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Filtered Search Results
Medchemexpress LLC HY-10395 5mg Medchemexpress, PD173955 CAS:260415-63-2 Purity:>98%
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Medchemexpress, HY-10395 5mg PD173955 CAS:260415-63-2 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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Enzo Life Sciences Fluphenazine-N-2-chloroethane . 2HCl (50mg). CAS: 83016-35-7
A potent irreversible inactivator of calmodulin. Possesses potent antiproliferative and cytotoxic activity. It is also an irreversible D2 dopamine receptor antagonist. Alternative name: SKF-7171A. Purity: ≥98%. Solubility: Soluble in DMSO (50mg/ml) or water (10mg/ml warm). Long Term Storage: Ambient.
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![eMolecules Medchem Express / NU6140 / 5mg / 482203877 / HY-107419 / / 444723-13-1 / [null] / 422.533 / C23H30N6O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502459968.PNG-250.jpg)
eMolecules Medchem Express / NU6140 / 5mg / 482203877 / HY-107419 / / 444723-13-1 / [null] / 422.533 / C23H30N6O2
Medchem Express / NU6140 / 5mg / 482203877 / HY-107419 / / 444723-13-1 / [null] / 422.533 / C23H30N6O2
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eMolecules Medchem Express / KW-2449 / 5mg / 446258113 / HY-10339 / / 1000669-72-6 / MFCD18385006 / 332.407 / C20H20N4O
Medchem Express / KW-2449 / 5mg / 446258113 / HY-10339 / / 1000669-72-6 / MFCD18385006 / 332.407 / C20H20N4O
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eMolecules Medchem Express / BAY-678 / 5mg / 437899129 / HY-111457A / / 675103-36-3 / MFCD29924806 / 400.361 / C20H15F3N4O2
Medchem Express / BAY-678 / 5mg / 437899129 / HY-111457A / / 675103-36-3 / MFCD29924806 / 400.361 / C20H15F3N4O2
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AdipoGen Tetracycline hydrochloride, 64-75-5, MFCD00078142, 5 g
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MF: C22H24N2O8 . HCl, MW: 480.9, ≥99%, Appearance: Yellow to orange powder. Tetracycline is a broad-spectrum antibiotic that prevents bacterial growth by inhibiting protein synthesis. It binds to a single site in the 30S ribosomal subunit which prevents attachment of aminoacyl tRNA to the ribosomal acceptor site. It is used in cell biology as a selective agent in cell culture systems. Tetracycline is toxic to prokaryotic and eukaryotic cells and selects for cells harboring the bacterial tetR gene, which are resistant to the antibiotic.
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eMolecules 5-Methylhydantoin | 616-03-5 | MFCD00022398 | 25g
Apollo Scientific | 5-Methylhydantoin | 25g | 562438593 | OR451305 | 95.000 | 616-03-5 | MFCD00022398 | 114.104 | C4H6N2O2
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Medchemexpress LLC HY-100036 2mg Medchemexpress, MK-4101 CAS:935273-79-3 Purity:>98%
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Medchemexpress, HY-100036 2mg MK-4101 CAS:935273-79-3 MK-4101 is a Smoothened (SMO) antagonist ( IC 50 of 1.1 µM for 293 cells ) and also a potent inhibitor of the hedgehog pathway ( IC 50 of 1.5 µM for mouse cells; IC 50 of 1 µM for KYSE180 oesophageal cancer cells). MK-4101 has robust antitumor activity that inhibits tumor cell proliferation and induces extensive apoptosis [1] . 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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eMolecules Medchem Express / Rbin-1 / 5mg / 446256136 / HY-100816 / / 328023-11-6 / MFCD02369534 / 256.330 / C13H12N4S
Medchem Express / Rbin-1 / 5mg / 446256136 / HY-100816 / / 328023-11-6 / MFCD02369534 / 256.330 / C13H12N4S
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Medchemexpress LLC HY-13861 100mg Medchemexpress, GW7647 CAS:265129-71-3 Purity:98%
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Medchemexpress,HY-13861 100mg GW7647 CAS:265129-71-3 Formula:C29H46N2O3S GW7647 is a potent PPARα agonist, with EC50s of 6 nM, 1.1 μM, and 6.2 μM for human PPARα, PPARγ and PPARδ, respectively. 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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eMolecules Medchem Express / SU 5402 / 5mg / 446258554 / HY-10407 / / 215543-92-3 / MFCD08235144 / 296.326 / C17H16N2O3
Medchem Express / SU 5402 / 5mg / 446258554 / HY-10407 / / 215543-92-3 / MFCD08235144 / 296.326 / C17H16N2O3
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Medchemexpress LLC Cefetamet (Ro 15-8074) | 65052-63-3 | 99.1% | C14H15N5O5S2 | 50 MG
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Cefetamet (Ro 15-8074) is a cephalosporin antibiotic and the active metabolite of Cefetamet pivoxil. It functions by binding to bacterial penicillin-binding protein (PBP), with an IC50 for PBP3 in *Escherichia coli* W3110 of 2.5 μg/mL.
- Demonstrates significant activity against various Gram-negative bacteria (including Enterobacteriaceae, Neisseria species, and Haemophilus influenzae) and Gram-positive bacteria such as Streptococcus.
- Exhibits high in vitro activity against most members of Enterobacteriaceae, Haemophilus influenzae, Neisseria spp., and Streptococcus pneumoniae (MIC90 ≤ 2 μg/mL).
- Kills and lyses Treponema pallidum.
- Can be utilized in research for respiratory tract, urinary tract, ear, nose, and throat infections, and syphilis.
- In vivo studies show it can cure experimental syphilis in rabbits (1-30 mg/kg; i.m.; once).
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Medchemexpress LLC Zuclopenthixol-d4 succinate | 1246833-97-5 | 99.0% | C26H27D4ClN2O5S | 1 MG
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Zuclopenthixol-d4 succinate is the deuterium labeled Zuclopenthixol. Zuclopenthixol is a thioxanthene derivative which acts as a mixed dopamine D1/D2 receptor antagonist. It is for research use only and not sold to patients. Deuteration has gained attention because of its potential to affect 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
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eMolecules Medchem Express / Fluopyram / 10mg / 455326178 / HY-119459 / / 658066-35-4 / MFCD17166960 / 396.720 / C16H11ClF6N2O
Medchem Express / Fluopyram / 10mg / 455326178 / HY-119459 / / 658066-35-4 / MFCD17166960 / 396.720 / C16H11ClF6N2O
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Medchemexpress LLC Daptomycin | 103060-53-3 | >99.7% | C72H101N17O26 | 50 MG
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Daptomycin is a lipopeptide antibiotic characterized by its rapid in vitro bactericidal activity specifically against gram-positive organisms. This compound plays a crucial role in anti-infection pathways, functioning as an effective bacterial inhibitor for research applications.
- Lipopeptide antibiotic
- Rapid in vitro bactericidal activity
- Effective against gram-positive organisms
- Inhibitor target
- Suitable for research use
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