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Inflammation
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ALX-340-038 Revised 08-Sep-08
Leukotriene B4
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SYNONYMS LTB4
5,12-Dihydroxy-[S-[R*,S*-(E,Z,Z,E)]]-6,8,10,14-eicosatetraenoic acid
PRODUCT LINE Inflammation
PRODUCT CATEGORY Leukotrienes
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-340-038-C025   25 µg 170.00 USD Add To Cart
Product Specification
FORMULA: C20H32O4
MW: 336.5
CAS NUMBER: 71160-24-2
MERCK INDEX: 14: 5455
CONCENTRATION: 0.1mg/ml
PURITY: ≥97%
FORMULATION: Liquid. Solution in ethanol.
SOLUBILITY: Soluble in DMSO or dimethyl formamide; slightly soluble in PBS, pH 7.2 (1mg/ml). Solvents should be free of oxygen, transition metal ions, and redox active compounds.
SHIPPING: SHIPPED ON BLUE ICE
LONG TERM STORAGE: -20°C
USE/STABILITY: Stable for at least 1 year after receipt when stored at -20°C. We do not recommend storing aqueous solutions for more than one day.
HANDLING: Protect from light and oxygen.

Product Description
Activator of PPARα. Stimulates a number of leukocyte functions, including aggregation, stimulation of ion fluxes, enhancement of lysosomal enzyme release, superoxide anion production, chemotaxis, and chemokinesis.
Product Specific Literature References
Leukotriene B4 and inflammatory disease: R.M. McMillan & S.J. Foster; Agents Actions 24, 114 (1988) Abstract
The PPARalpha-leukotriene B4 pathway to inflammation control: P.R. Devchand, et al.; Nature 384, 39 (1996) Abstract
Leukotriene B4: S.W. Crooks & R.A. Stockley; Int. J. Biochem. Cell Biol. 30, 173 (1998), (Review) Abstract
The peroxisome proliferator-activated receptor alpha (PPARalpha) ligand WY 14,643 does not interfere with leukotriene B4 induced adhesion of neutrophils to endothelial cells: M. Heimbürger & J. Palmblad; BBRC 249, 371 (1998) Abstract
Ligand selectivity of the peroxisome proliferator-activated receptor alpha: Q. Lin, et al.; Biochemistry 38, 185 (1999) Abstract
General Information
BACKGROUND/TECHNICAL INFORMATION To change the solvent, evaporate the ethanol under a gentle stream of nitrogen and immediately add the solvent of choice.
Further Categories Containing This Product:
PPAR Agonists
 
 
ALX-340-043 Revised 08-Sep-08
Leukotriene C4
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SYNONYMS LTC4
5S-Hydroxy-6R-(S-glutathionyl)-7E,9E,11Z,14Z-eicosatetraenoic acid
PRODUCT LINE Inflammation
PRODUCT CATEGORY Leukotrienes
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-340-043-C025   25 µg 157.00 USD Add To Cart
ALX-340-043-C050   50 µg 298.00 USD Add To Cart
ALX-340-043-C100   100 µg 563.00 USD Add To Cart
Product Specification
FORMULA: C30H47N3O9S
MW: 625.8
CAS NUMBER: 72025-60-6
MERCK INDEX: 14: 5455
CONCENTRATION: 0.1mg/ml
PURITY: ≥97%
FORMULATION: Liquid. Solution in ethanol:water (95:5).
SOLUBILITY: 50mg/ml soluble in DMSO or dimethyl formamide; slightly soluble in PBS, pH 7.2 (100µg/ml).
SHIPPING: SHIPPED ON DRY ICE
LONG TERM STORAGE: -80°C
USE/STABILITY: Stable for at least 1 year after receipt when stored at -80°C. We do not recommend storing aqueous solutions for more than one day.

General Information
BACKGROUND/TECHNICAL INFORMATION To change the solvent, evaporate the ethanol:water (95:5) under a gentle stream of nitrogen and immediately add the solvent of choice.
 
 
ALX-270-090 Revised 14-May-03
Dapsone
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SYNONYMS 4,4'-Diaminodiphenyl sulfone
DDS
PRODUCT LINE Inflammation
PRODUCT CATEGORY Leukotrienes Other Products
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ALX-270-090-G001   1 g 10.00 USD Add To Cart
ALX-270-090-G005   5 g 20.00 USD Add To Cart
Product Specification
FORMULA: C12H12N2O2S
MW: 248.3
CAS NUMBER: 80-08-0
MERCK INDEX: 14: 2822
PURITY: ≥96%
APPEARANCE: Off-white solid.
SOLUBILITY: Soluble in  100% ethanol, DMSO or methanol.
SHIPPING: AMBIENT
LONG TERM STORAGE: +20°C
HAZARD: TOXIC.

Product Description
Leukotriene B4 (LTB4) antagonist. Inhibits LTB4 induced lysozyme release.
Product Specific Literature References
Dapsone inhibits LTB4 binding and bioresponse at the cellular and physiologic levels: B.L. Maloff, et al.; Eur. J. Pharmacol. 158, 85 (1988) Abstract
 
 
ALX-340-021 Revised 04-Jun-08
MK-571 . sodium salt
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PRODUCT LINE Inflammation
PRODUCT CATEGORY Leukotrienes Other Products
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ALX-340-021-M005   5 mg 45.00 USD Add To Cart
ALX-340-021-M025   25 mg 190.00 USD Add To Cart
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Product Specification
FORMULA: C26H26ClN2O3S2 . Na
MW: 514.1 . 23.0
CAS NUMBER: 115104-28-4
PURITY: ≥97% (HPLC)
APPEARANCE: Off-white to light yellow solid.
SOLUBILITY: Soluble in water (20mg/ml), aqueous buffers, 100% ethanol (10mg/ml) or DMSO.
SHIPPING: SHIPPED ON BLUE ICE
LONG TERM STORAGE: -20°C
USE/STABILITY: Aqueous stock solutions may be stable for more than 24 hours but we recommend making a fresh preparation before use.
HANDLING: Hygroscopic.
IDENTITY: Identity determined by 1H-NMR.

Product Description
Leukotriene LTD4 receptor antagonist that potently inhibits MRP1.
Product Specific Literature References
The leukotriene LTD4 receptor antagonist MK571 specifically modulates MRP associated multidrug resistance: V. Gekeler, et al.; BBRC 208, 345 (1995) Abstract
Resistance of human multidrug resistance-associated protein 1-overexpressing lung tumor cells to the anticancer drug arsenic trioxide: L. Vernhet, et al.; Biochem. Pharmacol. 61, 1387 (2001) Abstract
Overexpression of glutathione S-transferase II and multidrug resistance transport proteins is associated with acquired tolerance to inorganic arsenic: J. Liu, et al.; Mol. Pharmacol. 60, 302 (2001) Abstract
P-Glycoprotein and transporter MRP1 reduce HIV protease inhibitor uptake in CD4 cells: potential for accelerated viral drug resistance?: K. Jones, et al.; Aids 15, 1353 (2001) Abstract
Impact of BCRP/MXR, MRP1 and MDR1/P-Glycoprotein on thermoresistant variants of atypical and classical multidrug resistant cancer cells: U. Stein, et al.; Int. J. Cancer 97, 751 (2002) Abstract
Further Categories Containing This Product:
MDR Inhibitors
 
 
ALX-340-026 Revised 16-Jun-06
LY-171,883
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SYNONYMS 1-[2-Hydroxy-3-propyl-4-[4-(1H-tetrazol-5-yl)butoxy]phenyl]ethanone
PRODUCT LINE DNA Regulation / Transcription
PRODUCT CATEGORY PPAR Antagonists
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ALX-340-026-M010   10 mg 68.00 USD Add To Cart
Product Specification
FORMULA: C16H22N4O3
MW: 318.4
CAS NUMBER: 88107-10-2
PURITY: ≥98%
APPEARANCE: White to off-white crystalline solid.
SOLUBILITY: Soluble in 100% ethanol, DMSO or dimethyl formamide. Also soluble in 0.5M aqueous sodium bicarbonate.
SHIPPING: AMBIENT
LONG TERM STORAGE: +4°C
USE/STABILITY: Organic stock solutions are stable for at least six months when stored at –20°C.

Product Description
Competitive leukotriene D4 (LTD4) antagonist. Has also been shown to bind to the γ-isofom of the peroxisome proliferator activated receptor (PPARγ).
Product Specific Literature References
LY171883, 1-less than 2-hydroxy-3-propyl-4-less than 4-(1H-tetrazol-5- yl) butoxy greater than phenyl greater than ethanone, an orally active leukotriene D4 antagonist: J.H. Fleisch, et al.; J. Pharmacol. Exp. Ther. 233, 148 (1985) Abstract
Formation of sulphidopeptide-leukotrienes by cell-cell interaction causes coronary vasoconstriction in isolated, cell-perfused heart of rabbit: A. Sala, et al.; Br. J. Pharmacol. 110, 1206 (1993) Abstract
Stimulation of adipogenesis in fibroblasts by PPAR gamma 2, a lipid- activated transcription factor: P. Tontonoz, et al.; Cell 79, 1147 (1994) Abstract
15-Deoxy-delta 12, 14-prostaglandin J2 is a ligand for the adipocyte determination factor PPAR gamma: B.M. Forman, et al.; Cell 83, 803 (1995) Abstract
Further Categories Containing This Product:
Leukotrienes Other Products
 
 
ALX-430-063 Revised 10-Oct-07
Anthralin
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SYNONYMS Dithranol
PRODUCT LINE Inflammation
PRODUCT CATEGORY Leukotrienes Other Products
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ALX-430-063-G001   1 g 25.00 USD Add To Cart
Product Specification
FORMULA: C14H10O3
MW: 226.2
CAS NUMBER: 1143-38-0
MERCK INDEX: 14: 684
RTECS: CB8927000
PURITY: ≥97% (HPLC)
APPEARANCE: Yellow powder.
SOLUBILITY: Soluble in acetic acid.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HAZARD: MAY BE MUTAGENIC. IRRITANT.

Product Description
Leukotriene biosynthesis inhibitor. Inhibits LTB4 ω-oxidation.
Product Specific Literature References
Anthralin (1,8-dihydroxyanthrone) is a potent inhibitor of leukotriene production and LTB4-omega oxidation by human neutrophils: J.M. Schröder; J. Invest. Dermatol. 87, 624 (1986) Abstract
Further Categories Containing This Product:
Carcinogens & Tumor Promoters Other Products • Cancer Other Products
 
 
ALX-340-020 Revised 24-Nov-08
Prostaglandin F2α
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SYNONYMS Dinoprost
9α,11α,15S-Trihydroxy-prosta-5Z,13E-dien-1-oic acid
PRODUCT LINE Inflammation
PRODUCT CATEGORY Prostaglandins & Prostaglandin Analogs
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ALX-340-020-M001   1 mg 36.00 USD Add To Cart
ALX-340-020-M005   5 mg 162.00 USD Add To Cart
Product Specification
FORMULA: C20H34O5
MW: 354.5
CAS NUMBER: 551-11-1
PURITY: ≥99%
APPEARANCE: White to off-white crystalline solid.
SOLUBILITY: 100mg/ml soluble in 100% ethanol, DMSO or dimethyl formamide; also soluble in aqueous buffers (10mg/ml in PBS, pH 7.2).
SHIPPING: SHIPPED ON BLUE ICE
LONG TERM STORAGE: -20°C
USE/STABILITY: Stable for at least 2 years after receipt when stored at –20°C. We do not recommend storing aqueous solutions for more than one day.

Product Description
Widely distributed prostaglandin occurring in many species.
 
 
ALX-340-022 Revised 29-Aug-08
Prostaglandin J2, 15-Deoxy-Δ12,14-
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PRODUCT LINE Inflammation
PRODUCT CATEGORY Prostaglandins & Prostaglandin Analogs
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-340-022-C500   500 µg 85.00 USD Add To Cart
ALX-340-022-M001   1 mg 150.00 USD Add To Cart
Product Specification
FORMULA: C20H28O3
MW: 316.4
CAS NUMBER: 87893-55-8, 89886-60-2
CONCENTRATION: 1mg/ml
PURITY: ≥97%
FORMULATION: Liquid. Solution in mehtyl acetate.
SOLUBILITY: 20mg/ml soluble in 100% ethanol, DMSO or dimethyl formamide; 2.7mg/ml soluble in PBS, pH 7.2
SHIPPING: SHIPPED ON BLUE ICE
LONG TERM STORAGE: -20°C
USE/STABILITY: Stable for at least 1 year after receipt when stored at -20°C. May polymerize in basic solutions. Keep aqueous solutions on ice and use within 12 hours.
HAZARD: IRRITANT. FLAMMABLE.

Product Description
Suggested natural ligand for the γ-isoform of the nuclear peroxisome proliferator activated receptor (PPARγ).
Product Specific Literature References
Albumin-catalyzed metabolism of prostaglandin D2. Identification of products formed in vitro: F.A. Fitzpatrick and M.A. Wynalda; J. Biol. Chem. 258, 11713 (1983) Abstract; Full Text
9-Deoxy-delta 9, delta 12-13,14-dihydroprostaglandin D2, a metabolite of prostaglandin D2 formed in human plasma: Y. Kikawa, et al.; PNAS 81, 1317 (1984) Abstract
15-Deoxy-delta 12, 14-prostaglandin J2 is a ligand for the adipocyte determination factor PPAR gamma: B.M. Forman, et al.; Cell 83, 803 (1995) Abstract
A prostaglandin J2 metabolite binds peroxisome proliferator-activated receptor gamma and promotes adipocyte differentiation: S.A. Kliewer, et al.; Cell 83, 813 (1995) Abstract
General Information
BACKGROUND/TECHNICAL INFORMATION To change the solvent, evaporate the methyl acetate under a gentle stream of nitrogen and immediately add the solvent of choice.
Further Categories Containing This Product:
PPAR Agonists
 
 
ALX-340-025 Revised 11-Jul-08
8-iso Prostaglandin F2α
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SYNONYMS 8-epi Prostaglandin F2α
8-Isoprostane
PRODUCT LINE Inflammation
PRODUCT CATEGORY Prostaglandins & Prostaglandin Analogs
Ordering Information
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ALX-340-025-M001   1 mg 162.00 USD Add To Cart
ALX-340-025-M005   5 mg 728.00 USD Add To Cart
Product Specification
FORMULA: C20H34O5
MW: 354.5
CAS NUMBER: 27415-26-5
PURITY: ≥99%
APPEARANCE: White to off-white crystalline solid.
SOLUBILITY: 100mg/ml soluble in 100% ethanol, DMSO or dimethyl formamide; also soluble in aqueous buffers (10mg/ml in PBS, pH 7.2).
SHIPPING: SHIPPED ON BLUE ICE
LONG TERM STORAGE: -20°C
USE/STABILITY: Stable for at least 2 years after receipt when stored at -20°C. Stock solutions in organic solvents are stable for 6 months at -20°C. We do not recommend storing aqueous solutions for more than one day. 


Product Description
Potent vasoconstrictor in rat lung and kidney where its effects seem to be mediated through thromboxane receptors. However, evidence exists for a separate and distinct isoprostane receptor. It is also a mitogen in 3T3 cells and in vascular smooth muscle cells; may play a role in pulmonary oxygen toxicity. Thought to be formed via non-enzymatic, free-radical-induced oxidation of unsaturated fatty acids in membrane phospholipids.
Product Specific Literature References
Receptor-mediated mitogenic effect of thromboxane A2 in vascular smooth muscle cells: K. Hanasaki, et al.; Biochem. Pharmacol. 40, 2535 (1990) Abstract
Effects of a novel prostaglandin, 8-epi-PGF2 alpha, in rabbit lung in situ: M. Banerjee, et al.; Am. J. Physiol. 263, H660 (1992) Abstract
Glomerular actions of a free radical-generated novel prostaglandin, 8- epi-prostaglandin F2 alpha, in the rat. Evidence for interaction with thromboxane A2 receptors: K. Takahashi, et al.; J. Clin. Invest. 90, 136 (1992) Abstract
Evidence for the existence of F2-isoprostane receptors on rat vascular smooth muscle cells: M. Fukunaga, et al.; Am. J. Physiol. 264, C1619 (1993) Abstract
Role of nonenzymatically generated prostanoid, 8-iso-PGF2 alpha, in pulmonary oxygen toxicity: C.A. Vacchiano & G.E. Tempel; J. Applied Physiol. 77, 2912 (1994) Abstract
Molecular and functional evidence for the distinct nature of F2- isoprostane receptors from those of thromboxane A2: T. Yura, et al.; Adv. Prostaland. Thromb. Leukotr. 23, 237 (1995) Abstract
 
 
ALX-340-028 Revised 25-Aug-08
Prostaglandin E2
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SYNONYMS Dinoprostone
PRODUCT LINE Inflammation
PRODUCT CATEGORY Prostaglandins & Prostaglandin Analogs
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-340-028-M001   1 mg 28.00 USD Add To Cart
ALX-340-028-M005   5 mg 123.00 USD Add To Cart
ALX-340-028-M010   10 mg 218.00 USD Add To Cart
Product Specification
FORMULA: C20H32O5
MW: