NP-MRD: Showing NP-Card for Multiflorine N-oxide (NP0055151)

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Record Information

Version

2.0

Created at

2022-04-28 01:16:42 UTC

Updated at

2022-04-28 01:16:42 UTC

NP-MRD ID

NP0055151

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Multiflorine N-oxide

Description

(1R,2S,7R,9R,10R)-7λ⁵,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]Heptadec-13-ene-7,12-dione belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative. Multiflorine N-oxide is found in Lupinus hirsutus and Lupinus pilosus. Based on a literature review very few articles have been published on (1R,2S,7R,9R,10R)-7λ⁵,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]Heptadec-13-ene-7,12-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 44  0  0  0  0  0  0  0  0999 V2000
   -5.5908   -0.4689   -0.2645 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4171   -0.0254   -0.2187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1821    1.3298   -0.6876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9265    1.7049   -0.8397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8380    0.8337   -0.5615 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5025    1.3735   -0.7453 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2222    1.2273    0.5587 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6254    0.5146    1.6075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9736   -0.8141    1.0103 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1868   -1.6175    0.5469 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3056   -0.9277    0.0474 N   0  0  2  0  0  4  0  0  0  0  0  0
    1.3488   -1.0643   -1.3217 O   0  0  0  0  0  1  0  0  0  0  0  0
    2.5309   -1.6293    0.4826 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6533   -1.0285   -0.3374 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8527    0.4400   -0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5210    1.1262   -0.3532 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4749    0.4209    0.4708 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9779   -0.5301   -0.1156 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3613   -0.8905    0.2997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9788    2.0272   -0.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7595    2.7302   -1.1943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5137    2.4283   -1.0898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0464    0.7928   -1.5701 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5060    2.2457    0.9095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5507    1.0695    1.7819 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0055    0.4160    2.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5231   -1.3914    1.7901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2102   -2.3317   -0.2352 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4968   -2.3071    1.3873 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6911   -1.4818    1.5708 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4635   -2.6968    0.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6156   -1.5572   -0.1873 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3352   -1.0870   -1.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6632    0.8264   -0.6358 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0048    0.6111    1.0737 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6149    2.1734    0.0349 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3179    1.1512   -1.4199 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8977    0.3822    1.5192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7089   -1.2054   -0.9814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3966   -0.8209    1.4268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6255   -1.9493    0.0790 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 12  1  6
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 18  1  0
 18 19  1  0
 19  2  1  0
  2  1  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
 17 11  1  0
  6  7  1  0
 10 11  1  0
  5 18  1  0
 13 30  1  0
 13 31  1  0
 14 32  1  0
 14 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 17 38  1  1
  7 24  1  1
  8 25  1  0
  8 26  1  0
  9 27  1  1
 10 28  1  0
 10 29  1  0
 18 39  1  6
 19 40  1  0
 19 41  1  0
  3 20  1  0
  4 21  1  0
  6 22  1  0
  6 23  1  0
M  CHG  2  11   1  12  -1
M  END


  Mrv1652304282203162D          

 19 22  0  0  1  0            999 V2000
    6.3404    2.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0549    2.4469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3404    1.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6259    0.7969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9114    1.2094    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9114    2.0344    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6259    2.4469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3281    2.6178    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1646    1.5188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5031    0.6260    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3281    0.6260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9197    1.2094    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9197    2.0344    0.0000 N   0  3  2  0  0  0  0  0  0  0  0  0
    3.5031    2.6178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2053    2.4469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4908    2.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4908    1.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2053    0.7969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8120    2.8523    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  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  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 18  1  6  0  0  0
 13 19  1  6  0  0  0
M  CHG  2  13   1  19  -1
M  END
> <DATABASE_ID>
NP0055151

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[O-][N@@+]12CCCC[C@H]1[C@@H]1C[C@H](C2)[C@H]2CC(=O)C=CN2C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H22N2O2/c18-13-4-5-16-9-11-7-12(14(16)8-13)10-17(19)6-2-1-3-15(11)17/h4-5,11-12,14-15H,1-3,6-10H2/t11-,12-,14-,15+,17-/m1/s1

> <INCHI_KEY>
JFDGIEYDTGTBET-YTHJTJSOSA-N

> <FORMULA>
C15H22N2O2

> <MOLECULAR_WEIGHT>
262.353

> <EXACT_MASS>
262.168127956

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
28.812093433519003

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,7R,9R,10R)-12-oxo-7,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadec-13-en-7-ium-7-olate

> <ALOGPS_LOGP>
-0.13

> <JCHEM_LOGP>
0.25186621966666567

> <ALOGPS_LOGS>
-2.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.95519246176382

> <JCHEM_PKA_STRONGEST_BASIC>
3.8185445494304813

> <JCHEM_POLAR_SURFACE_AREA>
43.370000000000005

> <JCHEM_REFRACTIVITY>
74.4251

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.06e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,7R,9R,10R)-12-oxo-7,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadec-13-en-7-ium-7-olate

> <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      11.835   3.798   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      13.169   4.568   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      11.835   2.258   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.502   1.488   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       9.168   2.258   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       9.168   3.798   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.502   4.568   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.079   4.886   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.774   2.835   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.539   1.169   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.079   1.169   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.450   2.258   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       5.450   3.798   0.000  0.00  0.00           N+1
HETATM   14  C   UNK     0       6.539   4.886   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.116   4.568   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.783   3.798   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.783   2.258   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.116   1.488   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.249   5.324   0.000  0.00  0.00           O-1
CONECT    1    2    3    7                                                  
CONECT    2    1                                                            
CONECT    3    1    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    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   18                                                  
CONECT   13   12   14   15   19                                             
CONECT   14   13    8                                                       
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   12                                                       
CONECT   19   13                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂N₂O₂

Average Mass

262.3530 Da

Monoisotopic Mass

262.16813 Da

IUPAC Name

(1R,2S,7R,9R,10R)-12-oxo-7,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadec-13-en-7-ium-7-olate

Traditional Name

(1R,2S,7R,9R,10R)-12-oxo-7,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadec-13-en-7-ium-7-olate

CAS Registry Number

Not Available

SMILES

[O-][N@@+]12CCCC[C@H]1[C@@H]1C[C@H](C2)[C@H]2CC(=O)C=CN2C1

InChI Identifier

InChI=1S/C15H22N2O2/c18-13-4-5-16-9-11-7-12(14(16)8-13)10-17(19)6-2-1-3-15(11)17/h4-5,11-12,14-15H,1-3,6-10H2/t11-,12-,14-,15+,17-/m1/s1

InChI Key

JFDGIEYDTGTBET-YTHJTJSOSA-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 hirsutus	Plant	KNApSAcK
Lupinus pilosus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolizidines

Sub Class

Not Available

Direct Parent

Quinolizidines

Alternative Parents

Substituents

Quinolizidine
Tetrahydropyridine
Piperidine
Trialkyl amine oxide
Vinylogous amide
Cyclic ketone
Tertiary aliphatic amine
Tertiary amine
Ketone
Allylamine
Azacycle
Trisubstituted n-oxide
Enamine
N-oxide
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organic zwitterion
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
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	-0.13	ALOGPS
logP	0.25	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	17.96	ChemAxon
pKa (Strongest Basic)	3.82	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	43.37 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	74.43 m³·mol⁻¹	ChemAxon
Polarizability	28.81 Å³	ChemAxon
Number of Rings	4	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163184630

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Multiflorine N-oxide (NP0055151)

MOL for NP0055151 (Multiflorine N-oxide)

3D MOL for NP0055151 (Multiflorine N-oxide)

3D SDF for NP0055151 (Multiflorine N-oxide)

3D-SDF for NP0055151 (Multiflorine N-oxide)

PDB for NP0055151 (Multiflorine N-oxide)

3D PDB for NP0055151 (Multiflorine N-oxide)

SMILES for NP0055151 (Multiflorine N-oxide)

INCHI for NP0055151 (Multiflorine N-oxide)

Structure for NP0055151 (Multiflorine N-oxide)

3D Structure for NP0055151 (Multiflorine N-oxide)