NP-MRD: Showing NP-Card for Daldinone A (NP0004463)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2020-12-09 01:57:00 UTC

Updated at

2021-07-15 16:49:15 UTC

NP-MRD ID

NP0004463

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Daldinone A

Provided By

NPAtlas

Description

(2R,11S,12R)-2,7,17-trihydroxypentacyclo[10.7.1.0²,¹¹.0³,⁸.0¹⁶,²⁰]Icosa-1(20),3(8),4,6,16,18-hexaene-9,15-dione belongs to the class of organic compounds known as fluorenes. Fluorenes are compounds containing a fluorene moiety, which consists of two benzene rings connected through either a cyclopentane, cyclopentene, or cyclopenta-1,3-diene. Daldinone A is found in Annulohypoxylon stygium, Daldinia concentrica and Daldinia sp.. Daldinone A was first documented in 2002 (PMID: 12502330). Based on a literature review very few articles have been published on (2R,11S,12R)-2,7,17-trihydroxypentacyclo[10.7.1.0²,¹¹.0³,⁸.0¹⁶,²⁰]Icosa-1(20),3(8),4,6,16,18-hexaene-9,15-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118063D          

 41 45  0  0  0  0            999 V2000
    2.8151   -2.6245    1.0919 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1197   -1.6498    0.7296 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6423   -1.7599    0.7292 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1643   -1.3361   -0.6238 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3482   -1.2766   -0.6882 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0360   -2.1422    0.3359 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5224   -1.9181    0.2081 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8525   -0.4693    0.3147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0002   -0.0405    0.4983 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7673    0.5255    0.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9052    1.8487    0.5638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1372    2.2559    1.0537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8246    2.7064    0.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6211    2.2507   -0.0629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4585    0.9106   -0.4409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5664    0.1278   -0.2804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6140    0.0689   -0.9797 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5151    0.1571   -2.3884 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9616    0.3956   -0.5355 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5255    1.5768   -0.9661 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8082    1.9514   -0.5675 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5262    1.1475    0.2596 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9846   -0.0661    0.7199 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7213   -0.8451    1.5436 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7155   -0.4006    0.3032 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2110   -1.1592    1.5506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3777   -2.8197    0.8617 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5737   -2.0189   -1.3802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7298   -1.4973   -1.6934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7997   -3.2016    0.2432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7507   -1.7273    1.3467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9975   -2.3966    1.1131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9492   -2.3852   -0.7007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3222    3.2017    1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9237    3.7406    0.7129 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2447    2.8823   -0.1822 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5983    1.1248   -2.5854 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    2.2764   -1.6268 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2587    2.8767   -0.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5324    1.3931    0.6013 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5700   -1.6838    1.9822 H   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  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
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 25  2  1  0  0  0  0
 17  4  1  0  0  0  0
 25 19  1  0  0  0  0
 16  5  1  0  0  0  0
 16 10  1  0  0  0  0
  3 26  1  0  0  0  0
  3 27  1  0  0  0  0
  4 28  1  6  0  0  0
  5 29  1  6  0  0  0
  6 30  1  0  0  0  0
  6 31  1  0  0  0  0
  7 32  1  0  0  0  0
  7 33  1  0  0  0  0
 12 34  1  0  0  0  0
 13 35  1  0  0  0  0
 14 36  1  0  0  0  0
 18 37  1  0  0  0  0
 20 38  1  0  0  0  0
 21 39  1  0  0  0  0
 22 40  1  0  0  0  0
 24 41  1  0  0  0  0
M  END

     RDKit          3D

 41 45  0  0  0  0  0  0  0  0999 V2000
    2.8151   -2.6245    1.0919 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1197   -1.6498    0.7296 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6423   -1.7599    0.7292 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1643   -1.3361   -0.6238 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3482   -1.2766   -0.6882 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0360   -2.1422    0.3359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5224   -1.9181    0.2081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8525   -0.4693    0.3147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0002   -0.0405    0.4983 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7673    0.5255    0.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9052    1.8487    0.5638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1372    2.2559    1.0537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8246    2.7064    0.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6211    2.2507   -0.0629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4585    0.9106   -0.4409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5664    0.1278   -0.2804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6140    0.0689   -0.9797 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5151    0.1571   -2.3884 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9616    0.3956   -0.5355 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5255    1.5768   -0.9661 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8082    1.9514   -0.5675 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5262    1.1475    0.2596 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9846   -0.0661    0.7199 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7213   -0.8451    1.5436 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7155   -0.4006    0.3032 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2110   -1.1592    1.5506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3777   -2.8197    0.8617 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5737   -2.0189   -1.3802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7298   -1.4973   -1.6934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7997   -3.2016    0.2432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7507   -1.7273    1.3467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9975   -2.3966    1.1131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9492   -2.3852   -0.7007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3222    3.2017    1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9237    3.7406    0.7129 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2447    2.8823   -0.1822 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5983    1.1248   -2.5854 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    2.2764   -1.6268 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2587    2.8767   -0.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5324    1.3931    0.6013 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5700   -1.6838    1.9822 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  6
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 25  2  1  0
 17  4  1  0
 25 19  1  0
 16  5  1  0
 16 10  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  6
  5 29  1  6
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
 12 34  1  0
 13 35  1  0
 14 36  1  0
 18 37  1  0
 20 38  1  0
 21 39  1  0
 22 40  1  0
 24 41  1  0
M  END


  Mrv1652306242118063D          

 41 45  0  0  0  0            999 V2000
    2.8151   -2.6245    1.0919 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1197   -1.6498    0.7296 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6423   -1.7599    0.7292 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1643   -1.3361   -0.6238 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3482   -1.2766   -0.6882 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0360   -2.1422    0.3359 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5224   -1.9181    0.2081 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8525   -0.4693    0.3147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0002   -0.0405    0.4983 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7673    0.5255    0.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9052    1.8487    0.5638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1372    2.2559    1.0537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8246    2.7064    0.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6211    2.2507   -0.0629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4585    0.9106   -0.4409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5664    0.1278   -0.2804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6140    0.0689   -0.9797 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5151    0.1571   -2.3884 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9616    0.3956   -0.5355 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5255    1.5768   -0.9661 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8082    1.9514   -0.5675 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5262    1.1475    0.2596 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9846   -0.0661    0.7199 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7213   -0.8451    1.5436 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7155   -0.4006    0.3032 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2110   -1.1592    1.5506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3777   -2.8197    0.8617 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5737   -2.0189   -1.3802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7298   -1.4973   -1.6934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7997   -3.2016    0.2432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7507   -1.7273    1.3467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9975   -2.3966    1.1131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9492   -2.3852   -0.7007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3222    3.2017    1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9237    3.7406    0.7129 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2447    2.8823   -0.1822 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5983    1.1248   -2.5854 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    2.2764   -1.6268 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2587    2.8767   -0.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5324    1.3931    0.6013 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5700   -1.6838    1.9822 H   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  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
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 25  2  1  0  0  0  0
 17  4  1  0  0  0  0
 25 19  1  0  0  0  0
 16  5  1  0  0  0  0
 16 10  1  0  0  0  0
  3 26  1  0  0  0  0
  3 27  1  0  0  0  0
  4 28  1  6  0  0  0
  5 29  1  6  0  0  0
  6 30  1  0  0  0  0
  6 31  1  0  0  0  0
  7 32  1  0  0  0  0
  7 33  1  0  0  0  0
 12 34  1  0  0  0  0
 13 35  1  0  0  0  0
 14 36  1  0  0  0  0
 18 37  1  0  0  0  0
 20 38  1  0  0  0  0
 21 39  1  0  0  0  0
 22 40  1  0  0  0  0
 24 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0004463

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C3=C(C([H])=C1[H])[C@@]1(O[H])C4=C([H])C([H])=C([H])C(O[H])=C4C(=O)C([H])([H])[C@@]1([H])[C@@]3([H])C([H])([H])C([H])([H])C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H16O5/c21-13-3-1-2-10-18(13)16(24)8-12-9-4-6-14(22)19-15(23)7-5-11(17(9)19)20(10,12)25/h1-3,5,7,9,12,21,23,25H,4,6,8H2/t9-,12+,20+/m1/s1

> <INCHI_KEY>
OYRYUFABCKQXTO-HGCCHXFOSA-N

> <FORMULA>
C20H16O5

> <MOLECULAR_WEIGHT>
336.343

> <EXACT_MASS>
336.099773615

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
34.20448234689399

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,11S,12R)-2,7,17-trihydroxypentacyclo[10.7.1.0^{2,11}.0^{3,8}.0^{16,20}]icosa-1(20),3,5,7,16,18-hexaene-9,15-dione

> <ALOGPS_LOGP>
2.43

> <JCHEM_LOGP>
2.8597127259999997

> <ALOGPS_LOGS>
-3.30

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.886783852730543

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.284414022470063

> <JCHEM_PKA_STRONGEST_BASIC>
-3.726130813153877

> <JCHEM_POLAR_SURFACE_AREA>
94.83000000000001

> <JCHEM_REFRACTIVITY>
90.79190000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.70e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,11S,12R)-2,7,17-trihydroxypentacyclo[10.7.1.0^{2,11}.0^{3,8}.0^{16,20}]icosa-1(20),3,5,7,16,18-hexaene-9,15-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 41 45  0  0  0  0  0  0  0  0999 V2000
    2.8151   -2.6245    1.0919 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1197   -1.6498    0.7296 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6423   -1.7599    0.7292 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1643   -1.3361   -0.6238 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3482   -1.2766   -0.6882 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0360   -2.1422    0.3359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5224   -1.9181    0.2081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8525   -0.4693    0.3147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0002   -0.0405    0.4983 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7673    0.5255    0.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9052    1.8487    0.5638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1372    2.2559    1.0537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8246    2.7064    0.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6211    2.2507   -0.0629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4585    0.9106   -0.4409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5664    0.1278   -0.2804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6140    0.0689   -0.9797 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5151    0.1571   -2.3884 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9616    0.3956   -0.5355 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5255    1.5768   -0.9661 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8082    1.9514   -0.5675 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5262    1.1475    0.2596 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9846   -0.0661    0.7199 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7213   -0.8451    1.5436 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7155   -0.4006    0.3032 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2110   -1.1592    1.5506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3777   -2.8197    0.8617 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5737   -2.0189   -1.3802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7298   -1.4973   -1.6934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7997   -3.2016    0.2432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7507   -1.7273    1.3467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9975   -2.3966    1.1131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9492   -2.3852   -0.7007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3222    3.2017    1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9237    3.7406    0.7129 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2447    2.8823   -0.1822 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5983    1.1248   -2.5854 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    2.2764   -1.6268 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2587    2.8767   -0.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5324    1.3931    0.6013 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5700   -1.6838    1.9822 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  6
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 25  2  1  0
 17  4  1  0
 25 19  1  0
 16  5  1  0
 16 10  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  6
  5 29  1  6
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
 12 34  1  0
 13 35  1  0
 14 36  1  0
 18 37  1  0
 20 38  1  0
 21 39  1  0
 22 40  1  0
 24 41  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  O   UNK     0       2.815  -2.624   1.092  0.00  0.00           O+0
HETATM    2  C   UNK     0       2.120  -1.650   0.730  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.642  -1.760   0.729  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.164  -1.336  -0.624  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.348  -1.277  -0.688  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.036  -2.142   0.336  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.522  -1.918   0.208  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.853  -0.469   0.315  0.00  0.00           C+0
HETATM    9  O   UNK     0      -5.000  -0.041   0.498  0.00  0.00           O+0
HETATM   10  C   UNK     0      -2.767   0.526   0.198  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.905   1.849   0.564  0.00  0.00           C+0
HETATM   12  O   UNK     0      -4.137   2.256   1.054  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.825   2.706   0.430  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.621   2.251  -0.063  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.459   0.911  -0.441  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.566   0.128  -0.280  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.614   0.069  -0.980  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.515   0.157  -2.388  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.962   0.396  -0.536  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.526   1.577  -0.966  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.808   1.951  -0.568  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.526   1.147   0.260  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.985  -0.066   0.720  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.721  -0.845   1.544  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.716  -0.401   0.303  0.00  0.00           C+0
HETATM   26  H   UNK     0       0.211  -1.159   1.551  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.378  -2.820   0.862  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.574  -2.019  -1.380  0.00  0.00           H+0
HETATM   29  H   UNK     0      -1.730  -1.497  -1.693  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.800  -3.202   0.243  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.751  -1.727   1.347  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.998  -2.397   1.113  0.00  0.00           H+0
HETATM   33  H   UNK     0      -3.949  -2.385  -0.701  0.00  0.00           H+0
HETATM   34  H   UNK     0      -4.322   3.202   1.343  0.00  0.00           H+0
HETATM   35  H   UNK     0      -1.924   3.741   0.713  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.245   2.882  -0.182  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.598   1.125  -2.585  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.033   2.276  -1.627  0.00  0.00           H+0
HETATM   39  H   UNK     0       4.259   2.877  -0.901  0.00  0.00           H+0
HETATM   40  H   UNK     0       5.532   1.393   0.601  0.00  0.00           H+0
HETATM   41  H   UNK     0       4.570  -1.684   1.982  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4   26   27                                             
CONECT    4    3    5   17   28                                             
CONECT    5    4    6   16   29                                             
CONECT    6    5    7   30   31                                             
CONECT    7    6    8   32   33                                             
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   16                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11   34                                                       
CONECT   13   11   14   35                                                  
CONECT   14   13   15   36                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15    5   10                                                  
CONECT   17   15   18   19    4                                             
CONECT   18   17   37                                                       
CONECT   19   17   20   25                                                  
CONECT   20   19   21   38                                                  
CONECT   21   20   22   39                                                  
CONECT   22   21   23   40                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23   41                                                       
CONECT   25   23    2   19                                                  
CONECT   26    3                                                            
CONECT   27    3                                                            
CONECT   28    4                                                            
CONECT   29    5                                                            
CONECT   30    6                                                            
CONECT   31    6                                                            
CONECT   32    7                                                            
CONECT   33    7                                                            
CONECT   34   12                                                            
CONECT   35   13                                                            
CONECT   36   14                                                            
CONECT   37   18                                                            
CONECT   38   20                                                            
CONECT   39   21                                                            
CONECT   40   22                                                            
CONECT   41   24                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   90    0
END

RDKit          3D

41 45  0  0  0  0  0  0  0  0999 V2000
    2.8151   -2.6245    1.0919 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1197   -1.6498    0.7296 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6423   -1.7599    0.7292 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1643   -1.3361   -0.6238 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3482   -1.2766   -0.6882 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0360   -2.1422    0.3359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5224   -1.9181    0.2081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8525   -0.4693    0.3147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0002   -0.0405    0.4983 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7673    0.5255    0.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9052    1.8487    0.5638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1372    2.2559    1.0537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8246    2.7064    0.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6211    2.2507   -0.0629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4585    0.9106   -0.4409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5664    0.1278   -0.2804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6140    0.0689   -0.9797 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5151    0.1571   -2.3884 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9616    0.3956   -0.5355 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5255    1.5768   -0.9661 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8082    1.9514   -0.5675 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5262    1.1475    0.2596 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9846   -0.0661    0.7199 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7213   -0.8451    1.5436 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7155   -0.4006    0.3032 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2110   -1.1592    1.5506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3777   -2.8197    0.8617 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5737   -2.0189   -1.3802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7298   -1.4973   -1.6934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7997   -3.2016    0.2432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7507   -1.7273    1.3467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9975   -2.3966    1.1131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9492   -2.3852   -0.7007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3222    3.2017    1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9237    3.7406    0.7129 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2447    2.8823   -0.1822 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5983    1.1248   -2.5854 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    2.2764   -1.6268 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2587    2.8767   -0.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5324    1.3931    0.6013 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5700   -1.6838    1.9822 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  6
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 25  2  1  0
 17  4  1  0
 25 19  1  0
 16  5  1  0
 16 10  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  6
  5 29  1  6
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
 12 34  1  0
 13 35  1  0
 14 36  1  0
 18 37  1  0
 20 38  1  0
 21 39  1  0
 22 40  1  0
 24 41  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₀H₁₆O₅

Average Mass

336.3430 Da

Monoisotopic Mass

336.09977 Da

IUPAC Name

(2R,11S,12R)-2,7,17-trihydroxypentacyclo[10.7.1.0^{2,11}.0^{3,8}.0^{16,20}]icosa-1(20),3,5,7,16,18-hexaene-9,15-dione

Traditional Name

(2R,11S,12R)-2,7,17-trihydroxypentacyclo[10.7.1.0^{2,11}.0^{3,8}.0^{16,20}]icosa-1(20),3,5,7,16,18-hexaene-9,15-dione

CAS Registry Number

Not Available

SMILES

OC1=CC=CC2=C1C(=O)C[C@H]1[C@H]3CCC(=O)C4=C(O)C=CC(=C34)[C@@]21O

InChI Identifier

InChI=1S/C20H16O5/c21-13-3-1-2-10-18(13)16(24)8-12-9-4-6-14(22)19-15(23)7-5-11(17(9)19)20(10,12)25/h1-3,5,7,9,12,21,23,25H,4,6,8H2/t9-,12+,20+/m1/s1

InChI Key

OYRYUFABCKQXTO-HGCCHXFOSA-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
Annulohypoxylon stygium	LOTUS Database	35616633
Daldinia concentrica	Fungi	KNApSAcK
Daldinia sp.	NPAtlas	12502330

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fluorenes. Fluorenes are compounds containing a fluorene moiety, which consists of two benzene rings connected through either a cyclopentane, cyclopentene, or cyclopenta-1,3-diene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Fluorenes

Sub Class

Not Available

Direct Parent

Fluorenes

Alternative Parents

Substituents

Fluorene
Tetralin
Indane
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Tertiary alcohol
Vinylogous acid
Ketone
Polyol
Organooxygen compound
Alcohol
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
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	2.43	ALOGPS
logP	2.86	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	8.28	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	90.79 m³·mol⁻¹	ChemAxon
Polarizability	34.2 Å³	ChemAxon
Number of Rings	5	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

NPAtlas ID

NPA009625

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

552719

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

637058

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Quang DN, Hashimoto T, Tanaka M, Baumgartner M, Stadler M, Asakawa Y: Chemical constituents of the ascomycete Daldinia concentrica. J Nat Prod. 2002 Dec;65(12):1869-74. doi: 10.1021/np020301h. [PubMed:12502330 ]

Showing NP-Card for Daldinone A (NP0004463)

MOL for NP0004463 (Daldinone A)

3D MOL for NP0004463 (Daldinone A)

3D SDF for NP0004463 (Daldinone A)

3D-SDF for NP0004463 (Daldinone A)

PDB for NP0004463 (Daldinone A)

3D PDB for NP0004463 (Daldinone A)

SMILES for NP0004463 (Daldinone A)

INCHI for NP0004463 (Daldinone A)

Structure for NP0004463 (Daldinone A)

3D Structure for NP0004463 (Daldinone A)