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Filtered Search Results
Thermo Scientific Chemicals Cycloheximide, 95%
CAS: 66-81-9 Molecular Formula: C15H23NO4 Molecular Weight (g/mol): 281.35 MDL Number: MFCD00082346 InChI Key: YPHMISFOHDHNIV-QTEFRXOUNA-N Synonym: cycloheximide,actidione,cycloheximide,naramycin a,kaken,actidion,actidone,hizarocin,naramycin,neocycloheximide PubChem CID: 6197 ChEBI: CHEBI:27641 IUPAC Name: 4-[(2R)-2-[(1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione SMILES: [H][C@]1(C[C@@H](C)C[C@H](C)C1=O)[C@H](O)CC1CC(=O)NC(=O)C1
| PubChem CID | 6197 |
|---|---|
| CAS | 66-81-9 |
| Molecular Weight (g/mol) | 281.35 |
| ChEBI | CHEBI:27641 |
| MDL Number | MFCD00082346 |
| SMILES | [H][C@]1(C[C@@H](C)C[C@H](C)C1=O)[C@H](O)CC1CC(=O)NC(=O)C1 |
| Synonym | cycloheximide,actidione,cycloheximide,naramycin a,kaken,actidion,actidone,hizarocin,naramycin,neocycloheximide |
| IUPAC Name | 4-[(2R)-2-[(1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione |
| InChI Key | YPHMISFOHDHNIV-QTEFRXOUNA-N |
| Molecular Formula | C15H23NO4 |
2-Azetidinone, 98%
CAS: 930-21-2 Molecular Formula: C3H5NO Molecular Weight (g/mol): 71.08 MDL Number: MFCD00013328 InChI Key: MNFORVFSTILPAW-UHFFFAOYSA-N Synonym: 2-azetidinone,beta-propiolactam,azetidinone,propiolactam,azetan-2-one,beta-lactam,2-azetdinone,azetidine-2-one,acmc-209xab PubChem CID: 136721 ChEBI: CHEBI:327119 IUPAC Name: azetidin-2-one SMILES: C1CNC1=O
| PubChem CID | 136721 |
|---|---|
| CAS | 930-21-2 |
| Molecular Weight (g/mol) | 71.08 |
| ChEBI | CHEBI:327119 |
| MDL Number | MFCD00013328 |
| SMILES | C1CNC1=O |
| Synonym | 2-azetidinone,beta-propiolactam,azetidinone,propiolactam,azetan-2-one,beta-lactam,2-azetdinone,azetidine-2-one,acmc-209xab |
| IUPAC Name | azetidin-2-one |
| InChI Key | MNFORVFSTILPAW-UHFFFAOYSA-N |
| Molecular Formula | C3H5NO |
(S)-(-)-2-Pyrrolidone-5-carboxylic acid, 98%
CAS: 98-79-3 Molecular Formula: C5H7NO3 Molecular Weight (g/mol): 129.12 MDL Number: MFCD00005272 InChI Key: ODHCTXKNWHHXJC-UHFFFAOYNA-N Synonym: l-pyroglutamic acid,pyroglutamic acid,pidolic acid,5-oxo-l-proline,h-pyr-oh,5-oxoproline,s-5-oxopyrrolidine-2-carboxylic acid,2s-5-oxopyrrolidine-2-carboxylic acid,l-5-oxoproline,l-proline, 5-oxo PubChem CID: 7405 ChEBI: CHEBI:18183 IUPAC Name: (2S)-5-oxopyrrolidine-2-carboxylic acid SMILES: OC(=O)C1CCC(=O)N1
| PubChem CID | 7405 |
|---|---|
| CAS | 98-79-3 |
| Molecular Weight (g/mol) | 129.12 |
| ChEBI | CHEBI:18183 |
| MDL Number | MFCD00005272 |
| SMILES | OC(=O)C1CCC(=O)N1 |
| Synonym | l-pyroglutamic acid,pyroglutamic acid,pidolic acid,5-oxo-l-proline,h-pyr-oh,5-oxoproline,s-5-oxopyrrolidine-2-carboxylic acid,2s-5-oxopyrrolidine-2-carboxylic acid,l-5-oxoproline,l-proline, 5-oxo |
| IUPAC Name | (2S)-5-oxopyrrolidine-2-carboxylic acid |
| InChI Key | ODHCTXKNWHHXJC-UHFFFAOYNA-N |
| Molecular Formula | C5H7NO3 |
(S)-(-)-2-Pyrrolidinone-5-carboxylic acid, 98+%
CAS: 98-79-3 Molecular Formula: C5H7NO3 Molecular Weight (g/mol): 129.12 MDL Number: MFCD00005272 InChI Key: ODHCTXKNWHHXJC-UHFFFAOYNA-N Synonym: l-pyroglutamic acid,pyroglutamic acid,pidolic acid,5-oxo-l-proline,h-pyr-oh,5-oxoproline,s-5-oxopyrrolidine-2-carboxylic acid,2s-5-oxopyrrolidine-2-carboxylic acid,l-5-oxoproline,l-proline, 5-oxo PubChem CID: 7405 ChEBI: CHEBI:18183 SMILES: OC(=O)C1CCC(=O)N1
| PubChem CID | 7405 |
|---|---|
| CAS | 98-79-3 |
| Molecular Weight (g/mol) | 129.12 |
| ChEBI | CHEBI:18183 |
| MDL Number | MFCD00005272 |
| SMILES | OC(=O)C1CCC(=O)N1 |
| Synonym | l-pyroglutamic acid,pyroglutamic acid,pidolic acid,5-oxo-l-proline,h-pyr-oh,5-oxoproline,s-5-oxopyrrolidine-2-carboxylic acid,2s-5-oxopyrrolidine-2-carboxylic acid,l-5-oxoproline,l-proline, 5-oxo |
| InChI Key | ODHCTXKNWHHXJC-UHFFFAOYNA-N |
| Molecular Formula | C5H7NO3 |
DL-Aminoglutethimide, 99%
CAS: 125-84-8 Molecular Formula: C13H16N2O2 Molecular Weight (g/mol): 232.283 MDL Number: MFCD00010122 InChI Key: ROBVIMPUHSLWNV-UHFFFAOYSA-N Synonym: aminoglutethimide,dl-aminoglutethimide,cytadren,orimeten,p-aminoglutethimide,elipten,3-4-aminophenyl-3-ethylpiperidine-2,6-dione,aminoglutetimida,3-4-aminophenyl-3-ethyl-2,6-piperidinedione,aminoglutethimidum PubChem CID: 2145 ChEBI: CHEBI:2654 IUPAC Name: 3-(4-aminophenyl)-3-ethylpiperidine-2,6-dione SMILES: CCC1(CCC(=O)NC1=O)C2=CC=C(C=C2)N
| PubChem CID | 2145 |
|---|---|
| CAS | 125-84-8 |
| Molecular Weight (g/mol) | 232.283 |
| ChEBI | CHEBI:2654 |
| MDL Number | MFCD00010122 |
| SMILES | CCC1(CCC(=O)NC1=O)C2=CC=C(C=C2)N |
| Synonym | aminoglutethimide,dl-aminoglutethimide,cytadren,orimeten,p-aminoglutethimide,elipten,3-4-aminophenyl-3-ethylpiperidine-2,6-dione,aminoglutetimida,3-4-aminophenyl-3-ethyl-2,6-piperidinedione,aminoglutethimidum |
| IUPAC Name | 3-(4-aminophenyl)-3-ethylpiperidine-2,6-dione |
| InChI Key | ROBVIMPUHSLWNV-UHFFFAOYSA-N |
| Molecular Formula | C13H16N2O2 |
Glutarimide, 98%
CAS: 1121-89-7 Molecular Formula: C5H7NO2 Molecular Weight (g/mol): 113.12 MDL Number: MFCD00006670 InChI Key: KNCYXPMJDCCGSJ-UHFFFAOYSA-N Synonym: glutarimide,2,6-piperidinedione,2,6-diketopiperidine,2,6-dioxopiperidine,acetylglycinamide impurity b,piperidin-2,6-dione,acmc-2099da,5-21-09-00557 beilstein handbook reference,2,6-piperidinedione 9ci PubChem CID: 70726 ChEBI: CHEBI:5435 IUPAC Name: piperidine-2,6-dione SMILES: O=C1CCCC(=O)N1
| PubChem CID | 70726 |
|---|---|
| CAS | 1121-89-7 |
| Molecular Weight (g/mol) | 113.12 |
| ChEBI | CHEBI:5435 |
| MDL Number | MFCD00006670 |
| SMILES | O=C1CCCC(=O)N1 |
| Synonym | glutarimide,2,6-piperidinedione,2,6-diketopiperidine,2,6-dioxopiperidine,acetylglycinamide impurity b,piperidin-2,6-dione,acmc-2099da,5-21-09-00557 beilstein handbook reference,2,6-piperidinedione 9ci |
| IUPAC Name | piperidine-2,6-dione |
| InChI Key | KNCYXPMJDCCGSJ-UHFFFAOYSA-N |
| Molecular Formula | C5H7NO2 |
Alkali Scientific Cycloheximide, 100 G
Cycloheximide is a potent inhibitor of eukaryotic protein synthesis commonly used in microbiological and biochemical research. It acts by interfering with ribosomal translocation, preventing elongation of peptide chains during translation. This property makes it highly effective as an antifungal agent in laboratory media, where it selectively suppresses molds and yeasts while allowing bacterial growth. Cycloheximide is frequently used in selective culture media, contamination control protocols, and experimental studies focused on gene expression and protein synthesis. The compound is also utilized in research investigating cellular metabolism, stress responses, and mechanisms of translation inhibition in eukaryotic cells under controlled laboratory conditions.
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Alkali Scientific Cycloheximide, 5 G
Cycloheximide is an antifungal and protein synthesis inhibitor widely used in microbiology and laboratory research. It works by blocking translation in eukaryotic ribosomes, preventing the production of proteins necessary for fungal growth. This selective action allows it to be used in culture media to suppress molds and yeasts while permitting bacterial growth. Cycloheximide is commonly included in selective agar formulations, environmental monitoring media, and research protocols where fungal contamination must be controlled. It is also used in molecular and cellular biology studies to investigate protein synthesis and cellular responses to translational inhibition under controlled experimental conditions.
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Alkali Scientific Cycloheximide, 25 G
Cycloheximide is a widely used laboratory reagent that inhibits protein synthesis in eukaryotic organisms by blocking ribosomal function. This mechanism makes it particularly effective for suppressing fungal growth in microbiological media while allowing bacterial cultures to develop. It is commonly incorporated into selective media to prevent contamination by molds and yeasts during bacterial isolation procedures. In addition to its antifungal applications, cycloheximide is used in research studies examining cellular processes such as protein synthesis, gene expression, and metabolic regulation. Its ability to rapidly halt translation makes it a valuable tool in experimental biology and biochemical investigations.
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Alkali Scientific Cycloheximide, 1 G
Cycloheximide is a protein synthesis inhibitor widely used in microbiology and cell biology laboratories as an antifungal agent. It functions by blocking the translocation step in eukaryotic ribosomes, effectively preventing protein synthesis in fungi and other eukaryotic organisms. This selective inhibition makes it useful in culture media where suppression of fungal growth is required while allowing bacterial growth to proceed. Cycloheximide is commonly incorporated into selective agar formulations and research protocols to control contamination by molds and yeasts. It is also used in molecular biology studies to investigate protein synthesis mechanisms and cellular responses to translational inhibition in experimental systems.
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AG Scientific Inc Cycloheximide 25 G
Cycloheximide is an antibiotic produced by Streptomyces sp. that activates against yeasts and fungi. It inhibits protein synthesis thru DNA translation arrest in eukaryotes. Cycloheximide also inhibits chain initiation and chain elongation by acting on 60S subunits of eukaryote ribosome.
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AG Scientific Inc Cycloheximide 10 G
Cycloheximide is an antibiotic produced by Streptomyces sp. that activates against yeasts and fungi. It inhibits protein synthesis thru DNA translation arrest in eukaryotes. Cycloheximide also inhibits chain initiation and chain elongation by acting on 60S subunits of eukaryote ribosome.
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AG Scientific Inc Cycloheximide 1 G
Cycloheximide is an antibiotic produced by Streptomyces sp. that activates against yeasts and fungi. It inhibits protein synthesis thru DNA translation arrest in eukaryotes. Cycloheximide also inhibits chain initiation and chain elongation by acting on 60S subunits of eukaryote ribosome.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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AG Scientific Inc Cycloheximide 5 G
Cycloheximide is an antibiotic produced by Streptomyces sp. that activates against yeasts and fungi. It inhibits protein synthesis thru DNA translation arrest in eukaryotes. Cycloheximide also inhibits chain initiation and chain elongation by acting on 60S subunits of eukaryote ribosome.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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