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Catalog | name | Description | price |
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R-R-4927 | Adenosine-d CAS No.109923-50-4 | Adenosine-d/CAS No.109923-50-4 is the deuterium labeled Adenosine. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation. | price> |
R-C-3258 | ORM-10103 CAS:488847-28-5 | ORM-10103 is a specific inhibitor of the Na+/Ca2+ exchanger(NCX),which decreases the NCX current with estimated IC50s of 55 and 67nM at -80 and at 20mV,respectively.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4928 | 5-ODMT cEt N-Bz A Phosphoramidite (Amidite) CAS No.1197033-19-4 | 5-ODMT cEt N-Bz A Phosphoramidite Amidite/CAS No.1197033-19-4 is a locked nucleic acid (LNA) analogue. 5-ODMT cEt N-Bz A Phosphoramidite Amidite possesses hybridization and mismatch discrimination attributes similar to those of LNA and shows resistance to exonuclease digestion. | price> |
R-C-3259 | YHO-13177 CAS:912287-56-0 | YHO-13177 is a potent and specific inhibitor of BCRP;potentiated the cytotoxicity of SN-38 in cancer cells and no effect on P-glycoprotein–mediated paclitaxel resistance in MDR1-transduced human leukemia K562 cells.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4929 | 2-O,4-C-Methyleneadenosine CAS No.206055-70-1 | 2-O,4-C-Methyleneadenosine (LNA-A)/CAS No.206055-70-1 is a locked nucleic acid (LNA) and is also an adenosine analog. | price> |
R-C-3260 | Tenapanor CAS:1234423-95-0 | Tenapanor acts as an inhibitor of the sodium-proton exchanger NHE3. This antiporter protein is found in the kidney and intestines, and normally acts to regulate the levels of sodium absorbed and secreted by the body.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4930 | 5-ODMT cEt G Phosphoramidite (Amidite) CAS No.945628-66-0 | 5-ODMT cEt G Phosphoramidite Amidite/CAS No.945628-66-0 is a potent nucleic acid analog. 5-ODMT cEt G Phosphoramidite Amidite shows excellent safety and antisense activity. | price> |
R-C-3261 | Rimeporide CAS:187870-78-6 | Rimeporide(EMD-87580)is a potent and selective inhibitor of the Na+/H+ exchanger (NHE-1).Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4931 | 9-(β-D-Xylofuranosyl)adenine CAS No.524-69-6 | 9-(β-D-Xylofuranosyl)adenine/CAS No.524-69-6 is an adenosine analog. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. Its popular products are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277). | price> |
R-C-3262 | NHE3-IN-1 CAS:632355-68-1 | NHE3-IN-1 is a sodium/proton exchanger type 3(NHE-3)inhibitor extracted from patent WO 2011019784 A1.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4932 | 2-Fluoro-2-deoxy-ara-A(Bz)-3-phosphoramiditeCAS No.329187-86-2 | 2-Fluoro-2-deoxy-ara-A(Bz)-3-phosphoramidite/CAS No.329187-86-2 is an adenosine analog. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. Its popular products are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277). | price> |
R-C-3263 | GZ-793A CAS:1356447-90-9 | GZ-793A is a selective inhibitor of vesicular monoamine transporter 2(VMAT2),which transports the monoamine neurotransmitters from cellular cytosol into synaptic vesicles.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4933 | Nucleoside-Analog-1 CAS No.876707-99-2 | Nucleoside-Analog-1/CAS No.876707-99-2 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups. | price> |
R-C-3264 | NBI-98782 CAS:85081-18-1 | NBI-98782(alpha-dihydrotetrabenazine)is a vesicular monoamine transporter(VMAT2) inhibtior with an Ki value of 0.97nM.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4934 | AzddMeC CAS No.87190-79-2 | AzddMeC (CS-92)/CAS No.87190-79-2 is an antiviral nucleoside analogue and a potent potent, selective and orally active HIV-1 reverse transcriptase and HIV-1 replication inhibitor. In HIV-1-infected human PBM cells and HIV-1-infected human macrophages, the EC50 values of AzddMeC are 9 nM and 6 nM, respectively. AzddMeC is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups. | price> |
R-C-3265 | U18666A CAS:3039-71-2 | U18666A, an intra-cellular cholesterol transport inhibitor, inhibits replication of Ebola virus, dengue virus, and human hepatitis C virus.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4935 | 3-Deoxycytidine CAS No.7057-33-2 | 3-Deoxycytidine/4-Amino-1-((2R,3R,5S)-3-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one/CAS No.7057-33-2 is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc. | price> |
R-C-3166 | TUG-770 CAS:1402601-82-4 | TUG-770 is a Highly Potent Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonist for Treatment of Type 2 Diabetes.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-C-3266 | TAK-441 CAS:1186231-83-3 | TAK-441 is a pyrrolo[3,2-c]pyridine derivative,as a highly potent and orally active hedgehog signaling inhibitor.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4936 | Peldesine CAS No.133432-71-0 | Peldesine (BCX 34)/CAS No.133432-71-0 is a potent, competitive, reversible and orally active purine nucleoside phosphorylase (PNP) inhibitor with IC50s of 36 nM, 5 nM, and 32 nM for human, rat, and mouse red blood cell (RBC) PNP, respectively. Peldesine is also a T-cell proliferation inhibitor with an IC50 of 800 nM. Peldesine has the potential for cutaneous T-cell lymphoma, psoriasis and HIV infection research.At equivalent molar concentrations, both the salt and free forms of a compound exhibit comparable biological activity. Nevertheless, the salt form (Peldesine dihydrochloride) usually boasts enhanced water solubility and stability. | price> |