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T2477UNBS-5162UNBS-5162,UNBS5162,UNBS 5162
UNBS-5162 is a novel naphthalimide that decreases CXCL chemokine expression in experimental prostate cancers.
价 格:¥电议型 号:T2477产 地:美洲
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T2576Brivanib AlaninateBrivanib Alaninate,BMS-582664,
Brivanib Alaninate is the alaninate salt of a vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor with potential antineoplastic activity. Brivanib strongly binds to and inhibits VEGFR2, a tyrosine kinase receptor expressed almost exclusively
价 格:¥电议型 号:T2576产 地:美洲
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T4598BMS-5BMS-5,BMS5,BMS 5
BMS-5 is a potent LIMK inhibitor with IC50s of 7 nM and 8 nM for LIMK1 and LIMK2, respectively.
价 格:¥电议型 号:T4598产 地:美洲
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T6103VS-5584VS-5584,VS5584,VS 5584
VS-5584 is a pan-PI3K/mTOR kinase inhibitor.
价 格:¥电议型 号:T6103产 地:美洲
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T8495Alobresib;化合物AlobresibVorolanib|||GS-5829;Vorolanib|||GS-5829
Alobresib (Vorolanib) is an inhibitor of BET bromodomain,is an antineoplastic drug candidate.
价 格:¥电议型 号:T8495产 地:中国大陆
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T839096-hydroxy Buspirone;化合物 6-hydroxy BuspironeBMY 28674|||BMS-52821;BMY 28674|||BMS-52821
6-Hydroxy Buspirone, an active metabolite of the anxiolytic compound buspirone, is produced via the cytochrome P450 (CYP) isoform CYP3A4. This compound exhibits affinity for the serotonin (5-HT) receptor subtype 5-HT1A, demonstrating efficacy in the rat hippocampus and dorsal raphe with half-maximal effective concentrations (EC50s) of 4 and 1 ?M, respectively. Furthermore, 6-Hydroxy Buspirone acts as a potent antagonist against dopamine D2, D3, and D4 receptors with half-maximal inhibitory conce
价 格:¥电议型 号:T83909产 地:中国大陆
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T833403α-Acetoxyurs-5:12-dien-24-oic acid;化合物 3α-Acetoxyurs-5:12-dien-24-oic acid3α-Acetoxyurs-5:12-dien-2
3α-Acetoxyurs-5:12-dien-24-oic acid, a natural compound, is isolatable from Boswellia sacra Fluckiger [1].
价 格:¥电议型 号:T83340产 地:中国大陆
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T8240Cis-5-Dodecenoic Acid;顺式 -5-十二碳烯酸Cis-5-Dodecenoic Acid
Cis-5-Dodecenoic Acid is a monounsaturated fatty acid that has a C12 chain as a backbone and a cis double bond at the C5 position.
价 格:¥电议型 号:T8240产 地:中国大陆
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T79303IACS-52825;化合物 IACS-52825IACS-52825
IACS-52825 is a potent, selective DLK inhibitor, exhibiting a dissociation constant (Kd) of 1.3 nM, and is valuable for researching chemotherapy-induced peripheral neuropathy (CIPN) [1].
价 格:¥电议型 号:T79303产 地:中国大陆
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T77761BMS-502;化合物 BMS-502BMS-502
BMS-502 is a potent dual inhibitor of diacylglycerol kinase (DGK) α and ζ that induces immune responses in human and mouse T cells and blocks intracellular checkpoint signaling in T cells. BMS-502 stimulates immune responses in a dose-dependent manner and can be used to study immune-related diseases.
价 格:¥电议型 号:T77761产 地:中国大陆
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T7766Remdesivir;瑞德西韦GS-5734;瑞德西韦|||GS-5734
Remdesivir (GS-5734) is a nucleoside analog, a broad-spectrum antiviral compound that exerts its activity by inhibiting the RNA-dependent RNA polymerase of viruses. Remdesivir is active against Ebola, SARS, and MERS viruses, and is potentially therapeutic against COVID-19.
价 格:¥电议型 号:T7766产 地:中国大陆
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T76856Andecaliximab;Andecaliximab单抗GS-5745;GS-5745
Andecaliximab is a recombinant IgG4 monoclonal antibody targeting matrix metalloproteinase 9 (MMP9). Andecaliximab showed antifibrotic effects in a mouse model of idiopathic pulmonary fibrosis. Andecaliximab can be used to study gastric adenocarcinoma and idiopathic pulmonary fibrosis (IPF), as well as dengue virus.
价 格:¥电议型 号:T76856产 地:中国大陆
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T75241Ledipasvir hydrochloride;盐酸雷迪帕韦GS-5885 hydrochloride;GS-5885 hydrochloride
Ledipasvir hydrochloride (GS-5885) is a hepatitis C virus NS5A inhibitor, displaying potent activity with EC50 values of 34 pM for genotype 1a replicon and 4 pM for genotype 1b replicon. Additionally, it acts as a SARS-CoV 3CL pro inhibitor with an IC50 of 1.62 ?M [3].
价 格:¥电议型 号:T75241产 地:中国大陆
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T73778cis-5-Tetradecenoic acid;化合物 cis-5-Tetradecenoic acidcis-5-Tetradecenoic acid
Cis-5-Tetradecenoic acid, an intrinsic metabolite found in blood, serves as a research tool for Long Chain 3-Hydroxyacyl CoA Dehydrogenase Deficiency [1] [2].
价 格:¥电议型 号:T73778产 地:中国大陆
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T72868ADAMTS-5-IN-2;化合物 ADAMTS-5-IN-2ADAMTS-5-IN-2
ADAMTS-5-IN-2 is a potent inhibitor of ADAMTS-5, exhibiting an IC50 of 0.71 ?M, and holds potential for osteoarthritis research.
价 格:¥电议型 号:T72868产 地:中国大陆
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T71641BMS-593214;化合物 BMS-593214BMS-593214
BMS-593214 is an active site-directed factor (F) VIIa inhibitor that exhibits antithrombotic and antihaemostatic properties. It acts as a direct competitive inhibitor of human FVIIa and a non-competitive inhibitor of Viia-activated substrate FX. Moreover, BMS-593214 effectively prevents electroinduced carotid artery thrombosis (AT) and wire-induced vena cava thrombosis (VT).
价 格:¥电议型 号:T71641产 地:中国大陆
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T70925GS-5759;化合物 GS-5759GS-5759
GS-5759 is a bifunctional ?2-Adrenoceptor Agonist and Phosphodiesterase 4 Inhibitor for Chronic Obstructive Pulmonary Disease with a Unique Mode of Action.
价 格:¥电议型 号:T70925产 地:中国大陆
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T6S1538Neochlorogenic acid;新绿原酸trans-5-O-Caffeoylquinic acid|||Neochlorogenate|||5-O-Caffeoylquinic acid;新绿
Neochlorogenic acid (trans-5-O-Caffeoylquinic acid) is an antioxidant compound used in the treatment of oxidative stress and related afflictions.
价 格:¥电议型 号:T6S1538产 地:中国大陆
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T69890PS-519;化合物 PS-519PS-519
PS-519 is a human tissue plasminogen activator and proteasome inhibitor.
价 格:¥电议型 号:T69890产 地:中国大陆
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T69411CNS-5788;化合物 CNS-5788CNS-5788
CNS-5788 is a potential ischemia-selective N-methyl-D-aspartate (NMDA) receptor ion-channel blocker
价 格:¥电议型 号:T69411产 地:中国大陆