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：3795958
自主品牌
已选条件
-
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
-
T11119Duocarmycin DM free base；化合物 T11119Duocarmycin；Duocarmycin
Duocarmycin is a DNA minor groove binding alkylating agent and explored as drug–antibody conjugates (ADCs) . Duocarmycin is based on its characteristic curved indole structure and a spirocyclopropylcyclohexadienone electrophile to act anticancer activity.
价 格：￥电议型 号：T11119产 地：中国大陆
-
T11118Duocarmycin SA；化合物 T11118Duocarmycin SA
Duocarmycin SA is an extremely potent cytotoxic agent and antitumor antibiotic that induces sequence-selective alkylation of duplex DNA, with an IC50 of 10 pM. It demonstrates synergistic cytotoxicity against glioblastoma multiforme (GBM) cells when combined with proton radiation in vitro.
价 格：￥电议型 号：T11118产 地：中国大陆
-
T11117Duocarmycin MB；倍癌霉素 MBDuocarmycin MB
Duocarmycin MB can be used against multi-drug resistant cell lines. Duocarmycin MB is an antibody drug conjugates (ADCs) toxin. Duocarmycin is a DNA alkylating agent that binds in the minor groove.
价 格：￥电议型 号：T11117产 地：中国大陆
-
T11116Duocarmycin MA；倍癌霉素 MADuocarmycin MA
Duocarmycin MA can be used against multi-drug resistant cell lines.Duocarmycin MA is an antibody drug conjugates (ADCs) toxin. Duocarmycin is a DNA alkylating agent that binds in the minor groove.
价 格：￥电议型 号：T11116产 地：中国大陆
-
T11115Duocarmycin GA；倍癌霉素 GADuocarmycin GA
Duocarmycin GA, an antibody drug conjugate (ADC) toxin and a DNA alkylating agent, effectively targets and binds in the minor groove of DNA. It is particularly potent against multi-drug resistant cell lines, offering a strategic approach in combating resistance.
价 格：￥电议型 号：T11115产 地：中国大陆
-
T11114Duloxetine metabolite Para-Naphthol Duloxetine；度洛西汀代谢物Para-Naphthol duloxetine；度洛西汀代谢物|||Para-Naphth
Para-Naphthol Duloxetine is a serotonin-norepinephrine reuptake inhibitor (SNRI),is a metabolite of Duloxetine.
价 格：￥电议型 号：T11114产 地：中国大陆
-
T11113Duloxetine D3 hydrochloride；化合物 T11113(S)-Duloxetine D3 hydrochloride|||LY248686 D3 hydrochloride；(S
Duloxetine D3 hydrochloride is a serotonin-norepinephrine reuptake inhibitor (SNRI) with a Ki of 4.6 nM, used for treatment of major depressive disorder and generalized anxiety disorder (GAD).Duloxetine D3 hydrochloride ((S)-Duloxetine D3 hydrochloride) is a deuterium labeled Duloxetine hydrochloride.
价 格：￥电议型 号：T11113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
-
T11111DUB-IN-2；化合物DUB-IN-2DUB-IN-2
Dub-in-2, with an IC50 value of 0.28 for USP8, is an effective deubiquitinase inhibitor.
价 格：￥电议型 号：T11111产 地：中国大陆
-
T11110DUB-IN-1；化合物DUB-IN-1DUB-IN-1
DUB-IN-1, with an IC50 value of 0.24 for USP8, is an active inhibitor of ubiquitin-specific protease (USPs).
价 格：￥电议型 号：T11110产 地：中国大陆
-
T1111Pralidoxime Chloride吡啶醛肟甲氯2-PAM chloride|||吡啶醛肟甲氯|||2-Pyridinealdoxime methochloride|||2-PAM (chlori
Pralidoxime Chloride (2-PAM chloride) is a useful agent in the treatment of organophosphate poisoning. Pralidoxime binds to organophosphate-inactivated acetylcholinesterase, used to combat poisoning by organophosphates or acetylcholinesterase inhibitors (nerve agents).
价 格：￥电议型 号：T1111产 地：中国大陆
-
-
T11108DSR-6434；化合物DSR-6434DSR-6434
DSR-6434 is a selective agonist of TLR7 with antitumor effect. DSR-6434 exhibits EC50s of 7.2 nM and 4.6 nM for human and mouse.
价 格：￥电议型 号：T11108产 地：中国大陆
-
T11107DSP-1053；化合物 T11107DSP-1053
Dsp-1053 is a powerful SERT (Ki=1.02 nM) inhibitor with partial 5-HT1A receptor (Ki=5.05 nM) agonizing activity.
价 格：￥电议型 号：T11107产 地：中国大陆
-
T11105DS88790512；化合物 T11105DS88790512
DS88790512, IC50 at 11 nM, is an effective, selective, oral bioeffective TRPC6 inhibitor.
价 格：￥电议型 号：T11105产 地：中国大陆
-
T11104DS21360717；化合物 T11104DS21360717
DS21360717 is an effective oral tyrosine kinase inhibitor with anticancer activity and IC50 of 0.49 nM.
价 格：￥电议型 号：T11104产 地：中国大陆
-
T11103DS18561882；化合物 DS18561882DS18561882
DS18561882 is an orally available, selective and potent inhibitor of methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) with antitumor activity, inhibits MTHFD1 activity and can be used in the study of breast cancer.
价 格：￥电议型 号：T11103产 地：中国大陆
-
T11101DS08210767；化合物DS08210767DS08210767
DS08210767 is a highly potent, orally bioavailable PTHR1 antagonist with IC50 of 90 nM.
价 格：￥电议型 号：T11101产 地：中国大陆
