NP-MRD: Showing NP-Card for (-)-O7-Methylsalsolinol (NP0051024)

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Record Information

Version

2.0

Created at

2022-04-27 22:28:33 UTC

Updated at

2022-04-27 22:28:33 UTC

NP-MRD ID

NP0051024

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-O7-Methylsalsolinol

Description

(-)-Salsoline, also known as salsoline or D-salosine, belongs to the class of organic compounds known as tetrahydroisoquinolines. (-)-O7-Methylsalsolinol is found in Alangium lamarckii, Salsola collina , Salsola richteri and Xylosalsola paletzkiana. (-)-O7-Methylsalsolinol was first documented in 1980 (PMID: 6935920). These are tetrahydrogenated isoquinoline derivatives (-)-Salsoline is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 29 30  0  0  0  0  0  0  0  0999 V2000
    3.8321    1.1833   -0.3793 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3069   -0.0787   -0.1113 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9702   -0.4053   -0.0627 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0043    0.5348   -0.2857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3534    0.1819   -0.2316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7044   -1.1132    0.0466 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3112   -2.0523    0.2702 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6452   -1.7166    0.2196 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6096   -2.6987    0.4518 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1052   -1.5854    0.1248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0232   -0.4062    0.0992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6043    0.6032   -0.8518 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3743    1.2293   -0.4779 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5223    2.0514    0.7926 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1715    1.9957   -0.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269    1.2988    0.1100 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0004    1.2609   -1.4875 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2286    1.5735   -0.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0295   -3.0729    0.4894 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5940   -2.4718    0.4190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3295   -2.3332   -0.6611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2026   -2.1592    1.0935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1205    0.0892    1.0843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0307   -0.7495   -0.2230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5907    0.2834   -1.8269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0200    1.8435   -1.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7536    2.8541    0.7440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2575    1.4057    1.6600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5383    2.4543    0.8791 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8  3  1  0
 13  5  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  4 18  1  0
 10 21  1  0
 10 22  1  0
 11 23  1  0
 11 24  1  0
 12 25  1  0
 13 26  1  6
 14 27  1  0
 14 28  1  0
 14 29  1  0
  7 19  1  0
  9 20  1  0
M  END


  Mrv0541 02251208042D          

 14 15  0  0  1  0            999 V2000
   12.3367  -13.4937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1942  -13.4937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3367  -11.0189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6221  -11.4313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7657  -11.0189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7657  -12.6687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3367  -12.6687    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.0512  -11.4313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0512  -12.2562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4797  -11.4313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4797  -12.2562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6221  -12.2562    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.1942  -11.0189    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.1942  -12.6687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  1  1  6  0  0  0
  2 14  1  0  0  0  0
  3  8  1  0  0  0  0
  3  4  1  0  0  0  0
  4 12  1  0  0  0  0
  5 10  2  0  0  0  0
  5  8  1  0  0  0  0
  6  9  1  0  0  0  0
  6 11  2  0  0  0  0
  7  9  1  0  0  0  0
  7 12  1  0  0  0  0
  8  9  2  0  0  0  0
 10 11  1  0  0  0  0
 10 13  1  0  0  0  0
 11 14  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0051024

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(CCN[C@H]2C)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C11H15NO2/c1-7-9-6-11(14-2)10(13)5-8(9)3-4-12-7/h5-7,12-13H,3-4H2,1-2H3/t7-/m0/s1

> <INCHI_KEY>
YTPRLBGPGZHUPD-ZETCQYMHSA-N

> <FORMULA>
C11H15NO2

> <MOLECULAR_WEIGHT>
193.2423

> <EXACT_MASS>
193.110278729

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
21.296754736261757

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S)-7-methoxy-1-methyl-1,2,3,4-tetrahydroisoquinolin-6-ol

> <ALOGPS_LOGP>
0.92

> <JCHEM_LOGP>
1.1372350989211433

> <ALOGPS_LOGS>
-1.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.097057373401725

> <JCHEM_PKA_STRONGEST_BASIC>
9.072264497646431

> <JCHEM_POLAR_SURFACE_AREA>
41.489999999999995

> <JCHEM_REFRACTIVITY>
55.478500000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.51e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
salsoline

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-FEB-12         0                                  
HETATM    1  C   UNK     0      23.029 -25.188   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      28.363 -25.188   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      23.029 -20.569   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      21.695 -21.338   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      25.696 -20.569   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      25.696 -23.648   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      23.029 -23.648   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      24.362 -21.338   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      24.362 -22.878   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      27.029 -21.338   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      27.029 -22.878   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      21.695 -22.878   0.000  0.00  0.00           N+0
HETATM   13  O   UNK     0      28.363 -20.569   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      28.363 -23.648   0.000  0.00  0.00           O+0
CONECT    1    7                                                            
CONECT    2   14                                                            
CONECT    3    8    4                                                       
CONECT    4    3   12                                                       
CONECT    5   10    8                                                       
CONECT    6    9   11                                                       
CONECT    7    1    9   12                                                  
CONECT    8    3    5    9                                                  
CONECT    9    6    7    8                                                  
CONECT   10    5   11   13                                                  
CONECT   11    6   10   14                                                  
CONECT   12    4    7                                                       
CONECT   13   10                                                            
CONECT   14    2   11                                                       
MASTER        0    0    0    0    0    0    0    0   14    0   30    0
END

View in JSmol

Synonyms

Value	Source
(1S)-7-Methoxy-1-methyl-1,2,3,4-tetrahydroisoquinolin-6-ol	HMDB
Salsoline	HMDB
(+)-Salsoline	HMDB
Salsoline (-)-form	HMDB
Salsoline hydrochloride, hydrate (4:4:1)	HMDB
1(R),2(N)-Dimethyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline	HMDB
D-Salosine	HMDB
Salsoline hydrochloride, (R)-isomer	HMDB
Salsoline hydrochloride, (S)-isomer	HMDB
(S)-Salsoline	HMDB
7-O-Methylsalsolinol	HMDB
N-Methyl-(R)-salsolinol	HMDB
Methylsalsolinol	HMDB
Salsoline hydrochloride	HMDB

Chemical Formula

C₁₁H₁₅NO₂

Average Mass

193.2423 Da

Monoisotopic Mass

193.11028 Da

IUPAC Name

(1S)-7-methoxy-1-methyl-1,2,3,4-tetrahydroisoquinolin-6-ol

Traditional Name

salsoline

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(CCN[C@H]2C)C=C1O

InChI Identifier

InChI=1S/C11H15NO2/c1-7-9-6-11(14-2)10(13)5-8(9)3-4-12-7/h5-7,12-13H,3-4H2,1-2H3/t7-/m0/s1

InChI Key

YTPRLBGPGZHUPD-ZETCQYMHSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Alangium lamarckii	Plant	KNApSAcK
Salsola collina	Plant	KNApSAcK
Salsola richteri	Plant	KNApSAcK
Xylosalsola paletzkiana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydroisoquinolines. These are tetrahydrogenated isoquinoline derivatives.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrahydroisoquinolines

Sub Class

Not Available

Direct Parent

Tetrahydroisoquinolines

Alternative Parents

Substituents

Tetrahydroisoquinoline
Anisole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
Benzenoid
Secondary aliphatic amine
Ether
Secondary amine
Azacycle
Organooxygen compound
Organonitrogen compound
Amine
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

isoquinolines (CHEBI:112 )

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	0.92	ALOGPS
logP	1.14	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	10.1	ChemAxon
pKa (Strongest Basic)	9.07	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	41.49 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	55.48 m³·mol⁻¹	ChemAxon
Polarizability	21.3 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0012469

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

442356

PDB ID

Not Available

ChEBI ID

761542

Good Scents ID

Not Available

References

General References

Borg S, Kvande H, Magnuson E, Sjoqvist B: Salsolinol and salsoline in cerebrospinal lumbar fluid of alcoholic patients. Acta Psychiatr Scand Suppl. 1980;286:171-7. doi: 10.1111/j.1600-0447.1980.tb08064.x. [PubMed:6935920 ]

Showing NP-Card for (-)-O7-Methylsalsolinol (NP0051024)

MOL for NP0051024 ((-)-O7-Methylsalsolinol)

3D MOL for NP0051024 ((-)-O7-Methylsalsolinol)

3D SDF for NP0051024 ((-)-O7-Methylsalsolinol)

3D-SDF for NP0051024 ((-)-O7-Methylsalsolinol)

PDB for NP0051024 ((-)-O7-Methylsalsolinol)

3D PDB for NP0051024 ((-)-O7-Methylsalsolinol)

SMILES for NP0051024 ((-)-O7-Methylsalsolinol)

INCHI for NP0051024 ((-)-O7-Methylsalsolinol)

Structure for NP0051024 ((-)-O7-Methylsalsolinol)

3D Structure for NP0051024 ((-)-O7-Methylsalsolinol)