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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences Doxycycline Hydrochloride, Ready Made Solution , 10592-13-9
Doxycycline Hydrochloride, Ready Made Solution
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Cayman Chemical DCPIP asy Reagent 700UG
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An analytical reference standard categorized as a quinazolinone intended for research and forensic applications
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Medchemexpress LLC HY-B0568 5g Medchemexpress, Deferiprone CAS:30652-11-0 Purity:98%
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Medchemexpress,HY-B0568 5g Deferiprone CAS:30652-11-0 Formula:C7H9NO2 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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Selleck Chemical LLC Ribostamycin Sulfate S4215-50mg
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Ribostamycin Sulfate(Vistamycin Sulfate Landamycine) is an aminoglycoside antibiotic containing a neutral sugar moiety and is produced by Streptomyces ribosidi cus
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Ambeed AMBEED
5000885979 AZITHROMYCIN 10G
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Medchemexpress LLC Umeclidinium bromide | 869113-09-7 | 99.7% | 25MG
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Umeclidinium bromide | 869113-09-7 | 99.7% | 25MG
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Selleck Chemical LLC THZ2
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THZ2 a THZ1 analog is a selective inhibitor of CDK7 with IC50 of 13 9 nM THZ2 efficiently suppresses the clonogenic growth of TNBC cells with IC50 of 10 nM
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Alkali Scientific Tobramycin [O 3 Amino 3 deoxy α D glucopyranosyl (1 6) O [2, 6 diamino 2, 3, 6 trideoxy α D ribohexopyranosyl (1 4)] 2 deoxy D streptamine], 1 Gram
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Tobramycin is an aminoglycoside antibiotic used to treat serious bacterial infections, particularly those caused by Gram-negative organisms. The 1 gram powder form is commonly used in clinical settings for preparing injectable solutions. Tobramycin works by binding to bacterial ribosomes, disrupting protein synthesis, and ultimately causing cell death. It is frequently used in the treatment of infections such as pneumonia, urinary tract infections, and sepsis. In laboratory research, tobramycin is used to study bacterial resistance mechanisms and to evaluate the effectiveness of new antibiotic formulations in combating multi-drug resistant organisms.
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Medchemexpress LLC Vortioxetine hydrobromide | 960203-27-4 | C18H23BrN2S | 500 MG
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Vortioxetine hydrobromide is a multimodal serotonergic agent that acts as an antagonist for 5-HT3A and 5-HT7 receptors, an inhibitor of the 5-hydroxytryptamine transporter (SERT), a 5-HT1A agonist, and a partial 5-HT1B agonist. It is intended for research use.
- Antagonist for 5-HT3A and 5-HT7 receptors
- Inhibitor of 5-hydroxytryptamine transporter (SERT)
- Agonist for 5-HT1A receptors
- Partial agonist for 5-HT1B receptors
- Increases cell proliferation and survival
- Stimulates maturation of immature granule cells in hippocampus
- Does not cause cognitive or psychomotor impairment
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Medchemexpress LLC Vortioxetine (hydrobromide) | 960203-27-4 | C18H23BrN2S | 200 MG
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Vortioxetine hydrobromide is an antagonist of 5-HT3A and 5-HT7 receptors and an inhibitor of the 5-hydroxytryptamine transporter (SERT). It also acts as a 5-HT1A agonist and a partial 5-HT1B agonist. This compound is intended for research use only.
- Antagonist of 5-HT3A and 5-HT7 receptors
- Inhibitor of 5-hydroxytryptamine transporter (SERT)
- 5-HT1A agonist
- Partial 5-HT1B agonist
- Intended for research use only
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Medchemexpress LLC Vortioxetine | 508233-74-7 | C18H22N2S | 500 MG
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Vortioxetine (Lu AA 21004) is an antagonist of 5-HT3A and 5-HT7 receptors (Ki: 3.7 nM, 19 nM) and an inhibitor of serotonin transporter (SERT) (Ki: 1.6 nM). It also acts as a 5-HT1A agonist and a partial agonist of 5-HT1B (Ki: 15 nM, 33 nM).
- Antagonistic properties at 5-HT3A and 5-HT7 receptors.
- Partial agonist properties at 5-HT1B receptors.
- Agonistic properties at 5-HT1A receptors.
- Potent inhibition of SERT.
- Significantly increases cell proliferation and cell survival, and stimulates maturation of immature granule cells in the sub granular zone of the dentate gyrus of the hippocampus after 21 days of treatment.
- Does not cause cognitive or psychomotor impairment.
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Alkali Scientific Carbenicillin, Disodium Salt, 1 G
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Carbenicillin Disodium Salt is a beta-lactam antibiotic used in microbiological research for its ability to inhibit bacterial cell wall synthesis. It interferes with the formation of peptidoglycan cross-links, leading to weakened cell walls and bacterial lysis. Carbenicillin is commonly used in molecular biology for the selection of plasmid-containing bacteria, particularly in cloning and transformation experiments. Compared to ampicillin, it offers improved stability and reduced satellite colony formation. This compound is widely applied in cell culture and microbiology laboratories for maintaining selective pressure in bacterial cultures and supporting studies involving gene expression, recombinant DNA technology, and antimicrobial activity.
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eMolecules 515-64-0 | Sulfisomidine | Combi-Blocks | MFCD00010567 | 278.330 | C12H14N4O2S | 95.000 | Cc1cc(NS(=O)(=O)c2ccc(N)cc2)nc(C)n1 | 5g | 290703365
Sulfisomidine | Combi-Blocks | 515-64-0 | MFCD00010567 | 278.330 | C12H14N4O2S | 95.000 | Cc1cc(NS(=O)(=O)c2ccc(N)cc2)nc(C)n1 | 5g | 290703365
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TARGETMOL CHEMICALS INC Tacrolimus 50mg
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Tacrolimus can bind FKBP12 to form a high-affinity complex (Ki: 0.2 nM) which inhibits the activity of the calcium/calmodulin-dependent protein phosphatase.
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Medchemexpress LLC Lyn-1604 dihydrochloride | 2310109-38-5 | 99.6% | 657.54 g/mol | C33H45Cl4N3O2 | 25 MG
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LYN-1604 dihydrochloride is a potent small-molecule activator of UNC-51-like kinase 1 (ULK1) used in preclinical research, including studies of triple-negative breast cancer. The compound exhibits strong activity (reported EC50 18.94 nM) and is supplied as the dihydrochloride salt to improve handling and solubility. For research use only.
- Potent ULK1 activation (EC50 18.94 nM).
- High purity (≈99.6%).
- Supplied as a dihydrochloride salt for improved solubility.
- Solid form; stable when stored sealed at 4°C; in solution store at -80°C (up to 6 months) or -20°C (up to 1 month) per guidance.
- Available in multiple small research pack sizes suitable for preclinical studies.
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