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Two-carbon nitrogen ring bases (adenine and guanine) covalently linked to a sugar (ribose or deoxyribose) and one to three phosphate groups; can function as extracellular messengers, antimetabolites, and chain terminators that inhibit viral DNA polymerase.
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Motesanib diphosphate is a small-molecule, ATP-competitive inhibitor of vascular endothelial growth factor receptors VEGFR1, VEGFR2, and VEGFR3 that also inhibits Kit. The diphosphate salt is supplied for research and analytical applications.
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Coenzyme A (CoA, CoASH, HSCoA) is a coenzyme that facilitates enzymatic acyl-group transfer reactions and supports the synthesis and oxidation of fatty acids. CoA is involved in the mechanisms of a wide variety of enzymes.
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Exists as a 557AkDa hexadecamer composed of eight heavy chains each with a molecular weight of approximately 56AkDa and eight light chains of molecular weight 14AkDa. Each molecule contains one magnesium ion. pH optimum ~7.9. KM for CO2 ~0.45 mM. Ribulose diphosphate becomes inhibitory at concentrations exceeding 0.7 mM. Orthophosphate and ammonium sulfate are competitive inhibitors. 3-Phosphoglycerate is a noncompetitive inhibitor.
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MW 392.15 Da, Purity >95%. Potent, specific adenosine kinase inhibitor (IC₅₀ = 26 nM). Inhibits platelet aggregation and spreading, and interferes with adenosine and adenine nucleotide metabolism. Additionally inhibits other kinases such as ERK2 (Ki = 525 nM).
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Motesanib diphosphate is the diphosphate salt of a small-molecule ATP-competitive inhibitor of vascular endothelial growth factor receptors (VEGFR1/2/3). It is supplied as a research-grade analytical standard for biochemical assays, pathway studies, and method development. The compound should be stored sealed and protected from moisture; in solvent, stability is -80°C for up to six months and -20°C for up to one month.
High purity (~99.9%).
Potent VEGFR1/2/3 inhibition with IC50s 2-6 nM.
Molecular formula C22H29N5O9P2, molecular weight 569.44 g/mol.
Suitable for biochemical assays and analytical method development.
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Inosine 5'-diphosphate sodium is a purine ribonucleoside 5'-diphosphate that features inosine as its nucleobase. This compound is known for its role in intracellular energy metabolism and signal transduction processes.
A purine ribonucleoside 5'-diphosphate
Inosine is the nucleobase
Participates in intracellular energy metabolism
Involved in signal transduction processes
Relevant to respiratory disease research
Applicable to metabolic or endocrine disease studies
Used in pulmonary disease research
Investigated in lung fibrosis studies
Can be classified as an oligonucleotide
Functions as a nucleotide analog
Related to inosine compounds
Identified as a nucleoside
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Inosine 5'-diphosphate sodium is a purine ribonucleoside 5'-diphosphate with inosine as the nucleobase. It participates in intracellular energy metabolism and signal transduction processes.
Purine ribonucleoside 5'-diphosphate
Contains inosine as the nucleobase
Participates in intracellular energy metabolism
Involved in signal transduction processes
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Sonidegib diphosphate is the diphosphate salt of sonidegib, a potent and selective Smoothened (Smo) antagonist used in research to inhibit Hedgehog pathway signaling. It shows low-nanomolar binding potency in Smo assays and is supplied for laboratory use with supporting datasheet and safety documents.
Potent Smo antagonist with low-nanomolar binding (mouse 1.3 nM; human 2.5 nM).
Diphosphate salt form suitable for aqueous assay conditions.
Supplied as a 10 mg vial for research use.
Molecular weight 681.49 g·mol^-1; formula C26H32F3N3O11P2.
Storage: sealed, away from moisture; in solvent: -80°C (6 months), -20°C (1 month).
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Also available in 5 mg 10 mg 25 mg 50 mg 200 mg 500 mg and bulk. Please contact Fisher for quotes. Guanosine 5'-diphosphate (GDP) as Potential Iron Mobilizer Preventing the Hepcidin-Ferroportin Interaction and Modulating the Interleukin-6/Stat-3 Pathway. purity: 98%
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3AE-phosphoadenosine 5AE-phosphate (PAP) a 3AE-phosphorylated nucleotide is found in almost all organisms and is obtained as a by-product of sulfur and lipid metabolism.
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Motesanib Diphosphate (AMG-706 CAS 857876-30-3) is an oral small-molecule ATP-competitive inhibitor that targets vascular endothelial growth factor receptors (VEGFR1/2/3) platelet-derived growth factor receptor (PDGFR) c-Kit and Ret with reported IC50 values of 2 84 nM It demonstrates over 1000-fold selectivity for VEGFRs relative to EGFR Src and p38 kinases In vitro Motesanib Diphosphate potently inhibits VEGF-induced proliferation of human endothelial cells (IC50 10 nM) and blocks PDGF- and SCF-induced signaling while showing minimal effects on bFGF-stimulated proliferation In preclinical studies it suppresses angiogenesis and induces regression in tumor xenograft models Motesanib is under investigation in anti-angiogenic cancer research
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Coenzyme A (CoA, CoASH, HSCoA) is a coenzyme that facilitates enzymatic acyl-group transfer reactions and supports the synthesis and oxidation of fatty acids. CoA is involved in the mechanisms of a wide variety of enzymes.
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