588-46-5
Chemical Structure
N-Benzylacetamide
Synonym(s): N-Acetylbenzylamine
- CAS No.: 588-46-5
- Formula:C9H11NO
- Molecular Weight:149.19
IUPAC Name: N-benzylacetamide
InChIKey: UZJLYRRDVFWSGA-UHFFFAOYSA-N
SMILES: CC(NCC1=CC=CC=C1)=O
Biological Activity: N-Benzylacetamide (N-Acetylbenzylamine), as an endogenous metabolite, is the major component of the plasma metabolic profile of Benznidazole (HY-B1548)[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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N-Benzylacetamide | 99.35% | N-Benzylacetamide (N-Acetylbenzylamine), as an endogenous metabolite, is the major component of the plasma metabolic profile of Benznidazole (HY-B1548). | ||||||||||||||||||||
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N-Benzylacetamide (Standard) | ≥98% | N-Benzylacetamide (Standard) is the analytical standard of N-Benzylacetamide (HY-W052051). This product is intended for research and analytical applications. N-Benzylacetamide (N-Acetylbenzylamine), as an endogenous metabolite, is the major component of the plasma metabolic profile of Benznidazole (HY-B1548). | ||||||||||||||||||||
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N-Benzylacrylamide | 97.47% | N-Benzylacrylamide (Benzyl acrylamide) is a hydrophobic monomer. N-Benzylacrylamide can form hydrophobic microdomains that act as physical cross-linking sites to connect polymer chains to each other into a three-dimensional network; dynamically reversible hydrophobic interactions enable the spontaneous reformation of physical cross-linking sites after contact of fractured surfaces, thereby achieving autonomous self-healing. N-Benzylacrylamide can promote the synthesis of carboxymethyl cellulose-modified amphiphilic copolymers, and enhance the intermolecular association, viscoelasticity, thermal stability, as well as fire resistance/fire extinguishing performance of the resulting hydrogels. | ||||||||||||||||||||
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N-Methylbenzamide | 99.93% | N-Methylbenzamide is a potent phosphodiesterase 10A (PDE10A) inhibitor. N-Methylbenzamide has anti-cancer activity. | ||||||||||||||||||||
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Beclamide | 98.86% | Beclamide is an active molecule with anticonvulsant activity, used as an anticonvulsant drug. | ||||||||||||||||||||
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N-Methylbenzylamine | 98.16% | N-methylbenzylamine is a member of phenylmethylamines. N-methylbenzylamine can be found in carrot, which makes N-methylbenzylamine a potential biomarker for the consumption of these food products. | ||||||||||||||||||||
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Benzylurea | 99.94% | Benzylurea is an anti-inflammatory agent. Benzylurea inhibits LPS (HY-D1056)-induced upregulation of MTCH2 expression and regulates pathways associated with mitochondrial function, inflammation and cell survival. Benzylurea alleviates LPS-induced proliferation inhibition and apoptosis of periodontal ligament fibroblasts, as well as the release of proinflammatory cytokines. Benzylurea can be used in studies related to periodontitis. | ||||||||||||||||||||
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2-(Benzylamino)acetic acid | 98.46% | 2-(Benzylamino)acetic acid is a Glycine (HY-Y0966) derivative. | ||||||||||||||||||||
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2-Phenylacetamide | 99.92% | 2-Phenylacetamide is a estrogen-like compound that can be isolated from Lepidium apetalum seeds. 2-Phenylacetamide inhibits p38 MAPK signaling pathway, exhibits anti-inflammatory, antioxidant, anti-hypertensive, and anti-fibrosis effects. 2-Phenylacetamide is orally active. | ||||||||||||||||||||
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N-(2-hydroxy-2-phenylethyl)acetamide | N-(2-hydroxy-2-phenylethyl)acetamide is isolated from the solid rice cultures of the endophytic fungus Diaporthe eucalyptorum KY-9. N-(2-hydroxy-2-phenylethyl)acetamide exhibits antifungal activities against Alternaria solani. | |||||||||||||||||||||
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N-Benzylacetamidine hydrobromide | N-Benzylacetamidine (hydrobromide) is a acetamidine compound. N-Benzylacetamidine (hydrobromide) is a selective inducible nitric oxide synthase (iNOS) inhibitor with an IC50 of 0.20 μM. | |||||||||||||||||||||
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Acetophenone-13C8 | Acetophenone-13C8 (1-Phenylethan-1-One-13C8) is the 13C-labeled Acetophenone (HY-Y0989). Acetophenone (1-Phenylethan-1-One) is an organic compound with simple structure. Acetophenone can be bioreduced to phenylethanol (PEA). | |||||||||||||||||||||
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