| Name | monensin A |
|---|---|
| Synonyms |
17-8 Monensin
Monensic acid, Lilly 67314, A 3223A Monensin premix MONENSIN SODIUM MONENSINSODIUMSALT EINECS 244-941-7 monelan Monensin A MONENSIN a3823a 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-beta-methoxy-alpha,gamma,2,8-tetramethyl-1,6-dioxaspirodecane-7-butyric acid elancoban 4-[2-(5-ethyl-5-{5-[6-hydroxy-6-(hydroxyMethyl)-3,5-diMethyloxan-2-yl]-3-Methyloxolan-2-yl}oxolan-2-yl)-9-hydroxy-2,8-diMethyl-1,6-dioxaspirodecan-7-yl]-3-Methoxy-2-Methylpentanoic acid (2S,3R,4S)-4-[(2S,5R,7S,8R,9S)-2-{(2S,2'R,3'S,5R,5'R)-2-Ethyl-5'-[(2S,3S,5R,6R)-6-hydroxy-6-(hydroxymethyl)-3,5-dimethyltetrahydro-2H-pyran-2-yl]-3'-methyloctahydro-2,2'-bifuran-5-yl}-9-hydroxy-2,8-dimethyl-1,6-dioxaspiro[4.5]dec-7-yl]-3-methoxy-2-methylpentanoic acid MONENSIN NA monensicacid 2-(5-ethyltetrahydro-5-(tetrahydro-dioxaspirodecane-7-butyricacid MONENSIN A SODIUM SALT Elancoban Monelan Romensin 4-[2-[2-Ethyl-5-(6-hydroxy-6-hydroxymethyl-3,5-dimethyltetrahydropyran-2-yl)-3-methyloctahydro-[2,2]bifuranyl-5-yl]-9-hydroxy-2,8-dimethyl-1,6-dioxaspirodec-7-yl]-3-methoxy-2-methylpentanoic acid MONENSIN(PURE) MFCD00077826 gamma,2,8-tetramethyl-furyl)-2-furyl)-9-hydroxy-beta-methoxy-alph 4-[3-[5-ETHYL-5-[5-[6-HYDROXY-6-(HYDROXYMETHYL)-3,5-DIMETHYL-TETRAHYDROPYRAN-2-YL]-3-METHYL-TETRAHYDROFURAN-2-YL]-TETRAHYDROFURAN-2-YL]-9-HYDROXY-3,8-DIMETHYL-4,6-DIOXASPIRODEC-7-YL]-3-METHOXY-2-METHYL-PENTANOATE Monensin //BP Monensine sodium Monensin:Monesin Sodium 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-methoxy-a,2,8-tetramethyl-1,6-dioxaspirodecane-7-butyric Acid |
| Description | Monensin is a lipid-soluble naturally occurring bioactive ionophore produced by Streptomyces spp. Monensin can bind protons and monovalent cations. Monensin exhibits a broad spectrum activity against opportunistic pathogens of humans in both drug sensitive and resistant strains. Monensin also induces apoptosis in multiple cancer cell lines[1][2]. |
|---|---|
| Related Catalog | |
| References |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 766.3±60.0 °C at 760 mmHg |
| Melting Point | 103-105°C |
| Molecular Formula | C36H61NaO11 |
| Molecular Weight | 670.871 |
| Flash Point | 229.2±26.4 °C |
| Exact Mass | 670.429199 |
| PSA | 156.20000 |
| LogP | 3.72 |
| Vapour Pressure | 0.0±5.9 mmHg at 25°C |
| Index of Refraction | 1.546 |
| Storage condition | 2-8°C |
| Hazard Codes | T: Toxic; |
|---|---|
| Risk Phrases | R25 |
| Safety Phrases | S36/37/39-S45 |
| RIDADR | UN 3462 6.1/PG 2 |
| WGK Germany | 3 |
| RTECS | JH2830000 |
| Packaging Group | II |
| Hazard Class | 6.1(a) |
| Precursor 1 | |
|---|---|
| DownStream 2 | |