NP-MRD: Showing NP-Card for (1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol (NP0141373)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-01 19:41:23 UTC

Updated at

2022-09-01 19:41:23 UTC

NP-MRD ID

NP0141373

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol

Description

Pughiinin A belongs to the class of organic compounds known as 1-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 1-position. (1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol was first documented in 2002 (PMID: 12451493). Based on a literature review very few articles have been published on Pughiinin A (PMID: 34976955).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309012221412D          

 26 28  0  0  1  0            999 V2000
    1.1002   -2.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2131   -1.6196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5618   -1.1131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6465   -0.2143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1836    0.4686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4472   -0.0632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4112    1.0403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6900    1.1199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4659    0.8395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3161    1.1430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9674    0.6365    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0803    1.4538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7316    0.9473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3829    0.4409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1471    0.7517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7984    0.2453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5626    0.5561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6854   -0.5719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9212   -0.8827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8083   -1.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2700   -0.3763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5057   -0.6871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8545   -0.1807    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0903   -0.4915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9773   -1.3087    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6286   -1.8152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  5  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 11 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  1  0  0  0
M  END

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
   -2.8180   -3.5247   -0.8596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3128   -2.2679   -0.1695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1668   -1.3673    0.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7239   -0.1406    0.9080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2561    1.1129    0.2780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8379    0.8172   -1.1147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5405    1.4357    1.1006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3923    2.3010    0.2683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1636    2.5935    0.4404 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0825    1.8750    0.7515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7382    1.2212   -0.4578 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0039    1.6346   -1.7038 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0325    1.8160   -0.5762 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1950    1.2025   -0.2010 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2536    1.8866    0.3256 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3913    1.1773    0.6766 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4954    1.8263    1.2162 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4637   -0.1879    0.5024 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3720   -0.8826   -0.0390 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3794   -2.3486   -0.2542 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2564   -0.1749   -0.3813 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0805   -0.8096   -0.9475 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8456   -0.2739   -0.2839 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3200   -1.0310   -0.8765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8762   -2.0704    0.0340 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4858   -1.9562    1.3663 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8726   -3.7028   -0.6475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5581   -3.4744   -1.9317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2125   -4.3521   -0.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2221   -1.5187    0.0866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1317   -0.2605    1.9737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6737   -0.0356    1.0632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9231    0.8532   -1.1559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4678    1.6361   -1.7654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4177   -0.1246   -1.5371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1038    0.5147    1.2645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1491    1.8299    2.0591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1558    2.1770    0.5530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0421    3.2295    0.0325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8964    3.7073    0.3262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8492    2.6308    1.1838 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0592    1.1664    1.5973 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2933    2.7094   -1.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0798    1.6421   -1.6449 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2941    1.0301   -2.5884 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2215    2.9558    0.4718 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4968    2.8263    1.3656 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3252   -0.7738    0.7609 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4279   -2.7079   -0.2791 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9408   -2.6090   -1.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7863   -2.8467    0.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0672   -1.9264   -0.8156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0845   -0.6512   -2.0454 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9432   -0.4702    0.8050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0662   -0.3115   -1.1864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0180   -1.5530   -1.8380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3523   -3.0401   -0.2661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1427   -2.4143    1.9124 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  5  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  6
 11 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 14 21  1  0
 11 23  1  0
 20 49  1  0
 20 50  1  0
 20 51  1  0
 22 52  1  0
 22 53  1  0
 23 54  1  1
 24 55  1  0
 24 56  1  0
 25 57  1  6
 26 58  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  6 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 12 43  1  0
 12 44  1  0
 12 45  1  0
 15 46  1  0
 17 47  1  0
 18 48  1  0
M  END


  Mrv1652309012221412D          

 26 28  0  0  1  0            999 V2000
    1.1002   -2.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2131   -1.6196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5618   -1.1131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6465   -0.2143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1836    0.4686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4472   -0.0632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4112    1.0403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6900    1.1199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4659    0.8395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3161    1.1430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9674    0.6365    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0803    1.4538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7316    0.9473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3829    0.4409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1471    0.7517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7984    0.2453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5626    0.5561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6854   -0.5719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9212   -0.8827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8083   -1.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2700   -0.3763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5057   -0.6871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8545   -0.1807    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0903   -0.4915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9773   -1.3087    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6286   -1.8152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  5  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 11 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0141373

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C2C[C@@H]3C[C@@H](O)\C(C)=C/CC(C)(C)\C=C\C[C@@]3(C)OC2=CC(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O3/c1-15-7-10-22(3,4)8-6-9-23(5)17(13-20(15)25)12-19-16(2)11-18(24)14-21(19)26-23/h6-8,11,14,17,20,24-25H,9-10,12-13H2,1-5H3/b8-6+,15-7-/t17-,20-,23-/m1/s1

> <INCHI_KEY>
QTNDIUYXNQSFIE-HGRUNDETSA-N

> <FORMULA>
C23H32O3

> <MOLECULAR_WEIGHT>
356.506

> <EXACT_MASS>
356.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
41.655576089565365

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,3R,4Z,8E,11R)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0^{13,18}]nonadeca-4,8,13(18),14,16-pentaene-3,15-diol

> <ALOGPS_LOGP>
6.59

> <JCHEM_LOGP>
5.173993898666666

> <ALOGPS_LOGS>
-4.64

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.613504847488095

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.92868112846496

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9678569049206995

> <JCHEM_POLAR_SURFACE_AREA>
49.69

> <JCHEM_REFRACTIVITY>
108.36469999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.08e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3R,4Z,8E,11R)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0^{13,18}]nonadeca-4,8,13(18),14,16-pentaene-3,15-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 01-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-SEP-22         0                                  
HETATM    1  C   UNK     0       2.054  -4.549   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.264  -3.023   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.049  -2.078   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.207  -0.400   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.343   0.875   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.835  -0.118   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.768   1.942   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.288   2.090   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.736   1.567   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.323   2.134   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.539   1.188   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.750   2.714   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.966   1.768   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.181   0.823   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.608   1.403   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.824   0.458   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      12.250   1.038   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.613  -1.068   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.186  -1.648   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.975  -3.173   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.971  -0.702   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.544  -1.283   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.328  -0.337   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.902  -0.917   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.691  -2.443   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.907  -3.388   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7    8                                             
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   23                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   14   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   11   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24    2   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₂O₃

Average Mass

356.5060 Da

Monoisotopic Mass

356.23514 Da

IUPAC Name

(1R,3R,4Z,8E,11R)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0^{13,18}]nonadeca-4,8,13(18),14,16-pentaene-3,15-diol

Traditional Name

(1R,3R,4Z,8E,11R)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0^{13,18}]nonadeca-4,8,13(18),14,16-pentaene-3,15-diol

CAS Registry Number

Not Available

SMILES

CC1=C2C[C@@H]3C[C@@H](O)\C(C)=C/CC(C)(C)\C=C\C[C@@]3(C)OC2=CC(O)=C1

InChI Identifier

InChI=1S/C23H32O3/c1-15-7-10-22(3,4)8-6-9-23(5)17(13-20(15)25)12-19-16(2)11-18(24)14-21(19)26-23/h6-8,11,14,17,20,24-25H,9-10,12-13H2,1-5H3/b8-6+,15-7-/t17-,20-,23-/m1/s1

InChI Key

QTNDIUYXNQSFIE-HGRUNDETSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 1-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

1-benzopyrans

Alternative Parents

Substituents

1-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Benzenoid
Secondary alcohol
Oxacycle
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
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	6.59	ALOGPS
logP	5.17	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	9.93	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	49.69 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	108.36 m³·mol⁻¹	ChemAxon
Polarizability	41.66 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	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

78437833

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10021199

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Pittayakhajonwut P, Theerasilp M, Kongsaeree P, Rungrod A, Tanticharoen M, Thebtaranonth Y: Pughiinin A, a sesquiterpene from the fungus Kionochaeta pughii BCC 3878. Planta Med. 2002 Nov;68(11):1017-9. doi: 10.1055/s-2002-35653. [PubMed:12451493 ]
Wang FR, Yang L, Kong FD, Ma QY, Xie QY, Wu YG, Dai HF, Chen P, Xiao N, Zhao YX: Humulane-Type Macrocyclic Sesquiterpenoids From the Endophytic Fungus Penicillium sp. of Carica papaya. Front Chem. 2021 Dec 16;9:797858. doi: 10.3389/fchem.2021.797858. eCollection 2021. [PubMed:34976955 ]
LOTUS database [Link]

Showing NP-Card for (1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol (NP0141373)

MOL for NP0141373 ((1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol)

3D MOL for NP0141373 ((1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol)

3D SDF for NP0141373 ((1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol)

3D-SDF for NP0141373 ((1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol)

PDB for NP0141373 ((1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol)

3D PDB for NP0141373 ((1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol)

SMILES for NP0141373 ((1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol)

INCHI for NP0141373 ((1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol)

Structure for NP0141373 ((1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol)

3D Structure for NP0141373 ((1r,3r,4z,8e,11r)-4,7,7,11,17-pentamethyl-12-oxatricyclo[9.8.0.0¹³,¹⁸]nonadeca-4,8,13,15,17-pentaene-3,15-diol)