NP-MRD: Showing NP-Card for Condidymic acid (NP0071054)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 16:28:14 UTC

Updated at

2022-04-28 16:28:14 UTC

NP-MRD ID

NP0071054

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Condidymic acid

Description

5-Hydroxy-11-methoxy-3,13-dipentyl-8-oxatricyclo[7.4.0.0²,⁷]Trideca-1(9),2(7),3,5,10,12-hexaene-4-carboxylic acid belongs to the class of organic compounds known as dibenzofurans. Dibenzofurans are compounds containing a dibenzofuran moiety, which consists of two benzene rings fused to a central furan ring. Condidymic acid is found in Cladonia didyma, Cladonia rangiferina and Cladonia rigida. 5-Hydroxy-11-methoxy-3,13-dipentyl-8-oxatricyclo[7.4.0.0²,⁷]Trideca-1(9),2(7),3,5,10,12-hexaene-4-carboxylic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171514352D          

 29 31  0  0  0  0            999 V2000
    5.1736   -0.9006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3531   -0.9868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8682   -0.3194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0477   -0.4056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5628    0.2618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7423    0.1756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4068   -0.5781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5863   -0.6643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2507   -1.4180    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5697   -1.5042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1014    0.0031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4369    0.7568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1014    1.5105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2574    0.8430    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  1  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  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 18 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 28  1  0  0  0  0
 14 28  2  0  0  0  0
 28 29  1  0  0  0  0
  6 29  1  0  0  0  0
 12 29  2  0  0  0  0
M  END

     RDKit          3D

 59 61  0  0  0  0  0  0  0  0999 V2000
   -0.7055    3.2514   -1.3085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5904    2.1506   -0.7564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9578    1.1423   -1.7941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8503    0.4031   -2.4278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0486   -0.4604   -1.3411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0287   -1.4073   -0.7047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8745   -1.9791   -1.6330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1174   -2.4595   -1.2328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9188   -3.0160   -2.1975 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5432   -3.1184   -3.5444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4738   -2.3569    0.0763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6248   -1.7984    1.0092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7460   -1.6265    2.2865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6397   -1.0911    2.7629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3409   -0.7932    4.0399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0905   -0.2890    4.3796 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0988   -0.0220    5.6790 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8368   -0.1093    3.3425 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1333    0.3218    3.7951 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1229    0.5481    3.1005 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3659    0.5267    5.1809 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5325   -0.4012    1.9961 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6563   -0.1768    1.1004 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9943    1.2161    0.7104 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2344    1.3419   -0.1465 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1451    0.6002   -1.4477 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4439    0.8242   -2.2185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7183   -0.8786    1.7265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3650   -1.3184    0.5932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3015    4.0266   -1.7987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1701    3.7296   -0.4607 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0946    2.8259   -1.9626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1941    1.7458    0.1728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5537    2.6724   -0.4748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6166    0.3917   -1.2856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6310    1.6486   -2.5180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0843    1.0326   -2.9120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2035   -0.3128   -3.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7256   -0.9607   -1.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1011    0.3643   -0.6694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5747   -2.0829   -2.6544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7059   -3.8367   -3.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2994   -2.1268   -3.9960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4439   -3.4774   -4.0981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4344   -2.7168    0.4044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1018   -0.9541    4.8184 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6696    0.2888    6.3287 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0973   -0.0738    5.5930 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7403   -0.9364    0.2528 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6277   -0.5598    1.6340 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0476    1.9542    1.5717 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1939    1.6849    0.1043 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4503    2.4064   -0.3854 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1040    0.9287    0.4325 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3490    1.0579   -2.0540 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9771   -0.4894   -1.2857 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5344    0.1013   -3.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2731    0.7781   -1.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3991    1.8658   -2.6515 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  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  8 11  2  0
 11 12  1  0
 12 29  2  0
 29 28  1  0
 28 14  2  0
 14 13  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 21  1  0
 19 20  2  0
 18 22  2  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 29  6  1  0
 22 28  1  0
 13 12  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  7 41  1  0
 10 42  1  0
 10 43  1  0
 10 44  1  0
 11 45  1  0
 15 46  1  0
 17 47  1  0
 21 48  1  0
 23 49  1  0
 23 50  1  0
 24 51  1  0
 24 52  1  0
 25 53  1  0
 25 54  1  0
 26 55  1  0
 26 56  1  0
 27 57  1  0
 27 58  1  0
 27 59  1  0
M  END


  Mrv1533004171514352D          

 29 31  0  0  0  0            999 V2000
    5.1736   -0.9006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3531   -0.9868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8682   -0.3194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0477   -0.4056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5628    0.2618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7423    0.1756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4068   -0.5781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5863   -0.6643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2507   -1.4180    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5697   -1.5042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1014    0.0031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4369    0.7568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1014    1.5105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2574    0.8430    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  1  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  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 18 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 28  1  0  0  0  0
 14 28  2  0  0  0  0
 28 29  1  0  0  0  0
  6 29  1  0  0  0  0
 12 29  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0071054

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC1=CC(OC)=CC2=C1C1=C(O2)C=C(O)C(C(O)=O)=C1CCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C24H30O5/c1-4-6-8-10-15-12-16(28-3)13-19-21(15)23-17(11-9-7-5-2)22(24(26)27)18(25)14-20(23)29-19/h12-14,25H,4-11H2,1-3H3,(H,26,27)

> <INCHI_KEY>
JJNLMPAFVQRTIH-UHFFFAOYSA-N

> <FORMULA>
C24H30O5

> <MOLECULAR_WEIGHT>
398.499

> <EXACT_MASS>
398.209324066

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
45.64700787149019

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-hydroxy-11-methoxy-3,13-dipentyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-4-carboxylic acid

> <ALOGPS_LOGP>
6.09

> <JCHEM_LOGP>
7.580985516333333

> <ALOGPS_LOGS>
-4.91

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.675309986532884

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.1402715523284566

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8429550086053816

> <JCHEM_POLAR_SURFACE_AREA>
79.9

> <JCHEM_REFRACTIVITY>
113.81749999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.93e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-11-methoxy-3,13-dipentyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-4-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       9.657  -1.681   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.126  -1.842   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.221  -0.596   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.689  -0.757   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.784   0.489   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.252   0.328   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.626  -1.079   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.094  -1.240   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.468  -2.647   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.064  -2.808   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.189   0.006   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.816   1.413   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.189   2.820   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334   5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.667   7.700   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.001   5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.668   5.390   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       5.335   7.700   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.668   0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.002   3.080   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.667   3.080   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.347   1.574   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   29                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12                                                       
CONECT   12   11   13   29                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   28                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   22                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   18   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   22   14   29                                                  
CONECT   29   28    6   12                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Value	Source
5-Hydroxy-11-methoxy-3,13-dipentyl-8-oxatricyclo[7.4.0.0,]trideca-1(9),2(7),3,5,10,12-hexaene-4-carboxylate	Generator

Chemical Formula

C₂₄H₃₀O₅

Average Mass

398.4990 Da

Monoisotopic Mass

398.20932 Da

IUPAC Name

5-hydroxy-11-methoxy-3,13-dipentyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-4-carboxylic acid

Traditional Name

5-hydroxy-11-methoxy-3,13-dipentyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-4-carboxylic acid

CAS Registry Number

Not Available

SMILES

CCCCCC1=CC(OC)=CC2=C1C1=C(O2)C=C(O)C(C(O)=O)=C1CCCCC

InChI Identifier

InChI=1S/C24H30O5/c1-4-6-8-10-15-12-16(28-3)13-19-21(15)23-17(11-9-7-5-2)22(24(26)27)18(25)14-20(23)29-19/h12-14,25H,4-11H2,1-3H3,(H,26,27)

InChI Key

JJNLMPAFVQRTIH-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Cladonia didyma	LOTUS Database	35616633
Cladonia rangiferina	Fungi	KNApSAcK
Cladonia rigida	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dibenzofurans. Dibenzofurans are compounds containing a dibenzofuran moiety, which consists of two benzene rings fused to a central furan ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzofurans

Sub Class

Dibenzofurans

Direct Parent

Dibenzofurans

Alternative Parents

Substituents

Dibenzofuran
Hydroxybenzoic acid
Salicylic acid or derivatives
Anisole
Phenol ether
Phenol
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Vinylogous acid
Furan
Heteroaromatic compound
Oxacycle
Ether
Carboxylic acid
Carboxylic acid derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
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	6.09	ALOGPS
logP	7.58	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	3.14	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	79.9 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	113.82 m³·mol⁻¹	ChemAxon
Polarizability	45.65 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

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

71405159

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Condidymic acid (NP0071054)

MOL for NP0071054 (Condidymic acid)

3D MOL for NP0071054 (Condidymic acid)

3D SDF for NP0071054 (Condidymic acid)

3D-SDF for NP0071054 (Condidymic acid)

PDB for NP0071054 (Condidymic acid)

3D PDB for NP0071054 (Condidymic acid)

SMILES for NP0071054 (Condidymic acid)

INCHI for NP0071054 (Condidymic acid)

Structure for NP0071054 (Condidymic acid)

3D Structure for NP0071054 (Condidymic acid)