Tricarboxylic acids and derivatives
![Alkali Scientific 4 Methylumbelliferyl B D glucopyranoside Monohydrate [Methylumbelliferyl B D glucoside], 250 Mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000660008.jpg-250.jpg)
Alkali Scientific 4 Methylumbelliferyl B D glucopyranoside Monohydrate [Methylumbelliferyl B D glucoside], 250 Mg
Methylumbelliferyl β-D Glucopyranoside Monohydrate, 250 mg is a high-purity biochemical reagent used to assess glucosidase enzyme activity. The reagent is cleaved by glucosidase enzymes to release a fluorescent product that can be quantified in enzyme assays, making it useful for studying enzyme kinetics and metabolic pathways. It is commonly used in microbiological research, clinical diagnostics, and enzymatic analysis to detect glucosidase activity. This substrate offers high sensitivity and accuracy, ensuring reliable results in applications requiring precise enzyme activity measurements, such as microbial testing, genetic research, and metabolic studies.
Medchemexpress LLC IACS-8803 diammonium | 98.8% | 50 MG
IACS-8803 diammonium is a highly potent cyclic dinucleotide STING agonist known for its robust systemic antitumor efficacy. It has demonstrated superior antitumor activity in in-vivo studies, specifically in mice bearing bilateral B16-OVA melanomas with a 10 μg intra-tumoral injection.
- Highly potent cyclic dinucleotide STING agonist
- Robust systemic antitumor efficacy
- Molecular weight: 726.60
- Molecular formula: C20H29FN12O9P2S2
- Appearance: Solid
- Color: White to off-white
Medchemexpress LLC diMal-O-CH2COOH | 1620837-47-9 | 96.8% | C13H12N2O7 | 5 MG
diMal-O-CH2COOH is a cleavable ADC linker, intended for research use only.
- Solid appearance, white to off-white color.
- Shipping at room temperature in continental US.
- Store at 4°C, protected from light and under nitrogen.
- In solvent, store at -80°C for 6 months or -20°C for 1 month, protected from light and under nitrogen.
- Relevant for cancer and cancer targeted therapy research.
eMolecules 60981-68-2 | Bis(diphenylphosphino)(isopropyl)amine | ChemScene427.468 | C27H27NP2 | 97.000 | CC(C)N(P(c1ccccc1)c1ccccc1)P(c1ccccc1)c1ccccc1 | 100mg | 694122838
Bis(diphenylphosphino)(isopropyl)amine | ChemScene | 60981-68-2427.468 | C27H27NP2 | 97.000 | CC(C)N(P(c1ccccc1)c1ccccc1)P(c1ccccc1)c1ccccc1 | 100mg | 694122838
eMolecules 467-62-9 | Tris(4-aminophenyl)methanol | Ambeed | MFCD00036222 | 305.381 | C19H19N3O | 95.000 | Nc1ccc(cc1)C(O)(c1ccc(N)cc1)c1ccc(N)cc1 | 1g | 603089382
Tris(4-aminophenyl)methanol | Ambeed | 467-62-9 | MFCD00036222 | 305.381 | C19H19N3O | 95.000 | Nc1ccc(cc1)C(O)(c1ccc(N)cc1)c1ccc(N)cc1 | 1g | 603089382
Apexbio Technology LLC Amfenac Sodium Monohydrate 61618-27-7 10mM (in 1mL DMSO)
Amfenac Sodium Monohydrate (CAS 61618-27-7) is a synthetic non-steroidal anti-inflammatory compound structurally characterized by an acetic acid moiety It functions by inhibiting cyclooxygenase (COX) enzymes consequently suppressing prostaglandin synthesis and mitigating inflammatory processes and pain signaling Amfenac Sodium Monohydrate is utilized in biomedical research to investigate inflammatory pathways and to evaluate non-steroidal analgesic drug effects in cellular and animal models of inflammation Its well-defined inhibitory mechanism makes it a valuable tool for elucidating COX-mediated physiological and pathological responses
![eMolecules 68-04-2 | Sodium citrate | Combi-Blocks | MFCD00012462 | 258.068 | C6H5Na3O7 | 98.000 | [Na+].[Na+].[Na+].OC(CC([O-])=O)(CC([O-])=O)C([O-])=O | 1kg | 290693721](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000129299.jpg-250.jpg)
eMolecules 68-04-2 | Sodium citrate | Combi-Blocks | MFCD00012462 | 258.068 | C6H5Na3O7 | 98.000 | [Na+].[Na+].[Na+].OC(CC([O-])=O)(CC([O-])=O)C([O-])=O | 1kg | 290693721
Sodium citrate | Combi-Blocks | 68-04-2 | MFCD00012462 | 258.068 | C6H5Na3O7 | 98.000 | [Na+].[Na+].[Na+].OC(CC([O-])=O)(CC([O-])=O)C([O-])=O | 1kg | 290693721