The ribonucleotide reductase R1 inhibitor N-acetyl-N,Ο-di(propylcarbamoyl)hydroxylamine, an analogue of caracemide

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Standard

The ribonucleotide reductase R1 inhibitor N-acetyl-N,Ο-di(propylcarbamoyl)hydroxylamine, an analogue of caracemide. / Nielsen, Bettina Bryde; Frydenvang, Karla; Larsen, Ingrid Kjøller.

In: Acta Crystallographica Section C: Crystal Structure Communications, Vol. 52, No. 2, 15.02.1996, p. 387-390.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Nielsen, BB, Frydenvang, K & Larsen, IK 1996, 'The ribonucleotide reductase R1 inhibitor N-acetyl-N,Ο-di(propylcarbamoyl)hydroxylamine, an analogue of caracemide', Acta Crystallographica Section C: Crystal Structure Communications, vol. 52, no. 2, pp. 387-390. https://doi.org/10.1107/S0108270195012236

APA

Nielsen, B. B., Frydenvang, K., & Larsen, I. K. (1996). The ribonucleotide reductase R1 inhibitor N-acetyl-N,Ο-di(propylcarbamoyl)hydroxylamine, an analogue of caracemide. Acta Crystallographica Section C: Crystal Structure Communications, 52(2), 387-390. https://doi.org/10.1107/S0108270195012236

Vancouver

Nielsen BB, Frydenvang K, Larsen IK. The ribonucleotide reductase R1 inhibitor N-acetyl-N,Ο-di(propylcarbamoyl)hydroxylamine, an analogue of caracemide. Acta Crystallographica Section C: Crystal Structure Communications. 1996 Feb 15;52(2):387-390. https://doi.org/10.1107/S0108270195012236

Author

Nielsen, Bettina Bryde ; Frydenvang, Karla ; Larsen, Ingrid Kjøller. / The ribonucleotide reductase R1 inhibitor N-acetyl-N,Ο-di(propylcarbamoyl)hydroxylamine, an analogue of caracemide. In: Acta Crystallographica Section C: Crystal Structure Communications. 1996 ; Vol. 52, No. 2. pp. 387-390.

Bibtex

@article{9f21a3efe3434723a1b1636b7df4268e,
title = "The ribonucleotide reductase R1 inhibitor N-acetyl-N,Ο-di(propylcarbamoyl)hydroxylamine, an analogue of caracemide",
abstract = "The molecular structure of the caracemide analogue N-acetyl-N,Ο-di(propylcarbamoyl)hydroxylamine (Chemical Abstracts nomenclature: N-[(propylamino)carbonyl]-N-{[(propylamino)carbonyl]oxy}acetamide), C10H19N3O4, is comparable to the structure of the parent compound N-acetyl-N,Ο-di(methylcarbamoyl)hydroxylamine. The caracemide moiety of the compound consists of two nearly planar moieties, which are almost perpendicular to each other as in the crystal structure of caracemide itself. The two propyl groups in each of the two molecules (A and B) in the asymmetric unit have different conformations. One of these groups adopts the gauche conformation, with torsion angles of 49.1 (6) and -61.3(4)° for molecules A and B, respectively, while the other adopts a fully extended conformation, with respective torsion angles of 179.2 (3) and 176.5 (3)°. The main differences in bond lengths, angles and torsion angles between molecules A and B are found in one of the propyl groups.",
author = "Nielsen, {Bettina Bryde} and Karla Frydenvang and Larsen, {Ingrid Kj{\o}ller}",
year = "1996",
month = feb,
day = "15",
doi = "10.1107/S0108270195012236",
language = "English",
volume = "52",
pages = "387--390",
journal = "Acta crystallographica. Section C, Structural chemistry",
issn = "2053-2296",
publisher = "Wiley",
number = "2",

}

RIS

TY - JOUR

T1 - The ribonucleotide reductase R1 inhibitor N-acetyl-N,Ο-di(propylcarbamoyl)hydroxylamine, an analogue of caracemide

AU - Nielsen, Bettina Bryde

AU - Frydenvang, Karla

AU - Larsen, Ingrid Kjøller

PY - 1996/2/15

Y1 - 1996/2/15

N2 - The molecular structure of the caracemide analogue N-acetyl-N,Ο-di(propylcarbamoyl)hydroxylamine (Chemical Abstracts nomenclature: N-[(propylamino)carbonyl]-N-{[(propylamino)carbonyl]oxy}acetamide), C10H19N3O4, is comparable to the structure of the parent compound N-acetyl-N,Ο-di(methylcarbamoyl)hydroxylamine. The caracemide moiety of the compound consists of two nearly planar moieties, which are almost perpendicular to each other as in the crystal structure of caracemide itself. The two propyl groups in each of the two molecules (A and B) in the asymmetric unit have different conformations. One of these groups adopts the gauche conformation, with torsion angles of 49.1 (6) and -61.3(4)° for molecules A and B, respectively, while the other adopts a fully extended conformation, with respective torsion angles of 179.2 (3) and 176.5 (3)°. The main differences in bond lengths, angles and torsion angles between molecules A and B are found in one of the propyl groups.

AB - The molecular structure of the caracemide analogue N-acetyl-N,Ο-di(propylcarbamoyl)hydroxylamine (Chemical Abstracts nomenclature: N-[(propylamino)carbonyl]-N-{[(propylamino)carbonyl]oxy}acetamide), C10H19N3O4, is comparable to the structure of the parent compound N-acetyl-N,Ο-di(methylcarbamoyl)hydroxylamine. The caracemide moiety of the compound consists of two nearly planar moieties, which are almost perpendicular to each other as in the crystal structure of caracemide itself. The two propyl groups in each of the two molecules (A and B) in the asymmetric unit have different conformations. One of these groups adopts the gauche conformation, with torsion angles of 49.1 (6) and -61.3(4)° for molecules A and B, respectively, while the other adopts a fully extended conformation, with respective torsion angles of 179.2 (3) and 176.5 (3)°. The main differences in bond lengths, angles and torsion angles between molecules A and B are found in one of the propyl groups.

UR - http://www.scopus.com/inward/record.url?scp=3242846558&partnerID=8YFLogxK

U2 - 10.1107/S0108270195012236

DO - 10.1107/S0108270195012236

M3 - Journal article

AN - SCOPUS:3242846558

VL - 52

SP - 387

EP - 390

JO - Acta crystallographica. Section C, Structural chemistry

JF - Acta crystallographica. Section C, Structural chemistry

SN - 2053-2296

IS - 2

ER -

ID: 382748571