Cell Culture Media, Supplements, and Reagents
Medchemexpress LLC Ulipristal | 159811-51-5 | ≥98.0% | 433.58 | 50 MG
Ulipristal is a selective progesterone receptor modulator (SPRM) that binds to the progesterone receptor, inhibiting PR-mediated gene expression and interfering with progesterone activity in the reproductive system.
- Selective progesterone receptor modulator (SPRM)
- Binds to the progesterone receptor
- Inhibits PR-mediated gene expression
- Interferes with progesterone activity in the reproductive system
- May suppress the growth of uterine leiomyomatosis
- Can be used as emergency contraception by inhibiting or delaying ovulation and affecting endometrial tissue
Medchemexpress LLC ILK-IN-3 50mg | 6975-75-3 | 50 MG
ILK-IN-3 is an orally active integrin-linked kinase (ILK) inhibitor supplied as a 50 mg research reagent. It is used in preclinical studies to modulate ILK activity and has been reported to enhance the anticancer efficacy of docetaxel in orthotopic LCC6 models. For research use only.
- Orally active ILK inhibitor suitable for in vitro and in vivo studies.
- Reported to improve docetaxel anticancer efficacy in LCC6 model.
- High purity (>99% by LCMS) for reproducible results.
- Supplied as a solid powder with recommended cold storage for stability.
- Provided with certificate of analysis and datasheet for quality and handling information.
Apexbio Technology LLC Azomycin 527-73-1 250mg
Azomycin (CAS 527-73-1) is a small-molecule inhibitor that interferes with electron transport pathways in aerobic Gram-positive and Gram-negative bacteria It is designed to disrupt cellular electron transfer processes thereby inhibiting bacterial respiratory function Azomycin exerts its biological activity primarily through inhibition of microbial electron transport In in vitro assays Azomycin demonstrates inhibitory activity with IC50 values typically in the micromolar concentration range though specific values may vary depending on bacterial strain and experimental conditions Based on these pharmacological properties Azomycin holds research potential in studies of bacterial metabolic pathways antimicrobial resistance mechanisms and novel antibacterial therapeutic strategies
Medchemexpress LLC Ulipristal | 159811-51-5 | ≥98.0% | 433.58 | 100 MG
Ulipristal is a selective progesterone receptor modulator (SPRM). It functions by binding to the progesterone receptor, which inhibits PR-mediated gene expression and interferes with progesterone activity in the reproductive system.
- May suppress the growth of uterine leiomyomatosis.
- Can be used as an emergency contraception.
- Inhibits or delays ovulation.
- Affects endometrial tissue.
eMolecules Medchem Express / Fanapanel / 10mg / 446264956 / HY-15069 / / 161605-73-8 / MFCD07364000 / 409.258 / C14H15F3N3O6P
Medchem Express / Fanapanel / 10mg / 446264956 / HY-15069 / / 161605-73-8 / MFCD07364000 / 409.258 / C14H15F3N3O6P
Medchemexpress LLC Cefetamet | 65052-63-3 | 99.1% | C14H15N5O5S2 | 5 MG
Cefetamet is a cephalosporin antibiotic and the active metabolite of Cefetamet pivoxil. It targets bacterial penicillin-binding protein (PBP) and exhibits significant activity against a range of Gram-negative bacteria, including Enterobacteriaceae and *Haemophilus influenzae*, as well as Gram-positive bacteria like Streptococcus. This compound effectively kills and lyses *Treponema pallidum*.
- Cephalosporin antibiotic
- Active against Gram-negative and Gram-positive bacteria
- Targets bacterial penicillin-binding protein (PBP)
- Kills and lyses *Treponema pallidum*
- Used in research for bacterial infections
Medchemexpress LLC Abiraterone-d4 | 2122245-62-7 | 98.0% | C24H27D4NO | 1 MG
Abiraterone-d4 is a deuterium-labeled version of Abiraterone, acting as a potent, irreversible inhibitor of CYP17A1. It exhibits antiandrogen activity by inhibiting 17α-hydroxylase and 17,20-lyase activities of CYP17 (IC50 values of 2.5 nM and 15 nM, respectively). Intended for research use only, it serves as a tracer or internal standard for quantitative analysis methods like NMR, GC-MS, or LC-MS. Deuteration aids quantitation in drug development and can influence pharmacokinetic and metabolic profiles.
- Potent, irreversible CYP17A1 inhibitor
- Antiandrogen activity, inhibiting 17α-hydroxylase and 17,20-lyase activities of CYP17
- For research use only
- Tracer or internal standard for quantitative analysis (NMR, GC-MS, LC-MS)
- Deuteration for quantitation in drug development and influencing pharmacokinetic profiles
Medchemexpress LLC Vortioxetine (Standard) | 508233-74-7 | MFCD22380814 | C18H22N2S | 100 MG
Vortioxetine (Lu AA 21004) is a multimodal serotonergic agent with antagonistic properties at 5-HT3A and 5-HT7 receptors, partial agonist properties at 5-HT1B receptors, and agonistic properties at 5-HT1A receptors. It also acts as a potent inhibitor of the serotonin transporter (SERT). This product is intended for research and analytical applications, and does not cause cognitive or psychomotor impairment.
- Antagonist of 5-HT3A and 5-HT7 receptors
- Inhibitor of serotonin transporter (SERT)
- Agonist of 5-HT1A receptors
- Partial agonist of 5-HT1B receptors
- Increases cell proliferation and survival
- Stimulates maturation of immature granule cells
- Intended for research and analytical applications
Apexbio Technology LLC Tobramycin 32986-56-4 10mM (in 1mL H20)
Tobramycin (CAS 32986-56-4) is a small-molecule inhibitor targeting the bacterial ribosomal 30S subunit It is designed to interfere with protein synthesis thereby inhibiting bacterial growth Tobramycin exerts its biological activity primarily through specific binding to the 30S subunit preventing translation and subsequent bacterial proliferation In in vitro and in vivo studies Tobramycin demonstrates inhibitory activity with reported IC50 values ranging from 0 2 g/mL to 4 g/mL depending on the bacterial strain and experimental conditions Based on these pharmacological properties Tobramycin holds research potential in the investigation of bacterial infection mechanisms including studies of Pseudomonas aeruginosa and models of bacterial pneumonia as well as in the exploration of bacterial resistance mechanisms
Medchemexpress LLC HY-11087 10mg Medchemexpress, SD 0006 CAS:271576-80-8 Purity:>98%
Medchemexpress, HY-11087 10mg SD 0006 CAS:271576-80-8 SD 0006 (SD-06) is an orally active, selective, ATP-competitive and potent diaryl pyrazole inhibitor of p38α MAP kinase, with an IC50 of 110 nM for p38α. 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.