Sulbactam
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Category | Enzyme inhibitors |
Catalog number | BBF-03931 |
CAS | 68373-14-8 |
Molecular Weight | 233.24 |
Molecular Formula | C8H11NO5S |
Purity | >98% |
Online Inquiry
Description
Sulbactam is a β-lactamase inhibitor. This drug is given in combination with β-lactam antibiotics to inhibit β-lactamase, an enzyme produced by bacteria that destroys the antibiotics.
Specification
Related CAS | 69388-84-7 (sodium) |
Synonyms | RO-1-9213; RO 1-9213; RO1-9213 |
Storage | Store at -20°C |
IUPAC Name | (2S,5R)-3,3-dimethyl-4,4,7-trioxo-4lambda6-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid |
Canonical SMILES | CC1(C(N2C(S1(=O)=O)CC2=O)C(=O)O)C |
InChI | InChI=1S/C8H11NO5S/c1-8(2)6(7(11)12)9-4(10)3-5(9)15(8,13)14/h5-6H,3H2,1-2H3,(H,11,12)/t5-,6+/m1/s1 |
InChI Key | FKENQMMABCRJMK-RITPCOANSA-N |
Source | Semi-synthetic |
Properties
Appearance | White Solid |
Boiling Point | 356°C |
Melting Point | >130°C |
Flash Point | 297.1°C |
Density | 1.62 g/cm3 |
Solubility | Soluble in ethanol, methanol, DMF, DMSO |
LogP | 0.22370 |
Reference Reading
1.Analysis of drug resistance in 1,861 strains of Acinetobacter baumannii.
Jin H1, Qiu F2, Ji HJ1, Lu Q1. Biomed Rep. 2016 Apr;4(4):463-466. Epub 2016 Feb 15.
Acinetobacter baumannii is an emerging human pathogen that causes hospital-acquired infections. The trend in increased antimicrobial resistance limits the choice of effective antimicrobial agents. The present study reports the resistance to Acinetobacter baumannii and analyzes the associations between antibiotic use and resistance rates at a general hospital between 2010 and 2014. A total of 1,861 isolates were obtained from clinical cultures, accounting for 10.33% of all detected bacteria (1,861/18,016). The strains were mainly from respiratory samples (1,628 isolates, 87.5%) and the intensive care unit (696 isolates, 37.4%). The resistance rates of Acinetobacter baumannii to the majority of antibiotics were >50%, particularly the resistance rate to cefoperazone/sulbactam increased from 47.37 in 2011 to 89.25% in 2014. However, the rates of imipenem and cilastatin sodium decreased from 81.03 to 69.44% due to the antibiotic policy. There were Pearson significant associations between the use of three antibiotics and resistance in Acinetobacter baumannii to this drug, piperacillin/tazobactam (r=0.
2.Rice-Field Drowning-Associated Pneumonia in which Pseudomonas spp., Aspergillus fumigatus, and Cunninghamella sp. Are Isolated.
Yamawaki S1, Nakashima K, Suzuki F, Otsuki A, Watanabe J, Takai M, Katsurada M, Katsurada N, Ohkuni Y, Misawa M, Kaneko N, Otsuka Y, Aoshima M. Intern Med. 2016;55(7):825-9. doi: 10.2169/internalmedicine.55.4454. Epub 2016 Apr 1.
We herein report the case of an 84-year-old who developed pneumonia after drowning in a rice field. Besides Aspergillus fumigatus, many pathogens previously not reported in drowning-associated pneumonia (such as Pseudomonas fluorescens, Pseudomonas putida, Nocardia niigatensis, and Cunninghamella sp.) were isolated from his sputum. He received sulbactam/ampicillin, trimethoprim/sulfamethoxazole, voriconazole, levofloxacin and liposomal amphotericin B, but died due to respiratory failure. Because the patient had drowned in a contaminated stagnant rice field and had multiple lung cavities, zygomycosis was suspected. This report provides invaluable information for the consideration of zygomycosis after an individual drowning in a rice field, even in an immunocompetent patient.
3.Treatment for patients with multidrug resistant Acinetobacter baumannii pulmonary infection.
Pan T1, Liu X1, Xiang S1, Ji W1. Exp Ther Med. 2016 Apr;11(4):1345-1347. Epub 2016 Feb 8.
Bacterial infections are common but have become increasingly resistant to drugs. The aim of the present study was to examine the combined treatment of traditional Chinese and Western medicine in 30 cases of pulmonary infection with multidrug resistant Acinetobacter baumannii. Patients were divided into groups A and B according to drug treatments. Cefoperazone or sulbactam and tanreqing were administered in group A, and cefoperazone or sulbactam in group B. The curative effect and prognosis of the two groups were recorded and the remaining treatments were performed routinely in the clinic. For the combined therapy group, which was administered sulperazone and tanreqing, 8 patients were recovered, 6 patients had significant effects, 3 patients exhibited some improvement and 1 patient had no response. One of the patients did not survive after 28 days. By contrast, there were 4 patients that were successfully treated, 3 patients with significant effects, 2 patients with some improvement and 2 patients had no response in the sulperazone group, and 4 patients did not survive after 28 days.
4.Prospective open-label randomized comparative, non-inferiority study of two initial antibiotic strategies for patients with nursing- and healthcare-associated pneumonia: Guideline-concordant therapy versus empiric therapy.
Matsuda S1, Ogasawara T2, Sugimoto S3, Kato S4, Umezawa H5, Yano T2, Kasamatsu N2. J Infect Chemother. 2016 Apr 6. pii: S1341-321X(16)30013-7. doi: 10.1016/j.jiac.2016.03.003. [Epub ahead of print]
BACKGROUND AND OBJECTIVE: The nursing- and healthcare-associated pneumonia guideline, proposed by the Japan Respiratory Society, recommends that patients at risk of exposure to drug-resistant pathogens, classified as treatment category C, be treated with antipseudomonal antibiotics. This study aimed to prove the non-inferiority of empirical therapy in our hospital compared with guideline-concordant therapy.
Recommended Products
BBF-05781 | Emodepside | Inquiry |
BBF-05877 | Coenzyme Q10 | Inquiry |
BBF-03880 | Cyclopamine | Inquiry |
BBF-03753 | Baicalin | Inquiry |
BBF-05808 | Triptolide | Inquiry |
BBF-03816 | Milbemycin oxime | Inquiry |
Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳