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Filtered Search Results
![eMolecules 130-14-3 | Sodium naphthalene-1-sulphonate | Apollo Scientific | MFCD00064964 | 230.210 | C10H7NaO3S | 95.000 | [Na+].[O-]S(=O)(=O)c1cccc2ccccc12 | 25g | 562424623](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502160226.JPG-250.jpg)
eMolecules 130-14-3 | Sodium naphthalene-1-sulphonate | Apollo Scientific | MFCD00064964 | 230.210 | C10H7NaO3S | 95.000 | [Na+].[O-]S(=O)(=O)c1cccc2ccccc12 | 25g | 562424623
Sodium naphthalene-1-sulphonate | Apollo Scientific | 130-14-3 | MFCD00064964 | 230.210 | C10H7NaO3S | 95.000 | [Na+].[O-]S(=O)(=O)c1cccc2ccccc12 | 25g | 562424623
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Medchemexpress LLC Rotigotine Hydrochloride | 125572-93-2 | 99.5% | C19H26ClNOS | 100 MG
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Rotigotine Hydrochloride (N-0923 Hydrochloride) is a full agonist of the dopamine receptor, a partial agonist of the 5-HT1A receptor, and an antagonist of the α2B-adrenergic receptor. It exhibits Ki values of 0.71 nM for the dopamine D3 receptor, 4-15 nM for D2, D5, and D4 receptors, and 83 nM for the dopamine D1 receptor.
- Full agonist at dopamine receptors, partial agonist at 5-HT1A receptor, and antagonist at α2B-adrenergic receptor.
- Shows selectivity for D3 receptors (10-fold over D2, D4, D5, and 100-fold over D1).
- Functionally acts as a full agonist at all dopamine receptors.
- Decreases THir neurons in primary mesencephalic cell culture.
- Neuroprotective effects against MPP+ toxicity and rotenone-induced cell death.
- Inhibits ROS production by rotenone.
- For research use only.
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Aobchem AOBCHEM
5000866158 1-IODO-4-METHOXYNAPHTHALENE 50
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Medchemexpress LLC 4-(4-((dimethylamino)methyl)-2,5-dimethoxyphenyl)-2-methyl-2,7-naphthyridin-1(2H)-one | 1883429-22-8 | >98.0% | 353.17 Da | C20H23N3O3 | 100 MG
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BI-9564 is a potent, selective, and cell-permeable small-molecule inhibitor of the BRD9 bromodomain, with weaker activity against BRD7. Developed through structure-guided design, it binds BRD9 in the low-nanomolar range and has been used as a chemical probe in cellular assays and in vivo studies, including reported oral efficacy in preclinical AML models.
- High affinity for BRD9 with weaker activity against BRD7.
- Demonstrated cellular potency (AlphaScreen IC50 ≈ 75 nM).
- Cell-permeable and suitable for cellular and in vivo studies.
- Validated structural data available (PDB: 5F1H).
- Useful as a research chemical probe to study chromatin remodeling biology.
- Available from multiple research suppliers in small-mass packaging.
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eMolecules 29671-92-9 | Chloroformamidine hydrochloride | Chem-Impex | MFCD00035527 | 114.960 | CH4Cl2N2 | 99.000 | Cl.NC(Cl)=N | 25g | 386903867
Chloroformamidine hydrochloride | Chem-Impex | 29671-92-9 | MFCD00035527 | 114.960 | CH4Cl2N2 | 99.000 | Cl.NC(Cl)=N | 25g | 386903867
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Cambridge Isotope Laboratories Dechlorane 602 (unlabeled) 100 ug/mL in nonane 1 2 mL
Dechlorane 602 (unlabeled) 100 ug/mL in nonane 1 2 mL
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Apexbio Technology LLC Linagliptin (BI-1356) 668270-12-0 100mg
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Linagliptin (BI-1356 CAS 668270-12-0) is a potent competitive inhibitor of dipeptidyl peptidase-4 (DPP-4) demonstrating IC50 values of 0 4 1 1 nM in multiple in vitro assays using DPP-4 extracted from Caco-2 cells DPP-4 is a membrane-bound and soluble protease involved in the degradation of incretin hormones such as GLP-1 which enhance pancreatic -cell glucose sensitivity and insulin secretion Linagliptin displays marked selectivity for DPP-4 over related peptidases and serine proteases In vivo linagliptin dose-dependently inhibits plasma DPP-4 activity and sustains glycemic control with prolonged effects observed at pharmacologically relevant doses This compound is widely utilized in studies of glucose metabolism and -cell function
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000700927 A-NAPHTHOLBENZEIN 500MG
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Medchemexpress LLC Valnemulin hydrochloride | 133868-46-9 | 98.1% | C31H53ClN2O5S | 100 MG
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Valnemulin hydrochloride is an orally effective truncated pleurotin antibiotic that inhibits protein synthesis in bacteria by binding to peptidyl transferase in the 50s ribosome subunit.
- Effective in eliminating Mycobacterium bovis from the lungs in experimental bovine models.
- Reduces mortality associated with epidemic rabbit enteropathy without adversely affecting growth performance.
- Controls experimental infection in calves, diminishing clinical signs, restoring appetite, and reversing weight loss.
- Reduces the isolation of Pasteurella multocida from infected calves' lungs.
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Aobchem AOBCHEM
5000872631 ETHYL 2- NAPHTHALEN-1-YL BENZO
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Aobchem AOBCHEM
5000872627 ETHYL 2- NAPHTHALEN-1-YL BENZO
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Aobchem AOBCHEM
5000865529 6-BROMO-1-CHLORO-2-NAPHTHOL 50
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Medchemexpress LLC Alizapride hydrochloride | 59338-87-3 | 99.8% | C16H22ClN5O2 | 1 ML
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Alizapride is a potent antiemetic that functions as a dopamine receptor antagonist. It is also utilized in the treatment of human digestive disorders.
- Potent antiemetic properties
- Functions as a dopamine receptor antagonist
- Useful in treating human digestive disorders
- Significantly reduces bound IgG-sensitized erythrocytes with splenic macrophages
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Sigma Aldrich Fine Chemicals Biosciences Menadione United States Pharmacopeia (USP) Reference Standard | 58-27-5 | MFCD00001681 | 200MG
Menadione United States Pharmacopeia (USP) Reference Standard | Mol Wt: 172.18 | 58-27-5 | MFCD00001681 | 200MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000656209 DFHBI-BI 1MG
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