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：3737257
自主品牌
已选条件
-
T26636Antifolate C2化合物Antifolate C2AGF 154|||AGF154|||AGF-154
Antifolate C2 (AGF 154) has antitumor activity with an IC of 0.14 nM measured in a growth inhibition assay of human tumor cells.Antifolate C2 can be used for the study of cancer and autoimmune diseases.
价 格：￥电议型 号：T26636产 地：中国大陆
-
T26444A 76154；化合物 T26444A-76154|||A76154；A-76154|||A76154
A 76154 is an antagonist of leutenizing hormone releasing hormone (LHRH).
价 格：￥电议型 号：T26444产 地：中国大陆
-
T26154RU 45144；化合物 T26154RU45144|||RU-45144；RU45144|||RU-45144
RU 45144 is an estradiol derivative with antiestrogenic activity.
价 格：￥电议型 号：T26154产 地：中国大陆
-
T25917Palmitoyl rhizoxin；化合物 T25917RS 1541|||RS1541|||RS-1541；RS 1541|||RS1541|||RS-1541
Palmitoyl rhizoxin is a highly lipophilic antitumor compound that acts by inhibiting tubulin polymerization and has stronger in vivo activity than rhizoxin.
价 格：￥电议型 号：T25917产 地：中国大陆
-
T25808MI 1544；化合物 T25808Attcpl-LHRH|||AttcplLHRH|||MI-1544|||MI1544|||Attcpl LHRH；Attcpl-LHRH|||AttcplLHRH
MI 1544 is a LHRH antagonist.
价 格：￥电议型 号：T25808产 地：中国大陆
-
T25537Iomazenil；化合物 T25537RO-16-0154|||RO 16-0154；RO-16-0154|||RO 16-0154
Iomazenil is an antagonist and partial inverse agonist of benzodiazepine and potential therapy for alcohol abuse.
价 格：￥电议型 号：T25537产 地：中国大陆
-
T25154Bim 21009；化合物 T25154LHRH-Ncpapa|||Bim-21009|||Bim21009|||LHRHNcpapa|||LHRH Ncpapa；LHRH-Ncpapa|||Bim-
Bim 21009 is an inhibitor of gonadorelin.
价 格：￥电议型 号：T25154产 地：中国大陆
-
T24461Mevinolinic acid；化合物 T24461L 154819|||L-154819|||MK 819|||MSD 803 acid|||Monacolinic K acid；L 154819
Mevinolinic acid is an active metabolite of Lovastatin. Lovastatin is an HMG-CoA reductase inhibitor.
价 格：￥电议型 号：T24461产 地：中国大陆
-
T24157Ici D1542；化合物 T24157D 1542|||D1542|||Ici-D1542|||ZD 1542；D 1542|||D1542|||Ici-D1542|||ZD 1542
Ici D1542 is a drug that exhibits both potent, selective TXS inhibition and TXA2 receptor antagonism. Ici D1542 is an effective thromboxane A2 synthase inhibitor and receptor antagonist in vitro.
价 格：￥电议型 号：T24157产 地：中国大陆
-
T24154I942；化合物I942I 942|||I-942；I 942|||I-942
I942 is a novel, selective ACyclic nucleotide (NCN) EPAC1 agonist that activates exchange proteins to regulate inflammatory gene expression in human umbilical blood tubes and inhibit pro-inflammatory cytokine signaling associated with cardiovascular disease.
价 格：￥电议型 号：T24154产 地：中国大陆
-
T23931D 15413；化合物 T23931D-15413|||D15413；D-15413|||D15413
D 15413 is an inhibitor of estrogen-dependent mammary tumors.
价 格：￥电议型 号：T23931产 地：中国大陆
-
T23514VU-1545；化合物VU 1545VU 1545；VU 1545
VU-1545 is mGlu5 positive allosteric modulator.
价 格：￥电议型 号：T23514产 地：中国大陆
-
T23154Piclamilast；吡拉米司特RPR 73401|||RP 73401；RPR 73401|||RP 73401|||吡拉米司特
Piclamilast (RP 73401) is a PDE4 inhibitor.
价 格：￥电议型 号：T23154产 地：中国大陆
-
T23131PE 154；化合物PE 154PE 154
PE 154 is a potent fluorescent inhibitor of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) with IC50s of 280 pM and 16 nM respectively. PE 154 is commonly used to label β-amyloid plaques in histochemical analysis.
价 格：￥电议型 号：T23131产 地：中国大陆
-
T22994ML 154；化合物ML 154ML 154
ML 154 is a potent neuropeptide S receptor (NPSR) antagonist.
价 格：￥电议型 号：T22994产 地：中国大陆
-
-
T22801GNE-617 hydrochloride (1362154-70-8 free base)；化合物 T22801GNE-617 hydrochloride；GNE-617 hydrochloride
GNE-617 hydrochloride is a potent and competitive inhibitor of nicotinamide phosphoribosyltransferase (IC50: 5nM). GNE-617 hydrochloride reduces the NAD levels in a > 95% reduction in both NAPRT1-deficient and NAPRT1-proficient cell lines and exerts (EC50: 0.54nM to 4.69nM).
价 格：￥电议型 号：T22801产 地：中国大陆
-
-
T22633CCT251545 analogue, Compound 51；化合物 T22633CCT251545 analogue, Compound 51
CCT251545 analog is a potent and selective CDK8/19 inhibitor (IC50: 5.1 nM and 5.6 nM, respectively). Mediator complex-associated kinases CDK8 and CDK19 are involved in the regulation of multiple transcription pathways. CDK8 plays as an oncogene in gastric and colorectal cancers through the activation of WNT signaling.
价 格：￥电议型 号：T22633产 地：中国大陆
-
T22154SR 2595；化合物 T22154SR 2595
SR2595 is an inverse agonist of nuclear receptor PPARγ with an IC 50 of 30 nM [1].
价 格：￥电议型 号：T22154产 地：中国大陆
