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Monensin sodium

Monensin sodium structure

Monensin sodium 

structure
  • CAS No:

    22373-78-0

  • Formula:

    C36H62O11.Na

  • Chemical Name:

    Monensin sodium

  • Synonyms:

    Monensin,sodium salt (1:1);1,6-Dioxaspiro[4.5]decane-7-butyric acid,2-[5-ethyltetrahydro-5-[tetrahydro-3-methyl-5-[tetrahydro-6-hydroxy-6-(hydroxymethyl)-3,5-dimethyl-2H-pyran-2-yl]-2-furyl]-2-furyl]-9-hydroxy-β-methoxy-α,γ,2,8-tetramethyl-,monosodium salt;Monensin,monosodium salt;Monensin sodium salt;Monensin sodium;Rumensin;Sodium monensin;Coban 45;Coban;Monensin A sodium salt;NSC 343257;CRC Rumensin;Kexxtone;22136-43-2;1174161-37-5;1192220-11-3;1191082-56-0

  • Categories:

    Active Pharmaceutical Ingredients  >  Antiparasitic Drugs

Description

Monensin sodium salt is an antibiotic secreted by the bacteria Streptomyces cinnamonensis.


An antiprotozoal agent produced by Streptomyces cinnamonensis. It exerts its effect during the development of first-generation trophozoites into first-generation schizonts within the intestinal epithelial cells. It does not interfere with hosts' development of acquired immunity to the majority of coccidial species. Monensin is a sodium and proton selective ionophore and is widely used as such in biochemical studies.

Monensin sodium Basic Attributes

710.86800

710.42200

244-941-7

1GS872GAFV

DTXSID2045573

29419090

Characteristics

165.43000

2.87390

almost white solid.

267-269 °C

766.3ºC at 760 mmHg

229.2ºC

2-8ºC

4.13E-27mmHg at 25°C

Safety Information

II

6.1(a)

UN 3462 6.1/PG 2

3

R25

S45

JH2830000

T

Stable under normal temperatures and pressures.

P264-P301 + P310

H300

|Danger|H300 (98.99%): Fatal if swallowed [Danger Acute toxicity, oral]|P264, P270, P301+P310, P321, P330, P405, and P501|Aggregated GHS information provided by 198 companies from 3 notifications to the ECHA C&L Inventory.|H300: Fatal if swallowed [Danger Acute toxicity, oral]|P260, P264, P270, P301+P310, P309+P311, P314, P321, P330, P405, and P501|P260, P261, P264, P270, P272, P280, P301+P310, P302+P352, P307+P311, P312, P314, P321, P322, P330, P333+P313, P361, P363, P405, and P501

Drug Information

Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues. (See all compounds classified as Antifungal Agents.)|Substances that are destructive to protozoans. (See all compounds classified as Antiprotozoal Agents.)|Agents useful in the treatment or prevention of COCCIDIOSIS in man or animals. (See all compounds classified as Coccidiostats.)|Chemical agents that increase the permeability of CELL MEMBRANES to PROTONS. (See all compounds classified as Proton Ionophores.)|Chemical agents that increase the permeability of CELL MEMBRANES to SODIUM ions. (See all compounds classified as Sodium Ionophores.)

Coban

Monensin sodium Use and Manufacturing

Uses

1. Poliether antibiotic. Coccidiostat.
2. Antifungal
3. Antibacterial

Animal Drugs -> FDA Approved Animal Drug Products (Green Book) -> Active Ingredients

Computed Properties

Molecular Weight:692.9
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:10
Exact Mass:692.41115704
Monoisotopic Mass:692.41115704
Topological Polar Surface Area:156
Heavy Atom Count:48
Complexity:1110
Defined Atom Stereocenter Count:17
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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