-
1
-
-
75149163461
-
Therapeutic agents from the sea: biodiversity, chemo-evolutionary insight and advances to the end of Darwin's 200th year
-
Newman D.J., et al. Therapeutic agents from the sea: biodiversity, chemo-evolutionary insight and advances to the end of Darwin's 200th year. Diving Hyperb. Med. 2009, 39:216-225.
-
(2009)
Diving Hyperb. Med.
, vol.39
, pp. 216-225
-
-
Newman, D.J.1
-
2
-
-
65649101923
-
Chemotherapy of acute leukemia in adults
-
Thomas X. Chemotherapy of acute leukemia in adults. Expert Opin. Pharmacother. 2009, 10:221-237.
-
(2009)
Expert Opin. Pharmacother.
, vol.10
, pp. 221-237
-
-
Thomas, X.1
-
3
-
-
65549094616
-
Treatment strategies for pediatric acute myeloid leukemia
-
Absalon M.J., et al. Treatment strategies for pediatric acute myeloid leukemia. Expert Opin. Pharmacother. 2009, 10:57-79.
-
(2009)
Expert Opin. Pharmacother.
, vol.10
, pp. 57-79
-
-
Absalon, M.J.1
-
4
-
-
77953683703
-
-
MARTINDALE The Complete Drug Reference (database on the internet). Cytarabine. Thomson MICROMEDEX, 2009. Available at: Accessed December 1, 2009. Micromedex Health Care, Martindale-The Complete Drug Reference ()
-
MARTINDALE (2009) The Complete Drug Reference (database on the internet). Cytarabine. Thomson MICROMEDEX, 2009. Available at: Accessed December 1, 2009. Micromedex Health Care, Martindale-The Complete Drug Reference (). http://www.micromedex.com/.
-
(2009)
-
-
-
5
-
-
2542542709
-
Neonatal herpes simplex infection
-
Whitley R. Neonatal herpes simplex infection. Curr. Opin. Infect. Dis. 2004, 17:243-246.
-
(2004)
Curr. Opin. Infect. Dis.
, vol.17
, pp. 243-246
-
-
Whitley, R.1
-
6
-
-
77953688193
-
-
MARTINDALE (2009) The Complete Drug Reference (database on the internet). Vidarabine. Thomson MICROMEDEX, Available at: Accessed December 1, 2009. Micromedex Health Care, Martindale-The Complete Drug Reference ()
-
MARTINDALE (2009) The Complete Drug Reference (database on the internet). Vidarabine. Thomson MICROMEDEX, 2009. Available at: Accessed December 1, 2009. Micromedex Health Care, Martindale-The Complete Drug Reference (). http://www.micromedex.com/.
-
(2009)
-
-
-
7
-
-
0002224261
-
W-Conotoxin MVIIA: from marine snail venom to analgesic drug
-
Karger, N. Fusetani (Ed.)
-
Olivera B.M. w-Conotoxin MVIIA: from marine snail venom to analgesic drug. Drugs from the Sea 2000, 75-85. Karger. N. Fusetani (Ed.).
-
(2000)
Drugs from the Sea
, pp. 75-85
-
-
Olivera, B.M.1
-
8
-
-
71449089152
-
Drugs from slugs - past, present and future perspectives of omega-conotoxin research
-
Bingham J.P., et al. Drugs from slugs - past, present and future perspectives of omega-conotoxin research. Chem. Biol. Interact. 2010, 183:1-18.
-
(2010)
Chem. Biol. Interact.
, vol.183
, pp. 1-18
-
-
Bingham, J.P.1
-
9
-
-
0021242718
-
A venom peptide with a novel presynaptic blocking action
-
Kerr L.M., Yoshikami D. A venom peptide with a novel presynaptic blocking action. Nature 1984, 308:282-284.
-
(1984)
Nature
, vol.308
, pp. 282-284
-
-
Kerr, L.M.1
Yoshikami, D.2
-
10
-
-
9144272640
-
Ziconotide: neuronal calcium channel blocker for treating severe chronic pain
-
Miljanich G.P. Ziconotide: neuronal calcium channel blocker for treating severe chronic pain. Curr. Med. Chem. 2004, 11:3029-3040.
-
(2004)
Curr. Med. Chem.
, vol.11
, pp. 3029-3040
-
-
Miljanich, G.P.1
-
11
-
-
33645329856
-
Targeting N-type and T-type calcium channels for the treatment of pain
-
McGivern J.G. Targeting N-type and T-type calcium channels for the treatment of pain. Drug Discov. Today 2006, 11:245-253.
-
(2006)
Drug Discov. Today
, vol.11
, pp. 245-253
-
-
McGivern, J.G.1
-
12
-
-
0033972437
-
Interactions of intrathecally administered ziconotide, a selective blocker of neuronal N-type voltage-sensitive calcium channels, with morphine on nociception in rats
-
Wang Y.X., et al. Interactions of intrathecally administered ziconotide, a selective blocker of neuronal N-type voltage-sensitive calcium channels, with morphine on nociception in rats. Pain 2000, 84:271-281.
-
(2000)
Pain
, vol.84
, pp. 271-281
-
-
Wang, Y.X.1
-
13
-
-
0027968002
-
Calcium channel antagonist peptides define several components of transmitter release in the hippocampus
-
Gaur S., et al. Calcium channel antagonist peptides define several components of transmitter release in the hippocampus. Neuropharmacology 1994, 33:1211-1219.
-
(1994)
Neuropharmacology
, vol.33
, pp. 1211-1219
-
-
Gaur, S.1
-
14
-
-
9144230737
-
Intrathecal ziconotide in the treatment of refractory pain in patients with cancer or AIDS - A randomized controlled trial
-
Staats P.S., et al. Intrathecal ziconotide in the treatment of refractory pain in patients with cancer or AIDS - A randomized controlled trial. J. Am. Med. Assoc. 2004, 291:63-70.
-
(2004)
J. Am. Med. Assoc.
, vol.291
, pp. 63-70
-
-
Staats, P.S.1
-
15
-
-
70349803503
-
Intrathecal ziconotide for neuropathic pain: a review
-
Rauck R.L., et al. Intrathecal ziconotide for neuropathic pain: a review. Pain Pract. 2009, 9:327-337.
-
(2009)
Pain Pract.
, vol.9
, pp. 327-337
-
-
Rauck, R.L.1
-
16
-
-
46749141315
-
Ziconotide: an update and review
-
Williams J.A., et al. Ziconotide: an update and review. Expert Opin. Pharmacother. 2008, 9:1575-1583.
-
(2008)
Expert Opin. Pharmacother.
, vol.9
, pp. 1575-1583
-
-
Williams, J.A.1
-
17
-
-
0025070774
-
-
Rinehart, K.L. et al. Ecteinascidins 729, 743, 745, 759A, 759B, and 770: potent antitumor agents from the Caribbean tunicate Ecteinascidia turbinata [erratum to document cited in CA113(9):75189d]. J. Org. Chem 55, 4512-4515; Erratum: Rinehart, K.L. et al. (1991) J. Org. Chem. 56, 1676.
-
Rinehart, K.L. et al. (1990) Ecteinascidins 729, 743, 745, 759A, 759B, and 770: potent antitumor agents from the Caribbean tunicate Ecteinascidia turbinata [erratum to document cited in CA113(9):75189d]. J. Org. Chem 55, 4512-4515; Erratum: Rinehart, K.L. et al. (1991) J. Org. Chem. 56, 1676.
-
(1990)
-
-
-
18
-
-
0024995421
-
Antitumor tetrahydroisoquinoline alkaloids from the colonial ascidian Ecteinascidia turbinata
-
Wright A.E., et al. Antitumor tetrahydroisoquinoline alkaloids from the colonial ascidian Ecteinascidia turbinata. J. Org. Chem. 1990, 55:4508-4512.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 4508-4512
-
-
Wright, A.E.1
-
19
-
-
67650309276
-
Soft tissue sarcoma trials: one size no longer fits all
-
Verweij J. Soft tissue sarcoma trials: one size no longer fits all. J. Clin. Oncol. 2009, 27:3085-3087.
-
(2009)
J. Clin. Oncol.
, vol.27
, pp. 3085-3087
-
-
Verweij, J.1
-
20
-
-
60749137451
-
Beyond chemotherapy: targeted therapies in ovarian cancer
-
Yap T.A., et al. Beyond chemotherapy: targeted therapies in ovarian cancer. Nat. Rev. Cancer 2009, 9:167-181.
-
(2009)
Nat. Rev. Cancer
, vol.9
, pp. 167-181
-
-
Yap, T.A.1
-
21
-
-
61549104994
-
® (trabectedin, ET-743). A semisynthetic process solves the supply problem
-
® (trabectedin, ET-743). A semisynthetic process solves the supply problem. Nat. Prod. Rep. 2009, 26:322-327.
-
(2009)
Nat. Prod. Rep.
, vol.26
, pp. 322-327
-
-
Cuevas, C.1
Francesch, A.2
-
22
-
-
0034814388
-
Differential rates of reversibility of ecteinascidin 743-DNA covalent adducts from different sequences lead to migration to favored bonding sites
-
Zewail-Foote M., Hurley L.H. Differential rates of reversibility of ecteinascidin 743-DNA covalent adducts from different sequences lead to migration to favored bonding sites. J. Am. Chem. Soc. 2001, 123:6485-6495.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 6485-6495
-
-
Zewail-Foote, M.1
Hurley, L.H.2
-
23
-
-
17944374027
-
Antiproliferative activity of ecteinascidin 743 is dependent upon transcription-coupled nucleotide-excision repair
-
Takebayashi Y., et al. Antiproliferative activity of ecteinascidin 743 is dependent upon transcription-coupled nucleotide-excision repair. Nat. Med. 2001, 7:961-966.
-
(2001)
Nat. Med.
, vol.7
, pp. 961-966
-
-
Takebayashi, Y.1
-
24
-
-
34548706418
-
Replication and homologous recombination repair regulate DNA double-strand break formation by the antitumor alkylator ecteinascidin 743
-
Soares D.G., et al. Replication and homologous recombination repair regulate DNA double-strand break formation by the antitumor alkylator ecteinascidin 743. Proc. Natl. Acad. Sci. U. S. A. 2007, 104:13062-13067.
-
(2007)
Proc. Natl. Acad. Sci. U. S. A.
, vol.104
, pp. 13062-13067
-
-
Soares, D.G.1
-
25
-
-
33748035692
-
S, cross-talk between nucleotide excision and homologous recombination DNA repair pathways in the mechanism of action of antitumor trabectedin
-
Herrero A.B., et al. S, cross-talk between nucleotide excision and homologous recombination DNA repair pathways in the mechanism of action of antitumor trabectedin. Cancer Res. 2006, 66:8155-8162.
-
(2006)
Cancer Res.
, vol.66
, pp. 8155-8162
-
-
Herrero, A.B.1
-
26
-
-
0035146702
-
Ecteinascidin-743 (ET-743), a natural marine compound, with a unique mechanism of action
-
Erba E., et al. Ecteinascidin-743 (ET-743), a natural marine compound, with a unique mechanism of action. Eur. J. Cancer 2001, 37:97-105.
-
(2001)
Eur. J. Cancer
, vol.37
, pp. 97-105
-
-
Erba, E.1
-
27
-
-
64449085620
-
Phase I clinical and pharmacokinetic study of trabectedin and doxorubicin in advanced soft tissue sarcoma and breast cancer
-
Sessa C., et al. Phase I clinical and pharmacokinetic study of trabectedin and doxorubicin in advanced soft tissue sarcoma and breast cancer. Eur. J. Cancer 2009, 45:1153-1161.
-
(2009)
Eur. J. Cancer
, vol.45
, pp. 1153-1161
-
-
Sessa, C.1
-
28
-
-
67650651992
-
The Halichondrins and E7389
-
Jackson K., et al. The Halichondrins and E7389. Chem. Rev. 2009, 109:3044-3079.
-
(2009)
Chem. Rev.
, vol.109
, pp. 3044-3079
-
-
Jackson, K.1
-
29
-
-
17344374835
-
Comparative antitumor activities of halichondrins and vinblastine against human tumor xenografts
-
Fodstad O., et al. Comparative antitumor activities of halichondrins and vinblastine against human tumor xenografts. J. Exp. Ther. Oncol. 1996, 1:119-125.
-
(1996)
J. Exp. Ther. Oncol.
, vol.1
, pp. 119-125
-
-
Fodstad, O.1
-
30
-
-
0035110756
-
In vitro and in vivo anticancer activities of synthetic macrocyclic ketone analogues of halichondrin B
-
Towle M.J., et al. In vitro and in vivo anticancer activities of synthetic macrocyclic ketone analogues of halichondrin B. Cancer Res. 2001, 61:1013-1021.
-
(2001)
Cancer Res.
, vol.61
, pp. 1013-1021
-
-
Towle, M.J.1
-
31
-
-
84975897156
-
Discovery of E7389, a fully synthetic macrocyclic ketone analog of halichondrin B
-
CRC Press, Taylor and Francis Group, Boca Raton, Fl. G.M. Cragg, D.G.I. Kingston, D.J. Newman (Eds.)
-
Yu M.J., et al. Discovery of E7389, a fully synthetic macrocyclic ketone analog of halichondrin B. Anticancer Agents from Natural Products 2005, 241-265. CRC Press, Taylor and Francis Group, Boca Raton, Fl. G.M. Cragg, D.G.I. Kingston, D.J. Newman (Eds.).
-
(2005)
Anticancer Agents from Natural Products
, pp. 241-265
-
-
Yu, M.J.1
-
32
-
-
23144433687
-
The primary antimitotic mechanism of action of the synthetic halichondrin E7389 is suppression of microtubule growth
-
Jordan M.A., et al. The primary antimitotic mechanism of action of the synthetic halichondrin E7389 is suppression of microtubule growth. Mol. Cancer Ther. 2005, 4:1086-1095.
-
(2005)
Mol. Cancer Ther.
, vol.4
, pp. 1086-1095
-
-
Jordan, M.A.1
-
33
-
-
51049119664
-
Inhibition of centromere dynamics by eribulin (E7389) during mitotic metaphase
-
Okouneva T., et al. Inhibition of centromere dynamics by eribulin (E7389) during mitotic metaphase. Mol. Cancer Ther. 2008, 7:2003-2011.
-
(2008)
Mol. Cancer Ther.
, vol.7
, pp. 2003-2011
-
-
Okouneva, T.1
-
34
-
-
4143052665
-
Induction of morphological and biochemical apoptosis following prolonged mitotic blockage by halichondrin B macrocyclic ketone analog E7389
-
Kuznetsov G., et al. Induction of morphological and biochemical apoptosis following prolonged mitotic blockage by halichondrin B macrocyclic ketone analog E7389. Cancer Res. 2004, 64:5760-5766.
-
(2004)
Cancer Res.
, vol.64
, pp. 5760-5766
-
-
Kuznetsov, G.1
-
35
-
-
67449147109
-
A phase I study of eribulin mesylate (E7389), a mechanistically novel inhibitor of microtubule dynamics, in patients with advanced solid malignancies
-
Goel S., et al. A phase I study of eribulin mesylate (E7389), a mechanistically novel inhibitor of microtubule dynamics, in patients with advanced solid malignancies. Clin. Cancer Res. 2009, 15:4207-4212.
-
(2009)
Clin. Cancer Res.
, vol.15
, pp. 4207-4212
-
-
Goel, S.1
-
36
-
-
67449123315
-
Phase I study of eribulin mesylate administered once every 21 days in patients with advanced solid tumors
-
Tan A.R., et al. Phase I study of eribulin mesylate administered once every 21 days in patients with advanced solid tumors. Clin. Cancer Res. 2009, 15:4213-4219.
-
(2009)
Clin. Cancer Res.
, vol.15
, pp. 4213-4219
-
-
Tan, A.R.1
-
37
-
-
67649908927
-
Phase II study of eribulin mesylate, a halichondrin B analog, in patients with metastatic breast cancer previously treated with an anthracycline and a taxane
-
Vahdat L.T., et al. Phase II study of eribulin mesylate, a halichondrin B analog, in patients with metastatic breast cancer previously treated with an anthracycline and a taxane. J. Clin. Oncol. 2009, 27:2954-2961.
-
(2009)
J. Clin. Oncol.
, vol.27
, pp. 2954-2961
-
-
Vahdat, L.T.1
-
38
-
-
59149099068
-
Phase II study of eribulin mesylate E7389 in patients with locally advanced or metastatic breast cancer previously treated with anthracyclin, taxane, and capecitabine therapy
-
May 20
-
Vahdat L.T., et al. Phase II study of eribulin mesylate E7389 in patients with locally advanced or metastatic breast cancer previously treated with anthracyclin, taxane, and capecitabine therapy. J. Clin. Oncol. 2008, 26(May 20 Suppl.):1084.
-
(2008)
J. Clin. Oncol.
, vol.26
, Issue.SUPPL.
, pp. 1084
-
-
Vahdat, L.T.1
-
39
-
-
34547685818
-
Comparison of the antivascular and cytotoxic activities of TZT-1027 (Soblidotin) with those of other anticancer agents
-
Watanabe J., et al. Comparison of the antivascular and cytotoxic activities of TZT-1027 (Soblidotin) with those of other anticancer agents. Anticancer Drugs 2007, 18:905-911.
-
(2007)
Anticancer Drugs
, vol.18
, pp. 905-911
-
-
Watanabe, J.1
-
40
-
-
33845286942
-
Vascular disrupting agents
-
Lippert J.W. Vascular disrupting agents. Bioorg. Med. Chem. 2007, 15:605-615.
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 605-615
-
-
Lippert, J.W.1
-
41
-
-
77953683267
-
-
cf.
-
cf. (2009). http://clinicaltrials.gov/.
-
(2009)
-
-
-
42
-
-
33646758595
-
The nemertine toxin anabaseine and its derivative DMXBA (GTS-21): chemical and pharmacological properties
-
Kem W.R., et al. The nemertine toxin anabaseine and its derivative DMXBA (GTS-21): chemical and pharmacological properties. Marine Drugs 2006, 4:255-273.
-
(2006)
Marine Drugs
, vol.4
, pp. 255-273
-
-
Kem, W.R.1
-
43
-
-
9144251593
-
Hydroxy metabolites of the Alzheimer's drug candidate 3-[(2,4-dimethoxy)benzylidene]-anabaseine dihydrochloride (GTS-21): their molecular properties, interactions with brain nicotinic receptors, and brain penetration
-
Kem W.R., et al. Hydroxy metabolites of the Alzheimer's drug candidate 3-[(2,4-dimethoxy)benzylidene]-anabaseine dihydrochloride (GTS-21): their molecular properties, interactions with brain nicotinic receptors, and brain penetration. Mol. Pharmacol. 2004, 65:56-67.
-
(2004)
Mol. Pharmacol.
, vol.65
, pp. 56-67
-
-
Kem, W.R.1
-
44
-
-
20544460348
-
Long-lasting cognitive improvement with nicotinic receptor agonists: mechanisms of pharmacokinetic-pharmacodynamic discordance
-
Buccafusco J.J., et al. Long-lasting cognitive improvement with nicotinic receptor agonists: mechanisms of pharmacokinetic-pharmacodynamic discordance. Trends Pharmacol. Sci. 2005, 26:352-360.
-
(2005)
Trends Pharmacol. Sci.
, vol.26
, pp. 352-360
-
-
Buccafusco, J.J.1
-
45
-
-
34548684581
-
Treating schizophrenia symptoms with an alpha7 nicotinic agonist, from mice to men
-
Olincy A., Stevens K.E. Treating schizophrenia symptoms with an alpha7 nicotinic agonist, from mice to men. Biochem. Pharmacol. 2007, 74:1192-1201.
-
(2007)
Biochem. Pharmacol.
, vol.74
, pp. 1192-1201
-
-
Olincy, A.1
Stevens, K.E.2
-
46
-
-
63849213473
-
Nicotinic acetylcholine receptor signalling: roles in Alzheimer's disease and amyloid neuroprotection
-
Buckingham S., et al. Nicotinic acetylcholine receptor signalling: roles in Alzheimer's disease and amyloid neuroprotection. Pharmacol. Rev. 2009, 61:39-61.
-
(2009)
Pharmacol. Rev.
, vol.61
, pp. 39-61
-
-
Buckingham, S.1
-
47
-
-
24644466288
-
Septal innervation regulates the function of alpha7 nicotinic receptors in CA1 hippocampal interneurons
-
Thinschmidt J.S., et al. Septal innervation regulates the function of alpha7 nicotinic receptors in CA1 hippocampal interneurons. Exp. Neurol. 2005, 195:342-352.
-
(2005)
Exp. Neurol.
, vol.195
, pp. 342-352
-
-
Thinschmidt, J.S.1
-
48
-
-
63149095488
-
Nicotinic receptor-mediated neuroprotection in neurodegenerative disease models
-
Shimohama S. Nicotinic receptor-mediated neuroprotection in neurodegenerative disease models. Biol. Pharm. Bull. 2009, 32:332-336.
-
(2009)
Biol. Pharm. Bull.
, vol.32
, pp. 332-336
-
-
Shimohama, S.1
-
49
-
-
34247125289
-
Selective alpha7-nicotinic acetylcholine receptor agonist GTS-21 improves survival in murine endotoxemia and severe sepsis
-
Pavlov V.A., et al. Selective alpha7-nicotinic acetylcholine receptor agonist GTS-21 improves survival in murine endotoxemia and severe sepsis. Crit. Care Med. 2007, 35:1139-1144.
-
(2007)
Crit. Care Med.
, vol.35
, pp. 1139-1144
-
-
Pavlov, V.A.1
-
50
-
-
67650391166
-
The selective alpha7 agonist GTS-21 attenuates cytokine production in human whole blood and human monocytes activated by ligands for TLR2, TLR3, TLR4, TLR9, and RAGE
-
Rosas-Ballina M., et al. The selective alpha7 agonist GTS-21 attenuates cytokine production in human whole blood and human monocytes activated by ligands for TLR2, TLR3, TLR4, TLR9, and RAGE. Mol. Med. 2009, 15:195-202.
-
(2009)
Mol. Med.
, vol.15
, pp. 195-202
-
-
Rosas-Ballina, M.1
-
51
-
-
45249125112
-
Cholinergic agonists attenuate renal ischemia-reperfusion injury in rats
-
Yeboah M.M., et al. Cholinergic agonists attenuate renal ischemia-reperfusion injury in rats. Kidney Int. 2008, 74:62-69.
-
(2008)
Kidney Int.
, vol.74
, pp. 62-69
-
-
Yeboah, M.M.1
-
52
-
-
77449083458
-
Alpha7 cholinergic-agonist prevents systemic inflammation and improves survival during resuscitation
-
Cai B., et al. Alpha7 cholinergic-agonist prevents systemic inflammation and improves survival during resuscitation. J. Cell. Mol. Med. 2008, 13:3774-3785.
-
(2008)
J. Cell. Mol. Med.
, vol.13
, pp. 3774-3785
-
-
Cai, B.1
-
53
-
-
0038690569
-
Safety, pharmacokinetics, and effects on cognitive function of multiple doses of GTS-21 in healthy, male volunteers
-
Kitagawa H., et al. Safety, pharmacokinetics, and effects on cognitive function of multiple doses of GTS-21 in healthy, male volunteers. Neuropsychopharmacology 2003, 28:542-551.
-
(2003)
Neuropsychopharmacology
, vol.28
, pp. 542-551
-
-
Kitagawa, H.1
-
54
-
-
33744911665
-
Proof-of-concept trial of an alpha7 nicotinic agonist in schizophrenia
-
Olincy A., et al. Proof-of-concept trial of an alpha7 nicotinic agonist in schizophrenia. Arch. Gen. Psychiatry 2006, 63:630-638.
-
(2006)
Arch. Gen. Psychiatry
, vol.63
, pp. 630-638
-
-
Olincy, A.1
-
55
-
-
48949099564
-
Initial phase 2 trial of a nicotinic agonist in schizophrenia
-
Freedman R., et al. Initial phase 2 trial of a nicotinic agonist in schizophrenia. Am. J. Psychiatry 2008, 165:1040-1047.
-
(2008)
Am. J. Psychiatry
, vol.165
, pp. 1040-1047
-
-
Freedman, R.1
-
56
-
-
0346036093
-
Aplidin induces apoptosis in human cancer cells via glutathione depletion and sustained activation of the epidermal growth factor receptor, Src, JNK, and p38 MAPK
-
Cuadrado A., et al. Aplidin induces apoptosis in human cancer cells via glutathione depletion and sustained activation of the epidermal growth factor receptor, Src, JNK, and p38 MAPK. J. Biol. Chem. 2003, 278:241-250.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 241-250
-
-
Cuadrado, A.1
-
57
-
-
3042781436
-
Aplidin induces the mitochondrial apoptotic pathway via oxidative stress-mediated JNK and p38 activation and protein kinase C delta
-
Garcia-Fernandez L.F., et al. Aplidin induces the mitochondrial apoptotic pathway via oxidative stress-mediated JNK and p38 activation and protein kinase C delta. Oncogene 2002, 21:7533-7544.
-
(2002)
Oncogene
, vol.21
, pp. 7533-7544
-
-
Garcia-Fernandez, L.F.1
-
58
-
-
48549097751
-
Aplidin, a marine organism-derived compound with potent antimyeloma activity in vitro and in vivo
-
Mitsiades C.S., et al. Aplidin, a marine organism-derived compound with potent antimyeloma activity in vitro and in vivo. Cancer Res. 2008, 68:5216-5225.
-
(2008)
Cancer Res.
, vol.68
, pp. 5216-5225
-
-
Mitsiades, C.S.1
-
59
-
-
36749071496
-
Aplidine: a paradigm of how to handle the activity and toxicity of a novel marine anticancer poison
-
Le Tourneau C., et al. Aplidine: a paradigm of how to handle the activity and toxicity of a novel marine anticancer poison. Curr. Pharm. Des. 2007, 13:3427-3439.
-
(2007)
Curr. Pharm. Des.
, vol.13
, pp. 3427-3439
-
-
Le Tourneau, C.1
-
60
-
-
0027296890
-
Kahalalide F: A bioactive depsipeptide from the sacoglossan mollusk Elysia rufescens and the green alga Bryopsis sp
-
Hamann M.T., Scheuer P.J. Kahalalide F: A bioactive depsipeptide from the sacoglossan mollusk Elysia rufescens and the green alga Bryopsis sp. J. Am. Chem. Soc. 1993, 115:5825-5826.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 5825-5826
-
-
Hamann, M.T.1
Scheuer, P.J.2
-
61
-
-
0035930006
-
Synthesis and structure determination of kahalalide F (1,2)
-
Lopez-Macia A., et al. Synthesis and structure determination of kahalalide F (1,2). J. Am. Chem. Soc. 2001, 123:11398-11401.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 11398-11401
-
-
Lopez-Macia, A.1
-
62
-
-
67149096306
-
Molecular pharmacodynamics of PM02734 (elisidepsin) as single agent and in combination with erlotinib; synergistic activity in human non-small cell lung cancer cell lines and xenograft models
-
Ling Y.H., et al. Molecular pharmacodynamics of PM02734 (elisidepsin) as single agent and in combination with erlotinib; synergistic activity in human non-small cell lung cancer cell lines and xenograft models. Eur. J. Cancer 2009, 45:1855-1864.
-
(2009)
Eur. J. Cancer
, vol.45
, pp. 1855-1864
-
-
Ling, Y.H.1
-
63
-
-
0036558479
-
Chemistry and biology of the tetrahydroisoquinoline antitumor antibiotics
-
Scott J.D., Williams R.M. Chemistry and biology of the tetrahydroisoquinoline antitumor antibiotics. Chem. Rev. 2002, 102:1669-1730.
-
(2002)
Chem. Rev.
, vol.102
, pp. 1669-1730
-
-
Scott, J.D.1
Williams, R.M.2
-
64
-
-
65649141676
-
Molecular pharmacology and antitumor activity of Zalypsis in several human cancer cell lines
-
Leal J.F., et al. Molecular pharmacology and antitumor activity of Zalypsis in several human cancer cell lines. Biochem. Pharmacol. 2009, 78:162-170.
-
(2009)
Biochem. Pharmacol.
, vol.78
, pp. 162-170
-
-
Leal, J.F.1
-
65
-
-
77953683416
-
-
Fenical, W. et al. Halimide, a cytotoxic marine natural product, and derivatives thereof. WO/1999/048889, The Regents of the University of California, September 30, 1999.
-
Fenical, W. et al. (1999) Halimide, a cytotoxic marine natural product, and derivatives thereof. WO/1999/048889, The Regents of the University of California, September 30, 1999.
-
(1999)
-
-
-
66
-
-
0030697347
-
(-)-Phenylahistin: A new mammalian cell cycle inhibitor produced by Aspergillus ustus
-
Kanoh K., et al. (-)-Phenylahistin: A new mammalian cell cycle inhibitor produced by Aspergillus ustus. Bioorg. Med. Chem. Lett. 1997, 7:2847-2852.
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 2847-2852
-
-
Kanoh, K.1
-
67
-
-
33646118484
-
NPI-2358 is a tubulin-depolymerizing agent: in-vitro evidence for activity as a tumor vascular-disrupting agent
-
Nicholson B., et al. NPI-2358 is a tubulin-depolymerizing agent: in-vitro evidence for activity as a tumor vascular-disrupting agent. Anticancer Drugs 2006, 17:25-31.
-
(2006)
Anticancer Drugs
, vol.17
, pp. 25-31
-
-
Nicholson, B.1
-
68
-
-
59649086041
-
Tubulin photoaffinity labeling with biotin-tagged derivatives of potent diketopiperazine antimicrotubule agents
-
Yamazaki Y., et al. Tubulin photoaffinity labeling with biotin-tagged derivatives of potent diketopiperazine antimicrotubule agents. ChemBioChem 2008, 9:3074-3081.
-
(2008)
ChemBioChem
, vol.9
, pp. 3074-3081
-
-
Yamazaki, Y.1
-
69
-
-
77953683048
-
-
Pilat, M.J. et al. Phase I trial of NPI-2358 (a novel vascular disrupting agent) in patients with solid tumors or lymphomas. In Proceedings of the 100th Annual Meeting of the American Association for Cancer Research, April 18-22, 2009, Denver, Colorado (CO), Abstract nr. 3598.
-
Pilat, M.J. et al. (2009) Phase I trial of NPI-2358 (a novel vascular disrupting agent) in patients with solid tumors or lymphomas. In Proceedings of the 100th Annual Meeting of the American Association for Cancer Research, April 18-22, 2009, Denver, Colorado (CO), Vol. 50, Abstract nr. 3598.
-
(2009)
, vol.50
-
-
-
70
-
-
34248592567
-
Mechanism of action of the microtubule-targeted antimitotic depsipeptide tasidotin (formerly ILX651) and its major metabolite tasidotin C-carboxylate
-
Ray A., et al. Mechanism of action of the microtubule-targeted antimitotic depsipeptide tasidotin (formerly ILX651) and its major metabolite tasidotin C-carboxylate. Cancer Res. 2007, 67:3767-3776.
-
(2007)
Cancer Res.
, vol.67
, pp. 3767-3776
-
-
Ray, A.1
-
71
-
-
58849164924
-
Intracellular activation and deactivation of tasidotin, an analog of dolastatin 15: correlation with cytotoxicity
-
Bai R., et al. Intracellular activation and deactivation of tasidotin, an analog of dolastatin 15: correlation with cytotoxicity. Mol. Pharmacol. 2009, 75:218-226.
-
(2009)
Mol. Pharmacol.
, vol.75
, pp. 218-226
-
-
Bai, R.1
-
72
-
-
0022907680
-
The pseudopterosins: A new class of anti-inflammatory and analgesic diterpene pentosides from the marine sea whip Pseudopterogorgia elisabethae (Octocorallia)
-
Look S.A., et al. The pseudopterosins: A new class of anti-inflammatory and analgesic diterpene pentosides from the marine sea whip Pseudopterogorgia elisabethae (Octocorallia). J. Org. Chem. 1986, 51:5140-5145.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 5140-5145
-
-
Look, S.A.1
-
73
-
-
0025004467
-
New anti-inflammatory pseudopterosins from the marine octocoral Pseudopterogorgia elisabethae
-
Roussis V., et al. New anti-inflammatory pseudopterosins from the marine octocoral Pseudopterogorgia elisabethae. J. Org. Chem. 1990, 55:4916-4922.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 4916-4922
-
-
Roussis, V.1
-
74
-
-
27644474606
-
Atomarianones A and B: two cytotoxic meroditerpenes from the brown alga Taonia atomaria
-
Abatis D., et al. Atomarianones A and B: two cytotoxic meroditerpenes from the brown alga Taonia atomaria. Tetrahedron Lett. 2005, 46:8525-8529.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 8525-8529
-
-
Abatis, D.1
-
75
-
-
0000355156
-
The pseudopterosins: anti-inflammatory and analgesic natural products from the sea whip Pseudopterogorgia elisabethae
-
Look S.A., et al. The pseudopterosins: anti-inflammatory and analgesic natural products from the sea whip Pseudopterogorgia elisabethae. Proc. Natl. Acad. Sci. U. S. A. 1986, 83:6238-6240.
-
(1986)
Proc. Natl. Acad. Sci. U. S. A.
, vol.83
, pp. 6238-6240
-
-
Look, S.A.1
-
76
-
-
0023185918
-
Effect of pseudopterosin A on cell division, cell cycle progression, DNA, and protein synthesis in cultured sea urchin embryos
-
Ettouati W.S., Jacobs R.S. Effect of pseudopterosin A on cell division, cell cycle progression, DNA, and protein synthesis in cultured sea urchin embryos. Mol. Pharmacol. 1987, 31:500-505.
-
(1987)
Mol. Pharmacol.
, vol.31
, pp. 500-505
-
-
Ettouati, W.S.1
Jacobs, R.S.2
-
77
-
-
0032557396
-
Pharmacological characterization of the pseudopterosins: novel anti- inflammatory natural products isolated from the Caribbean soft coral, Pseudopterogorgia elisabethae
-
Mayer A.M., et al. Pharmacological characterization of the pseudopterosins: novel anti- inflammatory natural products isolated from the Caribbean soft coral, Pseudopterogorgia elisabethae. Life Sci. 1998, 62:L401-L407.
-
(1998)
Life Sci.
, vol.62
-
-
Mayer, A.M.1
-
78
-
-
33746083559
-
Pseudopterosin A inhibits phagocytosis and alters intracellular calcium turnover in a pertussis toxin sensitive site in Tetrahymena thermophila
-
Moya C.E., Jacobs R.S. Pseudopterosin A inhibits phagocytosis and alters intracellular calcium turnover in a pertussis toxin sensitive site in Tetrahymena thermophila. Comp. Biochem. Physiol. C. Toxicol. Pharmacol. 2006, 143:436-443.
-
(2006)
Comp. Biochem. Physiol. C. Toxicol. Pharmacol.
, vol.143
, pp. 436-443
-
-
Moya, C.E.1
Jacobs, R.S.2
-
79
-
-
52449098970
-
Synthesis and an evaluation of the bioactivity of the C-glycoside of pseudopterosin A methyl ether
-
Zhong W., et al. Synthesis and an evaluation of the bioactivity of the C-glycoside of pseudopterosin A methyl ether. J. Org. Chem. 2008, 73:7011-7016.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 7011-7016
-
-
Zhong, W.1
-
80
-
-
0001889852
-
Adenosine regulation of neutrophil function and inhibition of inflammation via adenosine receptors
-
Wiley-Liss, K.A. Jacobson, M.F. Jarvis (Eds.)
-
Cronstein B.N. Adenosine regulation of neutrophil function and inhibition of inflammation via adenosine receptors. Purinergic Approaches in Experimental Therapeutics 1997, 285-299. Wiley-Liss. K.A. Jacobson, M.F. Jarvis (Eds.).
-
(1997)
Purinergic Approaches in Experimental Therapeutics
, pp. 285-299
-
-
Cronstein, B.N.1
-
81
-
-
0030698058
-
Wound healing is accelerated by agonists of adenosine A2 (G alpha s-linked) receptors
-
Montesinos M.C., et al. Wound healing is accelerated by agonists of adenosine A2 (G alpha s-linked) receptors. J. Exp. Med. 1997, 186:1615-1620.
-
(1997)
J. Exp. Med.
, vol.186
, pp. 1615-1620
-
-
Montesinos, M.C.1
-
82
-
-
77953685911
-
-
IND 60606 New drug application VM301 for use in phase I/IIA clinical trials. IND 60606. filed July 12, 2000.
-
IND 60606 (2000) New drug application VM301 for use in phase I/IIA clinical trials. IND 60606. filed July 12, 2000.
-
(2000)
-
-
-
83
-
-
84900067626
-
The bryostatins
-
Taylor and Francis, G.M. Cragg (Ed.)
-
Newman D.J. The bryostatins. Anticancer Agents from Natural Products 2005, 137-150. Taylor and Francis. G.M. Cragg (Ed.).
-
(2005)
Anticancer Agents from Natural Products
, pp. 137-150
-
-
Newman, D.J.1
-
84
-
-
33847029508
-
Identification of the putative bryostatin polyketide synthase gene cluster from " Candidatus Endobugula sertula" , the uncultivated microbial symbiont of the marine bryozoan Bugula neritina
-
Sudek S., et al. Identification of the putative bryostatin polyketide synthase gene cluster from " Candidatus Endobugula sertula" , the uncultivated microbial symbiont of the marine bryozoan Bugula neritina. J. Nat. Prod. 2007, 70:67-74.
-
(2007)
J. Nat. Prod.
, vol.70
, pp. 67-74
-
-
Sudek, S.1
-
85
-
-
0028305511
-
Hemiasterlin and geodiamolide TA: two new cytotoxic peptides from the marine sponge Hemiasterella minor
-
Talpir R., et al. Hemiasterlin and geodiamolide TA: two new cytotoxic peptides from the marine sponge Hemiasterella minor. Tetrahedron Lett. 1994, 35:4453-4456.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 4453-4456
-
-
Talpir, R.1
-
86
-
-
70350213204
-
Synthetic analogs of the marine natural product hemiasterlin: Optimization and discovery of E7974, a novel and potent antitumor agent
-
Abstract # 1212
-
Kowalczyk J., et al. Synthetic analogs of the marine natural product hemiasterlin: Optimization and discovery of E7974, a novel and potent antitumor agent. Proc. Am. Assoc. Cancer Res. 2005, 46. Abstract # 1212.
-
(2005)
Proc. Am. Assoc. Cancer Res.
, vol.46
-
-
Kowalczyk, J.1
-
87
-
-
70350231755
-
Tubulin-based antimitotic mechanism of E7974, a novel analogue of the marine sponge natural product hemiasterlin
-
Kuznetsov G., et al. Tubulin-based antimitotic mechanism of E7974, a novel analogue of the marine sponge natural product hemiasterlin. Mol. Cancer Ther. 2009, 8:2852-2860.
-
(2009)
Mol. Cancer Ther.
, vol.8
, pp. 2852-2860
-
-
Kuznetsov, G.1
-
88
-
-
45349107667
-
A phase I trial of E7974 administered on days 1 and 15 of a 28-day cycle in patients with solid malignancies
-
June 20
-
Madajewicz S., et al. A phase I trial of E7974 administered on days 1 and 15 of a 28-day cycle in patients with solid malignancies. J. Clin. Oncol. 2007, 25(June 20 Suppl.):2550.
-
(2007)
J. Clin. Oncol.
, vol.25
, Issue.SUPPL.
, pp. 2550
-
-
Madajewicz, S.1
-
89
-
-
45349097727
-
A phase I trial of E7974 administered on days 1, 8, and 15 of a 28-day cycle in patients with solid malignancies
-
June 20
-
Zojwalla N., et al. A phase I trial of E7974 administered on days 1, 8, and 15 of a 28-day cycle in patients with solid malignancies. J. Clin. Oncol. 2007, 25(June 20 Suppl.):2543.
-
(2007)
J. Clin. Oncol.
, vol.25
, Issue.SUPPL.
, pp. 2543
-
-
Zojwalla, N.1
-
90
-
-
77953685432
-
-
Rocha Lima, C. et al. A phase I trial of E7974 administered on day 1 of a 21-day cycle in patient with advanced tumors. In Proceedings of the 2008 ASCO Gastrointestinal Cancers Symposium Abstract # 326.
-
Rocha Lima, C. et al. (2008) A phase I trial of E7974 administered on day 1 of a 21-day cycle in patient with advanced tumors. In Proceedings of the 2008 ASCO Gastrointestinal Cancers Symposium Abstract # 326.
-
(2008)
-
-
-
91
-
-
0037455147
-
Salinosporamide A: a highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus Salinospora
-
Feling R.H., et al. Salinosporamide A: a highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus Salinospora. Angew. Chem. Int. Ed. Engl. 2003, 42:355-357.
-
(2003)
Angew. Chem. Int. Ed. Engl.
, vol.42
, pp. 355-357
-
-
Feling, R.H.1
-
92
-
-
62149103377
-
Discovery and development of the anticancer agent salinosporamide A (NPI-0052)
-
Fenical W., et al. Discovery and development of the anticancer agent salinosporamide A (NPI-0052). Bioorg. Med. Chem. 2009, 17:2175-2180.
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 2175-2180
-
-
Fenical, W.1
-
93
-
-
33646137808
-
Crystal structures of salinosporamide A (NPI-0052) and B (NPI-0047) in complex with the 20S proteasome reveal important consequences of β-lactone ring opening and a mechanism for irreversible binding
-
Groll M., et al. Crystal structures of salinosporamide A (NPI-0052) and B (NPI-0047) in complex with the 20S proteasome reveal important consequences of β-lactone ring opening and a mechanism for irreversible binding. J. Am. Chem. Soc. 2006, 128:5136-5141.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 5136-5141
-
-
Groll, M.1
-
94
-
-
33750209537
-
A novel proteasome inhibitor NPI-0052 as an anticancer therapy
-
Chauhan D., et al. A novel proteasome inhibitor NPI-0052 as an anticancer therapy. Br. J. Cancer 2006, 95:961-965.
-
(2006)
Br. J. Cancer
, vol.95
, pp. 961-965
-
-
Chauhan, D.1
-
95
-
-
77952564354
-
From natural product to clinical trials: NPI-0052 (salinosporamide A), a marine actinomycete-derived anticancer agent
-
Royal Society of Chemistry, A.D. Buss, M.S. Butler (Eds.)
-
Lam K.S. From natural product to clinical trials: NPI-0052 (salinosporamide A), a marine actinomycete-derived anticancer agent. Natural Products Chemistry for Drug Discovery 2010, 355-373. Royal Society of Chemistry. 18th edn. A.D. Buss, M.S. Butler (Eds.).
-
(2010)
Natural Products Chemistry for Drug Discovery
, pp. 355-373
-
-
Lam, K.S.1
-
96
-
-
52649173202
-
Proteasome inhibition activates epidermal growth factor receptor (EGFR) and EGFR-independent mitogenic kinase signaling pathways in pancreatic cancer cells
-
Sloss C.M., et al. Proteasome inhibition activates epidermal growth factor receptor (EGFR) and EGFR-independent mitogenic kinase signaling pathways in pancreatic cancer cells. Clin. Cancer Res. 2008, 14:5116-5123.
-
(2008)
Clin. Cancer Res.
, vol.14
, pp. 5116-5123
-
-
Sloss, C.M.1
-
97
-
-
54249139074
-
Marine pharmacology in 2005-2006: antitumour and cytotoxic compounds
-
Mayer A.M., Gustafson K.R. Marine pharmacology in 2005-2006: antitumour and cytotoxic compounds. Eur. J Cancer 2008, 44:2357-2387.
-
(2008)
Eur. J Cancer
, vol.44
, pp. 2357-2387
-
-
Mayer, A.M.1
Gustafson, K.R.2
-
98
-
-
67349092463
-
Marine pharmacology in 2005-6: marine compounds with anthelmintic, antibacterial, anticoagulant, antifungal, anti-inflammatory, antimalarial, antiprotozoal, antituberculosis, and antiviral activities; affecting the cardiovascular, immune and nervous systems, and other miscellaneous mechanisms of action
-
Mayer A.M., et al. Marine pharmacology in 2005-6: marine compounds with anthelmintic, antibacterial, anticoagulant, antifungal, anti-inflammatory, antimalarial, antiprotozoal, antituberculosis, and antiviral activities; affecting the cardiovascular, immune and nervous systems, and other miscellaneous mechanisms of action. Biochim. Biophys. Acta 2009, 1790:283-308.
-
(2009)
Biochim. Biophys. Acta
, vol.1790
, pp. 283-308
-
-
Mayer, A.M.1
-
99
-
-
67649491097
-
A renaissance in marine pharmacology: from preclinical curiosity to clinical reality
-
Glaser K.B., Mayer A.M. A renaissance in marine pharmacology: from preclinical curiosity to clinical reality. Biochem. Pharmacol. 2009, 78:440-448.
-
(2009)
Biochem. Pharmacol.
, vol.78
, pp. 440-448
-
-
Glaser, K.B.1
Mayer, A.M.2
|