SCOPUS 정보 검색 플랫폼

Volumn 3, Issue 5, 1993, Pages 803-808

The free energy change of restricting a bond rotation in the binding of peptide analogues to vancomycin group antibiotics

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE DERIVATIVE; N FUMARYL DEXTRO ALANINE; N SUCCINYL DEXTRO ALANINE; RISTOCETIN A; UNCLASSIFIED DRUG; VANCOMYCIN DERIVATIVE;

COMPLEX FORMATION; CONFERENCE PAPER; MATHEMATICS; PROTEIN BINDING; STRUCTURE ACTIVITY RELATION; ULTRAVIOLET SPECTROPHOTOMETRY;

EID: 0027241298 PISSN: 0960894X EISSN: None Source Type: Journal
DOI: 10.1016/S0960-894X(00)80670-8 Document Type: Article

Times cited : (25)

References (20)

4
- 0019407381
- On the attribution and additivity of binding energies
- (1978) Proceedings of the National Academy of Sciences , vol.78 , pp. 4046
- Jencks¹

5
- 0015101706
- (1971) Proc. Natl. Acad. Sci. U.S.A. , vol.68 , pp. 1678
- Page¹ Jencks²

6
- 0021745755
- (1984) J. Med. Chem. , vol.27 , pp. 1648
- Andrews¹ Craik² Martin³

7
- 0003481596
- Second Edition, W.H. Freeman, New York
- (1985) Enzyme Structure and Mechanism
- Ferst¹

8
- 84913182091
- N-succinyl-D-alanine (NSDA) and N-fumaryl-D-alanine (NFDA) were both prepared from D-alanine methyl ester, and mono-methyl succinate or mono-methyl fumarate, respectively. The N-succinyl-D-alanine dimethyl ester (N-fumaryl-D-alanine dimethyl ester) was prepared by stirring a 1:1 mixture of D-lanine methyl ester and mono-methyl succinate (mono-methyl fumarate) with N-methylmorpholine, hydroxybenzotriazole and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (8:1:2) in dichloromethane for 10 hours at room temperature. The solvent was evaporated and the residue dissolved in ethyl acetate. The solution was washed with water, sodium hydrogen carbonate solution, citric acid solution, and again with water, dried over potassium carbonate, filtered, and the solvent then evaporated under vacuum. Final purification by flash column chromatography using silica gel/ethyl acetate gave pure N-succinyl-D-alanine dimethyl ester (N-fumaryl-D-alanine dimethyl ester), typical yields [[Truncated]]

9
- 84913182090
- Gerhard, U.; Williams D.H.; University of Cambridge, unpublished results.

10
- 84942700429
- 1H n.m.r. studies of the structure of ristocetin A and of its complexes with bacterial cell wall analogues in aqueous solution
- (1985) Journal of the Chemical Society, Perkin Transactions 1 , pp. 949
- Williamson¹ Williams²

11
- 34250653849
- max for both ligands was determined to be 286nm. Titration was carried out at the previously determined wavelength in a 2-cell arrangement, where buffer and ristocetin A solutions were placed in the reference and sample beam respectively. Equal [[Truncated]]
- (1989) Numerical Recipes in Pascal
- Press¹ Flannery² Tenkolsky³ Vetterling⁴

12
- 84986437005
- Macromodel?an integrated software system for modeling organic and bioorganic molecules using molecular mechanics
- (1990) Journal of Computational Chemistry , vol.11 , pp. 440
- Mohamadi¹ Richards² Guida³ Liskamp⁴ Lipton⁵ Caufield⁶ Chang⁷ Hendrickson⁸ Still⁹

13
- 0003421978
- Plenum Press, London
- (1977) Critical Stability Constants III , pp. 108
- Martell¹ Smith²

14
- 0003421978
- Plenum Press, London
- (1977) Critical Stability Constants III , pp. 115
- Martell¹ Smith²

16
- 3643136615
- Average structures of butadiene, acrolein, and glyoxal determined by gas electron diffraction and spectroscopy
- Journal of Molecular Structure , vol.1 , pp. 463
- Kuchitsu¹ Fukuyama² Morino³

17
- 0141935319
- Wiley & Sons, New York
- (1961) Molecular Orbital Theory , pp. 165-172
- Streitwieser¹

18
- 0003719955
- Oxford University Press
- (1985) The Physical Basis of Organic Chemistry , pp. 77-114
- Maskill¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.