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Filtered Search Results
Medchemexpress LLC Azido-PEG3-C-Boc | 250MG
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Azido-PEG3-C-Boc | 250MG
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Medchemexpress LLC (R)-1-Boc-3-propylpiperazine | 928025-57-4 | 228.34 | 100 MG
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(R)-1-Boc-3-propylpiperazine is a drug intermediate for synthesis of various active compounds. This product has not been fully validated for medical applications and is for research use only.
- Target: drug intermediate
- Pathway: others
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Medchemexpress LLC Recombinant human carbonic anhydrase 9 (His-tag) | >95.0% | 100UG
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Recombinant human carbonic anhydrase 9 (CA9) produced in HEK293 cells and supplied as a lyophilized preparation with a C-terminal 6xHis tag. The protein corresponds to amino acids Q38-D414 of human CA9, is glycosylated (apparent molecular weight 45-60 kDa), and is purified to >95% by reducing SDS-PAGE. It is formulated in PBS (pH 7.4) or PBS with 8% trehalose and intended for research use in biochemical and cell biology studies involving CA9.
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Medchemexpress LLC Carbonic anhydrase 9 protein, cynomolgus (HEK293, His) | 10UG
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Recombinant cynomolgus carbonic anhydrase IX (CA9) expressed in HEK293 cells with a C-terminal His tag. The enzyme catalyzes reversible hydration of CO2 and is supplied as a lyophilized powder from PBS (pH 7.4) with 8% trehalose; reconstitute to ≥100 μg/mL in ddH2O for recommended use. Suitable for biochemical and cell biology studies of pH regulation and CA9-related pathways.
- Recombinant protein expressed in HEK293 cells.
- C-terminal His tag for purification and detection.
- Lyophilized from PBS (pH 7.4) with 8% trehalose for stability.
- Recommended reconstitution concentration ≥100 μg/mL in ddH2O.
- Useful for studies of carbon dioxide transport and pH regulation.
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Medchemexpress LLC Boc-NH-PEG7-azide | 50MG
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Boc-NH-PEG7-azide | 50MG
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Medchemexpress LLC 1-Phenyl-2-pyrrolidi 10mM 1mL
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1-Phenyl-2-pyrrolidinone (1-Phenylpyrrolidin-2-one) is a phenyl analogue of GABA with sedative effect decreasing the exploratory behavior of rats at 50-100 mg/kg (i v ) 1-Phenyl-2-pyrrolidinone also has been proved to inhibit emotional reactions in dogs and cats 1-Phenyl-2-pyrrolidinone induces decreases in the pressor reaction to emotional stress without accompanied by normalization of the function of baroreceptor reflexes[1][2]
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Medchemexpress LLC N-(Azido-PEG2)-N-Boc-PEG4-acid | 2093153-82-1 | C22H42N4O10 | 100 MG
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N-(Azido-PEG2)-N-Boc-PEG4-acid is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent due to its Azide group, which allows it to undergo copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules containing Alkyne groups. It can also participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups.
- Utilized in the synthesis of PROTACs
- Functions as a click chemistry reagent with an Azide group
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions
- Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions
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Medchemexpress LLC N-Boc-biocytin | 62062-43-5 | MFCD00133628 | >98.0% | 472.60 g·mol⁻¹ | C21H36N4O6S | 100 MG
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N-Boc-Biocytin is a Boc-protected biotin-PEG linker containing a carboxylic acid and a Boc-protected primary amine. It permits formation of stable amide bonds with primary amines and, after acidic removal of the Boc group, provides a free amine for further conjugation. The reagent is intended for biotinylation and affinity tagging of biomolecules.
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Medchemexpress LLC N-Boc-PEG1-bromide | 164332-88-1 | 97.9% | 268.15 | C9H18BrNO3 | 250 MG
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N-Boc-PEG1-bromide is a Boc-protected PEG1 bromide reagent used as a short, hydrophilic linker for conjugation chemistry, including antibody-drug conjugate (ADC) and PROTAC linker synthesis. It provides a terminal bromide for alkylation or nucleophilic substitution and a Boc-protected amino group for orthogonal protection strategies.
- Provides a short PEG spacer to increase solubility.
- Contains a terminal bromide for alkylation and substitution reactions.
- Includes a Boc-protected amino group for orthogonal deprotection.
- Used in ADC and PROTAC linker synthesis and general conjugation chemistry.
- Supplied in multiple package sizes for research use.
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Medchemexpress LLC {Boc}-Met-Leu-Phe | 67247-12-5 | MFCD00037435 | 99.9% | 509.66 g/mol | C25H39N3O6S | 5 MG
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Boc-MLF (Boc-Met-Leu-Phe-OH) is a Boc-protected tripeptide that acts as a formyl peptide receptor (FPR) antagonist. It reduces fMLF-induced superoxide production with a reported IC50 of 0.63 μM and is supplied as a purified powder for research use. The compound is readily soluble in DMSO and can be formulated for in vivo dosing using common co-solvents.
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Ambeed AMBEED
5000887639 Z-11-TETRADECEN-1-YLACET 100MG
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Medchemexpress LLC E/Z-HA155 25mg | 1229652-22-5 | 463.29 | C24H19BFNO5S | 25 MG
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A potent autotaxin (ATX) type I inhibitor for laboratory research, (E/Z)-HA155 is used to study cancer, fibrotic disease, inflammation, pain, and angiogenesis. The product is supplied as a high-purity solid and includes supporting structural and stability data for experimental use.
- Potent autotaxin (ATX) type I inhibitor for mechanistic and pharmacology studies.
- High purity suitable for analytical and biological assays.
- Supplied as a solid 25 mg quantity for small-scale experiments.
- Stable when stored as a powder at -20°C for extended periods.
- Structural identifiers and formula provided for computational and analytical workflows.
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Medchemexpress LLC E Z -MitoTam iodid 10mg | 10MG
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E Z -MitoTam iodid 10mg | 10MG
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Cayman Chemical 9 Z 11 E 13 EOctadecatrienoic
A fatty acid agonist of PPARγ; activates PPARγ transcriptional activity in a reporter assay using RAW 264.7 cells at 10 µM; an inhibitor of DNA polymerase α, -β, -γ, -Δ, and -ε (IC50s = 10.7, 13.4, 10.6, 14, and 22 µM, respectively); an inhibitor of topoisomerase I and -II (IC50s = 20 and 5 µM, respectively); reduces the viability of, and induces apoptosis in, MCF-7 breast cancer cells in a concentration-dependent manner; induces ferroptosis in MDA-MB-231 breast cancer cells in an ACSL1-dependent manner; reduces clinical signs of disease in a model of DSS-induced IBD in PPARγ-expressing, but not PPARγ-knockout, mice
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STA Pharmaceutical DNA C(Bz) amidite | 1 g | CAS 102212-98-6 | MDL MFCD00036315
DNA C(Bz) amidite is a Amidite reagent (Subcategory: Cytosine Series) sold by WuXi TIDES. Offered in 1 g. Store at -20 °C. SDS available for reference.
Specifications
- CAS: 102212-98-6
- MDL: MFCD00036315
- InChIKey: PGTNFMKLGRFZDX-SALLYJDFSA-N
- Molecular Weight: 833.922761998
- Molecular Formula: C46H52N5O8P
- Purity: ≥99%
- Container Type: 15 mL HDPE
- Pack Size: 1 g
- Net Weight: 1 g
- Gross Weight: 7.8 g
- Commodity Code: 29349990
- Country Of Origin: China
- IUPAC: (2R,3S,5R)-5-(4-benzamido-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
- SMILES: CC(N(P(O[C@H]1C[C@H](N2C(N=C(C=C2)NC(C3=CC=CC=C3)=O)=O)O[C@@H]1COC(C4=CC=C(C=C4)OC)(C5=CC=C(C=C5)OC)C6=CC=CC=C6)OCCC#N)C(C)C)C
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