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：3878819
自主品牌
已选条件
-
T25302Deltakephalin；化合物 T25302DTLET|||Enkephalin leu, thr(2)-thr(6)-；DTLET|||Enkephalin leu, thr(2)-thr(6)
Deltakephalin is a synthetic, potent specific opiate delta receptors agonist.
价 格：￥电议型 号：T25302产 地：中国大陆
-
T24850Takeda103A；化合物Takeda103ACMPD103A|||Takeda-103A|||Takeda-103-A|||CMPD-103A|||Takeda 103 A；CMPD103A|||
Takeda103A (CMPD103A) is the GRK2-dependent bovine tubulin oxidation effective inhibitor.
价 格：￥电议型 号：T24850产 地：中国大陆
-
T2404Vonoprazan fumarate；富马酸沃诺拉赞TAK-438；富马酸沃诺拉赞|||TAK-438
Vonoprazan fumarate (TAK-438) is a novel P-CAB (potassium-competitive acid blocker) that reversibly inhibits H+/K+, ATPase.
价 格：￥电议型 号：T2404产 地：中国大陆
-
T2351LTAK-875 Hemihydrate；化合物TAK-875 HemihydrateTAK-875|||Fasiglifam；TAK-875|||Fasiglifam
TAK-875 Hemihydrate (Fasiglifam) is a selective GPR40 agonist with EC50 of 14 nM, 400-fold more potent than oleic acid.
价 格：￥电议型 号：T2351L产 地：中国大陆
-
T2351Fasiglifam；化合物TAK875TAK875；TAK875
Fasiglifam (TAK875) is a potent, selective and orally bioavailable GPR40 agonist.
价 格：￥电议型 号：T2351产 地：中国大陆
-
-
T22436Takeda-6d；化合物Takeda-6dTakeda-6d
Takeda-6d is a novel, potent DFG-out RAF/vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor with IC50 of 7.0 nM and 2.2 nM, respectively.
价 格：￥电议型 号：T22436产 地：中国大陆
-
T21417Dihydrotachysterol；双氢速甾醇Hytakerol|||HSDB-3314|||HSDB3314|||Parterol|||HSDB 3314；Hytakerol|||HSDB-331
Dihydrotachysterol (DHT) is a biologically active synthetic analog of vitamin D. It promotes intestinal absorption of active calcium and phosphate . It is also beneficial in the treatment of hypoparathyroidism.
价 格：￥电议型 号：T21417产 地：中国大陆
-
T21254Vonoprazan Fumarate；富马酸沃诺拉赞TAK-438|||TAK 438|||Vonoprazan Fumurate|||TAK438；TAK-438|||TAK 438|||Vono
Vonoprazan Fumarate (TAK438) , a novel potassium-competitive acid blocker, inhibits gastric acid secretion. Vonoprazan Fumarate (TAK438) inhibited H+,K+-ATPase activity in porcine gastric microsomes with IC50 value of 19 nM at pH 6.5.
价 格：￥电议型 号：T21254产 地：中国大陆
-
T21062TAK-659；化合物 T21062TAK 659|||TAK659；TAK 659|||TAK659
TAK-659 is a spleen tyrosine kinase (SYK) inhibitor.
价 格：￥电议型 号：T21062产 地：中国大陆
-
-
T1838Sapanisertib；沙帕色替TAK-228|||MLN0128|||INK 128；沙帕色替|||TAK-228|||MLN0128|||INK 128
Sapanisertib (INK 128) is an orally bioavailable inhibitor of raptor-mTOR (TOR complex 1 or TORC1) and rictor-mTOR (TOR complex 2 or TORC2) with potential antineoplastic activity.
价 格：￥电议型 号：T1838产 地：中国大陆
-
T1745Balipodect；化合物TAK-063TAK063|||TAK-063|||TAK 063；TAK063|||TAK-063|||TAK 063
Balipodect (TAK063) is a highly effective and selective PDE10A inhibitor (IC50: 0.30 nM); Its selectivity is >15000-fold over other PDEs.
价 格：￥电议型 号：T1745产 地：中国大陆
-
T17289ZED-1227；化合物ZED-1227ZED-101|||TAK-227；ZED-101|||TAK-227
ZED-1227 (TAK-227) is an orally active, selective and potent transglutaminase 2 (TG2) inhibitor with anticancer activity that blocks inflammation-induced TG2 expression and activation for the treatment of Celiac Disease.
价 格：￥电议型 号：T17289产 地：中国大陆
-
T16976TAK-915；化合物 T16976TAK-915
TAK-915 is a potent, selective, and brain-penetrant phosphodiesterase 2A (PDE2A) inhibitor (IC50: 0.61 nM). TAK-915 is >4100-fold more selectivity for PDE2A than PDE1A.
价 格：￥电议型 号：T16976产 地：中国大陆
-
T16975TAK-593；化合物TAK-593TAK-593
TAK-593 is an effective VEGFR and PDGFR family inhibitor (IC50s: 3.2, 0.95, 1.1, 4.3, and 13 nM for VEGFR1, VEGFR2, VEGFR3, PDFGRα, and PDFGRβ, respectively).
价 格：￥电议型 号：T16975产 地：中国大陆
-
T16974TAK-243；化合物TAK-243MLN7243；MLN7243
TAK-243 (MLN7243) is a selective inhibitor of the ubiquitin-activating enzyme UAE (IC50=1 nM). TAK-243 blocks ubiquitin binding and disrupts mono-ubiquitin signaling as well as overall protein ubiquitination. TAK-243 exhibits antitumor activity and promotes apoptosis.
价 格：￥电议型 号：T16974产 地：中国大陆
-
T16973TAK-220；化合物 T16973TAK-220
TAK-220 is a selective and orally bioavailable CCR5 antagonist (IC50s: 3.5 nM and 1.4 nM for inhibition on the binding of RANTES and MIP-1α to CCR5, respectively).
价 格：￥电议型 号：T16973产 地：中国大陆
-
T15709Lapaquistat acetate；化合物 T15709TAK-475；TAK-475
Lapaquistat acetate is a squalene synthase inhibitor. It also blocks the conversion of farnesyl diphosphate (FPP) to squalene. Lapaquistat acetate is used to Mevalonate Kinase Deficiency (MKD), it is effective at lowering low-density lipoprotein cholesterol, but it might cause liver damage.
价 格：￥电议型 号：T15709产 地：中国大陆
-
T15567Imiglitazar；伊格列扎TAK-559；TAK-559
Imiglitazar (TAK559) is a potent PPAR-β/δ receptor agonist with hypoglycemic effects.
价 格：￥电议型 号：T15567产 地：中国大陆
