Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C12H15NO8 |
Molecular Weight | 301.2494 |
Optical Activity | ( - ) |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC[C@H]1O[C@@H](OC2=CC=CC=C2[N+]([O-])=O)[C@H](O)[C@@H](O)[C@H]1O
InChI
InChIKey=KUWPCJHYPSUOFW-YBXAARCKSA-N
InChI=1S/C12H15NO8/c14-5-8-9(15)10(16)11(17)12(21-8)20-7-4-2-1-3-6(7)13(18)19/h1-4,8-12,14-17H,5H2/t8-,9+,10+,11-,12-/m1/s1
Molecular Formula | C12H15NO8 |
Molecular Weight | 301.2494 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: Beta-galactosidase (Lactobacillus helveticus) Sources: https://www.ncbi.nlm.nih.gov/pubmed/30813223 |
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Target ID: Beta-galactosidase (Aspergillus oryzae) Sources: https://www.ncbi.nlm.nih.gov/pubmed/24435763 |
PubMed
Title | Date | PubMed |
---|---|---|
Two β-galactosidases from the human isolate Bifidobacterium breve DSM 20213: molecular cloning and expression, biochemical characterization and synthesis of galacto-oligosaccharides. | 2014 |
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Expression and characterization of two β-galactosidases from Klebsiella pneumoniae 285 in Escherichia coli and their application in the enzymatic synthesis of lactulose and 1-lactulose. | 2014 Nov-Dec |
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Antibacterial activity of phenyllactic acid against Listeria monocytogenes and Escherichia coli by dual mechanisms. | 2017 Aug 1 |
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In Vitro Screening of Indigenous Lactobacillus Isolates for Selecting Organisms with Better Health-Promoting Attributes. | 2018 Aug |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:35:44 GMT 2023
by
admin
on
Sat Dec 16 17:35:44 GMT 2023
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Record UNII |
8RFX6AT9WP
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Record Status |
Validated (UNII)
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Record Version |
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28347-45-7
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369-07-3
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8RFX6AT9WP
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ortho-Nitrophenyl-β-galactoside
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83631
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DB01920
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DTXSID10861907
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103737-63-9
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96647
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