NP-MRD: Showing NP-Card for (1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde (NP0190893)

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Record Information

Version

2.0

Created at

2022-09-04 07:38:49 UTC

Updated at

2022-09-04 07:38:50 UTC

NP-MRD ID

NP0190893

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde

Description

Euglobal G1 belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring. (1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde is found in Eucalyptus grandis. Based on a literature review very few articles have been published on Euglobal G1.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042209382D          

 28 31  0  0  1  0            999 V2000
    5.6793    3.5542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9991    3.0874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2547    3.4430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0633    2.2649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3832    1.7980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6387    2.1536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4474    0.9755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1918    0.6199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8720    1.0868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2561   -0.2026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0005   -0.5582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0647   -1.3807    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5759   -0.6695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6401   -1.4920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8315   -0.3139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7672    0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0228    0.8642    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3426    0.3973    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0871    0.0417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4069   -0.4252    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1513   -0.7808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7267   -0.8921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9823   -0.5364    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2177    0.1094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5982    0.7529    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9180    0.2860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4277    0.9495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0938    0.2505    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 15 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 25 24  1  1  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
    4.8393   -0.4002    0.7650 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5332   -1.6241   -0.0645 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0763   -2.7216    0.8297 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5636   -1.3151   -1.1954 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2935   -0.8054   -0.7131 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5978   -1.6642   -0.0419 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7438    0.4880   -0.8886 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3710    1.5332   -1.5834 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6030    1.2984   -2.1255 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7614    2.7850   -1.7223 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3915    3.8645   -2.4303 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5021    3.7679   -2.9598 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5004    2.9728   -1.1470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1116    4.1999   -1.2760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1488    1.9584   -0.4516 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4823    0.7572   -0.3422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1815   -0.2205    0.3477 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4416   -0.1062    0.9766 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1256   -0.0975    2.4801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2274    1.0937    0.6164 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4594    2.2604    0.1107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3673    0.8342   -0.3460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6694   -0.6104   -0.5350 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3470   -1.2903   -0.9201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1391   -1.4189    0.5999 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6009   -1.4192    0.7414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2718   -0.8677    1.9325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1363   -2.8246    0.4494 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2043    0.4698    0.5297 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6719   -0.6182    1.8589 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9091   -0.0691    0.6567 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5008   -1.9131   -0.5672 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2379   -3.3182    0.4054 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9121   -3.4482    0.9578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8528   -2.3647    1.8703 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3703   -2.3196   -1.7298 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1184   -0.7507   -1.9430 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2477    1.8009   -2.6341 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8997    4.8247   -2.5253 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1572    5.0247   -1.7085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0759    0.2781    2.6613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1235   -1.1308    2.8824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7699    0.6020    3.0309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7342    1.4521    1.5671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0357    2.8195   -0.6851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2959    3.0517    0.9019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2953    1.3942   -0.0554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0901    1.2472   -1.3541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4991   -0.8004   -1.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4367   -2.2239   -1.4634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6374   -0.6148   -1.4214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5546   -2.2863    0.8965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7233    0.1309    1.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6755   -0.8316    2.8463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1911   -1.4661    2.2192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1535   -2.6565   -0.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4892   -3.4137   -0.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3324   -3.2978    1.4426 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 10 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  1
 18 25  1  0
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 20  1  0
 20 21  1  0
 23 26  1  0
 26 27  1  0
 26 28  1  0
 16  7  2  0
 20 18  1  0
 21 15  1  0
 26 25  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  9 38  1  0
 11 39  1  0
 14 40  1  0
 19 41  1  0
 19 42  1  0
 19 43  1  0
 25 52  1  6
 24 50  1  0
 24 51  1  0
 23 49  1  6
 22 47  1  0
 22 48  1  0
 20 44  1  1
 21 45  1  0
 21 46  1  0
 27 53  1  0
 27 54  1  0
 27 55  1  0
 28 56  1  0
 28 57  1  0
 28 58  1  0
M  END


  Mrv1652309042209382D          

 28 31  0  0  1  0            999 V2000
    5.6793    3.5542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9991    3.0874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2547    3.4430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0633    2.2649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3832    1.7980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6387    2.1536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4474    0.9755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1918    0.6199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8720    1.0868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2561   -0.2026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0005   -0.5582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0647   -1.3807    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5759   -0.6695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6401   -1.4920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8315   -0.3139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7672    0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0228    0.8642    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3426    0.3973    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0871    0.0417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4069   -0.4252    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1513   -0.7808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7267   -0.8921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9823   -0.5364    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2177    0.1094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5982    0.7529    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9180    0.2860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4277    0.9495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0938    0.2505    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 15 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 25 24  1  1  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0190893

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC(=O)C1=C(O)C(C=O)=C(O)C2=C1O[C@]1(C)[C@@H]3C[C@H](C[C@@H]1C2)C3(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C23H30O5/c1-11(2)6-16(25)18-20(27)15(10-24)19(26)14-8-13-7-12-9-17(22(12,3)4)23(13,5)28-21(14)18/h10-13,17,26-27H,6-9H2,1-5H3/t12-,13+,17+,23-/m0/s1

> <INCHI_KEY>
SFBXDLHLJDQOFR-UTNBYVNNSA-N

> <FORMULA>
C23H30O5

> <MOLECULAR_WEIGHT>
386.488

> <EXACT_MASS>
386.209324066

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
42.0547677275288

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,11R,13S)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0^{2,11}.0^{4,9}]pentadeca-4(9),5,7-triene-7-carbaldehyde

> <JCHEM_LOGP>
6.241427797999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.123253177058414

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.189778608888398

> <JCHEM_PKA_STRONGEST_BASIC>
-4.636696486193242

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
107.649

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,11R,13S)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0^{2,11}.0^{4,9}]pentadeca-4(9),5,7-triene-7-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      10.601   6.635   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.332   5.763   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.942   6.427   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.452   4.228   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.182   3.356   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       6.792   4.020   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.302   1.821   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.691   1.157   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      10.961   2.029   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.811  -0.378   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.201  -1.042   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      11.321  -2.577   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       8.542  -1.250   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.662  -2.785   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       7.152  -0.586   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.032   0.949   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.643   1.613   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.373   0.742   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.763   0.078   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.493  -0.794   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.882  -1.457   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.223  -1.665   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.834  -1.001   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.273   0.204   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.983   1.405   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.714   0.534   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.798   1.772   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.175   0.468   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   16                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   21                                                  
CONECT   16   15    7   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20   25                                             
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20   15                                                       
CONECT   22   20   23                                                       
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24   18   26                                                  
CONECT   26   25   23   27   28                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₀O₅

Average Mass

386.4880 Da

Monoisotopic Mass

386.20932 Da

IUPAC Name

(1R,2S,11R,13S)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0^{2,11}.0^{4,9}]pentadeca-4(9),5,7-triene-7-carbaldehyde

Traditional Name

(1R,2S,11R,13S)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0^{2,11}.0^{4,9}]pentadeca-4(9),5,7-triene-7-carbaldehyde

CAS Registry Number

Not Available

SMILES

CC(C)CC(=O)C1=C(O)C(C=O)=C(O)C2=C1O[C@]1(C)[C@@H]3C[C@H](C[C@@H]1C2)C3(C)C

InChI Identifier

InChI=1S/C23H30O5/c1-11(2)6-16(25)18-20(27)15(10-24)19(26)14-8-13-7-12-9-17(22(12,3)4)23(13,5)28-21(14)18/h10-13,17,26-27H,6-9H2,1-5H3/t12-,13+,17+,23-/m0/s1

InChI Key

SFBXDLHLJDQOFR-UTNBYVNNSA-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
Eucalyptus grandis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Xanthenes

Alternative Parents

Substituents

Xanthene
Butyrophenone
Aromatic monoterpenoid
Pinane monoterpenoid
Nopinane monoterpenoid
Monoterpenoid
Aryl alkyl ketone
Aryl ketone
Aryl-aldehyde
Phenol
Alkyl aryl ether
Benzenoid
Vinylogous acid
Ketone
Oxacycle
Ether
Aldehyde
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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	6.24	ChemAxon
pKa (Strongest Acidic)	7.19	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	107.65 m³·mol⁻¹	ChemAxon
Polarizability	42.05 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

10283304

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10068739

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde (NP0190893)

MOL for NP0190893 ((1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde)

3D MOL for NP0190893 ((1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde)

3D SDF for NP0190893 ((1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde)

3D-SDF for NP0190893 ((1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde)

PDB for NP0190893 ((1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde)

3D PDB for NP0190893 ((1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde)

SMILES for NP0190893 ((1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde)

INCHI for NP0190893 ((1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde)

Structure for NP0190893 ((1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde)

3D Structure for NP0190893 ((1r,2s,11r,13s)-6,8-dihydroxy-2,14,14-trimethyl-5-(3-methylbutanoyl)-3-oxatetracyclo[11.1.1.0²,¹¹.0⁴,⁹]pentadeca-4(9),5,7-triene-7-carbaldehyde)