NP-MRD: Showing NP-Card for mollicellin d (NP0287607)

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Record Information

Version

2.0

Created at

2022-09-09 16:51:19 UTC

Updated at

2022-09-09 16:51:19 UTC

NP-MRD ID

NP0287607

Secondary Accession Numbers

None

Natural Product Identification

Common Name

mollicellin d

Description

Mollicellin D belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone). Mollicellin D is an extremely weak basic (essentially neutral) compound (based on its pKa). mollicellin d is found in Ovatospora brasiliensis. Production by Chaetomium subspecies and mycotoxin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 05061307042D          

 28 30  0  0  0  0            999 V2000
    7.4228    2.9168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8440    1.5514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6366    3.5528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8390    3.5528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4509    1.8694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8461    2.4305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0859    1.1398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5733    0.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2393    2.1125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4530    2.7485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0226    2.7485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0578    2.1873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3897    1.1398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8742    1.3830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4811    1.7010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8109    2.5053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4178    2.1873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014    1.3830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6647    2.5053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9945    1.7010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3253    3.1503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3705    2.4305    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.3617    0.0923    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4790    0.8219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0034    0.8219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9673    3.8936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7378    1.3430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1503    3.1503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  9  1  1  0  0  0  0
  9  2  1  0  0  0  0
  9  5  2  0  0  0  0
 10  3  1  0  0  0  0
 11  4  1  0  0  0  0
 12  6  1  0  0  0  0
 12 10  2  0  0  0  0
 13  8  1  0  0  0  0
 14  7  2  0  0  0  0
 14 12  1  0  0  0  0
 15  7  1  0  0  0  0
 16 11  1  0  0  0  0
 17 11  2  0  0  0  0
 18 13  2  0  0  0  0
 18 17  1  0  0  0  0
 19 10  1  0  0  0  0
 19 15  2  0  0  0  0
 20 13  1  0  0  0  0
 20 16  2  0  0  0  0
 21 16  1  0  0  0  0
 22 17  1  0  0  0  0
 23  8  1  0  0  0  0
 24 14  1  0  0  0  0
 25 18  1  0  0  0  0
 26 21  2  0  0  0  0
 27 15  1  0  0  0  0
 27 20  1  0  0  0  0
 28 19  1  0  0  0  0
 28 21  1  0  0  0  0
M  END

     RDKit          3D

 49 51  0  0  0  0  0  0  0  0999 V2000
    6.1639   -1.0324    1.2543 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2923    0.0440    0.6932 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3983    1.3734    1.3212 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5041   -0.2028   -0.3031 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6102    0.7524   -0.9354 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1868    0.3245   -0.9696 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5993   -0.1685   -2.1233 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3876   -0.2470   -3.2636 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2827   -0.5705   -2.1553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4927   -0.4871   -1.0114 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0947    0.0028    0.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4371    0.4134    0.1660 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9392    0.9271    1.4664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5099    0.1699    1.3938 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8626    0.0036    1.6654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1509   -0.0664    2.8794 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0087   -0.1046    0.7723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1939    0.2669    1.3598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1916    0.7244    2.7428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3339    0.1843    0.5711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8405    0.6601    1.3291 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -5.3024   -0.2533   -0.7621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4938   -0.2821   -1.4090 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1005   -0.6173   -1.3202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9125   -1.0931   -2.6910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0570   -1.1627   -3.4439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9379   -0.5415   -0.5422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8022   -0.9490   -1.2698 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6693   -1.3826    2.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1491   -0.6308    1.5632 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2748   -1.8762    0.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1691    2.2191    0.6742 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6748    1.3893    2.1886 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3922    1.5023    1.8254 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5003   -1.2287   -0.7207 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9247    0.8651   -2.0170 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6141    1.7536   -0.4619 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9953   -0.6003   -4.1201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1895   -0.9596   -3.0561 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0911    1.1684    2.1399 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5377    0.1393    1.9649 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4894    1.8845    1.3465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2339    1.1986    2.8595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2921   -0.0344    3.5347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6027    1.6283    2.9835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7915   -0.5220   -2.2867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4561   -2.1100   -2.7129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2341   -0.3667   -3.2264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3872   -2.1058   -3.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6 12  2  0
 12 13  1  0
 12 11  1  0
 11 10  2  0
 10 28  1  0
 28 27  1  0
 27 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  2  0
 24 25  1  0
 25 26  1  0
 17 15  1  0
 15 16  2  0
 15 14  1  0
 10  9  1  0
  9  7  2  0
  7  8  1  0
  7  6  1  0
 14 11  1  0
 24 27  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  5 36  1  0
  5 37  1  0
 13 40  1  0
 13 41  1  0
 13 42  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
 23 46  1  0
 25 47  1  0
 25 48  1  0
 26 49  1  0
  9 39  1  0
  8 38  1  0
M  END


  Mrv0541 05061307042D          

 28 30  0  0  0  0            999 V2000
    7.4228    2.9168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8440    1.5514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6366    3.5528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8390    3.5528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4509    1.8694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8461    2.4305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0859    1.1398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5733    0.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2393    2.1125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4530    2.7485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0226    2.7485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0578    2.1873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3897    1.1398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8742    1.3830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4811    1.7010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8109    2.5053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4178    2.1873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014    1.3830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6647    2.5053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9945    1.7010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3253    3.1503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3705    2.4305    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.3617    0.0923    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4790    0.8219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0034    0.8219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9673    3.8936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7378    1.3430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1503    3.1503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  9  1  1  0  0  0  0
  9  2  1  0  0  0  0
  9  5  2  0  0  0  0
 10  3  1  0  0  0  0
 11  4  1  0  0  0  0
 12  6  1  0  0  0  0
 12 10  2  0  0  0  0
 13  8  1  0  0  0  0
 14  7  2  0  0  0  0
 14 12  1  0  0  0  0
 15  7  1  0  0  0  0
 16 11  1  0  0  0  0
 17 11  2  0  0  0  0
 18 13  2  0  0  0  0
 18 17  1  0  0  0  0
 19 10  1  0  0  0  0
 19 15  2  0  0  0  0
 20 13  1  0  0  0  0
 20 16  2  0  0  0  0
 21 16  1  0  0  0  0
 22 17  1  0  0  0  0
 23  8  1  0  0  0  0
 24 14  1  0  0  0  0
 25 18  1  0  0  0  0
 26 21  2  0  0  0  0
 27 15  1  0  0  0  0
 27 20  1  0  0  0  0
 28 19  1  0  0  0  0
 28 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0287607

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=C(C)C2=C(OC3=C(C(C)=C(Cl)C(O)=C3CO)C(=O)O2)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H21ClO6/c1-9(2)5-6-12-10(3)19-15(7-14(12)24)27-20-13(8-23)18(25)17(22)11(4)16(20)21(26)28-19/h5,7,23-25H,6,8H2,1-4H3

> <INCHI_KEY>
AINFZKIGIQBKDM-UHFFFAOYSA-N

> <FORMULA>
C21H21ClO6

> <MOLECULAR_WEIGHT>
404.841

> <EXACT_MASS>
404.102666111

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
42.015017793130625

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
13-chloro-5,14-dihydroxy-15-(hydroxymethyl)-7,12-dimethyl-6-(3-methylbut-2-en-1-yl)-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3(8),4,6,12,14-hexaen-10-one

> <ALOGPS_LOGP>
3.99

> <JCHEM_LOGP>
4.946696639333333

> <ALOGPS_LOGS>
-4.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.05263696490238

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.1500775703667765

> <JCHEM_PKA_STRONGEST_BASIC>
-3.208376831682645

> <JCHEM_POLAR_SURFACE_AREA>
96.22

> <JCHEM_REFRACTIVITY>
107.95139999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.32e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
13-chloro-5,14-dihydroxy-15-(hydroxymethyl)-7,12-dimethyl-6-(3-methylbut-2-en-1-yl)-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3(8),4,6,12,14-hexaen-10-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      13.856   5.445   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.642   2.896   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.655   6.632   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.566   6.632   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.042   3.490   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.913   4.537   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.627   2.128   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.937   0.626   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.513   3.943   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.312   5.131   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.909   5.131   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.441   4.083   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.594   2.128   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.099   2.582   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.498   3.175   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.380   4.677   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.780   4.083   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.123   2.582   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.841   4.677   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.723   3.175   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.341   5.881   0.000  0.00  0.00           C+0
HETATM   22 Cl   UNK     0      -0.692   4.537   0.000  0.00  0.00          Cl+0
HETATM   23  O   UNK     0       4.409   0.172   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      10.227   1.534   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -0.006   1.534   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       3.672   7.268   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       5.111   2.507   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       5.881   5.881   0.000  0.00  0.00           O+0
CONECT    1    9                                                            
CONECT    2    9                                                            
CONECT    3   10                                                            
CONECT    4   11                                                            
CONECT    5    6    9                                                       
CONECT    6    5   12                                                       
CONECT    7   14   15                                                       
CONECT    8   13   23                                                       
CONECT    9    1    2    5                                                  
CONECT   10    3   12   19                                                  
CONECT   11    4   16   17                                                  
CONECT   12    6   10   14                                                  
CONECT   13    8   18   20                                                  
CONECT   14    7   12   24                                                  
CONECT   15    7   19   27                                                  
CONECT   16   11   20   21                                                  
CONECT   17   11   18   22                                                  
CONECT   18   13   17   25                                                  
CONECT   19   10   15   28                                                  
CONECT   20   13   16   27                                                  
CONECT   21   16   26   28                                                  
CONECT   22   17                                                            
CONECT   23    8                                                            
CONECT   24   14                                                            
CONECT   25   18                                                            
CONECT   26   21                                                            
CONECT   27   15   20                                                       
CONECT   28   19   21                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₁ClO₆

Average Mass

404.8410 Da

Monoisotopic Mass

404.10267 Da

IUPAC Name

13-chloro-5,14-dihydroxy-15-(hydroxymethyl)-7,12-dimethyl-6-(3-methylbut-2-en-1-yl)-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3(8),4,6,12,14-hexaen-10-one

Traditional Name

13-chloro-5,14-dihydroxy-15-(hydroxymethyl)-7,12-dimethyl-6-(3-methylbut-2-en-1-yl)-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3(8),4,6,12,14-hexaen-10-one

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C(C)C2=C(OC3=C(C(C)=C(Cl)C(O)=C3CO)C(=O)O2)C=C1O

InChI Identifier

InChI=1S/C21H21ClO6/c1-9(2)5-6-12-10(3)19-15(7-14(12)24)27-20-13(8-23)18(25)17(22)11(4)16(20)21(26)28-19/h5,7,23-25H,6,8H2,1-4H3

InChI Key

AINFZKIGIQBKDM-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
Ovatospora brasiliensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Depsides and depsidones

Sub Class

Not Available

Direct Parent

Depsides and depsidones

Alternative Parents

Substituents

Depsidone
Diaryl ether
1-hydroxy-2-unsubstituted benzenoid
1,4-dioxepine
Dioxepine
Aryl chloride
Aryl halide
Benzenoid
Carboxylic acid ester
Lactone
Monocarboxylic acid or derivatives
Ether
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Organochloride
Organohalogen compound
Alcohol
Aromatic alcohol
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Primary 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	3.99	ALOGPS
logP	4.95	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	7.15	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	107.95 m³·mol⁻¹	ChemAxon
Polarizability	42.02 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	No	ChemAxon

External Links

HMDB ID

HMDB0033343

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB011371

KNApSAcK ID

Not Available

Chemspider ID

134712

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

152840

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for mollicellin d (NP0287607)

MOL for NP0287607 (mollicellin d)

3D MOL for NP0287607 (mollicellin d)

3D SDF for NP0287607 (mollicellin d)

3D-SDF for NP0287607 (mollicellin d)

PDB for NP0287607 (mollicellin d)

3D PDB for NP0287607 (mollicellin d)

SMILES for NP0287607 (mollicellin d)

INCHI for NP0287607 (mollicellin d)

Structure for NP0287607 (mollicellin d)

3D Structure for NP0287607 (mollicellin d)