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：3872513
自主品牌
已选条件
-
T15418GS-6201；化合物GS-6201CVT-6883；CVT-6883
GS-6201 (CVT-6883) is a selective antagonist of adenosine A2B receptor. GS-6201 shows high affinity and selectivity for the human adenosine A2B receptors with a Ki of 22 nM.
价 格：￥电议型 号：T15418产 地：中国大陆
-
T15021CV-159；化合物 T15021CV-159
CV-159 is a unique dihydropyridine Ca2+ antagonist with antiinflammatory activities. It has an anti-calmodulin (CaM) action.
价 格：￥电议型 号：T15021产 地：中国大陆
-
T15011Creatine riboside；化合物 T15011Creatine riboside|||Creatine riboside；Creatine riboside|||Creatine ribos
Creatine riboside, a urinary metabolite, is a diagnostic and prognostic biomarker of lung cancer.
价 格：￥电议型 号：T15011产 地：中国大陆
-
T15008CP 316311；化合物 CP 316311CP 316311
CP 316311 is a specific CRF1 receptor antagonist with potential antidepressant activity and may be used in the study of depression.
价 格：￥电议型 号：T15008产 地：中国大陆
-
T14999CORM-401；化合物 CORM-401CORM-401
CORM-401 is a carbonyl complex and carbon monoxide releasing molecule with angiogenic and antimicrobial activities.
价 格：￥电议型 号：T14999产 地：中国大陆
-
T14991CMS-121；化合物CMS-121CMS121；CMS121
CMS-121, a quinolone derivative, is an orally active acetyl-CoA carboxylase 1 (ACC1) inhibitor. CMS-121 protects HT22 cells against ischemia and oxidative damage (EC50: 7 nM and 200 nM). CMS-121 shows strong neuroprotective, antioxidative, anti-inflammatory, and renoprotective activities.
价 格：￥电议型 号：T14991产 地：中国大陆
-
T14989CMPD101；化合物CMPD101CMPD101
CMPD101 is a membrane-permeable small-molecule inhibitor of GRK2/3 (IC50: 18 nM and 5.4 nM). Which can be used for the study of heart failure. CMPD101 exhibits less selectively against GRK1, GRK5, ROCK-2 and PKCα with IC50s of 3.1 μM , 2.3 μM, 1.4 μM and 8.1 μM, respectively.
价 格：￥电议型 号：T14989产 地：中国大陆
-
T14988CMPD1；化合物CMPD1CMPD1
CMPD1 is a non-ATP-competitive p38 MAPK-mediated MK2 phosphorylation inhibitor(apparent Ki (Kiapp): 330?nM).
价 格：￥电议型 号：T14988产 地：中国大陆
-
T14969CINPA1；化合物CINPA1CINPA-1|||CINPA 1；CINPA-1|||CINPA 1
CINPA1 (CINPA 1) is a selective inhibitor of constitutive androstane receptor (CAR) with an IC50 of 70 nM for CAR-mediated transcription. CINPA1 can be used in studies about CAR function.
价 格：￥电议型 号：T14969产 地：中国大陆
-
T14960Chroman 1；化合物Chroman 1Chroman 1
Chroman 1 is a potent inhibitor of ROCK1 (IC50?= 52 pM) and ROCK2 (IC50?= 1 pM).
价 格：￥电议型 号：T14960产 地：中国大陆
-
T14913CD38 inhibitor 1；化合物CD38 inhibitor 1CD38 inhibitor 1
CD38 inhibitor 1 is an inhibitor of CD38. For hCD38 and mouse CD38, the IC50s are 7.3 nM and 1.9 nM.
价 格：￥电议型 号：T14913产 地：中国大陆
-
T14901CCT-251921；化合物CCT-251921CCT-251921
CCT-251921 is a potent, selective, and orally bioavailable CDK8 inhibitor (IC50: 2.3 nM).
价 格：￥电议型 号：T14901产 地：中国大陆
-
T14891Cbz-NH-PEG6-C2-acid；化合物 T14891Cbz-NH-PEG6-C2-acid
Cbz-NH-PEG6-C2-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：T14891产 地：中国大陆
-
T14860CaMKII-IN-1；化合物CaMKII-IN-1CaMKII-IN-1
CaMKII-IN-1 is a potent and highly selective inhibitor of CaMKII (IC50 = 63 nM). CaMKII-IN-1 exhibited more than 100-fold higher selectivity for CaMKII over CaMKIV, MLCK, p38a, Akt1, and PKC.
价 格：￥电议型 号：T14860产 地：中国大陆
-
T14851C2-Bis-phosphoramidic acid diethyl ester；化合物 T14851C2-Bis-phosphoramidic acid diethyl ester
C2-Bis-phosphoramidic acid diethyl ester is an alkyl chain-derived PROTAC linker utilized for the synthesis of PROTACs[1].
价 格：￥电议型 号：T14851产 地：中国大陆
-
T14735Boc-NH-PEG1-CH2COOH；化合物 T14735Boc-NH-PEG-1-CH2COOH|||BocNHPEG1CH2COOH|||Boc NH PEG1 CH2COOH|||Boc-NH
Boc-NH-PEG1-CH2COOH 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：T14735产 地：中国大陆
-
T14151AKR1C1-IN-1；化合物AKR1C1-IN-1AKR1C1-IN-1
AKR1C1-IN-1 is a human 20α-hydroxysteroid dehydrogenase (AKR1C1) inhibitor (Ki: 4 nM for AKR1C1).
价 格：￥电议型 号：T14151产 地：中国大陆
-
T13661Docosatrienoic Acid；化合物 T13661cis-13,16,19-docosatrienoic acid|||(13Z,16Z,19Z)-13,16,19-Docosatrieno
Docosatrienoic acid is a rare omega-3 fatty acid; Ki value is 5×M, which inhibits the binding of LTB4 to porcine neutrophil membrane.
价 格：￥电议型 号：T13661产 地：中国大陆
-
T13631c(phg-isoDGR-(NMe)k)；化合物 T13631c(phg-isoDGR-(NMe)k)
c (phg-isoDGR- (NMe) k) is a selective and effective α5β1-integrin ligand with IC50 of 2.9 nM.
价 格：￥电议型 号：T13631产 地：中国大陆
-
T13572Cancer-Targeting Compound 1；癌症靶向化合物1Cancer-Targeting Compound 1
Cancer-Targeting Compound 1 can be used in the study of hormone-related cancers, including the treatment or prevention of fibroids, uterine leiomyomas, polycystic ovarian syndrome, or hormone-dependent Cancer, among others.
价 格：￥电议型 号：T13572产 地：中国大陆
