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Merck

A7257

(−)-Norepinephrine

≥98% (TLC), crystalline, adrenergic neurotransmitter

Synonim(y):

(R)-4-(2-Amino-1-hydroxyethyl)-1,2-benzenediol, L-Arterenol, L-Noradrenaline, Levarterenol

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Wybierz wielkość

500 MG

1430,00 zł

1 G

1970,00 zł

5 G

7110,00 zł

1430,00 zł


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Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C8H11NO3
Numer CAS:
Masa cząsteczkowa:
169.18
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
200-096-6
MDL number:
Beilstein/REAXYS Number:
2804840
Assay:
≥98%
Form:
crystalline
Quality level:

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Nazwa produktu

(−)-Norepinephrine, ≥98%, crystalline

InChI key

SFLSHLFXELFNJZ-QMMMGPOBSA-N

InChI

1S/C8H11NO3/c9-4-8(12)5-1-2-6(10)7(11)3-5/h1-3,8,10-12H,4,9H2/t8-/m0/s1

SMILES string

NC[C@H](O)c1ccc(O)c(O)c1

assay

≥98%

form

crystalline

color

off-white to tan

storage temp.

−20°C

Quality Level

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Ta pozycja
SML0675489350A9512
assay

≥98%

assay

≥95% (HPLC)

assay

≥97% (LC/MS)

assay

≥99%

form

crystalline

form

powder

form

crystalline solid

form

solid

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

200

storage temp.

−20°C

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

-

color

off-white to tan

color

white to light brown

color

white

color

white

Gene Information

human ... ADRA1A(148), ADRA1B(147), ADRA1D(146), ADRA2A(150), ADRA2B(151), ADRA2C(152), ADRB1(153), ADRB2(154), ADRB3(155)
rat ... Adra1a(29412), Adra1d(29413), Adra2a(25083), Adrb1(24925), Adrb2(24176), Drd1a(24316), Drd2(24318)

Gene Information

-

Gene Information

-

Gene Information

-

General description

Norepinephrine is a neurotransmitter found in both the peripheral and central nervous systems. It triggers effects associated with the ′fight or flight′ response and is mediated by the family of adrenergic receptors. Structurally, it is a catecholamine due to the presence of the catechol moiety (consisting of two hydroxyl groups on a benzene ring) and an amine (NH2) group.[1] Norepinephrine exhibits pharmacologic effects on α1 and β1 adrenoceptors. It does not elevate heart rate. The primary advantage of norepinephrine is to improve organ perfusion by increasing vascular tone. Compared to dopamine, norepinephrine is more effective at achieving targeted endpoints, less metabolically active than epinephrine, and reduces serum lactate levels. Moreover, it notably enhances renal perfusion and splanchnic blood flow in sepsis, especially when used alongside dobutamine.[2] Norepinephrine is used in the treatment of hypotension, depression, schizophrenia, and attention deficit/hyperactivity disorders.

Application

(−)-Norepinephrine has been used:
  • as anαand β-AR agonist to stimulate mouse organoids to study the pathways that are activated upon intestinal epithelial adrenergic receptor (AR) stimulation[3],
  • to measure the monoamine levels in various limbic regions of mouse brains by high-performance liquid chromatography (HPLC) coupled with an electrochemical equipped with an auto-sampler[4],
  • as a dispersal agent in biofilm dispersion assay to study its effects on the dispersal of Mannheimia haemolytica biofilms[5]

Features and Benefits

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

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral

Klasa składowania

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

ppe

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


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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Role of the stress-associated chemicals norepinephrine, epinephrine and substance P in dispersal of Mannheimia haemolytica from biofilms
Pillai DK, et al.
Veterinary Microbiology, 215, 11-17 (2018)
Kelly Del Tredici et al.
Journal of neurology, neurosurgery, and psychiatry, 84(7), 774-783 (2012-10-16)
Although resting tremor, cogwheel rigidity, hypokinesia/bradykinesia and postural instability usually dominate the clinical picture of sporadic Parkinson's disease (PD), both clinical and epidemiological data reveal that a wide variety of additional symptoms impair patients' quality of life considerably, parallel to
Ophiocordyceps formosana improves hyperglycemia and depression-like behavior in an STZ-induced diabetic mouse model
Huang CW, et al.
BMC Complementary and Alternative Medicine, 16, 1-11 (2016)
Norepinephrine: not too much, too long
Martin C, et al.
Shock, 44, 305-309 (2015)
Infectious diseases and biologic weapons
Neligan P
The Journal of Biological Chemistry, 369-400 (2012)

Produkty

DISCOVER Bioactive Small Molecules for Neuroscience

Questions

1–4 of 4 Questions  
  1. How should Product A7257, (-)-Norepinephrine, be dissolved?

    1 answer
    1. This product is soluble in 0.5M HCl at a concentration of 50mg/mL, yielding a clear faint yellow solution.

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  2. How long is a solution of Product A7257, (-)-Norepinephrine, stable?

    1 answer
    1. A stock solution of 1 mg/ml or greater may be stored frozen in aliquots. Avoid freeze-thaw cycles. When the solution gets a pink cast, the product has degraded.

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  3. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

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  4. What are the differences between Product No. A7257, (-)-Norepinephrine and Product No. A0937, (±)-Norepinephrine (+)-bitartrate salt?

    1 answer
    1. Product No. A7257, is the free base form of the (-) isomer; it is not water soluble. Product No. A0937 is the bitartrate salt of the racemic (+/-) mixture; it is soluble in water at a concentration of 50 mg/mL.

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