NP-MRD: Showing NP-Card for (17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde (NP0239673)

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Record Information

Version

2.0

Created at

2022-09-06 23:19:18 UTC

Updated at

2022-09-06 23:19:19 UTC

NP-MRD ID

NP0239673

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde

Description

CHEMBL4069816 belongs to the class of organic compounds known as diarylethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups. (17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde is found in Hypotrachyna revoluta, Lobaria oregana and Xanthoparmelia verrucigera. Based on a literature review very few articles have been published on CHEMBL4069816.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072201192D          

 29 32  0  0  1  0            999 V2000
    5.5063    1.3180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6821    1.3533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3006    2.0848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7433    2.7809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3618    3.5124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8045    4.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5376    3.5478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0948    2.8516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4763    2.1201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0336    1.4240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4151    0.6925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2745    2.7637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6944    3.3503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7912    4.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1301    4.6631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2269    5.4824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3721    4.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2890    4.8308    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2753    3.5180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9364    3.0245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6713    2.2432    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1476    1.5696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8023    0.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1536    2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    3.0418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1796    3.3068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4921    4.6047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2693    4.3280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8559    4.9081    0.0000 O   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  2  0  0  0  0
 14 27  1  0  0  0  0
 27 28  1  0  0  0  0
  7 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END

     RDKit          3D

 45 48  0  0  0  0  0  0  0  0999 V2000
    4.4657    3.4880   -1.2261 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1100    3.2875   -0.8950 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6086    1.9937   -0.8956 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4030    0.9256   -1.2092 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9268   -0.3962   -1.2187 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7683   -1.5480   -1.5501 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5926   -0.5318   -0.8871 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7653    0.5415   -0.5659 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2768    1.8122   -0.5689 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4896    2.9655   -0.2288 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9841    4.1276   -0.2329 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6032    0.5170   -0.2193 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2323   -0.5624    0.4327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8403   -1.8829    0.4797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6167   -2.7804    1.1950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1973   -4.1907    1.2427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7572   -2.4008    1.8566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5558   -3.2710    2.5813 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1232   -1.0504    1.7860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3829   -0.1415    1.0863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0870    1.1558    1.1148 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7023    1.2643   -0.1504 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3325    2.3519   -0.8824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0559    1.0195    2.1074 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1948   -0.3080    2.4343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1009   -0.7945    3.1725 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2675   -2.5372   -0.0975 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2251   -1.9408   -0.9124 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8539   -2.6161   -1.7529 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7198    2.9761   -2.1793 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1602    3.1413   -0.4552 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6399    4.5858   -1.3789 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4475    1.0594   -1.4667 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8278   -1.1206   -1.4669 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8676   -2.3328   -0.7770 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8121   -1.8626   -2.5973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5499    2.9142    0.0468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1612   -4.2743    0.9178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2769   -4.5228    2.3159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8563   -4.8218    0.5938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2710   -4.2410    2.6169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3972    1.9738    1.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5322    3.3293   -0.3769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0494    2.3656   -1.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3359    2.3329   -1.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 21  1  0
 21 24  1  0
 24 25  1  0
 25 26  2  0
 25 19  1  0
 19 20  2  0
 20 13  1  0
 13 14  2  0
 14 27  1  0
 27 28  1  0
 28 29  2  0
 28  7  1  0
  7  5  2  0
  5  6  1  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  1  0
  3  9  1  0
  9 10  1  0
 10 11  2  0
  9  8  2  0
  8 12  1  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 20 21  1  0
 12 13  1  0
 17 19  1  0
  8  7  1  0
 23 43  1  0
 23 44  1  0
 23 45  1  0
 21 42  1  1
  6 34  1  0
  6 35  1  0
  6 36  1  0
  4 33  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 10 37  1  0
 16 38  1  0
 16 39  1  0
 16 40  1  0
 18 41  1  0
M  END


  Mrv1652309072201192D          

 29 32  0  0  1  0            999 V2000
    5.5063    1.3180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6821    1.3533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3006    2.0848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7433    2.7809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3618    3.5124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8045    4.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5376    3.5478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0948    2.8516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4763    2.1201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0336    1.4240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4151    0.6925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2745    2.7637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6944    3.3503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7912    4.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1301    4.6631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2269    5.4824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3721    4.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2890    4.8308    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2753    3.5180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9364    3.0245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6713    2.2432    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1476    1.5696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8023    0.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1536    2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    3.0418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1796    3.3068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4921    4.6047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2693    4.3280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8559    4.9081    0.0000 O   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  2  0  0  0  0
 14 27  1  0  0  0  0
 27 28  1  0  0  0  0
  7 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0239673

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1OC(=O)C2=C1C1=C(OC(=O)C3=C(C)C=C(OC)C(C=O)=C3O1)C(C)=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C20H16O9/c1-7-5-10(25-3)9(6-21)16-11(7)18(23)28-15-8(2)14(22)12-13(17(15)27-16)20(26-4)29-19(12)24/h5-6,20,22H,1-4H3/t20-/m0/s1

> <INCHI_KEY>
HQNHVWVEYNXZBJ-FQEVSTJZSA-N

> <FORMULA>
C20H16O9

> <MOLECULAR_WEIGHT>
400.339

> <EXACT_MASS>
400.079432095

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
38.244046675969976

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(17S)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0^{3,8}.0^{14,18}]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde

> <JCHEM_LOGP>
3.723437959

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.637598908405579

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.623781077737037

> <JCHEM_PKA_STRONGEST_BASIC>
-3.684584544575214

> <JCHEM_POLAR_SURFACE_AREA>
117.59000000000003

> <JCHEM_REFRACTIVITY>
99.51519999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(17S)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0^{3,8}.0^{14,18}]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      10.278   2.460   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.740   2.526   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.028   3.892   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.854   5.191   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.142   6.557   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.968   7.856   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.603   6.623   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.777   5.323   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.489   3.958   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.663   2.658   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.375   1.293   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       4.246   5.159   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.163   6.254   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.344   7.783   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.110   8.704   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.290  10.234   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.695   8.096   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.539   9.018   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.514   6.567   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.748   5.646   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.253   4.187   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.142   2.930   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.498   1.531   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.287   4.207   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -0.744   5.678   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.202   6.173   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       4.652   8.595   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.103   8.079   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       7.198   9.162   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   28                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8    3   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14   20                                                  
CONECT   14   13   15   27                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   25                                                  
CONECT   20   19   13   21                                                  
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25                                                       
CONECT   25   24   19   26                                                  
CONECT   26   25                                                            
CONECT   27   14   28                                                       
CONECT   28   27    7   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₆O₉

Average Mass

400.3390 Da

Monoisotopic Mass

400.07943 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CO[C@H]1OC(=O)C2=C1C1=C(OC(=O)C3=C(C)C=C(OC)C(C=O)=C3O1)C(C)=C2O

InChI Identifier

InChI=1S/C20H16O9/c1-7-5-10(25-3)9(6-21)16-11(7)18(23)28-15-8(2)14(22)12-13(17(15)27-16)20(26-4)29-19(12)24/h5-6,20,22H,1-4H3/t20-/m0/s1

InChI Key

HQNHVWVEYNXZBJ-FQEVSTJZSA-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
Hypotrachyna revoluta	LOTUS Database	35616633
Lobaria oregana	LOTUS Database	35616633
Xanthoparmelia verrucigera	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diarylethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Diarylethers

Alternative Parents

Substituents

Diaryl ether
Isobenzofuranone
Benzofuranone
Phthalide
Isocoumaran
Anisole
1,4-dioxepine
Alkyl aryl ether
Aryl-aldehyde
Dioxepine
Benzenoid
Dicarboxylic acid or derivatives
Vinylogous acid
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Acetal
Organic oxide
Hydrocarbon derivative
Aldehyde
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

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

76789024

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

137640253

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde (NP0239673)

MOL for NP0239673 ((17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde)

3D MOL for NP0239673 ((17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde)

3D SDF for NP0239673 ((17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde)

3D-SDF for NP0239673 ((17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde)

PDB for NP0239673 ((17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde)

3D PDB for NP0239673 ((17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde)

SMILES for NP0239673 ((17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde)

INCHI for NP0239673 ((17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde)

Structure for NP0239673 ((17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde)

3D Structure for NP0239673 ((17s)-13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde)