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：3552663
自主品牌
已选条件
-
T37082HS271HS271,HS-271
HS271 is a selective, highly potent and orally active IRAK4 inhibitor (IC50= 7.2 μM). HS271 shows excellent enzymatic and cellular activities, as well as excellent pharmacokinetic properties.
价 格：￥电议型 号：T37082产 地：中国大陆
-
T7847Apelin-13 triTFA(217082-58-1(free base))Apelin 13 triTFA(217082 58 1(free base)),Apelin13 triTFA(217
Apelin-13 triTFA is the endogenous ligand of the APJ receptor, activating this G protein-coupled receptor with an EC50 value of 0.37 nM.
价 格：￥电议型 号：T7847产 地：中国大陆
-
TP1501LCTTHWGFTLC, CYCLIC acetate(244082-19-7 free base)CTTHWGFTLC, CYCLIC acetate(244082197 free base),C
CTTHWGFTLC, CYCLIC acetate is an inhibitor for matrix metalloproteinases (MMP)-2 and MMP-9. It is also called type IV collagenase or gelatinase. Gelatinases are potential targets of therapeutic intervention in cancer, and inhibitors of these enzymes can prevent tumor progression.
价 格：￥电议型 号：TP1501L产 地：中国大陆
-
T60082HDAC-IN-40HDACIN40,HDAC IN 40
HDAC-IN-40 is a potent alkoxyamide-based HDAC inhibitor with Ki of 60 nM and 30 nM for HDAC2 and HDAC6, respectively. HDAC-IN-40 had antitumor effects
价 格：￥电议型 号：T60082产 地：中国大陆
-
T10824cis-Urocanic acid
cis-Urocanic acid is a 5-HT2A receptor agonist (Kd: 4.6 nM). It is an immune modulator that induces immunosuppression by binding to the 5-HT2A receptor.
价 格：￥电议型 号：T10824产 地：中国大陆
-
T15000Cort108297Cort108297,Cort-108297
Cort108297 is a specific antagonist of the glucocorticoid receptor with a high affinity for GRs (Ki: 0.45 nM).
价 格：￥电议型 号：T15000产 地：中国大陆
-
TQ0082AticaprantCERC 501,inhibit,LY2456302,Opioid Receptor,Aticaprant,Inhibitor,CERC501,LY 2456302
Aticaprant (CERC-501) is a potent and centrally-penetrant antagonist of the kappa-opioid receptor (Ki: 0.807 nM).
价 格：￥电议型 号：TQ0082产 地：中国大陆
-
T9825CORT-108297 EnantiomerCORT108297 Enantiomer,CORT 108297 Enantiomer
CORT-108297 Enantiomer is an enantiomer of CORT-108297 which is an antagonist of the Glucocorticoid Receptor.
价 格：￥电议型 号：T9825产 地：中国大陆
-
T30828CGP 35949
CGP 35949 is an LTD4 antagonist with phospholipase inhibitory activity.
价 格：￥电议型 号：T30828产 地：中国大陆
-
T10827CK2/ERK8-IN-1
CK2/ERK8-IN-1 is a dual inhibitor of casein kinase 2 (CK2) (Ki: 0.25 ?M) and ERK8 (IC50s: 0.50 μM) with pro-apoptotic efficacy. CK2/ERK8-IN-1 also binds to PIM1, DYRK1A, and HIPK2 (Kis: 8.65 ?M, 11.9 ?M, and 15.25 ?M).
价 格：￥电议型 号：T10827产 地：中国大陆
-
T7352PridopidineFR-310826,Dopamine Receptor,inhibit,Pridopidine,Inhibitor,ACR-16,ACR 16,ASP-2314,FR 31082
Pridopidine, a dopamine (DA) stabilizer, acts as a low affinity dopamine D2 receptor (D2R) antagonist, improves motor performance and shows neuroprotective effects in Huntington disease R6/2 mouse model.
价 格：￥电议型 号：T7352产 地：中国大陆
-
T8491VorolanibVEGFR,PDGFR,X82,Vascular endothelial growth factor receptor,CM 082,transporter,angiogenesis
Vorolanib is an orally active VEGFR/PDGFR dual inhibitor.
价 格：￥电议型 号：T8491产 地：中国大陆
-
TN2082PinostrobinThreonine proteases,Pinostrobin,inhibit,Serine proteases,Inhibitor,foxO3a,cholesterol,ant
Pinostrobin, a potent flavonoid inducer, exerts a neuroprotective effect against Aα2(25-35)-induced neurotoxicity in PC12 cells, at least in part, via inhibiting oxidative damage and calcium overload, as well as suppressing the mitochondrial pathway of cellular apoptosis.
价 格：￥电议型 号：TN2082产 地：中国大陆
-
TD0082Sodium 5-((2-aminoethyl)amino)naphthalene-1-sulfonatenucleic acid probes,DABCYL,Sodium 5((2aminoethy
Sodium 5-((2-aminoethyl)amino)naphthalene-1-sulfonate is a donor for developing FRET-based nucleic acid probes that is widely used in real time PCR assays.
价 格：￥电议型 号：TD0082产 地：中国大陆
-
T16766Ro 08-2750growth,MSI,Ro 082750,p75NTR,TRKA,RNA-binding,Nerve,NGF,Inhibitor,leukemia,Apoptosis,AML,Ro
Ro 08-2750 is a non-peptide and reversible nerve growth factor (NGF) inhibitor which binds to NGF, and with an IC50 of ~ 1 ?M. Ro 08-2750 is a selective MSI RNA-binding activity inhibitor, with an IC50 of 2.7 μM. Ro 08-2750 inhibits NGF binding to p75NTR selectively over TRKA.
价 格：￥电议型 号：T16766产 地：中国大陆
-
T90821,3-Benzoxazole-6-carboxylic acid1,3Benzoxazole6carboxylic acid,1,3 Benzoxazole 6 carboxylic acid
1,3-Benzoxazole-6-carboxylic acid is a chemical compound.
价 格：￥电议型 号：T9082产 地：中国大陆
-
T7082HDAC8-IN-1HDAC-8-IN-1,HDAC8IN1,Histone deacetylases,Inhibitor,inhibit,HDAC,HDAC8 IN 1
MDK-7933 (HDAC8-IN-1) is a HDAC8 inhibitor with an IC50 of 27.2 nM in cancer cell lines. MDK-7933 shows antiproliferative effects toward several human lung cancer cell lines (A549, H1299, and CL1-5). HDAC8-IN-1 exhibits cytotoxicity against human lung CL1-5 cells without significant cytotoxicity for normal IMR-90 cells[1].
价 格：￥电议型 号：T7082产 地：中国大陆
-
T11101DS08210767DS-08210767,DS08210767
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
-
TN7082demethyldaphnoretin-7-O-glucosidedemethyldaphnoretin 7 O glucoside,demethyldaphnoretin7Oglucoside
Demethyldaphnoretin-7-O-glucoside is a natural product that is isolated from Daphne oleoides Schreber subsp. kurdica (DOK). In Turkish traditional medicine, the aerial parts of DOK have been used to treat malaria, rheumatism and for wound healing.
价 格：￥电议型 号：TN7082产 地：中国大陆
-
T40823NCGC00029283NCGC00029283,NCGC-00029283
NCGC00029283 is a werner syndrome helicase-nuclease (WRN) helicase inhibitor with IC 50 s of 2.3 μM, 12.5 μM, and 3.4 μM for WRN, BLM and FANCJ helicase, respectively.
价 格：￥电议型 号：T40823产 地：中国大陆
