CAS No.: 4430-20-0 Molecular Formula:C19H12Cl2O5S MW:423.270

CAS No.: 4430-20-0 Molecular Formula: C19H12Cl2O5S MW:423.270

Chloramphenicol is a semisynthetic, broad-spectrum antibiotic derived from Streptomyces venequelae with primarily bacteriostatic activity. Chloramphenicol diffuses through the bacterial cell wall and reversibly binds to the bacterial 50S ribosomal subunit. The binding interferes with peptidyl transferase activity, thereby prevents transfer of amino acids to the growing peptide chains and blocks peptide bond formation. As a result, bacterial protein synthesis is blocked and impede bacterial cell proliferation. CAS Number: 56-75-7; Synonyms: Chloromycetin; Chlornitromycin; Chlorocid; Levomycetin; Molecular Formula: C11H12Cl2N2O5 Molecular Weight: 323.126 g/mol InChI Key: WIIZWVCIJKGZOK-RKDXNWHRSA-N

Chloramphenicol is a semisynthetic, broad-spectrum antibiotic derived from Streptomyces venequelae with primarily bacteriostatic activity. Chloramphenicol diffuses through the bacterial cell wall and reversibly binds to the bacterial 50S ribosomal subunit. The binding interferes with peptidyl transferase activity, thereby prevents transfer of amino acids to the growing peptide chains and blocks peptide bond formation. As a result, bacterial protein synthesis is blocked and impede bacterial cell proliferation. CAS Number: 56-75-7; Synonyms: Chloromycetin; Chlornitromycin; Chlorocid; Levomycetin; Molecular Formula: C11H12Cl2N2O5 Molecular Weight: 323.126 g/mol InChI Key: WIIZWVCIJKGZOK-RKDXNWHRSA-N

A non denaturing zwitterionic detergent with characteristics similar to CHAPS, although more soluble due to a more polar head group. Useful for the solubilization of integral membrane proteins. CHAPSO has been used in a study to assess the processes of liposome solubilization and reconstitution of two transport proteins. It has also been used in a study to investigate a novel bicelle system for orienting macromolecules over a wide temperature range. It can be used for solubilization of membrane proteins. Both CHAPS and CHAPSO have low light absorbance in the ultraviolet region of the electromagnetic spectrum, which is useful for monitoring ongoing chemical reactions or protein-protein binding with UV/Vis spectroscopy. CAS Number: 82473-24-3; Synonyms: MFCD00081079; CHAPS Hydroxy analog; BioXtra; AC1L3U2M; 3-((3-Cholamidopropyl)dimethylammonio)-2-hydroxy-1-propanesulfonate; Molecular Formula: C32H58N2O8S Molecular Weight: 630.882 g/mol (anhydrous basis) InChI Key: GUQQBLRVXOUDTN-XOHPMCGNSA-N

CHAPS is a zwitterionic surfactant used in the laboratory to solubilize biological macromolecules such as proteins. It has both hydrophilic and hydrophobic properties. It can be used for s olubilization of membrane proteins. Combines the properties of both the sulfobetaine-type and bile-acid detergents. Both CHAPS and CHAPSO have low light absorbance in the ultraviolet region of the electromagnetic spectrum, which is useful for monitoring ongoing chemical reactions or protein-protein binding with UV/Vis spectroscopy. CAS Number: 75621-03-3; Synonyms: CHEBI:1418; 3-((3-Cholamidopropyl)dimethylammonium)-1-propanesulfonate; Molecular Formula: C32H58N2O7S Molecular Weight: 614.883 g/mol (anhydrous basis) InChI Key: UMCMPZBLKLEWAF-BCTGSCMUSA-N

CHAPS is a zwitterionic surfactant used in the laboratory to solubilize biological macromolecules such as proteins. It has both hydrophilic and hydrophobic properties. It can be used for s olubilization of membrane proteins. Combines the properties of both the sulfobetaine-type and bile-acid detergents. Both CHAPS and CHAPSO have low light absorbance in the ultraviolet region of the electromagnetic spectrum, which is useful for monitoring ongoing chemical reactions or protein-protein binding with UV/Vis spectroscopy. CAS Number: 75621-03-3; Synonyms: CHEBI:1418; 3-((3-Cholamidopropyl)dimethylammonium)-1-propanesulfonate; Molecular Formula: C32H58N2O7S Molecular Weight: 614.883 g/mol (anhydrous basis) InChI Key: UMCMPZBLKLEWAF-BCTGSCMUSA-N

CHAPS is a zwitterionic surfactant used in the laboratory to solubilize biological macromolecules such as proteins. It has both hydrophilic and hydrophobic properties. It can be used for s olubilization of membrane proteins. Combines the properties of both the sulfobetaine-type and bile-acid detergents. Both CHAPS and CHAPSO have low light absorbance in the ultraviolet region of the electromagnetic spectrum, which is useful for monitoring ongoing chemical reactions or protein-protein binding with UV/Vis spectroscopy. CAS Number: 75621-03-3; Synonyms: CHEBI:1418; 3-((3-Cholamidopropyl)dimethylammonium)-1-propanesulfonate; Molecular Formula: C32H58N2O7S Molecular Weight: 614.883 g/mol (anhydrous basis) InChI Key: UMCMPZBLKLEWAF-BCTGSCMUSA-N

CHAPS is a zwitterionic surfactant used in the laboratory to solubilize biological macromolecules such as proteins. It has both hydrophilic and hydrophobicproperties. It can be used for s olubilization of membrane proteins. Combines the propertiesof both the sulfobetaine-type and bile-acid detergents. Both CHAPS andCHAPSO have low light absorbance in the ultravioletregion of the electromagnetic spectrum, which is useful for monitoring ongoingchemical reactions or protein-protein binding with UV/Vis spectroscopy. CAS Number: 75621-03-3; Synonyms: CHEBI:1418; 3-((3-Cholamidopropyl)dimethylammonium)-1-propanesulfonate; Molecular Formula: C32H58N2O7S Molecular Weight: 614.883 g/mol (anhydrous basis) InChI Key: UMCMPZBLKLEWAF-BCTGSCMUSA-N

CAS Number: 7647-17-8; Synonyms: Caesium chloride; Cesium monochloride; Cesium chloride (CsCl); Dicesium dichloride; Molecular Formula: CsCl Molecular Weight: 168.355 g/mol InChI Key: AIYUHDOJVYHVIT-UHFFFAOYSA-M

CAS Number: 7647-17-8; Synonyms: Caesium chloride; Cesium monochloride; Cesium chloride (CsCl); Dicesium dichloride; Molecular Formula: CsCl Molecular Weight: 168.355 g/mol InChI Key: AIYUHDOJVYHVIT-UHFFFAOYSA-M

Cefsulodin Sodium is the sodium salt form of cefsuldin, a pyridinium-substituted semi-synthetic, third-generation cephalosporin antibiotic with a narrow spectrum of activity. Cefsulodin has activity against Pseudomonas aeruginosa and Staphylococcus aureus but little activity against other bacteria. CAS Number: 52152-93-9; Synonyms: Sulcephalosporin; Cefsulodin sodium; Cefsulodine sodium; Cefsulodin sodium salt hydrate; Molecular Formula: C22H19N4NaO8S2 Molecular Weight: 554.524 g/mol InChI Key: REACMANCWHKJSM-DWBVFMGKSA-M

Cefsulodin Sodium is the sodium salt form of cefsuldin, a pyridinium-substituted semi-synthetic, third-generation cephalosporin antibiotic with a narrow spectrum of activity. Cefsulodin has activity against Pseudomonas aeruginosa and Staphylococcus aureus but little activity against other bacteria. CAS Number: 52152-93-9; Synonyms: Sulcephalosporin; Cefsulodin sodium; Cefsulodine sodium; Cefsulodin sodium salt hydrate; Molecular Formula: C22H19N4NaO8S2 Molecular Weight: 554.524 g/mol InChI Key: REACMANCWHKJSM-DWBVFMGKSA-M

Cefotaxime Sodium is the sodium salt form of cefotaxime, a beta-lactam, third-generation cephalosporin antibiotic with bactericidal activity. Cefotaxime sodium binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. Inactivation of PBPs interferes with the cross-linking of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. Compared to the second and first generation cephalosporins, cefotaxime sodium is more active against gram-negative bacteria and less active against gram-positive bacteria. CAS Number: 64485-93-4; Synonyms: CEFOTAXIME SODIUM SALT; Sodium cefotaxime; Tolycar; Pretor; Molecular Formula: C16H16N5NaO7S2 Molecular Weight: 477.442 g/mol InChI Key: AZZMGZXNTDTSME-JUZDKLSSSA-M

Cefotaxime Sodium is the sodium salt form of cefotaxime, a beta-lactam, third-generation cephalosporin antibiotic with bactericidal activity. Cefotaxime sodium binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. Inactivation of PBPs interferes with the cross-linking of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. Compared to the second and first generation cephalosporins, cefotaxime sodium is more active against gram-negative bacteria and less active against gram-positive bacteria. CAS Number: 64485-93-4; Synonyms: CEFOTAXIME SODIUM SALT; Sodium cefotaxime; Tolycar; Pretor; Molecular Formula: C16H16N5NaO7S2 Molecular Weight: 477.442 g/mol InChI Key: AZZMGZXNTDTSME-JUZDKLSSSA-M

Cefotaxime Sodium is the sodium salt form of cefotaxime, a beta-lactam, third-generation cephalosporin antibiotic with bactericidal activity. Cefotaxime sodium binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. Inactivation of PBPs interferes with the cross-linking of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. Compared to the second and first generation cephalosporins, cefotaxime sodium is more active against gram-negative bacteria and less active against gram-positive bacteria. CAS Number: 64485-93-4; Synonyms: CEFOTAXIME SODIUM SALT; Sodium cefotaxime; Tolycar; Pretor; Molecular Formula: C16H16N5NaO7S2 Molecular Weight: 477.442 g/mol InChI Key: AZZMGZXNTDTSME-JUZDKLSSSA-M

Broad-spectrum semisynthetic penicillin derivative used parenterally. Carbenicillin disodium is susceptible to gastric juice and penicillinase and may damage platelet function. CAS Number: 4800-94-6; Synonyms: Carbenicillin sodium; Carbenicillin disodium salt; 4800-94-6; Carbecin; Sodium carbenicillin; Molecular Formula: C17H16N2Na2O6S Molecular Weight: 422.363 g/mol InChI Key: RTYJTGSCYUUYAL-YCAHSCEMSA-L

Broad-spectrum semisynthetic penicillin derivative used parenterally. Carbenicillin disodium is susceptible to gastric juice and penicillinase and may damage platelet function. CAS Number: 4800-94-6; Synonyms: Carbenicillin sodium; Carbenicillin disodium salt; 4800-94-6; Carbecin; Sodium carbenicillin; Molecular Formula: C17H16N2Na2O6S Molecular Weight: 422.363 g/mol InChI Key: RTYJTGSCYUUYAL-YCAHSCEMSA-L

Broad-spectrum semisynthetic penicillin derivative used parenterally. Carbenicillin disodium is susceptible to gastric juice and penicillinase and may damage platelet function. CAS Number: 4800-94-6; Synonyms: Carbenicillin sodium; Carbenicillin disodium salt; 4800-94-6; Carbecin; Sodium carbenicillin; Molecular Formula: C17H16N2Na2O6S Molecular Weight: 422.363 g/mol InChI Key: RTYJTGSCYUUYAL-YCAHSCEMSA-L

Broad-spectrum semisynthetic penicillin derivative used parenterally. Carbenicillin disodium is susceptible to gastric juice and penicillinase and may damage platelet function. CAS Number: 4800-94-6; Synonyms: Carbenicillin sodium; Carbenicillin disodium salt; 4800-94-6; Carbecin; Sodium carbenicillin; Molecular Formula: C17H16N2Na2O6S Molecular Weight: 422.363 g/mol InChI Key: RTYJTGSCYUUYAL-YCAHSCEMSA-L