Category: Reagents

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Reference: 14810-10
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17-phenyl trinor PGE2 is a synthetic analog of PGE2. It is an EP1 and EP3 receptor agonist.(3318,1025) 17-phenyl trinor PGE2 is an EP1 and EP3 receptor agonist.1,2 It causes contraction of the guinea pig ileum at a...
Reference: B2005-50
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immunostimulant
Reference: 14810-5
€0.00 (tax incl.)
17-phenyl trinor PGE2 is a synthetic analog of PGE2. It is an EP1 and EP3 receptor agonist.(3318,1025) 17-phenyl trinor PGE2 is an EP1 and EP3 receptor agonist.1,2 It causes contraction of the guinea pig ileum at a...
Reference: B2005-5.1
€0.00 (tax incl.)
immunostimulant
Reference: 14810-500
€0.00 (tax incl.)
17-phenyl trinor PGE2 is a synthetic analog of PGE2. It is an EP1 and EP3 receptor agonist.(3318,1025) 17-phenyl trinor PGE2 is an EP1 and EP3 receptor agonist.1,2 It causes contraction of the guinea pig ileum at a...
Reference: B2006-1000
€0.00 (tax incl.)
cyclic derivative of the neurotransmitter gamma-aminobutyric acid (GABA)
Reference: 14827-1
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A metabolite of estriol; binds to basolateral and canalicular liver plasma membranes (Kds = 85 and 164 µM, respectively); competitively inhibits 4Mu-GlcU hydrolysis and is a substrate for hydrolysis by KLFc
Reference: B2006-5000
€0.00 (tax incl.)
cyclic derivative of the neurotransmitter gamma-aminobutyric acid (GABA)
Reference: 14827-10
€0.00 (tax incl.)
A metabolite of estriol; binds to basolateral and canalicular liver plasma membranes (Kds = 85 and 164 µM, respectively); competitively inhibits 4Mu-GlcU hydrolysis and is a substrate for hydrolysis by KLFc
Reference: 14827-5
€0.00 (tax incl.)
A metabolite of estriol; binds to basolateral and canalicular liver plasma membranes (Kds = 85 and 164 µM, respectively); competitively inhibits 4Mu-GlcU hydrolysis and is a substrate for hydrolysis by KLFc
Reference: 14840-100
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Major urinary metabolite of PGE1 and PGE2 that is used as a marker of PGE2 biosynthesis
Reference: 14840-25
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Major urinary metabolite of PGE1 and PGE2 that is used as a marker of PGE2 biosynthesis
Reference: 14840-50
€0.00 (tax incl.)
Major urinary metabolite of PGE1 and PGE2 that is used as a marker of PGE2 biosynthesis
Reference: B2008-S
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metal halide with thyroid protecting and expectorant properties
Reference: 14910-1
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A PGE2 metabolite found in the semen of primates, including man; potent smooth muscle relaxant and a selective agonist for the EP2 receptor (EC50 = 200 nM for relaxing cat tracheal rings)
Reference: B2008-5.1
€0.00 (tax incl.)
metal halide with thyroid protecting and expectorant properties
Reference: 14910-100
€0.00 (tax incl.)
A PGE2 metabolite found in the semen of primates, including man; potent smooth muscle relaxant and a selective agonist for the EP2 receptor (EC50 = 200 nM for relaxing cat tracheal rings)
Reference: B2008-50
€0.00 (tax incl.)
metal halide with thyroid protecting and expectorant properties
Reference: 14910-50
€0.00 (tax incl.)
A PGE2 metabolite found in the semen of primates, including man; potent smooth muscle relaxant and a selective agonist for the EP2 receptor (EC50 = 200 nM for relaxing cat tracheal rings)
Reference: B2009-S
€0.00 (tax incl.)
selective antagonist of the cysteinyl leukotrienes (LT) C(4), LTD(4) and LTE(4),
Reference: 14910-500
€0.00 (tax incl.)
A PGE2 metabolite found in the semen of primates, including man; potent smooth muscle relaxant and a selective agonist for the EP2 receptor (EC50 = 200 nM for relaxing cat tracheal rings)
Reference: B2009-5.1
€0.00 (tax incl.)
selective antagonist of the cysteinyl leukotrienes (LT) C(4), LTD(4) and LTE(4),
Reference: 14938-100
€0.00 (tax incl.)
An inhibitor of 5α-reductase type II (IC50 = 4.2 nM); 100-fold selective for 5α-reductase type II over type I; does not affect the growth of androgen-refractory PC3 prostate cancer cells but increases the protein...
Reference: B2009-50
€0.00 (tax incl.)
selective antagonist of the cysteinyl leukotrienes (LT) C(4), LTD(4) and LTE(4),
Reference: 14938-250
€0.00 (tax incl.)
An inhibitor of 5α-reductase type II (IC50 = 4.2 nM); 100-fold selective for 5α-reductase type II over type I; does not affect the growth of androgen-refractory PC3 prostate cancer cells but increases the protein...
Reference: B2010-S
€0.00 (tax incl.)
non-steroidal COX inhibitor
Reference: 14938-50
€0.00 (tax incl.)
An inhibitor of 5α-reductase type II (IC50 = 4.2 nM); 100-fold selective for 5α-reductase type II over type I; does not affect the growth of androgen-refractory PC3 prostate cancer cells but increases the protein...
Reference: B2010-5.1
€0.00 (tax incl.)
non-steroidal COX inhibitor
Reference: 14940-1
€0.00 (tax incl.)
20-ethyl PGE2 is an analog of PGE2 in which the ω-chain has been extended by the addition of two methylene carbon atoms. The only well studied prostaglandin analog with this structural feature is unoprostone, an...
Reference: B2010-50
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non-steroidal COX inhibitor
Reference: 14940-10
€0.00 (tax incl.)
20-ethyl PGE2 is an analog of PGE2 in which the ω-chain has been extended by the addition of two methylene carbon atoms. The only well studied prostaglandin analog with this structural feature is unoprostone, an...
Reference: B2011-5.1
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anthelmintic
Reference: 14940-5
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20-ethyl PGE2 is an analog of PGE2 in which the ω-chain has been extended by the addition of two methylene carbon atoms. The only well studied prostaglandin analog with this structural feature is unoprostone, an...
Reference: B2011-5000
€0.00 (tax incl.)
anthelmintic
Reference: 14943-1
€0.00 (tax incl.)
An immediate precursor to cholesterol in the Bloch pathway of cholesterol biosynthesis; reported to activate liver X receptor-target genes in both the liver of cholesterol-free mice and in cholesterol-starved...
Reference: B2012-1000
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synthetic glucocorticoid
Reference: 14943-10
€0.00 (tax incl.)
An immediate precursor to cholesterol in the Bloch pathway of cholesterol biosynthesis; reported to activate liver X receptor-target genes in both the liver of cholesterol-free mice and in cholesterol-starved...
Reference: B2012-5.1
€0.00 (tax incl.)
synthetic glucocorticoid
Reference: 14943-25
€0.00 (tax incl.)
An immediate precursor to cholesterol in the Bloch pathway of cholesterol biosynthesis; reported to activate liver X receptor-target genes in both the liver of cholesterol-free mice and in cholesterol-starved...
Reference: B2012-5000
€0.00 (tax incl.)
synthetic glucocorticoid
Reference: 14943-5
€0.00 (tax incl.)
An immediate precursor to cholesterol in the Bloch pathway of cholesterol biosynthesis; reported to activate liver X receptor-target genes in both the liver of cholesterol-free mice and in cholesterol-starved...
Reference: 14950-1
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A CYP450 ω-oxidation metabolite of PGE2 that preceeds β-oxidation and the loss of up to four carbons from the lower side chain of PGE2
Reference: 14950-100
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A CYP450 ω-oxidation metabolite of PGE2 that preceeds β-oxidation and the loss of up to four carbons from the lower side chain of PGE2
Reference: 14950-50
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A CYP450 ω-oxidation metabolite of PGE2 that preceeds β-oxidation and the loss of up to four carbons from the lower side chain of PGE2
Reference: 14950-500
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A CYP450 ω-oxidation metabolite of PGE2 that preceeds β-oxidation and the loss of up to four carbons from the lower side chain of PGE2
Reference: B2014-S
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inhibitor of organic anion transport, MRP and pannexin-1 channel
Reference: 14990-1
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PGE3 is formed via the COX metabolism of EPA.(1145) In human ocular tissue, it comprises 2.4% of the COX products formed.(1145) When applied to the eyes of a rabbit, a 1 µg dose of PGE3 decreases IOP from 21 mmHg to...
Reference: B2014-1000
€0.00 (tax incl.)
inhibitor of organic anion transport, MRP and pannexin-1 channel
Reference: 14990-100
€0.00 (tax incl.)
PGE3 is formed via the COX metabolism of EPA.(1145) In human ocular tissue, it comprises 2.4% of the COX products formed.(1145) When applied to the eyes of a rabbit, a 1 µg dose of PGE3 decreases IOP from 21 mmHg to...
Reference: B2014-5000
€0.00 (tax incl.)
inhibitor of organic anion transport, MRP and pannexin-1 channel
Reference: 14990-50
€0.00 (tax incl.)
PGE3 is formed via the COX metabolism of EPA.(1145) In human ocular tissue, it comprises 2.4% of the COX products formed.(1145) When applied to the eyes of a rabbit, a 1 µg dose of PGE3 decreases IOP from 21 mmHg to...
Reference: B2014-5.1
€0.00 (tax incl.)
inhibitor of organic anion transport, MRP and pannexin-1 channel
Reference: 14990-500
€0.00 (tax incl.)
PGE3 is formed via the COX metabolism of EPA.(1145) In human ocular tissue, it comprises 2.4% of the COX products formed.(1145) When applied to the eyes of a rabbit, a 1 µg dose of PGE3 decreases IOP from 21 mmHg to...
Reference: B2015-S
€0.00 (tax incl.)
Antioxidant, anti-inflammatory and hypocholesterolemic agent
Reference: 14995-100
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17-trans PGE3 is an isomer of PGE3 which could theoretically result from the COX metabolism of dietary trans-fatty acids.(5470) There are no published reports on the biological activity of this compound.
Reference: B2015-50
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Antioxidant, anti-inflammatory and hypocholesterolemic agent
Reference: 14995-25
€0.00 (tax incl.)
17-trans PGE3 is an isomer of PGE3 which could theoretically result from the COX metabolism of dietary trans-fatty acids.(5470) There are no published reports on the biological activity of this compound.
Reference: B2015-5.1
€0.00 (tax incl.)
Antioxidant, anti-inflammatory and hypocholesterolemic agent
Reference: 14995-50
€0.00 (tax incl.)
17-trans PGE3 is an isomer of PGE3 which could theoretically result from the COX metabolism of dietary trans-fatty acids.(5470) There are no published reports on the biological activity of this compound.
Reference: B2016-S
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thioamide derivative with antitubercular activity
Reference: 15008-10
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A third generation, irreversible steroidal aromatase inhibitor (Ki = 10.2 nM; Kinact = 26 nM) that induces aromatase degradation, which leads to a decrease in estrogen levels in plasma
Reference: B2016-100
€0.00 (tax incl.)
thioamide derivative with antitubercular activity
Reference: 15008-25
€0.00 (tax incl.)
A third generation, irreversible steroidal aromatase inhibitor (Ki = 10.2 nM; Kinact = 26 nM) that induces aromatase degradation, which leads to a decrease in estrogen levels in plasma
Reference: B2016-5.1
€0.00 (tax incl.)
thioamide derivative with antitubercular activity
Reference: 15008-5
€0.00 (tax incl.)
A third generation, irreversible steroidal aromatase inhibitor (Ki = 10.2 nM; Kinact = 26 nM) that induces aromatase degradation, which leads to a decrease in estrogen levels in plasma
Reference: B2016-500
€0.00 (tax incl.)
thioamide derivative with antitubercular activity
Reference: 15008-50
€0.00 (tax incl.)
A third generation, irreversible steroidal aromatase inhibitor (Ki = 10.2 nM; Kinact = 26 nM) that induces aromatase degradation, which leads to a decrease in estrogen levels in plasma
Reference: B2017-S
€0.00 (tax incl.)
a form of vitamin B6
Reference: 15010-1
€0.00 (tax incl.)
PGF1α is the putative metabolite of DGLA via the COX pathway. Both PGF1α and PGF2α have been shown to act as priming pheromones for male Atlantic salmon with a threshold concentration of 10−11 M.(3467) PGF1α binds to...
Reference: B2017-5.1
€0.00 (tax incl.)
a form of vitamin B6
Reference: 15010-10
€0.00 (tax incl.)
PGF1α is the putative metabolite of DGLA via the COX pathway. Both PGF1α and PGF2α have been shown to act as priming pheromones for male Atlantic salmon with a threshold concentration of 10−11 M.(3467) PGF1α binds to...
Reference: B2017-100
€0.00 (tax incl.)
a form of vitamin B6
Reference: 15010-5
€0.00 (tax incl.)
PGF1α is the putative metabolite of DGLA via the COX pathway. Both PGF1α and PGF2α have been shown to act as priming pheromones for male Atlantic salmon with a threshold concentration of 10−11 M.(3467) PGF1α binds to...
Reference: B2017-500
€0.00 (tax incl.)
a form of vitamin B6
Reference: 15020-1
€0.00 (tax incl.)
PGF1α alcohol is an analog of PGF1α with a primary alcohol replacing the C-1 carboxyl group. There are no published reports on the biological activity of this compound; however, the corresponding PGE1 analog (Item No....
Reference: B2018-S
€0.00 (tax incl.)
cholecystokinin type 1 (CCK1) receptor inhibitor
Reference: 15020-10
€0.00 (tax incl.)
PGF1α alcohol is an analog of PGF1α with a primary alcohol replacing the C-1 carboxyl group. There are no published reports on the biological activity of this compound; however, the corresponding PGE1 analog (Item No....
Reference: B2018-5.1
€0.00 (tax incl.)
cholecystokinin type 1 (CCK1) receptor inhibitor
Reference: 15020-5
€0.00 (tax incl.)
PGF1α alcohol is an analog of PGF1α with a primary alcohol replacing the C-1 carboxyl group. There are no published reports on the biological activity of this compound; however, the corresponding PGE1 analog (Item No....
Reference: B2018-1000
€0.00 (tax incl.)
cholecystokinin type 1 (CCK1) receptor inhibitor
Reference: 15076-100
€0.00 (tax incl.)
A saturated DAG with lauric acid (12:0) side-chains attached at both the sn-1 and sn-2 positions
Reference: B2018-5000
€0.00 (tax incl.)
cholecystokinin type 1 (CCK1) receptor inhibitor
Reference: 15076-250
€0.00 (tax incl.)
A saturated DAG with lauric acid (12:0) side-chains attached at both the sn-1 and sn-2 positions
Reference: B2019-10
€0.00 (tax incl.)
Pleuromutilin antibiotic,protein synthesis inhibitor
Reference: 15076-500
€0.00 (tax incl.)
A saturated DAG with lauric acid (12:0) side-chains attached at both the sn-1 and sn-2 positions
Reference: B2019-5.1
€0.00 (tax incl.)
Pleuromutilin antibiotic,protein synthesis inhibitor
Reference: 15077-100
€0.00 (tax incl.)
A saturated DAG with myristic acid (14:0) side-chains attached at both the sn-1 and sn-2 positions
Reference: B2020-S
€0.00 (tax incl.)
rystalline pentose alcohol
Reference: 15077-250
€0.00 (tax incl.)
A saturated DAG with myristic acid (14:0) side-chains attached at both the sn-1 and sn-2 positions
Reference: B2020-5.1
€0.00 (tax incl.)
rystalline pentose alcohol
Reference: 15077-500
€0.00 (tax incl.)
A saturated DAG with myristic acid (14:0) side-chains attached at both the sn-1 and sn-2 positions
Reference: B2020-500
€0.00 (tax incl.)
rystalline pentose alcohol

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