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CAS 55598-85-1

:

49-({3-[(4-amino-5-hydroxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy]-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl}oxy)-5,15-dichloro-2,18,33,36,38-pentahydroxy-19-{[4-methyl-2-(methylamino)pentanoyl]amino}-20,24,27,43,45-pentaoxo-7,13-dioxa-21,

Description:
The chemical substance with the name "49-({3-[(4-amino-5-hydroxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy]-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl}oxy)-5,15-dichloro-2,18,33,36,38-pentahydroxy-19-{[4-methyl-2-(methylamino)pentanoyl]amino}-20,24,27,43,45-pentaoxo-7,13-dioxa-21" and CAS number "55598-85-1" is a complex organic compound characterized by multiple functional groups, including hydroxyl (-OH), amino (-NH2), and oxo (=O) groups, which contribute to its potential biological activity. The presence of dichloro and various hydroxy groups suggests that this compound may exhibit significant reactivity and solubility in polar solvents. Its intricate structure, featuring multiple tetrahydropyran rings, indicates potential for stereochemical diversity, which could influence its interaction with biological targets. Such compounds are often investigated for their pharmacological properties, including antimicrobial or antitumor activities. However, specific properties such as melting point, solubility, and stability would require empirical data for precise characterization.
Formula:C66H74Cl2N8O25
InChI:InChI=1/C66H74Cl2N8O25/c1-23(2)12-34(70-5)58(87)75-49-51(82)26-7-10-38(32(67)14-26)97-40-16-28-17-41(55(40)101-65-56(54(85)53(84)42(22-77)99-65)100-44-21-66(4,69)57(86)24(3)96-44)98-39-11-8-27(15-33(39)68)52(83)50-62(91)74-48(64(94)95)31-18-29(78)19-37(80)45(31)30-13-25(6-9-36(30)79)46(59(88)76-50)73-60(89)47(28)72-43(81)20-35(63(92)93)71-61(49)90/h6-11,13-19,23-24,34-35,42,44,46-54,56-57,65,70,77-80,82-86H,12,20-22,69H2,1-5H3,(H,71,90)(H,72,81)(H,73,89)(H,74,91)(H,75,87)(H,76,88)(H,92,93)(H,94,95)
SMILES:CC(C)CC(C(=NC1C(c2ccc(c(c2)Cl)Oc2cc3cc(c2OC2C(C(C(C(CO)O2)O)O)OC2CC(C)(C(C(C)O2)O)N)Oc2ccc(cc2Cl)C(C2C(=NC(c4cc(cc(c4c4cc(ccc4O)C(C(=N2)O)N=C(C3N=C(CC(C(=O)O)N=C1O)O)O)O)O)C(=O)O)O)O)O)O)NC
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