NP-MRD: Showing NP-Card for 5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione (NP0304397)

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Record Information

Version

2.0

Created at

2022-09-10 19:27:26 UTC

Updated at

2022-09-10 19:27:27 UTC

NP-MRD ID

NP0304397

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione

Description

5,9A-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-4,5,5a,5b,6,7,8,9,9a,10,11,11a-dodecahydro-1,12-dioxatetraphene-4,8-dione belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. 5,9A-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-4,5,5a,5b,6,7,8,9,9a,10,11,11a-dodecahydro-1,12-dioxatetraphene-4,8-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241510072D          

 31 34  0  0  0  0            999 V2000
   -0.0339   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7762   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3163   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1265   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666   -0.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4767   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7467   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5569   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269   -2.3841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0970   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0168   -0.0454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3670    0.4223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1771    0.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9071    1.0459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7172    0.8900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5274    0.7341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7974   -0.0454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3375    0.5782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6075   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6204    0.6235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4221   -0.0708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8776   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6877   -1.1368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3375   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5274   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2573   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7172   -1.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4472   -0.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9071   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1771   -1.9164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  4  3  1  4  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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
  6 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 14 29  1  0  0  0  0
 29 30  1  0  0  0  0
 10 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          3D

 63 66  0  0  0  0  0  0  0  0999 V2000
    9.1050    0.3635   -1.5038 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6867    0.0342   -1.1891 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9847    0.7691   -0.3532 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6093    0.4389   -0.0562 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9143    1.1787    0.7806 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5197    0.8299    1.0712 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7969    1.6097    1.9494 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4889    1.2858    2.2246 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8340    1.9962    3.0232 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9341    0.1809    1.6085 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6969   -0.5440    0.7555 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9599   -0.2257    0.4941 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0549   -1.6287    0.1882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3118   -1.5587   -0.2571 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5983   -2.9912   -0.6523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3414   -0.5969   -1.3970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2398    0.6156   -1.1324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5836    0.0519   -0.7887 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7739   -0.9450   -1.7956 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7637    0.9208   -0.9928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1026    1.0199   -2.4941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6908    2.3050   -0.4876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9159    0.1245   -0.4209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9708    0.7155   -0.3461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8383   -1.2547    0.0276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5078   -1.8161    0.3878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5354   -0.6342    0.5383 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0699    0.1332    1.6981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1305   -1.1048    0.9105 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4671   -0.2041    1.8864 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4126   -0.7473    3.1974 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3746   -0.1182   -2.4726 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7195   -0.0434   -0.6799 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2203    1.4685   -1.5471 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2283   -0.8357   -1.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4457    1.6171    0.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1452   -0.4333   -0.5322 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3512    2.0245    1.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2804    2.4838    2.4190 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3130   -3.6270   -0.7573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1320   -3.4422    0.2366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1383   -3.1184   -1.5879 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6646   -0.1521   -1.6307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6680   -1.1092   -2.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3317    1.1401   -2.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8208    1.3067   -0.4135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6007   -0.5771   -2.6881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5184    0.0908   -2.8797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8248    1.8772   -2.5818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1713    1.3572   -2.9938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6652    2.6443   -0.1837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9939    3.0858   -1.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4424    2.4781    0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4918   -1.3503    0.9449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3694   -1.8917   -0.7358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4800   -2.4004    1.3119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1601   -2.4095   -0.5090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1692   -0.0523    1.8996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6131   -0.2627    2.6498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9490    1.2032    1.7025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3442   -2.0643    1.4843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9974    0.7859    2.0158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1924    0.0029    3.8112 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  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  1  0
 14 15  1  6
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  6
 18 20  1  0
 20 21  1  0
 20 22  1  0
 20 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  1
 27 29  1  0
 29 30  1  0
 30 31  1  0
 12  6  1  0
 29 14  1  0
 30 10  1  0
 27 18  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  3 36  1  0
  4 37  1  0
  5 38  1  0
  7 39  1  0
 15 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  0
 17 46  1  0
 19 47  1  0
 21 48  1  0
 21 49  1  0
 21 50  1  0
 22 51  1  0
 22 52  1  0
 22 53  1  0
 25 54  1  0
 25 55  1  0
 26 56  1  0
 26 57  1  0
 28 58  1  0
 28 59  1  0
 28 60  1  0
 29 61  1  1
 30 62  1  1
 31 63  1  0
M  END


  Mrv1533004241510072D          

 31 34  0  0  0  0            999 V2000
   -0.0339   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7762   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3163   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1265   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666   -0.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4767   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7467   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5569   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269   -2.3841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0970   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0168   -0.0454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3670    0.4223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1771    0.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9071    1.0459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7172    0.8900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5274    0.7341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7974   -0.0454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3375    0.5782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6075   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6204    0.6235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4221   -0.0708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8776   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6877   -1.1368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3375   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5274   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2573   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7172   -1.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4472   -0.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9071   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1771   -1.9164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  4  3  1  4  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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
  6 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
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 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
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 20 23  1  0  0  0  0
 23 24  2  0  0  0  0
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 10 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0304397

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=CC=CC1=CC(=O)C2=C(O1)OC1(C)CCC3(O)C(C)(C)C(=O)CCC3(C)C1C2O

> <INCHI_IDENTIFIER>
InChI=1S/C25H32O6/c1-6-7-8-9-15-14-16(26)18-19(28)20-23(4)11-10-17(27)22(2,3)25(23,29)13-12-24(20,5)31-21(18)30-15/h6-9,14,19-20,28-29H,10-13H2,1-5H3

> <INCHI_KEY>
NFIWDODYYNWZLI-UHFFFAOYSA-N

> <FORMULA>
C25H32O6

> <MOLECULAR_WEIGHT>
428.525

> <EXACT_MASS>
428.21988875

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
47.418724877504744

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-4,5,5a,5b,6,7,8,9,9a,10,11,11a-dodecahydro-1,12-dioxatetraphene-4,8-dione

> <ALOGPS_LOGP>
3.31

> <JCHEM_LOGP>
3.2890626586666647

> <ALOGPS_LOGS>
-4.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.156639922468742

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.548458740973178

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2991743587110154

> <JCHEM_POLAR_SURFACE_AREA>
93.06000000000002

> <JCHEM_REFRACTIVITY>
129.74819999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.60e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -0.063  -2.704   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.449  -2.995   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.457  -1.831   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.969  -2.122   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.978  -0.958   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.490  -1.249   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.994  -2.704   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.506  -2.995   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       9.010  -4.450   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.514  -1.831   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.010  -0.376   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.498  -0.085   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      10.018   0.788   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      11.531   0.497   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.027   1.952   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.539   1.661   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.051   1.370   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.555  -0.085   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      15.563   1.079   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      16.067  -0.376   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      16.091   1.164   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      17.588  -0.132   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      16.571  -1.831   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      18.084  -2.122   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      15.563  -2.995   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.051  -2.704   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      13.547  -1.249   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.539  -2.413   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.035  -0.958   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.027  -2.122   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      11.531  -3.577   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   30                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11    6                                                       
CONECT   13   11   14                                                       
CONECT   14   13   15   16   29                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   27                                             
CONECT   19   18                                                            
CONECT   20   18   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   18   28   29                                             
CONECT   28   27                                                            
CONECT   29   27   14   30                                                  
CONECT   30   29   10   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₂O₆

Average Mass

428.5250 Da

Monoisotopic Mass

428.21989 Da

IUPAC Name

5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-4,5,5a,5b,6,7,8,9,9a,10,11,11a-dodecahydro-1,12-dioxatetraphene-4,8-dione

Traditional Name

5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione

CAS Registry Number

Not Available

SMILES

CC=CC=CC1=CC(=O)C2=C(O1)OC1(C)CCC3(O)C(C)(C)C(=O)CCC3(C)C1C2O

InChI Identifier

InChI=1S/C25H32O6/c1-6-7-8-9-15-14-16(26)18-19(28)20-23(4)11-10-17(27)22(2,3)25(23,29)13-12-24(20,5)31-21(18)30-15/h6-9,14,19-20,28-29H,10-13H2,1-5H3

InChI Key

NFIWDODYYNWZLI-UHFFFAOYSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
Alkyl aryl ether
Pyranone
Pyran
Cyclic alcohol
Heteroaromatic compound
Tertiary alcohol
Vinylogous ester
Ketone
Secondary alcohol
Cyclic ketone
Oxacycle
Ether
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	3.31	ALOGPS
logP	3.29	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	13.55	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	93.06 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	129.75 m³·mol⁻¹	ChemAxon
Polarizability	47.42 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

LOTUS database [Link]

Showing NP-Card for 5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione (NP0304397)

MOL for NP0304397 (5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione)

3D MOL for NP0304397 (5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione)

3D SDF for NP0304397 (5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione)

3D-SDF for NP0304397 (5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione)

PDB for NP0304397 (5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione)

3D PDB for NP0304397 (5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione)

SMILES for NP0304397 (5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione)

INCHI for NP0304397 (5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione)

Structure for NP0304397 (5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione)

3D Structure for NP0304397 (5,9a-dihydroxy-5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5,5a,6,7,10,11-hexahydro-1,12-dioxatetraphene-4,8-dione)