3168-01-2
3168-01-2
Chemical Structure
Hydroxyhexamide
Synonym(s): (±)-Hydroxyhexamid
- CAS No.: 3168-01-2
- Formula:C15H22N2O4S
- Molecular Weight:326.41
IUPAC Name: N-(cyclohexylcarbamoyl)-4-(1-hydroxyethyl)benzenesulfonamide
InChIKey: VQDAEOYLIBGCHE-UHFFFAOYSA-N
SMILES: O=S(C1=CC=C(C(O)C)C=C1)(NC(NC2CCCCC2)=O)=O
Biological Activity: Hydroxyhexamide is a pharmacologically active metabolite of Acetohexamide, used as a hypoglycemic agents.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Hydroxyhexamide | 99.60% | Hydroxyhexamide is a pharmacologically active metabolite of Acetohexamide, used as a hypoglycemic agents. | ||||||||||||||||||||
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Hydroxyhexamide (Standard) | ≥98% | Hydroxyhexamide (Standard) is an analytical standard for Hydroxyhexamide. This product is intended for research and analytical applications. Hydroxyhexamide is a pharmacologically active metabolite of Acetohexamide, used as a hypoglycemic agents. | ||||||||||||||||||||
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NSC23005 sodium (Standard) | ≥98% | NSC23005 (sodium) (Standard) is the analytical standard of NSC23005 (sodium) (HY-100791). This product is intended for research and analytical applications. NSC23005 sodium is a novel and effective p18 inhibitor (ED50=5.21 nM) in promoting Hematopoietic stem cells (HSCs) expansion in both murine and human models. | ||||||||||||||||||||
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INK4C-IN-2 | 98.35% | INK4C-IN-2 is a p18INK4C inhibitor. NK4C-IN-2 promotes hematopoietic stem cells (HSCs) division by inhibiting INK4C and activating CDK4/6, with an ED50 of 5.21 nM. INK4C-IN-2 shows no cytotoxic to normal 32D cells, HSCs, leukemia cell lines and myeloma cell lines. | ||||||||||||||||||||
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Cyclamide | Cyclamide (Cicloral), an oligopeptide, can be produced by cyanobacteria algae strains. Cyclamide can be used for the research of diabetes mellitus. | |||||||||||||||||||||
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Chlorcyclamide | Chlorcyclamide is a class of sulfonamide that can be used for the study of diabetes. | |||||||||||||||||||||
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Acetohexamide | 99.67% | Acetohexamide is an orally active first-generation sulfonylurea agent used in research related to type 2 diabetes and cancer. Acetohexamide exerts reductase activity in human erythrocytes. Acetohexamide stimulates the pancreas to secrete insulin. Acetohexamide inhibits ATP-sensitive potassium channels in the β cells of the pancreas. Acetohexamide can inhibit the formation of circular chemorepellent induced defects (CCIDs) in lymphendothelial cell (LEC) monolayers. Acetohexamide inhibits markers of epithelial-to-mesenchymal-transition and migration. Acetohexamide suppresses the synthesis of 12(S)-HETE. Acetohexamide can potentiate hypoglycaemic action. | ||||||||||||||||||||
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Glyhexamide | Glyhexamide is an effective hypoglycemic agent in adult diabetics. | |||||||||||||||||||||
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Glipizide impurity 11 | Glipizide impurity 11 is an impurity of Glipizide. | |||||||||||||||||||||
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Glipizide impurity 6 | Glipizide impurity 6 is an impurity of Glipizide. | |||||||||||||||||||||
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Glipizide impurity 1 | Glipizide impurity 1 is an impurity of Glipizide. | |||||||||||||||||||||
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Glipizide impurity 7 | Glipizide impurity 7 is an impurity of Glipizide. | |||||||||||||||||||||
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