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Filtered Search Results
Medchemexpress LLC 2-nitro-5-methylbenzoic acid | 3113-72-2 | MFCD00007368 | 99.9% | 181.15 g/mol | C8H7NO4 | 100 G
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5-Methyl-2-nitrobenzoic acid (2-nitro-5-methylbenzoic acid) is an aromatic carboxylic acid used as a biochemical reagent and as a building block in organic synthesis. Supplied as a solid, it is suitable for research, analytical standards, and intermediate synthesis in medicinal chemistry and analytical workflows.
- High purity: 99.90%
- Molecular weight: 181.15 g/mol
- Chemical formula: C8H7NO4
- Appearance: white to light yellow solid
- Soluble in DMSO (100 mg/mL; may require sonication)
- Storage: powder at -20°C (3 years) or 4°C (2 years)
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Medchemexpress LLC Exatecan intermediate 13 | 127452-30-6 | 98% | C19H26N2O6 | 250 MG
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Exatecan intermediate 13 is an analytical standard of Ethyl 2-(6-(acetamidomethyl)-5-oxo-2,3-dihydro-5H-spiro[indolizine-1,2'-dioxolan]-7-yl)butanoate. This product is intended for research and analytical applications, including qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS. It is an impurity of Exatecan.
- Used as an analytical standard (reference standard supplied assay)
- Suitable for HPLC, GC, and MS applications
- Intended for research and analytical applications
- Impurity of Exatecan
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Aobchem Methyl 3-propylbenzoate | 97% | CAS 81631-62-1 | C11H14O2 | 250mg
Methyl 3-propylbenzoate | 97% | CAS 81631-62-1 | C11H14O2 | 250mg
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Medchemexpress LLC Ethyl acetylglycinate | 1906-82-7 | MFCD00009173 | >98.0% | 145.16 g/mol | C6H11NO3 | 25 G
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Ethyl acetylglycinate is N-acetylglycine ethyl ester (CAS 1906-82-7), a glycine derivative used as an intermediate in peptide and fine-chemical synthesis and as a research reagent. It is supplied as a white to off-white solid in laboratory-scale quantities for synthetic and analytical applications.
- N-acetyl-protected glycine derivative suitable for peptide synthesis and coupling
- High purity (>98%) as supplied for research use
- White to off-white solid, stable under recommended storage conditions
- Available in small pack sizes convenient for laboratory work
- Versatile building block for pharmaceutical and biochemical research
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Medchemexpress LLC Anti-B7-H4 VTCN1 Ant 10mg | 10mg
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Anti-B7-H4/VTCN1 Antibody is a CHO-expressed human antibody that targets B7-H4/VTCN1 The Anti-B7-H4/VTCN1 Antibody contains a huIgG1 heavy chain and a hu light chain with a predicted molecular weight (MW) of 145 kDa The isotype control for Anti-B7-H4/VTCN1 Antibody can be referenced as Human IgG1 kappa Isotype Control (HY-P99001)
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Medchemexpress LLC N-Carbamoyl-DL-aspartic acid | 923-37-5 | 1 G
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N-Carbamoyl-DL-aspartic acid, also known as Ureidosuccinic acid, is a precursor of nucleic acid pyrimidines. It has demonstrated antitumor activities and is considered an endogenous metabolite, playing a role in metabolic enzyme/protease pathways.
- Precursor of nucleic acid pyrimidines
- Exhibits antitumor activities
- Effective in murine Lewis lung carcinoma models
- Reverses toxicity and antitumor activity of N-(phosphonacetyl)-L-aspartate
- Functions as a precursor of nucleic acid pyrimidines in normal and tumor-bearing mice
- Soluble in DMSO for in vitro studies
- Can be formulated for in vivo studies using various solvent systems
- Recommended storage for powder is -20°C for 3 years or 4°C for 2 years
- Recommended storage in solvent is -80°C for 2 years or -20°C for 1 year
- For research use only
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Medchemexpress LLC UC2288 | 1394011-91-6 | 99.8% | 481.82 | 250 MG
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UC2288 is a potent and orally active p21 attenuator with relatively selective activity for p21. It is synthesized based on Sorafenib and potently inhibits cancer cell growth by inducing apoptosis. UC2288 shows no inhibition of VEGFR2 and Raf kinases even at 10 μM.
- Potent and orally active p21 attenuator
- Induces apoptosis to inhibit cancer cell growth
- Relatively selective activity for p21
- No inhibition of VEGFR2 and Raf kinases at 10 μM
- Decreases p21 protein level and mRNA expression
- Suppresses tumor growth in vivo
- Ameliorates MPTP-induced Parkinson's disease progression
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![Medchemexpress LLC Pyrimido[4,5-d]pyrimidin-2(1H)-one, 7-[[2-methoxy-4-(1-methyl-4-piperidinyl)phenyl]amino]- | 1936529-65-5 | 99.8% | 600.11 | C32H34ClN7O3 | 250 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000211456.png-250.jpg)
Medchemexpress LLC Pyrimido[4,5-d]pyrimidin-2(1H)-one, 7-[[2-methoxy-4-(1-methyl-4-piperidinyl)phenyl]amino]- | 1936529-65-5 | 99.8% | 600.11 | C32H34ClN7O3 | 250 MG
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YKL-05-099 is a small-molecule salt-inducible kinase (SIK) inhibitor used as a research tool in biochemical and cell-based studies. It exhibits high potency for SIK1 and SIK3, with reported IC50 values in the low nanomolar range, and is applied for kinase assays, signaling investigations, and target validation. The compound has a molecular weight of 600.11 and a reported purity of 99.76%.
- Potent inhibition of SIK1 and SIK3 (IC50 ≈ 10 and 30 nM, respectively).
- Moderate activity against SIK2 (IC50 ≈ 40 nM).
- High chemical purity (99.76%).
- Suitable for biochemical kinase assays and cell-based signaling studies.
- Provided as a solid research compound for laboratory use.
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Medchemexpress LLC TCO-PNB ester | 1438415-89-4 | 98.5% | C15H17NO5 | 25 MG
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TCO-PNB ester is an amine-reactive building block used for the modification of amine-containing molecules. It contains a TCO group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing a Tetrazine group.
- Amine-reactive building block for modification of amine-containing molecules.
- The TCO group allows for iEDDA reaction with Tetrazine-containing molecules.
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Accela Chembio Inc Ethyl 4-pyrimidinecarboxylate | 1g | 62846-82-6 | MFCD09832999 | 97+% | Shelf Life: 1440 Days | Light Sensitive
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Ethyl 4-pyrimidinecarboxylate | 1g | 62846-82-6 | MFCD09832999 | 97+% | Shelf Life: 1440 Days | Light Sensitive
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Medchemexpress LLC Ethyl β-carboline-3-carboxylate | 74214-62-3 | MFCD00009730 | 99.8% | C14H12N2O2 | 10MG
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Ethyl β-carboline-3-carboxylate is a β-carboline derivative that functions as a ligand and short-acting antagonist at benzodiazepine receptors. It is used in preclinical research to probe benzodiazepine receptor pharmacology and to study interactions with diazepam, including modulation of cerebellar cGMP levels.
- Ligand and short-acting antagonist of benzodiazepine receptors.
- Useful for preclinical studies of benzodiazepine pharmacology and receptor modulation.
- Demonstrated interaction with diazepam affecting cerebellar cGMP levels.
- High purity (99.75%) suitable for research applications.
- Solid, off-white to light yellow appearance for easy handling.
- Storage: sealed and away from moisture; in solvent store at -80°C up to 6 months or -20°C up to 1 month.
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Medchemexpress LLC Hydroxypropyl tetrahydropyrantriol | 439685-79-7 | 98.0% | 192.21 g·mol⁻¹ | C8H16O5 | 250 MG
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Pro-xylane (30% in water) is an aqueous formulation of hydroxypropyl tetrahydropyrantriol used as a cosmetic active to support skin matrix remodeling. It promotes glycosaminoglycan biosynthesis in fibroblasts, enhances dermal collagen and hyaluronic acid production, and is intended for formulation and research use.
- Stimulates glycosaminoglycan synthesis in fibroblasts
- Enhances collagen and hyaluronic acid production in the dermis
- Improves skin hydration and elasticity
- Reduces appearance of wrinkles and supports skin firmness
- Supplied as a 30% aqueous solution with high purity
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eMolecules 1912399-75-7 | Omilancor | Ambeed528.576 | C30H24N8O2 | 98.000 | O=C(N1CCN(CC1)C(=O)c1cccc(n1)-c1nc2ccccc2[nH]1)c1cccc(n1)-c1nc2ccccc2[nH]1 | 250mg | 837386387
Omilancor | Ambeed | 1912399-75-7528.576 | C30H24N8O2 | 98.000 | O=C(N1CCN(CC1)C(=O)c1cccc(n1)-c1nc2ccccc2[nH]1)c1cccc(n1)-c1nc2ccccc2[nH]1 | 250mg | 837386387
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Medchemexpress LLC ZT-1a | 212135-62-1 | 99.8% | 445.73 | 250 MG
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ZT-1a is a potent, non-ATP-competitive, and selective SPAK inhibitor. It inhibits SPAK activity and decreases SPS1-related proline/alanine-rich kinase (SPAK)-dependent phosphorylation, thereby inhibiting Na-K-2Cl cotransporter (NKCC1) and stimulating K-Cl cotransporters (KCCs).
- Potent, non-ATP-competitive, and selective SPAK inhibitor
- Inhibits Na-K-2Cl cotransporter (NKCC1) activity
- Stimulates K-Cl cotransporters (KCCs) activity
- Inhibits SPAK-dependent cation-Cl cotransporters (CCC) phosphorylation in vivo
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Medchemexpress LLC Pyrimidine-4-carboxylic acid | 31462-59-6 | 124.10 | 10 G
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Pyrimidine-4-carboxylic acid is a biochemical reagent suitable for diverse life science research. It functions as both a biological material and an organic compound, and is also an important synthetic intermediate in pharmaceutical synthesis.
- Biological material
- Organic compound
- Useful for life science related research
- Synthetic intermediate for pharmaceutical synthesis
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