NP-MRD: Showing NP-Card for 3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),5',7',9',11'-pentaen-4-one (NP0175256)

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Record Information

Version

2.0

Created at

2022-09-03 12:40:03 UTC

Updated at

2022-09-03 12:40:03 UTC

NP-MRD ID

NP0175256

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),5',7',9',11'-pentaen-4-one

Description

3-Chloro-2,5-dihydroxy-3,4-dihydro-2H-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]Tridecane]-1'(12'),5',7',9'(13'),10'-pentaen-4-one belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane. Based on a literature review very few articles have been published on 3-chloro-2,5-dihydroxy-3,4-dihydro-2H-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]Tridecane]-1'(12'),5',7',9'(13'),10'-pentaen-4-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032214402D          

 26 30  0  0  0  0            999 V2000
    4.7837    2.5433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1213    2.0516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2159    1.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9730    0.9042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6354    1.3960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0676    0.0847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4052   -0.4071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6481   -0.0792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5535    0.7403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7964    1.0681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8911    0.2486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2286   -0.2431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3232   -1.0627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6608   -1.5544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9037   -1.2266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8091   -0.4071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0520   -0.0792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0426    0.7403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6198    1.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3769    0.9042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4715    0.0847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0393    1.3960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7018    1.8877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9447    2.2155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3642    2.3794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2696    3.1990    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  4  6  1  0  0  0  0
  6  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  1  0  0  0  0
 11 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  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 12 21  2  0  0  0  0
 16 21  1  0  0  0  0
 20 22  1  0  0  0  0
 10 22  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 39 43  0  0  0  0  0  0  0  0999 V2000
    3.3298    1.1741   -2.3769 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7381    1.1756   -1.2697 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5132   -0.1018   -0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3482   -1.1906   -0.7926 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4414   -0.9969   -1.6398 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0995   -2.3787   -0.1596 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0024   -2.4861    0.6566 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1302   -1.4417    0.8706 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4213   -0.2467    0.2050 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5385    0.9408    0.3651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1981    1.0803   -0.8375 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4604    0.5262   -1.0152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0341    0.4386   -2.2826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2866   -0.1240   -2.3660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9477   -0.5820   -1.2471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3868   -0.4988    0.0096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0566   -0.9602    1.1242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4985   -0.8786    2.3830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2428   -0.3112    2.4423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5515    0.1575    1.3461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1192    0.0676    0.1156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2784    0.7239    1.4708 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3615    2.1984    0.5231 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0329    2.1013    1.7406 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2817    2.4347   -0.6385 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7048    3.3201   -0.0405 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    5.0514   -1.7941   -1.7640 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7454   -3.2139   -0.2944 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7593   -3.4178    1.1870 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2671   -1.4988    1.5023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4601    0.8157   -3.1054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7499   -0.2044   -3.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9462   -1.0277   -1.3344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0498   -1.4028    1.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0209   -1.2407    3.2679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7718   -0.2307    3.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6387    3.0436    0.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8521    2.9291    2.2759 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8020    3.1007   -1.4016 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 25  1  0
 25 26  1  0
 25  2  1  0
  2  1  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 22  1  0
 20 21  2  0
 10 23  1  0
 22 10  1  0
  9  3  1  0
 21 12  1  0
 21 16  1  0
 24 38  1  0
 23 37  1  1
 25 39  1  6
  5 27  1  0
  6 28  1  0
  7 29  1  0
  8 30  1  0
 13 31  1  0
 14 32  1  0
 15 33  1  0
 17 34  1  0
 18 35  1  0
 19 36  1  0
M  END


  Mrv1652309032214402D          

 26 30  0  0  0  0            999 V2000
    4.7837    2.5433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1213    2.0516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2159    1.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9730    0.9042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6354    1.3960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0676    0.0847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4052   -0.4071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6481   -0.0792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5535    0.7403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7964    1.0681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8911    0.2486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2286   -0.2431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3232   -1.0627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6608   -1.5544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9037   -1.2266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8091   -0.4071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0520   -0.0792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0426    0.7403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6198    1.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3769    0.9042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4715    0.0847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0393    1.3960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7018    1.8877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9447    2.2155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3642    2.3794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2696    3.1990    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  4  6  1  0  0  0  0
  6  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  1  0  0  0  0
 11 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  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 12 21  2  0  0  0  0
 16 21  1  0  0  0  0
 20 22  1  0  0  0  0
 10 22  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0175256

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1C(Cl)C(=O)C2=C(O)C=CC=C2C11OC2=CC=CC3=CC=CC(O1)=C23

> <INCHI_IDENTIFIER>
InChI=1S/C20H13ClO5/c21-17-18(23)16-11(6-3-7-12(16)22)20(19(17)24)25-13-8-1-4-10-5-2-9-14(26-20)15(10)13/h1-9,17,19,22,24H

> <INCHI_KEY>
VERJQRRBSKVZER-UHFFFAOYSA-N

> <FORMULA>
C20H13ClO5

> <MOLECULAR_WEIGHT>
368.77

> <EXACT_MASS>
368.0451512

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
35.862996818352514

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-chloro-2,5-dihydroxy-3,4-dihydro-2H-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0^{5,13}]tridecane]-1'(12'),5',7',9'(13'),10'-pentaen-4-one

> <ALOGPS_LOGP>
3.80

> <JCHEM_LOGP>
4.612035665

> <ALOGPS_LOGS>
-3.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.293780116802461

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.380760324523116

> <JCHEM_PKA_STRONGEST_BASIC>
-4.154441716426761

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
93.7991

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.67e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0^{5,13}]tridecane]-1'(12'),5',7',9'(13'),10'-pentaen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  O   UNK     0       8.930   4.748   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       7.693   3.830   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.870   2.300   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.283   1.688   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      10.519   2.606   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.460   0.158   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.223  -0.760   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.810  -0.148   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.633   1.382   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.220   1.994   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.397   0.464   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.160  -0.454   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.337  -1.984   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.100  -2.902   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.687  -2.290   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.510  -0.760   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.097  -0.148   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.080   1.382   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.157   2.300   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.570   1.688   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.747   0.158   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.807   2.606   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.043   3.524   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.630   4.136   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.280   4.442   0.000  0.00  0.00           C+0
HETATM   26 Cl   UNK     0       6.103   5.971   0.000  0.00  0.00          Cl+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4    9                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    3   10                                                  
CONECT   10    9   11   22   23                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   21                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20   12   16                                                  
CONECT   22   20   10                                                       
CONECT   23   10   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    2   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₃ClO₅

Average Mass

368.7700 Da

Monoisotopic Mass

368.04515 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OC1C(Cl)C(=O)C2=C(O)C=CC=C2C11OC2=CC=CC3=CC=CC(O1)=C23

InChI Identifier

InChI=1S/C20H13ClO5/c21-17-18(23)16-11(6-3-7-12(16)22)20(19(17)24)25-13-8-1-4-10-5-2-9-14(26-20)15(10)13/h1-9,17,19,22,24H

InChI Key

VERJQRRBSKVZER-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Tetralins

Sub Class

Not Available

Direct Parent

Tetralins

Alternative Parents

Substituents

Tetralin
Naphthalene
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Ketal
Alpha-haloketone
Alpha-chloroketone
Vinylogous acid
Secondary alcohol
Ketone
Halohydrin
Chlorohydrin
Oxacycle
Organoheterocyclic compound
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organochloride
Organohalogen compound
Alkyl halide
Alkyl chloride
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

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

78434872

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139586084

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),5',7',9',11'-pentaen-4-one (NP0175256)

MOL for NP0175256 (3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),5',7',9',11'-pentaen-4-one)

3D MOL for NP0175256 (3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),5',7',9',11'-pentaen-4-one)

3D SDF for NP0175256 (3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),5',7',9',11'-pentaen-4-one)

3D-SDF for NP0175256 (3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),5',7',9',11'-pentaen-4-one)

PDB for NP0175256 (3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),5',7',9',11'-pentaen-4-one)

3D PDB for NP0175256 (3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),5',7',9',11'-pentaen-4-one)

SMILES for NP0175256 (3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),5',7',9',11'-pentaen-4-one)

INCHI for NP0175256 (3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),5',7',9',11'-pentaen-4-one)

Structure for NP0175256 (3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),5',7',9',11'-pentaen-4-one)

3D Structure for NP0175256 (3-chloro-2,5-dihydroxy-2,3-dihydro-2',4'-dioxaspiro[naphthalene-1,3'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),5',7',9',11'-pentaen-4-one)