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Filtered Search Results
Medchemexpress LLC 5-amino-1,3,4-thiadiazole-2-sulfonamide | 14949-00-9 | 98.0% | 180.21 g·mol⁻¹ | C2H4N4O2S2 | 5 MG
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CL 5343 (5-amino-1,3,4-thiadiazole-2-sulfonamide) is a small-molecule inhibitor of carbonic anhydrases, selectively inhibiting human carbonic anhydrase B (HCA-B) and isoforms I, II, IV, and VII. It is supplied for research use to support biochemical assays and early drug discovery studies involving carbonic anhydrase pathways.
- selective carbonic anhydrase inhibition profile
- documented molecular formula and molecular weight for assay planning
- available in small research pack sizes for assay development
- soluble in common solvents for stock solution preparation
- intended for research use only; not for therapeutic use
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Medchemexpress LLC 1-Undecanol (Undecyl alcohol) | 112-42-5 | 172.31 | 500 G
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1-Undecanol, also known as Undecyl alcohol, is a metabolite primarily generated from the degradation of 2-tridecanone by Pseudomonas bacteria found in soil. This compound has demonstrated the ability to enhance the attraction of Grapholita molesta to sex pheromone traps.
- Main product of 2-tridecanone degradation by Pseudomonas bacteria
- Enhances attraction of Grapholita molesta to sex pheromone traps
- Acts as a synergist for Grapholita molesta sex pheromone
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Medchemexpress LLC KY-556 | 110816-78-9 | 725.57 | 100 MG
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KY-556 is a promising and orally-active pro-agent of disodium cromoglycate (DSCG) against allergic diseases.
- Orally-active pro-agent of disodium cromoglycate (DSCG) against allergic diseases.
- Inhibits dose-dependently the 48-hr homologous passive cutaneous anaphylaxis (PCA) in rats.
- Longer duration of action than intravenous disodium cromoglycate (DSCG).
- Tends to inhibit histamine release from actively sensitized rat lung fragments.
- Shows prolongation of survival time in rat systemic anaphylaxis.
- Significantly inhibits increased airway resistance in experimental asthma in rats.
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Medchemexpress LLC 1-Undecanol | 112-42-5 | 172.31 | 1 G
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1-Undecanol, also known as Undecyl alcohol, is primarily formed from the degradation of 2-tridecanone by Pseudomonas bacteria. This compound has been observed to enhance the attraction of *Grapholita molesta* to sex pheromone traps, acting as a synergist.
- Main product from bacterial degradation of 2-tridecanone
- Enhances attraction to sex pheromone traps
- Acts as a synergist for *Grapholita molesta* sex pheromone
- Appearance is solid below 11°C and liquid above 11°C
- Colorless to light yellow
- Soluble in DMSO
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Medchemexpress LLC 1-Pentadecanol | 629-76-5 | MFCD00004759 | 228.41 | 25 G
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1-Pentadecanol is a long-chain fatty alcohol that can be used in skin care products due to its anti-comedone, moisturizing, and hydrating properties. It is also suitable for the production of surfactants, emulsifiers, and lubricants.
- Anti-comedone activity
- Moisturizing and hydrating properties
- Suitable for skin care applications
- Can be used in surfactants, emulsifiers, and lubricants
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eMolecules Ambeed / 1-(2-(Hydroxymethyl)phenyl)ethanol / 250mg / 714085116 / A276443 / / 57259-71-9 / MFCD07776856 / 152.193 / C9H12O2
Ambeed / 1-(2-(Hydroxymethyl)phenyl)ethanol / 250mg / 714085116 / A276443 / / 57259-71-9 / MFCD07776856 / 152.193 / C9H12O2
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eMolecules TRANS-4-(DIBENZYLAMINO)CYCLOHEXANOL | 149506-81-0 | MFCD22124591 | 1g
AstaTech | TRANS-4-(DIBENZYLAMINO)CYCLOHEXANOL | 1g | 482916407 | C11561 | 98.000 | 149506-81-0 | MFCD22124591 | 295.426 | C20H25NO
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![Medchemexpress LLC 3,5-bis(trifluoromethyl)benzyl azabicyclo[3.1.0]hexane carboxylate | 2162961-71-7 | ≥98.0% | 527.4 | C23H19F6N5O3 | 25MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000235851.png-250.jpg)
Medchemexpress LLC 3,5-bis(trifluoromethyl)benzyl azabicyclo[3.1.0]hexane carboxylate | 2162961-71-7 | ≥98.0% | 527.4 | C23H19F6N5O3 | 25MG
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BI-2545 is a small-molecule chemical probe developed for research that potently inhibits autotaxin (ATX) and is suitable for both in vitro and in vivo studies. It demonstrates single-digit nanomolar biochemical potency against ATX and has been shown to lower plasma lysophosphatidic acid (LPA) levels following oral dosing in rodents.
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eMolecules JW PharmLab LLC / 4-Benzyloxy-2-methyl-phenylamine / 250mg / 716242136 / 20R2476 / 97.000 / 4792-60-3 / MFCD08686869 / 213.280 / C14H15NO
JW PharmLab LLC / 4-Benzyloxy-2-methyl-phenylamine / 250mg / 716242136 / 20R2476 / 97.000 / 4792-60-3 / MFCD08686869 / 213.280 / C14H15NO
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Medchemexpress LLC Pkr-in-c51 (compound 51) | 1314594-23-4 | 99.8% | 367.45 g/mol | C23H21N5 | 25 MG
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PKR-IN-C51 (compound 51) is an ATP-competitive inhibitor of double-stranded RNA-activated protein kinase (PKR) that suppresses intracellular PKR activation in primary mouse macrophages. It has an IC50 of 9 μM and is supplied as a solid or as a DMSO solution for research use only.
- ATP-competitive PKR inhibitor; IC50 9 μM.
- Molecular weight 367.45 g/mol; formula C23H21N5.
- High purity (≈99.8%).
- Available as solid (25 MG) and as 10 mM solution in DMSO.
- Storage: solid at 4°C protected from light; in solvent store at -80°C (6 months) or -20°C (1 month).
- For research use only; not for human or clinical use.
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eMolecules AstaTech / 1-(5-BENZOFURANYL)-ETHANONE / 0.1g / 696739635 / 73876 / 95.000 / 190775-71-4 / MFCD12406299 / 160.172 / C10H8O2
AstaTech / 1-(5-BENZOFURANYL)-ETHANONE / 0.1g / 696739635 / 73876 / 95.000 / 190775-71-4 / MFCD12406299 / 160.172 / C10H8O2
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eMolecules AstaTech / 3-METHYLPHTHALIC ANHYDRIDE / 1g / 277518242 / 35862 / 95.000 / 4792-30-7 / MFCD00047316 / 162.144 / C9H6O3
AstaTech / 3-METHYLPHTHALIC ANHYDRIDE / 1g / 277518242 / 35862 / 95.000 / 4792-30-7 / MFCD00047316 / 162.144 / C9H6O3
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eMolecules Ambeed / But-3-en-1-ol / 1g / 490556995 / A355895 / / 627-27-0 / MFCD00002959 / 72.107 / C4H8O
Ambeed / But-3-en-1-ol / 1g / 490556995 / A355895 / / 627-27-0 / MFCD00002959 / 72.107 / C4H8O
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Medchemexpress LLC Luxeptinib | 1616428-23-9 | 99.0% | C25H17F4N5O2 | 10MG
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Luxeptinib is an orally active, reversible, non-covalent small-molecule inhibitor that targets FLT3 and BTK signaling pathways. Provided for research use, it inhibits downstream phosphorylation events (including STAT5, AKT, and ERK1/2), induces cell-cycle arrest and apoptosis in leukemic cells, and includes manufacturer guidance for preparation and storage.
- Orally active reversible pan-FLT3 and pan-BTK inhibitor.
- Inhibits phosphorylation of FLT3 and STAT5 in cellular assays.
- Induces cell-cycle arrest, apoptosis, and autophagy in leukemia models.
- Supplied as a powder with recommended storage conditions for stability.
- Manufacturer provides suggested in-vitro stock concentrations and assay guidance.
- Suitable for in-vitro cell proliferation assays at 0.1-10 μM.
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eMolecules Medchem Express / Acetyl-CoA Carboxylase-IN-1 / 5mg / 779534845 / HY-152117 / / 179343-23-8 / MFCD12828288 / 395.058 / C13H9Br2N5
Medchem Express / Acetyl-CoA Carboxylase-IN-1 / 5mg / 779534845 / HY-152117 / / 179343-23-8 / MFCD12828288 / 395.058 / C13H9Br2N5
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