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(8S,10S)-10-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy}-6,8,11-trihydroxy-8-[(1R)-1-hydroxyethyl]-1-methoxy-5,7,8,9,10,12-hexahydrotetracene-5,12-dione
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ChemBase ID:
165428
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Molecular Formular:
C27H31NO10
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Molecular Mass:
529.53574
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Monoisotopic Mass:
529.1947962
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SMILES and InChIs
SMILES:
c1cc(c2c(c1)C(=O)c1c(C2=O)c(c2c(c1O)C[C@@](C[C@@H]2O[C@H]1C[C@H]([C@@H]([C@@H](O1)C)O)N)(O)[C@H](O)C)O)OC
Canonical SMILES:
COc1cccc2c1C(=O)c1c(C2=O)c(O)c2c(c1O)[C@@H](O[C@H]1C[C@@H](N)[C@@H]([C@@H](O1)C)O)C[C@](C2)(O)[C@H](O)C
InChI:
InChI=1S/C27H31NO10/c1-10-22(30)14(28)7-17(37-10)38-16-9-27(35,11(2)29)8-13-19(16)26(34)21-20(24(13)32)23(31)12-5-4-6-15(36-3)18(12)25(21)33/h4-6,10-11,14,16-17,22,29-30,32,34-35H,7-9,28H2,1-3H3/t10-,11+,14-,16-,17-,22+,27-/m0/s1
InChIKey:
HJEZFVLKJYFNQW-OXCIRTNUSA-N
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Cite this record
CBID:165428 http://www.chembase.cn/molecule-165428.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
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IUPAC name
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(8S,10S)-10-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy}-6,8,11-trihydroxy-8-[(1R)-1-hydroxyethyl]-1-methoxy-5,7,8,9,10,12-hexahydrotetracene-5,12-dione
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IUPAC Traditional name
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Synonyms
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(8S,10S)-10-[(3-Amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-[1-hydroxyethyl]-1-methoxy-5,12-naphthacenedione
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13-Dihydrodaunorubicin
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Duborimycin
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Leukaemomycin D
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Daunorubicinol (Mixture of Diastereomers)
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
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Data Source
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Data ID
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Price
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TRC
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CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
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Acid pKa
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9.736299
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H Acceptors
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11
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H Donor
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6
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LogD (pH = 5.5)
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-1.0412652
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LogD (pH = 7.4)
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-0.02799974
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Log P
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1.2748721
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Molar Refractivity
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133.8167 cm3
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Polarizability
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52.490555 Å3
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Polar Surface Area
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189.0 Å2
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Rotatable Bonds
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4
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Lipinski's Rule of Five
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false
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DETAILS
DETAILS
TRC
REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google Books
- • Mizuno, N.S., et al.: Cancer Res., 35, 1542 (1975)
- • Munger, C., et al.: Cancer Res., 48, 2404 (1975)
- • Kobayashi, Y., et al.: J. Biol. Chem., 275, 17639 ( 2000), Burke, B., et al.: Cardiovasc. Toxicol., 2, 41 (1975)
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PATENTS
PATENTS
PubChem Patent
Google Patent