Phenylcarbamic acid esters
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Filtered Search Results
Chemscene ChemScene | Boc-4-Abz-OH | 100G | CS-W007493 | 0.98 | 66493-39-8| MFCD00037428 | 237.25
ChemScene | Boc-4-Abz-OH | 100G | CS-W007493 | 0.98 | 66493-39-8| MFCD00037428 | 237.25
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Medchemexpress LLC N-Acetyldesloratadin 1mg | 117796-52-8 | 1 MG
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N-acetyldesloratadine is a research reagent that functions as a dual antagonist of platelet-activating factor (PAF) and histamine. It inhibits PAF-induced aggregation of human platelets (IC50 ≈ 0.6 μM) and is used in studies of allergic disease, platelet aggregation, and inflammation-related signaling. The compound is a white to off-white solid with molecular formula C21H21ClN2O and molecular weight 352.86.
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Medchemexpress LLC N-(Boc-PEG2)-N-bis(PEG3-azide) | 2353409-46-6 | >98% | C28H53N7O11 | 250 MG
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N-(Boc-PEG2)-N-bis(PEG3-azide) is a PEG-based PROTAC linker designed for the synthesis of PROTACs. It acts as a versatile click chemistry reagent, containing an azide group that enables participation in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne groups, and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Functions as a click chemistry reagent
- Features an azide group
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions
- Facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) reactions
- Appears as a colorless to light yellow viscous liquid
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Medchemexpress LLC β-N-Acetylhexosaminidase, Streptococcus pneumoniae | 9012-33-3 | 10 U
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β-N-Acetylhexosaminidase (EC 3.2.1.52) is an exoglycosidase that catalyzes the hydrolysis of terminal non-reducing β-N-acetylgalactosamine and glucosamine residues in oligosaccharides for epigenetic applications.
- Exoglycosidase enzyme
- Catalyzes hydrolysis of terminal non-reducing β-N-acetylgalactosamine and glucosamine residues
- Useful for epigenetic applications
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Medchemexpress LLC N-Phenethylbenzamide | 3278-14-6 | 99.56% | 225.29 | 1 ML
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N-Phenethylbenzamide is an active compound extracted from *Liriodendron tulipifera*. It is used for the research of inflammatory diseases.
- Active compound from natural source
- Suitable for inflammatory disease research
- High purity
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Medchemexpress LLC (S)-1-Boc-2-(aminomethyl)pyrrolidine | 119020-01-8 | 98.3% | 200.28 | 10 G
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(S)-1-Boc-2-(aminomethyl)pyrrolidine is a biochemical reagent used as a biological material or organic compound for life science related research. It serves as an intermediate in organic synthesis and acts as a chiral and heterocyclic building block in synthetic chemistry.
- Can be used as a biological material
- Functions as an organic compound for life science research
- Acts as an intermediate in organic synthesis
- Used as a chiral and heterocyclic building block in synthetic chemistry
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Medchemexpress LLC Boc-N-Amido-PEG3-azide | 642091-68-7 | C13H26N4O5 | 250 MG
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Boc-N-Amido-PEG3-azide is a PEG-based PROTAC linker employed in the synthesis of PROTACs. This click chemistry reagent features an azide group that enables participation in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne-containing molecules, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups. It contributes to the formation of PROTACs, which utilize the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Functions as a click chemistry reagent
- Contains an azide group for click chemistry reactions
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Facilitates strain-promoted alkyne-azide cycloaddition (SPAAC)
- Colorless to light yellow liquid appearance
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Medchemexpress LLC N-(n-butyl)thiophosphoric triamide | 94317-64-3 | MFCD00269941 | 99.8% | 167.21 g·mol⁻¹ | C4H14N3PS | 1 ML
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N-(n-Butyl)thiophosphoric triamide (NBPT) is a urease inhibitor used to slow enzymatic hydrolysis of urea in soil, reducing ammonia volatilization and improving nitrogen fertilizer efficiency. It binds the nickel active site of urease, delaying urea conversion to ammonium and helping to retain nitrogen in the crop root zone.
- Potent urease inhibitor that delays urea hydrolysis.
- Reduces ammonia volatilization from urea-based fertilizers.
- Improves nitrogen use efficiency and crop nitrogen uptake.
- Available as a 10 mM solution in DMSO and as solid formulations.
- High purity suitable for agricultural research and analytical applications.
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Medchemexpress LLC C-C motif chemokine 6 (rat), N-terminal His-tag | 100UG
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Recombinant rat CCL6 chemokine with an N-terminal His tag, expressed in E. coli and supplied as a lyophilized powder for biochemical and cell-based research. The protein shows documented biological activity, low endotoxin, and is formulated for stability and storage at -20°C.
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Medchemexpress LLC TMEM173 Human N-Hi 500ug
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Recombinant human TMEM173 (STING) protein with an N-terminal SUMO fusion and N-terminal 6xHis affinity tag, expressed in Escherichia coli and supplied as a purified research reagent for biochemical and signaling studies, including investigations of the cGAS-STING pathway.
- N-terminal SUMO and 6xHis purification tags.
- Expressed in Escherichia coli for bacterial expression.
- Supplied as purified recombinant protein for research use.
- Suitable for biochemical assays and signaling pathway studies.
- Available in a 500 μg package for assay development and characterization.
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Medchemexpress LLC CEACAM1 Human N-Hi 10ug
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Recombinant human CEACAM1 protein with an N-terminal His tag, expressed in E. coli and supplied as a lyophilized powder. The protein is suitable for biochemical and cell signaling studies involving insulin receptor-mediated pathways, hepatic lipogenesis, and modulation of cell proliferation. Supplied as 10 μg with >95% purity and low endotoxin, it includes recommended storage and reconstitution instructions.
- Expressed in E. coli for high-yield production.
- N-terminal His tag enabling straightforward purification and detection.
- Lyophilized format for convenient storage and transport.
- High purity for reliable biochemical assays.
- Low endotoxin to support cell-based experiments.
- Stable when aliquoted and frozen for long-term storage.
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Medchemexpress LLC Acid-PEG3-C2-Boc | 1807539-06-5 | ≥97.0% | 1 G
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Acid-PEG3-C2-Boc is a PEG- and Alkyl/ether-based PROTAC linker that can be utilized in the synthesis of PROTACs for the degradation of EGFR and the inhibition of mTOR.
- Molecular formula: C14H26O7
- Molecular weight: 306.35
- Appearance: Liquid, colorless to light yellow
- Solubility: Soluble in DMSO at ≥ 175 mg/mL
- Functions as a PROTAC linker
- Used in the synthesis of PROTACs for degradation of EGFR and inhibition of mTOR
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Medchemexpress LLC GSTM2 protein, human (N-His) | ≥98.0% | 50 UG
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Recombinant full-length human Glutathione S-transferase Mu 2 (GSTM2) with an N-terminal 6xHis tag, expressed in E. coli and supplied lyophilized for research applications. Characterized for purity, activity, and low endotoxin to support biochemical and immunological assays.
- Recombinant full-length human protein with N-terminal 6xHis tag.
- Expressed in E. coli expression system.
- Lyophilized formulation with trehalose and Tween-80 for stability.
- Purity ≥98.0% by reducing SDS-PAGE.
- Bioactivity 10-15 U/mg (CDNB substrate assay).
- Endotoxin level <1 EU/μg.
- Not recommended to reconstitute below 100 μg/mL.
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Medchemexpress LLC OGG1 Human N-His 5ug
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The OGG1 protein is a DNA repair enzyme specifically designed to cleave DNA at the 8-oxoG residue and plays a key role in maintaining genome integrity It demonstrates the ability to excise damaged bases such as 7 8-dihydro-8-oxoguanine and 2 6-diamino-4-hydroxy-5-N-methylformamidopyrimidine from the DNA structure (FAPY) OGG1 Protein Human (N-His) is the recombinant human-derived OGG1 protein expressed by E coli with N-6 His labeled tag
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Medchemexpress LLC 4,7,10,13-Tetraoxapentadecanoic acid, 15-oxo-, 1,1-dimethylethyl ester | 1415329-20-2 | ≥97.0% | C15H28O7 | 25 MG
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Ald-CH2-PEG4-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- PROTACs contain two different ligands connected by a linker
- Ligand for an E3 ubiquitin ligase and a ligand for the target protein
- Exploits the intracellular ubiquitin-proteasome system to selectively degrade target proteins
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