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：3308851
自主品牌
已选条件
-
T15168DRF-1042；化合物 DRF-1042DRF-1042
DRF-1042 is an orally active camptothecin analog with antitumor activity and inhibits DNA topoisomerase I. It is used in the study of refractory tumors.
价 格：￥电议型 号：T15168产 地：中国大陆
-
T15167Draflazine；化合物 T15167R-75231；R-75231
Draflazine is an ENT1 inhibitor. It completely reverses the hypersensitivity in the complete Freund’s adjuvant (CFA) model of mechanical hyperalgesia. Draflazine also completely reverses the hypersensitivity of the carrageenan inflammation model of thermal and mechanical hyperalgesia.
价 格：￥电议型 号：T15167产 地：中国大陆
-
T15166DPM-1001；化合物 T15166DPM-1001
DPM-1001 is an orally bioavailable and non-competitive protein-tyrosine phosphatase (PTP1B) inhibitor (IC50: 100 nM) with the anti-diabetic property.
价 格：￥电议型 号：T15166产 地：中国大陆
-
T15165DPI-3290；化合物 T15165Org 41793；Org 41793
DPI-3290 is a specific agonist of opioid receptors (Ki: 0.18 nM, 0.46 nM, and 0.62 nM for δ-, μ-, and κ-opioid receptors, respectively) with potent antinociceptive activity. DPI-3290 is one of a series of novel centrally acting agents.
价 格：￥电议型 号：T15165产 地：中国大陆
-
T15164DPH；化合物DPHDPH
DPH is a potent cell permeable activator of c-Abl. It shows potent enzymatic and cellular activity in stimulating c-Abl activation.
价 格：￥电议型 号：T15164产 地：中国大陆
-
T15163DPC-681；化合物 T15163DPH-153893；DPH-153893
DPC-681 is a potent and selective HIV protease inhibitor (IC90s: 4 to 40 nM for wild-type HIV-1).
价 格：￥电议型 号：T15163产 地：中国大陆
-
T15162DPA-714；化合物DPA-714DPA-714
DPA-714 is a high affinity translocator protein (TSPO) ligand (Ki=7 nM). It is designed with a fluorine atom in its structure, allowing labelling with fluorine -18 and in vivo imaging using positron emission tomography. [18F]DPA-714 successfully assesses for the specific imaging of inflammation in various models of neuroinflammation and in a brain tumor model.
价 格：￥电议型 号：T15162产 地：中国大陆
-
T15161Doxorubicin-SMCC；化合物 T15161Doxorubicin-SMCC
Doxorubicin-SMCC is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15161产 地：中国大陆
-
T15160Dotinurad；化合物Dotinurad(3,5-dichloro-4-hydroxyphenyl)(1,1-dioxidobenzo[d]thiazol-3(2H)-yl)methanone；(
Dotinurad ((3,5-dichloro-4-hydroxyphenyl)(1,1-dioxidobenzo[d]thiazol-3(2H)-yl)methanone) is a potent agent of uricosuric (IC50: 3.6 μM for uric acid).
价 格：￥电议型 号：T15160产 地：中国大陆
-
T1516Curcumin；姜黄素Diferuloylmethane|||Natural Yellow 3|||Indian Saffron|||Turmeric yellow；Diferuloylmethan
Curcumin (Natural Yellow 3) is a phenolic natural product, an inhibitor of histone acetyltransferase p300/CREB (IC50=25 μM) with specificity. Curcumin has a wide range of pharmacological activities such as antitumor, anti-inflammatory and antioxidant.
价 格：￥电议型 号：T1516产 地：中国大陆
-
T15159Dorzagliatin化合物DorzagliatinHMS5552
Dorzagliatin (HMS5552) is a dual-acting glucokinase (GK) activator. It also improves glycaemic control and pancreatic β-cell function in type 2 diabetes.
价 格：￥电议型 号：T15159产 地：中国大陆
-
T15158Dolastatin 15；化合物 T15158DLS 15；DLS 15
Dolastatin 15, a depsipeptide derived from Dolabella auricularia, is a potent antimitotic agent structurally related to the anti-tubulin agent Dolastatin 10. Dolastatin 15 can be used as an ADC cytotoxin and it induces cell cycle arrest and apoptosis in multiple myeloma cells.
价 格：￥电议型 号：T15158产 地：中国大陆
-
T15157Dodecanoylcarnitine；月桂酰肉碱Lauroylcarnitine；Lauroylcarnitine
Dodecanoylcarnitine ((-)-Lauroylcarnitine) has been associated with disturbances in fatty acid oxidation, and the use of Dodecanoylcarnitine resulted in an increase in the permeability of salmon calcitonin.
价 格：￥电议型 号：T15157产 地：中国大陆
-
T15156Dodecaethylene glycol；化合物 T15156HO-PEG12-OH；HO-PEG12-OH
Dodecaethylene glycol is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15156产 地：中国大陆
-
T15155Docebenone；化合物 T15155AA 861；AA 861
Docebenone is a selective and orally active inhibitor of 5-LO.
价 格：￥电议型 号：T15155产 地：中国大陆
-
T15154DNP-PEG4-NHS ester；化合物 T15154DNP-PEG4-NHS ester
DNP-PEG4-NHS ester is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15154产 地：中国大陆
-
T15153DNP-PEG4-alcohol；化合物 T15153DNP-PEG4-alcohol
DNP-PEG4-alcohol is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15153产 地：中国大陆
-
T15152DNP-PEG4-acid；化合物 T15152DNP-PEG4-acid
DNP-PEG4-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15152产 地：中国大陆
-
T15151DNP-PEG3-DNP；化合物 T15151DNP-PEG3-DNP
DNP-PEG3-DNP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15151产 地：中国大陆
-
T15150DNP-PEG3-azide；化合物 T15150DNP-PEG3-azide
DNP-PEG3-azide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15150产 地：中国大陆
