NP-MRD: Showing NP-Card for (+)-Phenaceatrovenetinone C (NP0351295)

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Record Information

Version

2.0

Created at

2025-07-08 21:59:56 UTC

Updated at

2025-07-29 03:36:09 UTC

NP-MRD ID

NP0351295

Natural Product DOI

https://doi.org/10.57994/4287

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Phenaceatrovenetinone C

Description

Based on a literature review very few articles have been published on (+)-Phenaceatrovenetinone C.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 01122315102D          

 36 40  0  0  1  0            999 V2000
    3.5724    1.2375    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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   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
    2.8579    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
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0214   -2.2461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8419   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6669   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -0.1576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0714   -1.9049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   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
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4323   -2.0127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6283   -1.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4408   -1.5830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9711   -2.2150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7835   -2.0717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3138   -2.7037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0657   -1.2964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8782   -1.1532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5354   -0.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7229   -0.8077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3461   -2.5015    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 11  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
  9 15  1  0  0  0  0
 11 16  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
  7 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 20  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 25 32  1  0  0  0  0
 24 33  2  0  0  0  0
 21 34  1  0  0  0  0
  6 34  1  0  0  0  0
 34 35  2  0  0  0  0
 20 36  2  0  0  0  0
M  END


  Mrv2104 01122315102D          

 36 40  0  0  1  0            999 V2000
    3.5724    1.2375    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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   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
    2.8579    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
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0214   -2.2461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8419   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6669   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -0.1576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0714   -1.9049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   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
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4323   -2.0127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6283   -1.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4408   -1.5830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9711   -2.2150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7835   -2.0717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3138   -2.7037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0657   -1.2964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8782   -1.1532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5354   -0.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7229   -0.8077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3461   -2.5015    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 11  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
  9 15  1  0  0  0  0
 11 16  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
  7 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 20  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 25 32  1  0  0  0  0
 24 33  2  0  0  0  0
 21 34  1  0  0  0  0
  6 34  1  0  0  0  0
 34 35  2  0  0  0  0
 20 36  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0351295

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1OC2=C(C(O)=C3C(=O)[C@@](O)(CC(=O)C4=CC(O)=C(O)C=C4)C(=O)C4=C(O)C=C(C)C2=C34)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C27H24O9/c1-10-7-15(30)18-19-17(10)23-21(26(3,4)11(2)36-23)22(32)20(19)25(34)27(35,24(18)33)9-16(31)12-5-6-13(28)14(29)8-12/h5-8,11,28-30,32,35H,9H2,1-4H3/t11-,27-/m1/s1

> <INCHI_KEY>
NXKBIFVMVUMPLS-DQQVXTMASA-N

> <FORMULA>
C27H24O9

> <MOLECULAR_WEIGHT>
492.48

> <EXACT_MASS>
492.142032353

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
48.21082224044763

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5R,9R)-5-[2-(3,4-dihydroxyphenyl)-2-oxoethyl]-3,5,7-trihydroxy-1,8,8,9-tetramethyl-4H,5H,6H,8H,9H-phenaleno[1,2-b]furan-4,6-dione

> <JCHEM_LOGP>
4.664552379

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.07780109316145

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.561164908389996

> <JCHEM_PKA_STRONGEST_BASIC>
-4.585777775089336

> <JCHEM_POLAR_SURFACE_AREA>
161.59

> <JCHEM_REFRACTIVITY>
128.94429999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(5R,9R)-5-[2-(3,4-dihydroxyphenyl)-2-oxoethyl]-3,5,7-trihydroxy-1,8,8,9-tetramethyl-9H-phenaleno[1,2-b]furan-4,6-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-JAN-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-JAN-23         0                                  
HETATM    1  C   UNK     0       6.668   2.310   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  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+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  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.133  -2.786   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.507  -4.193   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.038  -1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.578  -1.540   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.133  -0.294   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.467  -3.556   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.807  -3.757   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -0.183  -2.043   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.173  -3.222   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.689  -2.955   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.679  -4.135   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.196  -3.867   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -6.186  -5.047   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -5.723  -2.420   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -7.239  -2.153   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -4.733  -1.240   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -3.216  -1.508   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -0.646  -4.669   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       0.000  -0.000   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   34                                                  
CONECT    7    6    8   19                                                  
CONECT    8    7    2    9                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11   17                                                  
CONECT   11   10   12   13   16                                             
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    9                                                       
CONECT   16   11                                                            
CONECT   17   10   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17    7   20                                                  
CONECT   20   19   21   36                                                  
CONECT   21   20   22   23   34                                             
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   33                                                  
CONECT   25   24   26   32                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   25                                                       
CONECT   33   24                                                            
CONECT   34   21    6   35                                                  
CONECT   35   34                                                            
CONECT   36   20                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₂₄O₉

Average Mass

492.4800 Da

Monoisotopic Mass

492.14203 Da

IUPAC Name

(5R,9R)-5-[2-(3,4-dihydroxyphenyl)-2-oxoethyl]-3,5,7-trihydroxy-1,8,8,9-tetramethyl-4H,5H,6H,8H,9H-phenaleno[1,2-b]furan-4,6-dione

Traditional Name

(5R,9R)-5-[2-(3,4-dihydroxyphenyl)-2-oxoethyl]-3,5,7-trihydroxy-1,8,8,9-tetramethyl-9H-phenaleno[1,2-b]furan-4,6-dione

CAS Registry Number

Not Available

SMILES

C[C@H]1OC2=C(C(O)=C3C(=O)[C@@](O)(CC(=O)C4=CC(O)=C(O)C=C4)C(=O)C4=C(O)C=C(C)C2=C34)C1(C)C

InChI Identifier

InChI=1S/C27H24O9/c1-10-7-15(30)18-19-17(10)23-21(26(3,4)11(2)36-23)22(32)20(19)25(34)27(35,24(18)33)9-16(31)12-5-6-13(28)14(29)8-12/h5-8,11,28-30,32,35H,9H2,1-4H3/t11-,27-/m1/s1

InChI Key

NXKBIFVMVUMPLS-DQQVXTMASA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	maihieu@snu.ac.kr	Seoul National University	Van-Hieu, MAI	2025-07-08	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 126 MHz, C3D6O, experimental)	maihieu@snu.ac.kr	Seoul National University	Van-Hieu, MAI	2025-07-08	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, C3D6O, experimental)	maihieu@snu.ac.kr	Seoul National University	Van-Hieu, MAI	2025-07-08	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, C3D6O, experimental)	maihieu@snu.ac.kr	Seoul National University	Van-Hieu, MAI	2025-07-08	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, C3D6O, experimental)	maihieu@snu.ac.kr	Seoul National University	Van-Hieu, MAI	2025-07-08	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Penicillium sp. CNUFC-EML-48		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	4.66	ChemAxon
pKa (Strongest Acidic)	7.56	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	161.59 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	128.94 m³·mol⁻¹	ChemAxon
Polarizability	48.21 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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 (+)-Phenaceatrovenetinone C (NP0351295)

MOL for NP0351295 ((+)-Phenaceatrovenetinone C)

3D MOL for NP0351295 ((+)-Phenaceatrovenetinone C)

3D SDF for NP0351295 ((+)-Phenaceatrovenetinone C)

3D-SDF for NP0351295 ((+)-Phenaceatrovenetinone C)

PDB for NP0351295 ((+)-Phenaceatrovenetinone C)

3D PDB for NP0351295 ((+)-Phenaceatrovenetinone C)

SMILES for NP0351295 ((+)-Phenaceatrovenetinone C)

INCHI for NP0351295 ((+)-Phenaceatrovenetinone C)

Structure for NP0351295 ((+)-Phenaceatrovenetinone C)

3D Structure for NP0351295 ((+)-Phenaceatrovenetinone C)