Glyhexamide structure
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Common Name | Glyhexamide | ||
|---|---|---|---|---|
| CAS Number | 451-71-8 | Molecular Weight | 322.42200 | |
| Density | 1.3g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C16H22N2O3S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of GlyhexamideGlyhexamide is an effective hypoglycemic agent in adult diabetics. |
| Name | 1-cyclohexyl-3-(2,3-dihydro-1H-inden-5-ylsulfonyl)urea |
|---|---|
| Synonym | More Synonyms |
| Description | Glyhexamide is an effective hypoglycemic agent in adult diabetics. |
|---|---|
| Related Catalog | |
| In Vivo | Glyhexamide, a new cyclic sulfonylurea, is an effective hypoglycemic agent in adult diabetics, this activity is unaccompanied by increases in serum (immunoreactive) insulin concentrations. |
| References |
| Density | 1.3g/cm3 |
|---|---|
| Molecular Formula | C16H22N2O3S |
| Molecular Weight | 322.42200 |
| Exact Mass | 322.13500 |
| PSA | 83.65000 |
| LogP | 4.35850 |
| Index of Refraction | 1.602 |
| InChIKey | NFRPNQDSKJJQGV-UHFFFAOYSA-N |
| SMILES | O=C(NC1CCCCC1)NS(=O)(=O)c1ccc2c(c1)CCC2 |
| Storage condition | 2-8℃ |
| HS Code | 2935009090 |
|---|
| HS Code | 2935009090 |
|---|---|
| Summary | 2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0% |
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100
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Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101
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|
Name: Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
Source: Broad Institute
Target: N/A
External Id: 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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Name: Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
Source: Broad Institute
Target: N/A
External Id: 7124-01_Inhibitor_SinglePoint_HTS_Activity
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Name: qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
Source: NCGC
Target: apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id: AMA1100
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Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id: ABHD4_INH_FP_1536_1X%INH PRUN
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| HZ 21 |
| Subose |
| SQ 15,860 |
| GLYHEXAMIDE |
| Serbose |