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Filtered Search Results
Medchemexpress LLC Tiviciclovir hydroch 10mM 1mL | 10MM 1ML
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Tiviciclovir (AM188) hydrochloride is an antiviral guanosine analog and a hepatitis B virus inhibitor[1
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Medchemexpress LLC MEDCHEMEXPRESS LLC
5000406331 ALMOTRIPTAN HYDROCH 5MG
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Bioss GST-Tag HRP conjugated 2C1 Mon
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GST-Tag HRP conjugated 2C1 Monoclonal Antibody
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Bioss RNA polymerase II / POLR2A Mon
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RNA polymerase II / POLR2A Monoclonal Antibody
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Medchemexpress LLC Anisylacetone 100g | 104-20-1 | 100 G
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Anisylacetone (p-methoxybenzylacetone) is a liquid research reagent used as a male fruit fly attractant and as a fragrance and flavor intermediate. It is supplied for laboratory research and reference use with documented purity and storage recommendations.
- High purity: 99.40% (product page) and 99.87% (purity documentation).
- Appearance: colorless to light yellow liquid; density 1.046 g/cm3.
- Available as a solution (10 mM in DMSO, 1 mL) and bulk quantities (50 g, 100 g, larger by quote).
- Storage recommendations: pure form -20°C (up to 3 years) or 4°C (up to 2 years); in solvent store at -80°C (up to 6 months) or -20°C (up to 1 month).
- Intended for research use only; SDS and analytical documentation are provided.
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Chem-Impex International, Inc. 2-Bromo-4-fluorophenol | MFCD00010614 | 100G
2-Bromo-4-fluorophenol, MFCD00010614, 100G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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5000379293 TOFOGLIFLOZIN HYDRA 100MG
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Accela Chembio Inc 2-bromo-4-nitrophenol | 25g | 5847-59-6 | MFCD06656567 | 97+% | Shelf Life: 1800 Days | Light Sensitive
2-bromo-4-nitrophenol | 25g | 5847-59-6 | MFCD06656567 | 97+% | Shelf Life: 1800 Days | Light Sensitive
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Medchemexpress LLC Luseogliflozin hydrate | 1152425-66-5 | 99.2% | 452.56 g/mol | C23H32O7S | 25 MG
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Luseogliflozin hydrate is a research-grade sodium-glucose cotransporter 2 (SGLT2) inhibitor provided as the hydrate form. It is a potent and selective compound used in preclinical studies of glucose homeostasis and type 2 diabetes mellitus. The material is supplied as a high-purity solid suitable for in vitro and in vivo research applications.
- Potent SGLT2 inhibition (IC50 ≈ 2.26 nM).
- High purity (99.2%) suitable for research use.
- Hydrate form for consistent physicochemical properties.
- Molecular weight 452.56 g/mol; formula C23H32O7S.
- White to off-white solid, typically supplied in 25 MG quantities.
- Suitable for in vitro and in vivo studies of glucose transport and metabolism.
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eMolecules 1-METHYLCYCLOPROPANAMINE H 10G
5000189524 1-METHYLCYCLOPROPANAMINE H 10G
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eMolecules HOAT 25G
5000189216 HOAT 25G
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eMolecules DMTMM 100G
5000189120 DMTMM 100G
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Medchemexpress LLC (4R)-4-[(1S)-1-fluoroethyl]-3-[2-[[(1S)-1-[4-methyl-5-[2-(trifluoromethyl)-4-pyridinyl]... | 1628805-46-8 | MFCD31630851 | 99.2% | 490.45 g·mol⁻¹ | C23H22F4N6O2 | 1 ML
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IDH-305 is an orally available, mutant-selective, brain-penetrant inhibitor of isocitrate dehydrogenase 1 (IDH1) that targets R132 mutations. It is provided for research use in biochemical and cellular assays and is supplied as a 10 mM solution in DMSO (1 mL) or as solid quantities.
- Potent, mutant-selective inhibition of IDH1 (R132).
- Brain-penetrant, enabling central nervous system studies.
- Supplied as 10 mM solution in DMSO and as solid packs for flexibility.
- High purity for research-grade applications.
- Defined storage conditions to preserve stability.
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Medchemexpress LLC Methyl 4-(2-(3,4-dichlorophenyl)acetyl)-3-(1-pyrrolidinylmethyl)-1-piperazinecarboxylate fumarate | 126766-32-3 | MFCD00274044 | 99.9% | 530.4 | C23H29Cl2N3O7 | 1 ML
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GR 89696 (fumarate) is a potent, selective kappa-opioid receptor agonist used in preclinical pharmacology and pruritus research. It is provided as a fumarate salt and offered in solid form or as a ready-to-use 10 mM solution in DMSO, with solubility and storage data to support in vitro and in vivo studies.
- Highly selective kappa-opioid receptor agonist with reported kappa2 preference.
- Available as solid or ready-to-use 10 mM solution in DMSO.
- High solubility in DMSO (≥ 50 mg/mL) for convenient stock preparation.
- Provides storage and handling recommendations for stability.
- Suitable for in vitro and in vivo pharmacology and pruritus models.
- Supplied with standard chemical identifiers and characterization data.
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Medchemexpress LLC Crinecerfont hydrochloride | 321839-75-2 | 98.0% | 519.50 | C27H29Cl2FN2OS | 5 MG
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Crinecerfont hydrochloride is the hydrochloride salt of crinecerfont (SSR-125543), a potent, orally active, non-peptide corticotropin-releasing factor 1 (CRF1) receptor antagonist supplied for preclinical pharmacology research. It is provided as a high-purity solid with documented solubility and storage recommendations for laboratory use.
- Potent CRF1 receptor antagonist for preclinical research.
- High purity (98.0%).
- Molecular weight 519.50 g/mol.
- Soluble in DMSO at 100 mg/mL; in vivo formulation protocols available.
- Available in small research quantities, such as 5 mg.
- Store sealed away from moisture and light; follow cold storage guidance for solutions.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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