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| Product | Description | |
|---|---|---|
| Chromomycin A2 | Chromomycin A2 is produced by the strain of Streptomyces olivochromogenes 69895. A minor, more hydrophobic analogue of the chromomycin complex of the aureolic acid class; originally isolated from S. Aburaviensis and named aburamycin; exhibits a broad biological profile as an antibacterial, antifungal and antitumor agent. Synonyms: Aburamycin A; NSC 131187. Grades: >98% by HPLC. CAS No. 6992-70-7. Molecular formula: C59H86O26. Mole weight: 1211.30. |  |
| Chromomycin A3 | Chromomycin A3 is an aureolic acid-type antitumor antibiotic. Chromomycin A3 forms dimeric complexes with divalent cations, such as Mg 2+ , which strongly binds to the GC rich sequence of DNA to inhibit DNA replication and transcription. Chromomycin A3 has a variety of utilities as a staining agent for human sperm chromatin, autophagy inducing agent, and apoptosis inhibitor [1]. Uses: Scientific research. Group: Natural products. CAS No. 7059-24-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-W040129. |  |
| Chromomycin A3 | Chromomycin A3 is produced by the strain of Streptomyces olivochromogenes 69895. The major component of the chromomycin complex of the aureolic acid class; isolated from several streptomyces species; exhibits a broad biological profile as an antibacterial, antifungal and antitumour agent; binds reversibly to GC-specific DNA ligand in the minor groove which inhibits transcription, DNA gyrase and topoisomerase II activity. Synonyms: Aburamycin; Toyomycin; NSC 58514; B 599-III; SR1768E. Grades: >98% by HPLC. CAS No. 7059-24-7. Molecular formula: C57H82O26. Mole weight: 1183.24. | |
| Chromomycin A3 | Chromomycin A3 is the major component of the chromomycin complex of the aureolic acid class, isolated from several Streptomyces species and first reported in 1960. Chromomycin A3 exhibits a broad biological profile as an antibacterial, antifungal and antitumor agent. It binds reversibly to GC-specific DNA ligand in the minor groove which inhibits transcription, DNA gyrase and topoisomerase II. The intense UV spectrum and strong fluorescence makes chromomycin a useful stain for DNA. Group: Biochemicals. Grades: Highly Purified. CAS No. 7059-24-7. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Chromomycin a3 from streptomyces griseus | Chromomycin a3 from streptomyces griseus. Group: Biochemicals. Grades: Highly Purified. CAS No. 7059-24-7. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. US Biological Life Sciences. | Worldwide |
| Deacetylchromomycin A3 | It is produced by the strain of marine-derived Streptomyces sp. SNB-005. Synonyms: Deacetyl Chromomycin A3; (2R,3R,4R,6S)-6-(((6S,7S)-7-((1S,3S,4R)-3,4-dihydroxy-1-methoxy-2-oxopentyl)-6-(((2S,4S,5R,6R)-4-(((2S,4S,5R,6R)-4-(((2S,4R,5S,6S)-4,5-dihydroxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-4,10-dihydroxy-3-methyl-5-oxo-5,6,7,8-tetrahydroanthracen-2-yl)oxy)-4-(((2R,4R,5S,6R)-4-hydroxy-5-methoxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-2-methyltetrahydro-2H-pyran-3-yl acetate; (1S)-1-C-[(2S,3S)-7-{[4-O-Acetyl-2,6-dideoxy-3-O-(2,6-dideoxy-4-O-methyl-alpha-D-arabino-hexopyranosyl)-beta-D-arabino-hexopyranosyl]oxy}-3-{[2,6-dideoxy-3-C-methyl-alpha-L-ribo-hexopyranosyl-(1->3)-2,6-dideoxy-beta-D-ribo-hexopyranosyl-(1->3)-2,6-dideoxy-beta-D-ribo-hexopyranosyl]oxy}-5,10-dihydroxy-6-methyl-4-oxo-1,2,3,4-tetrahydro-2-anthracenyl]-5-deoxy-1-O-methyl-D-xylulose; Olivomycin D, 3D-O-(2,6-Dideoxy-3-C-methyl-α-L-arabino-hexopyranosyl)-7-methyl-; NSC 270051. CAS No. 6992-71-8. Molecular formula: C55H80O25. Mole weight: 1141.21. | |
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