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| Product | Description | |
|---|---|---|
| Gilvocarcin M | It is produced by the strain of Streptomyces gilvotanareus, Str. anandii. It has anti-gram-positive bacterial activity and can inhibit sarcoma 180 and P388 leukemia cells. Synonyms: 6H-Benzo(d)naphtho(1,2-b)pyran-6-one, 4-(6-deoxy-alpha-galactofuranosyl)-1-hydroxy-10,12-dimethoxy-8-methyl-; 4-(6-Deoxy-α-L-galactofuranosyl)-1-hydroxy-10,12-dimethoxy-8-methyl-6H-benzo[d]naphtho[1,2-b]pyran-6-one; Anandimycin B; ToroMycin B; Antibiotic 1072A. Grades: >95% by HPLC. CAS No. 77879-89-1. Molecular formula: C26H26O9. Mole weight: 482.48. |  |
| Gilvocarcin M (Anandimycin B, Toromycin B, Antibiotic 1072A) | Gilvocarcin M is the minor analogue of a complex of C-glycoside antitumor actives isolated from a Streptomyces sp. Gilvocarcin M contains a methyl group in the 8-position and is less active than the vinyl analogue (gilvocarcin V), which is thought to act as an inhibitor of human topoisomerase II. Gilvocarcin M displays potent antibacterial, antifungal, antiviral and antitumor activity. Recent research on the gilvocarcins suggests that they act as photoactivated crosslinkers of DNA to histones. Group: Biochemicals. Alternative Names: Anandimycin B, Toromycin B, Antibiotic 1072A. Grades: Highly Purified. CAS No. 77879-89-1. Pack Sizes: 500ug. US Biological Life Sciences. |  Worldwide |
| Gilvocarcin V (Anandimycin A, Toromycin B, Antibiotic 1072B) | Gilvocarcin V is the major analogue of a complex of C-glycoside antitumor actives isolated from a Streptomyces sp. Gilvocarcin V contains a vinyl group in the 8-position and is the most potent analogue of the complex. It is thought to act as an inhibitor of the catalytic activity of human topoisomerase II. The metabolite displays potent antibacterial, antifungal, antiviral and antitumor activity. Recent research on the gilvocarcins suggests that they act as photoactiviated crosslinkers of DNA to histones. Group: Biochemicals. Alternative Names: Anandimycin A, Toromycin B, Antibiotic 1072B. Grades: Highly Purified. CAS No. 77879-90-4. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Chrysomycin A (Chrysomycin V, Virenomycin V, Albacarcin V) | Chrysomycin A is the major analogue in a complex of C-glycoside antitumor actives isolated from Streptomyces. Chrysomycin A, with a vinyl group in the 8-position, is the most potent analogue of the complex, which is thought to act as an inhibitor of the catalytic activity of human topoisomerase II. Chrysomyin A has a potent antibacterial, antifungal, antiviral and antitumor profile. More recent research on related metabolites, the gilvocarcins, suggests that chrysomycins may act as photoactivated, crosslinkers of DNA to histones. Group: Biochemicals. Alternative Names: Chrysomycin V, Virenomycin V, Albacarcin V. Grades: Highly Purified. CAS No. 82196-88-1. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Chrysomycin B (Chrysomycin M, Virenomycin M, Albacarcin M) | Chrysomycin B is a minor analogue in a complex of C-glycoside antitumor actives isolated from Streptomyces. Chrysomycin B, containing a methyl group in the 8-position, is less active than its vinyl analogue (Chrysomycin A), albeit still a potent antitumor active and an inhibitor of the catalytic activity of human topoisomerase II. More recent research on related metabolites, the gilvocarcins, suggests that chrysomycins may act as photoactivated crosslinkers of DNA to histones. Group: Biochemicals. Alternative Names: Chrysomycin M, Virenomycin M, Albacarcin M. Grades: Highly Purified. CAS No. 83852-56-6. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Defucogilvocarcin V | Defucogilvocarcin V is a gilvocarcin antibiotic produced by Streptomyces arenas 2046. Activity against gram-positive bacteria. Synonyms: 6H-Benzo(d)naphtho(1,2-b)pyran-6-one, 8-ethenyl-1-hydroxy-10,12-dimethoxy-; Gilvocarcin V aglycone. CAS No. 80155-95-9. Molecular formula: C21H16O5. Mole weight: 348.35. | |
| Gilvocarcin V | Gilvocarcin V is an antibiotic with antibacterial activity and can be isolated from Actinomycete. Gilvocarcin V also has anti-tumor activity and can be used in cancer research [1]. Uses: Scientific research. Group: Natural products. CAS No. 77879-90-4. Pack Sizes: 100 μg; 250 μg. Product ID: HY-129307. |  |
| O-Deacetyl-ravidomycin (Antibiotic AY 26623) | O-deacetyl-ravidomycin is the more active and stable analogue of the ravidomycin complex produced by Streptomyces ravidus. The metabolite shows potent, light dependent antitumour activity. Microbial Screening Technologies in-house bioassays detected weak antibacterial and antifungal activity. O-Deacetyl-ravidomycin, like the related gilvocarcins and chrysomycins, is thought to act as a topoisomerase II inhibitor. Group: Biochemicals. Alternative Names: Antibiotic AY 26623. Grades: Highly Purified. CAS No. 88580-27-2. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Gilvocarcin E | It is produced by the strain of Streptomyces gilvotanareus, Str. anandii. It has anti-gram-positive bacterial activity and can inhibit sarcoma 180 and P388 leukemia cells. Synonyms: 8-Ethyl-4-(6-deoxy-α-L-galactofuranosyl)-1-hydroxy-10,12-dimethoxy-6H-benzo[d]naphtho[1,2-b]pyran-6-one; Anandimycin C; Toromycin C; dihydrotoromycin; 4-Fucofuranosyl-1-hydroxy-10,12-dimethoxy-8-ethyl-6H-benzo(d)naphtho(1,2b)pyran-6-one; 1,4-Anhydro-6-deoxy-1-(8-ethyl-1-hydroxy-10,12-dimethoxy-6-oxo-6H-benzo[d]naphtho[1,2-b]pyran-4-yl)hexitol. CAS No. 80937-34-4. Molecular formula: C27H28O9. Mole weight: 496.50. | |
| Gilvocarcin V | Antibiotic. Antitumor compound. Weakly active against Gram-positive bacteria and fungi. Mediates a unique cross-linking reaction between DNA and histone H3 by light. Single strand scission and covalent binding to DNA after photoactivation. Source:Streptomyces sp. Gö 3592. Group: Biochemicals. Alternative Names: 4-(6-Deoxy-α-D-galactofuranosyl)-8-ethenyl-1-hydroxy-10,12-dimethoxy-6H-benzo[d]naphtho[1,2-b]pyran-6-one; Antibiotic 1072B; NSC 338943; NSC 348115. Grades: Highly Purified. CAS No. 77879-90-4. Pack Sizes: 100ug, 250ug, 1mg. Molecular Formula: C??H??O?. US Biological Life Sciences. | Worldwide |
| Gilvocarcin V | It is produced by the strain of Streptomyces gilvotanareus, Str. anandii. It has anti-gram-positive bacteria, negative bacteria, fungal activity and can inhibit sarcoma 180 and P388 leukemia cells. Synonyms: DC-38-V; Anandimycin A; Toromycin; Antibiotic 1072B; Antibiotic B21085; Antibiotic DC 38A; Antibiotic DC 38V; 4-(6-Deoxy-α-D-galactofuranosyl)-8-ethenyl-1-hydroxy-10,12-dimethoxy-6H-benzo[d]naphtho[1,2-b]pyran-6-one; NSC 338943; NSC 348115. Grades: >95% by HPLC. CAS No. 77879-90-4. Molecular formula: C27H26O9. Mole weight: 494.49. | |
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