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58331-17-2

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58331-17-2 Usage

Uses

Different sources of media describe the Uses of 58331-17-2 differently. You can refer to the following data:
1. Narasin sodium is prepared from narasin taking advantage of the carboxylic acid which ionises and readily forms the salt in sodium hydroxide solutions. Narasin shows broad spectrum activity against Gram positive bacteria including anaerobes and mycoplasma, and also possesses antiviral and limited antifungal activity. Narasin is used in the animal health industry as an in-feed antibiotic and growth promotant.
2. Narasin sodium is an antibacterial and limited antifungal agent.

Biological Activity

narasin, isolated from certain streptomyces sp. is an ionophore antibiotic. as a coccidiostat, it can be used in veterinary practice for gastrointestinal parasites. narasin has been shown to induce tumor necrosis factor-related apoptosis-induced ligand (trail)-mediated apoptosis by er stress in glioma cells and to dampen nf-κb signaling by suppressing the phosphorylation of iκbα. nf-κb, as a transcription factor, plays a vital role across many cellular processes which are involved in neuronal and embryonic development, cell proliferation, apoptosis, and immune responses to infection and inflammation.

in vitro

narasin caused suicidal erythrocyte death or eryptosis. when human erythrocytes were exposed to narasin, it was shown that narasin resulted in the increase of annexin-v-binding indicating cell membrane scrambling with phosphatidylserine translocation to the erythrocyte surface and the decrease of forward scatter reflecting cell shrinkage, which indicated the death of erythrocyte [1]. narasin blocked nf-κb signaling via inhibition of iκbα phosphorylation at a lower concentration [2].

in vivo

new zealand white rabbits were given narasin 4-48 p. p. m, in pelleted feed. after 4 weeks, the experiments indicated that narasin protected rabbits from severe coccidiosis induced by e. flavescens, e. perforans e. magna, e. intestinalis, and e. stiedai. in addition, narasin reduced oocyst output in a highly effective fashion [3].

IC 50

3.2 μm: blocks nf-κb signaling via inhibition of iκbα phosphorylation

references

[1]. bouguerra, g., bissinger, r., abbes, s., & lang, f. stimulation of eryptosis by narasin. cellular physiology and biochemistry. 2015; 37(5):1807-1816. [2]. miller, s., huang, r., sakamuru, s., shukla, s., attene-ramos, m., & shinn, p. et al. identification of known drugs that act as inhibitors of nf-κb signaling and their mechanism of action. biochemical pharmacology. 2010; 79(9): 1272-1280. [3]. peeters, j., geeroms, r., antoine, o., mammerickx, m., & halen, p. efficacy of narasin against hepatic and intestinal coccidiosis in rabbits. parasitology. 1981; 83(02): 293-301.

Check Digit Verification of cas no

The CAS Registry Mumber 58331-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,3 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58331-17:
(7*5)+(6*8)+(5*3)+(4*3)+(3*1)+(2*1)+(1*7)=122
122 % 10 = 2
So 58331-17-2 is a valid CAS Registry Number.

58331-17-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name naransin sodium

1.2 Other means of identification

Product number -
Other names natriumnarasin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58331-17-2 SDS

58331-17-2Synthetic route

naransin sodium
58331-17-2

naransin sodium

A

5-<5-ethyltetrahydro-5-hydroxy-6-methylpyran-2-yl>dihydro-5-methyl-2H-furan-2-one
65171-42-8

5-<5-ethyltetrahydro-5-hydroxy-6-methylpyran-2-yl>dihydro-5-methyl-2H-furan-2-one

B

α-ethyl-6-<5-ethyl-9-(2-furanyl)-2,6-dihydroxy-1,3,7-trimethyl-4-oxodecyl>tetrahydro-3,5-dimethyl-2H-pyran-2-acetic acid

α-ethyl-6-<5-ethyl-9-(2-furanyl)-2,6-dihydroxy-1,3,7-trimethyl-4-oxodecyl>tetrahydro-3,5-dimethyl-2H-pyran-2-acetic acid

Conditions
ConditionsYield
With formic acid In tetrahydrofuran for 0.5h;A n/a
B 48%

58331-17-2Upstream product

58331-17-2Downstream Products

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