CAS 16846-24-5
:Josamicina
Descrição:
Josamicina é um antibiótico macrolídeo que é derivado principalmente da fermentação da bactéria Streptomyces narbonensis. É caracterizado pela sua capacidade de inibir a síntese de proteínas bacterianas ligando-se à subunidade ribossomal 50S, impedindo assim o crescimento de bactérias suscetíveis. Josamicina exibe um amplo espectro de atividade contra várias bactérias Gram-positivas e alguns organismos Gram-negativos, tornando-o eficaz no tratamento de infecções do trato respiratório, infecções de pele e certas doenças sexualmente transmissíveis. O composto é tipicamente administrado por via oral e é conhecido por suas favoráveis propriedades farmacocinéticas, incluindo boa penetração nos tecidos e uma meia-vida relativamente longa. Josamicina também é notável por seu baixo perfil de toxicidade, o que contribui para seu uso terapêutico. No entanto, como outros antibióticos, pode levar ao desenvolvimento de resistência a antibióticos se mal utilizado. Sua estrutura química inclui um grande anel de lactona, que é uma característica comum dos antibióticos macrolídeos, contribuindo para sua atividade biológica e estabilidade.
Fórmula:C42H69NO15
InChI:InChI=1/C42H69NO15/c1-23(2)19-32(47)56-40-27(6)53-34(22-42(40,8)50)57-37-26(5)54-41(36(49)35(37)43(9)10)58-38-29(17-18-44)20-24(3)30(46)16-14-12-13-15-25(4)52-33(48)21-31(39(38)51-11)55-28(7)45/h12-14,16,18,23-27,29-31,34-41,46,49-50H,15,17,19-22H2,1-11H3/b13-12+,16-14+/t24-,25-,26?,27?,29+,30+,31-,34?,35?,36?,37?,38+,39+,40?,41?,42?/m1/s1
Chave InChI:InChIKey=XJSFLOJWULLJQS-NGVXBBESSA-N
SMILES:O([C@@H]1[C@@H](OC)[C@H](OC(C)=O)CC(=O)O[C@H](C)C\C=C\C=C\[C@H](O)[C@H](C)C[C@@H]1CC=O)[C@H]2[C@H](O)[C@@H](N(C)C)[C@H](O[C@H]3C[C@@](C)(O)[C@@H](OC(CC(C)C)=O)[C@H](C)O3)[C@@H](C)O2
Sinónimos:- (2S,3R,4R,6S)-6-{[(2R,3S,4R,5R,6S)-6-{[(4R,6S,7R,9R,10R,11E,13E,16R)-4-(acetyloxy)-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)oxacyclohexadeca-11,13-dien-6-yl]oxy}-4-(dimethylamino)-5-hydroxy-2-methyltetrahydro-2H-pyran-3-yl]oxy}-4-hydroxy-2,4-dimethyltetrahydro-2H-pyran-3-yl 3-methylbutanoate (non-preferred name)
- (2S,3S,4R,6S)-6-{[(2R,3S,4R,5R,6S)-6-{[(4R,5S,6S,7R,9R,10R,11E,13E,16R)-4-(acetyloxy)-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)oxacyclohexadeca-11,13-dien-6-yl]oxy}-4-(dimethylamino)-5-hydroxy-2-methyltetrahydro-2H-pyran-3-yl]oxy}-4-hydroxy-2,4-dimethyltetrahydro-2H-pyran-3-yl 3-methylbutanoate (non-preferred name)
- 6-{[6-{[(4R,5S,6S,7R,9R,10R,11E,13E,16R)-4-(acetyloxy)-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)oxacyclohexadeca-11,13-dien-6-yl]oxy}-4-(dimethylamino)-5-hydroxy-2-methyltetrahydro-2H-pyran-3-yl]oxy}-4-hydroxy-2,4-dimethyltetrahydro-2H-pyran-3-yl 3-methylbutanoate (non-preferred name)
- Antibiotic YL 704A3
- Antibiotic YL 704A<sub>3</sub>
- En 141
- Iosalide
- Jomybel
- Josacine
- Josamicina
- Josamina
- Josamycin solution
- Josamycine
- Kitasamycin A3
- Kitasamycin A<sub>3</sub>
- Leucomycin A3
- Leucomycin A<sub>3</sub>
- Leucomycin V, 3-acetate 4<sup>B</sup>-(3-methylbutanoate)
- Leucomycin V, 3-acetate 4B-(3-methylbutanoate)
- Oxacyclohexadecane, leucomycin V deriv.
- Turimycin A5
- Turimycin A<sub>5</sub>
- Vilprafen
- Wilprafen
- JOSAMYCIN
- turimycina5
- 3-acetate4(supb)-(3-methylbutanoate)
- Leucomycin A3 (>90%)
- [(2S,3S,4R,6S)-6-[(2R,3S,4R,5R,6S)-6-[[(4R,5S,6S,7R,9R,10R,11E,13E,16R)-4-acetyloxy-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-1-oxacyclohexadeca-11,13-dien-6-yl]oxy]-4-(dimethylamino)-5-hydroxy-2-methyloxan-3-yl]oxy-4-hydroxy-2,4-dimethyloxa
- (4R,5S,6S,7R,9R,10R,11E,13E,16R)-4-(acetyloxy)-6-[[3,6-dideoxy-4-O-[2,6-dideoxy-3-C-methyl-4-O-(3-methylbutanoyl)-α-L-ribo-hexopyranosyl]-3-(dimethylamino)-β-D-glucopyranosyl]oxy]-10-hydroxy-5-methoxy-9,16-dimethyl-7-(2-oxoethyl)oxacyclohexadeca-11,13-dien-2-one (josamycin)
- LEUCOMYCIN V,3-AC-ETA 4B-(3-METHYLBUTANOATE)
- C12662
- (2S,3S,4R,6S)-6-(((2R,3S,4R,5R,6S)-6-(((4R,5S,6S,7R,9R,10R,11E,13E,16R)-4-Acetoxy-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)oxacyclohexadeca-11,13-dien-6-yl)oxy)-4-(dimethylamino)-5-hydroxy-2-methyltetrahydro-2H-pyran-3-yl)oxy)-4-hydroxy-2,4-
- Josamycin Standard
- 3-Acetate 4B-(3-Methylbutanoate)leucoMycin V
- JOSAMYCIN(16846-24-5)
- Leucomycin V, 3-acetate 4B-(3-methylbutanoate) (9CI)
- LEUCOMYCIN V,3-ACETA 4BETA-(3-METHYL BUTANOATE)
- kitasamycina3
- Josamycin for peak identification CRS
- antibioticyl-704a3
- JOSAMYCIN USP/EP/BP
- lucamycin
- LEUCOMYCIN V,3-ACETA 4β-(3-METHYL BUTANOATE)
- Josamycin Solution, 100ppm
- YL-704A3
- Leucomycin A3 (8CI)
- Leucomycin V 3-acetate 4''-(3-methylbutanoate)
- Pre-validation
- Josamycin for peak identification
- leucomycinv,3-acetate4(supb)-(3-methylbutanoate)
- Josamycin CRS
- Sparsentan Impurity 65
- Josamycin solution solution,1000ppm
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Pureza (%)
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16 produtos.
Josamycin, 98%
CAS:<p>Macrolide antibiotic</p>Fórmula:C42H69NO15Pureza:98%Cor e Forma:White, PowderPeso molecular:827.99JOSAMYCIN FOR PEAK IDENTIFICATION CRS
CAS:JOSAMYCIN FOR PEAK IDENTIFICATION CRSFórmula:C42H69NO15Peso molecular:827.995Leucomycin V, 3-acetate 4B-(3-methylbutanoate)
CAS:Fórmula:C42H69NO15Pureza:95%Cor e Forma:SolidPeso molecular:827.9950(2S,3S,4R,6S)-6-(((2R,3S,4R,5R,6S)-6-(((4R,5S,6S,7R,9R,10R,11E,13E,16R)-4-Acetoxy-10-Hydroxy-5-Methoxy-9,16-Dimethyl-2-Oxo-7-(2-Oxoethyl)Oxacyclohexadeca-11,13-Dien-6-Yl)Oxy)-4-(Dimethylamino)-5-Hydro
CAS:(2S,3S,4R,6S)-6-(((2R,3S,4R,5R,6S)-6-(((4R,5S,6S,7R,9R,10R,11E,13E,16R)-4-Acetoxy-10-Hydroxy-5-Methoxy-9,16-Dimethyl-2-Oxo-7-(2-Oxoethyl)Oxacyclohexadeca-11,13-Dien-6-Yl)Oxy)-4-(Dimethylamino)-5-HydroPureza:98%Peso molecular:828g/molJosamycin 1000 µg/mL in Acetonitrile
CAS:Produto ControladoFórmula:C42H69NO15Cor e Forma:Single SolutionPeso molecular:828.00GB 31660.1-2019 Macrolide Antibiotics Mixture 167 100 µg/mL in Methanol
CAS:Produto ControladoCor e Forma:MixtureJOSAMYCIN
CAS:Josamycin (EN-141) is a macrolide antibiotic exhibiting antimicrobial activity. The dissociation constant Kd from ribosome for Josamycin is 5.5 nM.Fórmula:C42H69NO15Pureza:91.38% - 99.88%Cor e Forma:SolidPeso molecular:827.99Leucomycin A3
CAS:<p>Applications A 16-membered ring macrolide antibiotic with antimicrobial activity against a wide range of pathogens. Particularly used in the treatment of Mycoplasma infection.<br>References Osono, T. et al.: J. Antibiot., 27, 366 (1974); Kuriaki, K. et al.: Jpn. J. Antibiot., 22, 232 (1969); Tan K. et al.: Zhonghua Yiyuamganranxue Zazhi, 16, 235 (2006);<br></p>Fórmula:C42H69NO15Pureza:>90%Cor e Forma:NeatPeso molecular:828.00Leucomycin A3
CAS:<p>Leucomycin A3 is a macrolide antibiotic with a mode of action that inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit. It is used for treating bacterial infections and has shown potential antiviral activity.</p>Fórmula:C42H69NO15Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:828 g/molJosamycin 10 µg/mL in Acetonitrile
CAS:Fórmula:C42H69NO15Cor e Forma:Colourless LiquidPeso molecular:828.00











