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| Product | Description | |
|---|---|---|
| 40S ribosomal protein S30 | 40S ribosomal protein S30 is an antimicrobial peptide produced by Oncorhynchus mykiss (Rainbow trout, Salmo gairdneri). It has antibacterial activity against Gram-positive bacteria and low activity against Gram-negative bacteria. Synonyms: Lys-Val-His-Gly-Ser-Leu-Ala-Arg-Ala-Gly-Lys. Grades: >95%. Molecular formula: C48H86N18O13. Mole weight: 1123.32. |  |
| 50S ribosomal protein L1 | 50S ribosomal protein L1 is an antimicrobial peptide produced by Helicobacter pylori. It has antibacterial and antifungal activity. Synonyms: Ala-Lys-Lys-Val-Phe-Lys-Arg-Leu-Glu-Lys-Leu-Phe-Ser-Lys-Ile-Gln-Asn-Asp-Lys. Grades: >98%. | |
| 50S ribosomal protein L16 3-hydroxylase | The enzyme, characterized from the bacterium Escherichia coli, hydroxylates an arginine residue on the 50S ribosomal protein L16, and is involved in regulation of bacterial ribosome assembly. Group: Enzymes. Synonyms: ycfD (gene name). Enzyme Commission Number: EC 1.14.11.47. 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-0666; 50S ribosomal protein L16 3-hydroxylase; EC 1.14.11.47; ycfD (gene name). Cat No: EXWM-0666. |  |
| Recombinant Ribosomal-protein-alanine acetyltransferase from E. coli | Ribosomal-protein-alanine acetyltransferase is an enzyme that catalyzes the chemical reaction: acetyl-CoA + ribosomal-protein L-alanine <-> CoA + ribosomal-protein N-acetyl-L-alanine. Group: Enzymes. Synonyms: ribosomal-protein-alanine N-acetyltransferase; RimJ; EC 2.3.1.128; 113383-52-1. Enzyme Commission Number: EC 2.3.1.128. CAS No. 113383-52-1. Purity: > 80 %. RimJ. Mole weight: 23 kDa. Appearance: Colourless clear liquid. Storage: Store at -20 degree C, for extended storage, conserve at -20 degree C or -80 degree C. Source: E. coli. Species: E. coli. ribosomal-protein-alanine N-acetyltransferase; RimJ; EC 2.3.1.128; 113383-52-1. Cat No: NATE-1019. | |
| Recombinant Ribosomal-protein-serine acetyltransferase from E. coli | This enzyme acetylates the N-terminal serine of ribosomal protein L7/L12. Group: Enzymes. Synonyms: RimL. Purity: > 80 %. RimL. Mole weight: 21 kDa. Appearance: Colourless clear liquid. Storage: Store at -20 degree C, for extended storage, conserve at -20 degree C or -80 degree C. Source: E. coli. Species: E. coli. RimL; Ribosomal-protein-serine acetyltransferase. Cat No: NATE-1020. | |
| ribosomal-protein-alanine N-acetyltransferase | A group of enzymes in Escherichia coli that acetylate the N-terminal alanine residues of specific ribosomal proteins. cf. EC 2.3.1.88, peptide α-N-acetyltransferase. Group: Enzymes. Synonyms: ribosomal protein S18 acetyltransferase. Enzyme Commission Number: EC 2.3.1.128. CAS No. 113383-52-1. RimJ. 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-2065; ribosomal-protein-alanine N-acetyltransferase; EC 2.3.1.128; 113383-52-1; ribosomal protein S18 acetyltransferase. Cat No: EXWM-2065. | |
| ribosomal protein L3 N5-glutamine methyltransferase | Modifies the glutamine residue in the glycylglycylglutamine (GGQ) motif of ribosomal protein L3 (Gln150 in the protein from the bacterium Escherichia coli). The enzyme does not act on peptide chain release factor 1 or 2. Group: Enzymes. Synonyms: YfcB; PrmB. Enzyme Commission Number: EC 2.1.1.298. 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-1905; ribosomal protein L3 N5-glutamine methyltransferase; EC 2.1.1.298; YfcB; PrmB. Cat No: EXWM-1905. | |
| [ribosomal protein S12] (aspartate89-C3)-methylthiotransferase | This bacterial enzyme binds two [4Fe-4S] clusters. A bridge of five sulfur atoms is formed between the free Fe atoms of the two [4Fe-4S] clusters. In the first reaction the enzyme transfers a methyl group from AdoMet to the external sulfur ion of the sulfur bridge. In the second reaction the enzyme catalyses the reductive fragmentation of a second molecule of AdoMet, yielding a 5'-deoxyadenosine radical, which then attacks the methylated sulfur atom of the polysulfide bridge, resulting in the transfer of a methylthiol group to aspartate89. The enzyme is a member of the superfamily of S-adenosyl-L-methionine-dependent radical (radical AdoMet) enzymes. Group: Enzymes. Synonyms: RimO; [ribosomal protein S12]-Asp89:sulfur-(sulfur carrier),S-adenosyl-L-methionine C3-methylthiotransferase. Enzyme Commission Number: EC 2.8.4.4. 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-3430; [ribosomal protein S12] (aspartate89-C3)-methylthiotransferase; EC 2.8.4.4; RimO; [ribosomal protein S12]-Asp89:sulfur-(sulfur carrier),S-adenosyl-L-methionine C3-methylthiotransferase. Cat No: EXWM-3430. | |
| Ribosomal protein S26 (47-61) | Ribosomal protein S26 (47-61) is a bioactive peptide of Ribosomal protein S26 which is encoded by the RPS26 gene. This gene encodes a ribosomal protein that is a component of the 40S subunit. And the protein belongs to the S26E family of ribosomal proteins. Synonyms: Small ribosomal subunit protein eS26 (47-61). | |
| S6K1 Inhibitor, PF-4708671 ((2-((4-(5-Ethylpyrimidin-4-yl)piperazin-1-yl)methyl)-5-(trifluoromethyl)-1H-benzo[d]imidazole, p70 Ribosomal S6 Kinase 1 Inhibitor) | A cell-permeable piperazinyl-pyrimidine compound that acts as an inhibitor against S6K1 (Ki=20nM; IC50=160nM) and MSK1 (IC50=950nM) kinase activity, exhibiting little or much reduced potency against 85 other protein and lipid kinases ( IC50=4.7, 9.2, 65uM, respectively, against RSK1, RSK2, and S6K2; <27% inhibition of the rest at 1uM). Shown to selectively inhibit IGF1- and PMA-stimulated S6K1 substrates phosphorylation in HEK-293 cells in a dose-dependent manner (up to 10uM) in vitro and alleviate heart remodeling and functional damage in a MI (myocardial infarction) model in mice in vivo (75/mg/kg/daily i.p.). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. Molecular Formula: C??H??F?N?, Molecular Weight: 390.4. US Biological Life Sciences. |  Worldwide |
| 10-DEBC hydrochloride | 10-DEBC hydrochloride is a selective and reversible Akt/PKB inhibitor suppressing the IGF-1-stimulated phosphorylation and activation of Akt (complete inhibition at 2.5 μM), and inhibiting downstream activation of mTOR, p70 S6 kinase and S6 ribosomal protein. 10-DEBC hydrochloride inhibits cell growth (IC50 ~ 2-6 μM) and leads to apoptosis in rhabdomyosarcoma cells. Synonyms: 10H-Phenoxazine-10-butanamine, 2-chloro-N,N-diethyl-, hydrochloride (1:1); Akt Inhibitor X; 2-Chloro-N,N-diethyl-10H-phenoxazine-10-butanamine hydrochloride; 10-[4'-(N,N-Diethylamino)butyl]-2-chlorophenoxazine hydrochloride; 4-(2-chloro-10H-phenoxazin-10-yl)-N,N-diethylbutan-1-amine hydrochloride. Grades: ≥99% by HPLC. CAS No. 925681-41-0. Molecular formula: C20H25N2OCl.HCl. Mole weight: 381.34. | |
| 10-DEBC hydrochloride | Selective inhibitor of Akt/PKB. Inhibits IGF-1-stimulated phosphorylation and activation of Akt (complete inhibition at 2.5uM), suppressing downstream activation of mTOR, p70 S6 kinase and S6 ribosomal protein. Shows no activity at PDK1, SGK1 or PI 3-kinase. Inhibits cell growth (IC50 ~ 2-6uM) and induces apoptosis in rhabdomyosarcoma cells. Group: Biochemicals. Grades: Highly Purified. CAS No. 925681-41-0. Pack Sizes: 10mg, 50mg. Molecular Formula: C20H25N2OCl.HCl, Method for Determining. US Biological Life Sciences. | Worldwide |
| 16S rRNA (adenine1518-N6/adenine1519-N6)-dimethyltransferase | KsgA introduces the most highly conserved ribosomal RNA modification, the dimethylation of adenine1518 and adenine1519 in 16S rRNA. Strains lacking the methylase are resistant to kasugamycin. Group: Enzymes. Synonyms: S-adenosylmethionine-6-N',N'-adenosyl (rRNA) dimethyltransferase; KsgA; ksgA methyltransferase. Enzyme Commission Number: EC 2.1.1.182. 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-1781; 16S rRNA (adenine1518-N6/adenine1519-N6)-dimethyltransferase; EC 2.1.1.182; S-adenosylmethionine-6-N',N'-adenosyl (rRNA) dimethyltransferase; KsgA; ksgA methyltransferase. Cat No: EXWM-1781. | |
| 16S rRNA (guanine527-N7)-methyltransferase | The enzyme specifically methylates guanine527 at N7 in 16S rRNA. Group: Enzymes. Synonyms: ribosomal RNA small subunit methyltransferase G; 16S rRNA methyltransferase RsmG; GidB; rsmG (gene name). Enzyme Commission Number: EC 2.1.1.170. 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-1768; 16S rRNA (guanine527-N7)-methyltransferase; EC 2.1.1.170; ribosomal RNA small subunit methyltransferase G; 16S rRNA methyltransferase RsmG; GidB; rsmG (gene name). Cat No: EXWM-1768. | |
| 16S rRNA pseudouridine516 synthase | The enzyme is specific for uridine516 in 16S rRNA. In vitro, the enzyme does not modify free 16S rRNA. The preferred substrate is a 5'-terminal fragment of 16S rRNA complexed with 30S ribosomal proteins. Group: Enzymes. Synonyms: 16S RNA pseudouridine516 synthase; 16S PsiI516 synthase; 16S RNA ψ516 synthase; RNA pseudouridine synthase RsuA; RsuA; 16S RNA pseudouridine 516 synthase. Enzyme Commission Number: EC 5.4.99.19. 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-5558; 16S rRNA pseudouridine516 synthase; EC 5.4.99.19; 16S RNA pseudouridine516 synthase; 16S PsiI516 synthase; 16S RNA ψ516 synthase; RNA pseudouridine synthase RsuA; RsuA; 16S RNA pseudouridine 516 synthase. Cat No: EXWM-5558. | |
| 20-Deoxo-20-(1-piperidinyl)tylosin | 20-Deoxo-20-(1-piperidinyl)tylosin, a formidable antibiotic with exceptional potency, finds its purpose in combating an array of bacterial infections. Its unrivaled capacity to impede bacterial protein synthesis materializes through binding with the 50S ribosomal subunit. Synonyms: Tylosin, 20-deoxo-20-(1-piperidinyl)-; 1003024-00-7; (4R,5S,6S,7R,9R,15R,16S)-6-[(2R,3S,4R,5S,6R)-5-[(2S,4R,5S,6S)-4,5-dihydroxy-4,6-dimethyloxan-2-yl]oxy-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-16-ethyl-4-hydroxy-15-[[(2R,3R,4S,5R,6R)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxymethyl]-5,9,13-trimethyl-7-(2-piperidin-1-ylethyl)-1-oxacyclohexadeca-11,13-diene-2,10-dione. CAS No. 1003024-00-7. Molecular formula: C51H88N2O16. Mole weight: 985.25. | |
| 23S rRNA (adenine1618-N6)-methyltransferase | The recombinant YbiN protein is able to methylate partially deproteinized 50 S ribosomal subunit, but neither the completely assembled 50 S subunits nor completely deproteinized 23 S rRNA. Group: Enzymes. Synonyms: rRNA large subunit methyltransferase F; YbiN protein; rlmF (gene name); m6A1618 methyltransferase. Enzyme Commission Number: EC 2.1.1.181. 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-1780; 23S rRNA (adenine1618-N6)-methyltransferase; EC 2.1.1.181; rRNA large subunit methyltransferase F; YbiN protein; rlmF (gene name); m6A1618 methyltransferase. Cat No: EXWM-1780. | |
| 23S rRNA (adenine2030-N6)-methyltransferase | The recombinant RlmJ protein is most active in methylating deproteinized 23S ribosomal subunit, and does not methylate the completely assembled 50S subunits. Group: Enzymes. Synonyms: YhiR protein; rlmJ (gene name); m6A2030 methyltransferase. Enzyme Commission Number: EC 2.1.1.266. 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-1871; 23S rRNA (adenine2030-N6)-methyltransferase; EC 2.1.1.266; YhiR protein; rlmJ (gene name); m6A2030 methyltransferase. Cat No: EXWM-1871. | |
| 23S rRNA (guanine1835-N2)-methyltransferase | The enzyme methylates 23S rRNA in vitro, assembled 50S subunits are not a substrate. The enzyme specifically methylates guanine1835 at N2 in 23S rRNA. Group: Enzymes. Synonyms: ygjO (gene name); rlmG (gene name); ribosomal RNA large subunit methyltransferase G. Enzyme Commission Number: EC 2.1.1.174. 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-1772; 23S rRNA (guanine1835-N2)-methyltransferase; EC 2.1.1.174; ygjO (gene name); rlmG (gene name); ribosomal RNA large subunit methyltransferase G. Cat No: EXWM-1772. | |
| 23S rRNA (guanine2535-N1)-methyltransferase | Streptomyces viridochromogenes produces the antibiotic avilamycin A which binds to the 50S ribosomal subunit to inhibit protein synthesis. To protect itself from the antibiotic, Streptomyces viridochromogenes utilizes two methyltransferases, 23S rRNA (guanine2535-N1)-methyltransferase and EC 2.1.1.208 [23S rRNA (uridine2479-2-O)-methyltransferase], whose actions confer avilamycin resistance to the RNA. Group: Enzymes. Synonyms: AviRa. Enzyme Commission Number: EC 2.1.1.209. 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-1810; 23S rRNA (guanine2535-N1)-methyltransferase; EC 2.1.1.209; AviRa. Cat No: EXWM-1810. | |
| 23S rRNA (guanine745-N1)-methyltransferase | The enzyme specifically methylates guanine745 at N1 in 23S rRNA. Group: Enzymes. Synonyms: Rlma(I); Rlma1; 23S rRNA m1G745 methyltransferase; YebH; RlmAI methyltransferase; ribosomal RNA(m1G)-methylase (ambiguous); rRNA(m1G)methylase (ambiguous); RrmA (ambiguous); 23S rRNA:m1G745 methyltransferase. Enzyme Commission Number: EC 2.1.1.187. 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-1786; 23S rRNA (guanine745-N1)-methyltransferase; EC 2.1.1.187; Rlma(I); Rlma1; 23S rRNA m1G745 methyltransferase; YebH; RlmAI methyltransferase; ribosomal RNA(m1G)-methylase (ambiguous); rRNA(m1G)methylase (ambiguous); RrmA (ambiguous); 23S rRNA:m1G745 methyltransferase. Cat No: EXWM-1786. | |
| 23S rRNA (uridine2479-2'-O)-methyltransferase | Streptomyces viridochromogenes produces the antibiotic avilamycin A which binds to the 50S ribosomal subunit to inhibit protein synthesis. To protect itself from the antibiotic, Streptomyces viridochromogenes utilizes two methyltransferases, 23S rRNA (uridine2479-2'-O)-methyltransferase and EC 2.1.1.209 [23S rRNA (guanine2535-N1)-methyltransferase], whose actions confer avilamycin resistance to the RNA. Group: Enzymes. Synonyms: AviRb. Enzyme Commission Number: EC 2.1.1.208. 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-1809; 23S rRNA (uridine2479-2'-O)-methyltransferase; EC 2.1.1.208; AviRb. Cat No: EXWM-1809. | |
| 23S rRNA (uridine2552-2'-O)-methyltransferase | The enzyme catalyses the 2'-O-methylation of the universally conserved U2552 in the A loop of 23S rRNA. Group: Enzymes. Synonyms: Um(2552) 23S ribosomal RNA methyltransferase; heat shock protein RrmJ; RrmJ; FTSJ; Um2552 methyltransferase. Enzyme Commission Number: EC 2.1.1.166. 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-1763; 23S rRNA (uridine2552-2'-O)-methyltransferase; EC 2.1.1.166; Um(2552) 23S ribosomal RNA methyltransferase; heat shock protein RrmJ; RrmJ; FTSJ; Um2552 methyltransferase. Cat No: EXWM-1763. | |
| 25S rRNA (cytosine2870-C5)-methyltransferase | The enzyme, found in eukaryotes, is specific for cytosine2870 of the 25S ribosomal RNA. The numbering corresponds to the enzyme from the yeast Saccharomyces cerevisiae. Group: Enzymes. Synonyms: NOP2 (gene name). Enzyme Commission Number: EC 2.1.1.310. 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-1918; 25S rRNA (cytosine2870-C5)-methyltransferase; EC 2.1.1.310; NOP2 (gene name). Cat No: EXWM-1918. | |
| 2-Methylthio-N6-iso-pentenyladenosine | 2-Methylthio-N6-isopentenyladenosine is located at position 37 in tRNAs that read codons starting with uridine. 2-Methylthio-N6-isopentenyladenosine in trpT(Su9) suppressor tRNA increase the efficiency of the tRNA by protecting it from ribosomal proofreading which is induced by codon context. Synonyms: Adenosine, N-(3-methyl-2-butenyl)-2-(methylthio)-; 2-Methyl-thio-N6-isopentyladenosine; N6-Isopentenyl-2-thiomethyladenosine; N-(3-Methyl-2-buten-1-yl)-2-(methylsulfanyl)adenosine; (2R,3S,4R,5R)-2-(Hydroxymethyl)-5-(6-((3-methylbut-2-en-1-yl)amino)-2-(methylthio)-9H-purin-9-yl)tetrahydrofuran-3,4-diol. Grades: ≥95%. CAS No. 20859-00-1. Molecular formula: C16H23N5O4S. Mole weight: 381.45. | |
| 2-Methylthio-N6-isopentenyladenosine-d6 | Isotope labelled 2-Methylthio-N6-isopentenyladenosine is located at position 37 in tRNAs that read codons starting with uridine. 2-Methylthio-N6-isopentenyladenosine in trpT(Su9) suppressor tRNA increase the efficiency of the tRNA by protecting it from ribosomal proofreading which is induced by codon context. Group: Biochemicals. Grades: Highly Purified. CAS No. 1258839-12-1. Pack Sizes: 1mg, 10mg. Molecular Formula: C16H17D6N5O4S, Molecular Weight: 387.49. US Biological Life Sciences. | Worldwide |
| 2'-O-MethylpseudoUridine-5'-Triphosphate Lithium | 2'-O-MethylpseudoUridine-5'-Triphosphate Lithium is a nucleotide analog commonly used in molecular biology research to investigate RNA modification and translation. It has been shown to enhance ribosomal reading efficiency and suppress frameshifting during translation. It may also play a role in regulating immune function and has potential therapeutic applications in autoimmunity and inflammatory diseases. Synonyms: 2'-O-Methylpseudo-UTP tetralithium salt. Grades: ≥90% by AX-HPLC. Molecular formula: C10H13Li4N2O15P3. Mole weight: 521.89. | |
| 5-Fluorocytidine | 5-Fluorocytidine is a member of cytidines, inhibits maturation of the 45S ribosomal RNA precursor [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2341-22-2. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-W039722. |  |
| 7-Propargylamino-7-deaza-ddATP - ATTO-425 | 7-Propargylamino-7-deaza-ddATP - ATTO-425 is a fluorescent nucleotide analog extensively used in biomedical research for labeling and detecting DNA fibers dynamics. It has been employed to study the molecular basis of DNA replications, identifying remotely induced mutations, and studying ribosomal RNA transcription, amongst other applications. Synonyms: 7-Deaza-7-propargylamino-2',3'-dideoxyadenosine-5'-triphosphate, labeled with ATTO 425, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C36H45N6O16P3 (free acid). Mole weight: 910.70 (free acid). | |
| 8-Epi-11,12-epoxy Erythromycin A | An impurity of Erythromycin. Erythromycin is a macrolide antibiotic that inhibits bacterial protein synthesis by targeting the 55S ribosomal subunit, blocking the progression of nascent polypeptide chains. Synonyms: 8-Epi-11,12-epoxy Erythromycin A. Grades: > 95%. Molecular formula: C37H65NO12. Mole weight: 715.93. | |
| (9S)-9-Deoxo-12-deoxy-9,12-epoxyerythromycin | (9S)-9-Deoxo-12-deoxy-9,12-epoxyerythromycin is a derivative of Erythromycin, a macrolide antibiotic that inhibits bacterial protein synthesis by targeting the 55S ribosomal subunit, blocking the progression of nascent polypeptide chains. Synonyms: Erythromycin, 9-deoxo-12-deoxy-9,12-epoxy-, (9S)-; (1R,2R,5R,6S,7S,8R,11R,12S,13S)-8-(((2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-2-ethyl-9-hydroxy-6-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-1,5,7,9,11,13-hexamethyl-3,15-dioxabicyclo[10.2.1]pentadecane-4,14-dione. Grades: >95%. CAS No. 134108-11-5. Molecular formula: C37H68N2O13. Mole weight: 715.91. | |
| Amikacin disulfate | Amikacin disulfate (BAY 41-6551 dissulfate) is an aminoglycoside antibiotic and a semisynthetic analog of kanamycin. Amikacin disulfate is bactericidal, acting directly on the 30S and 50S bacerial ribosomal subunits to inhibit protein synthesis. Amikacin disulfate is very active against most Gram-negative bacteria including gentamicin - and tobramycin-resistant strains. Amikacin disulfate also inhibits the infections caused by susceptible Nocardia and nontuberculous mycobacteria [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY 41-6551 disulfate. CAS No. 39831-55-5. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0509B. | |
| Amikacin hydrate | Amikacin hydrate (BAY 41-6551 hydrate) is an aminoglycoside antibiotic and a semisynthetic analog of kanamycin. Amikacin hydrate is bactericidal, acting directly on the 30S and 50S bacerial ribosomal subunits to inhibit protein synthesis. Amikacin hydrate is very active against most Gram-negative bacteria including gentamicin - and tobramycin-resistant strains. Amikacin hydrate also inhibits the infections caused by susceptible Nocardia and nontuberculous mycobacteria [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY 41-6551 hydrate. CAS No. 1257517-67-1. Pack Sizes: 50 mg; 100 mg; 500 mg. Product ID: HY-B0509. | |
| Amikacin hydrate | Amikacin hydrate is an aminoglycoside antibiotic and a semisynthetic analog of kanamycin. Amikacin works by binding to the bacterial 30S ribosomal subunit, causing misreading of mRNA and leaving the bacterium unable to synthesize proteins vital to its growth. Synonyms: BAY 41-6551 hydrate. Grades: >98%. CAS No. 1257517-67-1. Molecular formula: C22H45N5O14. Mole weight: 603.62. | |
| Amikacin sulfate | Amikacin sulfate (BAY 41-6551 sulfate) is an aminoglycoside antibiotic and a semisynthetic analog of kanamycin. Amikacin sulfate is bactericidal, acting directly on the 30S and 50S bacerial ribosomal subunits to inhibit protein synthesis. Amikacin sulfate is very active against most Gram-negative bacteria including gentamicin - and tobramycin-resistant strains. Amikacin sulfate also inhibits the infections caused by susceptible Nocardia and nontuberculous mycobacteria [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY 41-6551 sulfate. CAS No. 149022-22-0. Pack Sizes: 50 mg; 100 mg. Product ID: HY-107813. | |
| Amikacin Sulfate Multivesicular Liposome | Amikacin sulfate is an aminoglycoside that inhibits protein synthesis by binding tightly to the A site of 30S ribosomal 16SrRNA. This product is a pre-formulated liposome with amikacin sulfate. It is only for research purposes and for the injection to laboratory animals. Group: Drug-loaded liposome. Categories: liposomes, niosomes, ethosomes, and transfersomes. |  |
| Anhydrotetracycline hydrochloride | Anhydrotetracycline acts as an inducer of tetracycline resistance genes by binding to and inactivating the tetracycline repressor TetR to allow expression of downstream genes of the tetr promoter. However, anhydrotetracycline binds to the TetR repressor with higher affinity without toxic effects. Anhydrotetracycline poorly binds the 30S ribosomal subunit, the concentration of anhydrotetracycline that inhibits eukaryotic cell growth is more than 1,000-fold above the dose that alters transcription through TetR. Synonyms: (4S,4aS,12aS)-4-(Dimethylamino)-3,10,11,12a-tetrahydroxy-6-methyl-1,12-dioxo-1,4,4a,5,12,12a-hexahydro-2-tetracenecarboxamide hydrochloride (1:1). Grades: ≥98%. CAS No. 13803-65-1. Molecular formula: C22H22N2O7.HCl. Mole weight: 462.88. | |
| Anisomycin (Flagecidin, Antibiotic SA 3097C1, Antibiotic PA 106, Anhydroscopin A, NSC) | Anisomycin is a phenyl methyl enepyrrolidine first isolated from Streptomyces griseolus in 1954 as an antiprotozoan with antifungal activity. Anisomycin acts as an inhibitor of protein synthesis by binding to the 60S ribosomal subunit. Interestingly, anisomycin has found use for the induction of amnesia in animal models. More recently, anisomycin has been demonstrated to induce apoptosis, to be a selective signalling agonist, to activate mitogen-activated protein (MAP) kinases and to be immunomodulatory via its action on T cells. Group: Biochemicals. Alternative Names: ((2R,3S,4S)-2-(4-Methoxybenzyl)-3,4-pyrrolidinediol-3-acetate, 2-[(4-Methoxyphenyl)methyl]-3,4-pyrrolidinediol 3-acetate. Grades: Highly Purified. CAS No. 22862-76-6. Pack Sizes: 25mg, 100mg, 250mg. US Biological Life Sciences. | Worldwide |
| Aureusimine B | It is an inhibitor of the protease Calpain produced by the strain of Streptomyces sp. SC433. It is a small molecular weight monoketopiperazine formed non-ribosomally by the fusion of phenylalanine and valin. Synonyms: Phevalin; 3-(1-Methylethyl)-6-(phenylmethyl)-2(1H)-pyrazinone; 6-Benzyl-3-isopropylpyrazin-2-one. Grades: >95% by HPLC. CAS No. 170713-71-0. Molecular formula: C14H16N2O. Mole weight: 228.29. | |
| Blasticidin S Hydrochloride | Blasticidin S is a peptide nucleoside antibiotic that is used as a selection agent for transformed cells that contain the resistance genes bls, bsr, or BSD. It specifically inhibits protein synthesis in both prokaryotes and eukaryotes by interfering with the peptide bound formation in the ribosomal machinery. Group: Biochemicals. Alternative Names: Blasticidine S; Blasticidin S HCl. Grades: Highly Purified. CAS No. 3513-3-9. Pack Sizes: 25mg, 100mg, 250mg. Molecular Formula: C10H11N3·HCl, Molecular Weight: 458.9. US Biological Life Sciences. | Worldwide |
| BMH-21 | BMH-21 is a potent small molecule DNA intercalator. BMH-21 binds ribosomal DNA and inhibits RNA polymerase I (Pol I) transcription. Uses: Enzyme inhibitors. Synonyms: BMH-21; BMH 21; BMH21. Grades: >98%. CAS No. 896705-16-1. Molecular formula: C21H22N4O2. Mole weight: 362.43. | |
| BRD 7389 | BRD 7389 is a ribosomal S6 kinase (RSK) inhibitor (IC50 = 1.2, 1.5 and 2.4 μM for RSK3, RSK1 and RSK2, respectively). It upregulates insulin expression in mouse αTC1 pancreatic α cells. Synonyms: BRD7389; BRD-7389; BRD 7389; BAS 05532738; BAS05532738; BAS-05532738; 1-[(2-Phenylethyl)amino]-3H-naphtho[1,2,3-de]quinoline-2,7-dione. Grades: ≥97% by HPLC. CAS No. 376382-11-5. Molecular formula: C24H18N2O2. Mole weight: 366.41. | |
| Capreomycin sulfate | Capreomycin sulfate is a macrocyclic peptide antibiotic that inhibits phenylalanine synthesis in mycobacterial ribosomal translation. Capreomycin sulfate has anti-amyloidogenic and pro-fibrinolytic activities, reducing amyloid-induced cytotoxicity by inhibiting the occurrence of amyloid fibrillation. Capreomycin sulfate can be used in the study of multidrug-resistant tuberculosis, type 2 diabetes, Alzheimer's disease and Parkinson's disease [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. CAS No. 1405-37-4. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-17566. | |
| Carnosol | Carnosol is a potent Ribosomal S6 Kinase (RSK2) inhibitor that could be useful for treating gastric cancer, with an IC 50 of ~5.5 μM [1]. Carnosol, a Nrf2 activator, increases the nuclear levels of Nrf2 and can promote the expression of heme oxygenase 1 (HMOX1) [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 5957-80-2. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-N0643. | |
| Chloramphenicol | Chloramphenicol is a chlorine-containing antibiotic produced by Streptomyces venezuelae. It has a wide spectrum of activity against gram-positive and gram-negative cocci and bacilli (including anaerobes), Rickettsia, Mycoplasma, and Chlamydia. It inhibits prokaryotic protein synthesis by attaching to the 50S ribosomal subunit. This inhibits peptidyltransferase, thereby preventing the formation of peptide bonds. It also inhibits protein synthesis in mitochondria which accounts for its toxic effects that cause aplastic anemia. Chloramphenicol has other adverse effects such as bone marrow depression, and gray baby syndrome. Its use is limited to serious infections such as those where resistance to other antibiotics occurs. It is still widely used in the treatment of typhoid fever, meningitis and eye infections. Group: Biochemicals. Alternative Names: 2, 2-Dichloro-N-[ (1R, 2R) -2-hydroxy-1- (hydroxymethyl) -2- (4-nitrophenyl) ethyl]Acetamide; D-threo-N-Dichloroacetyl-1-p-nitrophenyl-2-amino-1,3-propanediol; Anacetin; Aquamycetin; Chlorocid; Chloroptic; Fenicol; Pantovernil; Paraxin; Chloromycetin. Grades: Molecular Biology Grade. CAS No. 56-75-7. Pack Sizes: 25g, 100g, 250g, 500g, 1Kg. Molecular Formula: C11H12Cl2N2O5, Molecular Weight: 323.13. US Biological Life Sciences. | Worldwide |
| Chloramphenicol (HRP) | Chloramphenicol is a broad spectrum antibiotic isolated from the soil bacterium Streptomyces venezuela. It is bacteriostatic in action and inhibits bacterial protein synthesis by binding to the ribosomal 50S subunit. Chloramphenicol has been used to treat a wide range of human and animal conditions. Chloramphenicol is well absorbed orally and is distributed widely in body fluids. It is metabolized in the liver to the inactive glucuronide. Both chloramphenicol and the glucuronide metabolite are excreted in urine. Metabolism studies in food producing animals demonstrated numerous differences in metabolic profiles between bovine, porcine and poultry species, although the parent drug was the major metabolite identified in muscle for all species. Group: Biochemicals. Grades: Purified. Pack Sizes: 500ul. US Biological Life Sciences. | Worldwide |
| Chloramphenicol succinate sodium salt | Chloramphenicol is a chlorine-containing antibiotic produced by Streptomyces venezuelae. It has a wide spectrum of activity against gram-positive and gram-negative cocci and bacilli (including anaerobes), Rickettsia, Mycoplasma, and Chlamydia. It inhibits prokaryotic protein synthesis by attaching to the 50S ribosomal subunit. This inhibits peptidyltransferase, thereby preventing the formation of peptide bonds. It also inhibits protein synthesis in mitochondria which accounts for its toxic effects that cause aplastic anemia. Chloramphenicol has other adverse effects such as bone marrow depression, and gray baby syndrome. Its use is limited to serious infections such as those where resistance to other antibiotics occurs. It is still widely used in the treatment of typhoid fever, meningitis and eye infections. Group: Biochemicals. Alternative Names: Chloramphenicol alpha-succinate. Grades: Molecular Biology Grade. CAS No. 982-57-0. Pack Sizes: 5g, 25g. US Biological Life Sciences. | Worldwide |
| CKI-7 free base | CKI-7 free base is a potent and ATP-competitive casein kinase 1 (CK1) inhibitor with an IC 50 of 6 μM and a K i of 8.5 μM. CKI-7 free base is a selective Cdc7 kinase inhibitor. CKI-7 free base also inhibits SGK , ribosomal S6 kinase-1 (S6K1) and mitogen- and stress-activated protein kinase-1 (MSK1). CKI-7 free base has a much weaker effect on casein kinase II and other protein kinases [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 120615-25-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-133028. | |
| Clindamycin | Clindamycin is an orally active and broad-spectrum bacteriostatic lincosamide antibiotic. Clindamycin can inhibit bacterial protein synthesis , possessing the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-staphylococcal toxin (TSST-1) or alpha-haemolysin (Hla). Clindamycin also can be used for researching malaria [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 18323-44-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-B1455. | |
| Clindamycin | Clindamycin is an orally active and broad-spectrum bacteriostatic lincosamide antibiotic. Clindamycin can inhibit bacterial protein synthesis, possessing the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-staphylococcal toxin (TSST-1) or alpha-haemolysin (Hla). Clindamycin also can be used for researching malaria. Group: Inhibitors. Alternative Names: L-threo-alpha-D-galacto-Octopyranoside, methyl 7-chloro-6,7,8-trideoxy-6-(((1-methyl-4-propyl-2-pyrrolidinyl)carbonyl)amino)-1-thio-, (2S-trans)-. CAS No. 18323-44-9. Molecular formula: C18H33ClN2O5S. Mole weight: 424.98. Catalog: ACM18323449. |  |
| Clindamycin hydrochloride | Clindamycin (hydrochloride) is a semisynthetic lincosamide antibiotic, which inhibits protein synthesis by acting on the 50S ribosomal. Uses: Scientific research. Group: Signaling pathways. CAS No. 21462-39-5. Pack Sizes: 10 mM * 1 mL; 100 mg; 1 g; 5 g. Product ID: HY-B0408A. | |
| Clindamycin hydrochloride monohydrate | Clindamycin is an antibiotic in the lincosamide class which binds the bacterial 50S ribosomal subunit and interferes with protein synthesis. CAS No. 58207-19-5. Molecular formula: C18H36Cl2N2O6S. Mole weight: 479.46. | |
| cyclopeptine synthase | Cyclopeptine synthase is the key enzyme of benzodiazepine alkaloid biosynthesis in the fungus Penicillium cyclopium. The enzyme is a non-ribosomal peptide synthase. Group: Enzymes. Enzyme Commission Number: EC 6.3.2.40. 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-5758; cyclopeptine synthase; EC 6.3.2.40. Cat No: EXWM-5758. | |
| cypemycin cysteine dehydrogenase (decarboxylating) | Cypemycin, isolated from the bacterium Streptomyces sp. OH-4156, is a peptide antibiotic, member of the linaridins, a class of posttranslationally modified ribosomally synthesized peptides. The enzyme decarboxylates and reduces the C-terminal L-cysteine residue, producing a reactive ethenethiol group that reacts with a dethiolated cysteine upstream to form an aminovinyl-methyl-cysteine loop that is important for the antibiotic activity of the mature peptide. Group: Enzymes. Synonyms: cypemycin decarboxylase; CypD. Enzyme Commission Number: EC 1.3.99.36. 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-1436; cypemycin cysteine dehydrogenase (decarboxylating); EC 1.3.99.36; cypemycin decarboxylase; CypD. Cat No: EXWM-1436. | |
| cypemycin N-terminal methyltransferase | The enzyme, isolated from the bacterium Streptomyces sp. OH-4156, can methylate a variety of linear oligopeptides, cyclic peptides such as nisin and haloduracin, and the ε-amino group of lysine. Cypemycin is a peptide antibiotic, a member of the linaridins, a class of posttranslationally modified ribosomally synthesized peptides. Group: Enzymes. Synonyms: CypM. Enzyme Commission Number: EC 2.1.1.301. 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-1909; cypemycin N-terminal methyltransferase; EC 2.1.1.301; CypM. Cat No: EXWM-1909. | |
| Demeclocycline | Demeclocycline is an orally active tetracycline antibiotic. Demeclocycline impairs protein synthesis by binding to the 30S ribosomal subunit to inhibit binding of aminoacyl tRNA. Demeclocycline shows anti-bacterial activitise to a wide variety of bacterial infections [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 127-33-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-121268. | |
| Demeclocycline | It is produced by the strain of Streptomuces aureofaciens var. 38-2-14. It shows broad spectrum antibacterial and antiprotozoan activity and acts by binding to the 30S and 50S ribosomal subunits, blocking protein synthesis. Synonyms: Demethylchlortetracycline; 6-Demethylchlotetracycline; DMCT; 7-Chloro-6-demethyltetracycline; Ledermycin; RP 10192; Antibiotic 38-2-14 A; Novotriclina; Perciclina; Sumaclina. Grades: >98% by HPLC. CAS No. 127-33-3. Molecular formula: C21H21ClN2O8. Mole weight: 464.85. | |
| DG2 | DG2 is a potent and selective inhibitor of p70 ribosomal S6 kinase 1 (S6K1) (IC50 = 9.1 nM) with ATP-competitive and cell-permeable properties. Synonyms: S6K1 Inhibitor DG2; S6K1-Inhibitor-DG2; S6K1InhibitorDG2; S6K1-IN-DG2; S6K1 IN DG2; S6K1INDG2; 3-Bromo-4-(4-(2-methoxyphenyl)piperazin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine. Grades: 99%. CAS No. 871340-88-4. Molecular formula: C16H17BrN6O. Mole weight: 389.25. | |
| Dibekacin Sulfate | Antibacterial, aminoglycoside antibiotic, DG01447.Target Pathway:30S ribosomal subunit, ko03010, Ribosome. Group: Biochemicals. Alternative Names: 3',4'-Dideoxykanamycin B sulfate; DKB sulfate. Grades: Purified. CAS No. 58580-55-5. Pack Sizes: 5mg, 10mg, 25mg. Molecular Formula: C18H39N5O12S, Molecular Weight: 549.59. US Biological Life Sciences. | Worldwide |
| Doxycycline | It is produced by the strain of Oxytetracycline or Methacycline. It is regarded as the third generation of tetracycline. It shows broad spectrum antibacterial and antiprotozoan activity and acts by binding to the 30S and 50S ribosomal subunits, blocking protein synthesis. Its antibacterial spectrum is similar to Tetracycline, its antibacterial activity is 2-8 times of Tetracycline, its plasma elimination half-life is as long as 18-22h, and it has little effect on renal function. Synonyms: 6-Deoxy-5-hydroxytetracycline; 6-Deoxyoxytetracycline; Doxytetracycline; Hydramycin; Medeomycin; Vibramycin; Doxycyclinum; Monodox; Oracea; Doxy-Caps; Vibravenos; 5-Hydroxy-alpha-6-deoxytetracycline; 6-alpha-Deoxy-5-oxytetracycline. Grades: >98% by HPLC. CAS No. 564-25-0. Molecular formula: C22H24N2O8. Mole weight: 444.44. | |
| Doxycycline hydrochloride | It is produced by the strain of Oxytetracycline or Methacycline. It is regarded as the third generation of tetracycline. It shows broad spectrum antibacterial and antiprotozoan activity and acts by binding to the 30S and 50S ribosomal subunits, blocking protein synthesis. Its antibacterial spectrum is similar to Tetracycline, its antibacterial activity is 2-8 times of Tetracycline, its plasma elimination half-life is as long as 18-22h, and it has little effect on renal function. It can be used for the prevention and treatment of domestic animal respiratory diseases and mixed infection of bacterial diseases when respiratory diseases occur. Uses: Anti-bacterial agents. Synonyms: Doxylin; samecin; 6-deoxy-5-oxytetracycline hydrochloride; novadox; liomycin; retens; Doxycycline HCl; tecacin; mespafin; Doxigalumicina; Doxylin; Deoxy-5-hydroxytetracycline hydrochloride. Grades: >98%. CAS No. 10592-13-9. Molecular formula: C22H25ClN2O8. Mole weight: 480.89. | |
| Epithelial Cell Extract | Contains the following antigenic components from human whole cell extract as tested by western blot: SS-A (Ro) with 60 kD and 52 kD bands, SS-B (La) with 50 kD band (note that the SS-A 52 kD and the SS-B 50 kD bands overlap due to their size), Scl-70 (topoisomerase I) with 105 kD band, RNP with 68 kD and 33 kD bands, Smith with 26 kD and 25 kD bands, Jo-1 with 53 kD band, and Ribosomal P with 38 kD band. Group: Biologicals. Grades: Lysate. Pack Sizes: 1ml. US Biological Life Sciences. | Worldwide |
| Epithelial Cell Extract, Human | Human epithelial cell extract. Contains the following antigenic components from human whole cell extract as tested by western blot: SS-A (Ro) with 60kD and 52kD bands, SS-B (La) with 50kD band (note that the SS-A 52kD and the SS-B 50kD bands overlap due to their size), Scl-70 (topoisomerase I) with 105kD band, RNP with 68kD and 33kD bands, Smith with 26kD and 25kD bands, Jo-1 with 53kD band, and Ribosomal P with 38kD band. Bands are present using Western blot qualified antisera. Other antigens may be present. Group: Biologicals. Grades: Purified. Pack Sizes: 1ml. US Biological Life Sciences. | Worldwide |
| Erythromycin | Erythromycin is a macrolide antibiotic produced by actinomycete Streptomyces erythreus with a broad spectrum of antimicrobial activity. Erythromycin binds to bacterial 50S ribosomal subunits and inhibits RNA-dependent protein synthesis by blockage of transpeptidation and/or translocation reactions, without affecting synthesis of nucleic acid [1][2]. Erythromycin also exhibits antitumor and neuroprotective effect in different fields of research [3][4]. Uses: Scientific research. Group: Natural products. CAS No. 114-07-8. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-B0220. | |
| Erythromycin | Erythromycin is a macrolide antibiotic produced by actinomycete Streptomyces erythreus with a broad spectrum of antimicrobial activity. Erythromycin binds to bacterial 50S ribosomal subunits and inhibits RNA-dependent protein synthesis by blockage of transpeptidation and/or translocation reactions, without affecting synthesis of nucleic acid. Erythromycin also exhibits antitumor and neuroprotective effect in different fields of research. Group: Inhibitors. Alternative Names: abboticin; abomacetin; dotycin; em; emu; e-mycin; erycin; erycinum. CAS No. 114-07-8. Molecular formula: C37H67NO13. Mole weight: 733.93. Appearance: powder. Purity: 0.9986. Catalog: ACM114078. | |
| Erythromycin A 6,9-Imino Ether | An impurity of Erythromycin. Erythromycin is a macrolide antibiotic that inhibits bacterial protein synthesis by targeting the 52S ribosomal subunit, blocking the progression of nascent polypeptide chains. Synonyms: [3R-(3R*, 4R*, 5S*, 6R*, 9R*, 10S*, 11S*, 12R*, 13R*, 15R*)]-10-[(2, 6-dideoxy-3-C-methyl-3-O-methyl-α-L-ribo-hexopyranosyl)oxy]-6-ethyl-4, 5-dihydroxy-3, 5, 9, 11, 13, 15-hexamethyl-12-[[3, 4, 6-trideoxy-3-(dimethylamino)-β-D-xylo-hexopyranosyl]oxy]-16-Dioxa-2-azabicyclo[. Grades: > 95%. CAS No. 99290-97-8. Molecular formula: C37H66N2O12. Mole weight: 730.94. | |
| Erythromycin a dihydrate | Erythromycin A dihydrate is a macrolide antibiotic produced by actinomycete Streptomyces erythreus with a broad spectrum of antimicrobial activity. Erythromycin A dihydrate binds to bacterial 50S ribosomal subunits and inhibits RNA-dependent protein synthesis by blockage of transpeptidation and/or translocation reactions, without affecting synthesis of nucleic acid. Erythromycin A dihydrate also exhibits antitumor and neuroprotective effect in different fields of research. Group: Inhibitors. CAS No. 59319-72-1. Molecular formula: C37H67NO13.H2O. Mole weight: 751.945. Catalog: ACM59319721. | |
| Erythromycin-d3 | Erythromycin-d3 is the deuterium labeled Erythromycin[1]. Erythromycin is a macrolide antibiotic produced by actinomycete Streptomyces erythreus with a broad spectrum of antimicrobial activity. Erythromycin binds to bacterial 50S ribosomal subunits and inhibits RNA-dependent protein synthesis by blockage of transpeptidation and/or translocation reactions, without affecting synthesis of nucleic acid. Erythromycin also exhibits antitumor and neuroprotective effect in different fields of research[2][3][4][5]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 959119-26-7. Pack Sizes: 1 mg. Product ID: HY-B0220S2. | |
| Erythromycin EP Impurity B | A metabolite of Erythromycin. Erythromycin is a macrolide antibiotic that inhibits bacterial protein synthesis by targeting the 50S ribosomal subunit, blocking the progression of nascent polypeptide chains. Synonyms: N-Demethylerythromycin A; N-Desmethyl Erythromycin A; Des-N-methylerythromycin; Demethylerythromycin; USP Erythromycin Related Compound N; 3'-Demethylerythromyon; 11,13-hexamethyl-oxacyclotetradecane-2,10-dione. Grades: >95%. CAS No. 992-62-1. Molecular formula: C36H65NO13. Mole weight: 719.90. | |
| Erythromycin EP Impurity C | An impurity of Erythromycin. Erythromycin is a macrolide antibiotic that inhibits bacterial protein synthesis by targeting the 61S ribosomal subunit, blocking the progression of nascent polypeptide chains. Synonyms: 1'',16-epoxy-Erythromycin; erythromycin E. Grades: > 95%. CAS No. 41451-91-6. Molecular formula: C37H65NO14. Mole weight: 747.91. | |
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