Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H11BrN2O2 |
| Molecular Weight | 271.111 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(C)C(=O)N2N1C(CBr)=C(C)C2=O
InChI
InChIKey=AHEWZZJEDQVLOP-UHFFFAOYSA-N
InChI=1S/C10H11BrN2O2/c1-5-7(3)12-8(4-11)6(2)10(15)13(12)9(5)14/h4H2,1-3H3
| Molecular Formula | C10H11BrN2O2 |
| Molecular Weight | 271.111 |
| 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 |
|---|---|---|
| Caged fluorescent haptens reveal the generation of cryptic epitopes in allergic contact dermatitis. | 2011-07 |
|
| Essential role of glutathione in acclimation to environmental and redox perturbations in the cyanobacterium Synechocystis sp. PCC 6803. | 2010-12 |
|
| Cytosolic action of phytochelatin synthase. | 2010-05 |
|
| Acrosome stability in the spermatozoa of dasyurid marsupials. | 2008 |
|
| Reactivity of zinc finger cysteines: chemical modifications within labile zinc fingers in estrogen receptor. | 2005-12 |
|
| Identification and characterization of a Pi isoform of glutathione S-transferase (GSTP1) as a zeaxanthin-binding protein in the macula of the human eye. | 2004-11-19 |
|
| Monobromobimane occupies a distinct xenobiotic substrate site in glutathione S-transferase pi. | 2003-11 |
|
| Interaction of S100A8/S100A9-arachidonic acid complexes with the scavenger receptor CD36 may facilitate fatty acid uptake by endothelial cells. | 2001-01-09 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:43:44 GMT 2025
by
admin
on
Mon Mar 31 19:43:44 GMT 2025
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| Record UNII |
V23UK0CYXL
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| Record Status |
Validated (UNII)
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| Record Version |
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V23UK0CYXL
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71418-44-5
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Monobromobimane
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62825
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608544
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114810
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DTXSID70221609
Created by
admin on Mon Mar 31 19:43:44 GMT 2025 , Edited by admin on Mon Mar 31 19:43:44 GMT 2025
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