Carboxylic acids and derivatives
Apexbio Technology LLC Moxalactam (sodium salt) 64953-12-4 1g
Moxalactam sodium salt (CAS 64953-12-4) is a small-molecule -lactam antibiotic belonging to the oxacephem subclass It is designed to inhibit bacterial cell wall biosynthesis by targeting penicillin-binding proteins (PBPs) Moxalactam sodium salt exerts its biological activity by interfering with PBPs thereby preventing cell wall synthesis In in vitro studies Moxalactam sodium salt demonstrates broad-spectrum inhibition of various Gram-positive Gram-negative and anaerobic bacteria including Klebsiella pneumoniae Escherichia coli Haemophilus influenzae and Neisseria gonorrhoeae Typical MIC values for susceptible organisms are generally in the low microgram-per-milliliter range Based on these pharmacological properties Moxalactam sodium salt holds research potential in antibacterial susceptibility assays studies on antibiotic resistance mechanisms and investigations of bacterial cell-wall synthesis pathways
Apexbio Technology LLC Cefotaxime (sodium salt)(Synonyms: Claforan, Cefotaxime Sodium, Cefotaxim sodium salt, Cefotaxime Na, Sodium cefotaxime), 10mM (in 1mL DMSO), CAS: 64485-93-4.
Cefotaxime sodium (CAS 64485-93-4) is a third-generation cephalosporin antibiotic belonging to the -lactam group characterized by inhibition of bacterial cell-wall synthesis through binding to penicillin-binding proteins In vitro analyses show strong inhibitory efficacy against various bacterial species notably cefotaxime exhibits an MIC below 0 1 g/ml against Streptococcus pneumoniae It also demonstrates high activity against Haemophilus influenzae including -lactamase-producing strains In vivo mouse model studies revealed that combination therapy of cefotaxime with minocycline enhanced survival following Vibrio vulnificus infection compared to single-agent treatments Clinically cefotaxime has been evaluated in pneumonia therapy demonstrating good tolerance and therapeutic utility in targeting susceptible bacterial pathogens
TARGETMOL CHEMICALS INC BUCINDOLOL FORMATE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Bucindolol Formatel is a blocker of (beta)1-adrenergic receptor. Bucindolol exhibits intrinsic sympathomimetic activity. Bucindolol can be used in the research of heart failure.
TARGETMOL CHEMICALS INC CARBENOXOLONE DISODIUM 100MG
Also available in 5 mg 10 mg 25 mg 50 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Carbenoxolone disodium (Duogastrone) salt is an agent derived from licorice root. It is used for the treatment of digestive tract ulcers especially in the stomach. Antidiuretic side effects are frequent but otherwise the drug is low in toxicity. purity: 98%
eMolecules 5855-79-8 | 3-Amino-5-sulfobenzoic acid | Combi-Blocks | MFCD01825295 | 217.200 | C7H7NO5S | 95.000 | Nc1cc(cc(c1)S(O)(=O)=O)C(O)=O | 1g | 482930410
3-Amino-5-sulfobenzoic acid | Combi-Blocks | 5855-79-8 | MFCD01825295 | 217.200 | C7H7NO5S | 95.000 | Nc1cc(cc(c1)S(O)(=O)=O)C(O)=O | 1g | 482930410
Cayman Chemical FR900098 sodium salt
A derivative of fosmidomycin that has antimalarial activity; inhibits DOXP reductoisomerase in vitro in a dose-dependent manner; exhibits in vitro antimalarial activity against three P. falciparum strains (IC50s = 170, 170, and 90 nM for HB3, A2, and Dd2 strains, respectively); FR900098 (>10 mg/kg, i.p.) eradicated P. vinckei parasites within four days in mice
eMolecules Medchem Express | MethADP (triammonium) | 5mg | 784543728 | HY-112502C | 476.324 | C11H26N8O9P2
Medchem Express | MethADP (triammonium) | 5mg | 784543728 | HY-112502C | | 476.324 | C11H26N8O9P2
Apexbio Technology LLC AVE 0991 sodium salt 306288-04-0 5mg
AVE 0991 sodium salt (CAS 306288-04-0) is a synthetic non-peptide agonist of the angiotensin-(1-7) receptor Mas Acting as a functional mimic of angiotensin-(1-7) AVE 0991 competitively binds to endothelial cell membranes with an IC50 of 21 35 nM in bovine aortic endothelial cells In vitro treatment with AVE 0991 promotes nitric oxide release to levels significantly greater than angiotensin-(1-7) In vivo AVE 0991 reduces urine volume and increases urine osmolality in mice effects reversed by angiotensin II antagonists indicating receptor specificity It also inhibits atherogenesis in ApoE knockout mice supporting its application in cardiovascular and renal research
![eMolecules 187227-45-8 | Oseltamivir acid | Medchem Express | MFCD00953940 | 284.356 | C14H24N2O4 | 98 | CCC(CC)O[C@@H]1C=C(C[C@H](N)[C@H]1NC(C)=O)C(O)=O | 50mg | 446262752](https://assets.fishersci.com/TFS-Assets/CCG/product-images/NC1643246.jpg-250.jpg)
eMolecules 187227-45-8 | Oseltamivir acid | Medchem Express | MFCD00953940 | 284.356 | C14H24N2O4 | 98 | CCC(CC)O[C@@H]1C=C(C[C@H](N)[C@H]1NC(C)=O)C(O)=O | 50mg | 446262752
Ambeed | (5R5aR8aR9S)-9-(((2R4aR6R7R8R8aS)-78-Dihydroxy-2-(thiophen-2-yl)hexahydropyrano[32-d][13]dioxin-6-yl)oxy)-5-(4-hydroxy-35-dimethoxyphenyl)-55a8a9-tetrahydrofuro[3467]naphtho[23-d][13]dioxol-6(8H)-one | 1mg | 761012304 | A102576 | 29767-20-2 | MFCD00866516 | 656.660 | C32H32O13S
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Alkali Scientific Oxacillin Sodium Salt Monohydrate, 1 G
Oxacillin Sodium Salt Monohydrate, 1G, is a laboratory-grade antibiotic used primarily for antimicrobial testing and research applications. As a penicillin-class antibiotic, it is effective against a variety of Gram-positive bacteria, particularly Staphylococcus species. Oxacillin works by inhibiting bacterial cell wall synthesis, which leads to cell death. This product is widely used in laboratory settings for studying bacterial resistance, particularly for assessing methicillin resistance in staphylococci. The 1g quantity is ideal for smaller scale studies and testing applications where precise antibiotic measurement is needed for microbial assays, including disk diffusion and dilution testing methods.
TARGETMOL CHEMICALS INC BMT-124110 FORMATE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. BMT-124110 Formate is a selective AAK1 inhibitor (IC50 0.9 nM) with anti-injury sensory activity.BMT-124110 Formate inhibits the BMP-2-inducible protein kinase BIKE with an IC50 17 nM.BMT-124110 Formate inhibits the cell-cycle protein G-related BMT-124110 Formate inhibits the cell cycle protein G-associated kinase GAK with an IC5099 nM.
![eMolecules Ambeed / Aluminum tristearate / 100g / 642079666 / A1150294 / / 637-12-7 / [null] / 877.410 / C54H105AlO6](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502427309.JPG-250.jpg)
eMolecules Ambeed / Aluminum tristearate / 100g / 642079666 / A1150294 / / 637-12-7 / [null] / 877.410 / C54H105AlO6
Ambeed / Aluminum tristearate / 100g / 642079666 / A1150294 / / 637-12-7 / [null] / 877.410 / C54H105AlO6
