Sulfaproxiline
CAS No. 116-42-7
Sulfaproxiline( Sulfaproxylin | Sulfaproxyline | Sulphaproxyline )
Catalog No. M26469 CAS No. 116-42-7
Sulfaproxiline is a synthetic antibacterial drug of sulfonamide.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 46 | In Stock |
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| 5MG | 39 | In Stock |
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| 10MG | 63 | In Stock |
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| 25MG | 107 | In Stock |
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| 50MG | 155 | In Stock |
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| 100MG | 231 | In Stock |
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| 200MG | 343 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameSulfaproxiline
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NoteResearch use only, not for human use.
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Brief DescriptionSulfaproxiline is a synthetic antibacterial drug of sulfonamide.
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DescriptionSulfaproxiline is a synthetic antibacterial drug of sulfonamide.
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In Vitro——
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In Vivo——
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SynonymsSulfaproxylin | Sulfaproxyline | Sulphaproxyline
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PathwayGPCR/G Protein
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TargetAntibacterial
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RecptorPDE4
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Research Area——
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Indication——
Chemical Information
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CAS Number116-42-7
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Formula Weight334.39
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Molecular FormulaC16H18N2O4S
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Purity>98% (HPLC)
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Solubility——
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SMILESCC(C)Oc1ccc(cc1)C(=O)NS(=O)(=O)c1ccc(N)cc1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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3-Hydroxy-C4-HSL
3-Hydroxy-C4-HSL (N-3-hydroxybutyryl-L-Homoserine lactone) is an N-acyl homoserine lactone obtained from pathogenic Vibrio vulnificus in fish and is a bacterial group sensing (QS) inducer that modulates bacterial signaling and can be used in the study of bacterial infections.
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Chebulinic acid
Chebulinic acid is a potent inhibitor of M. tuberculosis DNA gyrase. It also can inhibit SMAD-3 phosphorylation and H+ K+-ATPase activity.Chebulinic acid obviously inhibited HQ/Cu(II)- and H(2)O(2)/Cu(II)-mediated pBR322 DNA strand breaks. When MRC-5 cells were treated with HQ/Cu(II), the presence of Chebulinic acid inhibited HQ/Cu(II)-mediated double-strand breaks of genomic DNA.
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Retapamulin
An pleuromutilin antibiotic, specifically a protein synthesis inhibitor by interacting on the 50S subunit of the bacterial ribosome.
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