Direkt zum Inhalt
Merck
Alle Fotos(1)

Wichtige Dokumente

Gesamtdokumentation anzeigen

17809

Sigma-Aldrich

(−)-Epinephrin -(+)-bitartratsalz

tested according to Ph. Eur.

Synonym(e):

Adrenalini tartras, L-3,4-Dihydroxy-α-(methylaminomethyl)benzylalkohol-Wasserstoff D -bitartrat (Salz), L-Adrenalin -(+)-bitartratsalz, L-Adrenalin D-bitartrat, L-Epinephrin D-bitartrat

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(1)

About This Item

Empirische Formel (Hill-System):
C9H13NO3 · C4H6O6
CAS-Nummer:
51-42-3
Molekulargewicht:
333.29
EG-Nummer:
200-097-1
MDL-Nummer:
MFCD00035077
UNSPSC-Code:
12352200
PubChem Substanz-ID:
57647680

Agentur

tested according to Ph. Eur.

Qualitätsniveau

100

Löslichkeit

water: soluble 1 gm in 3 ml
alcohol: slightly soluble
chloroform: insoluble
diethyl ether: insoluble

Anwendung(en)

pharmaceutical (small molecule)

SMILES String

O[C@H]([C@@H](O)C(O)=O)C(O)=O.CNC[C@H](O)c1ccc(O)c(O)c1

InChI

1S/C9H13NO3.C4H6O6/c1-10-5-9(13)6-2-3-7(11)8(12)4-6;5-1(3(7)8)2(6)4(9)10/h2-4,9-13H,5H2,1H3;1-2,5-6H,(H,7,8)(H,9,10)/t9-;1-,2-/m01/s1

InChIKey

YLXIPWWIOISBDD-NDAAPVSOSA-N

Angaben zum Gen

human ... ADRA1A(148) , ADRA1B(147) , ADRA1D(146) , ADRA2A(150) , ADRA2B(151) , ADRA2C(152) , ADRB1(153) , ADRB2(154) , ADRB3(155)

Suchen Sie nach ähnlichen Produkten? Aufrufen Leitfaden zum Produktvergleich

Anwendung

(-)-Epinephrine (+)-bitartrate salt has been used for studying the active calcium uptake by rainbow trout skin. It has also been used in oxygen-derived oxidant assays for assessing the susceptibility of C. neoformans biofilms to antimicrobial molecules.

Biochem./physiol. Wirkung

(-)-Epinephrine (+)-bitartrate salt is an α,β-adrenergic receptor agonist. It inhibits the lipolysis completely and can overcome the antilipolytic impact of insulin in perifused isolated fat cell.
Adrenergischer Rezeptoragonist.

Piktogramme

Skull and crossbones
GHS06

Signalwort

Danger

H-Sätze

H300

Gefahreneinstufungen

Acute Tox. 1 Oral

Lagerklassenschlüssel

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

S S Solomon et al.
The Journal of laboratory and clinical medicine, 88(6), 984-994 (1976-12-01)
Development of a perifusion system utilizing isolated fat cells (IFC) has converted the static incubation system into one capable of measuring dynamic changes in adipose tissue metabolism. Using this new system, we have studied the initiation by epinephrine and inhibition
Luis R Martinez et al.
Infection and immunity, 74(11), 6118-6123 (2006-10-24)
The human pathogenic fungus Cryptococcus neoformans can form biofilms on polystyrene plates and medical devices in a process that requires capsular polysaccharide release. Although biofilms are known to be less susceptible to antimicrobial drugs, little is known about their susceptibility
W S Marshall et al.
The Journal of experimental biology, 166, 297-316 (1992-05-01)
The skin overlying the cleithrum bone of freshwater-acclimated rainbow trout contains numerous mitochondria-rich (MR) cells, as detected by DASPEI fluorescence. This tissue was mounted in vitro in an Ussing-style chamber with fresh water on the mucosal surface and saline supplemented
Yangjie Wei et al.
AAPS PharmSciTech, 16(2), 455-465 (2014-11-02)
Several attempts have been made to mask the bitter taste of oral formulations, but none have been made for injectable formulations. This study aims to mask the bitter taste of dental lidocaine HCl (LID) injection using hydroxypropyl-β-cyclodextrin (HP-β-CD) and sodium
Margot Van der Jeught et al.
Cellular reprogramming, 17(3), 170-180 (2015-06-09)
In mice, inhibition of both the fibroblast growth factor (FGF) mitogen-activated protein kinase kinase/extracellular-signal regulated kinase (MEK/Erk) and the Wnt signaling inhibitor glycogen synthase-3β (GSK3β) enables the derivation of mouse embryonic stem cells (mESCs) from nonpermissive strains in the presence
Alle zugehörigen Dokumente anzeigen

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

Setzen Sie sich mit dem technischen Dienst in Verbindung.