NP-MRD: Showing NP-Card for Ormosianine K (NP0331874)

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Record Information

Version

2.0

Created at

2023-09-27 00:36:18 UTC

Updated at

2024-09-03 04:17:17 UTC

NP-MRD ID

NP0331874

Natural Product DOI

https://doi.org/10.57994/0980

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Ormosianine K

Description

Ormosianine K belongs to the class of organic compounds known as n-acylpiperidines. N-acylpiperidines are compounds containing an N-acyethanolamine moiety, which is characterized by an acyl group is linked to the nitrogen atom of a piperidine. Based on a literature review very few articles have been published on Ormosianine K.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 09272300362D          

 19 21  0  0  1  0            999 V2000
   -0.4853    1.0283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2523    0.6588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1931   -0.1641    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5897   -0.4243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7558   -1.2324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5387   -1.4927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7047   -2.3008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7332   -0.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8760    1.1988    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6989    1.1397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2389    0.5160    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9811    0.8762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6642    0.4135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6050   -0.4094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8628   -0.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1797   -0.3069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5561   -0.8469    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4717    0.2609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0403    1.6990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  6  7  2  0  0  0  0
  3  8  1  0  0  0  0
  9  2  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 17 16  1  0  0  0  0
 17  8  1  0  0  0  0
 17 18  1  1  0  0  0
  9 18  1  1  0  0  0
 12 19  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0331874

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C=CCCN1C[C@@H]2C[C@@H](CN3C(=O)CCC=C23)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H20N2O2/c1-2-3-7-16-9-11-8-12(15(16)19)10-17-13(11)5-4-6-14(17)18/h2,5,11-12H,1,3-4,6-10H2/t11-,12-/m0/s1

> <INCHI_KEY>
FGHFLRKPEJJAJZ-RYUDHWBXSA-N

> <FORMULA>
C15H20N2O2

> <MOLECULAR_WEIGHT>
260.337

> <EXACT_MASS>
260.152477892

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
28.507713256367744

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,9S)-11-(but-3-en-1-yl)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridec-2-ene-6,10-dione

> <JCHEM_LOGP>
0.19391255566666663

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6464047359720302

> <JCHEM_POLAR_SURFACE_AREA>
40.620000000000005

> <JCHEM_REFRACTIVITY>
74.7206

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,9S)-11-(but-3-en-1-yl)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridec-2-ene-6,10-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-SEP-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-SEP-23         0                                  
HETATM    1  O   UNK     0      -0.906   1.920   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       0.471   1.230   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       0.361  -0.306   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      -1.101  -0.792   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.411  -2.301   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.872  -2.786   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.182  -4.295   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.369  -1.471   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.635   2.238   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.171   2.127   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       4.179   0.963   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       5.565   1.636   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.840   0.772   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.729  -0.764   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.344  -1.437   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.069  -0.573   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.905  -1.581   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.747   0.487   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.675   3.172   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    3   17                                                       
CONECT    9    2   10   18                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13   19                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11   17                                                  
CONECT   17   16    8   18                                                  
CONECT   18   17    9                                                       
CONECT   19   12                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₀N₂O₂

Average Mass

260.3370 Da

Monoisotopic Mass

260.15248 Da

IUPAC Name

(1S,9S)-11-(but-3-en-1-yl)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridec-2-ene-6,10-dione

Traditional Name

(1S,9S)-11-(but-3-en-1-yl)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridec-2-ene-6,10-dione

CAS Registry Number

Not Available

SMILES

C=CCCN1C[C@@H]2C[C@@H](CN3C(=O)CCC=C23)C1=O

InChI Identifier

InChI=1S/C15H20N2O2/c1-2-3-7-16-9-11-8-12(15(16)19)10-17-13(11)5-4-6-14(17)18/h2,5,11-12H,1,3-4,6-10H2/t11-,12-/m0/s1

InChI Key

FGHFLRKPEJJAJZ-RYUDHWBXSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
ROESY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	jinqiong@mail.kib.ac.cn	Not Available	Not Available	2023-09-27	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	jinqiong@mail.kib.ac.cn	Not Available	Not Available	2023-09-27	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	jinqiong@mail.kib.ac.cn	Not Available	Not Available	2023-09-27	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	jinqiong@mail.kib.ac.cn	Not Available	Not Available	2023-09-27	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCl3, experimental)	jinqiong@mail.kib.ac.cn	Not Available	Not Available	2023-09-27	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCl3, experimental)	jinqiong@mail.kib.ac.cn	Not Available	Not Available	2023-09-27	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCl3, experimental)	jinqiong@mail.kib.ac.cn	Not Available	Not Available	2023-09-27	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl3, experimental)	jinqiong@mail.kib.ac.cn	Not Available	Not Available	2023-09-27	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
yunnanensis		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as n-acylpiperidines. These are compounds containing an N-acyethanolamine moiety, which is characterized by an acyl group is linked to the nitrogen atom of a piperidine.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Piperidines

Sub Class

N-acylpiperidines

Direct Parent

N-acylpiperidines

Alternative Parents

Substituents

Piperidinecarboxamide
3-piperidinecarboxamide
N-acyl-piperidine
Tetrahydropyridine
Piperidinone
Delta-lactam
N-acyl-amine
Tertiary carboxylic acid amide
Lactam
Carboxamide group
Azacycle
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
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	0.19	ChemAxon
pKa (Strongest Basic)	-0.65	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	40.62 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	74.72 m³·mol⁻¹	ChemAxon
Polarizability	28.51 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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Ormosianine K (NP0331874)

MOL for NP0331874 (Ormosianine K)

3D MOL for NP0331874 (Ormosianine K)

3D SDF for NP0331874 (Ormosianine K)

3D-SDF for NP0331874 (Ormosianine K)

PDB for NP0331874 (Ormosianine K)

3D PDB for NP0331874 (Ormosianine K)

SMILES for NP0331874 (Ormosianine K)

INCHI for NP0331874 (Ormosianine K)

Structure for NP0331874 (Ormosianine K)

3D Structure for NP0331874 (Ormosianine K)