Cart
sales@molnova.com
Nifurpirinol
CAS No. 13411-16-0
Nifurpirinol( —— )
Catalog No. M36584 CAS No. 13411-16-0
Nifurpirinol (P-7138) is an antimicrobial compound that is acutely toxic to milkfish (Chanos chanos) species.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 117 | In Stock |
|
| 10MG | 188 | In Stock |
|
| 25MG | 363 | In Stock |
|
| 50MG | 529 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameNifurpirinol
-
NoteResearch use only, not for human use.
-
Brief DescriptionNifurpirinol (P-7138) is an antimicrobial compound that is acutely toxic to milkfish (Chanos chanos) species.
-
DescriptionNifurpirinol (P-7138) is a nitroaromatic antibiotic and acts as a novel substrate for the bacterial nitroreductase (NTR) enzyme. Nifurpirinol is a more potent proagent compared to Metronidazole to trigger cell-ablation in nitroreductase expressing transgenic models.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayCell Cycle/DNA Damage
-
TargetTopoisomerase
-
RecptorTopoisomerase | Antibiotic | Antibacterial
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number13411-16-0
-
Formula Weight246.22
-
Molecular FormulaC12H10N2O4
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : ≥ 20.83 mg/mL (84.60 mM)
-
SMILESO=[N+]([O-])C1=CC=C(/C=C/C2=CC=CC(CO)=N2)O1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. David Bergemann, et al. Nifurpirinol: A more potent and reliable substrate compared to metronidazole for nitroreductase-mediated cell ablations. Wound Repair Regen?
molnova catalog
related products
-
MC-DOXHZN
MC-DOXHZN is an albumin-binding prodrug of Doxorubicin (DNA topoisomerase II inhibitor), with acid-sensitive properties.
-
Proscillaridin A
Proscillaridin A is a natural product.It is a potent poison of topoisomerase I/II activity with IC50 values of 30 nM and 100 nM, respectively.
-
ARN-21934
ARN-21934 is a potent and selective inhibitor for human topoisomerase II α and topoisomerase II β. ARN-21934(IC50 = 2 μM) inhibits DNA relaxation as compared to the anticancer agent Etoposide (IC50=120 μM).
