Details
Stereochemistry | ACHIRAL |
Molecular Formula | C4H6OS |
Molecular Weight | 102.155 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1CCCS1
InChI
InChIKey=KMSNYNIWEORQDJ-UHFFFAOYSA-N
InChI=1S/C4H6OS/c5-4-2-1-3-6-4/h1-3H2
Molecular Formula | C4H6OS |
Molecular Weight | 102.155 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Thiolated dermal bovine collagen as a novel support for bioactive substances--conjugation with lysozyme. | 2001 Mar 9 |
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Design of inhibitors of scytalone dehydratase: probing interactions with an asparagine carboxamide. | 2002 Dec |
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Catalytic synthesis of thiobutyrolactones via CO insertion into the C-S bond of thietanes in the presence of a heterodinuclear organoplatinum-cobalt complex. | 2003 Aug 21 |
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Modification of cellulose fiber surfaces by use of a lipase and a xyloglucan endotransglycosylase. | 2005 Jan-Feb |
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Tiny droplets make a big splash. | 2006 Feb |
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Mechanism of hydrolysis and aminolysis of homocysteine thiolactone. | 2006 May 15 |
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Relations of lysophosphatidylcholine in low-density lipoprotein with serum lipoprotein-associated phospholipase A2, paraoxonase and homocysteine thiolactonase activities in patients with type 2 diabetes mellitus. | 2009 Nov |
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An improved synthesis of the selective EP4 receptor agonist ONO-4819. | 2009 Nov 6 |
|
The use of superporous Ac-CGGASIKVAVS-OH-modified PHEMA scaffolds to promote cell adhesion and the differentiation of human fetal neural precursors. | 2010 Aug |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:42:46 GMT 2023
by
admin
on
Fri Dec 15 19:42:46 GMT 2023
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Record UNII |
A3ERZ734SN
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Record Status |
Validated (UNII)
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Record Version |
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JECFA EVALUATION |
2-OXOTHIOLANE
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