NP-MRD: Showing NP-Card for 6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate (NP0315033)

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Record Information

Version

2.0

Created at

2022-09-11 13:27:49 UTC

Updated at

2022-09-11 13:27:49 UTC

NP-MRD ID

NP0315033

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate

Description

6,7,13-Trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]Icos-18-en-10-yl 4-methylpent-3-enoate belongs to the class of organic compounds known as conanine-type alkaloids. These are alkaloids with a structure based on the conanine skeleton. 6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate is found in Funtumia elastica and Holarrhena floribunda. 6,7,13-Trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]Icos-18-en-10-yl 4-methylpent-3-enoate is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161521522D          

 33 37  0  0  0  0            999 V2000
    6.0271   -1.6281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7048   -0.8687    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8860   -0.7681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3894   -1.4269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5706   -1.3263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2483   -0.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7517   -1.2256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4295   -0.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9329   -1.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1141   -1.0244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6175   -1.6832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9398   -2.4427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7586   -2.5433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4432   -3.1015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7449    0.0920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5637   -0.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  3  4  1  0  0  0  0
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  9 10  1  0  0  0  0
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 16 18  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
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 19 28  1  0  0  0  0
 28 29  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
  6 32  1  0  0  0  0
 32 33  1  0  0  0  0
  3 33  1  0  0  0  0
M  END

     RDKit          3D

 79 83  0  0  0  0  0  0  0  0999 V2000
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 33 78  1  0
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M  END


  Mrv1533004161521522D          

 33 37  0  0  0  0            999 V2000
    6.0271   -1.6281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  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  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 19 28  1  0  0  0  0
 28 29  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
  6 32  1  0  0  0  0
 32 33  1  0  0  0  0
  3 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0315033

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CNC1CCC2(C)C3CC(OC(=O)CC=C(C)C)C45CN(C)C(C)C4CCC5C3CC=C2C1

> <INCHI_IDENTIFIER>
InChI=1S/C29H46N2O2/c1-18(2)7-12-27(32)33-26-16-25-22(9-8-20-15-21(30-5)13-14-28(20,25)4)24-11-10-23-19(3)31(6)17-29(23,24)26/h7-8,19,21-26,30H,9-17H2,1-6H3

> <INCHI_KEY>
BJEAHAPLWWPUQZ-UHFFFAOYSA-N

> <FORMULA>
C29H46N2O2

> <MOLECULAR_WEIGHT>
454.699

> <EXACT_MASS>
454.355928729

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
54.32958236120989

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate

> <ALOGPS_LOGP>
4.44

> <JCHEM_LOGP>
4.327535829666666

> <ALOGPS_LOGS>
-5.43

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_BASIC>
10.70428471611713

> <JCHEM_POLAR_SURFACE_AREA>
41.57

> <JCHEM_REFRACTIVITY>
136.3516

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.69e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      11.251  -3.039   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      10.649  -1.622   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       9.120  -1.434   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.194  -2.664   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.665  -2.476   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.063  -1.058   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.137  -2.288   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.535  -0.870   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.608  -2.100   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.080  -1.912   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.153  -3.142   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.754  -4.560   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.283  -4.748   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.827  -5.789   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.429  -7.207   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.502  -8.437   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.104  -9.855   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.026  -8.249   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.478  -0.495   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.451  -2.034   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      -0.022  -2.484   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0      -0.523  -3.941   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.905  -1.223   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.445  -1.196   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.022   0.007   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.049   1.547   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.522   1.997   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.405   0.735   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.933   0.547   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.860   1.777   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.389   1.589   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.990   0.172   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.519  -0.016   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   33                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   32                                             
CONECT    7    6                                                            
CONECT    8    6    9   29                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   19                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   10   20   25   28                                             
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   19   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   19   29                                                  
CONECT   29   28    8   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31    6   33                                                  
CONECT   33   32    3                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Value	Source
6,7,13-Trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0,.0,.0,]icos-18-en-10-yl 4-methylpent-3-enoic acid	Generator
6,7,13-Trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoic acid	Generator

Chemical Formula

C₂₉H₄₆N₂O₂

Average Mass

454.6990 Da

Monoisotopic Mass

454.35593 Da

IUPAC Name

6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate

Traditional Name

6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate

CAS Registry Number

Not Available

SMILES

CNC1CCC2(C)C3CC(OC(=O)CC=C(C)C)C45CN(C)C(C)C4CCC5C3CC=C2C1

InChI Identifier

InChI=1S/C29H46N2O2/c1-18(2)7-12-27(32)33-26-16-25-22(9-8-20-15-21(30-5)13-14-28(20,25)4)24-11-10-23-19(3)31(6)17-29(23,24)26/h7-8,19,21-26,30H,9-17H2,1-6H3

InChI Key

BJEAHAPLWWPUQZ-UHFFFAOYSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Funtumia elastica	LOTUS Database	35616633
Holarrhena floribunda	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as conanine-type alkaloids. These are alkaloids with a structure based on the conanine skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal alkaloids

Direct Parent

Conanine-type alkaloids

Alternative Parents

Substituents

Conanine skeleton
Steroid ester
Azasteroid
Azaspirodecane
Alkaloid or derivatives
Fatty acid ester
Fatty acyl
N-alkylpyrrolidine
Pyrrolidine
Tertiary aliphatic amine
Tertiary amine
Amino acid or derivatives
Carboxylic acid ester
Azacycle
Secondary amine
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Secondary aliphatic amine
Amine
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Organooxygen 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	4.44	ALOGPS
logP	4.33	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Basic)	10.7	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	41.57 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	136.35 m³·mol⁻¹	ChemAxon
Polarizability	54.33 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

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

85425809

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate (NP0315033)

MOL for NP0315033 (6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate)

3D MOL for NP0315033 (6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate)

3D SDF for NP0315033 (6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate)

3D-SDF for NP0315033 (6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate)

PDB for NP0315033 (6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate)

3D PDB for NP0315033 (6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate)

SMILES for NP0315033 (6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate)

INCHI for NP0315033 (6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate)

Structure for NP0315033 (6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate)

3D Structure for NP0315033 (6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-10-yl 4-methylpent-3-enoate)