Indométhacine, > = 99% (TLC)

Code: i7378-25g D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Indomethacin has been used:as a medium supplement in osteogenic and adipogenic differentiation assays in human bone marrow stem cellsas a medium supplement in bov...


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Votre prix
£169.00 25G

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Indomethacin has been used:as a medium supplement in osteogenic and adipogenic differentiation assays in human bone marrow stem cellsas a medium supplement in bovine amniotic fluid stem cells (BAFSCs) culturein the inhibition of prostaglandin E2 (PGE2) in T cells

Biochem/physiol Actions

Cyclooxygenase (COX) inhibitor that is relatively selective for COX-1.

Features and Benefits

This compound was developed by Pfizer. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

This compound is featured on the Prostanoid Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

This compound is a featured product for ADME Tox research. Click here to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

General description

Indomethacin is an inhibitor of the enzyme cyclooxygenase 1 and 2. Indomethacin elicits side effects in gastrointestinal tract, kidney and cerebrum. Indomethacin, along with ibuprofen, is effective for treating patent ductus arteriosus (PDA) in infants with respiratory distress syndrome. Rectal indomethacin is effective in treating endoscopic retrograde cholangiography (ERCP) induced pancreatitis.

Packaging

10, 25, 100 g in glass bottle

assay98.5-100.5% (in accordance with EP)
biological sourcesynthetic
formpowder or crystals
Gene Informationhuman ... ALB(213), ALOX5(240), ELA2(1991), GPR44(11251), IL1A(3552), PLA2G1B(5319), PTGDR(5729), PTGS1(5742), PTGS2(5743)mouse ... Alox5(11689), Ptgdr(19214), Ptger1(19216), Ptger2(19217), Ptger3(19218), Ptger4(19219), Ptgs1(19224)rat ... Alox5(25290), Ptgs1(24693), Ptgs2(29527)
InChI keyCGIGDMFJXJATDK-UHFFFAOYSA-N
InChI1S/C19H16ClNO4/c1-11-15(10-18(22)23)16-9-14(25-2)7-8-17(16)21(11)19(24)12-3-5-13(20)6-4-12/h3-9H,10H2,1-2H3,(H,22,23)
loss≤0.5% loss on drying
mode of actionenzyme | inhibits
mp158-162 °C
originatorPfizer
Quality Level200
SMILES stringCOc1ccc2n(c(C)c(CC(O)=O)c2c1)C(=O)c3ccc(Cl)cc3
Code
Description
Unité de vente
Prix annoncé
Qté
I7378-5G
Unité:5G
Prix annoncé: £40.60
Source:Prix annoncé
I7378-100G
Unité:100G
Prix annoncé: £352.00
Source:Prix annoncé
I7378-10G
Unité:10G
Prix annoncé: £82.40
Source:Prix annoncé
Cas Number53-86-1
Hazard Class6.1
Un Number2811
Pack GroupI
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