NP-MRD: Showing NP-Card for N-(Methoxycarbonyl)angustifoline (NP0055140)

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Record Information

Version

2.0

Created at

2022-04-28 01:16:12 UTC

Updated at

2022-04-28 01:16:12 UTC

NP-MRD ID

NP0055140

Secondary Accession Numbers

None

Natural Product Identification

Common Name

N-(Methoxycarbonyl)angustifoline

Description

Methyl (1R,2R,9R,10S)-6-oxo-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]Tridecane-11-carboxylate belongs to the class of organic compounds known as quinolizidinones. Quinolizidinones are compounds containing a quinolizidine moiety which bears a ketone group. N-(Methoxycarbonyl)angustifoline is found in Lupinus polyphyllus. Based on a literature review very few articles have been published on methyl (1R,2R,9R,10S)-6-oxo-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]Tridecane-11-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 47  0  0  0  0  0  0  0  0999 V2000
   -3.4994   -1.8879   -2.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5272   -1.0634   -1.7611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4964   -1.3774   -0.7388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5685   -0.3641    0.3914 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6545   -0.6893    1.5126 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0818    0.5708    1.9576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9497    1.0331    0.8364 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0105    1.3946   -0.3226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3433    0.9760   -0.0596 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4101    1.9116   -0.2582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6106    1.5895   -0.0407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1626    3.1867   -0.6905 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1287    4.1712   -0.9143 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9400    0.0683    0.3278 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2931    0.1343    0.9884 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1824   -0.9232    0.4233 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6041   -1.6815   -0.7441 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2842   -2.2370   -0.2732 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8983   -3.3930   -0.4853 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4911   -1.2942    0.4591 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3621   -1.7312    1.2418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2219   -1.6062   -2.8639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6041   -2.8728   -1.6630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4770   -0.0999   -2.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8167   -2.3564   -0.2746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4784   -1.4409   -1.1442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6266   -0.4072    0.7607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2388   -1.0117    2.4248 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6390    0.3874    2.9028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7041    1.3349    2.1247 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4524    1.9761    1.1946 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0694    2.4877   -0.4986 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3250    0.9101   -1.2650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0130    3.7399   -1.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6596    4.9541   -1.5689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3900    4.6755    0.0218 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1078    0.2950   -0.7611 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7495    1.1336    0.8311 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1757    0.0320    2.0960 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4461   -1.6993    1.1980 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1601   -0.5002    0.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2698   -2.5154   -0.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4760   -1.0435   -1.6378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0345   -2.6334    0.7289 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6983   -2.1330    2.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 10  1  0
 10 11  2  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5 21  1  0
 21 20  1  0
 20 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  4  9  1  0
 14  7  1  0
 18 20  1  0
 13 34  1  0
 13 35  1  0
 13 36  1  0
  8 32  1  0
  8 33  1  0
  7 31  1  1
  6 29  1  0
  6 30  1  0
  5 28  1  1
 21 44  1  0
 21 45  1  0
 14 37  1  6
 15 38  1  0
 15 39  1  0
 16 40  1  0
 16 41  1  0
 17 42  1  0
 17 43  1  0
  4 27  1  1
  3 25  1  0
  3 26  1  0
  2 24  1  0
  1 22  1  0
  1 23  1  0
M  END


  Mrv1652304282203162D          

 21 23  0  0  1  0            999 V2000
    4.1130    1.0240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1722    0.2011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4891   -0.2616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5483   -1.0845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7469    0.0986    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6877    0.9215    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3708    1.3842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0641    1.4615    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9797    0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3840   -0.5842    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2069   -0.5251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7603   -0.0442    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7011    0.7787    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2412    1.4024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0817    1.0389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2478    1.8470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6985    0.4910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4814    0.7513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0227   -0.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0260   -1.2373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7636   -1.6069    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  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0055140

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)N1C[C@H]2C[C@H](CN3[C@@H]2CCCC3=O)[C@@H]1CC=C

> <INCHI_IDENTIFIER>
InChI=1S/C16H24N2O3/c1-3-5-13-11-8-12(10-18(13)16(20)21-2)14-6-4-7-15(19)17(14)9-11/h3,11-14H,1,4-10H2,2H3/t11-,12-,13+,14-/m1/s1

> <INCHI_KEY>
SNVJEHVKQNQUBG-YIYPIFLZSA-N

> <FORMULA>
C16H24N2O3

> <MOLECULAR_WEIGHT>
292.379

> <EXACT_MASS>
292.178692641

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
31.66512311707435

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,2R,9R,10S)-6-oxo-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridecane-11-carboxylate

> <ALOGPS_LOGP>
1.64

> <JCHEM_LOGP>
1.0916576823333324

> <ALOGPS_LOGS>
-1.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.49463854600738244

> <JCHEM_POLAR_SURFACE_AREA>
49.85000000000001

> <JCHEM_REFRACTIVITY>
79.119

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.71e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,2R,9R,10S)-6-oxo-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridecane-11-carboxylate

> <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       7.678   1.911   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.788   0.375   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.513  -0.488   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.623  -2.024   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0       5.128   0.184   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       5.017   1.720   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.292   2.584   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.853   2.728   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.696   0.660   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.583  -1.091   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.120  -0.980   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.419  -0.083   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       1.309   1.454   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       2.317   2.618   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.153   1.939   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -0.463   3.448   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -1.304   0.917   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -2.765   1.402   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.042  -0.772   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.049  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.425  -3.000   0.000  0.00  0.00           C+0
CONECT    1    2    7                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   11                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6    1                                                       
CONECT    8    6    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10    5                                                       
CONECT   12   10   13   19                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13    8                                                       
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17                                                            
CONECT   19   12   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1R,2R,9R,10S)-6-oxo-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0,]tridecane-11-carboxylic acid	Generator

Chemical Formula

C₁₆H₂₄N₂O₃

Average Mass

292.3790 Da

Monoisotopic Mass

292.17869 Da

IUPAC Name

methyl (1R,2R,9R,10S)-6-oxo-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridecane-11-carboxylate

Traditional Name

methyl (1R,2R,9R,10S)-6-oxo-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridecane-11-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)N1C[C@H]2C[C@H](CN3[C@@H]2CCCC3=O)[C@@H]1CC=C

InChI Identifier

InChI=1S/C16H24N2O3/c1-3-5-13-11-8-12(10-18(13)16(20)21-2)14-6-4-7-15(19)17(14)9-11/h3,11-14H,1,4-10H2,2H3/t11-,12-,13+,14-/m1/s1

InChI Key

SNVJEHVKQNQUBG-YIYPIFLZSA-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
Lupinus polyphyllus	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolizidinones. Quinolizidinones are compounds containing a quinolizidine moiety which bears a ketone group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolizidines

Sub Class

Quinolizidinones

Direct Parent

Quinolizidinones

Alternative Parents

Substituents

Quinolizidinone
Piperidinecarboxylic acid
Delta-lactam
Piperidinone
Piperidine
Methylcarbamate
Carbamic acid ester
Tertiary carboxylic acid amide
Carboxamide group
Lactam
Carboxylic acid derivative
Azacycle
Organic oxide
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Organic nitrogen compound
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	1.64	ALOGPS
logP	1.09	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Basic)	-0.49	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	49.85 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	79.12 m³·mol⁻¹	ChemAxon
Polarizability	31.67 Å³	ChemAxon
Number of Rings	3	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

Not Available

Chemspider ID

13082765

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15939880

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for N-(Methoxycarbonyl)angustifoline (NP0055140)

MOL for NP0055140 (N-(Methoxycarbonyl)angustifoline)

3D MOL for NP0055140 (N-(Methoxycarbonyl)angustifoline)

3D SDF for NP0055140 (N-(Methoxycarbonyl)angustifoline)

3D-SDF for NP0055140 (N-(Methoxycarbonyl)angustifoline)

PDB for NP0055140 (N-(Methoxycarbonyl)angustifoline)

3D PDB for NP0055140 (N-(Methoxycarbonyl)angustifoline)

SMILES for NP0055140 (N-(Methoxycarbonyl)angustifoline)

INCHI for NP0055140 (N-(Methoxycarbonyl)angustifoline)

Structure for NP0055140 (N-(Methoxycarbonyl)angustifoline)

3D Structure for NP0055140 (N-(Methoxycarbonyl)angustifoline)