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Tocris社 2013年7月新製品

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 New products are an essential component of our range. Introductions are made on an ongoing basis, with hundreds of new small molecules, peptides and antibodies being added every year. Our aim is to find the latest, otherwise unobtainable research tools, and bring them to the market as quickly as we can.

 

Cat.No. Product Name Activity
4990 Stavudine Nucleoside analog; antiviral
4985 Miglitol α-glucosidase inhibitor
4965 PD 180970 p210bcr/abl kinase inhibitor; also inhibits c-Src and KIT
4950 ICA 110381 KV7.2/7.3 activator; displays anticonvulsant properties
4942 Pitavastatin calcium HMG-CoA reductase inhibitor
4824 PD 334581 MEK1 inhibitor
4764 SIB 1553A hydrochloride Subunit selective nAChR agonist
4667 SB 706375 High affinity, non-peptide UT receptor antagonist
4987 Ethacrynic acid - d5 Deuterated ethacrynic acid
4981 Cystamine dihydrochloride Transglutaminase inhibitor; neuroprotective
4979 Methylmalonate Succinate dehydrogenase inhibitor
4960 AR-C155858 MCT1 and MCT2 inhibitor
4922 Purotoxin 1 Potent P2X3 modulator
4919 PG 106 Selective MC3 receptor antagonist
4891 I-CBP 112 Selective CREBBP/EP300 bromodomain inhibitor
4559 GNF 5837 Potent Trk inhibitor; inhibits TrkA, TrkB and TrkC
4932 RuBi-Dopa Caged dopamine; exhibits two-photon sensitivity
4921 Leukadherin 1 Allosteric activator of CD11b/CD18
4918 GSA 10 Smo receptor agonist
4914 Phrixotoxin 3 Potent modulator of NaV1.2, NaV1.3 and NaV1.5 channels
4887 OAC-1 Oct4 activator; enhances iPSC reprogramming efficiency
4844 HJC 0350 Selective Epac2 inhibitor
4816 Pentoxyresorufin Fluorometric cytochrome P450 substrate
4814 Methoxyresorufin Fluorometric CYP450 substrate
4801 QNZ 46 NR2C/NR2D-selective NMDA receptor non-competitive antagonist
4527 TC-I 15 Potent α2β1 inhibitor; displays antithrombotic activity in vivo
3412 (Z)-4-Hydroxytamoxifen Metabolite of tamoxifen (Cat. No. 0999)
3220 ShK-Dap22 Extremely potent and selective KV1.3 blocker; suppresses T cell activation in vitro
2983 GM 6001 Broad-spectrum MMP inhibitor
 

この製品に関するご意見・ご照会・お問合せはこちら

 


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