A0937

(±)-Norepinephrine (+)-bitartrate salt

Name: (±)-Norepinephrine (+)-bitartrate salt
Brand: SIGMA
Price: 126 USD
Availability: InStock

≥97% (TLC), powder, adrenergic neurotransmitter

Sinónimos:

(±)-Arterenol (+)-bitartrate salt, (±)-Noradrenalin (+)-bitartrate salt, 1-(3,4-Dihydroxyphenyl)-2-aminoethanol (+)-bitartrate salt, 3,4-Dihydroxyphenylethanolamine (+)-bitartrate salt

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1 G

$126.00

5 G

$480.00

$126.00

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Fórmula empírica (notación de Hill):

C₈H₁₁NO₃ · C₄H₆O₆

Número CAS:

3414-63-9

Peso molecular:

319.26

NACRES:

NA.77

PubChem Substance ID:

24278207

UNSPSC Code:

12352200

EC Number:

222-307-0

MDL number:

MFCD00132876

Form:

powder

Quality level:

200

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Nombre del producto

(±)-Norepinephrine (+)-bitartrate salt,

InChI

1S/C8H11NO3.C5H8O5/c9-4-8(12)5-1-2-6(10)7(11)3-5;1-2(4(7)8)3(6)5(9)10/h1-3,8,10-12H,4,9H2;2-3,6H,1H3,(H,7,8)(H,9,10)/t;2-,3-/m.1/s1

InChI key

PDZZSMDCBWCGRN-GEHKUQKJSA-N

SMILES string

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

form

powder

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Este artículo	A9512	N5785	489350
Sigma-Aldrich A0937 (±)-Norepinephrine (+)-bitartrate salt	Sigma-Aldrich A9512 L-(−)-Norepinephrine (+)-bitartrate salt monohydrate	Sigma-Aldrich N5785 L-(−)-Norepinephrine (+)-bitartrate salt monohydrate	Sigma-Aldrich 489350 L-(–)-Norepinephrine-(+)-bitartrate
form powder	form solid	form solid	form crystalline solid
Quality Level 200	Quality Level 200	Quality Level 200	Quality Level 100
Gene Information human ... ADRA1A(148), ADRA1B(147), ADRA1D(146), ADRA2A(150), ADRA2B(151), ADRA2C(152), ADRB1(153), ADRB2(154), ADRB3(155)	Gene Information -	Gene Information -	Gene Information -

Biochem/physiol Actions

Adrenergic neurotransmitter

Features and Benefits

This compound is featured on the α1-Adrenoceptors, α2-Adrenoceptors and β-Adrenoceptors pages of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

pictograms

GHS06

signalword

Danger

hcodes

H300 + H310 + H330

pcodes

P260 - P262 - P264 - P280 - P302 + P352 + P310 - P304 + P340 + P310

Hazard Classifications

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

Clase de almacenamiento

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

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Impact of diet and stress on the development of preeclampsia-like symptoms in p57kip2 mice.

Stéphanie Falcao et al.

American journal of physiology. Heart and circulatory physiology, 296(1), H119-H126 (2008-11-04)

The cyclin-dependent kinase inhibitor p57(kip2) regulates the cell cycle of trophoblastic cells. It has been established by a Japanese group that the heterozygous p57(kip2) knockout (p57(-/+)) mice are a good model of preeclampsia as they develop hypertension, proteinuria, and placental

[Hypovolemic shock during pregnancy].

E M Shifman

Anesteziologiia i reanimatologiia, (6)(6), 63-66 (2013-05-15)

Behavioral and plasma monoamine responses to high-speed railway noise stress in mice.

Guoqing Di et al.

Noise & health, 15(65), 217-223 (2013-06-19)

Studies have reported that railway noise causes stress responses. To evaluate the effects of high-speed railway (HSR) noise on behaviors and plasma monoamines. Institute of cancer research mice were exposed to previously recorded HSR noise for 53 days. The noise

[Tapentadol prolonged release for severe chronic pain. Results of a non-interventional study involving general practitioners and internists].

Andreas Schwittay

MMW Fortschritte der Medizin, 155(1), 64-64 (2013-04-12)

Assessment of the 18F-labeled PET tracer LMI1195 for imaging norepinephrine handling in rat hearts.

Takahiro Higuchi et al.

Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 54(7), 1142-1146 (2013-05-15)

A novel (18)F-labeled tracer, LMI1195 (N-[3-bromo-4-(3-(18)F-fluoro-propoxy)-benzyl]-guanidine), is being developed for sympathetic nerve imaging; its high specificity for neural uptake-1 mechanism has previously been demonstrated in cell associative studies and in rabbit and nonhuman primate studies assessing heart uptake. The aim

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(±)-Norepinephrine (+)-bitartrate salt