Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H7NO |
| Molecular Weight | 109.1259 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=C(N1)C=O
InChI
InChIKey=LFWLUDLUCDRDAF-UHFFFAOYSA-N
InChI=1S/C6H7NO/c1-5-2-3-6(4-8)7-5/h2-4,7H,1H3
| Molecular Formula | C6H7NO |
| Molecular Weight | 109.1259 |
| 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 |
|---|---|---|
| Chemoenzymatic formation of novel aminocoumarin antibiotics by the enzymes CouN1 and CouN7. | 2007-07-17 |
|
| Installation of the pyrrolyl-2-carboxyl pharmacophore by CouN1 and CouN7 in the late biosynthetic steps of the aminocoumarin antibiotics clorobiocin and coumermycin A1. | 2006-07-18 |
|
| Metabolic engineering of aminocoumarins: inactivation of the methyltransferase gene cloP and generation of new clorobiocin derivatives in a heterologous host. | 2005-08 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:03:48 GMT 2025
by
admin
on
Mon Mar 31 19:03:48 GMT 2025
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| Record UNII |
SP16VW48RI
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| Record Status |
Validated (UNII)
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| Record Version |
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