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：3521269
自主品牌
已选条件
-
T7336ICA-121431；化合物ICA-1214312,2-Diphenyl-N-[4-(thiazol-2-ylsulfamoyl；2,2-Diphenyl-N-[4-(thiazol-2-ylsulf
ICA-121431 (2,2-Diphenyl-N-[4-(thiazol-2-ylsulfamoyl) is a nanomolar potent small molecule Nav1.7 channel inhibitor with IC50 of 19 nM for rat Nav1.7, with little or no activity against human Nav1.5 or Nav1.7 channels.
价 格：￥电议型 号：T7336产 地：中国大陆
-
T73352,3-Diaminopropionic acid；L-2,3-二氨基丙酸L-2,3-Diaminopropionic acid；L-2,3-二氨基丙酸|||L-2,3-Diaminopropioni
2,3-Diaminopropionic acid (L-2,3-Diaminopropionic acid) is an amino acid that is a precursor of antibiotics and staphyloferrin B a siderophore produced by Staphylococcus aureus.
价 格：￥电议型 号：T7335产 地：中国大陆
-
T7292918:0-22:6 DG；化合物 18:0-22:6 DG1-Stearoyl-2-docosahexaenoyl-sn-glycerol；1-Stearoyl-2-docosahexaenoyl-s
1-Stearoyl-2-docosahexaenoyl-sn-glycerol (18:0-22:6 DG) is a diacylglycerol capable of binding to RasGRP and modulating the activation of MAP kinases.
价 格：￥电议型 号：T72929产 地：中国大陆
-
T71772Bicifadine free base；化合物 Bicifadine free baseCL-220075|||Bicifadine free base|||CL220075|||Bicifadin
Bicifadine, also known as DOV-220075, CL 220,075, is a SNDR inhibitor potentially for the treatment of lower back pain. Bicifadine has a non-opioid, non-NSAID mechanism for the treatment of pain, which should have less abuse potential than opioid drugs and less propensity to cause gastric ulcers than NSAID drugs. While the drug is purported to be a serotonin (SERT) and noradrenaline transporter (NET) inhibitor, it also has effects at the dopamine transporter (DAT), effectively making it a broad
价 格：￥电议型 号：T71772产 地：中国大陆
-
T71547MDL-25637；化合物 MDL-25637MDL-25637
MDL-25637 is a glucosidase inhibitor.
价 格：￥电议型 号：T71547产 地：中国大陆
-
T71505KAL-21404358；化合物 KAL-21404358KAL-21404358
KAL-21404358 is a Novel allosteric inhibitor of K-RasG12D, binding to the P110 site of K-RasG12D, impairing the K-RasG12D interaction with B-Raf, and disrupting the RAF-MEK-ERK and the PI3K-AKT signaling pathway.
价 格：￥电议型 号：T71505产 地：中国大陆
-
T71432MDL-27088；化合物 MDL-27088MDL-27088
MDL-27088 is an angiotensin-covering enzyme inhibitor.
价 格：￥电议型 号：T71432产 地：中国大陆
-
T71431MDL-27467A；化合物 MDL-27467AMDL-27467A
MDL-27467A is an ester derivative of a potent angiotensin converting enzyme inhibitor.
价 格：￥电议型 号：T71431产 地：中国大陆
-
T71430MDL-27210；化合物 MDL-27210MDL-27210
MDL-27210 is the ethyl ester prodrug of a potent angiotensin-converting enzyme inhibitor, MDL-27088.
价 格：￥电议型 号：T71430产 地：中国大陆
-
T71355MDL-27788；化合物 MDL-27788MDL-27788
MDL-27788 is a tricyclic inhibitor.
价 格：￥电议型 号：T71355产 地：中国大陆
-
T71140MDL-27048；化合物 MDL-27048MDL-27048
MDL-27048 is a powerful and reversible microtubule inhibitor.
价 格：￥电议型 号：T71140产 地：中国大陆
-
T71074MDL-29152；化合物 MDL-29152MDL-29152
MDL-29152 is a PKC specific inhibitor.
价 格：￥电议型 号：T71074产 地：中国大陆
-
T71039MDL-28753；化合物 MDL-28753MDL-28753
MDL-28753 is an antagonist of leukotriene D4 and antagonist of leukotrine C4.
价 格：￥电议型 号：T71039产 地：中国大陆
-
T71038MDL-28050；化合物 MDL-28050MDL-28050
MDL-28050 is a synthetic analog of hirudin 55-65 C-terminal fragment and a peptide inhibitor.
价 格：￥电议型 号：T71038产 地：中国大陆
-
T70850MDL-28133A；化合物 MDL-28133AMDL-28133A
MDL-28133A is a 5-HT2 receptor antagonist.
价 格：￥电议型 号：T70850产 地：中国大陆
-
T707578-Acetyl-2-(dipropylamino)tetralin；化合物 8-Acetyl-2-(dipropylamino)tetralin8-Acetyl-2-(dipropylamino)t
8-Acetyl-2-(dipropylamino)tetralin is a 5-HT(1A) receptor agonist; both isomers are active, but the (S)-isomer is the most potent.
价 格：￥电议型 号：T70757产 地：中国大陆
-
T69809NNL-2；化合物 NNL-2NNL-2
NNL-2 is a synthetic cannabinoid and T-type calcium channel inhibitor. This product is for research use only.
价 格：￥电议型 号：T69809产 地：中国大陆
-
T69048ML-236C；化合物 ML-236CML-236C
ML-236C is an inhibitor of cholesterogenesis.
价 格：￥电议型 号：T69048产 地：中国大陆
-
T69047ML-236A；化合物 ML-236AML-236A
ML-236A is an inhibitor of cholesterogenesis.
价 格：￥电议型 号：T69047产 地：中国大陆
-
T68878L-2286；化合物 L-2286L-2286
L-2286 is a novel PARP inhibitor. L-2286 exerted significant protective effect against ischemia-reperfusion-induced myocardial injury in both experimental models. More importantly, L-2286 facilitated the ischemia-reperfusion-induced activation of Akt, extracellular signal-regulated kinase, and p38-MAPK in both isolated hearts and in vivo cardiac injury.
价 格：￥电议型 号：T68878产 地：中国大陆
