NP-MRD: Showing NP-Card for 11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione (NP0163784)

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Record Information

Version

2.0

Created at

2022-09-02 22:31:39 UTC

Updated at

2022-09-02 22:31:39 UTC

NP-MRD ID

NP0163784

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione

Description

11-Chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]Heptadec-8-ene-7,15-dione belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. 11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione is found in Podocarpus macrophyllus. 11-Chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]Heptadec-8-ene-7,15-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171507112D          

 27 31  0  0  0  0            999 V2000
    0.6904   -2.8790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4097   -2.4749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1193   -2.8957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4193   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7097   -1.2291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7193   -0.4042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0097    0.0166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4386   -0.0001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1482   -0.4209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8674   -0.0168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1578    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8771    0.8082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1675    1.2290    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.5963    1.2123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6059    2.0373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3059    0.7915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0251    1.1956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2963   -0.0334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0881    0.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5770   -0.4376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5674   -1.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3490   -1.5266    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8417   -0.8649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6663   -0.8894    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8481   -1.6666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1289   -2.0708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1385   -1.2458    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  1  0  0  0  0
  6  7  2  0  0  0  0
  6  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
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  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
 18 20  1  0  0  0  0
 10 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  2  0  0  0  0
 21 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
  4 27  1  0  0  0  0
  9 27  1  0  0  0  0
 25 27  1  0  0  0  0
M  END

     RDKit          3D

 48 52  0  0  0  0  0  0  0  0999 V2000
    3.5036    1.5963   -1.4738 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8335    1.3860   -0.0123 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1980    1.0572    0.0160 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0172    0.2346    0.5311 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3847   -0.1055    1.8460 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7463   -1.2636    2.3190 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2844   -2.0231    3.1647 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3981   -1.5216    1.7520 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8216   -0.7428    0.8749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5360   -1.0000    0.3947 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3324   -1.6098    1.5042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7235   -1.8932   -0.7822 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5583   -1.4807   -1.9698 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -2.0943   -1.7527   -1.3694 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9092   -1.6493   -2.7640 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0365   -0.7432   -0.8118 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7016   -0.2288   -1.9788 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5032    0.4376   -0.1367 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8480    1.7668   -0.8152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7053    0.6571    1.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7704    0.5187    1.9567 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4658    1.0689    1.8780 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6884    1.4706    0.8229 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7728    1.5862    0.9009 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2287    1.3349   -0.5007 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5621    0.4291    0.4462 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0213    0.3206   -0.1414 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9690    0.7168   -1.8814 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8530    2.4780   -1.6626 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4313    1.6705   -2.1076 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5963    2.3234    0.5186 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3769    0.6445    0.8942 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2795   -0.6443   -0.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9537   -2.4292    2.1515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1313   -1.1708    2.4968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3868   -1.7652    1.3537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9508   -2.6806    1.5677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4882   -2.9370   -0.4525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5922   -2.7611   -1.2407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7439   -1.7640   -3.2617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9454   -1.2133   -0.3174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9616    0.1398   -2.5567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0379    2.0633   -1.4999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0833    2.5669   -0.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7867    1.6217   -1.4215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1094    2.3983    0.3887 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3162    2.3971    1.3883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5317    0.4951   -1.1010 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  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 26  1  0
 26 25  1  6
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 20  1  0
 20 21  2  0
 20 18  1  0
 18 19  1  6
 18 27  1  0
 27 10  1  0
 10 11  1  1
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 26  4  1  0
 24 26  1  0
 27 23  1  0
 10  9  1  0
 16 18  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  1
  3 32  1  0
  4 33  1  6
  8 34  1  0
 24 47  1  1
 23 46  1  6
 19 43  1  0
 19 44  1  0
 19 45  1  0
 27 48  1  6
 11 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  1
 14 39  1  6
 15 40  1  0
 16 41  1  1
 17 42  1  0
M  END


  Mrv1533004171507112D          

 27 31  0  0  0  0            999 V2000
    0.6904   -2.8790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4097   -2.4749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1193   -2.8957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4193   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7097   -1.2291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7193   -0.4042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0097    0.0166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4386   -0.0001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1482   -0.4209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8674   -0.0168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1578    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8771    0.8082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1675    1.2290    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.5963    1.2123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6059    2.0373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3059    0.7915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0251    1.1956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2963   -0.0334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0881    0.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5770   -0.4376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5674   -1.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3490   -1.5266    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8417   -0.8649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6663   -0.8894    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8481   -1.6666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1289   -2.0708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1385   -1.2458    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  1  0  0  0  0
  6  7  2  0  0  0  0
  6  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
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  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
 18 20  1  0  0  0  0
 10 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  2  0  0  0  0
 21 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
  4 27  1  0  0  0  0
  9 27  1  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0163784

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(O)C1OC(=O)C=C2C11OC1C1OC(=O)C3(C)C1C2(C)C(Cl)C(O)C3O

> <INCHI_IDENTIFIER>
InChI=1S/C18H21ClO8/c1-5(20)13-18-6(4-7(21)25-13)16(2)10-9(14(18)27-18)26-15(24)17(10,3)12(23)8(22)11(16)19/h4-5,8-14,20,22-23H,1-3H3

> <INCHI_KEY>
YXBBICUKBZSIMJ-UHFFFAOYSA-N

> <FORMULA>
C18H21ClO8

> <MOLECULAR_WEIGHT>
400.81

> <EXACT_MASS>
400.0924953

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
37.71669250188728

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione

> <ALOGPS_LOGP>
0.75

> <JCHEM_LOGP>
-0.3177183699999998

> <ALOGPS_LOGS>
-1.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.118230226156335

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.944374282510541

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0732097309684

> <JCHEM_POLAR_SURFACE_AREA>
125.82000000000002

> <JCHEM_REFRACTIVITY>
88.32639999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.38e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione

> <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       1.289  -5.374   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.631  -4.620   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.956  -5.405   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       2.649  -3.080   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.325  -2.294   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.343  -0.754   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.018   0.031   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.685  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.010  -0.786   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.353  -0.031   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.028   0.754   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.371   1.509   0.000  0.00  0.00           C+0
HETATM   13 Cl   UNK     0       4.046   2.294   0.000  0.00  0.00          Cl+0
HETATM   14  C   UNK     0       6.713   2.263   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.731   3.803   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.038   1.477   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       9.380   2.232   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.020  -0.062   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.498   0.370   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.677  -0.817   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.659  -2.357   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.118  -2.850   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.038  -1.614   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.577  -1.660   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.317  -3.111   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.974  -3.865   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.992  -2.326   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   27                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   27                                                  
CONECT   10    9   11   12   20                                             
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20   23                                             
CONECT   19   18                                                            
CONECT   20   18   10   21                                                  
CONECT   21   20   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   18   24                                                  
CONECT   24   23                                                            
CONECT   25   21   26   27                                                  
CONECT   26   25   27                                                       
CONECT   27   26    4    9   25                                             
MASTER        0    0    0    0    0    0    0    0   27    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₁ClO₈

Average Mass

400.8100 Da

Monoisotopic Mass

400.09250 Da

IUPAC Name

11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione

Traditional Name

11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione

CAS Registry Number

Not Available

SMILES

CC(O)C1OC(=O)C=C2C11OC1C1OC(=O)C3(C)C1C2(C)C(Cl)C(O)C3O

InChI Identifier

InChI=1S/C18H21ClO8/c1-5(20)13-18-6(4-7(21)25-13)16(2)10-9(14(18)27-18)26-15(24)17(10,3)12(23)8(22)11(16)19/h4-5,8-14,20,22-23H,1-3H3

InChI Key

YXBBICUKBZSIMJ-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Podocarpus macrophyllus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
Dihydropyranone
Oxepane
Dicarboxylic acid or derivatives
Gamma butyrolactone
Pyran
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Chlorohydrin
Halohydrin
Lactone
Secondary alcohol
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Alkyl chloride
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Alkyl halide
Carbonyl group
Organooxygen compound
Organohalogen compound
Organochloride
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	0.75	ALOGPS
logP	-0.32	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	12.94	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	125.82 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	88.33 m³·mol⁻¹	ChemAxon
Polarizability	37.72 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

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

74941536

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione (NP0163784)

MOL for NP0163784 (11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione)

3D MOL for NP0163784 (11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione)

3D SDF for NP0163784 (11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione)

3D-SDF for NP0163784 (11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione)

PDB for NP0163784 (11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione)

3D PDB for NP0163784 (11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione)

SMILES for NP0163784 (11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione)

INCHI for NP0163784 (11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione)

Structure for NP0163784 (11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione)

3D Structure for NP0163784 (11-chloro-12,13-dihydroxy-5-(1-hydroxyethyl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.0²,⁴.0⁴,⁹.0¹⁴,¹⁷]heptadec-8-ene-7,15-dione)