NP-MRD: Showing NP-Card for (+)-Jussiaeiine A (NP0074142)

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Record Information

Version

2.0

Created at

2022-04-28 19:18:41 UTC

Updated at

2022-04-28 19:18:41 UTC

NP-MRD ID

NP0074142

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Jussiaeiine A

Description

Jussiaeiine A belongs to the class of organic compounds known as alkyl aryl ethers. These are organic compounds containing the alkyl aryl ether functional group with the generic formula R-O-R' , where R is an alkyl group and R' is an aryl group. (+)-Jussiaeiine A is found in Ulex airensis, Ulex australis, Ulex densus, Ulex parviflorus and Ulex jussiaei. (+)-Jussiaeiine A was first documented in 2005 (PMID: 15651792). Based on a literature review very few articles have been published on Jussiaeiine A (PMID: 16876210).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 38  0  0  0  0  0  0  0  0999 V2000
    5.0610   -0.7187    1.3444 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9136    0.2012    0.2857 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6629    0.5575   -0.2125 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5991    1.4639   -1.2497 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3937    1.8605   -1.7905 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2492    1.3060   -1.2436 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3107    0.3960   -0.2025 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0281   -0.1127    0.2821 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7883   -0.8394   -0.7476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9976   -1.3738   -0.0049 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7987   -2.3340   -0.8389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8804   -2.7796   -0.1037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8042   -0.2448    0.5519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9554    0.5327    1.4229 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6623    1.5933    2.0961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7982    1.0620    0.7644 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5104    0.0588    0.2703 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6622   -0.2441    2.1727 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6095   -1.6028    0.9567 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0566   -1.0055    1.6863 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4905    1.9113   -1.6934 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3296    2.5757   -2.6100 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2845    1.6207   -1.6734 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2210   -0.8323    1.1159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2425   -1.6274   -1.2742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1947   -0.0749   -1.4729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5924   -1.9491    0.8719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1451   -3.2354   -1.0128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1184   -1.9116   -1.7901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6988   -2.8559   -0.6574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2874    0.3388   -0.2312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6003   -0.6961    1.1978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4927    2.0083    1.4909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9465    2.4237    2.2738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0255    1.2242    3.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1181    1.6373   -0.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2350    1.6661    1.4937 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  7  1  0
  7 17  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 10 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 17  3  1  0
 16  8  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  4 21  1  0
  5 22  1  0
  6 23  1  0
  8 24  1  1
  9 25  1  0
  9 26  1  0
 10 27  1  1
 11 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 13 32  1  0
 15 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
M  END


  Mrv1652304282221182D          

 17 18  0  0  1  0            999 V2000
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  4  9  1  6  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 11 15  1  0  0  0  0
 15 16  1  0  0  0  0
  2 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0074142

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=CC(=N1)[C@@H]1C[C@H](CO)CN(C)C1

> <INCHI_IDENTIFIER>
InChI=1S/C13H20N2O2/c1-15-7-10(9-16)6-11(8-15)12-4-3-5-13(14-12)17-2/h3-5,10-11,16H,6-9H2,1-2H3/t10-,11+/m0/s1

> <INCHI_KEY>
IGKQRFQWPBYAKH-WDEREUQCSA-N

> <FORMULA>
C13H20N2O2

> <MOLECULAR_WEIGHT>
236.315

> <EXACT_MASS>
236.152477892

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
26.915702597211325

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(3S,5R)-5-(6-methoxypyridin-2-yl)-1-methylpiperidin-3-yl]methanol

> <ALOGPS_LOGP>
1.67

> <JCHEM_LOGP>
0.9361140440000009

> <ALOGPS_LOGS>
-1.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.430345767396954

> <JCHEM_PKA_STRONGEST_BASIC>
8.277006479195059

> <JCHEM_POLAR_SURFACE_AREA>
45.59

> <JCHEM_REFRACTIVITY>
67.1431

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.94e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(3S,5R)-5-(6-methoxypyridin-2-yl)-1-methylpiperidin-3-yl]methanol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       2.667  -4.620   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      -1.334  -6.930   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   17                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    4   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15   11   16                                                       
CONECT   16   15                                                            
CONECT   17    2                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₂₀N₂O₂

Average Mass

236.3150 Da

Monoisotopic Mass

236.15248 Da

IUPAC Name

[(3S,5R)-5-(6-methoxypyridin-2-yl)-1-methylpiperidin-3-yl]methanol

Traditional Name

[(3S,5R)-5-(6-methoxypyridin-2-yl)-1-methylpiperidin-3-yl]methanol

CAS Registry Number

Not Available

SMILES

COC1=CC=CC(=N1)[C@@H]1C[C@H](CO)CN(C)C1

InChI Identifier

InChI=1S/C13H20N2O2/c1-15-7-10(9-16)6-11(8-15)12-4-3-5-13(14-12)17-2/h3-5,10-11,16H,6-9H2,1-2H3/t10-,11+/m0/s1

InChI Key

IGKQRFQWPBYAKH-WDEREUQCSA-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
Ulex airensis	Plant	KNApSAcK
Ulex australis	Plant	KNApSAcK
Ulex densus	Plant	KNApSAcK
Ulex parviflorus	LOTUS Database	35616633
Ulex parviflorus subsp. jussiaei	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl aryl ethers. These are organic compounds containing the alkyl aryl ether functional group with the generic formula R-O-R' , where R is an alkyl group and R' is an aryl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Alkyl aryl ethers

Alternative Parents

Substituents

Alkyl aryl ether
Aralkylamine
Piperidine
Pyridine
1,3-aminoalcohol
Heteroaromatic compound
Tertiary amine
Tertiary aliphatic amine
Azacycle
Organoheterocyclic compound
Primary alcohol
Hydrocarbon derivative
Organonitrogen compound
Amine
Organopnictogen compound
Organic nitrogen compound
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

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	1.67	ALOGPS
logP	0.94	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	15.43	ChemAxon
pKa (Strongest Basic)	8.28	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	45.59 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	67.14 m³·mol⁻¹	ChemAxon
Polarizability	26.92 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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00035120

Chemspider ID

554132

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

638637

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Maximo P, Lourenco A, Tei A, Wink M: Chemotaxonomy of Portuguese Ulex: quinolizidine alkaloids as taxonomical markers. Phytochemistry. 2006 Sep;67(17):1943-9. doi: 10.1016/j.phytochem.2006.05.037. Epub 2006 Jul 28. [PubMed:16876210 ]
Honda T, Takahashi R, Namiki H: Syntheses of (+)-cytisine, (-)-kuraramine, (-)-isokuraramine, and (-)-jussiaeiine A. J Org Chem. 2005 Jan 21;70(2):499-504. doi: 10.1021/jo048365f. [PubMed:15651792 ]

Showing NP-Card for (+)-Jussiaeiine A (NP0074142)

MOL for NP0074142 ((+)-Jussiaeiine A)

3D MOL for NP0074142 ((+)-Jussiaeiine A)

3D SDF for NP0074142 ((+)-Jussiaeiine A)

3D-SDF for NP0074142 ((+)-Jussiaeiine A)

PDB for NP0074142 ((+)-Jussiaeiine A)

3D PDB for NP0074142 ((+)-Jussiaeiine A)

SMILES for NP0074142 ((+)-Jussiaeiine A)

INCHI for NP0074142 ((+)-Jussiaeiine A)

Structure for NP0074142 ((+)-Jussiaeiine A)

3D Structure for NP0074142 ((+)-Jussiaeiine A)