2-(acetylamino)benzenecarboxamide

2-(acetylamino)benzenecarboxamide

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2-(acetylamino)benzenecarboxamide
Category Antibiotics
Catalog number BBF-03526
CAS 33809-77-7
Molecular Weight 178.19
Molecular Formula C9H10N2O2

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Description

2-(acetylamino)benzenecarboxamide is an antifungal antibiotic isolated from Streptomyces aurantiogriseus NPO-101.

Specification

Synonyms 2-(acetylamino)-benzamide; 2-(acetylamino)benzamide; 2'-carbamoyl-acetanilide; 2'-carbamoylacetanilide; NP 101A; NP-101A
IUPAC Name 2-acetamidobenzamide
Canonical SMILES CC(=O)NC1=CC=CC=C1C(=O)N
InChI InChI=1S/C9H10N2O2/c1-6(12)11-8-5-3-2-4-7(8)9(10)13/h2-5H,1H3,(H2,10,13)(H,11,12)
InChI Key WFKPHYKFAOXUTI-UHFFFAOYSA-N

Properties

Appearance White Powder
Antibiotic Activity Spectrum fungi
Melting Point 160-163°C

Reference Reading

1. Iodixanol (Optiprep), an improved density gradient medium for the iso-osmotic isolation of rat liver peroxisomes
P P Van Veldhoven, E Baumgart, G P Mannaerts Anal Biochem. 1996 May 15;237(1):17-23. doi: 10.1006/abio.1996.0194.
The suitability of Iodixanol {5,5'-[(2-hydroxy-1, 3-propanediyl)-bis(acetylamino)] bis-[N,N'-bis(2, 3-dihydroxypreopyl-2,4,6-triiodo-1,3-benzenecarboxamide)]}, a nonionic iodinated compound with a molecular weight of 1550, for the isolation of peroxisomes from rat liver was investigated. Centrifugation of light mitochondrial fractions in 20 to 40% (w/v) Iodixanol gradients, made iso-osmotic by the addition of sucrose, resulted in an excellent separation of peroxisomes from the remaining organelles, which were not able to enter the gradient. Peroxisomes banded around 30% (w/v) Iodixanol (d approximately 1.175) and, as revealed by marker enzyme analysis, were enriched 35- to 40-fold. Morphological examination of the peroxisomal fractions confirmed the near absence of other organelles and revealed structurally well-preserved peroxisomes. Free cores, also present in the starting fractions, migrated to higher densities and were trapped on a cushion. No interference of Iodixanol with marker enzyme determinations was observed, except for the UV-metric determination of urate oxidase and for the analysis of protein.

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