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：3734924
自主品牌
已选条件
-
T124147Quercetagetin 3,5,7-trimethyl ether；化合物 Quercetagetin 3,5,7-trimethyl etherQuercetagetin 3,5,7-trime
Quercetagetin 3,5,7-trimethyl ether is a useful organic compound for research related to life sciences. The catalog number is T124147 and the CAS number is 82784-42-7.
价 格：￥电议型 号：T124147产 地：中国大陆
-
T1240473,23-Dioxocycloart-24-en-26-oic acid；化合物 3,23-Dioxocycloart-24-en-26-oic acid3,23-Dioxocycloart-24-e
3,23-Dioxocycloart-24-en-26-oic acid is a useful organic compound for research related to life sciences and the catalog number is T124047.
价 格：￥电议型 号：T124047产 地：中国大陆
-
T123847Hexanorcucurbitacin F；化合物 Hexanorcucurbitacin FHexanorcucurbitacin F
Hexanorcucurbitacin F is a useful organic compound for research related to life sciences. The catalog number is T123847 and the CAS number is 96253-53-1.
价 格：￥电议型 号：T123847产 地：中国大陆
-
T12347p38-α MAPK-IN-1；化合物p38-α MAPK-IN-1p38-α MAPK-IN-1
p38-α MAPK-IN-1 is a MAPK14 (p38-α) inhibitor with IC50 of 2300 nM and 5500 nM in EFC displacement assay and HTRF assay,respectively.
价 格：￥电议型 号：T12347产 地：中国大陆
-
T12343Benzquinamide；苯喹胺BZQ|||P2647|||Benzoquinamide；BZQ|||P2647|||Benzoquinamide
Benzquinamide (P2647), an antiemetic agent with anticancer activity, inhibits p-glycoprotein-mediated drug efflux and potentiates the cytotoxicity of anticancer drugs in multidrug-resistant cells.The Ki values of Benzquinamide for α2A, α2B, and α2C adrenergic receptor (α2-AR) were 1,365, 691, and 545 nM, respectively. 545 nM, respectively.
价 格：￥电议型 号：T12343产 地：中国大陆
-
T12290OICR-0547；化合物 T12290OICR-0547
OICR-0547 is a closely related derivative of OICR-9429. OICR-9429 is a novel small-molecule Wdr5-MLL interaction antagonist.
价 格：￥电议型 号：T12290产 地：中国大陆
-
T12247NOT Receptor Modulator 1；化合物T122472-(3-(2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl)phenyl)propan-2
NOT Receptor Modulator 1 (2-(3-(2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl)phenyl)propan-2-ol) is a modulator of nuclear receptor NOT.
价 格：￥电议型 号：T12247产 地：中国大陆
-
T12193NCGC00247743；化合物 T12193NCGC00247743
NCGC00247743 is an inhibitor of histone lysine demethylase KDM4.
价 格：￥电议型 号：T12193产 地：中国大陆
-
T12147N-Desmethyl Clomipramine hydrochloride；化合物 T12147Desmethylclomipramine hydrochloride；Desmethylclomip
N-Desmethyl Clomipramine hydrochloride is a primary plasma N-desmethyl Clomipramine metabolite .
价 格：￥电议型 号：T12147产 地：中国大陆
-
T12063MK-447；化合物 T12063MK-447
MK-447 is a nonsteroidal antiinflammatory agent.
价 格：￥电议型 号：T12063产 地：中国大陆
-
T12051MIV-247；化合物 MIV-247MIV-247
MIV-247 is a selective and potent inhibitor of cathepsin S (Kis 2.1, 4.2, and 7.5 nM for human, mouse, and wild monkey cathepsin S, respectively), which attenuates mechanical anomalies in preclinical models of neuropathic pain, and can be used to study cardiac muscle injury.
价 格：￥电议型 号：T12051产 地：中国大陆
-
T12047Misoprostol acid；米索前列醇酸Misoprostol acid
Misoprostol acid is an active metabolite of Misoprostol,can be used for non-steroidal anti-inflammatory drug-induced (NSAID) gastric ulcers.
价 格：￥电议型 号：T12047产 地：中国大陆
-
T1203476751-0002；化合物 6751-00026751-0002
Glucagon-like peptide 1 receptor, Potency: 2238.7 nM
价 格：￥电议型 号：T120347产 地：中国大陆
-
T11947MARK4 inhibitor 1；化合物MARK4 inhibitor 1MARK4 inhibitor 1
MARK4 inhibitor 1 inhibits cancer cell proliferation, metastasis and induces apoptosis. MARK4 inhibitor 1 is a potent microtubule affinity-regulating kinase 4 (MARK4) inhibitor, with an IC50 of 1.54 μM.
价 格：￥电议型 号：T11947产 地：中国大陆
-
T11900LY-2584702 hydrochloride；化合物 T11900LY-2584702 hydrochloride
Ly-2584702 hydrochloride is a p70S6K selective ATP competitive inhibitor with IC50 of 4 nM.In the S6K1 enzyme assay, the IC50 of LY-2584702 was 2 nM.
价 格：￥电议型 号：T11900产 地：中国大陆
-
T11894Lusaperidone；芦沙哌酮R107474；R107474
Lusaperidone (R107474) is a potent α2-adrenergic receptor antagonist, a potential radioligand for the α (2)-adrenergic receptor, with inhibitory effects on α2A and α2C, with Ki values of 0.13 and 0.15 nM, respectively.
价 格：￥电议型 号：T11894产 地：中国大陆
-
T11847LLiarozole；利阿唑R75251 dihydrochloride；R75251 dihydrochloride|||利阿唑
Liarozole (R75251 dihydrochloride) is a cytochrome P450 (CYP450) dependent inhibitor, orally active, it also a potent inhibitor of estrogen (via inhibition of aromatase) and testicular androgen synthesis (inhibition of 17 ,20-lyase).Liarozole dihydrochloride is an imidazole derivative; it is being investigated as a non-hormonal agent in prostate cancer and in the treatment of various other cancers and skin disorders.
价 格：￥电议型 号：T11847L产 地：中国大陆
-
T11847Liarozole dihydrochloride；化合物 T11847R75251 dihydrochloride；R75251 dihydrochloride
Liarozole dihydrochloride is a cytochrome P450 (CYP450) dependent inhibitor, orally active, it also a potent inhibitor of estrogen (via inhibition of aromatase) and testicular androgen synthesis (inhibition of 17 ,20-lyase).Liarozole dihydrochloride is an imidazole derivative; it is being investigated as a non-hormonal agent in prostate cancer and in the treatment of various other cancers and skin disorders.
价 格：￥电议型 号：T11847产 地：中国大陆
-
T11747KD-3010；化合物KD-3010KD-3010
KD-3010 (Kalypsys) is an orally active potent and selective PPARδ agonist for the study of liver injury.
价 格：￥电议型 号：T11747产 地：中国大陆
-
T11725JNJ-47117096 hydrochloride；化合物 T11725MELK-T1 hydrochloride；MELK-T1 hydrochloride
JNJ-47117096 hydrochloride is potent and selective MELK inhibitor, with an IC50 of 23 nM, also effectively inhibits Flt3, with an IC50 of 18 nM.
价 格：￥电议型 号：T11725产 地：中国大陆
