NP-MRD: Showing NP-Card for 6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one (NP0303026)

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Record Information

Version

2.0

Created at

2022-09-10 17:00:36 UTC

Updated at

2022-09-10 17:00:36 UTC

NP-MRD ID

NP0303026

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one

Description

6-(Dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]Octadeca-1(18),2-dien-17-one belongs to the class of organic compounds known as buxus alkaloids. These are alkaloids with a triterpenoid-steroid pregnane type structure with C-4 methyl groups, a 9beta,10beta-cycloartenol system, and a degraded C-20 side chain. Structurally, they are derivatives of either a 9beta,10beta-cyclo-4,4,14alpha-trimethyl-5alpha-pregnane or a 9(10->19)abeo 4,4,14alpha-trimethyl-5alpha-pregnane system. 6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one is found in Buxus papillosa. 6-(Dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]Octadeca-1(18),2-dien-17-one is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241511382D          

 30 33  0  0  0  0            999 V2000
   -2.3461   -3.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6986   -2.6322    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9321   -2.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2846   -2.4261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3176   -1.6018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4562   -1.3157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9674   -1.9632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3511   -1.2329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1412   -1.2698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9436   -1.0781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5938   -1.5860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.4109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9622   -2.9318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
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 13 28  1  0  0  0  0
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 28 30  1  0  0  0  0
M  END

     RDKit          3D

 74 77  0  0  0  0  0  0  0  0999 V2000
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    4.6886   -0.3481   -1.5396 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6042   -0.1245   -0.0585 C   0  0  1  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004241511382D          

 30 33  0  0  0  0            999 V2000
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M  END
> <DATABASE_ID>
NP0303026

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CNC(C)C1CCC2(C)C3CCC4C(CCC(N(C)C)C4(C)C)=CC3=CC(=O)C12C

> <INCHI_IDENTIFIER>
InChI=1S/C27H44N2O/c1-17(28-6)20-13-14-26(4)22-11-10-21-18(9-12-23(29(7)8)25(21,2)3)15-19(22)16-24(30)27(20,26)5/h15-17,20-23,28H,9-14H2,1-8H3

> <INCHI_KEY>
GNCZDDWCBNDFIY-UHFFFAOYSA-N

> <FORMULA>
C27H44N2O

> <MOLECULAR_WEIGHT>
412.662

> <EXACT_MASS>
412.345364045

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
51.20170476520343

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one

> <ALOGPS_LOGP>
4.79

> <JCHEM_LOGP>
4.882727427333333

> <ALOGPS_LOGS>
-5.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_BASIC>
10.563859191944358

> <JCHEM_POLAR_SURFACE_AREA>
32.34

> <JCHEM_REFRACTIVITY>
127.93429999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.94e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -4.379  -5.868   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      -3.171  -4.913   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      -1.740  -5.483   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.518  -7.007   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.531  -4.529   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.593  -2.990   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.852  -2.456   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.806  -3.665   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.522  -2.301   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.343  -3.764   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.997  -2.370   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.495  -2.012   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.708  -2.961   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.724  -4.500   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.530  -5.473   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.025  -5.145   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.170  -6.426   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.633  -6.326   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.779  -7.608   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.951  -4.946   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.033  -6.130   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.065  -5.257   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.391  -4.474   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.376  -2.934   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0      10.701  -2.150   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      10.686  -0.610   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.043  -2.907   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.034  -2.177   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.744  -0.810   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.298  -0.825   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   20                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   20                                             
CONECT    9    8                                                            
CONECT   10    8   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   28                                                  
CONECT   14   13   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   10   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    5    8   21                                             
CONECT   21   20                                                            
CONECT   22   14   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   28                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   24   13   29   30                                             
CONECT   29   28                                                            
CONECT   30   28                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₄₄N₂O

Average Mass

412.6620 Da

Monoisotopic Mass

412.34536 Da

IUPAC Name

6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one

Traditional Name

6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one

CAS Registry Number

Not Available

SMILES

CNC(C)C1CCC2(C)C3CCC4C(CCC(N(C)C)C4(C)C)=CC3=CC(=O)C12C

InChI Identifier

InChI=1S/C27H44N2O/c1-17(28-6)20-13-14-26(4)22-11-10-21-18(9-12-23(29(7)8)25(21,2)3)15-19(22)16-24(30)27(20,26)5/h15-17,20-23,28H,9-14H2,1-8H3

InChI Key

GNCZDDWCBNDFIY-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
Buxus papillosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as buxus alkaloids. These are alkaloids with a triterpenoid-steroid pregnane type structure with C-4 methyl groups, a 9beta,10beta-cycloartenol system, and a degraded C-20 side chain. Structurally, they are derivatives of either a 9beta,10beta-cyclo-4,4,14alpha-trimethyl-5alpha-pregnane or a 9(10->19)abeo 4,4,14alpha-trimethyl-5alpha-pregnane system.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal alkaloids

Direct Parent

Buxus alkaloids

Alternative Parents

Substituents

Abeo-9(10->19)-4,4-14(alpha)-trimethyl-5(alpha)-pregnane-skeleton
Abeoabietane diterpenoid
Diterpenoid
Cyclohexenone
Ketone
Tertiary aliphatic amine
Tertiary amine
Secondary aliphatic amine
Secondary amine
Amine
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	4.79	ALOGPS
logP	4.88	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Basic)	10.56	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	32.34 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	127.93 m³·mol⁻¹	ChemAxon
Polarizability	51.2 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

LOTUS database [Link]

Showing NP-Card for 6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one (NP0303026)

MOL for NP0303026 (6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one)

3D MOL for NP0303026 (6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one)

3D SDF for NP0303026 (6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one)

3D-SDF for NP0303026 (6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one)

PDB for NP0303026 (6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one)

3D PDB for NP0303026 (6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one)

SMILES for NP0303026 (6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one)

INCHI for NP0303026 (6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one)

Structure for NP0303026 (6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one)

3D Structure for NP0303026 (6-(dimethylamino)-7,7,12,16-tetramethyl-15-[1-(methylamino)ethyl]tetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-17-one)