A.G. Scientific, Inc. Datasheets for Organic Chemicals
Organic chemicals are chemical compounds that contain carbon in their molecular structure.
Organic Chemicals: Learn more
| Product Name | Notes |
|---|---|
| A cephalosporin antibiotic, acts as an in hibitor to bacterial cell wall synthesis. Effective against Gram-negative and Gram-positive bacteria. Resistant to β-lactamase. | |
| A highly potent and selective ETA-receptor antagonist. | |
| A highly potent and selective ETB-receptor antagonist. | |
| A triterpenoid compound that exists widely in food, medicinal herbs and other plants. Displays anti-tumor, anti-inflammatory and antihyperlipidemic properties. Also displays TGR5 agonist activity (EC50 = 2.25 μM). | |
| A23187 is a widely used ionophore. It has the ability to increase the intracellular concentrations of cations and is widely used to increase the intracellular levels of calcium. Seeking published... | |
| Absorption Spectrum: λ max: 371 nm. Extincion: 33,000 M-1 cm-1. Emission Spectrum: λ max: 505 nm. Excitation: λ max: 380 nm | |
| Acts as a second terms potentiation in the nervous system. Product inhibits Ras-GAP. | |
| Agonist at Quisqualate / AMPA ionotropic receptors. Activity at metabotropic glutamate receptors. | |
| An aminoglycoside antibiotic, Tobramycin Sulfate Salt binds to 70S ribosomal subunit, inhibits translocation. Gram negative bacteria, reportedly not effective against Enterococci. ** Bulk & packaged quantities available, inquire with our... | |
| An inhibitor of the mitochondrial permeability transition. It acts as an inhibitory ligand of the mitochondrial adenine nucleotide translocator. Also inhibits apoptosis by preventing PARP cleavage and DEVDase activity. | |
| Anti-tumor, anti-HIV agent which induces apoptosis via activation of caspases. | |
| Antibiotic, Mycotoxin that induces DNA single-strand breaks. Anti-HIV Activity. | |
| Antineoplastic compound exhibiting anti-tumor, antiviral and antibacterial activity. Inhibits protein synthesis by suppression at the ribosome and may act as a mycotoxin. | |
| Boswellic acid derivative, which shows anti-tumor and anti-inflammatory activities. Potent non-redox, non-competitive 5-lipoxygenase and topoisomerase I and IIa inhibitor leading to apoptosis. Mobilizes intracellular Ca2+ and potently inhibits the MAP... | |
| Boswellic acid derivative, which shows anti-tumor and anti-inflammatory activities. Potent non-redox, noncompetitive 5-lipoxygenase and topoisomerase I and IIa inhibitor leading to apoptosis. Mobilizes intracellular Ca2+ and potently inhibits the MAP... | |
| Cefpodoxime free acid, a cephalosporin antibiotic. Active against most Gram positive and Gram negative organisms, with exception to Pseudomonas aeruginosa, Enterococcus, and Bacteroides fragilis. ** Product is available, for pricing... | |
| Cefsulodin Sodium Salt is a third generation cephalosporin antibiotic. Utilized in mIcrobiology with CIN ( Cefsulodin-Irgasan-N ovobiocin) Agar is used for the selective isolation of Yersinia enterocolitic. Also Cefsulodin chocolate... | |
| Cell-permeable. A potent, non-competitive inhibitor of p300 and PCAF (p300/CBP-associated factor) histone acetyltransferase (HAT) activities (IC50~8.5 μM and ~5 μM, respectively. Inhibits SUMOylation of RanGAP1-C2 with an IC50 = 2.2... | |
| Erlotinib is an inhibitor of human Epidermal growth factor receptor (EGFR) tyrosine kinase (IC50 = 2 nM) and decreases EGFR autophosphorylation in tumor cells (IC50 = 20 nM). Studies in... | |
| Excitatory amino acid receptor agonist selective for kainate receptor subtype; conformationally restricted analog of L-glutamic acid. | |
| Functions as Na+ ionophore by forming stable complexes with monovalent cations able to cross the plasma membrane. Blocks glycoprotein secretion; inhibits HDL to decrease cellular cholesterol esterification. Product has minimum... | |
| Immunosuppressive agent. Mycophenolic acid (MPA) has been tested extensively in renal transplant patients and has been shown to be effective in reducing the incidence of acute graft rejection. MPA is... | |
| Inhibitor of cyclin-dependent kinases (CDKs), with selectivity for CDK1/cyclin B (IC50=0.05 μm) and CDK5/p25 (IC50=0.065 μm) compared to GSK-3Beta (IC50=0.28 μM). | |
| Inhibitor of HSP90. Novobiocin interacts with the C-terminal ATP-binding domain of HSP90, unlike 17-AAG (A1256), Geldanamycin (G1047), Herbimycin A (H1050), or Radicicol (R1130) which all bind to the N-terminal ATP-binding... | |
| Inhibits apoptosis in various cell types induced by a variety of factors. Potent inhibitor of DNA topoisomerase II in vitro and protein-nucleic acid interactions. Stimulates the tyrosine phosphorylation of MAP... | |
| Inhibits lipid peroxidation induced by NADH or NADPH oxidation. Naturally-occurring phenolic compound with antioxidant properties. Isolated from Rosmarinus officinalis. | |
| Ionomycin, free acid, is a highly specific ionophore useful in studying Ca2+ transportation. From Streptomyces conglobatus. Highly specific ionophore useful in studying Ca2+ transportation. | |
| Kainic Acid is a marine product, derived from the red marine alga Digenea Simplex. Kainic Acid is an excitatory amino acid receptor agonist selective for kainate receptor subtype; conformationally restricted... | |
| Myristoleic acid is a cytotoxic component from the fruit extract of S. repens. It induces apoptosis and necrosis in human prostate cancer LNCaP cells at a rate of 8.8% and... | |
| Naturally-occurring polyphenolic compound with antioxidant and anti-inflammatory properties. Inhibits lipid peroxidation of rat liver microsomes by 90% at a concentration of 25μg/ml. Isolated from Rosmarinus officinalis. | |
| Polyether ionophore. Stimulates ATPase activity in mitochondria. | |
| Potent and selective AMPA/Kainate receptor antagonist. Neuroprotective and anti-convulsant agent in vivo. Water soluble form. See N1019 for non-salt form. NOTE: this product has specification changes related to appearance &... | |
| Potent modulator of growth, differentiation. Product for NON-human research use, not for clinical applications. | |
| Potent NMDA agonist. | |
| Product is high affinity ligand for retinoid X receptor (RXR). Able to destablize VDR=RXR heterodimer-DNA complex. | |
| Pseudomonic acid is a potent antibiotic produced by Pseudomonas fluorescens reported by Fuller et al. in 1971. Pseudomonic acid has broad spectrum activity against Gram positive bacteria and was approved... | |
| Reportedly more effectivethan A23187 as a Ca++ionophore. Highly specific ionophore useful in studying Ca2+ transportation. | |
| Reversible inhibitor of endoplasmic reticulum Ca2+ ATPase. Does not increase IP3 levels. Specific inhibitor of Ca2+- ATPase of sarcoplasmic reticulum, inhibiting the enzyme completely at 6-8 nmol/mg protein (at 0.5-2.0μM... | |
| Semi-synthetic antibiotic used for gene expression research utilizing carbenicillin-resist ant plasmids. | |
| Stable analog of Thalidomide with increased anti-tumor potency. | |
| Use for reporter gene assays, ATP assays, whole animal studies, DNA sequencing and others. Substrate for firefly luciferase. | |
| Use for reporter gene assays, ATP assays, whole animal studies, DNA sequencing and others. | |
| Used in cell activation experiments when calcium dose-response data are not required. Molar ratio Ca:Mg~1:1. Inquire for bulk pricing. Also available A23187 free acid & A23187 4-Bromo. |