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(1S,9S,10S)-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5-trien-4-ol; (2R,3R)-2,3-dihydroxybutanedioic acid
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ChemBase ID:
131003
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Molecular Formular:
C21H29NO7
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Molecular Mass:
407.45746
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Monoisotopic Mass:
407.19440227
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SMILES and InChIs
SMILES:
CN1CC[C@@]23CCCC[C@@H]2[C@H]1Cc1c3cc(cc1)O.[C@@H]([C@H](C(=O)O)O)(C(=O)O)O
Canonical SMILES:
OC(=O)[C@@H]([C@H](C(=O)O)O)O.Oc1ccc2c(c1)[C@@]13CCCC[C@@H]3[C@@H](C2)N(CC1)C
InChI:
InChI=1S/C17H23NO.C4H6O6/c1-18-9-8-17-7-3-2-4-14(17)16(18)10-12-5-6-13(19)11-15(12)17;5-1(3(7)8)2(6)4(9)10/h5-6,11,14,16,19H,2-4,7-10H2,1H3;1-2,5-6H,(H,7,8)(H,9,10)/t14-,16+,17+;1-,2-/m11/s1
InChIKey:
RWTWIZDKEIWLKQ-XCPWPWHNSA-N
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Cite this record
CBID:131003 http://www.chembase.cn/molecule-131003.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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(1S,9S,10S)-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5-trien-4-ol; (2R,3R)-2,3-dihydroxybutanedioic acid
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IUPAC Traditional name
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L(+)-tartaric acid; dextrorfano
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Synonyms
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(+)-3-Hydroxy-N-methylmorphinan (+)-tartrate salt
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Dextrorphan D-tartrate
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Dextrorphan tartrate
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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
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
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10.461597
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H Acceptors
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2
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H Donor
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1
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LogD (pH = 5.5)
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-0.095644645
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LogD (pH = 7.4)
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0.9349801
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Log P
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2.9030437
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Molar Refractivity
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78.0809 cm3
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Polarizability
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30.3868 Å3
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Polar Surface Area
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23.47 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 -
D127
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Biochem/physiol Actions Noncompetitive NMDA glutamate receptor antagonist that attenuates glutamate neurotoxicity in cortical cell cultures. |
PATENTS
PATENTS
PubChem Patent
Google Patent