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Filtered Search Results
Medchemexpress LLC Erythromycin estolate | 3521-62-8 | 100 MG
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Erythromycin estolate is a macrolide antibiotic derived from Erythromycin, utilized for treating a broad spectrum of bacterial infections. It has been noted to cause liver injury, often presenting as cholestatic hepatitis, with its toxicity linked to inhibiting bile acid transport. This compound also exhibits antiviral properties by inactivating viral particles and destroying their membrane integrity.
- Used as a macrolide antibiotic.
- Effective against a wide variety of bacterial infections.
- Causes liver injury, predominantly cholestatic hepatitis.
- Toxicity is associated with inhibiting bile acid transport.
- Inactivates viral particles by destroying viral membrane integrity.
- Inhibits various flaviviruses, including Zika, dengue, and yellow fever viruses.
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Medchemexpress LLC Clindamycin palmitate hydrochloride | 25507-04-4 | 98.2% | 1 ML
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Clindamycin palmitate hydrochloride is a hydrochloride salt of the ester of clindamycin and palmitic acid. It functions as an antibacterial agent. While it is inactive in vitro, it rapidly hydrolyzes in vivo to become the antibacterially active clindamycin.
- Functions as an antibacterial agent.
- Inactive in vitro, but rapidly converts to active clindamycin in vivo.
- Available in various forms, including solid and solution.
- Strict storage conditions ensure product stability and efficacy.
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Sigma Aldrich Fine Chemicals Biosciences (−)-Thalidomide | 841-67-8 | MFCD00210219 | 10mg
(−)-Thalidomide | Purity: 98% | Mol Wt: 258.23 | 841-67-8 | MFCD00210219 | 10mg
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Medchemexpress LLC HY-10585A 5g , Valproic acid (sodium salt) Sodium Valproate CAS:1069-66-5 Purity:98%
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Medchemexpress, HY-10585A 5g Valproic acid (sodium salt) Sodium Valproate CAS:1069-66-5 Formula:C8H15NaO2 IC 50 : 400 μM (HDAC1), 0.5-2 mM (HDAC) HDAC2 [6] Purity:98% Valproic acid sodium salt is an HDAC inhibitor, with IC 50 in the range of 0.5 and 2 mM, also inhibits HDAC1 ( IC 50 , 400 μM), and induces proteasomal degradation of HDAC2 ; Valproic acid sodium salt is used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches. Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-B0522A 5g , Ampicillin (sodium) D-(-)-α-Aminobenzylpenicillin sodium salt CAS:69-52-3 Purity:98%
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Medchemexpress, HY-B0522A 5g Ampicillin (sodium) D-(-)-α-Aminobenzylpenicillin sodium salt CAS:69-52-3 Formula:C16H18N3NaO4S Purity:98% Ampicillin sodium is a broad-spectrum beta-lactam antibiotic against a variety of gram-positive and gram-negative bacteria. Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Takara Bio Aureobasidin A, 10mg
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Aureobasidin A (AbA) is a cyclic depsipeptide antibiotic, isolated from the filamentous fungus Aureobasidium pullulans R106, which is toxic to yeast at low concentrations (0.10.5 g/ml). Sensitive species include Saccharomyces cerevisiae, Schizosaccharomyces pombe, Candida glabrata, Aspergillus nidulans and A. niger. AbA inhibits a yeast enzyme, inositol phosphorylceramide (IPC) synthase, which is expressed from the AUR1 gene. Expression of a mutant gene, AUR1-C, in transformed yeast confers resistance to the drug.
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Apexbio Technology LLC Carbenicillin, Disodium Salt(Synonyms: Carbenicillin disodium, Disodium carbenicillin, Carbenicillin sodium salt), 10mM (in 1mL H2O), CAS: 4800-94-6.
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Carbenicillin disodium salt (CAS 4800-94-6) is a semi-synthetic -lactam antibiotic commonly employed in biomedical research As a -lactam it inhibits bacterial cell-wall biosynthesis by irreversibly binding and inactivating bacterial transpeptidase enzymes thereby preventing the cross-linking of peptidoglycan layers required for cell wall integrity Carbenicillin is predominantly utilized against gram-negative bacteria although it also retains limited activity toward some gram-positive strains Due to its resistance to -lactamase-mediated degradation carbenicillin can substitute ampicillin for selecting plasmids encoding the bla (ampicillin resistance) gene in bacterial cultures
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Medchemexpress LLC Rifampicin | 13292-46-1 | 98.2% | 1 ML
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Rifampicin is a potent, broad-spectrum antibiotic effective against bacterial pathogens, and it also exhibits anti-influenza virus and anti-orthopoxvirus activities. It is intended for research use only.
- Potent, broad-spectrum antibiotic
- Effective against bacterial pathogens
- Exhibits anti-influenza virus activity
- Exhibits anti-orthopoxvirus activity
- Available as a 10 mM * 1 mL solution in DMSO
- Ready for reconstitution
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eMolecules 6-Nitropyridin-3-amine | 14916-65-5 | MFCD01646117 | 1g
Ambeed | 6-Nitropyridin-3-amine | 1g | 552553142 | A124465 | | 14916-65-5 | MFCD01646117 | 139.114 | C5H5N3O2
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Medchemexpress LLC Dydrogesterone-d6 | 152-62-5 | 1 MG
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Dydrogesterone-d6 is a deuterium-labeled version of Dydrogesterone. Dydrogesterone is an orally active and potent progestogen, used for various gynecological conditions resulting from progesterone deficiency. It is intended for research use only and not for patient use. Deuterium substitution in drug molecules is being explored for its potential to influence pharmacokinetic and metabolic profiles.
- Can be utilized as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
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Medchemexpress LLC Cefoperazone sodium salt | 62893-20-3 | 98.4% | 500 MG
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Cefoperazone sodium salt is a semisynthetic cephalosporin with a broad spectrum of antibacterial activity. It is intended for research use only.
- Semisynthetic cephalosporin with broad-spectrum antibacterial activity.
- Protects granulocytopenic mice from acute *Pseudomonas aeruginosa* pneumonia in in vitro studies.
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Medchemexpress LLC Enrofloxacin-d5 | 1173021-92-5 | 99.8% | 5 MG
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Enrofloxacin-d5 is a deuterium-labeled form of Enrofloxacin, an effective antibiotic with an MIC90 of 0.312 μg/mL for Mycoplasma bovis. Stable heavy isotopes have been incorporated into this drug molecule, primarily as tracers for quantitation during drug development. Deuteration can impact the pharmacokinetic and metabolic profiles of drugs.
- Can be used as a tracer
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- Deuterium labeling may affect pharmacokinetic and metabolic profiles
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Medchemexpress LLC MC-Val-Cit-PAB-Auristatin E | 2055896-77-8 | 97.0% | 1287.65 | C68H108N11O13 | 5 MG
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MC-Val-Cit-PAB-Auristatin E is an antibody-drug conjugate (ADC) linker-payload conjugate for research use. It links the cytotoxic tubulin inhibitor auristatin E to an MC-Val-Cit-PAB cleavable linker, enabling enzymatic release of the payload in target cells. The material is provided as a solid for preclinical and ADC development studies.
- cleavable val-cit dipeptide linker enabling enzymatic payload release
- contains auristatin E tubulin inhibitor as the payload
- molecular formula C68H108N11O13 and molecular weight 1287.65
- purity ~97.0% by HPLC (batch-specific certificate of analysis available)
- supplied as a solid with good solubility in DMSO for formulation
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Medchemexpress LLC Brilacidin (tetrahydrochloride) | 1224095-99-1 | 1082.75 | 5 MG
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Brilacidin tetrahydrochloride is an anti-infective antimicrobial. It demonstrates MIC90s of 1 and 8 μg/mL for Gram-positive bacteria such as *Streptococcus pneumonia* and *Streptococcus viridans*, and MIC90s of 8 and 4 μg/mL for Gram-negative bacteria including *Haemophilus influenza* and *Pseudomonas aeruginosa*. This compound acts as a defensin mimetic antibiotic.
- Functions as an anti-infective antimicrobial
- Acts as a defensin mimetic antibiotic compound
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Medchemexpress LLC Spectinomycin dihydrochloride | 21736-83-4 | 99.7% | 1 ML
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Spectinomycin dihydrochloride is a broad-spectrum antibiotic that inhibits the growth of various gram-positive and gram-negative organisms. It acts by selectively targeting the bacterial ribosome, thereby interrupting protein synthesis. It is also a noncompetitive inhibitor of td intron RNA with a Ki value of 7.2 mM.
- Inhibits protein synthesis in cells and Escherichia coli extracts
- Blocks the translocation of peptidyl-tRNAs from the A-site to the P-site
- Exhibits splicing inhibition dependent on pH changes and Mg2+ concentration
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