Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H12O2 |
| Molecular Weight | 116.1583 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)C(C)(C)C
InChI
InChIKey=CNMFHDIDIMZHKY-UHFFFAOYSA-N
InChI=1S/C6H12O2/c1-6(2,3)5(7)8-4/h1-4H3
| Molecular Formula | C6H12O2 |
| Molecular Weight | 116.1583 |
| 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 |
|---|---|---|
| Antimycobacterial activity of substituted isosteres of pyridine- and pyrazinecarboxylic acids. 2. | 2001 May 10 |
|
| AS-924, a novel, orally active, bifunctional prodrug of ceftizoxime: physicochemical properties, oral absorption in animals, and antibacterial activity. | 2001 Nov |
|
| Pivalase catalytic antibodies: towards abzymatic activation of prodrugs. | 2001 Nov 5 |
|
| Synthesis of helix 69 of Escherichia coli 23S rRNA containing its natural modified nucleosides, m(3)Psi and Psi. | 2002 Dec 13 |
|
| Cell handling, membrane-binding properties, and membrane-penetration modeling approaches of pivampicillin and phthalimidomethylampicillin, two basic esters of ampicillin, in comparison with chloroquine and azithromycin. | 2003 Apr |
|
| In situ observation of the four-step dehydration process of the 1 beta-methylcarbapenem antibiotic CS-834 crystal by X-rays. | 2003 Dec |
|
| Synthesis of acyloxymethyl ester prodrugs of the transferable protein farnesyl transferase substrate farnesyl methylenediphosphonate. | 2004 Oct 4 |
|
| Bioreversible quaternary N-acyloxymethyl derivatives of the poorly soluble tertiary amine Lu 28-179--synthesis, pharmaceutical chemical characterization and bioavailability studies in dogs. | 2005 Dec |
|
| Influence of esterification and modification of A-ring in a group of lupane acids on their cytotoxicity. | 2005 Oct 1 |
|
| Epigenetics of cervical cancer. An overview and therapeutic perspectives. | 2005 Oct 25 |
|
| Hydralazine target: from blood vessels to the epigenome. | 2006 Feb 28 |
|
| Prodrug forms of N-[(4-deoxy-4-amino-10-methyl)pteroyl]glutamate-gamma-[psiP(O)(OH)]-glutarate, a potent inhibitor of folylpoly-gamma-glutamate synthetase: synthesis and hydrolytic stability. | 2006 Jan 26 |
|
| Pivaloyloxymethyl-modified isoprenoid bisphosphonates display enhanced inhibition of cellular geranylgeranylation. | 2008 Apr 1 |
|
| (2SR,4aSR,8aSR)-6-Oxoperhydro-naphthalene-2-carboxylic acid. | 2008 Dec 20 |
|
| Synthesis and hybridization properties of oligonucleotides having 4-N-(pyrrol-2-ylcarbonyl)deoxycytidine. | 2009 |
|
| Chemical synthesis of RNA with base-labile 2'-o-(pivaloyloxymethyl)-protected ribonucleoside phosphoramidites. | 2010 Dec |
|
| [Synthetic studies of imidazole C-nucleosides toward biofunctional molecules]. | 2010 Dec |
|
| Enhanced stability and intracellular accumulation of quercetin by protection of the chemically or metabolically susceptible hydroxyl groups with a pivaloxymethyl (POM) promoiety. | 2010 Dec 23 |
|
| Synthesis of ester prodrugs of 9-(S)-[3-hydroxy-2-(phosphonomethoxy)propyl]-2,6-diaminopurine (HPMPDAP) as anti-poxvirus agents. | 2010 Oct 14 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:16:55 GMT 2023
by
admin
on
Sat Dec 16 02:16:55 GMT 2023
|
| Record UNII |
BFX9W386OX
|
| Record Status |
Validated (UNII)
|
| Record Version |
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| Code System | Code | Type | Description | ||
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209-959-1
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69027
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DTXSID4027234
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598-98-1
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BFX9W386OX
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Methyl pivalate
Created by
admin on Sat Dec 16 02:16:55 GMT 2023 , Edited by admin on Sat Dec 16 02:16:55 GMT 2023
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