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Nitrogenous bases covalently linked to a sugar with and without phosphate groups; used for synthesis, cell signaling, and as cofactors in enzymatic reactions; includes pyrimidine, purine, pyridine, flavin, pyrrolopyrimidine, and triazole varieties.
LDE225 Diphosphate (CAS 1218778-77-8) is a highly potent and selective antagonist of the Smoothened (Smo) receptor a seven-transmembrane protein involved in the Hedgehog (Hh) signaling pathway LDE225 inhibits Smo with IC50 values of 1 3 nM for murine and 2 5 nM for human Smo resulting in suppression of Hh signaling This pathway is implicated in cellular differentiation proliferation and oncogenesis In vitro LDE225 selectively binds Smo inhibiting Hh-dependent tumor cell growth In vivo it demonstrates dose-dependent antitumor efficacy in medulloblastoma xenograft mouse models LDE225 continues to be explored as a research tool and therapeutic candidate in Hh pathway-driven malignancies
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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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L-Adenosine is the L-enantiomer of adenosine, a metabolically stable nucleoside analog used as a research probe. It exhibits weak inhibitory activity against adenosine deaminase (ADA) and is used to study adenosine uptake and accumulation.
CAS number 3080-29-3.
Molecular formula C10H13N5O4; molecular weight 267.25.
Purity 99.82% (typical).
Physical form solid, white to off-white.
Storage: 4°C, protect from light; in solvent -80°C for 6 months, -20°C for 1 month.
Reported Ki for ADA: 385 μM.
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L-Adenosine is an enantiomeric nucleoside used as a biochemical probe for adenosine uptake and metabolism. It displays weak adenosine deaminase (ADA) inhibitory activity and is supplied in high-purity forms for laboratory research.
High purity (≈99.8%).
Molecular weight 267.25 g/mol.
CAS number 3080-29-3.
Available as solid and 10 mM DMSO solution formats.
Suitable for biochemical, uptake, and metabolism studies.
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Adenosine monophosphate (AMP) is an adenosine A1 receptor agonist and a key cellular metabolite involved in regulating energy homeostasis and signal transduction. It demonstrates significant antiviral activity against HSV-1 and HSV-2.
Acts as an adenosine A1 receptor agonist
Demonstrates significant antiviral activity against HSV-1 and HSV-2
Functions as a key cellular metabolite regulating energy homeostasis and signal transduction
Shows negligible cell toxicity at 25 to 400 μM in RAW264.7 cells
Significantly attenuates mRNA expression of TNF-α and IL-6 in RAW264.7 cells
Reduces recruitment of NF-κB p65 to TNF-α, IL-6, and IL-1β gene promoters
Increases hepatic adenosine levels in C57BL/6J mice
Improves survival rate and lowers serum AST and ALT levels in treated mice
Attenuates necrosis and reduces infiltration of inflammatory cells in vivo
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L-Guanosine is the L-configuration of Guanosine, a purine nucleoside with anti-herpesvirus activity. It can be utilized in the preparation of supramolecular hydrogel.
L-configuration of guanosine
Purine nucleoside with anti-herpesvirus activity
Utilized in the preparation of supramolecular hydrogel
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Adenosine receptor antagonist 3 is a small-molecule research compound that antagonizes adenosine receptors and is used in in vitro pharmacology and GPCR/G protein signaling studies. Supplied as a light-yellow solid and as a 10 mM solution in DMSO, it has a reported purity of 97.1% and molecular formula C16H14N6S.
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