Boronic acid derivatives
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Filtered Search Results
eMolecules 2820191-51-1 | TERT-BUTYL 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)AZEPANE-1-CARBOXYLATE | AstaTech | MFCD28101679 | 325.260 | C17H32BNO4 | 95.000 | CC(C)(C)OC(=O)N1CCCC(CC1)B1OC(C)(C)C(C)(C)O1 | 0.1g | 800787273
TERT-BUTYL 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)AZEPANE-1-CARBOXYLATE | AstaTech | 2820191-51-1 | MFCD28101679 | 325.260 | C17H32BNO4 | 95.000 | CC(C)(C)OC(=O)N1CCCC(CC1)B1OC(C)(C)C(C)(C)O1 | 0.1g | 800787273
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Medchemexpress LLC 3-Tolylboronic acid | 17933-03-8 | 135.96 | 100 G
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3-Tolylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
- For research use only
- Appearance: solid
- Color: white to off-white
- Shipping: room temperature in continental US (may vary elsewhere)
- Powder storage: -20°C for 3 years, 4°C for 2 years
- In solvent storage: -80°C for 6 months, -20°C for 1 month
- Documents available: data sheet, COA, SDS, handling instructions
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Cayman Chemical CAY10591 Fatty Acids and Deriv
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An activator of SIRT1 that decreases TNF-α levels from 325 pg/ml (control) to 104 and 53 pg/ml at 20 and 60 µM, respectively; exhibits a significant dose-dependent effect on fat mobilization in differentiated adipocytes
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Aobchem AOBCHEM
5000951904 2 5-DICHLORO-3-FLUOROPHENYLBOR
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Chem-Impex International, Inc. 4-Methoxyphenylboronic acid | MFCD00039139 | 5G
4-Methoxyphenylboronic acid, MFCD00039139, 5G
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Frontier Specialty Chemicals 25G 1-N-BOC-PYRROLE-2-BORONIC
1-N-Boc-pyrrole-2-boronic acid; CAS No: 135884-31-0
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Cayman Chemical CAY10434 Fatty Acids and Deriv
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A selective inhibitor of the 20-HETE synthase CYP4A11 (IC50 = 8.8 nM human renal microsomes)
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Cayman Chemical CAY10591 Fatty Acids and Deriv
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An activator of SIRT1 that decreases TNF-α levels from 325 pg/ml (control) to 104 and 53 pg/ml at 20 and 60 µM, respectively; exhibits a significant dose-dependent effect on fat mobilization in differentiated adipocytes
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Aobchem AOBCHEM
5000954463 4-METHYL-2-NITROPHENYLBORONIC
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Aobchem AOBCHEM
5000954993 4-METHYL-2-NITROPHENYLBORONIC
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Cayman Chemical CAY10462 Fatty Acids and Deriv
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A selective inhibitor of the 20-HETE synthase CYP4A11 (IC50 = 8.8 nM in human renal microsomes); 200-fold less potent as an inhibitor of 1A, 1C, and 3A CYP450 enzymes
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Medchemexpress LLC 3-aminophenylboronic acid | 30418-59-8 | MFCD00007755 | 99.9% | 136.94 g/mol | C6H8BNO2 | 500 G
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3-Aminophenylboronic acid is an organoboron reagent used in organic synthesis and biochemical research. It serves as a building block for cross-coupling chemistry and can be functionalized for biosensing applications, such as glycoprotein recognition when attached to nanomaterials. The compound is supplied at high purity and is suitable for analytical, preparative, and material science workflows.
- High purity suitable for analytical and synthetic applications.
- Serves as a boronic acid building block for cross-coupling reactions.
- Contains a reactive amino group for derivatization and bioconjugation.
- Applicable to sensor development for selective glycoprotein detection.
- Available in packaging sizes that support scale-up and bulk use.
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Cayman Chemical KT 5720 Inhibitors
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A potent inhibitor of PKA; blocks PKA signaling through competitive inhibition of ATP (Ki = 60 nM); inhibits phosphorylase kinase, PDK1, MEK, MSK1, PKBα, and GSK3β
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Cayman Chemical 19 SHETE Fatty Acids and Deriv
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Potent vasodilator of renal preglomerular vessels; 70% of the metabolite composition of arachidonic acid by CYP2E1; stimulates both renal sodium-potassium ATPase and volume absorption in the rabbit proximal straight tubule
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Cayman Chemical CAY10602 Fatty Acids and Deriv
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A SIRT1 activator; inhibits LPS-induced TNF-α release in THP-1 cells at 20 and 60 µM; decreases the expression of GPX4, SLC7A11, and SLC3A2, as well as increases the levels of iron and MDA, in A549, MDA-MB-231, and Hs 578T cells at 5 µM; reduces oleic acid-induced apoptosis and lipid accumulation in HepG2 cells when used at a concentration of 20 µM
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