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Revision as of 12:28, 19 April 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'UNII_Ref', 'ChemSpiderID_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEMBL_Ref', 'KEGG_Ref') per Chem/Drugbox validation (← Previous edit Latest revision as of 19:36, 31 January 2024 edit undoMichael7604 (talk | contribs)Extended confirmed users8,895 edits recategorized from Nitrobenzenes to Nitrobenzene derivatives 
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{{chembox {{chembox
| Verifiedfields = changed
| verifiedrevid = 400465036
| Watchedfields = changed
|Reference=<ref> at ]</ref>
| verifiedrevid = 424846904
|ImageFile=NS-398.png
| Reference=
|ImageSize=180px
| ImageFile=NS-398.png
|IUPACName=''N''-methanesulfonamide
| ImageSize=180px
|OtherNames=
| ImageFile1 = NS-398 molecule spacefill.png
| ImageAlt1 = Space-filling model of the NS-398 molecule
| PIN=''N''-methanesulfonamide
| OtherNames=
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo=123653-11-2 | CASNo=123653-11-2
| PubChem=4553
| ChEBI_Ref = {{ebicite|correct|EBI}}
| SMILES=CS(=O)(=O)NC1=C(C=C(C=C1)(=O))OC2CCCCC2
| ChEBI = 73458
| ChEMBL = 7162
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 4393
| DrugBank = DB14060
| IUPHAR_ligand = 8976
| PubChem=4553
| 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
| InChIKey = KTDZCOWXCWUPEO-UHFFFAOYAY
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 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
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = KTDZCOWXCWUPEO-UHFFFAOYSA-N
| SMILES=CS(=O)(=O)NC1=C(C=C(C=C1)(=O))OC2CCCCC2
}} }}
|Section2={{Chembox Properties |Section2={{Chembox Properties
| C=13|H=18|N=2|O=5|S=1 | C=13 | H=18 | N=2 | O=5 | S=1
| Appearance=Off-white solid | Appearance=Off-white solid
| Density= | Density=
| MeltingPt= | MeltingPt=
| BoilingPt= | BoilingPt=
| Solubility=Insoluble | Solubility=Insoluble
| SolubleOther = 5 mg/mL | SolubleOther = 5 mg/mL
| Solvent = ] | Solvent = ]
|
}} }}
|Section3={{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards= | MainHazards=
| FlashPt= | FlashPt=
| AutoignitionPt =
| Autoignition=
| GHS_ref=<ref>{{cite web |title=N194 NS-398 |url=https://www.sigmaaldrich.com/AU/en/product/sigma/n194 |publisher=Sigma-Aldrich |access-date=13 December 2021}}</ref>
| RPhrases =
| SPhrases = {{S22}} {{S24/25}} | GHSPictograms = {{GHS07}}
| GHSSignalWord = Warning
| HPhrases = {{H-phrases|302|312|332}}
| PPhrases = {{P-phrases|280}}
}} }}
}} }}


'''NS-398''' is a ] used in the study of the function of ]s.<ref>See for example: {{cite journal | journal = American Journal of Pathology | year = 2005 | volume = 167 | issue = 4 | pages = 1105–1117 | title = NS-398, a Cyclooxygenase-2-Specific Inhibitor, Delays Skeletal Muscle Healing by Decreasing Regeneration and Promoting Fibrosis | author = Wei Shen, Yong Li, Ying Tang, James Cummins and Johnny Huard | pmid = 16192645 | pmc = 1603662}}</ref> '''NS-398''' is a ] used in the study of the function of ]s.<ref>{{cite journal | journal = American Journal of Pathology | year = 2005 | volume = 167 | issue = 4 | pages = 1105–1117 | title = NS-398, a Cyclooxygenase-2-Specific Inhibitor, Delays Skeletal Muscle Healing by Decreasing Regeneration and Promoting Fibrosis |author1=Wei Shen |author2=Yong Li |author3=Ying Tang |author4=James Cummins |author5=Johnny Huard | pmid = 16192645 | pmc = 1603662 | doi = 10.1016/S0002-9440(10)61199-6}}</ref>

==See also==
*]
*] (JTE-522)


==References== ==References==
{{reflist}} {{Reflist}}

{{Prostanoidergics}}


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{{Organic-compound-stub}} {{Organic-compound-stub}}