NP-MRD: Showing NP-Card for (+)-(1S,3S)-Austrocortilutein (NP0074839)

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Record Information

Version

1.0

Created at

2022-04-28 20:09:39 UTC

Updated at

2022-04-28 20:09:39 UTC

NP-MRD ID

NP0074839

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-(1S,3S)-Austrocortilutein

Description

Austrocortilutein belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group. (+)-(1S,3S)-Austrocortilutein is found in Cortinarius, Cortinarius basirubescens and Dermocybe splendida. It was first documented in 2010 (PMID: 20392467). Based on a literature review very few articles have been published on Austrocortilutein.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 40  0  0  0  0  0  0  0  0999 V2000
    6.2516    0.5890    0.3753 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0410    1.3021    0.2296 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8210    0.6410    0.1240 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8067   -0.7229    0.1633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6130   -1.4403    0.0621 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6947   -2.7895    0.1108 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4309   -0.7540   -0.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4580    0.6340   -0.1186 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6506    1.3322   -0.0169 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2198    1.3492   -0.2673 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2477    2.6185   -0.3024 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0499    0.6364   -0.3765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1306   -0.6743   -0.3455 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1385   -1.4191   -0.1928 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1242   -2.6773   -0.1566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3844   -1.4479   -0.4511 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6840   -2.1356    0.7202 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5575   -0.5675   -0.7851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105    0.6822    0.0928 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6769    1.4686    0.1711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9994    0.3157    1.3740 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2723    1.4633   -0.5275 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0931    1.3026    0.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3274   -0.1641   -0.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1944    0.0595    1.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7504   -1.2703    0.2767 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0977   -3.5362    0.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6390    2.4110   -0.0504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2820   -2.2388   -1.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8821   -2.3930    1.2287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5240   -1.0306   -0.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4634   -0.2193   -1.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5065    0.7716    0.3881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5960    2.1578    1.0371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8927    2.0574   -0.7386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6248   -0.2979    1.8169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4998    1.5152   -1.6305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1628    2.4713   -0.1054 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  9  2  0
  9  8  1  0
  8  7  2  0
  7  5  1  0
  5  6  1  0
  5  4  2  0
  7 14  1  0
 14 15  2  0
 14 13  1  0
 13 12  2  0
 12 22  1  0
 22 19  1  0
 19 20  1  0
 19 21  1  1
 19 18  1  0
 18 16  1  0
 16 17  1  0
 12 10  1  0
 10 11  2  0
  4  3  1  0
 16 13  1  0
 10  8  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  9 28  1  0
  6 27  1  0
  4 26  1  0
 22 37  1  0
 22 38  1  0
 20 33  1  0
 20 34  1  0
 20 35  1  0
 21 36  1  0
 18 31  1  0
 18 32  1  0
 16 29  1  6
 17 30  1  0
M  END


  Mrv1652304282222092D          

 22 24  0  0  1  0            999 V2000
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4372   -0.6996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8245   -0.0288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  2  0  0  0  0
  6  9  1  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
  5 12  1  0  0  0  0
 12 13  1  6  0  0  0
 10 14  1  1  0  0  0
 10 15  1  6  0  0  0
  2 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
  1 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0074839

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C(O)=C1)C(=O)C1=C(C[C@](C)(O)C[C@@H]1O)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H16O6/c1-16(21)5-9-13(11(18)6-16)15(20)12-8(14(9)19)3-7(22-2)4-10(12)17/h3-4,11,17-18,21H,5-6H2,1-2H3/t11-,16-/m0/s1

> <INCHI_KEY>
LRHFZXBVDMVFCW-ZBEGNZNMSA-N

> <FORMULA>
C16H16O6

> <MOLECULAR_WEIGHT>
304.298

> <EXACT_MASS>
304.094688235

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
30.629746303573175

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3S)-1,3,8-trihydroxy-6-methoxy-3-methyl-1,2,3,4,9,10-hexahydroanthracene-9,10-dione

> <ALOGPS_LOGP>
1.83

> <JCHEM_LOGP>
0.4898468376666664

> <ALOGPS_LOGS>
-2.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.163449367680617

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.143981097821849

> <JCHEM_PKA_STRONGEST_BASIC>
-2.854450184035855

> <JCHEM_POLAR_SURFACE_AREA>
104.06

> <JCHEM_REFRACTIVITY>
78.52089999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.73e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3S)-1,3,8-trihydroxy-6-methoxy-3-methyl-2,4-dihydro-1H-anthracene-9,10-dione

> <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       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.816  -1.306   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.539  -0.054   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
CONECT    1    2    7   19                                                  
CONECT    2    1    3   16                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   12                                                  
CONECT    6    5    7    9                                                  
CONECT    7    6    1    8                                                  
CONECT    8    7                                                            
CONECT    9    6   10                                                       
CONECT   10    9   11   14   15                                             
CONECT   11   10   12                                                       
CONECT   12   11    5   13                                                  
CONECT   13   12                                                            
CONECT   14   10                                                            
CONECT   15   10                                                            
CONECT   16    2   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18    1                                                       
CONECT   20   18   21                                                       
CONECT   21   20                                                            
CONECT   22   16                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Value	Source
(1S,3S)-Austrocortilutein	MeSH

Chemical Formula

C₁₆H₁₆O₆

Average Mass

304.2980 Da

Monoisotopic Mass

304.09469 Da

IUPAC Name

(1S,3S)-1,3,8-trihydroxy-6-methoxy-3-methyl-1,2,3,4,9,10-hexahydroanthracene-9,10-dione

Traditional Name

(1S,3S)-1,3,8-trihydroxy-6-methoxy-3-methyl-2,4-dihydro-1H-anthracene-9,10-dione

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C(O)=C1)C(=O)C1=C(C[C@](C)(O)C[C@@H]1O)C2=O

InChI Identifier

InChI=1S/C16H16O6/c1-16(21)5-9-13(11(18)6-16)15(20)12-8(14(9)19)3-7(22-2)4-10(12)17/h3-4,11,17-18,21H,5-6H2,1-2H3/t11-,16-/m0/s1

InChI Key

LRHFZXBVDMVFCW-ZBEGNZNMSA-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
Cortinarius	LOTUS Database	35616633
Cortinarius basirubescens	LOTUS Database	35616633
Dermocybe splendida	Fungi	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Hydroxyanthraquinones

Alternative Parents

Substituents

Hydroxyanthraquinone
Anisole
Phenol ether
Aryl ketone
Quinone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Vinylogous acid
Tertiary alcohol
Ketone
Secondary alcohol
Ether
Polyol
Organic oxygen compound
Alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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	1.83	ALOGPS
logP	0.49	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	8.14	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	78.52 m³·mol⁻¹	ChemAxon
Polarizability	30.63 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

C00036337

Chemspider ID

9510649

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Austrocortilutein

METLIN ID

Not Available

PubChem Compound

11335703

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Beattie KD, Rouf R, Gander L, May TW, Ratkowsky D, Donner CD, Gill M, Grice ID, Tiralongo E: Antibacterial metabolites from Australian macrofungi from the genus Cortinarius. Phytochemistry. 2010 Jun;71(8-9):948-55. doi: 10.1016/j.phytochem.2010.03.016. Epub 2010 Apr 12. [PubMed:20392467 ]

Showing NP-Card for (+)-(1S,3S)-Austrocortilutein (NP0074839)

MOL for NP0074839 ((+)-(1S,3S)-Austrocortilutein)

3D MOL for NP0074839 ((+)-(1S,3S)-Austrocortilutein)

3D SDF for NP0074839 ((+)-(1S,3S)-Austrocortilutein)

3D-SDF for NP0074839 ((+)-(1S,3S)-Austrocortilutein)

PDB for NP0074839 ((+)-(1S,3S)-Austrocortilutein)

3D PDB for NP0074839 ((+)-(1S,3S)-Austrocortilutein)

SMILES for NP0074839 ((+)-(1S,3S)-Austrocortilutein)

INCHI for NP0074839 ((+)-(1S,3S)-Austrocortilutein)

Structure for NP0074839 ((+)-(1S,3S)-Austrocortilutein)

3D Structure for NP0074839 ((+)-(1S,3S)-Austrocortilutein)