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T76343-Hydroxymandelic Acidinhibit,3 Hydroxymandelic Acid,3-Hydroxymandelic Acid,Inhibitor,3Hydroxymandel
3-Hydroxymandelic Acid is a metabolite of Phenylephrine.
价 格:¥电议型 号:T7634产 地:中国大陆
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T6S1894LinderaneCYPs,Cytochrome P450,Linderane,inhibit,Inhibitor
1. Linderane was characterized as a mechanism-based inactivator of CYP2C9.
价 格:¥电议型 号:T6S1894产 地:中国大陆
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TP1380Galanin (1-16), mouse, porcine, ratGalanin (1-16), mouse, porcine, rat,Neuropeptide Y Receptor,Inhib
Galanin (1-16), mouse, porcine, rat is a hippocampal galanin receptor agonist(Kd = 3 nM) with high biological activity on locus coeruleus neurons.
价 格:¥电议型 号:TP1380产 地:中国大陆
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TN6782oroxylin A 7-O-β-d-glucuronideoroxylin A 7 O β d glucuronide,oroxylin A 7Oβdglucuronide
Oroxylin A 7-O-β-d-glucuronide was a new alkaloid which found in the bulbs of Lycoris radiata.
价 格:¥电议型 号:TN6782产 地:中国大陆
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T8930CID44216842diseases,neutrophils,ovarian,disorders,Cdc42,fibroblasts,breast,hepatitis C,CID 44216842,
CID44216842 is a potent Cdc42-selective guanine nucleotide binding lead inhibitor. The EC50s for Cdc42 WT and Cdc42Q61L mutant are 1.0 and 1.2 μM in GTP binding assay, respectively. The EC50s for Cdc42 WT and Cdc42Q61L mutant are 0.3 and 0.5 μM in GDP binding assay, respectively. Use as a molecular probe.
价 格:¥电议型 号:T8930产 地:中国大陆
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T9349IXA4endoplasmic reticulum (ER) proteostasis,UPR,protein secretion,Inhibitor,Inositol requiring enzym
IXA4 is a highly selective, nontoxic activator of IRE1/XBP1s and reduces APP secretion by activating IRE1. IXA4-stimulated IRE1 activation also enhanced pancreatic function.
价 格:¥电议型 号:T9349产 地:中国大陆
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T7903SaquinavirSARS-CoV,HIV,Human immunodeficiency virus,Inhibitor,inhibit,HIV Protease,SARS coronavirus,
Saquinavir is a potent HIV protease inhibitor, is an antiretroviral drug used together with other medications to treat or prevent HIV/AIDS.
价 格:¥电议型 号:T7903产 地:中国大陆
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T16845Sarolanerdog,Sarolaner,Parasite,PF 6450567,flea,Inhibitor,oral,inhibit,isoxazoline,tick,PF6450567
Sarolaner is an orally active and broad-spectrum ectoparasiticide (LC80: 0.3 μg/mL against C. felis and an LC100: 0.003 μg/mL against O. turicata).
价 格:¥电议型 号:T16845产 地:中国大陆
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T6700TenatoprazoleProton Pump,Inhibitor,gastric,ATPase,Tsg101,inhibit,virus,TU199,oral,TU 199,Tenatoprazo
Tenatoprazole, a prodrug of the proton pump inhibitor (PPI) class, can inhibit proton transport (IC50: 3.2 μM).
价 格:¥电议型 号:T6700产 地:中国大陆
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T7568LM22A-4LM-22A-4,Inhibitor,Trk Receptor,inhibit,LM22A4,LM22A-4,Tropomyosin related kinase receptor,LM
LM22A-4 is a brain-derived neurotrophic factor (BDNF) mimetic and agonist of the receptor tropomyosin-related kinase B (TrkB; IC50 : 47 nM in a fluorescence anisotropy assay)
价 格:¥电议型 号:T7568产 地:中国大陆
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TJS03127-hydroxy-4-methyl-8-nitrocoumarininhibit,7hydroxy4methyl8nitrocoumarin,Inhibitor,7 hydroxy 4 methyl
价 格:¥电议型 号:TJS0312产 地:中国大陆
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TN6848Piperonylic acidformation,virus,natural,inactivator,Cytochrome P450,Piperonylic acid,quasi-irreversi
Piperonylic acid is a natural molecule bearing a methylenedioxy function that closely mimics the structure of trans-cinnamic acid. Piperonylic acid selectively inactivate the CYP73A P450 subpopulation.
价 格:¥电议型 号:TN6848产 地:中国大陆
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TN2215Taurochenodeoxycholic acid sodiummRNA,Taurochenodeoxycholic acid,acid,Taurochenodeoxycholic acid sod
Sodium taurochenodeoxycholate is one of the main bioactive substances of animals´ bile acid. Sodium taurochenodeoxycholate induces apoptosis and shows obvious anti-inflammatory and immune regulation properties. It can increase glucose-induced insulin secretion and stimulate the electrical activity of α2-cells and enhance cytosolic Ca(2+) concentration ([Ca(2+)](c)).
价 格:¥电议型 号:TN2215产 地:中国大陆
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T600175-Bromo-4-chloro-3-indoxyl-beta-D-cellobioside5 Bromo 4 chloro 3 indoxyl beta D cellobioside,5Bromo4
5-Bromo-4-chloro-3-indoxyl-beta-D-cellobioside is a chromogenic compound used to detect cellobiohydrolases.
价 格:¥电议型 号:T60017产 地:中国大陆
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T9828N-[1-(Aminocarbonyl)-4-[(2-chloro-1-iminoethyl)amino]butyl]benzamideN[1(Aminocarbonyl)4[(2chloro1imi
N-[1-(Aminocarbonyl)-4-[(2-chloro-1-iminoethyl)amino]butyl]benzamide is a racemic form of Cl-amidine (S enantiomer). Cl-amidine is an orally active peptidylarginine deminase (PAD) inhibitor.
价 格:¥电议型 号:T9828产 地:中国大陆
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T60193CB-53391HIndole4carboxamide,2methyl1[5,6,7,8tetrahydro4[(phenylmethyl)amino]pyrido[2,3d]pyrimidin2yl
p97-IN-1 is a potent inhibitor of p97 with an IC 50 <30 nM [1].
价 格:¥电议型 号:T60193产 地:中国大陆
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T3696polygalaxanthone IIICYPs,Inhibitor,Cytochrome P450,inhibit,polygalaxanthone III
Polygalaxanthone III can significantly inhibit chlorzoxazone 6-hydroxylation catalyzed by CYP2E1.
价 格:¥电议型 号:T3696产 地:中国大陆
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TN6925Pristanehydrocarbon oil,Inhibitor,plants,Pristane,mineral oil,Norphytane,non-antigenic adjuvant,mari
Pristane is a natural product from shark liver oil and a non-antigenic adjuvant.
价 格:¥电议型 号:TN6925产 地:中国大陆
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T8375ML-210residue,Ferroptosis,inhibit,peroxidase,ML-210,Covalent,selenocysteine,Glutathione Peroxidase,M
ML-210 is a selective RAS and covalent glutathione peroxidase 4 (GPX4) inhibitor(GPX4, EC50 : 30 nM), with anti-cancer activity
价 格:¥电议型 号:T8375产 地:中国大陆
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TN1037GroenlandicineTopoisomerase,Groenlandicine,inhibit,Inhibitor
Groenlandicine is a protoberberine alkaloid from Coptidis Rhizoma. Groenlandicine exhibits moderate inhibitory effect with IC50 value of 154.2 μM for human recombinant aldose reductase (HRAR). Groenlandicine selectively induces topoisomerase I-mediated DNA cleavage;Groenlandicine may be a promising anti-Alzheimer´s disease agent due to its potent inhibitory activity of both ChEs and beta-amyloids formation, as well as marked ONOO(-) scavenging and good ROS inhibitory capacities.
价 格:¥电议型 号:TN1037产 地:中国大陆