NP-MRD: Showing NP-Card for (+)-Ningpeisine (NP0070199)

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Record Information

Version

2.0

Created at

2022-04-28 15:28:15 UTC

Updated at

2022-04-28 15:28:15 UTC

NP-MRD ID

NP0070199

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Ningpeisine

Description

(1S,2R,5S,7S,10S,11R,14R,15R,16S)-14-[(1S)-1-[(2R,5S)-1,5-dimethylpiperidin-2-yl]ethyl]-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadecan-8-one belongs to the class of organic compounds known as piperidines. Piperidines are compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms. (+)-Ningpeisine is found in Fritillaria ningguoensis. Based on a literature review very few articles have been published on (1S,2R,5S,7S,10S,11R,14R,15R,16S)-14-[(1S)-1-[(2R,5S)-1,5-dimethylpiperidin-2-yl]ethyl]-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadecan-8-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282217282D          

 31 35  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652304282217282D          

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 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
 28 30  1  6  0  0  0
 25 31  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0070199

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]([C@@H]1CC[C@@H]2[C@@H](C[C@H]3[C@H]2CC(=O)[C@H]2C[C@@H](O)CC[C@]32C)[C@H]1C)[C@H]1CC[C@H](C)CN1C

> <INCHI_IDENTIFIER>
InChI=1S/C28H47NO2/c1-16-6-9-26(29(5)15-16)18(3)20-7-8-21-22(17(20)2)13-24-23(21)14-27(31)25-12-19(30)10-11-28(24,25)4/h16-26,30H,6-15H2,1-5H3/t16-,17-,18-,19-,20+,21+,22-,23-,24-,25+,26+,28+/m0/s1

> <INCHI_KEY>
UBMXONPUBFQLKA-BQUVWSHHSA-N

> <FORMULA>
C28H47NO2

> <MOLECULAR_WEIGHT>
429.689

> <EXACT_MASS>
429.360679757

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
52.83340080962381

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,4aS,6aS,6bR,9R,10R,10aS,11aS,11bR)-9-[(1S)-1-[(2R,5S)-1,5-dimethylpiperidin-2-yl]ethyl]-3-hydroxy-10,11b-dimethyl-hexadecahydro-1H-cyclohexa[a]fluoren-5-one

> <ALOGPS_LOGP>
4.45

> <JCHEM_LOGP>
5.142023864333333

> <ALOGPS_LOGS>
-5.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
19.741107065115717

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.234295700131625

> <JCHEM_PKA_STRONGEST_BASIC>
9.899585807855182

> <JCHEM_POLAR_SURFACE_AREA>
40.540000000000006

> <JCHEM_REFRACTIVITY>
127.41699999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.12e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4aS,6aS,6bR,9R,10R,10aS,11aS,11bR)-9-[(1S)-1-[(2R,5S)-1,5-dimethylpiperidin-2-yl]ethyl]-3-hydroxy-10,11b-dimethyl-tetradecahydro-1H-cyclohexa[a]fluoren-5-one

> <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       5.372  -0.607   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.409   0.594   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.254   1.881   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.739   1.476   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.812  -0.063   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.181  -0.768   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.477   0.064   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.404   1.603   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.035   2.308   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.845  -0.641   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.141   0.191   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.068   1.729   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.363   2.562   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.732   1.856   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.805   0.318   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      13.510  -0.515   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      13.583  -2.053   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.028   2.689   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.919  -2.180   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.254  -2.307   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.561   3.257   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.024   3.345   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.331   4.720   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.179   2.057   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.871   0.682   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.026  -0.606   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.489  -0.517   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.204   0.858   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.641   2.146   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -1.741   0.946   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       3.564  -0.694   0.000  0.00  0.00           C+0
CONECT    1    2    5                                                       
CONECT    2    1    3   25                                                  
CONECT    3    2    4   21                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    1    6                                                  
CONECT    6    5    7   20                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8    4                                                       
CONECT   10    7   11   19                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   11   17                                                  
CONECT   17   16                                                            
CONECT   18   14                                                            
CONECT   19   10                                                            
CONECT   20    6                                                            
CONECT   21    3   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   29                                                  
CONECT   25   24    2   26   31                                             
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28   24                                                       
CONECT   30   28                                                            
CONECT   31   25                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₄₇NO₂

Average Mass

429.6890 Da

Monoisotopic Mass

429.36068 Da

IUPAC Name

(3S,4aS,6aS,6bR,9R,10R,10aS,11aS,11bR)-9-[(1S)-1-[(2R,5S)-1,5-dimethylpiperidin-2-yl]ethyl]-3-hydroxy-10,11b-dimethyl-hexadecahydro-1H-cyclohexa[a]fluoren-5-one

Traditional Name

(3S,4aS,6aS,6bR,9R,10R,10aS,11aS,11bR)-9-[(1S)-1-[(2R,5S)-1,5-dimethylpiperidin-2-yl]ethyl]-3-hydroxy-10,11b-dimethyl-tetradecahydro-1H-cyclohexa[a]fluoren-5-one

CAS Registry Number

Not Available

SMILES

C[C@@H]([C@@H]1CC[C@@H]2[C@@H](C[C@H]3[C@H]2CC(=O)[C@H]2C[C@@H](O)CC[C@]32C)[C@H]1C)[C@H]1CC[C@H](C)CN1C

InChI Identifier

InChI=1S/C28H47NO2/c1-16-6-9-26(29(5)15-16)18(3)20-7-8-21-22(17(20)2)13-24-23(21)14-27(31)25-12-19(30)10-11-28(24,25)4/h16-26,30H,6-15H2,1-5H3/t16-,17-,18-,19-,20+,21+,22-,23-,24-,25+,26+,28+/m0/s1

InChI Key

UBMXONPUBFQLKA-BQUVWSHHSA-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
Fritillaria ningguoensis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as piperidines. Piperidines are compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Piperidines

Sub Class

Not Available

Direct Parent

Piperidines

Alternative Parents

Substituents

Piperidine
Cyclic alcohol
Ketone
Secondary alcohol
Tertiary amine
Tertiary aliphatic amine
Azacycle
Carbonyl group
Amine
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Alcohol
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen 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	4.45	ALOGPS
logP	5.14	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	15.23	ChemAxon
pKa (Strongest Basic)	9.9	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	40.54 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	127.42 m³·mol⁻¹	ChemAxon
Polarizability	52.83 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

2340231

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3082876

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Ningpeisine (NP0070199)

MOL for NP0070199 ((+)-Ningpeisine)

3D MOL for NP0070199 ((+)-Ningpeisine)

3D SDF for NP0070199 ((+)-Ningpeisine)

3D-SDF for NP0070199 ((+)-Ningpeisine)

PDB for NP0070199 ((+)-Ningpeisine)

3D PDB for NP0070199 ((+)-Ningpeisine)

SMILES for NP0070199 ((+)-Ningpeisine)

INCHI for NP0070199 ((+)-Ningpeisine)

Structure for NP0070199 ((+)-Ningpeisine)

3D Structure for NP0070199 ((+)-Ningpeisine)