-
1
-
-
34948876455
-
Two new-class milbemycins from Streptomyces bingchenggensis Fermentation, isolation, structure elucidation and biological properties
-
Xiang, W. S., Wang, J. D., Wang, X. J. & Zhang, J. Two new-class milbemycins from Streptomyces bingchenggensis Fermentation, isolation, structure elucidation and biological properties. J. Antibiot. 60, 351-356 (2007).
-
(2007)
J. Antibiot.
, vol.60
, pp. 351-356
-
-
Xiang, W.S.1
Wang, J.D.2
Wang, X.J.3
Zhang, J.4
-
2
-
-
38749153988
-
Further new milbemycin antibiotics from Streptomyces bingchenggensis
-
Xiang, W. S., Wang, J. D., Wang, X. J., Zhang, J. & Wang, Z. Further new milbemycin antibiotics from Streptomyces bingchenggensis. J. Antibiot. 60, 608-613 (2007).
-
(2007)
J. Antibiot.
, vol.60
, pp. 608-613
-
-
Xiang, W.S.1
Wang, J.D.2
Wang, X.J.3
Zhang, J.4
Wang, Z.5
-
3
-
-
44649176384
-
New Seco-milbemycins from Streptomyces bingchenggensis: Fermentation, isolation and structure elucidation
-
Xiang, W. S., Wang, J. D., Fan, H. M., Wang, X. J. & Zhang, J. New Seco-milbemycins from Streptomyces bingchenggensis: fermentation, isolation and structure elucidation. J. Antibiot. 60, 27-32 (2008).
-
(2008)
J. Antibiot.
, vol.60
, pp. 27-32
-
-
Xiang, W.S.1
Wang, J.D.2
Fan, H.M.3
Wang, X.J.4
Zhang, J.5
-
4
-
-
67249114338
-
A novel macrolide compound from Streptomyces bingchenggensis fermentation, isolation, structure elucidation and biological properties
-
Xiang, W. S., Wang, J. D., Wang, X. J. & Zhang, J. A novel macrolide compound from Streptomyces bingchenggensis fermentation, isolation, structure elucidation and biological properties. J. Antibiot. 62, 229-231 (2009).
-
(2009)
J. Antibiot.
, vol.62
, pp. 229-231
-
-
Xiang, W.S.1
Wang, J.D.2
Wang, X.J.3
Zhang, J.4
-
5
-
-
0032977819
-
Mechanism of inhibition of a poxvirus topoisomerase by the marine natural product sansalvamide
-
Hwang, Y. et al. Mechanism of inhibition of a poxvirus topoisomerase by the marine natural product sansalvamide. A. Mol. Pharmacol. 6, 1049-1053 (1999).
-
(1999)
A. Mol. Pharmacol.
, vol.6
, pp. 1049-1053
-
-
Hwang, Y.1
-
6
-
-
0034676534
-
Rapid high-yield, solid-phase synthesis of the antitumor antibiotic sansalvamide A using a side-chain-tethered phenylalanine building block
-
Lee, Y. & Silverman, R. B. Rapid, high-yield, solid-phase synthesis of the antitumor antibiotic sansalvamide A using a side-chain-tethered phenylalanine building block. Org. Lett. 2, 3743-3746 (2000).
-
(2000)
Org. Lett.
, vol.2
, pp. 3743-3746
-
-
Lee, Y.1
Silverman, R.B.2
-
7
-
-
0037078829
-
Solid-phase Pd-catalyzed siliconaryl carbon bond formation. Synthesis of sansalvamide A peptide
-
Gu, W., Liu, S. & Silverman, R. B. Solid-phase, Pd-catalyzed siliconaryl carbon bond formation. Synthesis of sansalvamide A peptide. Org. Lett. 4, 4171-4174 (2002).
-
(2002)
Org. Lett.
, vol.4
, pp. 4171-4174
-
-
Gu, W.1
Liu, S.2
Silverman, R.B.3
-
8
-
-
23944442706
-
Synthesis and cytotoxicity of novel sansalvamide A derivatives
-
Carroll, C. L. et al. Synthesis and cytotoxicity of novel sansalvamide A derivatives. Org. Lett. 7, 3481-3484 (2005).
-
(2005)
Org. Lett.
, vol.7
, pp. 3481-3484
-
-
Carroll, C.L.1
-
9
-
-
33244483270
-
Synthesis and novel structure-activity relationships of potent sansalvamide A derivatives
-
Otrubova, K. et al. Synthesis and novel structure-activity relationships of potent sansalvamide A derivatives. Chem. Commun. 9, 1033-1034 (2006).
-
(2006)
Chem. Commun.
, vol.9
, pp. 1033-1034
-
-
Otrubova, K.1
-
10
-
-
34247580055
-
Scaffold targeting drug-resistant colon cancers
-
Otrubova, K., McGuire, K. L. & McAlpine, S. R. Scaffold targeting drug-resistant colon cancers. J. Med. Chem. 9, 1999-2002 (2007).
-
(2007)
J. Med. Chem.
, vol.9
, pp. 1999-2002
-
-
Otrubova, K.1
McGuire, K.L.2
McAlpine, S.R.3
-
11
-
-
33645329115
-
Plant Cyclopeptides
-
Tan, N. H. & Zhou, J. Plant Cyclopeptides. Chem. Rev. 106, 840-895 (2006).
-
(2006)
Chem. Rev.
, vol.106
, pp. 840-895
-
-
Tan, N.H.1
Zhou, J.2
-
12
-
-
53149144247
-
Design and synthesis of cyclo[-Arg-Gly-Asp-c(triazole)-Gly-Xaa-] peptide analogues by click chemistry
-
Liu, Y. Q. et al. Design and synthesis of cyclo[-Arg-Gly-Asp-c(triazole)- Gly-Xaa-] peptide analogues by click chemistry. Tetrahedron 47, 10728-10734 (2008).
-
(2008)
Tetrahedron
, vol.47
, pp. 10728-10734
-
-
Liu, Y.Q.1
-
13
-
-
52049109838
-
Natural products in drug discovery
-
Harvey, A. L. Natural products in drug discovery. Drug Discov. Today 13, 895-901 (2008).
-
(2008)
Drug Discov. Today
, vol.13
, pp. 895-901
-
-
Harvey, A.L.1
-
14
-
-
39149096281
-
Comprehensive study of sansalvamide A derivatives and their structure-activity relationships against drug-resistant colon cancer cell lines
-
Otrubova, K., Lushington, G., McGuire, K. L. & McAlpine, S. R. Comprehensive study of sansalvamide A derivatives and their structure-activity relationships against drug-resistant colon cancer cell lines. J. Med. Chem. 3, 530-544 (2008).
-
(2008)
J. Med. Chem.
, vol.3
, pp. 530-544
-
-
Otrubova, K.1
Lushington, G.2
McGuire, K.L.3
McAlpine, S.R.4
-
15
-
-
38749144034
-
Synthesis and cytotoxicity of a new class of potent decapeptide macrocycles
-
Davis, M. R. et al. Synthesis and cytotoxicity of a new class of potent decapeptide macrocycles. Org. Lett. 2, 177-180 (2008).
-
(2008)
Org. Lett.
, vol.2
, pp. 177-180
-
-
Davis, M.R.1
-
16
-
-
34547855100
-
Identification of Sansalvamide A analog potent against pancreatic cancer cell lines
-
Pan, P. S., McGuire, K. L. & McAlpine, S. R. Identification of Sansalvamide A analog potent against pancreatic cancer cell lines. Bioorg. Med. Chem. Lett. 18, 5072-5077 (2007).
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 5072-5077
-
-
Pan, P.S.1
McGuire, K.L.2
McAlpine, S.R.3
-
17
-
-
33947246678
-
Synthesis of second-generation sansalvamide A derivatives: Novel templates as potential antitumor agents
-
Rodriguez, R. A. et al. Synthesis of second-generation sansalvamide A derivatives: novel templates as potential antitumor agents. J. Org. Chem. 6, 1980-2002 (2007).
-
(2007)
J. Org. Chem.
, vol.6
, pp. 1980-2002
-
-
Rodriguez, R.A.1
-
18
-
-
33745592766
-
Synthesis of Sansalvamide A derivatives and their cytotoxicity in the MSS colon cancer cell line HT-2
-
Styers, T. J. et al. Synthesis of Sansalvamide A derivatives and their cytotoxicity in the MSS colon cancer cell line HT-2. Bioorg. Med. Chem. 16, 5625-5631 (2006).
-
(2006)
Bioorg. Med. Chem.
, vol.16
, pp. 5625-5631
-
-
Styers, T.J.1
-
19
-
-
33244483270
-
Synthesis and novel structure-activity relationships of potent sansalvamide A derivatives
-
Otrubova, K. et al. Synthesis and novel structure-activity relationships of potent sansalvamide A derivatives. Chem. Commun. 9, 1033-1034 (2006).
-
(2006)
Chem. Commun.
, vol.9
, pp. 1033-1034
-
-
Otrubova, K.1
-
20
-
-
30544431590
-
A novel peptide sansalvamide analogue inhibits pancreatic cancer cell growth through G0/G1 cell-cycle arrest
-
Ujiki, M. B. et al. A novel peptide sansalvamide analogue inhibits pancreatic cancer cell growth through G0/G1 cell-cycle arrest. Biochem. Biophys. Res. Commun. 4, 1224-1228 (2006).
-
(2006)
Biochem. Biophys. Res. Commun.
, vol.4
, pp. 1224-1228
-
-
Ujiki, M.B.1
-
21
-
-
0034127813
-
Human oesophageal adenocarcinoma cell lines JROECL 47 and JROECL 50 are admixtures of the human colon carcinoma cell line HCT 11
-
Wijnhoven, B. P. et al. Human oesophageal adenocarcinoma cell lines JROECL 47 and JROECL 50 are admixtures of the human colon carcinoma cell line HCT 11. Br. J. Cancer. 9, 1510-1512 (2000).
-
(2000)
Br. J. Cancer.
, vol.9
, pp. 1510-1512
-
-
Wijnhoven, B.P.1
|