
T11967Mcl-1 antagonist 1;化合物 T11967Mcl-1 antagonist 1
Mcl-1 antagonist 1 is a Mcl-1 protein antagonist.
价 格:¥电议型 号:T11967产 地:中国大陆
-
T11966MCHR1 antagonist 2;化合物MCHR1 antagonist 2MCHR1 antagonist 2
MCHR1 antagonist 2 is an antagonist of melanin-concentratin hormone receptor 1(MCH1-R, IC50 = 65 nM) and also inhibits hERG.
价 格:¥电议型 号:T11966产 地:中国大陆
-
T11964MCH-1 antagonist 1;化合物 T11964MCH-1 antagonist 1
MCH-1 antagonist 1 also inhibits CYP3A4 (IC50: 10μM).MCH-1 antagonist 1 is a potent melanin concentrating hormone (MCH-1) antagonist (Ki: 2.6 nM).
价 格:¥电议型 号:T11964产 地:中国大陆
-
T11963MCB-3681;化合物 T11963MCB-3681
MCB-3681, active against gram-positive bacterium, is the antibacterial Oxaquin´s active substance.
价 格:¥电议型 号:T11963产 地:中国大陆
-
T11962MC3482;化合物MC3482MC3482
MC3482 is a specific inhibitor of sirtuin5 (SIRT5).
价 格:¥电议型 号:T11962产 地:中国大陆
-
T11961MBM-55S;化合物MBM-55SMBM-55S
MBM-55S is an effective inhibitor of Nek2 with an IC50 of 1 nM. MBM-55S indecus cell cycle arrest and apoptosis thereby inhibiting the proliferation of cancer cells. MBM-55S shows antitumor activities.
价 格:¥电议型 号:T11961产 地:中国大陆
-
T11960MBM-55;化合物MBM-55MBM-55
MBM-55 is an effective inhibitor of NIMA related kinase 2 (NEK2) with an IC50 of 1 nM. MBM-55 effectively inhibits the proliferation of cancer cells by inducing cell cycle arrest and apoptosis.
价 格:¥电议型 号:T11960产 地:中国大陆
-
T1196Iodixanol;碘克沙醇Visipaque|||Acupaque;碘克沙醇|||Visipaque|||Acupaque
Iodixanol (Visipaque) is a nonionic hydrophilic compound commonly used as a contrast agent during coronary angiography.
价 格:¥电议型 号:T1196产 地:中国大陆
-
T11909LY2444296化合物LY2444296FP3FBZ
LY2444296 (FP3FBZ) is an orally active and selective antagonist of kappa opioid receptor(Ki = 1 nM).
价 格:¥电议型 号:T11909产 地:中国大陆
-
T11896LV-320;化合物 T11896LV-320
LV-320 is a potent and uncompetitive ATG4B inhibitor with an IC 50 of 24.5 μM and a K d of 16 μM. LV-320 inhibits ATG4B enzymatic activity, blocks autophagic flux in cells, and is stable, non-toxic and active in vivo. These findings suggest that LV-320 will serve as a relevant chemical tool to study the various roles of ATG4B in cancer and other contexts [1].
价 格:¥电议型 号:T11896产 地:中国大陆
-
T11892Lurasidone D8 Hydrochloride;化合物 T11892SM-13496 D8;SM-13496 D8
Lurasidone D8 Hydrochloride is an inhibitor of Dopamine D2, 5-HT2A, 5-HT7, 5-HT1A and noradrenaline α2C, and is the deuterium labeled Lurasidone.
价 格:¥电议型 号:T11892产 地:中国大陆
-
T1188Mizoribine;咪唑立宾Bredinin|||NSC 289637|||HE 69;Bredinin|||NSC 289637|||咪唑立宾|||HE 69
Mizoribine (NSC-289637) belongs to the family of 1-Ribosyl-imidazolecarboxamides. Mizoribine has been investigated for the treatment of Rheumatoid Arthritis.
价 格:¥电议型 号:T1188产 地:中国大陆
-
T11859LLitronesib;化合物 T11859LKF-89617|||LY-2523355;KF-89617|||LY-2523355
Litronesib is a selective inhibitor of mitosis-specific kinesin Eg5. It also has antitumor activity.
价 格:¥电议型 号:T11859L产 地:中国大陆
-
T11859Litronesib Racemate化合物 T11859LY-2523355 Racemate|||KF-89617 Racemate
Litronesib is a selective, allosteric inhibitor of kinesin Eg5.Litronesib (Racemate) is the racemate of litronesib.
价 格:¥电议型 号:T11859产 地:中国大陆
-
T1185Rofecoxib;罗非考昔MK 966|||MK-0966;MK 966|||罗非昔布|||罗非考昔|||MK-0966
Rofecoxib (MK 966) binds to and inhibits the enzyme cyclooxygenase-2 (COX-2), resulting in an inhibition of the conversion of arachidonic acid to prostaglandins. Rofecoxib is a synthetic, nonsteroidal derivative of phenyl-furanone with anti-inflammatory, antipyretic and analgesic properties and potential antineoplastic properties. COX-related metabolic pathways may represent key regulators of cell proliferation and neo-angiogenesis. Some epithelial tumor cell types overexpress pro-angiogenic COX
价 格:¥电议型 号:T1185产 地:中国大陆
-
T118496TLC0873-0006;化合物 TLC0873-0006TLC0873-0006
Tyrosine-protein kinase FYN, Kd: 240 nM
价 格:¥电议型 号:T118496产 地:中国大陆
-
T11830LDN-192960 hydrochloride化合物 T11830LDN192960 hydrochloride|||LDN 192960 hydrochloride
LDN-192960 hydrochloride is an inhibitor of Dual-specificity Tyrosine-regulated Kinase 2 (DYRK2) and Haspin with IC50s of 48 nM and 10 nM, respectively.
价 格:¥电议型 号:T11830产 地:中国大陆