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143-98-6 molecular structure
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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

ChemBase ID: 131003
Molecular Formular: C21H29NO7
Molecular Mass: 407.45746
Monoisotopic Mass: 407.19440227
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

Cite this record

CBID:131003 http://www.chembase.cn/molecule-131003.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(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
IUPAC Traditional name
L(+)-tartaric acid; dextrorfano
Synonyms
(+)-3-Hydroxy-N-methylmorphinan (+)-tartrate salt
Dextrorphan D-tartrate
Dextrorphan tartrate
CAS Number
143-98-6
PubChem SID
162225281
24277974
PubChem CID
5484438

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
D127 external link Add to cart Please log in.
Data Source Data ID
PubChem 5484438 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 10.461597  H Acceptors
H Donor LogD (pH = 5.5) -0.095644645 
LogD (pH = 7.4) 0.9349801  Log P 2.9030437 
Molar Refractivity 78.0809 cm3 Polarizability 30.3868 Å3
Polar Surface Area 23.47 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Pharmacology Properties Bioassay(PubChem)
Solubility
H2O: >10 mg/mL expand Show data source
Apperance
white powder expand Show data source
RTECS
QD1930000 expand Show data source
European Hazard Symbols
Harmful Harmful (Xn) expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
22 expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H302 expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves expand Show data source
Gene Information
human ... GRIN1(2902), GRIN2A(2903), GRIN2B(2904), GRIN2C(2905), GRIN2D(2906), GRINA(2907) expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - D127 external link
Biochem/physiol Actions
Noncompetitive NMDA glutamate receptor antagonist that attenuates glutamate neurotoxicity in cortical cell cultures.

REFERENCES

REFERENCES

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PATENTS

PATENTS

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