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Filtered Search Results
eMolecules 39070-63-8 | (3,4-Diaminophenyl)(phenyl)methanone | Oakwood Chemical | MFCD00007727 | 212.252 | C13H12N2O | 97.000 | Nc1ccc(cc1N)C(=O)c1ccccc1 | 5g | 537719186
(3,4-Diaminophenyl)(phenyl)methanone | Oakwood Chemical | 39070-63-8 | MFCD00007727 | 212.252 | C13H12N2O | 97.000 | Nc1ccc(cc1N)C(=O)c1ccccc1 | 5g | 537719186
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Medchemexpress LLC HY-N7080 100mg Medchemexpress, Dihydroferulic acid CAS:1135-23-5 Purity:>98%
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Medchemexpress, HY-N7080 100mg Dihydroferulic acid CAS:1135-23-5 Dihydroferulic acid (Hydroferulic acid) is one of the main metabolites of curcumin and antioxidant/radical-scavenging properties with an IC50 value of 19.5 μM. Dihydroferulic acid is a metabolite of human gut microflora as well as a precursor of vanillic acid. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 933755-97-6 | 1-Ethynylcyclopropanecarboxylic acid | MFCD19231569 | 100mg
Ambeed | 1-Ethynylcyclopropanecarboxylic acid | 100mg | 490558615 | A379110 | 933755-97-6 | MFCD19231569 | 110.112 | C6H6O2
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Medchemexpress LLC JAK-IN-5 hydrochloride | 2751323-21-2 | 99.5% | 511.03 | 50 MG
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JAK-IN-5 hydrochloride is an inhibitor of JAK, extracted from patent US20170121327A1. It is intended for research use only.
- Inhibits JAK.
- Inhibits STAT6 phosphorylation by 60% in IL-13-induced lung tissue in a mouse model of pSTAT6 induction at 0.5 mg/mL (oral aspirate, 50 μL).
- Inhibits 88% of BALF eosinophils in a male C57 mice model of Alternaria alternata-induced eosinophilic inflammation of the lung at 0.1-1.0 mg/mL (oral aspirate, 50 μL).
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Medchemexpress LLC HY-N0700 1g Medchemexpress, alpha-Asarone CAS:2883-98-9 Purity:>98%
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Medchemexpress, HY-N0700 1g alpha-Asarone CAS:2883-98-9 alpha-Asarone (α-Asarone) is one of the main psychoactive compounds, and possesses an antidepressant-like activity in mice. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 133229-11-5 | Medchem Express | AM-92016 (hydrochloride) | 5mg | 482203787 | HY-101253 | MFCD00673947 | 483.83 | C19H25Cl3N2O4S
Medchem Express | ML401 | 5mg | 495799946 | HY-116814 | 1597489-14-9 | 419.750 | C20H20BrClN2O
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![eMolecules 100286-90-6 | Irinotecan HCl | Broadpharm590.721 | C33H42N4O6 | 0.000 | CCc1c2CN3C(CC4C(COC(=O)[C@]4(O)CC)C3=O)c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 100mg | 724438162](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502461873.JPG-250.jpg)
eMolecules 100286-90-6 | Irinotecan HCl | Broadpharm590.721 | C33H42N4O6 | 0.000 | CCc1c2CN3C(CC4C(COC(=O)[C@]4(O)CC)C3=O)c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 100mg | 724438162
Irinotecan HCl | Broadpharm | 100286-90-6590.721 | C33H42N4O6 | 0.000 | CCc1c2CN3C(CC4C(COC(=O)[C@]4(O)CC)C3=O)c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 100mg | 724438162
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Selleck Chemical LLC JNJ0966
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JNJ0966 is a highly selective compound that inhibits activation of MMP-9 zymogen and subsequent generation of catalytically active enzyme It has no effect on MMP-1 MMP-2 MMP-3 MMP-9 or MMP-14 catalytic activity and did not inhibit activation of the highly related MMP-2 zymogen
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Apexbio Technology LLC Phenoxybenzamine HCl 63-92-3 10mM (in 1mL DMSO)
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Phenoxybenzamine HCl (CAS number 63-92-3) is an irreversible nonselective antagonist of alpha-adrenergic receptors It covalently binds to these receptors producing sustained blockage and therefore preventing receptor-mediated vasoconstriction Due to this prolonged alpha-receptor antagonism phenoxybenzamine hydrochloride is frequently utilized in biomedical research to study sympathetic nervous system functions receptor pharmacology and cardiovascular-related pathophysiology
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Medchemexpress LLC Mal-VC-PAB-DM1 | 1464051-44-2 | MFCD10039825 | 99.4% | 1248.81 g/mol | C61H82ClN9O17 | 5 MG
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Mal-VC-PAB-DM1 is a drug-linker conjugate used in the construction of antibody-drug conjugates (ADCs). It links the cytotoxic payload DM1 to a cleavable valine-citrulline-p-aminobenzyl (vc-pab) linker to enable targeted delivery of the payload in ADC research. The compound is supplied as a high-purity material and is soluble in DMSO for research applications.
- Drug-linker conjugate for ADC research
- Contains DM1 microtubule-disrupting payload
- Cleavable valine-citrulline-p-aminobenzyl (vc-pab) linker
- High purity (99.4%)
- Molecular weight 1248.81 g/mol
- Soluble in DMSO
- CAS number 1464051-44-2
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Medchemexpress LLC Zanubrutinib | 1691249-45-2 | MFCD31567461 | 471.55 | C27H29N5O3 | 25 MG
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Zanubrutinib is a selective, irreversible small-molecule inhibitor of Bruton tyrosine kinase (BTK) used in research to study BTK signaling and pharmacology. The compound shows high biochemical potency and is supplied as a solid reagent suitable for analytical, biochemical, and cellular studies. This catalog item is provided for research use only.
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Medchemexpress LLC 1,4-dimethoxybenzene-d10 | 74079-00-8 | 98.0% | 148.23 g/mol | C8D10O2 | 25 MG
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1,4-Dimethoxybenzene-d10 is the deuterium-labeled form of 1,4-dimethoxybenzene used as an analytical standard and tracer in research. It is employed as an internal standard for NMR, GC-MS, and LC-MS applications, and in metabolic and aromatic profiling studies. The compound has formula C8D10O2 and high isotopic enrichment (about 98 atom % D).
- Deuterium-labeled internal standard for NMR, GC-MS, and LC-MS
- High isotopic enrichment for reliable quantitation
- Suitable tracer for metabolic and aromatic profiling studies
- Stable solid form for convenient storage and handling
- Compatible with common analytical solvents and methods
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Medchemexpress LLC Rg-12525 | 120128-20-3 | 98.3% | 423.47 g/mol | C25H21N5O2 | 50 MG
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RG-12525 (NID 525) is a small-molecule research compound that antagonizes peptidoleukotriene receptors (LTC4, LTD4, LTE4), exhibits PPAR-γ agonist activity, and inhibits cytochrome P450 enzymes. It is provided in high-purity solid form and as a DMSO solution for biochemical and pharmacological research, supporting both in vitro and in vivo investigations.
- Potent leukotriene receptor antagonist with low-nanomolar activity.
- Shows PPAR-γ agonist activity (≈60 nM).
- Inhibits CYP3A4 (Ki ≈0.5 μM), useful for metabolism studies.
- Available as solid and DMSO solution for flexible dosing.
- High purity suitable for biochemical and pharmacological assays.
- Applicable to in vitro and in vivo pharmacology research.
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Medchemexpress LLC Trimetazidine-d8 dihydrochloride | 1219795-37-5 | 99.9% | 1 MG
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Trimetazidine-d8 dihydrochloride is a deuterium labeled compound that acts as a selective long chain 3-ketoyl coenzyme A thiolase inhibitor with an IC50 of 75 nM, inhibiting β-oxidation of free fatty acid (FFA). It is an effective antianginal and cytoprotective agent, possessing anti-oxidant, anti-inflammatory, antinociceptive, and gastroprotective properties. It also triggers autophagy and is a 3-hydroxyacyl-CoA dehydrogenase (HADHA) inhibitor.
- Can be used as a tracer
- Internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- Stable isotope-labeled compound with deuterium incorporated
- Affects pharmacokinetic and metabolic profiles
- For research use only
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Medchemexpress LLC 7-Prenyloxycoumarin | 10387-50-5 | 5 MG
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7-Prenyloxycoumarin, also known as 7-O-Prenylumbelliferone, is a secondary metabolite. It is derived from the endophytic fungus of *Annulohypoxylon ilanense*. This compound is supplied as a white to off-white solid with a molecular weight of 230.26 and a formula of C14H14O3. It demonstrates varying levels of cytotoxicity against several human cancer cell lines, including BT-549 and LoVo, with IC50 values of 37 μM and 30 μM respectively, while showing higher IC50 values (>100 μM) against A549, PC-3, SK-MEL-28, and U-373MG ATCC cell lines. 7-Prenyloxycoumarin is intended for research use only.
- Derived from natural sources
- Exhibits antiproliferative activity against certain cancer cell lines
- Provided as a high-purity solid (99.87%)
- Available in various quantities for research needs
- Detailed solubility and storage information provided
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