NP-MRD: Showing NP-Card for Asteltoxin Q (NP0350959)

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Record Information

Version

2.0

Created at

2025-04-15 09:50:47 UTC

Updated at

2025-06-10 23:52:53 UTC

NP-MRD ID

NP0350959

Natural Product DOI

https://doi.org/10.57994/3944

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Asteltoxin Q

Description

Based on a literature review very few articles have been published on Asteltoxin Q.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 01262312172D          

 32 35  0  0  1  0            999 V2000
   -2.1538   -0.8631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3692   -1.1180    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1143   -1.9026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2893   -1.9026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3782   -2.3876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0456   -1.9026    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3005   -2.6873    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7907   -1.1180    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4581   -0.6331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1255   -1.1180    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9102   -0.8631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5232   -1.4151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3079   -1.1602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9210   -1.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7056   -1.4573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8771   -0.6503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3187   -2.0093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1472   -2.8163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1033   -1.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7164   -2.3064    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5010   -2.0514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2748   -0.9474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6617   -0.3954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8333    0.4116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8706   -1.9026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3555   -2.5701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5442   -2.6873    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0343   -1.1180    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2206   -0.3334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7018   -0.6331    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2968    0.0857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1068    0.0857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  4  3  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  0  0  0  0
  6  7  1  6  0  0  0
  8  6  1  0  0  0  0
  8  9  1  1  0  0  0
 10  9  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  2  0  0  0  0
 25 10  1  0  0  0  0
  6 25  1  0  0  0  0
 25 26  1  6  0  0  0
  4 27  1  6  0  0  0
 28  4  1  0  0  0  0
 28  8  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30  2  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  6  0  0  0
M  END


  Mrv2104 01262312172D          

 32 35  0  0  1  0            999 V2000
   -2.1538   -0.8631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3692   -1.1180    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1143   -1.9026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2893   -1.9026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3782   -2.3876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0456   -1.9026    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3005   -2.6873    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7907   -1.1180    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4581   -0.6331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1255   -1.1180    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9102   -0.8631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5232   -1.4151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3079   -1.1602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9210   -1.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7056   -1.4573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8771   -0.6503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3187   -2.0093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1472   -2.8163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1033   -1.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7164   -2.3064    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5010   -2.0514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2748   -0.9474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6617   -0.3954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8333    0.4116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8706   -1.9026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3555   -2.5701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5442   -2.6873    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0343   -1.1180    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2206   -0.3334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7018   -0.6331    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2968    0.0857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1068    0.0857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  4  3  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  0  0  0  0
  6  7  1  6  0  0  0
  8  6  1  0  0  0  0
  8  9  1  1  0  0  0
 10  9  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  2  0  0  0  0
 25 10  1  0  0  0  0
  6 25  1  0  0  0  0
 25 26  1  6  0  0  0
  4 27  1  6  0  0  0
 28  4  1  0  0  0  0
 28  8  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30  2  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0350959

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12O[C@H](C)[C@](C)(O)[C@@]1(C)[C@H]1O[C@@H](\C=C\C=C\C3=C(C)C(OC)=CC(=O)O3)[C@H](O)[C@@]1([H])O2

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O8/c1-11-13(28-16(23)10-15(11)26-5)8-6-7-9-14-17(24)18-19(29-14)21(3)20(30-18)27-12(2)22(21,4)25/h6-10,12,14,17-20,24-25H,1-5H3/b8-6+,9-7+/t12-,14+,17+,18-,19+,20-,21+,22+/m1/s1

> <INCHI_KEY>
AVOLRKQPXXFPLF-XLSHRNDUSA-N

> <FORMULA>
C22H28O8

> <MOLECULAR_WEIGHT>
420.458

> <EXACT_MASS>
420.178417862

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
42.92991187064888

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-[(1E,3E)-4-[(1R,2R,4S,5S,6R,8S,10R,11R)-5,11-dihydroxy-1,10,11-trimethyl-3,7,9-trioxatricyclo[6.3.0.0^{2,6}]undecan-4-yl]buta-1,3-dien-1-yl]-4-methoxy-5-methyl-2H-pyran-2-one

> <JCHEM_LOGP>
1.330019173666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.581022923348952

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.907564763532143

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4888271613942687

> <JCHEM_POLAR_SURFACE_AREA>
103.68

> <JCHEM_REFRACTIVITY>
109.78949999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
6-[(1E,3E)-4-[(1R,2R,4S,5S,6R,8S,10R,11R)-5,11-dihydroxy-1,10,11-trimethyl-3,7,9-trioxatricyclo[6.3.0.0^{2,6}]undecan-4-yl]buta-1,3-dien-1-yl]-4-methoxy-5-methylpyran-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-JAN-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-JAN-23         0                                  
HETATM    1  C   UNK     0      -4.021  -1.611   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.556  -2.087   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -2.080  -3.552   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -0.540  -3.552   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.706  -4.457   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.952  -3.552   0.000  0.00  0.00           C+0
HETATM    7  H   UNK     0       2.428  -5.016   0.000  0.00  0.00           H+0
HETATM    8  C   UNK     0       1.476  -2.087   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.722  -1.182   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.968  -2.087   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.432  -1.611   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.577  -2.642   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.041  -2.166   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.186  -3.196   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.650  -2.720   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      10.971  -1.214   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      11.795  -3.751   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.475  -5.257   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.259  -3.275   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      14.404  -4.305   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      15.869  -3.829   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.580  -1.768   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.435  -0.738   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      12.755   0.768   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.492  -3.552   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.397  -4.797   0.000  0.00  0.00           O+0
HETATM   27  H   UNK     0      -1.016  -5.016   0.000  0.00  0.00           H+0
HETATM   28  C   UNK     0      -0.064  -2.087   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.412  -0.622   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.310  -1.182   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.554   0.160   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -2.066   0.160   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   30                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   27   28                                             
CONECT    5    4    6                                                       
CONECT    6    5    7    8   25                                             
CONECT    7    6                                                            
CONECT    8    6    9   28                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   25                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15   23                                                       
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23                                                       
CONECT   23   22   16   24                                                  
CONECT   24   23                                                            
CONECT   25   10    6   26                                                  
CONECT   26   25                                                            
CONECT   27    4                                                            
CONECT   28    4    8   29   30                                             
CONECT   29   28                                                            
CONECT   30   28    2   31   32                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₈O₈

Average Mass

420.4580 Da

Monoisotopic Mass

420.17842 Da

IUPAC Name

6-[(1E,3E)-4-[(1R,2R,4S,5S,6R,8S,10R,11R)-5,11-dihydroxy-1,10,11-trimethyl-3,7,9-trioxatricyclo[6.3.0.0^{2,6}]undecan-4-yl]buta-1,3-dien-1-yl]-4-methoxy-5-methyl-2H-pyran-2-one

Traditional Name

6-[(1E,3E)-4-[(1R,2R,4S,5S,6R,8S,10R,11R)-5,11-dihydroxy-1,10,11-trimethyl-3,7,9-trioxatricyclo[6.3.0.0^{2,6}]undecan-4-yl]buta-1,3-dien-1-yl]-4-methoxy-5-methylpyran-2-one

CAS Registry Number

Not Available

SMILES

[H][C@]12O[C@H](C)[C@](C)(O)[C@@]1(C)[C@H]1O[C@@H](\C=C\C=C\C3=C(C)C(OC)=CC(=O)O3)[C@H](O)[C@@]1([H])O2

InChI Identifier

InChI=1S/C22H28O8/c1-11-13(28-16(23)10-15(11)26-5)8-6-7-9-14-17(24)18-19(29-14)21(3)20(30-18)27-12(2)22(21,4)25/h6-10,12,14,17-20,24-25H,1-5H3/b8-6+,9-7+/t12-,14+,17+,18-,19+,20-,21+,22+/m1/s1

InChI Key

AVOLRKQPXXFPLF-XLSHRNDUSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, CDCl3, experimental)	ruanhl@hust.edu.cn	Huazhong University of Science and Technology	Han-Li Ruan	2025-04-15	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, CDCl3, experimental)	ruanhl@hust.edu.cn	Huazhong University of Science and Technology	Han-Li Ruan	2025-04-15	View Spectrum
ROESY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, CDCl3, experimental)	ruanhl@hust.edu.cn	Huazhong University of Science and Technology	Han-Li Ruan	2025-04-15	View Spectrum
1D_DEPT NMR	¹³C NMR Spectrum (1D, 101 MHz, CDCl3, experimental)	ruanhl@hust.edu.cn	Huazhong University of Science and Technology	Han-Li Ruan	2025-04-15	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl3, experimental)	ruanhl@hust.edu.cn	Huazhong University of Science and Technology	Han-Li Ruan	2025-04-15	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, CDCl3, experimental)	ruanhl@hust.edu.cn	Huazhong University of Science and Technology	Han-Li Ruan	2025-04-15	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, CDCl3, experimental)	ruanhl@hust.edu.cn	Huazhong University of Science and Technology	Han-Li Ruan	2025-04-15	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Pochonia Pochonia bulbillosa KNI755		Not Available

Chemical Taxonomy

Classification

Not classified

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	1.33	ChemAxon
pKa (Strongest Acidic)	12.91	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	103.68 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	109.79 m³·mol⁻¹	ChemAxon
Polarizability	42.93 Å³	ChemAxon
Number of Rings	4	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

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

Showing NP-Card for Asteltoxin Q (NP0350959)

MOL for NP0350959 (Asteltoxin Q)

3D MOL for NP0350959 (Asteltoxin Q)

3D SDF for NP0350959 (Asteltoxin Q)

3D-SDF for NP0350959 (Asteltoxin Q)

PDB for NP0350959 (Asteltoxin Q)

3D PDB for NP0350959 (Asteltoxin Q)

SMILES for NP0350959 (Asteltoxin Q)

INCHI for NP0350959 (Asteltoxin Q)

Structure for NP0350959 (Asteltoxin Q)

3D Structure for NP0350959 (Asteltoxin Q)