Antibiotic 02-3G
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| Category | Antibiotics |
| Catalog number | BBF-02987 |
| CAS | 132243-20-0 |
| Molecular Weight | 1099.17 |
| Molecular Formula | C53H78O24 |
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Description
It is a tryptomycin antibiotic produced by the strain of Streptomyces avellaneus 02-3. It inhibits P388 murine leukemia cells with IC50 of 0.60 μg/mL.
Specification
| Synonyms | 02-3G; 4A,4E-Dideacetylchromomycin A3 |
| IUPAC Name | (2S,3S)-2-[(2S,4R,5R,6R)-4-[(2S,4R,5S,6R)-4-[(2S,4S,5S,6S)-4,5-dihydroxy-4,6-dimethyloxan-2-yl]oxy-5-hydroxy-6-methyloxan-2-yl]oxy-5-hydroxy-6-methyloxan-2-yl]oxy-3-[(1S,3R,4R)-3,4-dihydroxy-1-methoxy-2-oxopentyl]-8,9-dihydroxy-6-[(2S,4R,5S,6R)-5-hydroxy-4-[(2R,4R,5S,6S)-4-hydroxy-5-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-7-methyl-3,4-dihydro-2H-anthracen-1-one |
| Canonical SMILES | CC1C(C(CC(O1)OC2C(CC3=C(C2=O)C(=C4C(=C3)C=C(C(=C4O)C)OC5CC(C(C(O5)C)O)OC6CC(C(C(O6)C)OC)O)O)C(C(=O)C(C(C)O)O)OC)OC7CC(C(C(O7)C)O)OC8CC(C(C(O8)C)O)(C)O)O |
| InChI | InChI=1S/C53H78O24/c1-19-30(73-35-15-31(43(58)21(3)68-35)74-34-14-29(55)49(66-9)24(6)71-34)13-27-11-26-12-28(50(67-10)48(63)42(57)20(2)54)51(47(62)40(26)46(61)39(27)41(19)56)77-37-17-32(44(59)23(5)70-37)75-36-16-33(45(60)22(4)69-36)76-38-18-53(8,65)52(64)25(7)72-38/h11,13,20-25,28-29,31-38,42-45,49-52,54-61,64-65H,12,14-18H2,1-10H3/t20-,21-,22-,23-,24+,25+,28+,29-,31-,32-,33-,34-,35+,36+,37+,38+,42-,43+,44-,45+,49-,50+,51+,52+,53+/m1/s1 |
| InChI Key | UZZCFUQRSLEKFX-NRWDCYODSA-N |
Properties
| Appearance | Yellow Powder |
| Antibiotic Activity Spectrum | Neoplastics (Tumor) |
| Melting Point | 181-186°C |
| Solubility | Soluble in Methanol |
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Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳
