NP-MRD: Showing NP-Card for (3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one (NP0152922)

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Record Information

Version

2.0

Created at

2022-09-02 09:30:08 UTC

Updated at

2022-09-02 09:30:08 UTC

NP-MRD ID

NP0152922

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one

Description

(+)-Applanatumol G belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. (3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one is found in Ganoderma applanatum. Based on a literature review very few articles have been published on (+)-applanatumol G.

Structure

MOL 3D MOL SDF PDB SMILES InChI

  Mrv1652309022211302D          

 28 30  0  0  1  0            999 V2000
   -0.0473   -2.6631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2076   -1.8785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0146   -1.7070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695   -0.9224    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    0.1576    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0542    0.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3397    1.3951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6252    0.9826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3397    2.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6252    2.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6252    3.4576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0892    3.8701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3397    3.8701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    3.4576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    2.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7686    2.2201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0937    1.1971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3237   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388   -0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542   -0.6674    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0542   -1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7686   -1.9049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7686   -2.7299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3397   -1.9049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3397   -2.7299    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
  4  3  1  6  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  1  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  4 23  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
   -4.6548    0.7310   -1.9699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5683   -0.1943   -0.7658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4214   -0.9522   -0.7347 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2383   -0.2051   -0.7008 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5643   -0.5302   -2.0449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3856   -1.3961   -1.6735 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0633   -0.8131   -0.3408 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7235    0.4859   -0.5432 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9330    0.4263   -1.3848 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8664    0.2481   -2.6528 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2936    0.5624   -0.8786 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5469    0.7870    0.4491 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8421    0.9389    0.9530 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0536    1.1657    2.3079 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9086    0.8651    0.1142 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6612    0.6397   -1.2205 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3888    0.4885   -1.7279 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2322    0.2634   -3.0918 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7176   -1.8073    0.4928 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9087   -1.9114    0.8069 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2867   -2.6998    0.9189 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5654   -2.1543    0.7195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2974   -0.6916    0.3480 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3052    0.1657    1.5520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6642    0.1579    2.0206 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1467    1.4423    2.1946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5720   -0.3998    2.6132 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1554    0.5693    3.2489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9835    1.5914   -1.8143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3197    0.1706   -2.8530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7216    1.0319   -2.0582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7535    0.4247    0.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4116   -0.9296   -0.8984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4952    0.8470   -0.6501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2462   -1.0186   -2.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2340    0.4338   -2.4666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6993   -2.4510   -1.5039 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3793   -1.2974   -2.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0013    1.1884   -1.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9379    1.0465    0.3992 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7708    0.8593    1.1860 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9878    1.2756    2.6740 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9251    0.9837    0.5046 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5046    0.5779   -1.9038 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0530    0.2160   -3.6741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0515   -2.6671   -0.1196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1845   -2.1993    1.6515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0666    1.1902    1.4203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2170    1.3603    2.5579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2279    2.0243    1.2613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6447    2.0473    2.9471 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8865    1.1004    2.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5142    1.3715    3.6849 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7029    0.0877    4.1301 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
  7 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  1
 24 25  1  0
 25 26  1  0
 24 27  1  0
 27 28  1  0
 23  4  1  0
 23  7  1  0
 17 11  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  2 33  1  0
  4 34  1  1
  5 35  1  0
  5 36  1  0
  6 37  1  0
  6 38  1  0
  8 39  1  0
  8 40  1  0
 12 41  1  0
 14 42  1  0
 15 43  1  0
 16 44  1  0
 18 45  1  0
 22 46  1  0
 22 47  1  0
 24 48  1  0
 26 49  1  0
 26 50  1  0
 26 51  1  0
 28 52  1  0
 28 53  1  0
 28 54  1  0
M  END

  Mrv1652309022211302D          

 28 30  0  0  1  0            999 V2000
   -0.0473   -2.6631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2076   -1.8785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0146   -1.7070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695   -0.9224    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    0.1576    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0542    0.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3397    1.3951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6252    0.9826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3397    2.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6252    2.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6252    3.4576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0892    3.8701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3397    3.8701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    3.4576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    2.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7686    2.2201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0937    1.1971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3237   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388   -0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542   -0.6674    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0542   -1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7686   -1.9049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7686   -2.7299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3397   -1.9049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3397   -2.7299    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
  4  3  1  6  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  1  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  4 23  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0152922

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCO[C@@H]1CC[C@]2(CC(=O)C3=CC(O)=CC=C3O)C(=O)OC[C@]12C(OC)OC

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O8/c1-4-27-16-7-8-19(10-15(23)13-9-12(21)5-6-14(13)22)17(24)28-11-20(16,19)18(25-2)26-3/h5-6,9,16,18,21-22H,4,7-8,10-11H2,1-3H3/t16-,19+,20-/m1/s1

> <INCHI_KEY>
FKTBPUPWFHCNQN-LSTHTHJFSA-N

> <FORMULA>
C20H26O8

> <MOLECULAR_WEIGHT>
394.42

> <EXACT_MASS>
394.162767797

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
40.10787215987297

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aS,4R,6aR)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-hexahydro-1H-cyclopenta[c]furan-1-one

> <ALOGPS_LOGP>
1.97

> <JCHEM_LOGP>
2.3041849306666675

> <ALOGPS_LOGS>
-2.96

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.0096143782885

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.203110600657428

> <JCHEM_PKA_STRONGEST_BASIC>
-3.766498173225639

> <JCHEM_POLAR_SURFACE_AREA>
111.52000000000001

> <JCHEM_REFRACTIVITY>
98.41969999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.28e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aS,4R,6aR)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one

> <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      -0.088  -4.971   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.388  -3.507   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.894  -3.186   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       2.370  -1.722   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.465  -0.476   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.834   0.294   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.834   1.834   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.501   2.604   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.167   1.834   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.501   4.144   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.167   4.914   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.167   6.454   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.167   7.224   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.501   7.224   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.834   6.454   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.834   4.914   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.168   4.144   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.299   0.770   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.775   2.235   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       6.204  -0.476   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.299  -1.722   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.834  -1.246   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.834  -2.786   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.168  -3.556   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.168  -5.096   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.501  -3.556   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.501  -5.096   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   23                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   19   23                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   11   18                                                  
CONECT   18   17                                                            
CONECT   19    7   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    4    7   24                                             
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   28                                                       
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₆O₈

Average Mass

394.4200 Da

Monoisotopic Mass

394.16277 Da

IUPAC Name

(3aS,4R,6aR)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-hexahydro-1H-cyclopenta[c]furan-1-one

Traditional Name

(3aS,4R,6aR)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one

CAS Registry Number

Not Available

SMILES

CCO[C@@H]1CC[C@]2(CC(=O)C3=CC(O)=CC=C3O)C(=O)OC[C@]12C(OC)OC

InChI Identifier

InChI=1S/C20H26O8/c1-4-27-16-7-8-19(10-15(23)13-9-12(21)5-6-14(13)22)17(24)28-11-20(16,19)18(25-2)26-3/h5-6,9,16,18,21-22H,4,7-8,10-11H2,1-3H3/t16-,19+,20-/m1/s1

InChI Key

FKTBPUPWFHCNQN-LSTHTHJFSA-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
Ganoderma applanatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alkyl-phenylketones

Alternative Parents

Substituents

Alkyl-phenylketone
Aryl alkyl ketone
Hydroquinone
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Gamma butyrolactone
Monocyclic benzene moiety
Vinylogous acid
Tetrahydrofuran
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxide
Hydrocarbon derivative
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	1.97	ALOGPS
logP	2.3	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	9.2	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	111.52 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	98.42 m³·mol⁻¹	ChemAxon
Polarizability	40.11 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

78441189

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139586388

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one (NP0152922)

MOL for NP0152922 ((3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one)

3D MOL for NP0152922 ((3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one)

3D SDF for NP0152922 ((3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one)

3D-SDF for NP0152922 ((3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one)

PDB for NP0152922 ((3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one)

3D PDB for NP0152922 ((3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one)

SMILES for NP0152922 ((3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one)

INCHI for NP0152922 ((3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one)

Structure for NP0152922 ((3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one)

3D Structure for NP0152922 ((3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-ethoxy-tetrahydrocyclopenta[c]furan-1-one)