NP-MRD: Showing NP-Card for (1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one (NP0292681)

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Record Information

Version

2.0

Created at

2022-09-10 00:19:28 UTC

Updated at

2022-09-10 00:19:29 UTC

NP-MRD ID

NP0292681

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one

Description

Dinosterone belongs to the class of organic compounds known as gorgostanes and derivatives. These are steroids containing a gorgostane moiety, which a skeleton characterized by the presence. Thus, dinosterone is considered to be a sterol. (1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one is found in Crypthecodinium cohnii. Based on a literature review very few articles have been published on Dinosterone.

Structure

MOL 3D MOL SDF PDB SMILES InChI

  Mrv1652309102202192D          

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M  END

     RDKit          3D

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M  END

  Mrv1652309102202192D          

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 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  9 25  1  0  0  0  0
  6 25  1  0  0  0  0
 25 26  1  1  0  0  0
  2 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0292681

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H](C)C(\C)=C\C(C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4[C@H](C)C(=O)CC[C@]4(C)[C@H]3CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C30H50O/c1-18(2)21(5)19(3)17-20(4)24-11-12-26-23-9-10-25-22(6)28(31)14-16-30(25,8)27(23)13-15-29(24,26)7/h17-18,20-27H,9-16H2,1-8H3/b19-17+/t20?,21-,22+,23+,24-,25+,26+,27+,29-,30+/m1/s1

> <INCHI_KEY>
VQFPSNWXBZIBRL-WALVZZJISA-N

> <FORMULA>
C30H50O

> <MOLECULAR_WEIGHT>
426.729

> <EXACT_MASS>
426.38616623

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
55.1144931217028

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,6S,7S,10S,11S,14R,15R)-2,6,15-trimethyl-14-[(3E,5R)-4,5,6-trimethylhept-3-en-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-one

> <JCHEM_LOGP>
8.437414303333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.411870409953474

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
133.26009999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,6S,7S,10S,11S,14R,15R)-2,6,15-trimethyl-14-[(3E,5R)-4,5,6-trimethylhept-3-en-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       2.892  -8.295   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.417  -8.505   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.363  -7.289   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.782  -5.863   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.257  -5.652   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.727  -4.647   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.299  -3.168   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.574  -2.304   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.790  -3.249   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.306  -2.978   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.829  -1.529   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.345  -1.258   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.338  -2.436   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.854  -2.164   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.377  -0.716   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.846  -3.342   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      16.362  -3.071   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      14.323  -4.790   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.807  -5.061   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.814  -3.884   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.291  -5.332   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.299  -4.155   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.775  -5.603   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.259  -5.874   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.267  -4.697   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.595  -6.083   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.998  -9.932   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.523 -10.142   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.053 -11.147   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.633 -12.574   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.527 -10.937   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   27                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   25                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   25                                                  
CONECT   10    9   11   22                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   20                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   13   21   22                                             
CONECT   21   20                                                            
CONECT   22   20   10   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24    9    6   26                                             
CONECT   26   25                                                            
CONECT   27    2   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₅₀O

Average Mass

426.7290 Da

Monoisotopic Mass

426.38617 Da

IUPAC Name

(1S,2R,6S,7S,10S,11S,14R,15R)-2,6,15-trimethyl-14-[(3E,5R)-4,5,6-trimethylhept-3-en-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-one

Traditional Name

(1S,2R,6S,7S,10S,11S,14R,15R)-2,6,15-trimethyl-14-[(3E,5R)-4,5,6-trimethylhept-3-en-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-one

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H](C)C(\C)=C\C(C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4[C@H](C)C(=O)CC[C@]4(C)[C@H]3CC[C@]12C

InChI Identifier

InChI=1S/C30H50O/c1-18(2)21(5)19(3)17-20(4)24-11-12-26-23-9-10-25-22(6)28(31)14-16-30(25,8)27(23)13-15-29(24,26)7/h17-18,20-27H,9-16H2,1-8H3/b19-17+/t20?,21-,22+,23+,24-,25+,26+,27+,29-,30+/m1/s1

InChI Key

VQFPSNWXBZIBRL-WALVZZJISA-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
Crypthecodinium cohnii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gorgostanes and derivatives. These are steroids containing a gorgostane moiety, which a skeleton characterized by the presence.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Gorgostanes and derivatives

Direct Parent

Gorgostanes and derivatives

Alternative Parents

Substituents

Gorgostane-skeleton
3-oxo-5-alpha-steroid
Oxosteroid
3-oxosteroid
Cyclic ketone
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Ergosterols and C24-methyl derivatives (LMST01031045 )

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	8.44	ChemAxon
pKa (Strongest Basic)	-7.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	17.07 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	133.26 m³·mol⁻¹	ChemAxon
Polarizability	55.11 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

113385194

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

52931359

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one (NP0292681)

MOL for NP0292681 ((1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one)

3D MOL for NP0292681 ((1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one)

3D SDF for NP0292681 ((1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one)

3D-SDF for NP0292681 ((1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one)

PDB for NP0292681 ((1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one)

3D PDB for NP0292681 ((1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one)

SMILES for NP0292681 ((1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one)

INCHI for NP0292681 ((1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one)

Structure for NP0292681 ((1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one)

3D Structure for NP0292681 ((1r,3as,3bs,5as,6s,9ar,9bs,11ar)-6,9a,11a-trimethyl-1-[(3e,5r)-4,5,6-trimethylhept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthren-7-one)