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Filtered Search Results
Medchemexpress LLC Tert-butyl 3-(4-chloro-7h-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate | 1240301-66-9 | 96.2% | 322.80 | 250 MG
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tert-Butyl 3-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate is a chemical compound that serves as a drug intermediate for the synthesis of various active compounds. It is intended for research use only.
- Used as a drug intermediate.
- Suitable for synthesis of active compounds.
- For research use only.
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Medchemexpress LLC Cyclo(L-Phe-trans-4-OH-L-Pro) | 118477-06-8 | 260.29 | 5 MG
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Cyclo(L-Phe-trans-4-OH-L-Pro) is an antifungal peptide.
- Purity: 99.76%
- Appearance: Solid
- Color: White to off-white
- Target: Fungal
- Pathway: Anti-infection
- Initial source: Microorganisms, specifically Lactobacillus plantarum
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Medchemexpress LLC Ethanaminium, N,N,N-trimethyl-2-(phosphonooxy)-, chloride, sodium salt (1:1:2) | 16904-96-4 | MFCD00070597 | 98.0% | 263.57 g/mol | C5H13ClNNa2O4P | 500 MG
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Phosphocholine chloride disodium is the disodium salt form of phosphocholine used as a biochemical reagent for preparing aqueous solutions and studying phospholipid headgroup behavior, membrane models, and drug-delivery research. It is supplied as a solid with documented solubility, assay, and batch data to support reproducible experimental preparation.
- Biochemical reagent for membrane and lipid research.
- Supplied as a solid for preparing aqueous solutions.
- Documented solubility data for accurate molarity calculations.
- Batch certificate of analysis available to support quality control.
- Suitable for preparation of defined experimental concentrations.
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TARGETMOL CHEMICALS INC TRIFLUOROMETHYL-TUBERCID 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Trifluoromethyl-tubercidin (TFMT) inhibits host MTr1 and suppresses virus replication. TFMT inhibits MTr1 through interaction at its S-adenosyl-l-methionine binding pocket to restrict influenza virus replication. TFMT was effective in inhibiting viral replication in mice displayed little toxicity. purity: 99%
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Medchemexpress LLC 1H-Indazole, 5-[(1-methylcyclopropyl)oxy]- | 1626355-74-5 | 97.3% | 188.23 | 1 G
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5-(1-Methylcyclopropoxy)-1H-indazole is a chemical compound with a molecular formula of C11H12N2O and a molecular weight of 188.23. It typically appears as a light yellow to yellow solid and has a purity of 97.34% by HPLC. This product is intended for research use only and has not been fully validated for medical applications.
- CAS number: 1626355-74-5
- Molecular formula: C11H12N2O
- Molecular weight: 188.23
- Purity (HPLC): 97.34%
- Appearance: Light yellow to yellow solid
- Storage: Powder: -20°C for 3 years, 4°C for 2 years; In solvent: -80°C for 6 months, -20°C for 1 month
- Analytical data: 1H NMR and LCMS consistent with structure
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Apexbio Technology LLC Cyclo (-RGDfK) 161552-03-0 25mg
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Cyclo(-RGDfK) is a cyclic pentapeptide that functions as an inhibitor targeting the integrin v 3 Integrins are transmembrane receptors mediating cell adhesion by recognizing specific peptide sequences notably the Arg-Gly-Asp (RGD) motif Integrin v 3 is involved in cell adhesion processes such as angiogenesis tissue remodeling and tumor development and is abundantly expressed on activated endothelial cells and various tumor cells Cyclo(-RGDfK) specifically binds integrin v 3 disrupting integrin-mediated cell attachment Consequently it is frequently utilized in bioengineering applications to modify biomaterial surfaces for enhanced cellular adherence and integration Additionally cyclo(-RGDfK) serves as a targeting ligand in imaging probes aimed at localizing integrin-positive tissues in cancer research
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Medchemexpress LLC AZ 11645373 | 227088-94-0 | 99.54% | 463.51 | 1 ML
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AZ11645373 is a highly selective and potent antagonist at human but not rat P2X7 receptors. It inhibits ATP-evoked IL-1β release from lipopolysaccharide-activated THP-1 cells, with an IC50 value of 90 nM.
- Highly selective and potent antagonist at human P2X7 receptors.
- Inhibits ATP-evoked IL-1β release from lipopolysaccharide-activated THP-1 cells.
- Produces a concentration-dependent inhibition of BzATP-mediated calcium transients.
- No significant effect on basal levels of IL-1β in culture medium of LPS-treated cells at specified concentrations.
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Chemscene CHEMSCENE
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5000577776 QUINOLINE-3-CARBALDEHYDE 5G
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eMolecules EMOLECULES INC
5000841375 N2-FMOC-N6-ACETYL-N2-METHY 5G
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1 CLICK CHEMISTRY
NC3968409 1 DIFLUOROMETHYL 1H PYRAZO 10G
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eMolecules 1823846-51-0 | 1-[1-(trifluoromethyl)cyclopropyl]ethanamine hydrochloride | MFCD28040273 | 1g
ChemScene | 3-Bromo-4-fluorophthalic acid | 100mg | 769180520 | CS-0626213 | 2828433-78-7 | 263.018 | C8H4BrFO4
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eMolecules Building Block Tool<|a>
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Sigma Aldrich Fine Chemicals Biosciences SuperdexR 75 Prep Grade Cy
Superdex(R) 75 prep grade gel filtration medium offers very high reSOLUTIONon fractionation for separation polishing and product formulation of recombinant proteins.Superdex(R) prep grade is a preparative gel filtration medium with a composite matrix of dextran and agarose. This matrix combines the excellent gel filtration properties of cross-linked dextran (Sephadex) with the physical and chemical stabilities of highly cross-linked agarose to produce a separation medium with outstanding selectivity and high reSOLUTIONon. In addition its low non-specific interaction permits high recovery of biological material. Together these properties make Superdex(R) prep grade the first choice gel filtration media for all applications from laboratory to process scale.Superdex(R) prep grade is available in a range of different bulk pack sizes and convenient pre-packed formats for easy scale-up and process development.As a BioProcess medium
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Apexbio Technology LLC EUK 134 81065-76-1 50mg
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EUK 134 (CAS 81065-76-1) is a synthetic salen-manganese complex designed to mimic the antioxidant enzymes superoxide dismutase (SOD) and catalase By scavenging reactive oxygen species (ROS) EUK 134 diminishes oxidative stress and attenuates cellular damage In vitro this compound inhibits formation of amyloid fibrils reduces microglial proliferation induced by -amyloid and protects neuronal cells from oxidative injury via inhibition of MAPK signaling In vivo studies indicate that EUK 134 decreases infarct size and neuronal cell death in rodent models of ischemic stroke and kainate-induced neurotoxicity EUK 134 is thus a relevant tool in oxidative stress and neurodegeneration research
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eMolecules Ambeed (S)-( )-2 2-Dimethylcyclopropanecarboxylic Acid 250mg 525124281 A208996 0 000 14590-53-5 MFCD08460918 114 144 C6H10O2
Ambeed (S)-( )-2 2-Dimethylcyclopropanecarboxylic Acid 250mg 525124281 A208996 0 000 14590-53-5 MFCD08460918 114 144 C6H10O2
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Chemscene CHEMSCENE
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5000577591 4-BROMO-3-TRIFLUOROMETHYL B 5G
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