CAS Number12650-69-0
SynonymsPseudomonic acid; Bactoderm; MFCD03792664; Pseudomonic acid A; Mupirocin; EINECS 231-791-2; Turixin; BACTROBAN; Mupirocin [USAN:BAN:INN]; Mupirocina; trans-Pseudomonic Acid; Bactroban Nasal; Plasimine; Mupirocine; Mupirocinum; Centany
Molecular FormulaC26H44O9
Molecular Weight500.62
Purity920-1020 μg/mg (HPLC)%
Density1.2±0.1 g/cm3
Boiling Point672.3±55.0 °C at 760 mmHg
Melting Point77-780C
Appearancecrystalline
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| Chemical & Physical Properties | |
|---|---|
| CAS Number | 12650-69-0 |
| Catalog No. | 2A-9011521 |
| Chinese Name | 莫匹罗星 |
| Synonyms | Pseudomonic acid; Bactoderm; MFCD03792664; Pseudomonic acid A; Mupirocin; EINECS 231-791-2; Turixin; BACTROBAN; Mupirocin [USAN:BAN:INN]; Mupirocina; trans-Pseudomonic Acid; Bactroban Nasal; Plasimine; Mupirocine; Mupirocinum; Centany |
| Molecular Formula | C26H44O9 |
| Molecular Weight | 500.62 |
| Purity | 920-1020 μg/mg (HPLC) |
| Density | 1.2±0.1 g/cm3 |
| Boiling Point | 672.3±55.0 °C at 760 mmHg |
| Melting Point | 77-780C |
| Appearance | crystalline |
| Water Solubility | H2O: 12 mg/mL, soluble |
| Storage Condition | -20°C Freezer, Under Inert Atmosphere |
| Application | Mupirocin is an antibiotic compound. |
| HTC | 2941909000 |
| PubChem ID | 24724542 |
| MDL Number | MFCD01711620 |
| SMILES | [H][C@@]1(CO[C@@H](C\C(C)=C\C(=O)OCCCCCCCCC(O)=O)[C@H](O)[C@@H]1O)C[C@@H]2O[C@@]2([H])[C@@H](C)[C@H](C)O |
| InChI | 1S/C26H44O9/c1-16(13-23(30)33-11-9-7-5-4-6-8-10-22(28)29)12-20-25(32)24(31)19(15-34-20)14-21-26(35-21)17(2)18(3)27/h13,17-21,24-27,31-32H,4-12,14-15H2,1-3H3,(H,28,29)/b16-13+/t17-,18-,19-,20-,21-,24+,25-,26-/m0/s1 |
| InChI Key | MINDHVHHQZYEEK-HBBNESRFSA-N |
| NACRES Code | NA.77 |
| UNSPSC | 12352200 |
| MSDS | msds/11521_1_12650_69_0.pdf |
| Use of | Mupirocin(BRL-4910A) is an antibiotic of the monoxycarbolic acid class; effective against Gram-positive bacteria, including MRSA. Properties Articles98 Name mupirocin Synonym More Synonyms Mupirocin Biological Activity Description Mupirocin(BRL-4910A) is an antibiotic of the monoxycarbolic acid class; effective against Gram-positive bacteria, including MRSA. Related Catalog Signaling Pathways >> Anti-infection >> Bacterial Research Areas >> Infection References [1]. Hughes J, et al. Inhibition of isoleucyl-transfer ribonucleic acid synthetase in Escherichia coli by pseudomonic acid. Biochem J. 1978 Oct 15;176(1):305-18. [2]. Cookson BD. The emergence of mupirocin resistance: a challenge to infection control and antibiotic prescribing practice. J Antimicrob Chemother. 1998 Jan;41(1):11-8. Chemical & Physical Properties Molecular Formula C26H44O9 Exact Mass 500.298523 PSA 146.05000 Index of Refraction 1.524 InChIKey MINDHVHHQZYEEK-HBBNESRFSA-N Safety Information Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter Hazard Codes Xi Safety Phrases S2 RIDADR NONH for all modes of transport WGK Germany 2 RTECS RA6907000 HS Code 2941909000 Synthetic Route 12650-69-0 Literature: Tetrahedron Letters, , vol. 24, # 34 p. 3661 - 3664 1,5-Anhydro-D-a... 32742-34-0 12650-69-0 Literature: Tetrahedron Letters, , vol. 24, # 34 p. 3661 - 3664 (3S,4R)-3-METHY... 87614-58-2 12650-69-0 Literature: Tetrahedron Letters, , vol. 24, # 34 p. 3661 - 3664 Precursor & DownStream Precursor 10 CAS#:50-69-1 CAS#:32742-34-0 1,5-Anhydro-D-a... CAS#:87614-58-2 (3S,4R)-3-METHY... CAS#:87614-59-3 3-[2-(TERT-BUTY... DownStream 0 |
| Transport Info | Product Name: Mupirocin |
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