Valnemulin hydrochloride

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Valnemulin hydrochloride
Category Antibiotics
Catalog number BBF-03914
CAS 133868-46-9
Molecular Weight 601.28
Molecular Formula C31H53ClN2O5S
Purity >90%

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Description

The hydrochloride salt form of Valnemulin is a wide-spectrum antibiotic that has been found to have strong antibacterial activity especially against mycoplasma and spirochete, and is commonly used as a veterinary drug. It can prevent and control swine dysentery, ileitis, colitis and other intestinal diseases, as well as swine asthma and other respiratory diseases.

Specification

Related CAS 101312-92-9 (free base)
Synonyms Valnemulin HCl; UNII-W1GDP58BNQ; W1GDP58BNQ
Shelf Life As supplied, 2 years from the QC date provided on the Certificate of Analysis, when stored properly
Storage Store at -20°C
IUPAC Name [(1S,2R,3S,4S,6R,7R,8R,14R)-4-ethenyl-3-hydroxy-2,4,7,14-tetramethyl-9-oxo-6-tricyclo[5.4.3.01,8]tetradecanyl] 2-[1-[[(2R)-2-amino-3-methylbutanoyl]amino]-2-methylpropan-2-yl]sulfanylacetate;hydrochloride
Canonical SMILES CC1CCC23CCC(=O)C2C1(C(CC(C(C3C)O)(C)C=C)OC(=O)CSC(C)(C)CNC(=O)C(C(C)C)N)C.Cl
InChI InChI=1S/C31H52N2O5S.ClH/c1-10-29(8)15-22(38-23(35)16-39-28(6,7)17-33-27(37)24(32)18(2)3)30(9)19(4)11-13-31(20(5)26(29)36)14-12-21(34)25(30)31;/h10,18-20,22,24-26,36H,1,11-17,32H2,2-9H3,(H,33,37);1H/t19-,20+,22-,24-,25+,26+,29-,30+,31+;/m1./s1
InChI Key MFBPRQKHDIVLOJ-AFFLPQGKSA-N
Source Semi-synthetic

Properties

Appearance White to Off-white Powder
Antibiotic Activity Spectrum mycoplasma
Boiling Point 672.7°C at 760 mmHg
Solubility Soluble in Water, Ethanol

Reference Reading

1.Synthesis, characterization and in vitro release performance of the pegylated valnemulin prodrug.
Dong X;Shu X;Wang Y;Niu Z;Xu S;Zhang Y;Zhao S J Vet Med Sci. 2018 Feb 2;80(1):173-180. doi: 10.1292/jvms.17-0434. Epub 2017 Nov 28.
Valnemulin, successfully developed by Sandoz in 1984, is a new generation derivative of pleuromutilin related to tiamulin. Valnemulin has low water-solubility, a short half-life period, low bioavailability, and instability. The application of valnemulin was restricted. Therefore, finding a more moderate delivery system is necessary to improve the shortcomings of valnemulin. The purpose of the study was to improve the strong stability and the irritation caused by of valnemulin hydrochloride power through pegylated-valnemulin prodrug mode. The prepared pegylated-valnemulin prodrug was characterized and evaluated by in vitro release performance under buffer solutions with pH levels of 7.4 and 3.6. The loading rate of valnemulin in PEG-succinic-valnemulin prodrug was determined by ultraviolet spectrophotometer and high performance liquid chromatography (HPLC). HPLC with evaporative light scattering detector was applied to determine the amount of PEG-succinic acid. The loading rate of valnemulin in PEG-succinic-valnemulin prodrug was 6.46%. PEG-succinic-valnemulin prodrug demonstrated a satisfactory solubility of valnemulin with 523 mg·ml;-1; and excellent stability verified by the stability experiment.
2.Preparation of valnemulin hydrogen fumarate and its enhanced stability compared with valnemulin hydrochloride.
Zhu X;Xu S;Xu Q Pharm Dev Technol. 2016;21(3):338-45. doi: 10.3109/10837450.2014.1003656. Epub 2015 Jan 19.
CONTEXT: ;It is necessary to develop a new salt of valnemulin to replace the veterinary antibiotic, e.g. valnemulin hydrochloride, in order to overcome its instability during storage and preparation.;OBJECTIVE: ;The objective of this study was to prepare a novel organic acid salt, valnemulin hydrogen fumarate, and to investigate its stability compared with valnemulin hydrochloride.;MATERIALS AND METHODS: ;The crystal of valnemulin hydrogen fumarate was prepared by modified crystallization method; the enhanced stabilities of valnemulin hydrogen fumarate were conducted under irradiation and humid conditions, and the experimental results were simulated at AM1 level of calculations.;RESULTS: ;Valnemulin hydrogen fumarate was more stable than valnemulin hydrochloride. After irradiation for 180 days, the content of valnemulin hydrogen fumarate decreased slightly 2.7%, whereas the content of valnemulin hydrochloride had an obvious decrease of 32.8%. Meanwhile, valnemulin hydrogen fumarate showed better anti-RH (relative humidity) ability than valnemulin hydrochloride. Under conditions of 65% and 85% RH, the absorption values of valnemulin hydrogen fumarate towards water were 0.75% and 1.20% at 48 h, whereas those of valnemulin hydrochloride were 4.

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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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