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：3547190
自主品牌
已选条件
-
T10783CGS 15435CGS 15435
CGS 15435 is a potent inhibitor of thromboxane (TxA2) synthetase (IC50: 1 nM). It has a selectivity for Tx synthetase 100000-fold greater than that for PGI2 synthetase, cyclooxygenase, and lipoxygenase enzymes.
价 格：￥电议型 号：T10783产 地：中国大陆
-
T7197Fadrozole(Rac)-FAD286,inhibit,Fadrozole,CGS 16949A,Inhibitor,Aromatase
Fadrozole is a nonsteroidal aromatase inhibitor with potential antineoplastic activity(IC50 : 6.4 nM)
价 格：￥电议型 号：T7197产 地：中国大陆
-
T6441CGS 21680 HydrochlorideCGS-21680,Inhibitor,CGS 21680,inhibit,CGS21680,CGS 21680 Hydrochloride,Adenos
CGS 21680 HCl（ IC50=22 nM）, an adenosine receptor agonist, exhibits 140-fold potency in A2 receptor over A1 receptor.
价 格：￥电议型 号：T6441产 地：中国大陆
-
T3472CGS 27023A
CGS 27023A is a non-peptidic, potent, and orally active stromelysin inhibitor.
价 格：￥电议型 号：T3472产 地：中国大陆
-
T22654Selfotel塞福太；CGS 19755；LY-272541
CGS 19755 is a selective, competitive NMDA antagonist that inhibits [3H]-3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid binding to NMDA-type receptors with IC50 of 50 nM.
价 格：￥电议型 号：T22654产 地：中国大陆
-
T14944CGS 15943
CGS 15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor. In transfected CHO cells, its Ki for human A1, A2A, A2B, and A3 Adenosine Receptors are 3.5, 4.2, 16, and 50 nM , respectively.
价 格：￥电议型 号：T14944产 地：中国大陆
-
T12405PentiapineCGS 10746
Pentiapine is a novel inhibitor of dopamine release.
价 格：￥电议型 号：T12405产 地：中国大陆
-
T0180Benazepril hydrochloride盐酸贝那普利；CGS14824A；Benazepril HCl；CGS 14824A HCl
Benazepril is an angiotensin-converting enzyme (ACE) inhibitor widely used in the therapy of hypertension. Benazepril is associated with a low rate of transient serum aminotransferase elevations and has been linked to rare instances of acute liver injury.
价 格：￥电议型 号：T0180产 地：中国大陆
-
T0180Benazepril hydrochlorideBenazepril hydrochloride,CGS14824A,Benazepril HCl
Benazepril is an angiotensin-converting enzyme (ACE) inhibitor widely used in the therapy of hypertension. Benazepril is associated with a low rate of transient serum aminotransferase elevations and has been linked to rare instances of acute liver injury.
价 格：￥电议型 号：T0180产 地：美洲
-
T12405PentiapinePentiapine,CGS 10746,
Pentiapine is a novel inhibitor of dopamine release.
价 格：￥电议型 号：T12405产 地：美洲
-
T14944CGS 15943CGS 15943
CGS 15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor. In transfected CHO cells, its Ki for human A1, A2A, A2B, and A3 Adenosine Receptors are 3.5, 4.2, 16, and 50 nM , respectively.
价 格：￥电议型 号：T14944产 地：美洲
-
T15803LY223982LY223982,CGS23131,SKF107324
LY223982 is an effective and specific inhibitor of the leukotriene B4 receptor (IC50: 13.2 nM). It also can against [3H]LTB4 binding to LTB4 receptor.
价 格：￥电议型 号：T15803产 地：美洲
-
T6441CGS 21680 HClCGS 21680 HCl,CGS 21680 Hydrochloride,
CGS 21680 HCl（ IC50=22 nM），an adenosine receptor agonist, exhibits 140-fold potency in A2 receptor over A1 receptor.
价 格：￥电议型 号：T6441产 地：美洲
-
T7556Fadrozole hydrochloride；盐酸法倔唑CGS 16949A；CGS 16949A|||盐酸法倔唑
Fadrozole hydrochloride (CGS 16949A) is a model aromatase inhibitor that has been shown to suppress estrogen production in the ovaries of fish.
价 格：￥电议型 号：T7556产 地：中国大陆
-
T7197LFadrozole HCl hydrate；化合物 T7197LFadrozole|||CGS-16949A|||Fadrozole hydrochloride hemihydrate|||CGS16
Fadrozole is a selective inhibitor of aromatase. It also effective in the treatment of estrogen-dependent diseases including breast cancer.
价 格：￥电议型 号：T7197L产 地：中国大陆
-
T71637Cgs 18102A (HCl)；化合物 Cgs 18102A (HCl)Cgs 18102A (HCl)
Cgs 18102A (HCl) has 5-HT(1) agonist & 5-HT(2) antagonist properties.
价 格：￥电议型 号：T71637产 地：中国大陆
-
T71545Cgs 15696；化合物 Cgs 15696Cgs 15696
Cgs 15696 is an adenosine antagonist.
价 格：￥电议型 号：T71545产 地：中国大陆
-
T71410Cgs 18320B；化合物 Cgs 18320BCgs 18320B
Cgs 18320B is a non-steroidal aromatase inhibitor
价 格：￥电议型 号：T71410产 地：中国大陆
-
T71345Cgs 21197；化合物 Cgs 21197Cgs 21197
Cgs 21197 is an adenosine A2 receptor antagonist.
价 格：￥电议型 号：T71345产 地：中国大陆
-
T71221CGS 21595；化合物 CGS 21595CGS 21595
CGS 21595 inhibits the formation of 5-hydroxyeicosatetraenoic acid and leukotriene B4; rapidly metabolized to CGS 19213.
价 格：￥电议型 号：T71221产 地：中国大陆
