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(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{[(1S,5R,13R,14S)-14-hydroxy-4-methyl-12-oxa-4-azapentacyclo[9.6.1.01,13.05,17.07,18]octadeca-7(18),8,10,15-tetraen-10-yl]oxy}oxane-2-carboxylic acid
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ChemBase ID:
130690
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Molecular Formular:
C23H27NO9
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Molecular Mass:
461.46178
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Monoisotopic Mass:
461.16858145
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SMILES and InChIs
SMILES:
CN1CC[C@]23c4c5ccc(c4O[C@H]2[C@H](C=CC3[C@@H]1C5)O)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)C(=O)O)O)O)O
Canonical SMILES:
O[C@@H]1[C@@H](O)[C@@H](O[C@@H]([C@H]1O)C(=O)O)Oc1ccc2c3c1O[C@@H]1[C@@]43CCN([C@@H](C2)C4C=C[C@@H]1O)C
InChI:
InChI=1S/C23H27NO9/c1-24-7-6-23-10-3-4-12(25)20(23)32-18-13(5-2-9(14(18)23)8-11(10)24)31-22-17(28)15(26)16(27)19(33-22)21(29)30/h2-5,10-12,15-17,19-20,22,25-28H,6-8H2,1H3,(H,29,30)/t10?,11-,12+,15+,16+,17-,19+,20+,22-,23+/m1/s1
InChIKey:
WAEXKFONHRHFBZ-RURUVCMVSA-N
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Cite this record
CBID:130690 http://www.chembase.cn/molecule-130690.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{[(1S,5R,13R,14S)-14-hydroxy-4-methyl-12-oxa-4-azapentacyclo[9.6.1.01,13.05,17.07,18]octadeca-7(18),8,10,15-tetraen-10-yl]oxy}oxane-2-carboxylic acid
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IUPAC Traditional name
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(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{[(1S,5R,13R,14S)-14-hydroxy-4-methyl-12-oxa-4-azapentacyclo[9.6.1.01,13.05,17.07,18]octadeca-7(18),8,10,15-tetraen-10-yl]oxy}oxane-2-carboxylic acid
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Synonyms
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Morphine 3-β-D-glucuronide solution
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M3G
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Morphine 3-β-D-glucuronide
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吗啡 3-β-D-葡萄糖苷酸 溶液
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吗啡 3-β-D-葡萄糖苷酸
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CAS Number
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MDL Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
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2.673982
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H Acceptors
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10
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H Donor
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5
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LogD (pH = 5.5)
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-3.4821389
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LogD (pH = 7.4)
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-3.4876406
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Log P
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-3.4819388
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Molar Refractivity
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112.1342 cm3
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Polarizability
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44.3441 Å3
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Polar Surface Area
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149.15 Å2
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Rotatable Bonds
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3
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Lipinski's Rule of Five
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true
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DETAILS
DETAILS
Sigma Aldrich
Sigma Aldrich -
M6886
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Biochem/physiol Actions Metabolite of morphine that is devoid of antinociceptic activity; hyperglycemic and neuroexcitatory effects appear to be mediated via a non-opioid mechanism. |
PATENTS
PATENTS
PubChem Patent
Google Patent