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Filtered Search Results
Medchemexpress LLC D-alanine, N-[(1,1-dimethylethoxy)carbonyl]- | 7764-95-6 | MFCD00063123 | 99.9% | 189.21 | C8H15NO4 | 100g
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N-tert-Butoxycarbonyl-D-alanine is an alanine derivative[1]
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Boron Molecular 4-(4-Iodophenyl)piperazin 5GR
4-(4-Iodophenyl)piperazine-1-carboxylic acid tert-butyl ester
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Aobchem AOBCHEM
5000920614 3-METHYL-1- 3- 1-METHYLETHYL P
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Aobchem AOBCHEM
5000920896 1-METHYLETHYL 3-HYDROXY-4-METH
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Aobchem 2-Fluoro-5-[(1-methylethyl)thio]benzoic acid | ≥95% | CAS 138736-66-0 | C10H11FO2S | 250mg
2-Fluoro-5-[(1-methylethyl)thio]benzoic acid | ≥95% | CAS 138736-66-0 | C10H11FO2S | 250mg
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Aobchem (3-(Ethoxycarbonyl)thiophen-2-yl)boronic acid | ≥95% | CAS 632325-56-5 | C7H9BO4S | 500mg
(3-(Ethoxycarbonyl)thiophen-2-yl)boronic acid | ≥95% | CAS 632325-56-5 | C7H9BO4S | 500mg
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Aobchem 2-Fluoro-5-[(1-methylethyl)thio]benzoic acid | ≥95% | CAS 138736-66-0 | C10H11FO2S | 500mg
2-Fluoro-5-[(1-methylethyl)thio]benzoic acid | ≥95% | CAS 138736-66-0 | C10H11FO2S | 500mg
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Aobchem (3-(Ethoxycarbonyl)thiophen-2-yl)boronic acid | ≥95% | CAS 632325-56-5 | C7H9BO4S | 1g
(3-(Ethoxycarbonyl)thiophen-2-yl)boronic acid | ≥95% | CAS 632325-56-5 | C7H9BO4S | 1g
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Ambeed tertButyl 2aminoethyl carbama
tert-Butyl (2-aminoethyl)carbamate, 57260-73-8, 97%
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Ambeed tertButyl 2aminoethyl carbama
tert-Butyl (2-aminoethyl)carbamate, 57260-73-8, 97%
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Ambeed Benzyl piperazine1carboxylate
Benzyl piperazine-1-carboxylate, 31166-44-6, 97%
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Apexbio Technology LLC CGH 2466 dihydrochloride 1177618-54-0 10mg
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CGH 2466 dihydrochloride is a small-molecule antagonist targeting adenosine receptors with inhibitory activities against phosphodiesterase type 4 (PDE4) and p38 mitogen-activated protein kinase (MAPK) It is designed to block adenosine receptor signaling and inhibit key inflammatory enzymes thereby modulating inflammatory pathways CGH 2466 dihydrochloride exerts its biological activity primarily through selective inhibition of the PDE4D isoform (IC50 22 5 nM) and inhibition of p38 MAPK and isoforms (IC50 187 18 nM and 400 38 nM respectively) It shows comparable affinities to CGS15943 for the adenosine A1 A2B and A3 receptors but no activity at the A2A receptor Based on these pharmacological properties CGH 2466 dihydrochloride holds research potential in studies involving inflammatory mechanisms such as allergen-induced eosinophilic airway inflammation models
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Apexbio Technology LLC AY 9944 dihydrochloride(Synonyms: AY-9944, AY9944, AY 9944, trans-1,4-Bis(2-chlorobenzylaminomethyl)cyclohexane dihydrochloride), 5mg, CAS: 366-93-8.
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AY 9944 dihydrochloride (CAS 366-93-8) is a selective inhibitor of 7-sterol reductase (Dhcr7) an enzyme involved in cholesterol biosynthesis through NADPH-dependent conversion of 7-dehydrocholesterol to cholesterol AY 9944 dihydrochloride inhibits recombinant human 7-sterol reductase expressed in yeast cells with an IC50 of 13 nM In an SD rat model of Smith-Lemli-Opitz syndrome AY 9944 treatment leads to increased accumulation of 7-dehydrocholesterol and decreased cholesterol levels across various tissues Additionally in PBMCs isolated from AIDS patients AY 9944 intervention restored mitogenic responses and cytokine production suggesting research applications in immunological studies and cholesterol metabolism disorders
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Apexbio Technology LLC N4-Methyl-dCTP(Synonyms: N4-Methyl-2'-deoxycytidine-5'-triphosphate, N4-Me-dCTP, 4-Methyl-dCTP), 10ul (100 mM).
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N4-Methyl-dCTP is a cytosine-derived modified deoxynucleoside triphosphate capable of being enzymatically incorporated into DNA strands thereby introducing cytosine methylation modifications at specific genomic sites DNA methylation at the N4 position of cytosine is observed naturally across both prokaryotic and eukaryotic organisms and influences processes such as epigenetic gene expression regulation DNA replication and DNA damage repair Researchers use N4-Methyl-dCTP to incorporate defined methylation modifications enabling investigation into methylation-specific DNA-binding protein interactions DNA methylation patterning analyses and functional studies of epigenetic modification pathways
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Medchemexpress LLC Boc-piperazine-benzoic acid | 162046-66-4 | 97.4% | 306.36 | 10 G
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Boc-piperazine-benzoic acid is a PROTAC linker used in the synthesis of PROTACs. Compounds synthesized with this linker, such as certain androgen receptor (AR) degraders, are highly potent and orally bioavailable. These compounds effectively reduce AR protein, suppress AR-regulated genes in tumor tissues, and inhibit tumor growth without toxicity.
- PROTAC linker
- Used in the synthesis of PROTACs
- Can synthesize androgen receptor (AR) degraders
- Resulting compounds have potential for research into prostate cancer
- For research use only
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