Monosaccharides
![eMolecules 64350-24-9 | N-Isobutyrylguanosine | Broadpharm353.335 | C14H19N5O6 | 0.000 | CC(C)C(=O)Nc1nc(=O)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2[nH]1 | 10g | 761707411](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502462420.JPG-250.jpg)
eMolecules 64350-24-9 | N-Isobutyrylguanosine | Broadpharm353.335 | C14H19N5O6 | 0.000 | CC(C)C(=O)Nc1nc(=O)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2[nH]1 | 10g | 761707411
N-Isobutyrylguanosine | Broadpharm | 64350-24-9353.335 | C14H19N5O6 | 0.000 | CC(C)C(=O)Nc1nc(=O)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2[nH]1 | 10g | 761707411
Cambridge Isotope Laboratories URIDINE (RIBOSE-1-13C, 99%), 0.05 G
URIDINE (RIBOSE-1-13C, 99%), 0.05 G
Sigma Aldrich Fine Chemicals Biosciences DL-Arabinose >=98% | 147-81-9 | MFCD00135867 | 10G
DL-Arabinose >=98% | Purity: >=98% | Mol Wt: 150.13 | 147-81-9 | MFCD00135867 | 10G
Sigma Aldrich Fine Chemicals Biosciences L-(+)-Arabinose natural sourced | 5328-37-0 | MFCD00135866 | 1KG
L-(+)-Arabinose natural sourced | Mol Wt: 150.13 | 5328-37-0 | MFCD00135866 | 1KG
Accela Chembio Inc 6-chloropurine Riboside | 5g | 5399-87-1 | MFCD00005738 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4
6-chloropurine Riboside | 5g | 5399-87-1 | MFCD00005738 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4
Bioworld 5-Fluorouridine, 250 mg
SpecificationsA proapoptotic and cytotoxic nucleoside analogSynonyms: 5-Fluorouracil 1β-D-ribofuranoside, FUrdShipped at ambient temperatureAppearance: SolidDensity : ~1.8 g/cm3 (Predicted)Melting Point: 182 °C
Sigma Aldrich Fine Chemicals Biosciences D-(-)-Ribose BioReagent, suitable for cell culture | 50-69-1 | MFCD00135453 | 100G
D-(-)-Ribose BioReagent, suitable for cell culture | Purity: >=99% (GC) | Mol Wt: 150.13 | 50-69-1 | MFCD00135453 | 100G
Chem-Impex International, Inc. Adenosine-3',5'-cyclic monophosphate monosodium salt | 37839-81-9 | MFCD00069736 | 1G
Adenosine-3',5'-cyclic monophosphate monosodium salt, 37839-81-9, MFCD00069736, 1G
Sigma Aldrich Fine Chemicals Biosciences L-(+)-Arabinose natural sourced | 5328-37-0 | MFCD00135866 |
L-(+)-Arabinose natural sourced | Mol Wt: 150.13 | 5328-37-0 | MFCD00135866 |
Apexbio Technology LLC D-Ribose 50-69-1 100mg
D-Ribose (CAS 50-69-1) is a naturally occurring pentose monosaccharide involved in the pentose phosphate pathway where it serves as a crucial substrate for the biosynthesis of nucleotides and nucleic acids By facilitating the regeneration of adenosine triphosphate (ATP) D-Ribose supports cellular energy metabolism particularly under conditions of increased energy demand or compromised ATP production Preclinical and clinical research including ongoing trials examining the effects of D-Ribose on exercise performance investigate its capacity to enhance cellular bioenergetics D-Ribose is widely utilized in studies related to metabolic function myocardial energy balance and recovery from exercise-induced fatigue
Medchemexpress LLC Sitagliptin (phosphate) | 654671-78-0 | 99.6% | 505.31 | 200 MG
Sitagliptin phosphate is an orally active and highly selective DPP4 inhibitor that blocks the degradation of glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic peptide (GIP), thereby increasing active incretin levels. This compound has demonstrated protective effects on pancreatic islet grafts in type 1 diabetes models and is useful for the study of both type 1 and type 2 diabetes.
- Orally active and highly selective DPP4 inhibitor
- Blocks degradation of glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic peptide (GIP)
- Increases active incretin levels
- Directly stimulates GLP-1 secretion by intestinal L cells via cAMP/PKA and ERK1/2 pathways
- Shows protective effects on pancreatic islet grafts in type 1 diabetes models
- Suitable for studying type 1 and type 2 diabetes
Apexbio Technology LLC DL-α-Hydroxyglutaric acid disodium salt 40951-21-1 25mg
DL- -Hydroxyglutaric acid disodium salt (CAS 40951-21-1) is a small molecule analogue of -hydroxyglutaric acid a metabolite implicated in neurometabolic disorders In humans aberrant accumulation of D- -hydroxyglutaric acid occurs in D-2-hydroxyglutaric aciduria associated with mutations in isocitrate dehydrogenase (IDH) enzymes particularly IDH1 and IDH2 These mutations alter normal metabolic flux leading to overproduction of D- -hydroxyglutaric acid from 2-oxoglutarate In preclinical studies elevated levels of this metabolite are detectable in IDH1-mutant glioma models and non-invasive quantification is feasible via magnetic resonance spectroscopy DL- -Hydroxyglutaric acid disodium salt is utilized in research investigating metabolic dysregulation biomarker development and disease mechanisms linked to IDH mutations and gliomagenesis
Medchemexpress LLC Pemetrexed disodium hemipenta hydrate | 357166-30-4 | 99.78% | 1 ML
Pemetrexed disodium hemipenta hydrate is a CNS-penetrant antifolate. Its pentaglutamate form inhibits thymidylate synthase (TS) with a Ki value of 1.3 nM, dihydrofolate reductase (DHFR) with a Ki value of 7.2 nM, and glycinamide ribonucleotide formyltransferase (GARFT) with a Ki value of 65 nM. Its antitumor activity may stem from simultaneous and multiple inhibition of several key folate-requiring enzymes via its polyglutamated metabolites. It is a novel classical antifolate.
- CNS-penetrant antifolate
- Inhibits thymidylate synthase (TS), dihydrofolate reductase (DHFR), and glycinamide ribonucleotide formyltransferase (GARFT)
- Potential antitumor activity through polyglutamated metabolites
- Soluble at 10 mM in water
AdipoGen BQC
Chemical. CAS 207124-63-8. Formula C20H10K2N2O4 . 3H2O. MW 474.55. 2,2´-Biquinoline-4,4´-dicarboxylic acid dipotassium salt BQC is a water soluble biquinoline-based ligand. The oxidation of alcohols to the corresponding aldehydes and ketones, which can be performed by a variety of methods, remains one of the most important reactions in organic synthesis. BOC is used in the aerobic oxidation of alcohols primary, secondary and benzylic in the presence of palladium catalysts. The catalytic system composed of CuCl2 and BQC was found to be highly efficient for the selective oxidation of secondary benzylic, allylic and propargylic alcohols to the corresponding ketones, with aqueous t-butyl hydroperoxide under phase-transfer catalysis conditions. The catalytic system is stable and can be recycled and reused several times without loss of activity.