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：3436564
自主品牌
已选条件
-
T6819Desogestrel；去氧孕烯Org-2969|||Desogen|||Desogestrelum|||Cerazette；Org-2969|||去氧孕烯|||Desogen|||Desogestr
Desogestrel (Cerazette) is a synthetic progestational hormone used often as the progestogenic component of combined oral contraceptive agents.
价 格：￥电议型 号：T6819产 地：中国大陆
-
T64812Collagenase Type I胶原酶ICollagenase I|||Collagenase Type I (From microorganisms)
Collagenase Type I is a proteolytic enzyme that breaks down the peptide bonds in collagen, the main structural protein of connective tissue. Collagenase has been explored as a potential treatment option to break down herniated disc material, thereby reducing pressure on nearby nerves. Collagenase may aid in the breakdown and reorganization of excessive scar tissue, potentially improving tissue function and appearance. Collagenase has the potential to treat disc herniation, keloid, cellulite, lip
价 格：￥电议型 号：T64812产 地：中国大陆
-
T63572Org 43553；化合物 Org 43553Org 43553
Org 43553 is an orally active low molecular weight (LMW) luteinizing hormone receptor (LH-R) agonist capable of agonizing human LH (EC50: 3.7 nM) and FSH receptors (EC50: 110 nM).Org 43553 can be used for endocrine studies.
价 格：￥电议型 号：T63572产 地：中国大陆
-
T5S1054Wilforgine雷公藤精碱雷公藤晋碱|||雷公藤精碱
1. Wilforgine exhibits insecticidal activity of some degree.
价 格：￥电议型 号：T5S1054产 地：中国大陆
-
T5420LCycloguanil；环氯胍Cycloguanyl|||Chlorguanide triazine；Cycloguanyl|||Chlorguanide triazine|||环氯胍
Cycloguanil is an antimalarial.
价 格：￥电议型 号：T5420L产 地：中国大陆
-
T5326LSugammadex化合物 T5326LOrg-25969|||Org25969|||Org 25969|||361LPM2T56
Sugammadex is an agent for reversal of neuromuscular blockade by the agent rocuronium in general anaesthesia. It is the first selective relaxant binding agent (SRBA). Sugammadex is a modified γ-cyclodextrin, with a lipophilic core and a hydrophilic periphery. This gamma cyclodextrin has been modified from its natural state by placing eight carboxyl thio ether groups at the sixth carbon positions. These extensions extend the cavity size allowing greater encapsulation of the rocuronium molecule. T
价 格：￥电议型 号：T5326L产 地：中国大陆
-
T5326Sugammadex sodium；舒更葡糖钠Org25969|||Sugammadex (sodium)；Org25969|||Sugammadex (sodium)|||舒更葡糖钠
Sugammadex sodium (Org25969) , a synthetic derivative of γ-cyclodextrin, is a steroid-based neuromuscular blocker reversing agent.
价 格：￥电议型 号：T5326产 地：中国大陆
-
T50082Org 25543；化合物Org 25543Org 25543
Org 25543 is the development of an N-Acyl amino acid that selectively inhibits the glycine transporter 2 to produce analgesia in a rat model of chronic pain.
价 格：￥电议型 号：T50082产 地：中国大陆
-
T4408Elafibranor；化合物ElafibranorGFT505；GFT505
Elafibranor (GFT505) is an agonist of the peroxisome proliferator-activated receptor-α (PPAR-α) and peroxisome proliferator-activated receptor-δ (PPAR-δ) with EC50 values of 45 and 175 nM, respectively.
价 格：￥电议型 号：T4408产 地：中国大陆
-
T4382Proguanil hydrochloride；盐酸氯胍Paludrine hydrochloride|||Chlorguanide hydrochloride|||Chloroquanil；Palu
Proguanil hydrochloride (Chloroquanil) is a biguanide compound which metabolizes in the body to form cycloguanil, an anti-malaria agent.Upon hydrolysis, Proguanil hydrochloride is converted to its active cyclic triazine metabolite, cycloguanil, by a cytochrome P450 dependent reaction. Cycloguanil selectively inhibits the bifunctional dihydrofolate reductase-thymidylate synthase of plasmodium parasite, thereby disrupting deoxythymidylate synthesis and ultimately blocking DNA and protein synthesis
价 格：￥电议型 号：T4382产 地：中国大陆
-
T40469(+)-N-Formylnorglaucine；醛基去甲海罂粟碱；醛基去甲海碱(+)-N-Formylnorglaucine
(+)-N-Formylnorglaucine, an aporphine alkaloid found in the leaves of Unonopsis stipitata, features a formyl group that is connected to the nitrogen within its heterocyclic structure.
价 格：￥电议型 号：T40469产 地：中国大陆
-
T39633Navocaftor；NavocaftorGLPG 3067|||ABBV-3067；GLPG 3067|||ABBV-3067
Navocaftor, as a cystic fibrosis transmembrane regulator ( CFTR ), is a protein modulator (US 20200377491 Al, example 1).
价 格：￥电议型 号：T39633产 地：中国大陆
-
T3957Farampator；化合物FarampatorOrg24448|||CX-691；Org24448|||CX-691
Farampator (CX-691) (CX-691;Org24448) is a positive modulator of AMPA receptor.
价 格：￥电议型 号：T3957产 地：中国大陆
-
T37962Paeoniflorgenin；芍药苷元Paeoniflorgenin
Paeoniflorgenin is a deglucosylated metabolite of Paeoniflorin[1].
价 格：￥电议型 号：T37962产 地：中国大陆
-
T37700Org 24598 lithium salt；Org 24598 lithium saltOrg 24598 lithium salt
Org 24598 lithium salt is a GlyT-1 inhibitor of glycine transporter 1. Org 24598 lithium salt inhibits the specific binding of [3H]CHIBA-3007 to rat meninges (Ki=16.9 nM).
价 格：￥电议型 号：T37700产 地：中国大陆
-
T37699Org 24598；Org 24598Org 24598|||Org 24598；Org 24598|||Org 24598
Potent and selective inhibitor of the glial glycine transporter GlyT1b (IC50 = 6.9 nM). Displays negligible activity at GlyT-2, adrenoreceptors, dopamine, 5HT receptors and noradrenaline, dopamine, 5HT and GABA transporters (pIC50 in vivo.
价 格：￥电议型 号：T37699产 地：中国大陆
-
T376475α-dihydro Levonorgestrel；5α-dihydro Levonorgestrel5α-dihydro Levonorgestrel
5α-dihydro Levonorgestrel is a metabolite of the synthetic progestin levonorgestrel . It lacks in vitro and in vivo estrogenic activity, but induces copulatory behavior in male rats when administered at a dose of 1 mg per animal per day.
价 格：￥电议型 号：T37647产 地：中国大陆
-
T37577Glycogen Phosphorylase Inhibitor；Glycogen Phosphorylase InhibitorGlycogen Phosphorylase Inhibitor
Glycogen phosphorylase in the liver, muscle, and brain initiate glycogenolysis by releasing glucose-1-phosphate from glycogen. Glycogen phosphorylase inhibitor is a cell-permeable acyl urea first identified as an inhibitor of human liver glycogen phosphorylase (IC50 = 53 nM). It blocks glucagon-induced hepatic glycogenolysis in vivo. Glycogen phosphorylase inhibitor has been used to study glycogen utilization in human liver HepG2 cells, retinal explants, and human T lymphocyte Kit 225 cells.
价 格：￥电议型 号：T37577产 地：中国大陆
-
T37222GLS1 Inhibitor；GLS1 InhibitorGLS1 Inhibitor
GLS1 inhibitor is an inhibitor of glutaminase 1 (GLS1; IC50= 0.021 μM).1It inhibits the growth of NCI H1703 non-small cell lung cancer (NSCLC) cellsin vitro(GI50= 0.011 μM). GLS1 inhibitor (100 mg/kg) reduces tumor growth, increases tumor levels of glutamine, and decreases tumor levels of glutamate and aspartate in an NCI H1703 mouse xenograft model.
价 格：￥电议型 号：T37222产 地：中国大陆
-
T34328Rimexolone；化合物 T34328Rimexel|||Org-6216|||Vexol；Rimexel|||Org-6216|||Vexol
Rimexolone is a glucocorticoid steroid used to treat inflammation in the eye.
价 格：￥电议型 号：T34328产 地：中国大陆
