Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H16N2O2 |
| Molecular Weight | 172.2248 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=N)CCCCC(=N)OC
InChI
InChIKey=ZLFRJHOBQVVTOJ-UHFFFAOYSA-N
InChI=1S/C8H16N2O2/c1-11-7(9)5-3-4-6-8(10)12-2/h9-10H,3-6H2,1-2H3
| Molecular Formula | C8H16N2O2 |
| Molecular Weight | 172.2248 |
| 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 |
|---|---|---|
| An approach to peptide-based ATP receptors by a combination of random selection, rational design, and molecular imprinting. | 2009-11-15 |
|
| The Sir2-Sum1 complex represses transcription using both promoter-specific and long-range mechanisms to regulate cell identity and sexual cycle in the yeast Kluyveromyces lactis. | 2009-11 |
|
| Porin new light onto chromatin and nuclear organization. | 2008 |
|
| Substitution as a mechanism for genetic robustness: the duplicated deacetylases Hst1p and Sir2p in Saccharomyces cerevisiae. | 2007-08 |
|
| Effect of intracellular magnesium and oxygen tension on K+-Cl- cotransport in normal and sickle human red cells. | 2006 |
|
| Dynamic acetylation of all lysine 4-methylated histone H3 in the mouse nucleus: analysis at c-fos and c-jun. | 2005-12 |
|
| Genomic mapping of RNA polymerase II reveals sites of co-transcriptional regulation in human cells. | 2005 |
|
| ATP-dependent vesiculation in red cell membranes from different hereditary stomatocytosis variants. | 2003-03 |
|
| Preparation of well-defined bovine polyhemoglobin based on dimethyl adipimidate and glutaraldebyde cross-linkage. | 2002-05-10 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:52:54 GMT 2025
by
admin
on
Mon Mar 31 19:52:54 GMT 2025
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| Record UNII |
1NMY8K60OU
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID901319059
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25738
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13139-70-3
Created by
admin on Mon Mar 31 19:52:54 GMT 2025 , Edited by admin on Mon Mar 31 19:52:54 GMT 2025
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1NMY8K60OU
Created by
admin on Mon Mar 31 19:52:54 GMT 2025 , Edited by admin on Mon Mar 31 19:52:54 GMT 2025
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PRIMARY |