benzeneboronic acid, m carboxy

Benzeneboronic acid, m-carboxy- is a bioactive chemical.

Turanose is a naturally occurring isomer of sucrose found in honey. It has anti-inflammatory and fat-regulating activities. It has research potential for obesity and related chronic diseases.

m-PEG12-acid is a PEG-based PROTAC linker used in the synthesis of PROTACs.

Carbamic acid, N-mercapto-N-methyl-, m-isopropylphenyl ester is a bioactive chemical.

m-Cumenesulfonic acid is a bioactive chemical.

Carbanilic acid, m-heptyloxy-, 2-(dimethylamino)ethyl ester, hydrochloride is a bioactive chemical.

5-Carboxy-3,4-dihydro-2,4-dioxo-1(2H)-pyrimidine   acetic acid benzyl ester is a useful organic compound for research related to life sciences and the catalog number is TNU1477.

Carbanilic acid, m-((hexyloxy)methyl)-, 2-piperidinoethyl ester, hydrochloride is a bioactive chemical.

(S)-4-(Amino(carboxy)methyl)-3-methylbenzoic acid hydrochloride is a useful organic compound for research related to life sciences and the catalog number is T64800.

Carbanilic acid, m-ethoxy-N-phenyl-, 2-(diethylamino)ethyl ester is a bioactive chemical.

Carbamic acid, methyl(phenylthio)-, m-isopropylphenyl ester is a bioactive chemical.

N-(Diethylphosphorothioyl)-N-methylcarbamic acid, m-isopropylphenyl ester is a bioactive chemical.

Carbanilic acid, m-hydroxy-N-methyl-, methyl ester, dimethylcarbamate (ester) is a bioactive chemical.

m-Fluorocinnamic acid is a bioactive chemical.

m-PEG5-phosphonic acid ethyl ester, a polyethylene glycol (PEG)-derived linker, is commonly used in constructing proteolysis targeting chimeras (PROTACs) [1].

m-PEG4-phosphonic acid ethyl ester is a PEGylation-based linker used in the design and synthesis of PROTACs, which are heterobifunctional molecules that facilitate targeted protein degradation[1].

Bis-(m-PEG4)-amidohexanoic acid is a polyethylene glycol (PEG)-based linker utilized in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

Bis-(m-PEG8-amido)-hexanoic acid is a polyethylene glycol (PEG)-based linker used in synthesizing proteolysis targeting chimeras (PROTACs) [1].

N-(m-PEG4)-N'-(PEG4-acid)-Cy5 is a polyethylene glycol (PEG)-based PROTAC linker used in the synthesis of PROTACs[1].

m-PEG4-phosphonic acid is a PEG-based linker for PROTACs, joining two essential ligands crucial for forming PROTAC molecules. This linker facilitates selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-Tolylacetic acid, also known as 3-Methylbenzeneacetic acid, is a hydroaromatic dicarboxylic acid that is excreted in the urine as a metabolite of tolueneacetic acid.

(R)-2-Amino-3-(m-tolyl)propanoic acid is a valuable compound for life sciences research, catalog number T65696, CAS number 114926-39-5.

m-PEG2-acid is a PEG-based linker for PROTACs, joining two essential ligands crucial for forming PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.

m-PEG11-acid is a non-cleavable 11-unit polyethylene glycol (PEG) linker used in the synthesis of antibody-drug conjugates (ADCs) [1] and as a PEG-based linker for PROTAC synthesis [2].

m-PEG21-acid is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation through the ubiquitin-proteasome system within cells.

m-PEG5-phosphonic acid is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands necessary for PROTAC molecule formation. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

N-(m-PEG4)-3,3-Dimethyl-3H-indole-N'-(acid-PEG3)-benzothiazole is a PEG-based PROTAC linker suitable for synthesizing PROTACs [1].

20-carboxy Arachidonic acid (20-COOH-AA) is the major metabolite of 20-HETE that is produced in renal tubular epithelial, endothelial, and microvascular smooth muscle cell cultures. This ω-oxidation conversion can take place using purified alcohol dehydrogenases three and four or by microsomes containing recombinant human CYP4F3B. Like 20-HETE, 20-COOH-AA inhibits ion transport in the kidneys. It also produces vasorelaxation of porcine coronary microvessels constricted with endothelin. 20-COOH-AA binds to isolated ligand binding domains of peroxisome proliferator-activated receptor α (PPARα) (Kd = 0.87 ± 0.12 μM) and PPARγ (Kd = 1.7 ± 0.5 μM), and is a dual activator of PPARα and PPARγ in a transiently transfected COS-7 cell reporter system.

Benzoic acid, m-(2,3-dihydroxypropoxy)-, methyl ester is a bioactive chemical.

Benzoic acid, m-(2-(p-bromophenyl)-5-methylpyrrol-1-yl)- is a bioactive chemical.

Carbanilic acid, m-hydroxy-, 2-methoxyethyl ester, methylcarbamate is a bioactive chemical.

Carbanilic acid, m-((pentyloxy)methyl)-, 2-piperidinoethyl ester, hydrochloride is a bioactive chemical.

Benzoic acid, m-(2-methyl-5-phenylpyrrol-1-yl)-, compd. with 2-amino-2-methyl-1-propanol (1:1) is a bioactive chemical.

Benzoic acid, m-((p-methylaminophenyl)azo)- is a bioactive chemical.

Benzoic acid, m-(2-methyl-5-phenylpyrrol-1-yl)- is a bioactive chemical.

M-PEG1-acid is a PEG derivative containing a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. In the presence of activators (e.g. EDC, DCC), the terminal carboxylic acid can be reacted with primary amine groups t

Benzoic acid, m-(2-methyl-5-phenylpyrrol-1-yl)-, compd. with 2-aminoethanol (1:1) is a bioactive chemical.

Benzoic acid, m-iodo-, 2-phenylhydrazide is a bioactive chemical.

m-((4-((4-Hydroxy-m-tolyl)azo)-3-methoxyphenyl)azo)benzenesulphonic acid is a bioactive chemical.

Carbanilic acid, m-ethoxy-, 2-(dimethylamino)ethyl ester, hydrochloride is a bioactive chemical.

m-Phenylenediacetic acid is a bioactive chemical.

m-PEG4-C6-phosphonic acid ethyl ester, a polyethylene glycol (PEG)-based linker compound, is used for synthesizing proteolysis-targeting chimeras (PROTACs)[1].

m-PEG37-acid is a PEG-based linker for PROTACs that connects two essential ligands, critical for forming PROTAC molecules, thereby facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

N-(Propanoic acid)-N-bis(m-PEG12) is a polyethylene glycol (PEG) based linker used in PROTACs synthesis [1].

m-PEG12-NH-C2-acid is a PEG-based linker for PROTACs, joining two essential ligands necessary for the formation of PROTAC molecules. This linker enables selective protein degradation by utilizing the ubiquitin-proteasome system [within cells].

m-PEG12-COO-propanoic acid is a polyethylene glycol (PEG) derivative used as a PROTAC linker for synthesizing PROTAC compounds [1].

m-PEG8-C10-phosphonic acid is a PEG-based linker for PROTACs that joins two essential ligands, enabling selective protein degradation via the ubiquitin-proteasome system within cells [PROTACs].

m-PEG5-sulfonic acid is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG3-Sulfone-PEG3-acid is a polyethylene glycol (PEG)-based linker used in protein degradation via targeted chimera (PROTAC) [1].

Carboxy-PEG4-sulfonic acid is a PEG-based linker frequently used in PROTAC synthesis [1].