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S5272

Sigma-Aldrich

Sulfanitran

~85%

Sinónimos:

N4-Acetyl-N1-(4-nitrophenyl)sulfanilamide

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About This Item

Fórmula empírica (notación de Hill):
C14H13N3O5S
Número de CAS:
122-16-7
Peso molecular:
335.34
Beilstein/REAXYS Number:
2952955
MDL number:
MFCD00024598
UNSPSC Code:
51101500
PubChem Substance ID:
24899645

assay

~85%

form

powder

color

yellow to greenish yellow

antibiotic activity spectrum

neoplastics

mode of action

enzyme | interferes

SMILES string

CC(=O)Nc1ccc(cc1)S(=O)(=O)Nc2ccc(cc2)[N+]([O-])=O

InChI

1S/C14H13N3O5S/c1-10(18)15-11-4-8-14(9-5-11)23(21,22)16-12-2-6-13(7-3-12)17(19)20/h2-9,16H,1H3,(H,15,18)

InChI key

GWBPFRGXNGPPMF-UHFFFAOYSA-N

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Application

Sulfanitran is used to stimulate MRP2. It is used to stimulate the MRP2-mediated transport of lipophilic amphipathic drugs. It is used to study the efflux of chemotherapeutics in tumor cell lines.

Biochem/physiol Actions

Sulfanitran stimulates the ATP binding cassette family transporter multidrug resistance protein 2 (MRP2). Sulfanitran increases the affinity of MRP2 for estradiol-17-β-D-glucuronide. It stimulates the vectorial transport of saquinavir, a MRP2 substrate, across polarized MDCKII monolayers.

Other Notes

Keep container tightly closed in a dry and well-ventilated place.

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Jurjen S Lagas et al.
Drug metabolism and disposition: the biological fate of chemicals, 37(1), 129-136 (2008-10-11)
Diclofenac is an important analgesic and anti-inflammatory drug, widely used for treatment of postoperative pain, rheumatoid arthritis, and chronic pain associated with cancer. Consequently, diclofenac is often used in combination regimens and undesirable drug-drug interactions may occur. Because many drug-drug
Darko Ursic et al.
International journal of pharmaceutics, 381(2), 199-204 (2009-09-29)
Intestinal efflux transporters can significantly reduce the absorption of the drug after peroral application. In this work we studied secretion of glutathione conjugates triggered by glucose at the luminal side of the intestine. Glucose stimulated secretion of DNPSG, NEMSG and
Noam Zelcer et al.
The Journal of biological chemistry, 278(26), 23538-23544 (2003-04-19)
Multidrug resistance protein 2 (MRP2) belongs to the ATP binding cassette family of transporters. Its substrates include organic anions and anticancer drugs. We have used transport assays with vesicles derived from Sf9 insect cells overproducing MRP2 to study the interactions
Hehui Zheng et al.
Se pu = Chinese journal of chromatography, 25(2), 238-240 (2007-06-22)
A method for the determination of 12 sulfonamides (SAs) (sulfanilamide, sulfamonomethoxine, sulfacetamide, sulfamethoxazole, sulfadiazine, sulfisoxazole, sulfathiazole, sulfadi-methoxine, sulfamerazine, sulfaquinoxaline, sulfamethazine, sulfanitran) in cosmetics was developed by ultra performance liquid chromatography with photodiode array detector (UPLC-PDA). The chromatographic column used was
Marilyn J Schneider et al.
Analytical and bioanalytical chemistry, 407(15), 4423-4435 (2014-12-30)
Multiclass, multiresidue methods are becoming increasingly popular in regulatory monitoring programs due to their increased analytical scope and laboratory efficiency. In this work, we report the development and validation of a new high-throughput analytical method to monitor up to 131

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