NP-MRD: Showing NP-Card for 7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione (NP0154441)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 11:21:43 UTC

Updated at

2022-09-02 11:21:43 UTC

NP-MRD ID

NP0154441

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione

Description

7A-hydroxy-3,4,5a,8,8,11a-hexamethyl-1,5a,6,7,7a,8,9,10,11,11a,11b,12-dodecahydro-2,5-dioxatetraphene-1,9-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. 7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione is found in Aspergillus flocculosus. Based on a literature review very few articles have been published on 7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-1,5a,6,7,7a,8,9,10,11,11a,11b,12-dodecahydro-2,5-dioxatetraphene-1,9-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022213212D          

 27 30  0  0  0  0            999 V2000
    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 O   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7467    0.7341    0.0000 C   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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  2  8  2  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  0  0  0  0
  6 27  1  0  0  0  0
M  END

     RDKit          3D

 57 60  0  0  0  0  0  0  0  0999 V2000
    5.8289    2.2079    0.5243 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4140    1.7597    0.6695 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6400    2.1946    1.6569 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3876    1.7970    1.7844 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7389    2.2672    2.7531 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8651    0.9056    0.8689 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6121    0.4297   -0.1592 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9182    0.8568   -0.2754 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7214    0.3372   -1.3912 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0654   -0.4462   -1.0414 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8486   -1.1505   -0.8824 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2425   -2.6327   -0.9720 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0445   -0.8420   -2.1338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0413    0.1699   -1.8660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0241   -0.4363   -0.8508 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6456   -1.4437   -1.6443 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1168    0.5535   -0.6199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1970    1.6100   -1.7209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4967   -0.1276   -0.6379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0432    1.2808    0.6457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3846    2.4444    0.7581 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5374    0.6140    1.8731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9867   -0.7359    1.6595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3697   -1.0286    0.3205 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5426   -2.5674    0.2384 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1406   -0.8349    0.3910 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4614    0.4671    1.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9793    3.2275    0.9624 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4530    1.4561    1.0571 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1414    2.2536   -0.5353 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6271    0.9898   -2.2716 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4625   -0.7330   -1.6289 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7794    0.3228   -1.0869 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9859   -3.1729   -0.0375 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3372   -2.7791   -1.0952 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7965   -3.1186   -1.8793 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6781   -0.3991   -2.9524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4132   -1.7369   -2.5854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6951    1.1558   -1.5964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5844    0.2857   -2.8519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8731   -1.0418   -2.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4176    1.1653   -2.7071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3689    2.3140   -1.7002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1202    2.2113   -1.4638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8102   -0.4205    0.3795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4997   -1.0204   -1.2703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2727    0.5575   -1.0302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8521    1.3158    2.4154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4387    0.5828    2.5625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2092   -0.9314    2.4368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8068   -1.4686    1.9372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1106   -3.0602    1.1129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6628   -2.6954    0.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2999   -2.9657   -0.7325 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4843   -1.6294    1.1256 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3207    0.3662    2.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1538    1.3193    0.7279 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  8  2  0
  8  9  1  0
  8  7  1  0
  7  6  2  0
  6 27  1  0
 27 26  1  0
 26 11  1  0
 11 12  1  1
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  6
 15 17  1  0
 17 18  1  0
 17 19  1  0
 17 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  6
 11 10  1  0
  6  4  1  0
  4  5  2  0
  4  3  1  0
  3  2  1  0
 10  7  1  0
 24 26  1  0
 24 15  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  9 31  1  0
  9 32  1  0
  9 33  1  0
 27 56  1  0
 27 57  1  0
 26 55  1  1
 12 34  1  0
 12 35  1  0
 12 36  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  0
 14 40  1  0
 16 41  1  0
 18 42  1  0
 18 43  1  0
 18 44  1  0
 19 45  1  0
 19 46  1  0
 19 47  1  0
 22 48  1  0
 22 49  1  0
 23 50  1  0
 23 51  1  0
 25 52  1  0
 25 53  1  0
 25 54  1  0
M  END


  Mrv1652309022213212D          

 27 30  0  0  0  0            999 V2000
    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 O   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7467    0.7341    0.0000 C   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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  2  8  2  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  0  0  0  0
  6 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0154441

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C(C)C2=C(CC3C(C)(CCC4(O)C(C)(C)C(=O)CCC34C)O2)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O5/c1-12-13(2)26-18(24)14-11-15-20(5)8-7-16(23)19(3,4)22(20,25)10-9-21(15,6)27-17(12)14/h15,25H,7-11H2,1-6H3

> <INCHI_KEY>
BWYKQVIOFJIPNL-UHFFFAOYSA-N

> <FORMULA>
C22H30O5

> <MOLECULAR_WEIGHT>
374.477

> <EXACT_MASS>
374.209324066

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
41.190329017548734

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-1,5a,6,7,7a,8,9,10,11,11a,11b,12-dodecahydro-2,5-dioxatetraphene-1,9-dione

> <ALOGPS_LOGP>
3.29

> <JCHEM_LOGP>
3.0532335486666673

> <ALOGPS_LOGS>
-3.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.362866824782866

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.860574498185443

> <JCHEM_PKA_STRONGEST_BASIC>
-3.297181592367563

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
102.98109999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.81e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       4.978  -0.958   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.490  -1.249   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       6.994  -2.704   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       8.506  -2.995   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.010  -4.450   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.514  -1.831   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.010  -0.376   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.498  -0.085   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.994   1.370   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      10.018   0.788   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      11.531   0.497   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.027   1.952   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.539   1.661   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.051   1.370   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.555  -0.085   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      15.563   1.079   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      16.067  -0.376   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.091   1.164   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.588  -0.132   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      16.571  -1.831   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      18.084  -2.122   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      15.563  -2.995   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      14.051  -2.704   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.547  -1.249   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.539  -2.413   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.035  -0.958   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.027  -2.122   0.000  0.00  0.00           C+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   27                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    2    9                                                  
CONECT    9    8                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12   13   26                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17   24                                             
CONECT   16   15                                                            
CONECT   17   15   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   15   25   26                                             
CONECT   25   24                                                            
CONECT   26   24   11   27                                                  
CONECT   27   26    6                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₅

Average Mass

374.4770 Da

Monoisotopic Mass

374.20932 Da

IUPAC Name

7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-1,5a,6,7,7a,8,9,10,11,11a,11b,12-dodecahydro-2,5-dioxatetraphene-1,9-dione

Traditional Name

7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione

CAS Registry Number

Not Available

SMILES

CC1=C(C)C2=C(CC3C(C)(CCC4(O)C(C)(C)C(=O)CCC34C)O2)C(=O)O1

InChI Identifier

InChI=1S/C22H30O5/c1-12-13(2)26-18(24)14-11-15-20(5)8-7-16(23)19(3,4)22(20,25)10-9-21(15,6)27-17(12)14/h15,25H,7-11H2,1-6H3

InChI Key

BWYKQVIOFJIPNL-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

Species Name	Source	Reference
Aspergillus flocculosus	LOTUS Database	35616633

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
Pyranone
Alkyl aryl ether
Pyran
Heteroaromatic compound
Vinylogous ester
Tertiary alcohol
Cyclic alcohol
Cyclic ketone
Lactone
Ketone
Oxacycle
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	3.29	ALOGPS
logP	3.05	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	13.86	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	102.98 m³·mol⁻¹	ChemAxon
Polarizability	41.19 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

162992545

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione (NP0154441)

MOL for NP0154441 (7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione)

3D MOL for NP0154441 (7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione)

3D SDF for NP0154441 (7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione)

3D-SDF for NP0154441 (7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione)

PDB for NP0154441 (7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione)

3D PDB for NP0154441 (7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione)

SMILES for NP0154441 (7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione)

INCHI for NP0154441 (7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione)

Structure for NP0154441 (7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione)

3D Structure for NP0154441 (7a-hydroxy-3,4,5a,8,8,11a-hexamethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione)