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| Product | Description | |
|---|---|---|
| Penicillin V | An impurity of Penicillin V which is used to treat many different types of infections caused by bacteria, such as ear infections (use by mouth). Uses: Penicillins. Synonyms: penicillin v; Phenoxymethylpenicillin; Penicillin phenoxymethyl; Oracillin; 87-08-1; Phenopenicillin; Phenomycilline; V-Cillin; Vebecillin; Fenospen; Distaquaine V; Phenoxymethyl penicillin; Meropenin; Calcipen; Fenacilin; Phenocillin; Phenoxymethylenepenicillinic acid; Stabicillin; Apopen; Oratren; Rocilin; Ospen;6beta-Phenoxyacetamido-2,2-dimethylpenam-3alpha-carboxylic acid; Phenoxymethylpenicillin, Antibiotic for Culture Media Use Only; Penicillin V, United States Pharmacopeia (USP) Reference Standard; Phenoxymethylpenicillin, European Pharmacopoeia (EP) Reference Standard; 4-THIA-1-AZABICYCLO(3.2.0)HEPTANE-2-CARBOXYLIC ACID, 3,3-DIMETHYL-7-OXO-6-((PHENOXYACETYL)AMINO)-, (2S-(2ALPHA,5ALPHA,6.BETA)).-. Grades: > 95%. CAS No. 87-08-1. Molecular formula: C16H18N2O5S. Mole weight: 350.4. |  |
| Penicillin V | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. |  |
| Penicillin V β-Sulfoxide-d3 | Isotope labelled Penicillin V β-Sulfoxide, an intermediate in the synthesis of Penicillin V (P223500), an antibacterial agent. Group: Biochemicals. Alternative Names: 6-Phenoxyacetamidopenici llinic Acid-d3 1 β-Oxide; Penicillin-d3 V S-Oxide; [2S-(2α,4 β,5α,6 β )]-3, 3-Dimethyl-7-oxo-6-[(phenoxyacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid-d3 4-Oxide; (2S, 4S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid-d3 4-Oxide. Grades: Highly Purified. CAS No. 148680-07-3. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Penicillin V-d5 | Antibacterial. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenoxy-d5-acetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid; 6-(Phenoxy-d5-acetamido)penicillanic Acid; Phenoxy methyl penicillin-d5; Phenospen-d5; Oracilline-d5; V-Cillin-d5. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Penicillin V-d5 | Penicillin V-d 5 (Phenoxymethylpenicillin-d5) is the deuterium labeled Penicillin V. Penicillin V (Phenoxymethylpenicillin) is an orally active antibiotic. Penicillin V inhibits the growth of Streptococci, C. difficile and S. aureus. Penicillin V can be used for the research of otitis, sinusitis, pharyngitis and tonsillitis[1][2][3][4]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1356837-87-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-B0975AS. |  |
| Penicillin V-d5 potassium | Penicillin V-d 5 (potassium) is the deuterium labeled Penicillin V Potassium[1]. Penicillin V Potassium (Phenoxymethylpenicillin potassium salt) is an orally active antibiotic. Penicillin V Potassium inhibits the growth of Streptococci, C. difficile and S. aureus. Penicillin V Potassium can be used for the research of otitis, sinusitis, pharyngitis and tonsillitis[2][3][4][5]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: Phenoxymethylpenicillin-d5 potassium salt. CAS No. 2699607-22-0. Pack Sizes: 1 mg. Product ID: HY-B0975S1. | |
| Penicillin V potassium | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Penicillin V Potassium | Penicillin V Potassium (Phenoxymethylpenicillin potassium salt) is an orally active antibiotic. Penicillin V Potassium inhibits the growth of Streptococci , C. difficile and S. aureus. Penicillin V Potassium can be used for the research of otitis, sinusitis, pharyngitis and tonsillitis [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: Phenoxymethylpenicillin potassium salt. CAS No. 132-98-9. Pack Sizes: 5 g; 10 g. Product ID: HY-B0975. | |
| Penicillin V potassium salt | 100g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17KN2O5S. CAS No. 132-98-9. Prepack ID 55440700-100g. Molecular Weight 388.48. See USA prepack pricing. |  |
| Penicillin V potassium salt | 25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17KN2O5S. CAS No. 132-98-9. Prepack ID 55440700-25g. Molecular Weight 388.48. See USA prepack pricing. | |
| Penicillin V potassium salt | analytical standard. Group: Application areas. | |
| Penicillin V Potassium Salt | Antibacterial. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Potassium; 6- (Phenoxyacetamido) penicillanic Acid Potassium; Antibiocin. Grades: Highly Purified. CAS No. 132-98-9. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Penicillin V Potassium Salt | The Potassium Salt form of Penicillin V is an orally active penicillin that has been found to be an effective antibiotic against sorts of bacteria. Uses: Penicillins. Synonyms: (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Potassium; 6-(Phenoxyacetamido)penicillanic Acid Potassium; Antibiocin; Calciopen K; Cilacil; Fenoxypen; Vepicombin; 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-(2-phenoxyacetamido)-, (2S,5R,6R)-, Potassium salt. Grades: 96%. CAS No. 132-98-9. Molecular formula: C16H17KN2O5S. Mole weight: 388.48. | |
| Penicillin V Potassium USP | Phenoxymethylpenicillin Potassium, 3,3-dimethyl-7-oxo-6-(2-phenoxy-acetamido)-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid mono Potassium salt. Grades: USP. CAS No. 132-98-9. Product ID: 8-01823. Molecular formula: C16H17N2O5SK. Mole weight: 388.5. |  |
| 2-Ethoxynaphthaldehyde | 2-Ethoxynaphthaldehyde is used in the synthesis of various antistaphylococcic penicillins. Group: Biochemicals. Alternative Names: NSC 74560; 2-Ethoxy-1-naphthaldehyde; 2-Ethoxy-1-naphthalene carboxaldehyde. Grades: Highly Purified. CAS No. 19523-57-0. Pack Sizes: 2.5g. US Biological Life Sciences. | Worldwide |
| 2-Ethoxynaphthaldehyde | 2-Ethoxynaphthaldehyde is used to synthesize various antistaphylococcal penicillins. Synonyms: NSC 74560; 2-Ethoxy-1-naphthaldehyde; 2-Ethoxy-1-naphthalenecarboxaldehyde; 2-ethoxy-naphthalen-1-methylaldehyde. Grades: ≥95%. CAS No. 19523-57-0. Molecular formula: C13H12O2. Mole weight: 200.23. | |
| 2-Ethoxynaphthaldehyde-d5 | Isotope labelled 2-Ethoxynaphthaldehyde is used in the synthesis of various antistaphylococcic penicillins. Group: Biochemicals. Alternative Names: NSC 74560-d5; 2-Ethoxy-1-naphthaldehyde-d5; 2-Ethoxy-1-naphthalene carboxaldehyde-d5. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| 2-Ethoxynaphthalene-1-carboxylic Acid | 2-Ethoxynaphthalene-1-carboxylic Acid is used in the synthesis of various antistaphylococcic penicillins. Group: Biochemicals. Alternative Names: 2-Ethoxy-1-naphthoic Acid; 2-Ethoxy-1-naphthalenecarboxylic Acid. Grades: Highly Purified. CAS No. 2224-00-2. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 2-Ethoxynaphthalene-1-carboxylic Acid-d5 | Isotope labelled 2-Ethoxynaphthalene-1-carboxylic Acid is used in the synthesis of various antistaphylococcic penicillins. Group: Biochemicals. Alternative Names: 2-Ethoxy-1-naphthoic Acid-d5; 2-Ethoxy-1-naphthalenecarboxylic Acid-d5. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 3-Cyclohexen-1-ol | 3-Cyclohexen-1-ol, a versatile and dynamic organic molecule, finds its application in the synthesis of drugs, agrochemicals, fragrances as well as a flavoring agent. Its potential use as an anti-inflammatory and anticancer agent has sparked immense interest in the scientific community. In the pharmaceutical industry, this compound acts as a crucial raw material in the manufacture of key drugs such as penicillin and ibuprofen. The diverse and expansive utility of 3-Cyclohexen-1-ol in various industries makes it an invaluable component in the field of organic chemistry. Synonyms: Cyclohex-3-enol; 3-Cyclohexenol. Grades: 95%. CAS No. 822-66-2. Molecular formula: C6H10O. Mole weight: 98.14. | |
| Azlocillin sodium salt | Azlocillin is an acylampicillin antibiotic with an extended spectrum of activity and greater in vitro potency than the carboxy penicillins. Azlocillin is similar to mezlocillin and piperacillin. It demonstrates antibacterial activity against a broad spectrum of bacteria, including Pseudomonas aeruginosa and, in contrast to most cephalosporins, exhibits activity against enterococci. Uses: Anti-bacterial agents. Synonyms: Bayer Brand of Azlocillin; Sodium Azlocillin; Securopen; Bay-e 6905; Baye 6905; Bay e 6905; Azlocillin; Azlocillin Bayer Brand. Grades: >98%. CAS No. 37091-65-9. Molecular formula: C20H23N5O6SNa. Mole weight: 484.48. | |
| Benzylpenicillin | It is produced by the strain of Penicillum sp. Penicillin has a strong antibacterial effect on gram-positive bacteria, Neisseria, Haemophilus, anaerobes (except fragile bacilli), spirochetes and actinomycetes, but no effect on mycobacterium tuberculosis, rickettsia, fungi, protozoa and virus. Synonyms: penicillin g; Benzylpenicillinic acid; Pencillin G. Molecular formula: C16H18N2O4S. Mole weight: 334.39. | |
| Benzylpenicillinate-d7, Potassium Salt | Benzylpennicillin (penicillin G) is a widely used antibiotic in veterinary medicine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| β-lactamase | A group of enzymes of varying specificity hydrolysing β-lactams; some act more rapidly on penicillins, some more rapidly on cephalosporins. The latter were formerly listed as EC 3.5.2.8, cephalosporinase. Group: Enzymes. Synonyms: penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4508; β-lactamase; EC 3.5.2.6; 9073-60-3; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase. Cat No: EXWM-4508. |  |
| β-Lactamase Blend, Recombinant | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. Group: Enzymes. Synonyms: β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: 600-1500 IU beta-lactamase I per vial; 60-100 IU beta-lactamase II per vial. Storage: 2-8°C. Form: Lyophilized powder containing sodium chloride, potassium phosphate and sorbitol. Source: E. coli. β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Cat No: NATE-0776. | |
| Boc-L-Pen(pMeBzl)-OH | Boc-L-Pen(pMeBzl)-OH is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Boc-L-4-Methylbenzyl-L-Penicillamine; Boc-S-4-Methylbenzyl-L-penicillamine; L-Valine, N-[(1,1-dimethylethoxy)carbonyl]-3-[[(4-methylphenyl)methyl]thio]-; (2R) -3-methyl-3-[ (4-methylbenzyl) sulfanyl]-2- ({[ (2-methyl-2-propanyl) oxy]carbonyl}amino) butanoate; N-α-(t-Butoxycarbonyl)-S-(4-methylbenzyl)-L-penicillamine; Boc-β,β-dimethyl-L-Cys(pMeBzl)-OH; (R)-2-((tert-butoxycarbonyl)amino)-3-methyl-3-((4-methylbenzyl)thio)butanoic acid; N-(tert-Butoxycarbonyl)-3-[(4-methylbenzyl)sulfanyl]-L-valine. Grades: 95%. CAS No. 104323-41-3. Molecular formula: C18H27NO4S. Mole weight: 353.48. | |
| Boc-S-4-methoxybenzyl-D-penicillamine | Boc-S-4-methoxybenzyl-D-penicillamine is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Boc-D-Pen(pMeOBzl)-OH; Boc-β,β-dimethyl-D-Cys(pMeOBzl)-OH; Boc-D-Pen(Mob)-OH; (S)-2-((tert-Butoxycarbonyl)amino)-3-((4-methoxybenzyl)thio)-3-methylbutanoic acid; 3-[(4-Methoxybenzyl)sulfanyl]-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-D-valine; N-α-(t-Butoxycarbonyl)-S-(4-methoxybenzyl)-D-penicillamine. Grades: ≥95%. CAS No. 106306-57-4. Molecular formula: C18H27NO5S. Mole weight: 369.48. | |
| Boc-S-4-methoxybenzyl-L-penicillamine | Boc-S-4-methoxybenzyl-L-penicillamine is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Boc-L-Pen(pMeOBzl)-OH; Boc-β,β-dimethyl-L-Cys(pMeOBzl)-OH; Boc-Pen(Mob)-OH; (R)-2-((tert-Butoxycarbonyl)amino)-3-((4-methoxybenzyl)thio)-3-methylbutanoic acid; 3-[(4-Methoxybenzyl)sulfanyl]-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-valine; L-Valine, N-[(1,1-dimethylethoxy)carbonyl]-3-[[(4-methoxyphenyl)methyl]thio]-. Grades: ≥95%. CAS No. 120944-75-4. Molecular formula: C18H27NO5S. Mole weight: 369.48. | |
| Boc-S-4-methylbenzyl-D-penicillamine dicyclohexylammonium salt | Boc-S-4-methylbenzyl-D-penicillamine dicyclohexylammonium salt is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Boc-D-Pen(pMeBzl)-OH DCHA; Boc-b,b-dimethyl-D-Cys(pMeBzl)-OH DCHA; N-tert-Butyloxycarbonyl-S-(4-methylbenzyl)-D-penicillamine dicyclohexylamine; D-Valine, N-[(1,1-dimethylethoxy)carbonyl]-3-[[(4-methylphenyl)methyl]thio]-, compd. with N-cyclohexylcyclohexanamine (1:1). Grades: ≥95%. CAS No. 198470-36-9. Molecular formula: C18H27NO4S.C12H23N. Mole weight: 534.80. | |
| Boc-S-acetamidomethyl-D-penicillamine | Boc-S-acetamidomethyl-D-penicillamine is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Boc-D-Pen(Acm)-OH; Boc-β,β-dimethyl-D-Cys(Acm)-OH; N-tert-butoxycarbonyl-S-acetamidomethyl-D-penicillamine; 3-[(Acetamidomethyl)sulfanyl]-N-(tert-butoxycarbonyl)-D-valine; (S)-3-((Acetamidomethyl)thio)-2-((tert-butoxycarbonyl)amino)-3-methylbutanoic acid; 3-[(Acetamidomethyl)sulfanyl]-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-D-valine. Grades: ≥95%. CAS No. 201421-14-9. Molecular formula: C13H24N2O5S. Mole weight: 320.41. | |
| Boc-S-acetamidomethyl-L-penicillamine | Boc-S-acetamidomethyl-L-penicillamine is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Boc-L-Pen(Acm)-OH; Boc-β,β-dimethyl-L-Cys(Acm)-OH; N-tert-butoxycarbonyl-S-acetamidomethyl-L-penicillamine; Boc-Cys(Me2)(Acm)-OH; (R)-3-((acetamidomethyl)thio)-2-((tert-butoxycarbonyl)amino)-3-methylbutanoic acid; 3-[(Acetamidomethyl)sulfanyl]-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-valine; L-Valine, 3-[[(acetylamino)methyl]thio]-N-[(1,1-dimethylethoxy)carbonyl]-. Grades: ≥95%. CAS No. 129972-45-8. Molecular formula: C13H24N2O5S. Mole weight: 320.41. | |
| Boc-S-methyl-L-penicillamine dicyclohexylammonium salt | Boc-S-methyl-L-penicillamine dicyclohexylammonium salt is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Boc-L-Pen(Me)-OH DCHA; Boc-β,β-dimethyl-L-Cys(Me)-OH DCHA; N-tert-butoxycarbonyl-S-methyl-L-penicillamine dicyclohexylamine; Dicyclohexylamine (R)-2-((tert-butoxycarbonyl)amino)-3-methyl-3-(methylthio)butanoate; N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-3-(methylsulfanyl)-L-valine N-cyclohexylcyclohexanamine (1:1); L-Valine, N-[(1,1-dimethylethoxy)carbonyl]-3-(methylthio)-, compd. with N-cyclohexylcyclohexanamine (1:1). Grades: ≥95%. CAS No. 112898-23-4. Molecular formula: C11H21NO4S.C12H23N. Mole weight: 444.68. | |
| Boc-S-trityl-D-penicillamine | Boc-S-trityl-D-penicillamine is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Boc-D-Pen(Trt)-OH; Boc-b,b-dimethyl-D-Cys(Trt)-OH; N-t-Butoxycarbonyl-S-trityl-D-penicillamine; N-(tert-Butoxycarbonyl)-3-[(triphenylmethyl)sulfanyl]-D-valine; (S)-2-(tert-Butoxycarbonylamino)-3-methyl-3-(tritylthio)butanoic acid; N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-3-(tritylsulfanyl)valine; N-[(1,1-Dimethylethoxy)carbonyl]-3-[(triphenylmethyl)thio]-D-valine. Grades: ≥95%. CAS No. 135592-14-2. Molecular formula: C29H33NO4S. Mole weight: 491.64. | |
| Boc-S-trityl-L-penicillamine | Boc-S-trityl-L-penicillamine is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Boc-L-Pen(Trt)-OH; Boc-β,β-dimethyl-L-Cys(Trt)-OH; Boc-Pen(Trt)-OH; N-[(1,1-Dimethylethoxy)carbonyl]-3-[(triphenylmethyl)thio]-L-valine; (R)-2-((tert-Butoxycarbonyl)amino)-3-methyl-3-(tritylthio)butanoic acid; N-alpha-t-Butoxycarbonyl-S-trityl-L-penicillamine; N-(tert-Butoxycarbonyl)-3-[(triphenylmethyl)sulfanyl]-L-valine; N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-3-(tritylsulfanyl)valine. Grades: ≥95%. CAS No. 135592-13-1. Molecular formula: C29H33NO4S. Mole weight: 491.64. | |
| Cadrofloxacin | Cadrofloxacin, also known as Caderofloxacin and CS-940, is a novel fluoroquinolone antibacterial. The activities of CS-940 against gram-positive cocci and gram-negative rods, including methicillin-susceptible Staphylococcus aureus and penicillin-resistant Streptococcus pneumoniae, were comparable to those of tosufloxacin, with MICs at which 90% of the strains were inhibited (MIC90s) of 0.5 microg/ml or less. Against methicillin-resistant S. aureus, CS-940 was as active as tosufloxacin, with a MIC90 of 16 microg/ml. The efficacy of CS-940 against murine respiratory infections due to S. pneumoniae or Haemophilus influenzae was better than those of tosufloxacin and sparfloxacin. The efficacy of oral doses of CS-940 reflected not only potent in vitro activity but also a high transmigration ratio from the bloodstream to lung tissues. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CS-940; CS 940; CS940; Cadrofloxacin; Caderofloxacin; Cadrofloxacin hydrochloride; Cadrofloxacin HCl. Product Category: Others. Appearance: Solid powder. CAS No. 153808-85-6. Molecular formula: C19H20F3N3O4. Mole weight: 411.38. Purity: >98%. IUPACName: (S)-1-cyclopropyl-8-(difluoromethoxy)-6-fluoro-7-(3-methylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid. Canonical SMILES: O=C(C1=CN(C2CC2)C3=C(C=C(F)C(N4C[C@H](C)NCC4)=C3OC(F)F)C1=O)O. Density: 1.458g/cm³. Product ID: ACM153808856. Alfa Chem |  |
| Ceforanide | It is produced by the strain of Semisynthetic second generation cephalosporin for injection. Ceforanide is a beta-lactam, broad-spectrum antibiotic. It has bactericidal activity and is used in the sterilization in various medical procedures. It causes inhibition of bacterial cell wall synthesis by inactivating penicillin binding proteins (PBPs) thereby interfering with the final transpeptidation step required for cross-linking of peptidoglycan units which are a component of the cell wall. It has a longer elimination half-life than any currently available cephalosporin. Uses: Ceforanide has bactericidal activity and is used in the sterilization in various medical procedures. Synonyms: Precef; Ceforanido; Ceforanidum; 7-(o-(Aminomethyl)phenylacetamido)-3-(((1-(carboxymethyl)-1H-tetrazol-5-yl)thio)methyl)-3-cephem-4-carboxylic acid; (6R,7R)-7-(2-(alpha-Amino-o-tolyl)acetamido)-3-(((1-(carboxymethyl)-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid; (6R-trans)-7-(((2-(Aminomethyl)phenyl)acetyl)amino)-3-(((1-(carboxymethyl)-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid; Antibiotic BL-S 786. Grades: 95%. CAS No. 60925-61-3. Molecular formula: C20H21N7O6S2. Mole weight: 519.55. | |
| Cefsulodin sodium | Cefsulodin (SCE-129) sodium is a third generation β lactam antibiotic and member of the cephems subgroup of antibiotics. Cefsulodin sodium inhibits cell wall synthesis by competitively inhibiting penicillin binding protein ( PBP ) cross-linking and transpeptidation of peptidogly. Cefsulodin sodium is a potent tyrosine phosphatase inhibitor against mPTPB , a virulent phosphatase from Mycobacterium tuberculosis , with an IC 50 value of 16 μM [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SCE-129 sodium. CAS No. 52152-93-9. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-13588. | |
| Ceftobiprole | Ceftobiprole (Ro 63-9141) is a broad-spectrum cephalosporin with high levels of in vitro activity against methicillin- (MRSA) and vancomycin-resistant staphylococci (VRSA) and penicillin-resistant streptococci with a MIC 90 value of 2 μg/mL for MRSA. Ceftobiprole also inhibits gram-positive and gram-negative pathogens. Ceftobiprole can be used for the study of hospital-acquired pneumonia (excluding ventilator-associated pneumonia) and community-acquired pneumonia [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 63-9141; BAL 9141. CAS No. 209467-52-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112579. | |
| Ceftobiprole | Ceftobiprole (Ro 63-9141) is a broad-spectrum cephalosporin with high levels of in vitro activity against methicillin- (MRSA) and vancomycin-resistant staphylococci (VRSA) and penicillin-resistant streptococci with a MIC90 value of 2 μg/mL for MRSA. Ceftobiprole also inhibits gram-positive and gram-negative pathogens. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Ceftobiprole;5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid,7-[[(2Z)-2-(5-aMino-1,2,4-thiadiazol-3-yl)-2-(hydroxyiMino)acetyl]aMino]-8-oxo-3-[(E)-[(3R)-2-oxo[1,3-bipyrrolidin]-3-ylidene]Methyl]-,(6R,7R)-. Product Category: Inhibitors. CAS No. 209467-52-7. Molecular formula: C20H22N8O6S2. Mole weight: 534.576. Purity: ≥95.0%. Product ID: ACM209467527. Alfa Chemistry ISO 9001:2015 Certified. | |
| Ceftobiprole medocaril sodium | Ceftobiprole medocaril (BAL5788) sodium is the parenteral proagent of Ceftobiprole (HY-112579). Ceftobiprole is a parenteral pyrrolidinone cephalosporin. Ceftobiprole is a broad-spectrum cephalosporin with high levels of in vitro activity against methicillin- (MRSA) and vancomycin-resistant staphylococci (VRSA) and penicillin-resistant streptococci. Ceftobiprole also inhibits gram-positive and gram-negative pathogens [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAL5788 sodium. CAS No. 252188-71-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-106574A. | |
| Ceftobiprole medocaril sodium | Ceftobiprole medocaril sodium is a water-soluble prodrug ceftobiprole, a 5th-generation cephalosporin for the treatment of hospital-acquired pneumonia (excluding ventilator-associated pneumonia) and community-acquired pneumonia. Ceftobiprole binds to penicillin-binding proteins (PBPs) and inhibits their transpeptidase activity. Synonyms: Ceftobiprole medocaril; BAL5788; BAL-5788. CAS No. 252188-71-9. Molecular formula: C26H25N8NaO11S2. Mole weight: 712.6. | |
| Ceftriaxone Sodium | Ceftriaxone Sodium is an antibiotic, a third-generation cephalosporin. It has broad-spectrum activity against Gram-positive bacteria and expanded Gram-negative coverage. lt is useful for the treatment of a number of bacterial infections, includeing ear infections, skin infections, urinary tract infections, pneumonia, gonorrhea, pelvic inflammatory disease, bone and joint infections, intra-abdominal infections, and meningitis and so on. It is used preoperatively to reduce the risk of postoperative infections. It inhibits bacterial cell wall synthesis by means of binding to the penicillin-binding proteins. It is a stimulator of EAAT2 expression with neuroprotective effects in both in ... stimulator of eaat2 expression with neuroprotective effects in both in vitro and in vivo models, which is based in part on its ability to inhibit neuronal cell death by glutamate excitotoxicity. Synonyms: 2,5,6-tetrahydro-2-methyl-5,6-dioxo-)(methoxyimino)acetyl)amino)-8-oxo-3-(((4-triazin-3-yl)thio)methyl)-,sodiumsalt,hydrate(2:4:7)(6r-(6-alpha,7-2;beta(z)))-; [6R-[6alpha, 7beta (Z)]]-7-[[ (2-Amino-4-thiazolyl) (methoxyimino)acetyl]amino]-8-oxo-3-[[ (1, 2, 5, 6-tetrahydro-2-methyl-5, 6-dioxo-1, 2, 4-triazin-3-yl)thio]methyl]-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic acid sodium salt. Grades: 98%. CAS No. 74578-69-1. Molecular formula: C18H16N8Na2O7S3. Mole weight: 598.54. | |
| Cephalexin | Cefalexin, also spelled cephalexin, is an antibiotic that can treat a number of bacterial infections. It kills gram-positive and some gram-negative bacteria by disrupting the growth of the bacterial cell wall. Cefalexin is a beta-lactam antibiotic within the class of first-generation cephalosporins. It works similarly to other agents within this class, including intravenous cefazolin, but can be taken by mouth.Cefalexin can treat certain bacterial infections, including those of the middle ear, bone and joint, skin, and urinary tract. It may also be used for certain types of pneumonia, strep throat, and to prevent bacterial endocarditis. Cefalexin is not effective against infections caused by methicillin-resistant Staphylococcus aureus (MRSA), Enterococcus, or Pseudomonas. Like other antibiotics, cefalexin cannot treat viral infections, such as the flu, common cold or acute bronchitis. Cefalexin can be used in those who have mild or moderate allergies to penicillin. However, it is not recommended in those with severe penicillin allergies.Common side effects include upset stomach and diarrhea. An allergic reaction and infection with Clostridium difficile, a type of diarrhea, is also possible. To date, no evidence of harm to the baby has been found when used during pregnancy or breast feeding. It can be used in children and those over 65 years of age. Those with kidney problems may require a decrease in dose.In 2012, cefalexin wa | |
| Cephalexin | Cephalexin (Cefalexin) is a potent, orally active semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefalexin; Cephacillin. CAS No. 15686-71-2. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g; 10 g. Product ID: HY-B0200. | |
| Cephalexin hydrochloride | Cephalexin (Cefalexin) hydrochloride is a potent, orally active new semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin (Cefalexin) hydrochloride has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin (Cefalexin) hydrochloride targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin (Cefalexin) hydrochloride is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefalexin hydrochloride; Cephacillin hydrochloride. CAS No. 59695-59-9. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B0200A. | |
| Cephalexin monohydrate | Cephalexin (Cefalexin) monohydrate is a potent, orally active new semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin (Cefalexin) monohydrate has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin (Cefalexin) monohydrate targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin (Cefalexin) monohydrate is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefalexin hydrate; Cephacillin hydrate. CAS No. 23325-78-2. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0200B. | |
| Cephalexin (Standard) | Cephalexin (Standard) is the analytical standard of Cephalexin. This product is intended for research and analytical applications. Cephalexin (Cefalexin) is a potent, orally active semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefalexin (Standard); Cephacillin (Standard). CAS No. 15686-71-2. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0200R. | |
| Cephapirin benzathine | Cephapirin benzathine is a first-generation cephalosporin with a broad spectrum of activity against gram-positive and gram-negative organisms. Its resistance to β-lactamase is higher than that of the penicillin family. commonly used in the veterinary field. Synonyms: Cefapirin benzathine. CAS No. 97468-37-6. Molecular formula: C50H54N8O12S4. Mole weight: 1087.27. | |
| Cephradine monohydrate | Cephradine (Cefradine) monohydrate is a broad-spectrum and orally active cephalosporin. Cephradine monohydrate is active against both grampositive and gram-negative pathogens and effective in eradicating most penicillinase-producing organisms known to be resistant to penicillin G, penicillin V, and ampicillin. Cephradine monohydrate has been used in the research of genitourinary, gastrointestinal and respiratory tract infections, and in infections of the skin and soft tissues. Cephradine monohydrate blocks solar-ultraviolet induced skin inflammation through direct inhibition of TOPK [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefradine monohydrate. CAS No. 75975-70-1. Pack Sizes: 100 mg; 500 mg. Product ID: HY-128449. | |
| Ciclacillin | Ciclacillin is produced by the strain of Semi-synthetic broad-spectrum penicillin. The antibacterial activity of cyclociline against 101 strains of Escherichia coli, 50 strains of Proteus and 59 strains of Staphylococcus aureus was lower than that of ampicillin and carboxpicillin. The blood concentration is higher than ampicillin, but excretion is fast. Synonyms: Aminocyclohexylpenicillin; Calthor; Ciclacillin; Ciclacillum; Citosarin; Cyclapen; (Aminocyclohexyl)penicillin; Syngacillin; Ultracillin; Vastcillin; Vatracin; Vipicil; Wy 4508; Wyvital; (1-Aminocyclohexyl)penicillin; 6- (1-Aminocyclohexanecarboxamido) penicillanic Acid; [2S-(2α,5α,6β)]-6-[[(1-Aminocyclohexyl)carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid; 6-(1-Aminocyclohexanecarboxamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid. Grades: 98%. CAS No. 3485-14-1. Molecular formula: C15H23N3O4S. Mole weight: 341.42. | |
| Dicloxacillin | Dicloxacillin, a β-lactamase resistant penicillin similar to oxacillin, used to treat infections caused by susceptible (non-resistant) Gram-positive bacteria. Uses: Used as an antibiotic especially against gram-positive bacteria and also be significant in biological studies. Synonyms: Veracillin, BRL1702; BRL 1702; BRL-1702;(2S,5R,6R)-6-[[3-(2,6-dichlorophenyl)-5-methyl-1,2-oxazole-4-carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid. Grades: ≥95%. CAS No. 3116-76-5. Molecular formula: C19H17Cl2N3O5S. Mole weight: 470.32. | |
| Dicloxacillin Sodium | Dicloxacillin is a β-lactamase resistant penicillin similar to oxacillin and it has activity against gram-positive/negative aerobic and anaerobic bacteria. Synonyms: Veracillin, BRL1702; BRL 1702; BRL-1702. Grades: >98%. CAS No. 343-55-5. Molecular formula: C19H17Cl2N3NaO5S. Mole weight: 493.32. | |
| Dicloxacillin Sodium Salt Monohydrate | The sodium monohydrate salt form of Dicloxacillin, a β-Lactam compound, could be used as an antibiotic especially against Gram-positive bacteria and also be significant in biological studies. Synonyms: (2S,5R,6R)-6-[[[3-(2,6-Dichlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt Hydrate; 3-(2,6-Dichlorophenyl)-5-methyl-4-isoxazolyl Penicillin Sodium Salt Monohydrate; Dichlorstapenor Sodium; Dicloxacillin Sodium Hydrate; P1011; Sodium Dicloxacillin Monohydrate; BRL1702; BRL 1702; BRL-1702; P 1011; P-1011; P1011; 3-(2,6-DICHLOROPHENYL)-5-METHYL-4-ISOXAZOLYL PENICILLIN; DICLOXACILLIN SODIUM SALT HYDRATE VETRAN; DICLOXACILLIN SODIUM EPD(CRM STANDARD); DICLOXACILLIN SODIUM USP(CRM STANDARD); DICLOXACILLIN SODIUM WHO(CRM STANDARD); 4-Thia-1-azabicyclo3.2.0heptane-2-carbox. Grades: 97%. CAS No. 13412-64-1. Molecular formula: C19H16Cl2N3NaO5S.H2O. Mole weight: 510.32. | |
| DL-Penicillamine | DL-Penicillamine is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Uses: Antidotes. Synonyms: 3,3-Dimenthyl-DL-cysteine; DL-2-Amino-3-mercapto-3-methylbutanoic acid; 3-Mercapto-DL-valine; (±)-Penicillamine; 2-Amino-3-mercapto-3-methylbutyric Acid; 3,3-Dimethylcysteine; DL-3-Mercaptovaline; DL-β-Mercaptovaline; DMC; NSC 22880; NSC 44656; dl-DMC; β,β-Dimethylcysteine; β-Mercaptovaline; β-Thiovaline; 2-amino-3-methyl-3-sulfanylbutanoic acid. Grades: ≥95%. CAS No. 52-66-4. Molecular formula: C5H11NO2S. Mole weight: 149.21. | |
| D-Penicillamine 98+%. | A Penicillin metabolite used in the treatment of Wilsons disease, Cystinuria, Scleroderma and arsenic poisoning. Group: Biochemicals. Alternative Names: D-Pen-OH; 3-Mercapto-D-valine; (2S)-2-Amino-3-methyl-3-sulfanylbutanoic Acid; (S)-3,3-Dimethylcysteine; Cuprenil; Cuprimine; Cupripen; D-3-Mercaptovaline; D-Mercaptovaline; D-Penamine; Depamine; Depen; Kuprenil; Mercaptyl; Metalcaptase; NSC 81549. Grades: Highly Purified. CAS No. 52-67-5. Pack Sizes: 10g, 25g, 50g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| D-Penicillamine 99+%. | A Penicillin metabolite used in the treatment of Wilsons disease, Cystinuria, Scleroderma and arsenic poisoning. Group: Biochemicals. Alternative Names: D-Pen-OH; 3-Mercapto-D-valine; (2S)-2-Amino-3-methyl-3-sulfanylbutanoic Acid; (S)-3,3-Dimethylcysteine; Cuprenil; Cuprimine; Cupripen; D-3-Mercaptovaline; D-Mercaptovaline; D-Penamine; Depamine; Depen; Kuprenil; Mercaptyl; Metalcaptase; NSC 81549. Grades: Reagent Grade. CAS No. 52-67-5. Pack Sizes: 5g, 25g. US Biological Life Sciences. | Worldwide |
| Ertapenem | Ertapenem has in vitro activity against gram-positive and gram-negative aerobic and anaerobic bacteria. The bactericidal activity of ertapenem results from the inhibition of cell wall synthesis and is mediated through ertapenem binding to penicillin binding proteins (PBPs). In Escherichia coli, it has strong affinity toward PBPs 1a, 1b, 2, 3, 4 and 5 with preference for PBPs 2 and 3. Ertapenem is stable against hydrolysis by a variety of beta-lactamases, including penicillinases, and cephalosporinases and extended spectrum beta-lactamases. Ertapenem is hydrolyzed by metallo-beta-lactamases. Ertapenem has been shown to be active against most isolates of the following microorganisms in vitro and in clinical infections. Synonyms: (1R,5S,6S,8R,2'S,4'S)-2-(2-(3-carboxyphenylcarbamoyl)pyrrolidin-4-ylthio)-6-(1-hydroxyethyl)-1-methylcarbapenem-3-carboxylic acid; 1-Azabicyclo(3.2.0)hept-2-ene-2-carboxylic acid, 3-(((3S,5S)-5-(((3-carboxyphenyl)amino)carbonyl)-3-pyrrolidinyl)thio)-6-((1R)-1-hydroxyethyl-4-methyl-7-oxo-, (4R,5S,6S)-; 1-Azabicyclo(3.2.0)hept-2-ene-2-carboxylic acid, 3-((5-(((3-carboxyphenyl)amino)carbonyl)-3-pyrrolidinyl)thio)-6-(1-hydroxyethyl)-4-methyl-7-oxo-, (4R-(3(3S*, 5S*), 4α, 5β, 6β(R*)))-. Grades: 95%. CAS No. 153832-46-3. Molecular formula: C22H25N3O7S. Mole weight: 475.52. | |
| Ertapenem Sodium | Ertapenem Sodium is the sodium salt of ertapenem. Ertapenem has in vitro activity against gram-positive and gram-negative aerobic and anaerobic bacteria. The bactericidal activity of ertapenem results from the inhibition of cell wall synthesis and is mediated through ertapenem binding to penicillin binding proteins (PBPs). In Escherichia coli, it has strong affinity toward PBPs 1a, 1b, 2, 3, 4 and 5 with preference for PBPs 2 and 3. Ertapenem is stable against hydrolysis by a variety of beta-lactamases, including penicillinases, and cephalosporinases and extended spectrum beta-lactamases. Ertapenem is hydrolyzed by metallo-beta-lactamases. Ertapenem has been shown to be active against most isolates of the following microorganisms in vitro and in clinical infections. Synonyms: Invanz; Ertapenem sodium salt; MK-0826. Grades: 98%. CAS No. 153773-82-1. Molecular formula: C22H24N3NaO7S. Mole weight: 497.50. | |
| Flucloxacillin Sodium | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopypesticides & metabolitespharma & vet compounds & metabolitespesticides & metabolitespharma & vet compounds & metabolitesbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: Flucloxacillin sodium, NSC 277175, Monosodium flucloxacillin,4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, (2S,5R,6R)- (9CI), Sodium [3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]penicillin, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolecarboxamido]-3,3-dimethyl-7-oxo-, sodium salt (7CI), Floxapen, Floxapen sodium, Sodium flucloxacillin, Staphylex, Flucloxacillin sodium salt, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, [2S-(2?,5?,6?)]-, Floxacillin sodium, BRL-2039. | |
| Fmoc-S-acetamidomethyl-D-penicillamine | Fmoc-S-acetamidomethyl-D-penicillamine is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Fmoc-D-Pen(Acm)-OH; Fmoc-S-acetamidomethyl-β,β-dimethyl-D-Cys-OH; N-(fluorenylmethoxycarbonyl)-S-acetamidomethyl-D-penicillamine; (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-((acetamidomethyl)thio)-3-methylbutanoic acid; 3-[(Acetamidomethyl)sulfanyl]-N-{[(9H-fluoren-9-yl)methoxy]carbonyl}-D-valine. Grades: ≥95%. CAS No. 201531-77-3. Molecular formula: C23H26N2O5S. Mole weight: 442.53. | |
| Fmoc-S-acetamidomethyl-L-penicillamine | Fmoc-S-acetamidomethyl-L-penicillamine is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Fmoc-L-Pen(Acm)-OH; Fmoc-S-acetamidomethyl-β,β-dimethyl-L-Cys-OH; Fmoc-Pen(Acm)-OH; N-(fluorenylmethoxycarbonyl)-S-acetamidomethyl-L-penicillamine; (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-((acetamidomethyl)thio)-3-methylbutanoic acid; Fmoc-Cys(Me2)(Acm)-OH; 3-[(Acetamidomethyl)sulfanyl]-N-{[(9H-fluoren-9-yl)methoxy]carbonyl}-L-valine. Grades: ≥95%. CAS No. 201531-76-2. Molecular formula: C23H26N2O5S. Mole weight: 442.53. | |
| Fmoc-S-benzyl-D-penicillamine | Fmoc-S-benzyl-D-penicillamine is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Fmoc-D-Pen(Bzl)-OH; Fmoc-S-benzyl-β,β-dimethyl-D-Cys-OH; Fmoc-D-Pen(Bn)-OH; (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(benzylthio)-3-methylbutanoic acid; 3-(Benzylsulfanyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-valine; N-α-(9-Fluorenylmethoxycarbonyl)-S-benzyl-D-penicillamine. Grades: ≥95%. CAS No. 139551-73-8. Molecular formula: C27H27NO4S. Mole weight: 461.57. | |
| Fmoc-S-trityl-D-penicillamine | Fmoc-S-trityl-D-penicillamine is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Fmoc-D-Pen(Trt)-OH; Fmoc-S-trityl-β,β-dimethyl-D-Cys-OH; (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-methyl-3-(tritylthio)butanoic acid; N-alpha-(9-Fluorenylmethyloxycarbonyl)-S-trityl-D-penicillamine; N-{[(9H-Fluoren-9-yl)methoxy]carbonyl}-3-[(triphenylmethyl)sulfanyl]-D-valine. Grades: ≥95%. CAS No. 201532-01-6. Molecular formula: C39H35NO4S. Mole weight: 613.76. | |
| Fmoc-S-trityl-L-penicillamine | Fmoc-S-trityl-L-penicillamine is a derivative of D-Penicillamine, which is a penicillin metabolite used in the treatment of Wilson's disease, Cystinuria, Scleroderma and arsenic poisoning. Synonyms: Fmoc-L-Pen(Trt)-OH; Fmoc-S-trityl-β,β-dimethyl-L-Cys-OH; Fmoc-Pen(Trt)-OH; (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-methyl-3-(tritylthio)butanoic acid; N-Fmoc-3-(trityl-thio)-L-valine; N-{[(9H-Fluoren-9-yl)methoxy]carbonyl}-3-[(triphenylmethyl)sulfanyl]-L-valine; N-alpha-(9-Fluorenylmethyloxycarbonyl)-S-trityl-L-penicillamine. Grades: ≥95%. CAS No. 201531-88-6. Molecular formula: C39H35NO4S. Mole weight: 613.77. | |
| isopenicillin-N N-acyltransferase | Proceeds by a two stage mechanism via 6-aminopenicillanic acid. Different from EC 3.5.1.11, penicillin amidase. Group: Enzymes. Synonyms: acyl-coenzyme A:isopenicillin N acyltransferase; isopenicillin N:acyl-CoA: acyltransferase. Enzyme Commission Number: EC 2.3.1.164. CAS No. 54576-90-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2104; isopenicillin-N N-acyltransferase; EC 2.3.1.164; 54576-90-8; acyl-coenzyme A:isopenicillin N acyltransferase; isopenicillin N:acyl-CoA: acyltransferase. Cat No: EXWM-2104. | |
| Lactamase (Crude Enzyme) | Penicillinase from Bacillus cereushas been shown to contain three distinct species when purified and examined for homogeneity by sedimentation analysis, amino-terminal analysis, and vertical acrylamide gel electrophoresis. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Synthesis; medicine; biotechnology; pharmacology. Group: Enzymes. Synonyms: penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase. Pack: 100ml. Cat No: NATE-1839. | |
| L-Penicillamine Hydrochloride | L-Penicillamine Hydrochloride is a metabolite of Penicillin. Penicillin belongs to the β-lactam class of antibiotics, is a very common antibacterial drug. Synonyms: 3-Mercapto-L-valine Hydrochloride; NSC 81988; (R)-2-Amino-3-mercapto-3-methylbutanoic Acid Hydrochloride; Penicillamine DL-form hydrochloride; (+)-penicillamine hydrochloride. Grades: 95%. CAS No. 25526-04-9. Molecular formula: C5H12ClNO2S. Mole weight: 185.67. | |
| Moxifloxacin Hydrochloride | Moxifloxacin Hydrochloride is the hydrochloride salt preparation of Moxifloxacin, an 8-methoxy-fluoroquinone compound with broad-spectrum bactericidal activity against gram-positive and gram-negative strains. 8-methoxy-fluoroquinones are described to inhibit the activities of DNA gyrase and topoisomerase IV. The 8-methoxy group of Moxifloxacin is suggested to confer a lowered propensity for resistance development as compared to other C-8 substituted quinolones, and Moxifloxacin demonstrates potent activity against wild-type and first-step gyrase- and topoisomerase IV-resistant mutants. Moxifloxacin shows activity against methicillin-susceptible staphylococci, penicillin-susceptible and penicillin-resistant pneumococci, penicillin-susceptible and penicillin-resistant viridans group streptococci, group A streptococci, M. catarrhalis, and H. influenzae in vitro. Group: Biochemicals. Alternative Names: (1'S,6',S)-1-Cyclopropyl-7-(2,8-diazabicyclo[4.3.0]non-8-yl)-6-fluoro-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid hydrochloride; 1-Cyclopropyl-6-fluoro-8-methoxy-7-[(4aS,7aS)-octahydropyrrolo[3,4-b]pyridin-6-yl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid hydrochloride. Grades: Highly Purified. CAS No. 186826-86-8. Pack Sizes: 5g, 10g, 25g, 50g, 100g. US Biological Life Sciences. | Worldwide |
| muramoylpentapeptide carboxypeptidase | A bacterial enzyme that requires a divalent cation for activity. Does not cleave the C-terminal D-alanine from the product of the above reaction, UDP-N-acetyl-muramoyl-L-alanyl-γ-D-glutamyl-6-carboxy-L-lysyl-D-alanine. Competitively inhibited by penicillins and cephalosporins. Group: Enzymes. Synonyms: D-alanine carboxypeptidase I; DD-carboxypeptidase; D-alanine carboxypeptidase; D-alanyl-D-alanine carboxypeptidase; D-alanine-D-alanine-carboxypeptidase; carboxypeptidase D-alanyl-D-alanine; carboxypeptidase I; UDP-N-acetylmuramoyl-tetrapeptidyl-D-alanine alanine-hydrolase; D-alanyl-D-alanine peptidase; DD-peptidase; penicillin binding protein 5; PBP5; PdcA; VanY. Enzyme Commission Number: EC 3.4.17.8. CAS No. 9077-67-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4080; muramoylpentapeptide carboxypeptidase; EC 3.4.17.8; 9077-67-2; D-alanine carboxypeptidase I; DD-carboxypeptidase; D-alanine carboxypeptidase; D-alanyl-D-alanine carboxypeptidase; D-alanine-D-alanine-carboxypeptidase; carboxypeptidase D-alanyl-D-alanine; carboxypeptidase I; UDP-N-acetylmuramoyl-tetrapeptidyl-D-alanine alanine-hydrolase; D-alanyl-D-alanine peptidase; DD-peptidase; penicillin binding protein 5; PBP5; PdcA; VanY. Cat No: EXWM-4080. | |
| muramoyltetrapeptide carboxypeptidase | Variants are known from various microorganisms. Involved in peptidoglycan synthesis, catalysing both decarboxylation and transpeptidation. Stimulated by divalent cations such as Mg2+ and Ca2+, but not by Zn2+. Inhibited by thiol-blocking reagents, but unaffected by penicillin. Group: Enzymes. Synonyms: carboxypeptidase IIW; carboxypeptidase II; lysyl-D-alanine carboxypeptidase; L-lysyl-D-alanine carboxypeptidase; LD-carboxypeptidase. Enzyme Commission Number: EC 3.4.17.13. CAS No. 60063-80-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4065; muramoyltetrapeptide carboxypeptidase; EC 3.4.17.13; 60063-80-1; carboxypeptidase IIW; carboxypeptidase II; lysyl-D-alanine carboxypeptidase; L-lysyl-D-alanine carboxypeptidase; LD-carboxypeptidase. Cat No: EXWM-4065. | |
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