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Sparsomycin
Known as:
2-Propenamide, N-(1-(hydroxymethyl)-2-(((methylthio)methyl)sulfinyl)ethyl)-3-(1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinyl)-, (R-(R*,S*-(E)))-
, Sparsomycin [Chemical/Ingredient]
An antitumor antibiotic produced by Streptomyces sparsogenes. It inhibits protein synthesis in 70S and 80S ribosomal systems.
National Institutes of Health
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Related topics
Related topics
13 relations
Broader (2)
Antibiotics, Antineoplastic
Protein Synthesis Inhibitors
In Blood
agonists
analogs & derivatives
antagonists & inhibitors
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Narrower (4)
MDL 20828
deshydroxysparsomycin
ethyldeshydroxysparsomycin
octylsparsomycin
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
1989
1989
Lipophilic analogues of sparsomycin as strong inhibitors of protein synthesis and tumor growth: a structure-activity relationship study.
Leon A. G. M. Van den Broek
,
E. Lázaro
,
+7 authors
H. Ottenheijm
Journal of Medicinal Chemistry
1989
Corpus ID: 22695311
Fourteen derivatives of sparsomycin (1) were synthesized. Six of them were prepared following a novel synthetic route starting…
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Highly Cited
1985
Highly Cited
1985
A short route to chiral sulfoxides using titanium-mediated asymmetric oxidation
H. Kagan
,
Elisabet Duhach
,
C. Nemecek
,
P. Pitchen
,
O. Samuel
,
S.-H. Zhao
1985
Corpus ID: 5414939
Abstract
1984
1984
Structure-activity relationships of sparsomycin and its analogues. Octylsparsomycin: the first analogue more active than sparsomycin.
R. Liskamp
,
J. H. Colstee
,
H. Ottenheijm
,
P. Lelieveld
,
W. Akkerman
Journal of Medicinal Chemistry
1984
Corpus ID: 1819528
Nine analogues of sparsomycin were synthesized, and their cytostatic activity was studied in an in vitro clonogenic L1210 assay…
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1980
1980
Ribosomal resistance to the 12,13-epoxytrichothecene antibiotics in the producing organism Myrothecium verrucaria.
A. Hobden
,
E. Cundliffe
Biochemical Journal
1980
Corpus ID: 36751005
An extract of Myrothecium verrucaria, a fungus which produces a range of 12,13-epoxytrichothecene toxins, was found to be…
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1978
1978
Effect of sparsomycin analogues on the puromycin-peptidyl transferase reaction on ribosomes.
C. K. Lee
,
R. Vince
Journal of Medicinal Chemistry
1978
Corpus ID: 42814858
Sparsomycin analogues in which the unique -S(O)CH2SCH3 moiety was replaced by a variety of more easily accessible side chains…
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1977
1977
Pyrimidinylpropenamides as antitumor agents. Analogues of the antibiotic sparsomycin.
C. C. Lin
,
R. Dubois
Journal of Medicinal Chemistry
1977
Corpus ID: 977646
A series of pyrimidinylpropenamides 9 and their oxidation products 10 was prepared, as analogues of sparsomycin (1), for…
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1975
1975
Inhibitors of polypeptide elongation on yeast polysomes.
M. Barbacid
,
M. Fresno
,
D. Vazquez
Journal of antibiotics (Tokyo. )
1975
Corpus ID: 23526546
Yeast polysomes are very active for amino acid incorporation when supplemented with elongation factors and the different…
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1970
1970
Peptide chain termination. VII. The ribosomal and release factor requirements for peptide release.
R. Tompkins
,
E. Scolnick
,
C. T. Caskey
Proceedings of the National Academy of Sciences…
1970
Corpus ID: 25247869
Release factors participate in release of fMet from fMet-tRNA . AUG . ribosome intermediates upon binding to ribosomes. This…
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1968
1968
The action of sparsomycin and gougerotin on virus growth.
L. Thiry
Journal of General Virology
1968
Corpus ID: 45245384
Summary The incorporation of [14C]amino acids into the acid precipitable material of chick embryo fibroblasts was inhibited by…
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1966
1966
Toxic retinopathy following sparsomycin therapy.
J. R. McFarlane
,
M. Yanoff
,
H. Scheie
A M A Archives of Ophthalmology
1966
Corpus ID: 42261762
This paper presents the clinical and histologic ocular findings of two patients who developed toxic retinal changes while…
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