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1-[(2R,3R,4S,5S,6S)-6-carboxylato-3,4,5-trihydroxyoxan-2-yl]-3-[(2S)-1-(2H3)methylpyrrolidin-2-yl]-1λ5-pyridin-1-ylium
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ChemBase ID:
175120
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Molecular Formular:
C16H22N2O6
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Molecular Mass:
338.35568
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Monoisotopic Mass:
338.14778643
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SMILES and InChIs
SMILES:
c1c[n+](cc(c1)[C@@H]1CCCN1C)[C@@H]1O[C@H]([C@H]([C@@H]([C@@H]1O)O)O)C(=O)[O-]
Canonical SMILES:
CN1CCC[C@H]1c1ccc[n+](c1)[C@@H]1O[C@@H](C(=O)[O-])[C@H]([C@@H]([C@@H]1O)O)O
InChI:
InChI=1S/C16H22N2O6/c1-17-6-3-5-10(17)9-4-2-7-18(8-9)15-13(21)11(19)12(20)14(24-15)16(22)23/h2,4,7-8,10-15,19-21H,3,5-6H2,1H3/t10-,11-,12-,13+,14-,15+/m0/s1
InChIKey:
SAWAIULJDYFLPD-CTTWBBHYSA-N
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Cite this record
CBID:175120 http://www.chembase.cn/molecule-175120.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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1-[(2R,3R,4S,5S,6S)-6-carboxylato-3,4,5-trihydroxyoxan-2-yl]-3-[(2S)-1-(2H3)methylpyrrolidin-2-yl]-1λ5-pyridin-1-ylium
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IUPAC Traditional name
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1-[(2R,3R,4S,5S,6S)-6-carboxylato-3,4,5-trihydroxyoxan-2-yl]-3-[(2S)-1-(2H3)methylpyrrolidin-2-yl]-1λ5-pyridin-1-ylium
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Synonyms
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1-β-D-Glucopyranuronosyl-3-[(2S)-1-(methyl-d3)-2-pyrrolidinyl]pyridinium Inner Salt
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(S)-1-β-D-Glucopyranuronosyl-3-[1-(methyl-d3)-2-pyrrolidinyl]pyridinium Inner Salt
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Nicotine-d3 N-Glucuronide
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NNG-d3
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NIC GLUC-d3
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Nicotine-d3 N-β-D-Glucuronide
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CAS 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
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
Acid pKa
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2.5186102
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H Acceptors
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7
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H Donor
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3
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LogD (pH = 5.5)
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-6.926464
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LogD (pH = 7.4)
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-5.4127965
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Log P
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-7.2624025
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Molar Refractivity
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94.177 cm3
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Polarizability
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33.05497 Å3
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Polar Surface Area
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117.17 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
TRC
Toronto Research Chemicals -
N424595
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Labelled Nicotine N-β-D-Glucuronide (N424575). Nicotine N-β-D-Glucuronide is a Nicotine (N412420) metabolite in rat brain. Nicotine N-β-D-Glucuronide is used as a Nicotine biomarker in rat brain. |
REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google Books
- • Alexandrov, K., et al.: Toxicol. Lett., 198, 63 (2010)
- • Huang, L., et al.: J. Neurochem., 109, 826 (2010)
- • Quik, M., et al.: Biochem. Pharmacol., 78, 677 (2010)
- • Weems, J., et al.: Chem. Res. Toxicol., 23, 696 (2010)
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PATENTS
PATENTS
PubChem Patent
Google Patent