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Filtered Search Results
Medchemexpress LLC 1- Cbz-amino cyclope 5g
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1-(Cbz-amino)cyclopentanecarboxylic acid (Cbz-cycloleucine) is a biochemical reagent that can be used as a biological material or organic compound for life science related research
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Medchemexpress LLC 1- Cbz-amino cyclope 10g
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1-(Cbz-amino)cyclopentanecarboxylic acid (Cbz-cycloleucine) is a biochemical reagent that can be used as a biological material or organic compound for life science related research
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Medchemexpress LLC (Z,E)-9,12-tetradecadien-1-ol | 42521-46-0 | MFCD00270832 | >95.0% | 210.36 g/mol | C14H26O | 1mL
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(Z E)-9 12-Tetradecadienol is a synthetic enhancer of male Ephestia cautella attraction[1]
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Medchemexpress LLC 1- Cbz-amino cyclope 100g
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1-(Cbz-amino)cyclopentanecarboxylic acid (Cbz-cycloleucine) is a biochemical reagent that can be used as a biological material or organic compound for life science related research
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Apexbio Technology LLC Z-WEHD-FMK(Synonyms: Z-WEHD fluoromethyl ketone, Z-WEHD-FMK inhibitor, Caspase-5 inhibitor Z-WEHD-FMK), 5mg, CAS: 210345-00-9.
Z-WEHD-FMK (CAS 210345-00-9) is a peptide-based inhibitor primarily targeting inflammatory caspases including caspase-1 -4 and -5 It irreversibly blocks caspase-mediated proteolytic cleavage interfering with cellular signaling pathways involved in inflammation and apoptosis Studies demonstrate that Z-WEHD-FMK treatment prevents Chlamydia-induced fragmentation of the Golgi apparatus by inhibiting golgin-84 cleavage thereby decreasing bacterial proliferation and altering lipid trafficking to pathogen-containing inclusions This inhibitor is frequently utilized in cell biology and infectious disease research to investigate caspase-related cellular processes and microbial pathogenesis mechanisms
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Medchemexpress LLC (Z)-10-hydroxynortriptyline-d3 | 47132-19-4 | 99.0% | 282.40 | C19H18D3NO | 5 MG
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Deuterium-labeled (Z)-10-hydroxynortriptyline-d3 is a stable isotope internal standard of 10-hydroxynortriptyline, provided as a high-purity analytical reagent for use as a tracer and quantitative reference in research applications. It is intended for analytical workflows requiring precise quantitation of metabolites and drug substances.
- Stable isotope internal standard for accurate quantitation.
- Compatible with NMR, GC-MS, and LC-MS analytical methods.
- High purity suitable for analytical assays and calibration.
- Available in small research quantities for method development.
- Useful as an internal standard or tracer in pharmacokinetic studies.
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Medchemexpress LLC (E/Z)-Zotiraciclib citrate | 1204918-73-9 | C29H32N4O8 | 10 MM 1 ML
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(E/Z)-Zotiraciclib citrate is a potent inhibitor of CDK2, JAK2, and FLT3, intended for research use only. It appears as a solid with an off-white to light yellow color and has a high purity of 99.83%. It is soluble in DMSO at 250 mg/mL, with various in vivo dissolution protocols available.
- Potent CDK2 inhibitor
- Potent JAK2 inhibitor
- Potent FLT3 inhibitor
- For research use only
- Off-white to light yellow solid appearance
- High purity of 99.83%
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Medchemexpress LLC (Z)-Lanoconazole | 101529-65-1 | 98.7% | C14H10ClN3S2 | 25 MG
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(Z)-Lanoconazole is the Z configuration of Lanoconazole, a potent and orally active imidazole antifungal agent. It exhibits a broad spectrum of activity against fungi both in vitro and in vivo by interfering with ergosterol biosynthesis, specifically inhibiting sterol 14-alpha demethylase and blocking fungal membrane ergosterol biosynthesis. This agent is suitable for the investigation of dermatophytosis and onychomycosis.
- Potent and orally active imidazole antifungal agent
- Broad spectrum of activity against fungi in vitro and in vivo
- Interferes with ergosterol biosynthesis
- Inhibits sterol 14-alpha demethylase
- Blocks fungal membrane ergosterol biosynthesis
- Used for investigation of dermatophytosis and onychomycosis
- Suppresses TPA-induced irritant dermatitis in vivo
- Inhibits C. neoformans in vivo and reduces its growth in lungs and brains of MAIDS mice
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Apexbio Technology LLC Z-DQMD-FMK 767287-99-0 5mg
Z-DQMD-FMK is a small-molecule inhibitor targeting caspase-3 It is designed to selectively and irreversibly inhibit caspase-3 thereby modulating caspase-3-mediated signaling pathways and apoptotic processes Z-DQMD-FMK exerts its biological activity primarily through covalent binding to active thiol residues of caspase-3 via its fluoromethyl ketone group resulting in irreversible inhibition Based on these pharmacological properties Z-DQMD-FMK holds research potential in investigating apoptotic mechanisms caspase-3-dependent signaling and proteolytic processing events including protein kinase C isoform cleavage under zinc deficiency oxidative stress and ischemic injury
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Cayman Chemical 4 Z 7 Z-DecadIenoIc AcId 10mg
A PUFA; increased in the plasma of patients with an MCAD deficiency
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Medchemexpress LLC (E/Z)-Teriflunomide | 108605-62-5 | 99.9% | 270.21 | 10 MG
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(E/Z)-Teriflunomide is the active metabolite of Leflunomide. Leflunomide is an immunomodulatory agent that may exert effects by inhibiting the mitochondrial enzyme dihydroorotate dehydrogenase (DHODH). It can be used for the research of rheumatoid arthritis (RA).
- Active metabolite of Leflunomide
- Immunomodulatory agent
- Inhibits mitochondrial enzyme dihydroorotate dehydrogenase (DHODH)
- Suitable for rheumatoid arthritis (RA) research
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Apexbio Technology LLC Z-Guggulsterone 39025-23-5 5mg
Z-Guggulsterone (CAS 39025-23-5) is a small-molecule antagonist targeting multiple steroid hormone receptors including glucocorticoid (IC50 1740 nM) mineralocorticoid (IC50 1000 nM) androgen (IC50 220 nM) progesterone (EC50 1200 nM) estrogen (EC50 5000 nM) and farnesoid X (IC50 50000 nM) receptors It is designed to modulate these targets thereby influencing steroid receptor-mediated signaling pathways Z-Guggulsterone exerts its biological activity primarily through inhibition of receptor-mediated angiogenic processes In cell-based studies Z-Guggulsterone demonstrates dose- and time-dependent inhibition of cellular migration and tube formation in DU145 prostate cancer cells and human umbilical vein endothelial cells (HUVEC) Based on these pharmacological properties Z-Guggulsterone holds research potential in studies of tumor-associated angiogenesis and steroid receptor signaling
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eMolecules 65564-05-8 | 3-(Cbz-amino)propanal | Accela ChemBio | MFCD05664298 | 207.229 | C11H13NO3 | 96.000 | O=CCCNC(=O)OCc1ccccc1 | 1g | 786458677
3-(Cbz-amino)propanal | Accela ChemBio | 65564-05-8 | MFCD05664298 | 207.229 | C11H13NO3 | 96.000 | O=CCCNC(=O)OCc1ccccc1 | 1g | 786458677
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Medchemexpress LLC (E/Z)-SIS3 free base | 1009104-85-1 | MFCD24368989 | 99.5% | 453.53 | C28H27N3O3 | 100mg
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E/Z-SIS3 free base exhibits an inhibitory efficacy against smad3 exhibits an anti-fibrotic and anti-inflammatory effect through a TGF- /smad3 signaling pathway[1]
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Aobchem 4-Bromo-3-(hydroxymethyl)benzonitrile | ≥95% | CAS 905710-66-9 | C8H6BrNO | 1g
4-Bromo-3-(hydroxymethyl)benzonitrile | ≥95% | CAS 905710-66-9 | C8H6BrNO | 1g
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