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pancratistatin
A isoquinoline alkaloid from amaryllis with antineoplastic activity.
National Institutes of Health
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2 relations
Broader (2)
Amaryllidaceae Alkaloids
Isoquinolines
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Highly Cited
2009
Highly Cited
2009
Selective cytochrome P450 3A4 inhibitory activity of Amaryllidaceae alkaloids.
J. McNulty
,
J. Nair
,
Mohini Singh
,
D. Crankshaw
,
A. Holloway
,
J. Bastida
Bioorganic & Medicinal Chemistry Letters
2009
Corpus ID: 31052754
2009
2009
A flexible strategy based on a C2-symmetric pool of chiral substrates: concise synthesis of (+)-valienamine, key intermediate of (+)- pancratistatin, and conduramines A-1 and E.
Yuan-Kang Chang
,
Hong-Jay Lo
,
T. Yan
Organic Letters
2009
Corpus ID: 207624602
A new strategy invoking a new application of the [3,3] sigmatropic rearrangement of allylic azides and the presence of a C(2…
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2008
2008
Suzuki cross-coupling/reductive debenzyloxycarbonylation sequence for the syntheses of [c]annulated isoquinolines: application for the syntheses of pancratistatin-like isoquinolines.
G. Pandey
,
M. Balakrishnan
Journal of Organic Chemistry
2008
Corpus ID: 207677989
A two-step strategy involving Suzuki cross-coupling of boronic acids with a diverse array of alpha-iodoenones followed by…
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2008
2008
Sodium pancratistatin 3,4-o-cyclic phosphate, a water-soluble synthetic derivative of pancratistatin, is highly effective in a human colon tumor model.
S. Shnyder
,
P. Cooper
,
Nicola J Millington
,
J. Gill
,
M. Bibby
Journal of Natural Products
2008
Corpus ID: 39174250
Sodium pancratistatin 3,4- O-cyclic phosphate ( 2) is a novel water-soluble synthetic derivative of pancratistatin ( 1), a…
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2006
2006
Cyclotrimerization approach to unnatural structural modifications of pancratistatin and other amaryllidaceae constituents — Synthesis and biological evaluation
T. Hudlický
,
Michael Moser
,
Scott C. Banfield
,
U. Rinner
,
J. Chapuis
,
G. Pettit
2006
Corpus ID: 97751090
The phenanthridone core of pancratistatin lacking all aromatic oxygenation was prepared by cyclotrimerization of acetylene…
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2005
2005
Cyclotrimerization strategy toward analogues of amaryllidaceae constituents. synthesis of deoxygenated pancratistatin core.
Michael Moser
,
Xuetong Sun
,
T. Hudlický
Organic Letters
2005
Corpus ID: 8749193
[chemical reaction: see text]. A derivative of pancratistatin having no oxygenation in the aromatic ring was synthesized by a new…
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2005
2005
Induction of Apoptotic Cell Death Specifically in Rat and Human Cancer Cells by Pancratistatin
S. Pandey
,
N. Kekre
,
J. Naderi
,
J. McNulty
Artificial cells, blood substitutes, and…
2005
Corpus ID: 24736356
The major challenge in the battle against cancer is the specific targeting of cancer cells. Most chemotherapeutics and…
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Highly Cited
2004
Highly Cited
2004
Synthesis and biological activity of some structural modifications of pancratistatin.
U. Rinner
,
Heather Hillebrenner
,
D. Adams
,
T. Hudlický
,
G. Pettit
Bioorganic & Medicinal Chemistry Letters
2004
Corpus ID: 35474562
2004
2004
An approach to pancratistatins via ring-closing metathesis: efficient synthesis of novel 1-aryl-1-deoxyconduritols F. cv.
O. N. Nadein
,
A. Kornienko
Organic Letters
2004
Corpus ID: 10055045
Structurally novel cyclitols, 1-aryl-1-deoxyconduritols F, were efficiently prepared from d-xylose, utilizing RCM as a key step…
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1991
1991
Oversaturated solutions of drug in hydroxypropylcyclodextrins: parenteral preparation of pancratistatin.
J. Torres-Labandeira
,
P. Davignon
,
J. Pitha
Journal of Pharmacy and Science
1991
Corpus ID: 13392958
The effect of 15 cyclodextrin derivatives (polar-electroneutral, cationic, anionic, and lipophilic) and of three 2…
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