Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H10N2O2 |
Molecular Weight | 154.1665 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C=CC(=O)NCNC(=O)C=C
InChI
InChIKey=ZIUHHBKFKCYYJD-UHFFFAOYSA-N
InChI=1S/C7H10N2O2/c1-3-6(10)8-5-9-7(11)4-2/h3-4H,1-2,5H2,(H,8,10)(H,9,11)
Molecular Formula | C7H10N2O2 |
Molecular Weight | 154.1665 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Bis-acrylamide is the most frequently used cross-linking agent for protein separation applications in polyacrylamide gels. Bis-acrylamide 2% solution is a standard solution used in most electrophoresis applications. Bis-acrylamide is a cross linking agent that polymerizes with acrylamide and creates cross links within the polyacrylamide gel. It is capable of creating a network rather than linear chains which helps in maintaining the firmness of gel.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL2176812 Sources: https://www.ncbi.nlm.nih.gov/pubmed/2337777 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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PubMed
Title | Date | PubMed |
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The fractionation of high-molecular-weight ribonucleic acid by polyacrylamide-gel electrophoresis. | 1967 Jan |
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Polyneuropathies and CNS protein metabolism. III. Changes in protein synthesis rate induced by acrylamide intoxication. | 1978 Nov-Dec |
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Comparison of nucleic acid-protein interactions in solution and in polyacrylamide gels. | 1986 Feb 15 |
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Preparation and use of synthetic cell culture surfaces. A new reagent for the covalent immobilization of proteins and glycoproteins on a nonionic inert matrix. | 1986 Jun 25 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3190457
Mice: The sperm count and morphology, and testicular histopathology were studied in mice over a period of 75 days following a single oral administration of 50, 100, and 200 mg/kg Bis-acrylamide (MBA). With a 50 and 100 mg/kg dose, the sperm abnormality reached a maximum at 30 days, whereas the sperm count reached a minimum at 35 days. The abnormality and decrease in sperm count were both dose dependent. Following the administration of 200 mg/kg MBA, the appearance of abnormal sperm showed a diphase pattern, i.e., first at 7–15 days without any reduction of the sperm count and second at 30 days after treatment.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/12437947
Hydrogels based on poly(acrylic acid) and gelatin crosslinked with N,N'-methylene bisacrylamide (0.5mol%) and glutaraldehyde (4%), respectively, forming an interpenetrating network were employed as matrices, for studying the loading and release of gentamicin sulphate.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:05:53 GMT 2023
by
admin
on
Fri Dec 15 17:05:53 GMT 2023
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Record UNII |
EDK4RIE19C
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Record Status |
Validated (UNII)
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Record Version |
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DTXSID8025595
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406836
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110-26-9
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EDK4RIE19C
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203-750-9
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N,N'-Methylenebisacrylamide
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