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Wikipedia

NS-398

NS-398 is a COX-2 inhibitor used in the study of the function of cyclooxygenases.[2]

NS-398
Names
Preferred IUPAC name
N-[2-(Cyclohexyloxy)-4-nitrophenyl]methanesulfonamide
Identifiers
  • 123653-11-2 Y
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:73458 Y
ChEMBL
  • ChEMBL7162
ChemSpider
  • 4393 Y
DrugBank
  • DB14060
  • 8976
  • 4553
  • DTXSID8041084
  • InChI=1S/C13H18N2O5S/c1-21(18,19)14-12-8-7-10(15(16)17)9-13(12)20-11-5-3-2-4-6-11/h7-9,11,14H,2-6H2,1H3 Y
    Key: KTDZCOWXCWUPEO-UHFFFAOYSA-N N
  • InChI=1/C13H18N2O5S/c1-21(18,19)14-12-8-7-10(15(16)17)9-13(12)20-11-5-3-2-4-6-11/h7-9,11,14H,2-6H2,1H3
    Key: KTDZCOWXCWUPEO-UHFFFAOYAY
  • CS(=O)(=O)NC1=C(C=C(C=C1)[N+](=O)[O-])OC2CCCCC2
Properties
C13H18N2O5S
Molar mass 314.36 g·mol−1
Appearance Off-white solid
Insoluble
Solubility in DMSO 5 mg/mL
Hazards
GHS labelling:[1]
Warning
H302, H312, H332
P280
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)

See also edit

References edit

  1. ^ "N194 NS-398". Sigma-Aldrich. Retrieved 13 December 2021.
  2. ^ Wei Shen; Yong Li; Ying Tang; James Cummins; Johnny Huard (2005). "NS-398, a Cyclooxygenase-2-Specific Inhibitor, Delays Skeletal Muscle Healing by Decreasing Regeneration and Promoting Fibrosis". American Journal of Pathology. 167 (4): 1105–1117. doi:10.1016/S0002-9440(10)61199-6. PMC 1603662. PMID 16192645.

inhibitor, used, study, function, cyclooxygenases, namespreferred, iupac, name, cyclohexyloxy, nitrophenyl, methanesulfonamideidentifierscas, number, 123653, model, jsmol, interactive, imagechebi, chebi, 73458, ychembl, chembl7162chemspider, 4393, ydrugbank, d. NS 398 is a COX 2 inhibitor used in the study of the function of cyclooxygenases 2 NS 398 NamesPreferred IUPAC name N 2 Cyclohexyloxy 4 nitrophenyl methanesulfonamideIdentifiersCAS Number 123653 11 2 Y3D model JSmol Interactive imageChEBI CHEBI 73458 YChEMBL ChEMBL7162ChemSpider 4393 YDrugBank DB14060IUPHAR BPS 8976PubChem CID 4553CompTox Dashboard EPA DTXSID8041084InChI InChI 1S C13H18N2O5S c1 21 18 19 14 12 8 7 10 15 16 17 9 13 12 20 11 5 3 2 4 6 11 h7 9 11 14H 2 6H2 1H3 YKey KTDZCOWXCWUPEO UHFFFAOYSA N NInChI 1 C13H18N2O5S c1 21 18 19 14 12 8 7 10 15 16 17 9 13 12 20 11 5 3 2 4 6 11 h7 9 11 14H 2 6H2 1H3Key KTDZCOWXCWUPEO UHFFFAOYAYSMILES CS O O NC1 C C C C C1 N O O OC2CCCCC2PropertiesChemical formula C 13H 18N 2O 5SMolar mass 314 36 g mol 1Appearance Off white solidSolubility in water InsolubleSolubility in DMSO 5 mg mLHazardsGHS labelling 1 PictogramsSignal word WarningHazard statements H302 H312 H332Precautionary statements P280Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa N verify what is Y N Infobox referencesSee also editCelecoxib Tilmacoxib JTE 522 References edit N194 NS 398 Sigma Aldrich Retrieved 13 December 2021 Wei Shen Yong Li Ying Tang James Cummins Johnny Huard 2005 NS 398 a Cyclooxygenase 2 Specific Inhibitor Delays Skeletal Muscle Healing by Decreasing Regeneration and Promoting Fibrosis American Journal of Pathology 167 4 1105 1117 doi 10 1016 S0002 9440 10 61199 6 PMC 1603662 PMID 16192645 nbsp This article about an organic compound is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title NS 398 amp oldid 1201495896, wikipedia, wiki, book, books, library,

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