Cart
sales@molnova.com
2,2-Dihydroxy chalcone
CAS No. 15131-80-3
2,2-Dihydroxy chalcone( —— )
Catalog No. M37837 CAS No. 15131-80-3
2,2'-Dihydroxy chalcone is a potent inhibitor of β-glucuronidase (IC50=1.6±0.2 μM) and lysozyme (IC50=1.4±0.2 μM) release from rat neutrophils stimulated with fMLP/CB.2,2'-Dihydroxy chalcone has inhibitory activity against Escherichia coli, Shigella fowleri, Staphylococcus albicans and Staphylococcus aureus.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 296 | In Stock |
|
| 5MG | 409 | In Stock |
|
| 10MG | 604 | In Stock |
|
| 25MG | 908 | In Stock |
|
| 50MG | 1251 | In Stock |
|
| 100MG | 1647 | In Stock |
|
| 500MG | 3312 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product Name2,2-Dihydroxy chalcone
-
NoteResearch use only, not for human use.
-
Brief Description2,2'-Dihydroxy chalcone is a potent inhibitor of β-glucuronidase (IC50=1.6±0.2 μM) and lysozyme (IC50=1.4±0.2 μM) release from rat neutrophils stimulated with fMLP/CB.2,2'-Dihydroxy chalcone has inhibitory activity against Escherichia coli, Shigella fowleri, Staphylococcus albicans and Staphylococcus aureus.
-
Description2,2'-Dihydroxy chalcone is a potent inhibitor of β-glucuronidase (IC50=1.6±0.2 μM) and lysozyme (IC50=1.4±0.2 μM) release from rat neutrophils stimulated with fMLP/CB.2,2'-Dihydroxy chalcone has inhibitory activity against Escherichia coli, Shigella fowleri, Staphylococcus albicans and Staphylococcus aureus.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayAutophagy
-
TargetAutophagy
-
RecptorAutophagy | Antibacterial
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number15131-80-3
-
Formula Weight240.25
-
Molecular FormulaC15H12O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESOC1=C(\C=C\C(=O)C2=C(O)C=CC=C2)C=CC=C1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
CUR5g
CUR5g is an autophagy inhibitor that inhibits migration and colony formation in A549 cells and acts through a UVRAG-dependent mechanism by blocking the recruitment of STX17 to autophagosomes.
-
Sulfamethoxazole
Sulfamethoxazole is a sulfonamide bacteriostatic antibiotic.
-
LC3-mHTT-IN-AN1
LC3-mHTT-IN-AN1 (Compound AN1) is a mHTT-LC3 linker compound, which interacts with both mutant huntingtin protein (mHTT) and LC3B but not with wtHTT or irrelevant control proteins.
