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(8S,10S)-10-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy}-1,6,8,11-tetrahydroxy-8-(2-hydroxyacetyl)-5,7,8,9,10,12-hexahydrotetracene-5,12-dione; oxalic acid
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ChemBase ID:
170327
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Molecular Formular:
C28H29NO15
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Molecular Mass:
619.52756
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Monoisotopic Mass:
619.15371923
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SMILES and InChIs
SMILES:
c1ccc(c2c1C(=O)c1c(C2=O)c(c2c(c1O)C[C@](C[C@@H]2O[C@@H]1O[C@H]([C@@H](O)[C@@H](C1)N)C)(C(=O)CO)O)O)O.C(=O)(O)C(=O)O
Canonical SMILES:
OC(=O)C(=O)O.OCC(=O)[C@@]1(O)C[C@H](O[C@H]2C[C@@H](N)[C@@H]([C@@H](O2)C)O)c2c(C1)c(O)c1c(c2O)C(=O)c2c(C1=O)cccc2O
InChI:
InChI=1S/C26H27NO11.C2H2O4/c1-9-21(31)12(27)5-16(37-9)38-14-7-26(36,15(30)8-28)6-11-18(14)25(35)20-19(23(11)33)22(32)10-3-2-4-13(29)17(10)24(20)34;3-1(4)2(5)6/h2-4,9,12,14,16,21,28-29,31,33,35-36H,5-8,27H2,1H3;(H,3,4)(H,5,6)/t9-,12-,14-,16-,21+,26-;/m0./s1
InChIKey:
MPTUGNYPIWGZLI-BUBJVQHESA-N
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Cite this record
CBID:170327 http://www.chembase.cn/molecule-170327.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}-1,6,8,11-tetrahydroxy-8-(2-hydroxyacetyl)-5,7,8,9,10,12-hexahydrotetracene-5,12-dione; oxalic acid
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IUPAC Traditional name
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(8S,10S)-10-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy}-1,6,8,11-tetrahydroxy-8-(2-hydroxyacetyl)-9,10-dihydro-7H-tetracene-5,12-dione; oxalic acid
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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-1,6,8,11-tetrahydroxy-8-(hydroxyacetyl)-5,12-naphthacenedione Oxalate
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Desmethyldoxorubicin Oxalate
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14-Hydroxy Carminomycin Oxalate
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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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8.801472
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H Acceptors
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12
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H Donor
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7
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LogD (pH = 5.5)
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-0.9314278
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LogD (pH = 7.4)
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0.2615405
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Log P
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1.3126832
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Molar Refractivity
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130.1114 cm3
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Polarizability
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50.799023 Å3
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Polar Surface Area
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217.07 Å2
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Rotatable Bonds
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5
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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
- • Mossman, T., et al.: J. Immunol. Methods, 65, 55 (1983)
- • Janicke, R.U., et al.: J. Biol. Pharm., 273, 9357 (1983)
- • Sidorova, T.A., et al.: J. Med. Chem., 21, 5330 (1983)
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PATENTS
PATENTS
PubChem Patent
Google Patent