European journal of pharmacology
Chen J, Campbell AP, Wakelin LPG, Finch AM.
PMID: 34871559
Eur J Pharmacol. 2021 Dec 04;916:174659. doi: 10.1016/j.ejphar.2021.174659. Epub 2021 Dec 04.
The development of sub-type selective α
Cite
Chen J, Campbell AP, Wakelin LPG, et al. Characterisation of bis(4-aminoquinoline)s as α. Eur J Pharmacol. 2021;916:174659doi: 10.1016/j.ejphar.2021.174659.
Chen, J., Campbell, A. P., Wakelin, L. P. G., & Finch, A. M. (2021). Characterisation of bis(4-aminoquinoline)s as α. European journal of pharmacology, 916174659. https://doi.org/10.1016/j.ejphar.2021.174659
Chen, Junli, et al. "Characterisation of bis(4-aminoquinoline)s as α." European journal of pharmacology vol. 916 (2021): 174659. doi: https://doi.org/10.1016/j.ejphar.2021.174659
Chen J, Campbell AP, Wakelin LPG, Finch AM. Characterisation of bis(4-aminoquinoline)s as α. Eur J Pharmacol. 2021 Dec 04;916:174659. doi: 10.1016/j.ejphar.2021.174659. Epub 2021 Dec 04. PMID: 34871559.
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European journal of pharmacology
Chen J, Campbell AP, Wakelin LPG, Finch AM.
PMID: 34871559
Eur J Pharmacol. 2022 Feb 05;916:174659. doi: 10.1016/j.ejphar.2021.174659. Epub 2021 Dec 04.
The development of sub-type selective α
Cite
Chen J, Campbell AP, Wakelin LPG, et al. Characterisation of bis(4-aminoquinoline)s as α. Eur J Pharmacol. 2021;916:174659doi: 10.1016/j.ejphar.2021.174659.
Chen, J., Campbell, A. P., Wakelin, L. P. G., & Finch, A. M. (2022). Characterisation of bis(4-aminoquinoline)s as α. European journal of pharmacology, 916174659. https://doi.org/10.1016/j.ejphar.2021.174659
Chen, Junli, et al. "Characterisation of bis(4-aminoquinoline)s as α." European journal of pharmacology vol. 916 (2022): 174659. doi: https://doi.org/10.1016/j.ejphar.2021.174659
Chen J, Campbell AP, Wakelin LPG, Finch AM. Characterisation of bis(4-aminoquinoline)s as α. Eur J Pharmacol. 2022 Feb 05;916:174659. doi: 10.1016/j.ejphar.2021.174659. Epub 2021 Dec 04. PMID: 34871559.
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European journal of pharmacology
Chen J, Campbell AP, Wakelin LPG, Finch AM.
PMID: 34871559
Eur J Pharmacol. 2021 Dec 03;174659. doi: 10.1016/j.ejphar.2021.174659. Epub 2021 Dec 03.
The development of sub-type selective α
Cite
Chen J, Campbell AP, Wakelin LPG, et al. Characterisation of bis(4-aminoquinoline)s as α. Eur J Pharmacol. 2021;174659doi: 10.1016/j.ejphar.2021.174659.
Chen, J., Campbell, A. P., Wakelin, L. P. G., & Finch, A. M. (2021). Characterisation of bis(4-aminoquinoline)s as α. European journal of pharmacology, 174659. https://doi.org/10.1016/j.ejphar.2021.174659
Chen, Junli, et al. "Characterisation of bis(4-aminoquinoline)s as α." European journal of pharmacology vol. (2021): 174659. doi: https://doi.org/10.1016/j.ejphar.2021.174659
Chen J, Campbell AP, Wakelin LPG, Finch AM. Characterisation of bis(4-aminoquinoline)s as α. Eur J Pharmacol. 2021 Dec 03;174659. doi: 10.1016/j.ejphar.2021.174659. Epub 2021 Dec 03. PMID: 34871559.
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Acta crystallographica. Section D, Biological crystallography
Wilcock DJ, Adams A, Cardin CJ, Wakelin LP.
PMID: 15299669
Acta Crystallogr D Biol Crystallogr. 1996 May 01;52:481-5. doi: 10.1107/S0907444995016052.
d(ACGTACGT), C(78)H(84)N(30)O(32)P(7).20H(2)O, M(r) (DNA) = 2170, tetragonal, P4(3)2(1)2 (No 96), a = 42.845 (1), b = 42.845(1), c = 24.804 (1) A, V = 45532.5 (2) A(3), z = 8,lambda(MoKalpha) = 0.71069 A, micro (MoKalpha) = 0.10 mm(-1), T...
Cite
Wilcock DJ, Adams A, Cardin CJ, et al. Structure of the DNA octanucleotide d(ACGTACGT)2. Acta Crystallogr D Biol Crystallogr. 1996;52:481-5doi: 10.1107/S0907444995016052.
Wilcock, D. J., Adams, A., Cardin, C. J., & Wakelin, L. P. (1996). Structure of the DNA octanucleotide d(ACGTACGT)2. Acta crystallographica. Section D, Biological crystallography, 52481-5. https://doi.org/10.1107/S0907444995016052
Wilcock, D J, et al. "Structure of the DNA octanucleotide d(ACGTACGT)2." Acta crystallographica. Section D, Biological crystallography vol. 52 (1996): 481-5. doi: https://doi.org/10.1107/S0907444995016052
Wilcock DJ, Adams A, Cardin CJ, Wakelin LP. Structure of the DNA octanucleotide d(ACGTACGT)2. Acta Crystallogr D Biol Crystallogr. 1996 May 01;52:481-5. doi: 10.1107/S0907444995016052. PMID: 15299669.
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The Journal of organic chemistry
Howarth NM, Wakelin LP.
PMID: 27518596
J Org Chem. 2000 Jan 28;65(2):634. doi: 10.1021/jo974036u.
No abstract available.
Cite
Howarth NM, Wakelin LP. α-PNA: A Novel Peptide Nucleic Acid Analogue of DNA. J Org Chem. 2000;65(2):634doi: 10.1021/jo974036u.
Howarth, N. M., & Wakelin, L. P. (2000). α-PNA: A Novel Peptide Nucleic Acid Analogue of DNA. The Journal of organic chemistry, 65(2), 634. https://doi.org/10.1021/jo974036u
Howarth, N M, and Wakelin, L P. "α-PNA: A Novel Peptide Nucleic Acid Analogue of DNA." The Journal of organic chemistry vol. 65,2 (2000): 634. doi: https://doi.org/10.1021/jo974036u
Howarth NM, Wakelin LP. α-PNA: A Novel Peptide Nucleic Acid Analogue of DNA. J Org Chem. 2000 Jan 28;65(2):634. doi: 10.1021/jo974036u. PMID: 27518596.
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Biopolymers
Rowell KN, Thomas DS, Ball GE, Wakelin LPG.
PMID: 33207389
Biopolymers. 2021 Apr;112(4):e23409. doi: 10.1002/bip.23409. Epub 2020 Nov 18.
Dimers of 9-aminoacridine linked via the 9-amino group with polymethylene chains, termed diacridines, are known to bisintercalate into DNA when the linker comprises 6 or more methylene units. There are no literature reports of crystal or NMR solution structures...
Cite
Rowell KN, Thomas DS, Ball GE, et al. Molecular dynamic simulations of diacridine binding to DNA: Indications that C6 diacridine can bisintercalate spanning two base pairs. Biopolymers. 2020;112(4):e23409doi: 10.1002/bip.23409.
Rowell, K. N., Thomas, D. S., Ball, G. E., & Wakelin, L. P. G. (2021). Molecular dynamic simulations of diacridine binding to DNA: Indications that C6 diacridine can bisintercalate spanning two base pairs. Biopolymers, 112(4), e23409. https://doi.org/10.1002/bip.23409
Rowell, Keiran N, et al. "Molecular dynamic simulations of diacridine binding to DNA: Indications that C6 diacridine can bisintercalate spanning two base pairs." Biopolymers vol. 112,4 (2021): e23409. doi: https://doi.org/10.1002/bip.23409
Rowell KN, Thomas DS, Ball GE, Wakelin LPG. Molecular dynamic simulations of diacridine binding to DNA: Indications that C6 diacridine can bisintercalate spanning two base pairs. Biopolymers. 2021 Apr;112(4):e23409. doi: 10.1002/bip.23409. Epub 2020 Nov 18. PMID: 33207389.
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European journal of pharmacology
Chen J, Campbell AP, Wakelin LPG, Finch AM.
PMID: 34871559
Eur J Pharmacol. 2021 Dec 04;916:174659. doi: 10.1016/j.ejphar.2021.174659. Epub 2021 Dec 04.
The development of sub-type selective α
Cite
Chen J, Campbell AP, Wakelin LPG, et al. Characterisation of bis(4-aminoquinoline)s as α. Eur J Pharmacol. 2021;916:174659doi: 10.1016/j.ejphar.2021.174659.
Chen, J., Campbell, A. P., Wakelin, L. P. G., & Finch, A. M. (2021). Characterisation of bis(4-aminoquinoline)s as α. European journal of pharmacology, 916174659. https://doi.org/10.1016/j.ejphar.2021.174659
Chen, Junli, et al. "Characterisation of bis(4-aminoquinoline)s as α." European journal of pharmacology vol. 916 (2021): 174659. doi: https://doi.org/10.1016/j.ejphar.2021.174659
Chen J, Campbell AP, Wakelin LPG, Finch AM. Characterisation of bis(4-aminoquinoline)s as α. Eur J Pharmacol. 2021 Dec 04;916:174659. doi: 10.1016/j.ejphar.2021.174659. Epub 2021 Dec 04. PMID: 34871559.
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