Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H6O3 |
| Molecular Weight | 126.11 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(C)C(=O)OC1=O
InChI
InChIKey=MFGALGYVFGDXIX-UHFFFAOYSA-N
InChI=1S/C6H6O3/c1-3-4(2)6(8)9-5(3)7/h1-2H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Short synthesis of the seed germination inhibitor 3,4,5-trimethyl-2(5H)-furanone. | 2010-08-20 |
|
| A charge-switched nano-sized polymeric carrier for protein delivery. | 2010-06-15 |
|
| A tumor-acidity-activated charge-conversional nanogel as an intelligent vehicle for promoted tumoral-cell uptake and drug delivery. | 2010-05-10 |
|
| Synthesis and biological evaluation of a bioresponsive and endosomolytic siRNA-polymer conjugate. | 2009-04-08 |
|
| A dimethylmaleic acid-melittin-polylysine conjugate with reduced toxicity, pH-triggered endosomolytic activity and enhanced gene transfer potential. | 2007-09 |
|
| Reversible lipidization for the oral delivery of leu-enkephalin. | 2006-04 |
|
| Design of a pH-sensitive polymeric carrier for drug release and its application in cancer therapy. | 2004-04-01 |
|
| Interaction of bilirubin with native and protein-depleted human erythrocyte membranes. | 2003-04 |
|
| The total synthesis of (+/-)-merrilactone A. | 2002-03-13 |
|
| Selective enhancement of thrombopoietic activity of PEGylated interleukin 6 by a simple procedure using a reversible amino-protective reagent. | 2001-01 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
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Systematic Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Code | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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C007474
Created by
admin on Mon Mar 31 19:56:42 GMT 2025 , Edited by admin on Mon Mar 31 19:56:42 GMT 2025
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92512
Created by
admin on Mon Mar 31 19:56:42 GMT 2025 , Edited by admin on Mon Mar 31 19:56:42 GMT 2025
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212-165-8
Created by
admin on Mon Mar 31 19:56:42 GMT 2025 , Edited by admin on Mon Mar 31 19:56:42 GMT 2025
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5517
Created by
admin on Mon Mar 31 19:56:42 GMT 2025 , Edited by admin on Mon Mar 31 19:56:42 GMT 2025
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DTXSID6061103
Created by
admin on Mon Mar 31 19:56:42 GMT 2025 , Edited by admin on Mon Mar 31 19:56:42 GMT 2025
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6PP3N541QA
Created by
admin on Mon Mar 31 19:56:42 GMT 2025 , Edited by admin on Mon Mar 31 19:56:42 GMT 2025
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13010
Created by
admin on Mon Mar 31 19:56:42 GMT 2025 , Edited by admin on Mon Mar 31 19:56:42 GMT 2025
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766-39-2
Created by
admin on Mon Mar 31 19:56:42 GMT 2025 , Edited by admin on Mon Mar 31 19:56:42 GMT 2025
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PRIMARY |
SUBSTANCE RECORD
