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Cyclosporins
Known as:
Cyclosporine
, Cyclosporines
, Cyclosporins [Chemical/Ingredient]
A group of closely related cyclic undecapeptides from the fungi Trichoderma polysporum and Cylindocarpon lucidum. They have some antineoplastic and…
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National Institutes of Health
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Related topics
Related topics
31 relations
Narrower (22)
Debio088
IMM 125
SCY-635
SCY-641
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Broader (2)
Enzyme Inhibitors
Immunosuppressive Agents
In Blood
Process of secretion
agonists
antagonists & inhibitors
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2006
Review
2006
Cyclosporins. Structure-activity relationships.
H. Fliri
,
G. Baumann
,
+7 authors
M. Walkinshaw
Annals of the New York Academy of Sciences
2006
Corpus ID: 41552793
Cyclosporin A (Sandimmun) achieves immunosuppressive activity by complex formation with cyclophilin and subsequent binding of the…
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Review
2004
Review
2004
Pharmacologic circumvention of multidrug resistance
J. Ford
,
W. Hait
Cytotechnology (Dordrecht)
2004
Corpus ID: 12619001
The ability of malignant cells to develop resistance to chemotherapeutic drugs is a major obstacle to the successful treatment of…
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Highly Cited
2002
Highly Cited
2002
Cyclosporins: structure-activity relationships for the inhibition of the human MDR1 P-glycoprotein ABC transporter.
F. Loor
,
F. Tiberghien
,
T. Wenandy
,
A. Didier
,
R. Traber
Journal of Medicinal Chemistry
2002
Corpus ID: 43603690
Cyclic undecapeptide cyclo-[MeBmt(1)-Abu(2)-MeGly(3)-MeLeu(4)-Val(5)-MeLeu(6)-Ala(7)-D-Ala(8)-MeLeu(9)-MeLeu(10)-MeVal(11)], the…
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Highly Cited
2001
Highly Cited
2001
A phase I trial of doxorubicin, paclitaxel, and valspodar (PSC 833), a modulator of multidrug resistance.
R. Advani
,
G. Fisher
,
+4 authors
B. Sikic
Clinical Cancer Research
2001
Corpus ID: 8909742
PURPOSE P-glycoprotein is an efflux pump for many drugs including doxorubicin and paclitaxel. This study evaluated the…
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Review
2001
Review
2001
Cyclosporin H Is a Potent and Selective Formyl Peptide Receptor Antagonist Comparison with Nt-Butoxycarbonyl-~-phenylalanyl-L-leucyl-L-phenylalanyl-1-leucyl-L-phenylalanine and Cyclosporins
K. Wenzel‐Seifert
,
R. Seifert
2001
Corpus ID: 50992244
he cyclic undecapeptide, cyclosporin (Cs) H, is a potent inhibitor of FMLP-induced superoxide anion (02-) formation in human…
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Highly Cited
1989
Highly Cited
1989
Cell-free biosynthesis of new cyclosporins.
Alfons
,
Lawen
,
+5 authors
Horst Kleinkauf
Journal of antibiotics (Tokyo. )
1989
Corpus ID: 45054928
An enzyme preparation, isolated from extracts of the fungus Beauveria nivea (previously designated Tolypocladium inflatum), is…
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1989
1989
Enhancement of anthracycline growth inhibition in parent and multidrug-resistant Chinese hamster ovary cells by cyclosporin A and its analogues.
S. Chambers
,
W. Hait
,
B. Kacinski
,
S. Keyes
,
R. Handschumacher
Cancer Research
1989
Corpus ID: 31112539
Cyclosporins have been shown to sensitize multidrug-resistant cells to chemotherapeutic agents but, generally, have minimal…
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1988
1988
The weak immunosuppressant cyclosporine D as well as the immunologically inactive cyclosporine H are potent inhibitors in vivo of phorbol ester TPA-induced biological effects in mouse skin and of Ca2…
M. Gschwendt
,
W. Kittstein
,
F. Marks
Biochemical and Biophysical Research…
1988
Corpus ID: 25137217
1988
1988
The insecticidal activity of cyclosporines on mosquito larvae.
J. Weiser
,
V. Maťha
Journal of Invertebrate Pathology
1988
Corpus ID: 25942808
Highly Cited
1987
Highly Cited
1987
The cyclosporins inhibit lymphocyte activation at more than one site.
E. W. Gelfand
,
Roy K. Cheung
,
Gordon B. Mills
Journal of Immunology
1987
Corpus ID: 33622670
Cyclosporin A (CsA), a potent immunosuppressive agent, acts primarily by inhibiting T cell function. Although several potential…
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