NP-MRD: Showing NP-Card for Ormosianine P (NP0331879)

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Record Information

Version

2.0

Created at

2023-09-27 01:04:28 UTC

Updated at

2024-09-03 04:17:17 UTC

NP-MRD ID

NP0331879

Natural Product DOI

https://doi.org/10.57994/0985

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Ormosianine P

Description

Ormosianine P belongs to the class of organic compounds known as ormosia-type alkaloids. These are aloperine alkaloids with a structure based on the ormosanine skeleton. Based on a literature review very few articles have been published on Ormosianine P.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 09272301042D          

 30 34  0  0  1  0            999 V2000
   -0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5834   -0.5834    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7469    0.5156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4084   -0.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2295    0.3157    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4084    1.4084    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5834    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  0  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
    1.7241    2.1706    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2263    1.5160    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2218    2.8251    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4039    2.7174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0882    1.9552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0983    3.3719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5376    3.5873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3555    3.6950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8577    3.0404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5420    2.2782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4207    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4207    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  6  5  1  0  0  0  0
  6  7  1  1  0  0  0
  8  6  1  0  0  0  0
  8  9  1  0  0  0  0
  9  4  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 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
  2 15  1  0  0  0  0
  9 16  1  6  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 18 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 16 25  1  0  0  0  0
  8 26  1  6  0  0  0
  8 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  6 30  1  0  0  0  0
M  END


  Mrv2104 09272301042D          

 30 34  0  0  1  0            999 V2000
   -0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5834   -0.5834    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7469    0.5156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4084   -0.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2295    0.3157    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4084    1.4084    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5834    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  0  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
    1.7241    2.1706    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2263    1.5160    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2218    2.8251    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4039    2.7174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0882    1.9552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0983    3.3719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5376    3.5873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3555    3.6950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8577    3.0404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5420    2.2782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4207    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4207    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  6  5  1  0  0  0  0
  6  7  1  1  0  0  0
  8  6  1  0  0  0  0
  8  9  1  0  0  0  0
  9  4  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 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
  2 15  1  0  0  0  0
  9 16  1  6  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 18 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 16 25  1  0  0  0  0
  8 26  1  6  0  0  0
  8 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  6 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0331879

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12CCCCN1C[C@@]1(C[C@H]2C[C@@]2([H])CCCN[C@]12[H])[C@]1([H])CCCCN1C(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H37N3O/c1-16(26)25-12-5-3-9-20(25)22-14-18(13-17-7-6-10-23-21(17)22)19-8-2-4-11-24(19)15-22/h17-21,23H,2-15H2,1H3/t17-,18-,19-,20+,21+,22+/m1/s1

> <INCHI_KEY>
IBALPOZIWDWNBX-UQOPEDAQSA-N

> <FORMULA>
C22H37N3O

> <MOLECULAR_WEIGHT>
359.558

> <EXACT_MASS>
359.293662823

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
42.51096439013602

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[(2S)-2-[(1R,2S,7R,9R,10R)-3,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadecan-1-yl]piperidin-1-yl]ethan-1-one

> <JCHEM_LOGP>
2.035357119333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_BASIC>
10.284233876452383

> <JCHEM_POLAR_SURFACE_AREA>
35.58

> <JCHEM_REFRACTIVITY>
104.95589999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1-[(2S)-2-[(1R,2S,7R,9R,10R)-3,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadecan-1-yl]piperidin-1-yl]ethanone

> <JCHEM_VEBER_RULE>
1

$$$$

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  H   UNK     0      -1.334   0.770   0.000  0.00  0.00           H+0
HETATM    2  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.089  -1.089   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.394   0.963   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.629  -1.089   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.718   0.000   0.000  0.00  0.00           C+0
HETATM    7  H   UNK     0       2.295   0.589   0.000  0.00  0.00           H+0
HETATM    8  C   UNK     0       3.718   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.629   2.629   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.089   2.629   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       0.000   1.540   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.218   4.052   0.000  0.00  0.00           C+0
HETATM   17  H   UNK     0       4.156   2.830   0.000  0.00  0.00           H+0
HETATM   18  N   UNK     0       2.281   5.273   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       0.754   5.072   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.165   3.650   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.184   6.294   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.870   6.696   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.397   6.897   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.334   5.676   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.745   4.253   0.000  0.00  0.00           C+0
HETATM   26  H   UNK     0       5.052   0.770   0.000  0.00  0.00           H+0
HETATM   27  N   UNK     0       5.052   2.310   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0       6.385   1.540   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.385   0.000   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.052  -0.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   11   15                                             
CONECT    3    2    4    5                                                  
CONECT    4    3    9                                                       
CONECT    5    3    6                                                       
CONECT    6    5    7    8   30                                             
CONECT    7    6                                                            
CONECT    8    6    9   26   27                                             
CONECT    9    8    4   10   16                                             
CONECT   10    9   11                                                       
CONECT   11   10    2   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    2                                                       
CONECT   16    9   17   18   25                                             
CONECT   17   16                                                            
CONECT   18   16   19   22                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   18   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   16                                                       
CONECT   26    8                                                            
CONECT   27    8   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    6                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₇N₃O

Average Mass

359.5580 Da

Monoisotopic Mass

359.29366 Da

IUPAC Name

1-[(2S)-2-[(1R,2S,7R,9R,10R)-3,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadecan-1-yl]piperidin-1-yl]ethan-1-one

Traditional Name

1-[(2S)-2-[(1R,2S,7R,9R,10R)-3,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadecan-1-yl]piperidin-1-yl]ethanone

CAS Registry Number

Not Available

SMILES

[H][C@]12CCCCN1C[C@@]1(C[C@H]2C[C@@]2([H])CCCN[C@]12[H])[C@]1([H])CCCCN1C(C)=O

InChI Identifier

InChI=1S/C22H37N3O/c1-16(26)25-12-5-3-9-20(25)22-14-18(13-17-7-6-10-23-21(17)22)19-8-2-4-11-24(19)15-22/h17-21,23H,2-15H2,1H3/t17-,18-,19-,20+,21+,22+/m1/s1

InChI Key

IBALPOZIWDWNBX-UQOPEDAQSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
ROESY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, CD3OD, experimental)	jinqiong@mail.kib.ac.cn	Not Available	Not Available	2023-09-27	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, CD3OD, experimental)	jinqiong@mail.kib.ac.cn	Not Available	Not Available	2023-09-27	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, CD3OD, experimental)	jinqiong@mail.kib.ac.cn	Not Available	Not Available	2023-09-27	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, CD3OD, experimental)	jinqiong@mail.kib.ac.cn	Not Available	Not Available	2023-09-27	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CD3OD, experimental)	jinqiong@mail.kib.ac.cn	Not Available	Not Available	2023-09-27	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CD3OD, 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 ormosia-type alkaloids. These are aloperine alkaloids with a structure based on the ormosanine skeleton.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Lupin alkaloids

Sub Class

Aloperine and related alkaloids

Direct Parent

Ormosia-type alkaloids

Alternative Parents

Substituents

Ormosia-type alkaloid
Quinolidine
Quinolizidine
N-acyl-piperidine
Piperidine
Acetamide
Tertiary carboxylic acid amide
Tertiary aliphatic amine
Tertiary amine
Carboxamide group
Amino acid or derivatives
Azacycle
Organoheterocyclic compound
Secondary amine
Secondary aliphatic amine
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
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	2.04	ChemAxon
pKa (Strongest Basic)	10.28	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	35.58 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	104.96 m³·mol⁻¹	ChemAxon
Polarizability	42.51 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

Showing NP-Card for Ormosianine P (NP0331879)

MOL for NP0331879 (Ormosianine P)

3D MOL for NP0331879 (Ormosianine P)

3D SDF for NP0331879 (Ormosianine P)

3D-SDF for NP0331879 (Ormosianine P)

PDB for NP0331879 (Ormosianine P)

3D PDB for NP0331879 (Ormosianine P)

SMILES for NP0331879 (Ormosianine P)

INCHI for NP0331879 (Ormosianine P)

Structure for NP0331879 (Ormosianine P)

3D Structure for NP0331879 (Ormosianine P)