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：3550963
自主品牌
已选条件
-
T9890HIF1-IN-3?Hypoxia-inducible factors,HIF1 IN 3?,Inhibitor,HIFs,inhibit,HIF-PH,HIF1IN3?,Anticancer,HIF
HIF1-IN-3 is an effective inhibitor of HIF-1 (EC50 = 0.9 μM) and can be used in anticancer studies.
价 格：￥电议型 号：T9890产 地：中国大陆
-
T60158PBRM1-BD2-IN-3PBRM1BD2IN3
PBRM1-BD2-IN-3 (compound 12) is a potent PBRM1-BD2 inhibitor with an IC50 value of 1.1 μM. PBRM1-BD2 Inhibitor can be used to research anticancer.
价 格：￥电议型 号：T60158产 地：中国大陆
-
T93615-bromo-2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione5 bromo 2 (2,6 dioxopiperidin 3 yl)isoindole 1
5-bromo-2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione is a chemical compound.
价 格：￥电议型 号：T9361产 地：中国大陆
-
T64349Necroptosis-IN-3
Necroptosis-IN-3 (Compound 69) is a Necroptosis inhibitor that inhibits TNF-α induced necroptosis. Necroptosis-IN-3 (Compound STX1638) also inhibits 11β-HSD1.
价 格：￥电议型 号：T64349产 地：中国大陆
-
T6614Nutlin-3bNutlin 3b,Inhibitor,MDM-2/p53,Ubiquitin activating enzyme,Ubiquitin conjugating enzyme,inhi
Nutlin-3b is a p53/MDM2 antagonist or inhibitor (IC50: 13.6 μM), 150-fold less potent (+)-enantiomer of Nutlin-3 as in comparison with opposite (-)-enantiomer Nutlin-3a.
价 格：￥电议型 号：T6614产 地：中国大陆
-
T60185FGFR2-IN-3FGFR2IN3
FGFR2-IN-3 is an orally active selective FGFR2 inhibitor[1].
价 格：￥电议型 号：T60185产 地：中国大陆
-
TN2126Quercetin-3-O-glucose-6’’-acetateQuercetin3Oglucose6’’acetate,Quercetin 3 O glucose 6’’ acetate
Quercetin-3-O-glucose-6´´-acetate is an inhibitor of NADPH oxidase. Quercetin-3-O-glucose-6´´-acetate has antioxidant activities.
价 格：￥电议型 号：TN2126产 地：中国大陆
-
T8916WEE1-IN-3WEE1IN3,cycle,Inhibitor,inhibit,cell,Wee1,WEE-1-IN-3,WEE1 IN 3,Anticancer
JUN76288 is a potent Wee1 kinase inhibitor with an IC50 of <10 nM. It treatment of cancer and other proliferative diseases.
价 格：￥电议型 号：T8916产 地：中国大陆
-
TN7076herbacetin-3,8-diglucopyranosideherbacetin3,8diglucopyranoside,herbacetin 3,8 diglucopyranoside
herbacetin-3,8-diglucopyranoside is a natural product.
价 格：￥电议型 号：TN7076产 地：中国大陆
-
T7973BENZOFURAN-3-CARBALDEHYDEBENZOFURAN 3 CARBALDEHYDE,BENZOFURAN3CARBALDEHYDE
BENZOFURAN-3-CARBALDEHYDE is a natural product.
价 格：￥电议型 号：T7973产 地：中国大陆
-
T4404Methyl 2-(Boc-aMino)-2-(oxetan-3-yl)acetateMethyl 2 (Boc aMino) 2 (oxetan 3 yl)acetate,Methyl 2(Boca
Methyl 2-(Boc-aMino)-2-(oxetan-3-yl)acetate is a chemical compound.
价 格：￥电议型 号：T4404产 地：中国大陆
-
T67857(Z)-4-(5-((5-(4-bromophenyl)furan-2-yl)methylene)-4-oxo-2-thioxothiazolidin-3-yl)butanoic acid
(Z)-4-(5-((5-(4-bromophenyl)furan-2-yl)methylene)-4-oxo-2-thioxothiazolidin-3-yl)butanoic acid is an ASK1 inhibitor, IC50 = 0.2 μM.
价 格：￥电议型 号：T67857产 地：中国大陆
-
T67727MCT1-IN-3MCT1IN3
MCT1-IN-3 is a monocarboxylate transporter 1 (MCT1) inhibitor. The solute carrier (SLC) monocarboxylate transporter 1 (MCT1; SLC16A1) represents a promising target for the treatment of cancer. MCT1-IN-3 (compound 24) showed the highest MCT1 transport inhibition with an IC50 value of 81.0 Nm. MCT1-IN-3 has also significant inhibitivity against the multidrug transporter ABCB1.
价 格：￥电议型 号：T67727产 地：中国大陆
-
T9034MK2-IN-3MAPK activated protein kinase 2,Mitogen-activated protein kinase activated protein kinase 2,
MK2-IN-3 is a potent, cell-permeable inhibitor of mitogen-activated protein kinase-activated protein kinase 2 (MAPKAP-K2 or MK-2) and can be used for the treatment of rheumatoid arthritis
价 格：￥电议型 号：T9034产 地：中国大陆
-
T23316SB 218795constriction,SB-218795,Neurokinin Receptor,Inhibitor,neurokinin-3,NK receptor,pupillary,inh
SB 218795 is an effective and selective antagonist of NK3 with a Ki 13 nM for hNK3 which is about 90-fold and 7000-fold selectivity over hNK2 and hNK1.
价 格：￥电议型 号：T23316产 地：中国大陆
-
T10316AN3199AN3199,AN-3199
AN3199 is a selective inhibitor of PDE4 with an IC50 of 94.5 nM.
价 格：￥电议型 号：T10316产 地：中国大陆
-
T9360N-(2,6-dioxopiperidin-3-yl)-4-nitrophthalimideN (2,6 dioxopiperidin 3 yl) 4 nitrophthalimide,N(2,6di
N-(2,6-dioxopiperidin-3-yl)-4-nitrophthalimide exhibit inhibition of CRBN.
价 格：￥电议型 号：T9360产 地：中国大陆
-
T10791CHK1-IN-3CHK1IN3,CHK1 IN 3,CHK-1-IN-3
CHK1-IN-3 is an inhibitor of checkpoint kinase 1 (CHK1; IC50: 0.4 nM).
价 格：￥电议型 号：T10791产 地：中国大陆
-
T67883N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-5-ethyl-6-[ethyl(tetrahydropyran-4-yl)amino]-2-(1-pip
N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-5-ethyl-6-[ethyl(tetrahydropyran-4-yl)amino]-2-(1-piperidylmethyl)benzofuran-4-carboxamide is a specific inhibitor of histone modifier enhancer of zeste 2 (EZH2). EZH2 is aberrantly overexpressed in a number of human cancers that controls the adaptive response via regulation of Treg activity. Intratumoral EZH2 expression has also been shown to control the innate immunity
价 格：￥电议型 号：T67883产 地：中国大陆
-
T9141ERK-IN-3ERK1/2,inhibit,ERK,Inhibitor,ERK IN 3,RAS,Extracellular signal regulated kinases,cancer,ERKI
ERK-IN-3 is a potent and orally active inhibitor of ERK. It inhibits ERK1/2 with low single-digit nM IC50 values. It can be used for the research of cancers driven by RAS mutations.
价 格：￥电议型 号：T9141产 地：中国大陆
