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| Product | Description | |
|---|---|---|
| Nosiheptide | Nosiheptide. Group: Biochemicals. Alternative Names: Nosiheptide; 30, 32-Imino-8, 5: 18, 15: 40, 37-tri nitri lo-21, 36- ( [2, 4] -endo-thiazolomethanimino) -5H, 15H, 37H-pyrido [3, 2-w] [2, 11, 21, 27, 31, 7, 14, 17] benzoxatetrathiatri azacyclohexatri acontine nosiheptide deriv.; Multhiomycin; Multiomycin; NSC 307240; Primofax; RP 9671; [11S- [11R * (S * ) , 14Z, 21R * , 23R * , 29R * ] ] -N- [1- (Aminocarbonyl) ethenyl] -2- [14-ethylide ne -9, 10, 11, 12, 13, 14, 19, 20, 21, 22, 23, 24, 26, 33, 35, 36-hexadeca hydro-3, 23-di hydroxy-11- (1- hydroxyethyl) -31- methyl -9, 12, 19, 24, 33, 43-hexaoxo-30, 32-imino-8, 5: 18, 15: 40, 37-tri nitri lo-21, 36- ( [2, 4] -endo-thiazolomethanimino) -5H, 15H, 37H-pyrido [3, 2-w] [2, 11, 21, 27, 31, 7, 14, 17] benzoxatetrathiatri azacyclohexatri acontin-2-yl] -4-thiazolecarboxamide . Grades: Highly Purified. CAS No. 56377-79-8. Pack Sizes: 5mg. Molecular Formula: C51H43N13O12S6, Molecular Weight: 1226.32. US Biological Life Sciences. |  Worldwide |
| Nosiheptide | Nosiheptide (Multhiomycin), a thiopeptide antibiotic produced by Streptomyces actuosus , inhibits bacterial protein synthesis and bears a unique indole side ring system and regiospecific hydroxyl groups on the characteristic macrocyclic core. Nosiheptide has been widely used as a feed additive for animal growth [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Multhiomycin; RP 9671. CAS No. 56377-79-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-107486. |  |
| Nosiheptide | Nosiheptide (Multhiomycin), a thiopeptide antibiotic produced by Streptomyces actuosus, inhibits bacterial protein synthesis and bears a unique indole side ring system and regiospecific hydroxyl groups on the characteristic macrocyclic core. Nosiheptide has been widely used as a feed additive for animal growth. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Nosiheptide;N-[1-(Aminocarbonyl)ethenyl]-2-[(11S,14Z,21S,23S,29S)-14-ethylidene-9,10,11,12,13,14,19,20,21,22,23,24,26,33,35,36-hexadecahydro-3,23-dihydroxy-11-[(1R)-1-hydroxyethyl]-31-methyl-9,12,19,24,33,43-hexaoxo-30,32-imino-8,5:18,15:40,37-trinitrilo-21,36-([2,4]-endo-thiazolomethanimino)-5H,15H,37H-pyrido[3,2-w][2,11,21,27,31,7,14,17]benzoxatetrathiatriazacyclohexatriacontin-2-yl]-4-thiazolecarboxamide;Nosiheptide VETRANAL;priMofax. Product Category: Inhibitors. Appearance: Solid. CAS No. 56377-79-8. Molecular formula: C51H43N13O12S6. Mole weight: 1222.38. Purity: 0.9705. Canonical SMILES: OC1=C(C2=NC(C(NC(C(N)=O)=C)=O)=CS2)N=C(C3=CSC(C4NC(C5=CSC(C(CC(C(OCC6=C7C(C)=C(NC7=CC=C6)C(SC4)=O)=O)O)NC(C8=CSC(/C(NC(C(C(O)C)NC(C9=CSC%10=N9)=O)=O)=C\C)=N8)=O)=N5)=O)=N3)C%10=C1. Product ID: ACM56377798. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Nosiheptide precursor | Nosiheptide precursor is an antimicrobial peptide found in Streptomyces actuosus, and has antibacterial activity. Synonyms: Cys-Thr-Thr-Cys-Glu-Cys-Cys-Cys-Ser-Cys-Ser. Grades: ≥90%. |  |
| 23S rRNA (adenosine1067-2'-O)-methyltransferase | The methylase that is responsible for autoimmunity in the thiostrepton producer Streptomyces azureus, renders ribosomes completely resistant to thiostrepton. Group: Enzymes. Synonyms: 23S rRNA A1067 2'-methyltransferase; thiostrepton-resistance methylase; nosiheptide-resistance methyltransferase. Enzyme Commission Number: EC 2.1.1.230. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1833; 23S rRNA (adenosine1067-2'-O)-methyltransferase; EC 2.1.1.230; 23S rRNA A1067 2'-methyltransferase; thiostrepton-resistance methylase; nosiheptide-resistance methyltransferase. Cat No: EXWM-1833. |  |
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