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51-40-1

51-40-1 structure
51-40-1 structure
  • Name: Noradrenaline tartrate
  • Chemical Name: l-Noradrenaline tartrate
  • CAS Number: 51-40-1
  • Molecular Formula: C12H17NO9
  • Molecular Weight: 319.265
  • Catalog: API Circulatory system medication Anti-shock vasoactive drug
  • Create Date: 2018-09-30 22:02:23
  • Modify Date: 2024-01-04 11:36:26
  • Norepinephrine tartrate (Levarterenol tartrate), a naturally occurring chemical in the body that acts as both a stress hormone and neurotransmitter, is a β1-selective adrenergic receptor agonist with EC50 of 5.37 μM.

Name l-Noradrenaline tartrate
Synonyms Norepinephrine Bitartrate
l-noradrenalinetartrate
noradrenaline bitartrate
Levarterenolbitartrate
MFCD00036384
4-(2-Amino-1-hydroxyethyl)benzene-1,2-diol 2,3-dihydroxysuccinate (1:1)
Leverterenol bitartrate
noradrenalinetartrate
4-(2-Amino-1-hydroxyethyl)-1,2-benzenediol 2,3-dihydroxysuccinate (1:1)
1,2-Benzenediol, 4-(2-amino-1-hydroxyethyl)-, 2,3-dihydroxybutanedioate (1:1) (salt)
L-ARTERENOL BITARTRATE
Noradrenalineacidtartrate
4-(2-amino-1-hydroxyethyl)benzene-1,2-diol 2,3-dihydroxybutanedioate (1:1)
NORADRENALINE
EINECS 200-095-0
Levoarterenol bitartrate
Description Norepinephrine tartrate (Levarterenol tartrate), a naturally occurring chemical in the body that acts as both a stress hormone and neurotransmitter, is a β1-selective adrenergic receptor agonist with EC50 of 5.37 μM.
Related Catalog
Target

EC50: 5.37 μM (β1-selective adrenergic receptor)[1].

In Vitro Norepinephrine (NE) bitartrate monohydrate is generally considered to be a β1-subtype selective adrenergic agonist. Norepinephrine (NE) also has direct activity at the β2-adrenoceptor in higher concentrations[1]. Adipocytes from the inguinal fat pad (iWA) or the interscapular fat pad (BA) are isolated from neonatal wild-type C57BL/6J mice and cultured. To examine the effect of activating AT2 upon β-adrenergic signaling, cAMP production is first assessed in response to Norepinephrine (NE, 10 µM) with or without CGP (10 nM) co-treatment[2]. Norepinephrine (NE) increases cAMP as expected in iWA, and CGP does not alter this effect Norepinephrine (NE) is also known to induce lipolysis, and liberated fatty acids are required to functionally activate UCP1 protein and to stimulate heat production. CREB phosphorylation at Ser133 is increased after Norepinephrine (NE) treatment and significantly attenuated with CGP co-treatment in mouse iWA[2]. RT-PCR[2] Cell Line: Subcutaneous preadipocytes Adipocytes. Concentration: 10 μM. Incubation Time: 6 hours. Result: AT2 activation suppressed Norepinephrine induced UCP1 in white adipocytes (iWA)
References

[1]. MacGregor DA, et al. Relative efficacy and potency of beta-adrenoceptor agonists for generating cAMP in human lymphocytes. Chest. 1996 Jan;109(1):194-200.

[2]. Littlejohn NK, et al. Suppression of Resting Metabolism by the Angiotensin AT2 Receptor. Cell Rep. 2016 Aug 9;16(6):1548-60.

Boiling Point 442.6ºC at 760 mmHg
Molecular Formula C12H17NO9
Molecular Weight 319.265
Flash Point 221.5ºC
Exact Mass 319.090332
PSA 201.77000

CHEMICAL IDENTIFICATION

RTECS NUMBER :
DN6750000
CAS REGISTRY NUMBER :
51-40-1
LAST UPDATED :
199504
DATA ITEMS CITED :
6
MOLECULAR FORMULA :
C8-H11-N-O3.C4-H6-O6
MOLECULAR WEIGHT :
319.30
WISWESSER LINE NOTATION :
Z1YQR CQ DQ &OVYQYQVO

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
3987 ug/kg
TOXIC EFFECTS :
Behavioral - excitement
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
210 ug/kg
TOXIC EFFECTS :
Sense Organs and Special Senses (Eye) - lacrimation Behavioral - convulsions or effect on seizure threshold Lungs, Thorax, or Respiration - respiratory stimulation
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
26800 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1025 ug/kg
TOXIC EFFECTS :
Behavioral - convulsions or effect on seizure threshold Lungs, Thorax, or Respiration - dyspnea Lungs, Thorax, or Respiration - other changes

MUTATION DATA

TYPE OF TEST :
Mutation in mammalian somatic cells
TEST SYSTEM :
Rodent - mouse Lymphocyte
DOSE/DURATION :
100 mg/L
REFERENCE :
EMMUEG Environmental and Molecular Mutagenesis. (Alan R. Liss, Inc., 41 E. 11th St., New York, NY 10003) V.10- 1987- Volume(issue)/page/year: 11,523,1988 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X5302 No. of Facilities: 7 (estimated) No. of Industries: 1 No. of Occupations: 2 No. of Employees: 628 (estimated) No. of Female Employees: 314 (estimated)
Hazard Codes T+
Safety Phrases S22-S24/25
RIDADR UN 3249
Packaging Group III
Hazard Class 6.1(b)
HS Code 2922210000
HS Code 2922509090
Summary 2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%