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4-Phenoxybutan-1-amine
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4-Phenoxybutan-1-amine
Artikel-Nr:
(PRSI30-046)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
30-046
Lokale Artikelnummer::
PRSI30-046
Beschreibung:
Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes and ammonia in the presence of copper and quinone cofactor. The protein contains several conserved motifs including the active site of amine oxidases and the histidine residues that likely bind copper. It may be a critical modulator of signal transmission in retina, possibly by degrading the biogenic amines dopamine, histamine, and putrescine.Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes and ammonia in the presence of copper and quinone cofactor. This gene shows high sequence similarity to copper amine oxidases from various species ranging from bacteria to mammals. The protein contains several conserved motifs including the active site of amine oxidases and the histidine residues that likely bind copper. It may be a critical modulator of signal transmission in retina, possibly by degrading the biogenic amines dopamine, histamine, and putrescine. This gene may be a candidate gene for hereditary ocular diseases. Alternate splicing results in multiple transcript variants.
VE:
1 * 50 µG
Lieferant:
MACHEREY-NAGEL
Beschreibung:
Spezielle GC-Phase zur Analyse von Aminen.
Lieferant:
Sigma-Aldrich
Beschreibung:
2-Aminopurin, Sigma-Aldrich®
Lieferant:
FLUOROCHEM
Beschreibung:
5-Amino-2-chlorpyridin
Artikel-Nr:
(EDQMY0000769)
Lieferant:
EDQM
Hersteller-Artikelnummer::
Y0000769
Lokale Artikelnummer::
EDQMY0000769
Beschreibung:
Organic Standard, Promethazine impurity D, (2RS)-N,N-dimethyl-1-(10H-phenothiazin-10-yl)propan-2-amine S-oxide
VE:
1 * 15 mg
Artikel-Nr:
(EDQMY0000507)
Lieferant:
EDQM
Hersteller-Artikelnummer::
Y0000507
Lokale Artikelnummer::
EDQMY0000507
Beschreibung:
Organic Standard, Chlorpromazine impurity A, 3-(2-chloro-10H-phenothiazin-10-amine S-oxide (chlorpromazine, Ph. Eur. standard
VE:
1 * 15 mg
Lieferant:
BIONET RESEARCH
Beschreibung:
2-Amino-4-phenylthiazol
Lieferant:
Sigma-Aldrich
Beschreibung:
Adenin, Sigma-Aldrich®
Lieferant:
EDQM
Beschreibung:
Organic Standard, Azathioprine impurity A, 1-methyl-4-nitro-1H-imidazol-5-amine, Ph. Eur. standard
Artikel-Nr:
(BOSSBS-4176R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4176R-A750
Lokale Artikelnummer::
BOSSBS-4176R-A750
Beschreibung:
Functions as a polyspecific organic cation transporter, efficiently transporting many organic cations such as monoamine neurotransmitters 1-methyl-4-phenylpyridinium and biogenic amines including serotonin, dopamine, norepinephrine and epinephrine. May play a role in regulating central nervous system homeostasis of monoamine neurotransmitters. May be involved in luminal transport of organic cations in the kidney and seems to use luminal proton gradient to drive organic cation reabsorption. Does not seem to transport nucleoside and nucleoside analogs such as uridine, cytidine, thymidine, adenosine, inosine, guanosine, and azidothymidine. In (PubMed:16873718) adenosine is efficiently transported but in a fashion highly sensitive to extracellular pH, with maximal activity in the pH range 5.5 to 6.5. Glu-206 is essential for the cation selectivity and may function as the charge sensor for cationic substrates. Transport is chloride and sodium-independent but appears to be sensitive to changes in membrane potential. Weakly inhibited by the classical inhibitors of equilibrative nucleoside transport, dipyridamole, dilazep, and nitrobenzylthioinosine. May play a role in the regulation of extracellular adenosine concentrations in cardiac tissues, in particular during ischemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4176R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4176R-A555
Lokale Artikelnummer::
BOSSBS-4176R-A555
Beschreibung:
Functions as a polyspecific organic cation transporter, efficiently transporting many organic cations such as monoamine neurotransmitters 1-methyl-4-phenylpyridinium and biogenic amines including serotonin, dopamine, norepinephrine and epinephrine. May play a role in regulating central nervous system homeostasis of monoamine neurotransmitters. May be involved in luminal transport of organic cations in the kidney and seems to use luminal proton gradient to drive organic cation reabsorption. Does not seem to transport nucleoside and nucleoside analogs such as uridine, cytidine, thymidine, adenosine, inosine, guanosine, and azidothymidine. In (PubMed:16873718) adenosine is efficiently transported but in a fashion highly sensitive to extracellular pH, with maximal activity in the pH range 5.5 to 6.5. Glu-206 is essential for the cation selectivity and may function as the charge sensor for cationic substrates. Transport is chloride and sodium-independent but appears to be sensitive to changes in membrane potential. Weakly inhibited by the classical inhibitors of equilibrative nucleoside transport, dipyridamole, dilazep, and nitrobenzylthioinosine. May play a role in the regulation of extracellular adenosine concentrations in cardiac tissues, in particular during ischemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4176R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4176R-CY5.5
Lokale Artikelnummer::
BOSSBS-4176R-CY5.5
Beschreibung:
Functions as a polyspecific organic cation transporter, efficiently transporting many organic cations such as monoamine neurotransmitters 1-methyl-4-phenylpyridinium and biogenic amines including serotonin, dopamine, norepinephrine and epinephrine. May play a role in regulating central nervous system homeostasis of monoamine neurotransmitters. May be involved in luminal transport of organic cations in the kidney and seems to use luminal proton gradient to drive organic cation reabsorption. Does not seem to transport nucleoside and nucleoside analogs such as uridine, cytidine, thymidine, adenosine, inosine, guanosine, and azidothymidine. In (PubMed:16873718) adenosine is efficiently transported but in a fashion highly sensitive to extracellular pH, with maximal activity in the pH range 5.5 to 6.5. Glu-206 is essential for the cation selectivity and may function as the charge sensor for cationic substrates. Transport is chloride and sodium-independent but appears to be sensitive to changes in membrane potential. Weakly inhibited by the classical inhibitors of equilibrative nucleoside transport, dipyridamole, dilazep, and nitrobenzylthioinosine. May play a role in the regulation of extracellular adenosine concentrations in cardiac tissues, in particular during ischemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4176R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4176R-CY5
Lokale Artikelnummer::
BOSSBS-4176R-CY5
Beschreibung:
Functions as a polyspecific organic cation transporter, efficiently transporting many organic cations such as monoamine neurotransmitters 1-methyl-4-phenylpyridinium and biogenic amines including serotonin, dopamine, norepinephrine and epinephrine. May play a role in regulating central nervous system homeostasis of monoamine neurotransmitters. May be involved in luminal transport of organic cations in the kidney and seems to use luminal proton gradient to drive organic cation reabsorption. Does not seem to transport nucleoside and nucleoside analogs such as uridine, cytidine, thymidine, adenosine, inosine, guanosine, and azidothymidine. In (PubMed:16873718) adenosine is efficiently transported but in a fashion highly sensitive to extracellular pH, with maximal activity in the pH range 5.5 to 6.5. Glu-206 is essential for the cation selectivity and may function as the charge sensor for cationic substrates. Transport is chloride and sodium-independent but appears to be sensitive to changes in membrane potential. Weakly inhibited by the classical inhibitors of equilibrative nucleoside transport, dipyridamole, dilazep, and nitrobenzylthioinosine. May play a role in the regulation of extracellular adenosine concentrations in cardiac tissues, in particular during ischemia.
VE:
1 * 100 µl
Artikel-Nr:
(FLUO033441-1G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
033441-1G
Lokale Artikelnummer::
FLUO033441-1G
Beschreibung:
2-Amino-5-fluorbenzothiazol
VE:
1 * 1 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(MOLEM22156050)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M22156050
Lokale Artikelnummer::
MOLEM22156050
Beschreibung:
8-Bromadenin
VE:
1 * 250 mg
This is a MarketSource item. Additional charges may apply
Lieferant:
VARIAN
Beschreibung:
CP-Sil 8 CB für Amine ist eine basendeaktivierte 5% Phenylpolydimethylsiloxan-Säule, die für eine Vielzahl von Aminen verwendet werden kann.
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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