Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H16O4 |
| Molecular Weight | 164.1995 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COCCOCCOCCO
InChI
InChIKey=JLGLQAWTXXGVEM-UHFFFAOYSA-N
InChI=1S/C7H16O4/c1-9-4-5-11-7-6-10-3-2-8/h8H,2-7H2,1H3
| Molecular Formula | C7H16O4 |
| Molecular Weight | 164.1995 |
| 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 |
|---|---|---|
| Monoclonal antibody conjugates of doxorubicin prepared with branched peptide linkers: inhibition of aggregation by methoxytriethyleneglycol chains. | 2002 Sep 12 |
|
| New polyethyleneglycol-functionalized texaphyrins: synthesis and in vitro biological studies. | 2006 Apr 28 |
|
| Impact of the 3,6,9-trioxadecyloxy group on desazadesferrithiocin analogue iron clearance and organ distribution. | 2007 Jul 12 |
|
| Killing cancer cells by targeted drug-carrying phage nanomedicines. | 2008 Apr 3 |
|
| The impact of polyether chain length on the iron clearing efficiency and physiochemical properties of desferrithiocin analogues. | 2010 Apr 8 |
|
| Medium effect on the geometric isomerism of a centrosymmetrically disubstituted naphthalene derivative with flexible methoxytriethylene glycol chains. | 2010 Jun 24 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 20:11:01 GMT 2023
by
admin
on
Sat Dec 16 20:11:01 GMT 2023
|
| Record UNII |
DN0P4Q4I16
|
| Record Status |
Validated (UNII)
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| Record Version |
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97395
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8178
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DTXSID5026912
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9004-74-4
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