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Filtered Search Results
eMolecules 1364488-67-4 | Medchem Express | YH239-EE | 10mg | 446260943 | HY-12287 | MFCD28099816 | 504.41 | C25H27Cl2N3O4
Ambeed | 13-Difluoro-2-methyl-5-nitrobenzene | 250mg | 490505665 | A132644 | 170572-48-2 | MFCD03094192 | 173.119 | C7H5F2NO2
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eMolecules 13752-33-5 | Medchem Express | Panidazole | 5mg | 415686190 | HY-101715 | MFCD00866604 | 232.243 | C11H12N4O2
Ambeed | Barium 2266-tetramethyl-5-oxohept-3-en-3-olate | 1g | 601096364 | A983829 | 17594-47-7 | MFCD00058709 | 503.869 | C22H38BaO4
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Medchemexpress LLC HY-15510B 5mg Medchemexpress, Tenovin-6 (Hydrochloride) CAS:1011301-29-3 Purity:>98%
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Medchemexpress, HY-15510B 5mg Tenovin-6 (Hydrochloride) CAS:1011301-29-3 Tenovin-6 Hydrochloride, an analog of Tenovin-1 (HY-13423), is an activator of p53 transcriptional activity. Tenovin-6 Hydrochloride inhibits the protein deacetylase activities of purified human SIRT1, SIRT2, and SIRT3 with IC50s of 21 μM, 10 μM, and 67 μM, respectively. Tenovin-6 Hydrochloride also inhibits dihydroorotate dehydrogenase (DHODH)[2]. Purity:>98% 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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Cayman Chemical 1-AmInobenzotrIazole 250mg
A non-specific CYP inhibitor; acts as a suicide substrate, producing maximal destruction of hepatic and renal microsome CYP protein in vitro at 10 mM; effective in vivo, significantly reducing CYP content in both liver and kidney in rats within two hours
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Medchemexpress LLC Kasugamycin (hydrochloride hydrate) | 200132-83-8 | 99.9% | 500 MG
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Kasugamycin (Ksg) hydrochloride hydrate is an antibiotic that binds to 30s and 70s ribosomes but not to the 50s subunit, and has anti-infective activity. It mimics mRNA nucleotides, disrupts tRNA binding and inhibits canonical translation initiation. This product also increases the sensitivity of mycobacteria to Rifampicin in vitro and in mouse infection models.
- Antibiotic
- Binds to 30s and 70s ribosomes
- Anti-infective activity
- Mimics mRNA nucleotides
- Disrupts tRNA binding
- Inhibits canonical translation initiation
- Increases sensitivity of mycobacteria to Rifampicin
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Medchemexpress LLC IDH889 | 1429179-07-6 | 100.0% | 436.48 | 100 MG
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IDH889 is an orally available, brain penetrant, allosteric and mutant specific inhibitor of isocitrate dehydrogenase 1 (IDH1). It shows potent selectivity for IDH1 R132* mutations, with IC50s of 0.02 μM for IDH1R132H, 0.072 μM for IDH1R132C, and 1.38 μM for IDH1wt. IDH889 also demonstrates potent cellular inhibition of R-2-hydroxyglutarate (2-HG) production with an IC50 of 0.014 μM.
- Orally available
- Brain penetrant
- Allosteric and mutant specific IDH1 inhibitor
- Potent selectivity for IDH1 R132* mutations
- Potent cellular inhibition of R-2-hydroxyglutarate (2-HG) production
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Medchemexpress LLC N-desmethyl clomipramine hydrochloride | 29854-14-6 | MFCD00792880 | 100.0% | 337.29 g/mol | C18H22Cl2N2 | 100MG
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N-Desmethyl clomipramine hydrochloride is the primary N-desmethyl metabolite of clomipramine, supplied as the hydrochloride salt for use as an analytical reference standard in research on antidepressant metabolism and pharmacology. The product is provided as a solid powder in a range of pack sizes for analytical assays, method development, and reference material applications.
- Hydrochloride salt form
- Molecular weight 337.29 g/mol
- Chemical formula C18H22Cl2N2
- Provided as a solid powder
- Available in multiple pack sizes including 100 mg
- Intended for analytical and research use
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Cayman Chemical AzIthromycIn 250mg
A macrolide antibiotic; active against S. pneumoniae, S. aureus, N. gonorrhoeae, M. pneumoniae, H. pylori, C. trachomatis, and H. influenzae in vitro (MIC90s = S. pyogenes, S. pneumoniae, E. faecalis, or H. influenzae infection (ED50s = 0.78, 8.7, 12.7, and 30.3 mg/kg, respectively); decreases plasma levels of IL-6, TNF-α, and IL-1β and increases survival in mouse model of LPS-induced sepsis at 100 mg/kg
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Medchemexpress LLC 4-amino-2-[4-[1-(benzyloxycarbonyl)-2(S)-[(1,1-dimethylethyl)amino]carbonyl-piperazinyl]-6,7-dimethoxyqu | 189349-50-6 | 99.9% | 522.60 | C27H34N6O5 | 5 MG
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L-765314 is a research reagent: a selective α1B (alpha-1B) adrenergic receptor antagonist used to probe α1B-mediated signaling in pharmacology and neuroscience studies. It is supplied as a solid powder with documented affinity and high reported purity, suitable for in vitro and in vivo experiments.
- High affinity for α1B receptors (human Ki 2.0 nM; rat Ki 5.4 nM).
- High purity suitable for research (reported 99.92%).
- Solid powder form enabling flexible formulation and dosing.
- Molecular weight 522.60 and formula C27H34N6O5 for precise calculations.
- Stable under recommended storage conditions for long-term use.
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Bioworld Cefotaxime Sodium, 10 g
°°Cefotaxime SodiumBactericidal activityInhibits cell wall synthesisIn vitro activity against a wide range of gram-positive and gram-negative organismsHas a high degree of stability in the presence of -lactamases, both penicillinases and cephalosporinases, of gram-negative and gram-positive bacteriaSynonym: Cephotaxime; Sym-methoxyimino Cephalosporin; ClaforanFor in vitro lab use only. Not for human use or consumption.RTECS Number: XI0250000
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Medchemexpress LLC Streptomycin | 57-92-1 | 99.9% | 1 G
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Streptomycin is an effective antibiotic used in the research of tuberculosis (TB) against M. tuberculosis. It is also a bacteriocidal agent effective against a variety of bacterial infections. It strongly binds to nucleic acids, interfering with and blocking protein synthesis while still allowing RNA and DNA synthesis. Additionally, it functions as a common antibiotic in culture media and blocks stretch-activated and mechanosensitive ion channels in neurons and cardiac myocytes.
- Effective antibiotic against M. tuberculosis
- Bacteriocidal agent for research on various bacterial infections
- Interferes with and blocks protein synthesis
- Allows RNA and DNA synthesis to continue
- Common antibiotic in culture media
- Acts as a blocker of stretch-activated and mechanosensitive ion channels in neurons and cardiac myocytes
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Med Vet International Azithromycin Tablets, 250mg, 30ct
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Azithromycin is an antibiotic used to treat a range of bacterial infections. Azithromycin prevents bacteria from producing the proteins preventing them from multiplying
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Medchemexpress LLC Ipatasertib dihydrochloride | 1396257-94-5 | C24H34Cl3N5O2 | 2 MG
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Ipatasertib dihydrochloride is a highly selective, ATP-competitive pan-Akt inhibitor targeting Akt1, Akt2, and Akt3 with IC50s of 5, 18, and 8 nM, respectively. This compound demonstrates significant selectivity for Akt1 over PKA (more than 600-fold) and p70S6K (over 100-fold). In broader kinase profiling, it inhibits only PRKG1α, PRKG1β, and p70S6K by more than 70% at 1 μM concentration.
- Highly selective, ATP-competitive pan-Akt inhibitor
- Inhibits Akt1, Akt2, and Akt3 with high potency
- Demonstrates significant selectivity for Akt1 over PKA and p70S6K
- Inhibits PRKG1α, PRKG1β, and p70S6K at 1 μM
- Intended for research use only
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Sigma Aldrich Fine Chemicals Biosciences G 418 disulfate salt solution 50 mg/mL in H2O, 0.1 mum filtered, BioReagent, suitable for cell culture | Mol Wt: 692.71 | 108321-42-2 | MFCD00058314 | 50ML
G 418 disulfate salt solution 50 mg/mL in H2O, 0.1 mum filtered, BioReagent, suitable for cell culture | 108321-42-2 | MFCD00058314 | 50ML
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eMolecules 1125758-85-1 | A-804598 | 50mg
ChemScene | (2S4R)-tert-Butyl 4-(((benzyloxy)carbonyl)amino)-2-(hydroxymethyl)pyrrolidine-1-carboxylate | 100mg | 632321669 | CS-0150035 | 1194057-63-0 | MFCD18801151 | 350.415 | C18H26N2O5
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