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：3847622
自主品牌
已选条件
-
T10407Gartisertib；化合物 T10407ATR inhibitor 2；ATR inhibitor 2
ATR inhibitor 2 is an orally active, ATP-competitive, and selective ATR inhibitor (Ki <150 pM) with antitumor activity. ATR inhibitor 2 potently inhibits ATR-driven phosphorylated checkpoint kinase-1 (Chk1) phosphorylation (IC50: 8 nM).
价 格：￥电议型 号：T10407产 地：中国大陆
-
T10406Tuvusertib；化合物TuvusertibM1774|||ATR inhibitor 1；M1774|||ATR inhibitor 1
Tuvusertib (M1774) is an orally available ataxia telangiectasia and Rad3-related (ATR) kinase inhibitor (Ki< 1 ?Μ) with selective and potentially antitumor activity.Tuvusertib selectively inhibits ATR activity and blocks downstream phosphorylation of serine/threonine protein kinase checkpoint kinase 1 (CHK1), thereby inhibits DNA damage checkpoint activation, disrupting DNA damage repair and inducing apoptosis in tumor cells.
价 格：￥电议型 号：T10406产 地：中国大陆
-
T10405ATPA；化合物 T10405ATPA
ATPA is a selective glutamate receptor GluR5 activator (EC50s: 0.66, 1.4, 9.5, 23, 32, 18, and 14 μM for GluR5wt, GluR5(S721T), GluR5(S741M), GluR5(S721T, S741M), GluR5(S741A), GluR5(S741L), and GluR5(S741V)).
价 格：￥电议型 号：T10405产 地：中国大陆
-
T10404ATP synthase inhibitor 1；化合物ATP synthase inhibitor 1ATP synthase inhibitor 1
ATP synthase inhibitor 1 is an inhibitor of the c subunit of the F1/FO-ATP synthase complex. It inhibits mitochondrial permeability transition pore (mPTP) opening and does not affect ATP levels.
价 格：￥电议型 号：T10404产 地：中国大陆
-
T10403Atorvastatin ethyl ester；化合物 T10403Atorvastatin ethyl ester
Atorvastatin ethyl ester, a derivative of Atorvastatin, exhibits potent inhibition of 9-cis-RA-induced Gal4 reporter activity.
价 格：￥电议型 号：T10403产 地：中国大陆
-
T10402Atorvastatin Epoxy Tetrahydrofuran Impurity；化合物 T10402Atorvastatin Epoxy Tetrahydrofuran Impurity
Atorvastatin Epoxy Tetrahydrofuran Impurity is an impurity isolated oxidative degradation products of Atorvastatin. Atorvastatin is an orally active HMG-CoA reductase inhibitor.
价 格：￥电议型 号：T10402产 地：中国大陆
-
T10401Atorvastatin acetonide；化合物 T10401Atorvastatin acetonide
Atorvastatin acetonide is an impurity of Atorvastatin. Atorvastatin is an HMG-CoA reductase inhibitor and has the ability to effectively decrease blood lipids.
价 格：￥电议型 号：T10401产 地：中国大陆
-
T10400Atorvastatin acetonide tert-butyl ester；化合物 T10400Atorvastatin acetonide tert-butyl ester
Atorvastatin acetonide tert-butyl ester is a useful pharmaceutical intermediate in the preparation of Atorvastatin salts. Atorvastatin is an HMG-CoA reductase inhibitor.
价 格：￥电议型 号：T10400产 地：中国大陆
-
T10399Atorvastatin 3-Deoxyhept-2E-Enoic Acid；化合物 T10399(2E)-2,3-Dehydroxy Atorvastatin；(2E)-2,3-Dehydroxy
Atorvastatin 3-Deoxyhept-2E-Enoic Acid is an impurity of Atorvastatin. Atorvastatin is an HMG-CoA reductase inhibitor and has the ability to effectively decrease blood lipids.
价 格：￥电议型 号：T10399产 地：中国大陆
-
T10398ATN-161；化合物 T10398ATN-161
ATN-161 is a novel integrin α5β1 antagonist that inhibits angiogenesis and growth of liver metastases in a murine model.
价 格：￥电议型 号：T10398产 地：中国大陆
-
T10397ATN-161 trifluoroacetate salt；化合物ATN-161 trifluoroacetate saltATN-161 TFA salt；ATN-161 TFA salt
ATN-161 trifluoroacetate salt (ATN-161 TFA salt) is a novel integrin α5β1 antagonist that inhibits angiogenesis and growth of liver metastases and improves survival in a murine model.
价 格：￥电议型 号：T10397产 地：中国大陆
-
T10396ATM Inhibitor-1；化合物 T10396ATM Inhibitor-1
ATM Inhibitor-1 is a highly potent, selective and orally active ATM inhibito (IC50: 0.7 nM) anti-tumor activity. It shows weak activity against mTOR (IC50, 21 μM), DNAPK (IC50, 2.8 μM), PI3Kα (IC50, 3.8 μM), PI3Kβ (IC50, 10.3 μM), PI3Kγ (IC50, 3 μM) and PI3Kδ (IC50, 0.73 μM).
价 格：￥电议型 号：T10396产 地：中国大陆
-
T10395LATM-3507化合物 ATM-3507ATM3507|||ATM 3507
ATM-3507 is a protomyosin inhibitor with anticancer activity that inhibits human melanoma and can be used to study ovarian cancer.
价 格：￥电议型 号：T10395L产 地：中国大陆
-
T10395ATM-3507 trihydrochloride (1861449-70-8 free base)；化合物 T10395ATM-3507 trihydrochloride；ATM-3507 trih
ATM-3507 trihydrochloride is a potent tropomyosin inhibitor (IC50s: 3.83-6.84 μM in human melanoma cell lines).
价 格：￥电议型 号：T10395产 地：中国大陆
-
T10394LATB107 hydrochloride；化合物ATB107盐酸盐ATB107 hydrochloride(455325-51-6 Free base)；ATB107 hydrochloride(45
ATB107 hydrochloride is a novel and potent inhibitor of indole-3-glycerol phosphate synthase (IGPS) with a KD of 3 μM.
价 格：￥电议型 号：T10394L产 地：中国大陆
-
T10394ATB107；化合物 T10394ATB107
ATB107 is a potent and novel inhibitor of indole-3-glycerol phosphate synthase (IGPS, KD: 3 μM).
价 格：￥电议型 号：T10394产 地：中国大陆
-
T10393AT-007；化合物AT-007AT-007
AT-007 is an orally active CNS penetrant Aldose Reductase inhibitor for the treatment of Galactosemia (IC50: 100 pM). It reduces toxic galactitol levels and prevents disease complications in GALT deficiency rats.
价 格：￥电议型 号：T10393产 地：中国大陆
-
T10391Aspirin Aluminum阿司匹林铝Aluminum diacetylsalicylate|||阿司匹林铝
Aspirin Aluminum is an intermolecular compound that can inhibit gastrointestinal mucosal disorders induced by NSAIDs.
价 格：￥电议型 号：T10391产 地：中国大陆
-
T10390Asperphenamate；化合物AsperphenamateAsperphenamate
Asperphenamate is a fungal metabolite of Aspergillus flatiipes. The IC50s for T47D cells, MDA-MB-231 cells, and HL-60 cells are 92.3 μM, 96.5 μM, and 97.9 μM. Asperphenamate shows an anticancer effect.
价 格：￥电议型 号：T10390产 地：中国大陆
-
T10389LAspartyl-alanyl-diketopiperazine acetate；化合物T10389LDA-DKP|||Aspartyl-alanyl-diketopiperazine acetate
Aspartyl-alanyl-diketopiperazine acetate (DA-DKP) (DA-DKP) can modulate the inflammatory immune response through a molecular pathway implicated in T- lymphocyte anergy.
价 格：￥电议型 号：T10389L产 地：中国大陆
