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：3878895
自主品牌
已选条件
-
T11176Eliglustat hemitartrate；依利格鲁司特酒石酸盐Genz-112638|||Eliglustat tartrate；Genz-112638|||依利格鲁司特酒石酸盐|||Eligl
Eliglustat hemitartrate (Genz-112638) , with an IC50 of 24 nM, is a specific, potent, oral active glucocerebral glycosidase inhibitor.
价 格：￥电议型 号：T11176产 地：中国大陆
-
T11129LDuvelisib (R enantiomer) hydrochloride；杜韦利西布R对映体盐酸盐IPI-145 R enantiomer HCl|||Duvelisib (R enantiome
Duvelisib (R enantiomer) hydrochloride (INK1197 R enantiomer HCl) is a PI3K inhibitor. Duvelisib (R enantiomer) hydrochloride is the less active enantiomer of Duvelisib.
价 格：￥电议型 号：T11129L产 地：中国大陆
-
T11129Duvelisib (R enantiomer)化合物Duvelisib R entiomerDuvelisib R enantiomer|||IPI-145 R enantiomer|||INK11
Duvelisib R enantiomer (IPI-145 R enantiomer) is an enantiomer of Duvelisib with lower activity. Duvelisib is a PI3K inhibitor.
价 格：￥电议型 号：T11129产 地：中国大陆
-
T11128Dutogliptin；化合物 T11128PHX-1149 free base；PHX-1149 free base
Dutogliptin (PHX-1149 free base) is an oral, effective and selective dipeptide-peptide-4 (DPP4) inhibitor for the treatment of type 2 diabetes mellitus.
价 格：￥电议型 号：T11128产 地：中国大陆
-
T11127Dutogliptin tartrate；化合物 T11127PHX-1149；PHX-1149
Dutogliptin tartrate is an effective and selective oral dipeptide-peptide-4 (DPP4) inhibitor for the treatment of type 2 diabetes mellitus.
价 格：￥电议型 号：T11127产 地：中国大陆
-
T11126Durvalumab；度伐利尤单抗MEDI 4736；MEDI 4736
Durvalumab (MEDI 4736) is a humanized monoclonal antibody targeting PD-L1. It can block the interaction of PD-L1 with PD-1 and CD80, with IC50 values of 0.1 and 0.04 nM, respectively. Durvalumab is often used in combination with platinum-based compounds for the treatment of non-small cell lung cancer and advanced hepatocellular carcinoma cells.
价 格：￥电议型 号：T11126产 地：中国大陆
-
T11125Durlobactam sodium salt；化合物Durlobactam钠盐ETX2514 sodium salt；杜巴坦|||ETX2514 sodium salt|||杜洛巴坦
Durlobactam sodium salt (ETX2514 sodium salt) is an inhibitor of β-lactamase with IC50 values of 4 nM, 14 nM, and 190 nM for Class A KPC-2, Class C AmpC, and Class D OXA-24, respectively. Durlobactam sodium salt can be used in studies about drug-resistant Gram-negative bacteria including Acinetobacter baumannii.
价 格：￥电议型 号：T11125产 地：中国大陆
-
T11124Duramycin；化合物 T11124Lancovutide|||Moli1901；Lancovutide|||Moli1901
Duramycin is a cyclic peptide lantibiotic derived from Streptomyces cinnamoneuma. Duramycin interacts with phosphatidylethanolamine (PE) and has antibacterial, antiviral effects. Duramycin stimulates chloride secretion in airway epithelium and has the potential for cystic fibrosis treatment.
价 格：￥电议型 号：T11124产 地：中国大陆
-
T11123DuP 105；化合物DuP 105DuP 105
DuP 105 is an oral oxazolidinone, a novel synthetic antimicrobial compound effective against gram-positive bacteria.
价 格：￥电议型 号：T11123产 地：中国大陆
-
T11122DUPA(OtBu)-OH化合物DUPA(OtBu)-OH(S)-5-叔丁氧基-4-(3-((S)-1,5-二-叔丁氧基-1,5-二氧代-2-戊基)脲啶)-5-氧代戊酸
DUPA(OtBu)-OH is a DUPA precursor. DUPA is used as the targeting moiety to actively deliver Docetaxel (DTX) for treatment of Prostate-Specific Membrane Antigen (PSMA) expressing prostate cancer. PSMA has a high affinity for DUPA(Ki = 8 nM).
价 格：￥电议型 号：T11122产 地：中国大陆
-
T11121Duoperone；度奥哌隆Duoperone
Duoperone is a neuroleptic agent. Duoperone shows antiemetic activity in animal models.
价 格：￥电议型 号：T11121产 地：中国大陆
-
T11120Duocarmycin TM；化合物Duocarmycin TMDuocarmycin TM
Duocarmycin TM is a DNA alkylator. Duocarmycin TM is an exceptionally potent antitumor antibiotic.
价 格：￥电议型 号：T11120产 地：中国大陆
-
T11122-(Hydroxymethyl)pyridine吡啶甲醇吡啶甲醇|||Piconol
2-(Hydroxymethyl)pyridine (Piconol) is used as an organic synthesis and medicinal chemistry intermediate for the synthesis of the stimulant laxative bisacodyl, and as a pyridinol with hypoglycemic activity.
价 格：￥电议型 号：T1112产 地：中国大陆
-
T11112DUB-IN-3；化合物DUB-IN-3DUB-IN-3
DUB-IN-3 is a potent deubiquitinase (USP) enzyme inhibitor and the IC50 for USP8 is 0.56 μM.
价 格：￥电议型 号：T11112产 地：中国大陆
-
T10965DBPR112；化合物DBPR112DBPR112
DBPR112 is an orally active furanopyrimidine-based EGFR inhibitor with IC50s of 15 nM and 48 nM for EGFRWT and EGFRL858R/T790M, respectively. DBPR112 can occupy the ATP-binding site. DBPR112 has significant antitumor efficacy.
价 格：￥电议型 号：T10965产 地：中国大陆
-
T10495LBefiradol化合物 T10495LNLX-112|||F13640
Befiradol (NLX-112) is an agonist of 5-HT1A receptor.
价 格：￥电议型 号：T10495L产 地：中国大陆
-
T1044Clopidol；氯羟吡啶WR-61112；氯吡多|||氯羟吡啶|||WR-61112
Clopidol (WR-61112) is a very effective anticoccidial agent used in poultry.
价 格：￥电议型 号：T1044产 地：中国大陆
-
T10387ASP1126；化合物 T10387ASP1126
ASP1126 is a selective and orally active sphingosine-1-phosphate (S1P) agonist (EC50s: 7.12 nM, 517 nM for hS1P1 and hS1P3).
价 格：￥电议型 号：T10387产 地：中国大陆
-
T10203A 1120；化合物A 1120A 1120
A 1120 is a nonretinoid retinol-binding protein 4 (RBP4) antagonist (Ki: 8.3 nM), which disrupts the interaction between RBP4 and its binding partner transthyretin.
价 格：￥电议型 号：T10203产 地：中国大陆
-
T101123-Hydroxy-4-methoxyacetophenone异香草乙酮Acetoisovanillone|||4-甲氧基-3-羟基苯乙酮|||异香草乙酮
3-Hydroxy-4-methoxyacetophenone (Acetoisovanillone) is an active P. spinosa extract. It possesses anti-inflammatory activity and prevented injuries due to administration of acetic acid in the colon.
价 格：￥电议型 号：T10112产 地：中国大陆
