-
1
-
-
0038627550
-
Psammaplins from the sponge Pseudoceratina purpurea: Inhibition of both histone deacetylase and DNA methyltransferase
-
Piña, I.C.; Gautschi, J.T.; Wang, G.Y.S.; Miranda, L.S.; Francis, J.S.; Dennis, F.; Susan, C.K.; Lidia, C.S.; Stacy, W.R.; Larry, B.P.; Kenneth, W.B.; Phillip, C. Psammaplins from the sponge Pseudoceratina purpurea: inhibition of both histone deacetylase and DNA methyltransferase. J. Org. Chem. 2003, 68, 3866-3873.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 3866-3873
-
-
Pina, I.C.1
Gautschi, J.T.2
Wang, G.Y.S.3
Miranda, L.S.4
Francis, J.S.5
Dennis, F.6
Susan, C.K.7
Lidia, C.S.8
Stacy, W.R.9
Larry, B.P.10
Kenneth, W.B.11
Phillip, C.12
-
2
-
-
0032806308
-
Psammaplin A, a natural phenolic compound, has inhibitory effect on human topoisomerase II and is cytotoxic to cancer cells
-
Kim, D.; Lee, I.S.; Jung, J.H.; Lee, C.O.; Choi, S.U. Psammaplin A, a natural phenolic compound, has inhibitory effect on human topoisomerase II and is cytotoxic to cancer cells. Anticancer Res. 1999, 19, 4085-4090.
-
(1999)
Anticancer Res.
, vol.19
, pp. 4085-4090
-
-
Kim, D.1
Lee, I.S.2
Jung, J.H.3
Lee, C.O.4
Choi, S.U.5
-
3
-
-
0035477106
-
Combinatorial synthesis through disulfide exchange: Discovery of potent psammaplin A type antibacterial agents active against methicillin-resistant staphylococcus aureus (MRSA)
-
Nicolaou, K.C.; Hughes, R.; Pfefferkorn, J.A.; Barluenga, S.; Roecker, A.J. Combinatorial synthesis through disulfide exchange: discovery of potent psammaplin A type antibacterial agents active against methicillin-resistant staphylococcus aureus (MRSA). Chem. Eur. J. 2001, 7, 4280-4295.
-
(2001)
Chem Eur. J.
, vol.7
, pp. 4280-4295
-
-
Nicolaou, K.C.1
Hughes, R.2
Pfefferkorn, J.A.3
Barluenga, S.4
Roecker, A.J.5
-
4
-
-
0036166502
-
Psammaplin A, a chitinase inhibitor isolated from the Fijian marine sponge Aplysinella rhax
-
Tabudravu, J.N.; Eijsink, V.G.H.; Gooday, G.W.; Jaspars, M.; Komander, D.; Legg, M.; Synstad, B.; van Aalten, D.M.F. Psammaplin A, a chitinase inhibitor isolated from the Fijian marine sponge Aplysinella rhax. Bioorg. Med. Chem. 2002, 10, 1123-1128.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 1123-1128
-
-
Tabudravu, J.N.1
Eijsink, V.G.H.2
Gooday, G.W.3
Jaspars, M.4
Komander, D.5
Legg, M.6
Synstad, B.7
Van Aalten, D.M.F.8
-
5
-
-
0346094302
-
Psammaplin A, a marine natural product, inhibits aminopeptidase N and suppresses angiogenesis in vitro
-
Shim, J.S.; Lee, H.S.; Shin J.; Kwon, H.J. Psammaplin A, a marine natural product, inhibits aminopeptidase N and suppresses angiogenesis in vitro. Cancer Lett. 2004, 203, 163-169.
-
(2004)
Cancer Lett.
, vol.203
, pp. 163-169
-
-
Shim, J.S.1
Lee, H.S.2
Shin, J.3
Kwon, H.J.4
-
6
-
-
0026676620
-
A convenient synthesis of a bromotyrosine derived metabolite, psammaplin A, from psammaplysilla SP
-
Hoshino, O.; Murakata, M.; Yamada, K. A convenient synthesis of a bromotyrosine derived metabolite, psammaplin A, from psammaplysilla SP. Bioorg. Med. Chem. Lett. 1992, 2, 1561-1562.
-
(1992)
Bioorg. Med. Chem Lett.
, vol.2
, pp. 1561-1562
-
-
Hoshino, O.1
Murakata, M.2
Yamada, K.3
-
7
-
-
33646180176
-
An improved synthesis of psammaplin A
-
Godert, A.M.; Angelino, N.; Woloszynska-Read, A.; Morey, S.R.; James, S.R.; Karpf, A.R.; Sufrin, J.R. An improved synthesis of psammaplin A. Bioorg. Med. Chem. Lett. 2006, 16, 3330-3333.
-
(2006)
Bioorg. Med. Chem Lett.
, vol.16
, pp. 3330-3333
-
-
Godert, A.M.1
Angelino, N.2
Woloszynska-Read, A.3
Morey, S.R.4
James, S.R.5
Karpf, A.R.6
Sufrin, J.R.7
-
9
-
-
1542357995
-
Anticonvulsant activity of phenylmethylenehydantoins: A structure-activity relationship study
-
Thenmozhiyal, J.C.; Wong, P.T.H.; Chui, W.K. Anticonvulsant activity of phenylmethylenehydantoins: a structure-activity relationship study. J. Med. Chem. 2004, 47, 1527-1535.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 1527-1535
-
-
Thenmozhiyal, J.C.1
Wong, P.T.H.2
Chui, W.K.3
-
11
-
-
27844590858
-
A family of mycothiol analogues
-
Knapp, S.; Amorelli, B.; Darout, E.; Ventocilla, C.C.; Goldman, L.M.; Huhn, R.A.; Minnihan, E.C. A family of mycothiol analogues. J. Carbohydr. Chem. 2005, 24, 103-130.
-
(2005)
J. Carbohydr. Chem.
, vol.24
, pp. 103-130
-
-
Knapp, S.1
Amorelli, B.2
Darout, E.3
Ventocilla, C.C.4
Goldman, L.M.5
Huhn, R.A.6
Minnihan, E.C.7
-
12
-
-
5644266179
-
A very simple method for the preparation of symmetrical disulfides
-
Leino, R.; Lönnqvist, J.E. A very simple method for the preparation of symmetrical disulfides. Tetrahedron Lett. 2004, 45, 8489-8491.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 8489-8491
-
-
Leino, R.1
Lönnqvist, J.E.2
-
13
-
-
0026659612
-
Mixed-inhibitor-prodrug as a new approach toward systemically active inhibitors of enkephalindegrading enzymes
-
Fournie-Zaluski, M.C.; Coric, P.; Turcaud, S.; Lucas, E.; Noble, F.; Maldonado, R.; Roques, B.P. Mixed-inhibitor-prodrug as a new approach toward systemically active inhibitors of enkephalindegrading enzymes. J. Med. Chem. 1992, 35, 2473-2481.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 2473-2481
-
-
Fournie-Zaluski, M.C.1
Coric, P.2
Turcaud, S.3
Lucas, E.4
Noble, F.5
Maldonado, R.6
Roques, B.P.7
-
14
-
-
0343110277
-
Peptide synthesis by prior thiol capture. 4. Amide bond formation: The effect of a side-chain substituent on the rates of intramolecular O, N-acyl transfer
-
Kemp, D.S.; Galakatos, N.G.; Dranginis, S.; Ashton, C.; Fotouhi, N.; Curran, T.P. Peptide synthesis by prior thiol capture. 4. Amide bond formation: the effect of a side-chain substituent on the rates of intramolecular O, N-acyl transfer. J. Org. Chem. 1986, 51, 3320-3324.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 3320-3324
-
-
Kemp, D.S.1
Galakatos, N.G.2
Dranginis, S.3
Ashton, C.4
Fotouhi, N.5
Curran, T.P.6
-
15
-
-
33749529741
-
Synthesis of poly(β- amino esters) with thiol-reactive side chains for DNA delivery
-
Zugates, G.T.; Anderson, D.G.; Little, S.R.; Lawhorn, I.E.B.; Langer, R. Synthesis of poly(β- amino esters) with thiol-reactive side chains for DNA delivery. J. Am. Chem. Soc. 2006, 128, 12726-12734.
-
(2006)
J. Am. Chem Soc.
, vol.128
, pp. 12726-12734
-
-
Zugates, G.T.1
Anderson, D.G.2
Little, S.R.3
Lawhorn, I.E.B.4
Langer, R.5
-
16
-
-
20544478411
-
Efficient total synthesis of bastadin 6, an anti-angiogenic brominated tyrosine-derived metabolite from marine sponge
-
Kotoku, N.; Tsujita, H.; Hiramatsu, A.; Mori, C.; Koizumi, N.; Kobayashi, M. Efficient total synthesis of bastadin 6, an anti-angiogenic brominated tyrosine-derived metabolite from marine sponge. Tetrahedron 2005, 61, 7211-7218.
-
(2005)
Tetrahedron
, vol.61
, pp. 7211-7218
-
-
Kotoku, N.1
Tsujita, H.2
Hiramatsu, A.3
Mori, C.4
Koizumi, N.5
Kobayashi, M.6
-
17
-
-
12444304259
-
Designing molecules for PDT: Red light-induced DNA cleavage on disulfide bond activation in a dicopper (II) complex
-
Dhar, S.; Nethajiand, M.; Chakravarty, A.R. Designing molecules for PDT: red light-induced DNA cleavage on disulfide bond activation in a dicopper (II) complex. Dalton Trans. 2005, 344-348.
-
(2005)
Dalton Trans.
, pp. 344-348
-
-
Dhar, S.1
Nethajiand, M.2
Chakravarty, A.R.3
-
18
-
-
37049083933
-
Transition-metal chemistry of main-group hydrazides. Part 2. A new oxime thiosemicarbazide framework as a novel SN multifunctional tripodal ligand for palladium (II): Synthetic and X-ray crystal structural investigations
-
Katti, K.V.; Singh, P.R.; Barnes, C.L. Transition-metal chemistry of main-group hydrazides. Part 2. A new oxime thiosemicarbazide framework as a novel SN multifunctional tripodal ligand for palladium (II): synthetic and X-ray crystal structural investigations. J. Chem. Soc. Dalton Trans. 1993, 2153-2156.
-
(1993)
J. Chem. Soc. Dalton Trans.
, pp. 2153-2156
-
-
Katti, K.V.1
Singh, P.R.2
Barnes, C.L.3
-
19
-
-
0023236004
-
Brominated tyrosine metabolites from an unidentified sponge
-
Arabshahi, L.; Schmitz, F.J. Brominated tyrosine metabolites from an unidentified sponge. J. Org. Chem. 1987, 52, 3584-3586.
-
(1987)
J. Org. Chem.
, vol.52
, pp. 3584-3586
-
-
Arabshahi, L.1
Schmitz, F.J.2
-
21
-
-
0004150157
-
-
University of Göttingen: Göttingen, Germany
-
Sheldrick, G.M. SHELXL-97; University of Göttingen: Göttingen, Germany, 1997.
-
(1997)
SHELXL-97
-
-
Sheldrick, G.M.1
-
22
-
-
0004150157
-
-
University of Göttingen: Göttingen, Germany
-
Sheldrick, G.M. SHELXL-97; University of Göttingen: Göttingen, Germany, 1997.
-
(1997)
SHELXL-97
-
-
Sheldrick, G.M.1
-
23
-
-
37549039510
-
A short history of SHELXL
-
Sheldrick, G.M. A short history of SHELXL. Acta Cryst. 2008, A64, 112-122.
-
(2008)
Acta Cryst.
, vol.A64
, pp. 112-122
-
-
Sheldrick, G.M.1
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