NP-MRD: Showing NP-Card for 1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate (NP0288483)

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Record Information

Version

2.0

Created at

2022-09-09 18:12:12 UTC

Updated at

2022-09-09 18:12:13 UTC

NP-MRD ID

NP0288483

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate

Description

1,1,4A,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-tetradecahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 1,1,4A,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-tetradecahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004181502202D          

 35 37  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004181502202D          

 35 37  0  0  0  0            999 V2000
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  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  8  6  1  4  0  0  0
  8  9  2  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
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 12 26  1  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 32 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0288483

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CNCCOC(=O)C=C1CCC2C(C1C)C(=O)CC1C(C)(C)C(CCC21C)OC(=O)CC(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C28H45NO6/c1-17-18(14-23(31)34-13-12-29-7)8-9-19-25(17)20(30)15-21-27(4,5)22(10-11-28(19,21)6)35-24(32)16-26(2,3)33/h14,17,19,21-22,25,29,33H,8-13,15-16H2,1-7H3

> <INCHI_KEY>
CWEOPNAABDJTEA-UHFFFAOYSA-N

> <FORMULA>
C28H45NO6

> <MOLECULAR_WEIGHT>
491.669

> <EXACT_MASS>
491.324688173

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
56.188783308404325

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-tetradecahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate

> <ALOGPS_LOGP>
3.28

> <JCHEM_LOGP>
3.6247594816666657

> <ALOGPS_LOGS>
-5.08

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
19.751484079300855

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.129606590776078

> <JCHEM_PKA_STRONGEST_BASIC>
9.205981560131667

> <JCHEM_POLAR_SURFACE_AREA>
101.92999999999999

> <JCHEM_REFRACTIVITY>
134.57549999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.05e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0      13.337  -1.540   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      14.670  -2.310   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      16.004  -1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.338  -2.310   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      18.672  -1.540   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      20.005  -2.310   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      20.005  -3.850   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      21.339  -1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      22.673  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      22.673  -3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      24.006  -4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      25.340  -3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      25.340  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      24.006  -1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      24.006   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      26.674  -1.540   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      26.674   0.000   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      28.007  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      28.007  -3.850   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      29.341  -4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      29.868  -3.173   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      30.858  -4.887   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      29.341  -6.160   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      28.007  -6.930   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      26.674  -6.160   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      26.674  -4.620   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      25.340  -5.390   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      30.675  -6.930   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      32.008  -6.160   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      32.008  -4.620   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      33.342  -6.930   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      34.676  -6.160   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      36.009  -5.390   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      35.446  -7.494   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      33.906  -4.826   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   26                                                  
CONECT   13   12   14   16                                                  
CONECT   14   13    9   15                                                  
CONECT   15   14                                                            
CONECT   16   13   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   26                                                  
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   12   19   27                                             
CONECT   27   26                                                            
CONECT   28   23   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33   34   35                                             
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   32                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   74    0
END

View in JSmol

Synonyms

Value	Source
1,1,4a,8-Tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-tetradecahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoic acid	Generator

Chemical Formula

C₂₈H₄₅NO₆

Average Mass

491.6690 Da

Monoisotopic Mass

491.32469 Da

IUPAC Name

1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-tetradecahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate

Traditional Name

1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate

CAS Registry Number

Not Available

SMILES

CNCCOC(=O)C=C1CCC2C(C1C)C(=O)CC1C(C)(C)C(CCC21C)OC(=O)CC(C)(C)O

InChI Identifier

InChI=1S/C28H45NO6/c1-17-18(14-23(31)34-13-12-29-7)8-9-19-25(17)20(30)15-21-27(4,5)22(10-11-28(19,21)6)35-24(32)16-26(2,3)33/h14,17,19,21-22,25,29,33H,8-13,15-16H2,1-7H3

InChI Key

CWEOPNAABDJTEA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Cassane diterpenoid
Diterpenoid
Hydrophenanthrene
Phenanthrene
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Amino acid or derivatives
Carboxylic acid ester
Ketone
Secondary aliphatic amine
Carboxylic acid derivative
Secondary amine
Amine
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Alcohol
Organonitrogen compound
Organooxygen 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	3.28	ALOGPS
logP	3.62	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	15.13	ChemAxon
pKa (Strongest Basic)	9.21	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	101.93 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	134.58 m³·mol⁻¹	ChemAxon
Polarizability	56.19 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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 1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate (NP0288483)

MOL for NP0288483 (1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate)

3D MOL for NP0288483 (1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate)

3D SDF for NP0288483 (1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate)

3D-SDF for NP0288483 (1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate)

PDB for NP0288483 (1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate)

3D PDB for NP0288483 (1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate)

SMILES for NP0288483 (1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate)

INCHI for NP0288483 (1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate)

Structure for NP0288483 (1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate)

3D Structure for NP0288483 (1,1,4a,8-tetramethyl-7-{2-[2-(methylamino)ethoxy]-2-oxoethylidene}-9-oxo-decahydrophenanthren-2-yl 3-hydroxy-3-methylbutanoate)