NP-MRD: Showing NP-Card for Triptoquinone E (NP0075858)

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Record Information

Version

2.0

Created at

2022-04-28 21:04:44 UTC

Updated at

2022-04-28 21:04:44 UTC

NP-MRD ID

NP0075858

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Triptoquinone E

Description

(1S,4aS,10aR)-1,4a-dimethyl-5,8-dioxo-7-(propan-2-yl)-1,2,3,4,4a,5,8,9,10,10a-decahydrophenanthrene-1-carbaldehyde belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Triptoquinone E is found in Tripterygium hypoglaucum and Tripterygium wilfordii. Based on a literature review very few articles have been published on (1S,4aS,10aR)-1,4a-dimethyl-5,8-dioxo-7-(propan-2-yl)-1,2,3,4,4a,5,8,9,10,10a-decahydrophenanthrene-1-carbaldehyde.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 51  0  0  0  0  0  0  0  0999 V2000
    5.5408   -0.6120   -0.2274 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6673    0.5379    0.2309 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9741    1.7498   -0.6152 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2305    0.1751    0.0352 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8568   -0.9971   -0.4383 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4418   -1.2506   -0.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1177   -2.3805   -1.0465 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4003   -0.2458   -0.2350 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7914    0.8991    0.2269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1587    1.9923    0.6068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5804    1.7054    0.3064 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9199    0.2469    0.3895 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3678   -0.0203    0.1299 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2029    0.6825    1.2030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8475    0.4998   -1.1780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0192    1.7059   -1.3894 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6543   -1.5050    0.1531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5001   -2.2956    0.7107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1978   -2.0522   -0.0109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0291   -0.6123   -0.4327 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2927   -0.4612   -1.9248 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2412    1.1615    0.3841 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5820    2.2884    0.8381 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6028   -0.3222   -0.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3656   -1.5229    0.3782 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3650   -0.7900   -1.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8408    0.7453    1.3043 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9532    1.6059   -1.1435 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1729    1.8857   -1.3713 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9962    2.6588    0.0157 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6263   -1.7204   -0.6932 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0216    2.1596    1.7082 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1901    2.9489    0.1285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2127    2.2734    1.0200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8112    2.0671   -0.7163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7430   -0.0490    1.4661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1963    1.7634    1.0862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2824    0.3639    1.1034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7932    0.4100    2.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0783   -0.1405   -2.0315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5193   -1.6852    0.8235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9299   -1.9090   -0.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4162   -2.1138    1.8010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7468   -3.3708    0.5874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4073   -2.4032    0.6780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1499   -2.6797   -0.9228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3362   -0.6543   -2.4948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6098    0.5417   -2.2079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9755   -1.2748   -2.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  1
 13 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  6
 13 15  1  0
 15 16  2  0
  9 22  1  0
 22 23  2  0
 22  4  1  0
 20  8  1  0
 20 12  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  1
  3 28  1  0
  3 29  1  0
  3 30  1  0
  5 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 12 36  1  1
 14 37  1  0
 14 38  1  0
 14 39  1  0
 17 41  1  0
 17 42  1  0
 18 43  1  0
 18 44  1  0
 19 45  1  0
 19 46  1  0
 21 47  1  0
 21 48  1  0
 21 49  1  0
 15 40  1  0
M  END


  Mrv1652304282223042D          

 23 25  0  0  1  0            999 V2000
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3016   -0.7392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0300   -0.3518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6308   -1.1265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  6  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  2  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
  5 20  1  6  0  0  0
  3 21  1  6  0  0  0
 21 22  2  0  0  0  0
  3 23  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0075858

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=CC(=O)C2=C(CC[C@H]3[C@](C)(CCC[C@]23C)C=O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O3/c1-12(2)14-10-15(22)17-13(18(14)23)6-7-16-19(3,11-21)8-5-9-20(16,17)4/h10-12,16H,5-9H2,1-4H3/t16-,19+,20-/m0/s1

> <INCHI_KEY>
JMZHTRDGDKQYEC-DBVUQKKJSA-N

> <FORMULA>
C20H26O3

> <MOLECULAR_WEIGHT>
314.425

> <EXACT_MASS>
314.188194697

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
35.67390988499209

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4aS,10aR)-1,4a-dimethyl-5,8-dioxo-7-(propan-2-yl)-1,2,3,4,4a,5,8,9,10,10a-decahydrophenanthrene-1-carbaldehyde

> <ALOGPS_LOGP>
3.54

> <JCHEM_LOGP>
4.287403771000001

> <ALOGPS_LOGS>
-4.06

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.063928352412432

> <JCHEM_POLAR_SURFACE_AREA>
51.21

> <JCHEM_REFRACTIVITY>
91.4371

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.72e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4aS,10aR)-7-isopropyl-1,4a-dimethyl-5,8-dioxo-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde

> <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       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.206  -1.897   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.874   3.437   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -1.746   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.516   2.104   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.516  -0.564   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.030  -1.380   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       9.389  -0.657   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.777  -2.103   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   21   23                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   20                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   15                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4                                                       
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14    7   16                                                  
CONECT   16   15                                                            
CONECT   17   13   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20    5                                                            
CONECT   21    3   22                                                       
CONECT   22   21                                                            
CONECT   23    3                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₆O₃

Average Mass

314.4250 Da

Monoisotopic Mass

314.18819 Da

IUPAC Name

(1S,4aS,10aR)-1,4a-dimethyl-5,8-dioxo-7-(propan-2-yl)-1,2,3,4,4a,5,8,9,10,10a-decahydrophenanthrene-1-carbaldehyde

Traditional Name

(1S,4aS,10aR)-7-isopropyl-1,4a-dimethyl-5,8-dioxo-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde

CAS Registry Number

Not Available

SMILES

CC(C)C1=CC(=O)C2=C(CC[C@H]3[C@](C)(CCC[C@]23C)C=O)C1=O

InChI Identifier

InChI=1S/C20H26O3/c1-12(2)14-10-15(22)17-13(18(14)23)6-7-16-19(3,11-21)8-5-9-20(16,17)4/h10-12,16H,5-9H2,1-4H3/t16-,19+,20-/m0/s1

InChI Key

JMZHTRDGDKQYEC-DBVUQKKJSA-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
Tripterygium hypoglaucum	Plant	KNApSAcK
Tripterygium wilfordii	LOTUS Database	35616633

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

Diterpenoid
Abietane diterpenoid
Phenanthrene
Hydrophenanthrene
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
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	3.54	ALOGPS
logP	4.29	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Basic)	-7.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	51.21 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	91.44 m³·mol⁻¹	ChemAxon
Polarizability	35.67 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

8171362

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9995781

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Triptoquinone E (NP0075858)

MOL for NP0075858 (Triptoquinone E)

3D MOL for NP0075858 (Triptoquinone E)

3D SDF for NP0075858 (Triptoquinone E)

3D-SDF for NP0075858 (Triptoquinone E)

PDB for NP0075858 (Triptoquinone E)

3D PDB for NP0075858 (Triptoquinone E)

SMILES for NP0075858 (Triptoquinone E)

INCHI for NP0075858 (Triptoquinone E)

Structure for NP0075858 (Triptoquinone E)

3D Structure for NP0075858 (Triptoquinone E)