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| Product | Description | |
|---|---|---|
| TNP | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| TNP | TNP. Group: Biochemicals. Grades: Purified. CAS No. 519178-28-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| TNP | TNP is a cell-permeable inhibitor of IP6K1 and IP3K , with IC 50 values of 0.55 μM and 10.2 μM for IP3K, respectively. TNP binds to the ATP-binding sites of both enzymes [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 519178-28-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-110079. |  |
| TNP-470 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| TNP-470 | TNP-470 is a methionine aminopeptidase-2 inhibitor and also an angiogenesis inhibitor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AGM-1470. CAS No. 129298-91-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-101932. | |
| TNP-470 (AGM-1470, O-(Chloroacetyl-carbamoyl)fumagillol, AGM1470, MetAP-2 Inhibitor II, MetAP2 Inhibitor II, Methionine Aminopeptidase 2 Inhibitor II, TNP470) | A cell-permeable Fumagillin analog that inhibits MetAP2, but not MetAP1, methionine aminopeptidase activity (IC50 = 1nM against human MetAP2), without affecting the inhibitory activity of MetAP2 against HRI- (heme-regulated inhibitor kinase) catalyzed eIF-2alpha phosphorylation. A potent endothelial cytostasis inducer (IC50 = 25 pM and 37 pM, respectively, against HUVEC and bovine BAEC) in vitro and an effective anti-angiogenesis agent in vivo (2-100mg/kg in mice and rats; s.c.). Group: Biochemicals. Grades: Highly Purified. CAS No. 129298-91-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TNP-ATP triethylammonium salt | TNP-ATP triethylammonium salt. Group: Biochemicals. Grades: Purified. CAS No. 61368-63-6. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| TNP (N6-[ (4-nitrophenyl) methyl]-N2-[[3- (trifluoromethyl) phenyl]methyl]-9H-Purine-2, 6-diami ne) | Reversible inositol hexakisphosphate kinase (IP6K) inhibitor (IC50 = 0.47um for inhibition of InsP7 formation). Also inhibits inositol 1,4,5-trisphosphate 3-kinase (IP3K) (IC50 = 10.2um). Binds to the ATP binding site of IP3K (Ki = 4.3um). Group: Biochemicals. Grades: Highly Purified. CAS No. 519178-28-0. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Anti-TNPO2 (ab1) antibody produced in rabbit | affinity isolated antibody. Group: Fluorescence/luminescence spectroscopy. | |
| Anti-TNPO2 (ab2) antibody produced in rabbit | affinity isolated antibody. Group: Fluorescence/luminescence spectroscopy. | |
| Anti-TNPO2 (C-terminal) antibody produced in rabbit | ~1.0 mg/mL, affinity isolated antibody, buffered aqueous solution. Group: Fluorescence/luminescence spectroscopy. | |
| Monoclonal Anti-TNPO1 antibody produced in mouse | clone 3G2, purified immunoglobulin, buffered aqueous solution. Group: Fluorescence/luminescence spectroscopy. | |
| 2',3'-O-Trinitrophenyl-adenosine-5'-monophosphate triethylammonium salt | 2',3'-O-Trinitrophenyl-adenosine-5'-monophosphate triethylammonium salt, a powerful and discriminatory modulator employed within the biomedical sector, serves as a fundamental research instrument. Its widespread usage revolves around the exploration of adenosine receptor activation and its implications on diverse maladies, encompassing neurodegenerative ailments and enduring pain. The distinctive attributes of this substance render it indispensable for elucidating adenosine signaling pathways and constructing targeted remedies. The compound's unwavering purity and dependable availability guarantee precise and replicable findings, augmenting the realm of biomedical investigation. Synonyms: TNP-AMP. CAS No. 807261-75-2. Molecular formula: C16H15N8O13P·x(CH3CH2)3N. Mole weight: 558.31 (free acid). |  |
| 2'/3'-O-Trinitrophenyl-adenosine-5'-triphosphate triethylammonium salt | 2'/3'-O-Trinitrophenyl-adenosine-5'-triphosphate triethylammonium salt. Group: Biochemicals. Alternative Names: TNP-ATP. Grades: Highly Purified. CAS No. 61368-63-6,120360-48-7. Pack Sizes: 5mg, 10mg, 25mg, 50mg. Molecular Formula: C16H16N8O19P3. US Biological Life Sciences. | Worldwide |
| α-Conotoxin AuIB | α-Conotoxin AuIB is a selective antagonist of α3β4 nicotinic acetylcholine receptors. It shows > 100-fold selectivity over other receptor subunit combinations. Synonyms: alfa-Conotoxin AuIB; Gccsyppcfa tnpdc. CAS No. 216299-21-7. Molecular formula: C65H89N17O21S4. Mole weight: 1572.76. | |
| Rifasutenizol | Rifasutenizol (TNP-2198) is a dual-targeted antibacterial agent that has a good antibacterial effect on Helicobacter pylori infection. Rifasutenizol can be used in the study of microaerophilic and anaerobic bacterial infections [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TNP-2198. CAS No. 1001314-13-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-144300. | |
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