Benzothiazines
Apexbio Technology LLC Piroxicam 36322-90-4 1g
Piroxicam (CAS 36322-90-4) is a non-steroidal anti-inflammatory compound that acts as a dual inhibitor of cyclooxygenase isoforms COX-1 (human prostaglandin H synthase-1) and COX-2 (hPGHS-2) with greater potency toward COX-1 By suppressing prostaglandin synthesis piroxicam mediates anti-inflammatory effects and additionally blocks ADP-induced platelet aggregation This compound is utilized in research to study prostaglandin-mediated pathways evaluate cyclooxygenase inhibition profiles and investigate mechanisms underlying inflammation and platelet function
eMolecules 7-Methoxy-1,4-benzothiazin-3-one | 22726-30-3 | 5G | Purity: 95%
Combi-Blocks | 7-Methoxy-1,4-benzothiazin-3-one | 5G | 22726-30-3 | MFCD02660686
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eMolecules 7-Chloro-2h-1,4-benzothiazin-3(4h)-one | 5333-05-1 | MFCD00127344 | 5g
Combi-Blocks, Inc. | 7-Chloro-2h-1,4-benzothiazin-3(4h)-one | 5g | 603152985 | QF-8828 | 95.000 | 5333-05-1 | MFCD00127344 | 199.650 | C8H6ClNOS
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ALADDIN SCIENTIFIC CORPORATION Ethylene imine polymer, 25g
Ethylene imine polymer 99% M W 10000Cas-9002-98-6
![eMolecules 6-[(2-Amino-1,3-benzothiazol-5-yl)oxy]-1,3-benzothiazol-2-amine | | MFCD00972264 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502150442.JPG-250.jpg)
eMolecules 6-[(2-Amino-1,3-benzothiazol-5-yl)oxy]-1,3-benzothiazol-2-amine | | MFCD00972264 | 1g
Oakwood Chemicals | 6-[(2-Amino-1,3-benzothiazol-5-yl)oxy]-1,3-benzothiazol-2-amine | 1g | 480157615 | 182717 | | | MFCD00972264 | 314.380 | C14H10N4OS2
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Chemscene ChemScene | Methyl 3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate | 25G | CS-W002612 | 0.98 | 188614-01-9| MFCD00449104 | 223.25
ChemScene | Methyl 3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate | 25G | CS-W002612 | 0.98 | 188614-01-9| MFCD00449104 | 223.25
eMolecules N-Methyl-1,3-Benzothiazol-2-Amine | 16954-69-1 | MFCD00035877 | 250mg
WuXi AppTec | N-Methyl-1,3-Benzothiazol-2-Amine | 250mg | 583177465 | LN00002217 | | 16954-69-1 | MFCD00035877 | 164.230 | C8H8N2S
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Electron Microscopy Sciences Giemsa Working Solution 500 ML
Used in Wolbach's Giemsa Method, Wolbach, Todd, and Palfrey (1922) for the staining of : nuclei, collagen, riskettsia and bacteria. See references Wolbach, S.B., Todd, J.L., and Paltrey, F.W., The Etiology of Pathology Typhus, Harvard University Press, Cambridge, MA, p. 13-14, c. 1922 and Luna, L.G., (ed). Manual of Histologic Staining Methods od the AFIP, 3rd edition. McGraw-Hill, NY, p. 119, c. 1968.