NP-MRD: Showing NP-Card for Oblongifoliagarcinine C (NP0085948)

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Record Information

Version

2.0

Created at

2022-04-29 06:21:45 UTC

Updated at

2022-04-29 06:21:45 UTC

NP-MRD ID

NP0085948

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Oblongifoliagarcinine C

Description

2,2,2',2'-Tetramethyl-2H,2'H-[6,6'-bichromene]-8-ol belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position. Oblongifoliagarcinine C is found in Garcinia oblongifolia . 2,2,2',2'-Tetramethyl-2H,2'H-[6,6'-bichromene]-8-ol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161502112D          

 25 28  0  0  0  0            999 V2000
   -2.9559   -3.5692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4256   -4.4877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8545    0.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -0.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  2 12  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  2  0  0  0  0
 13 25  1  0  0  0  0
M  END

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
    6.5550    1.4594   -0.1786 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7845    0.1941    0.2780 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8608   -0.8512    0.5832 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0544    0.5592    1.4987 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7460    0.5122    1.5593 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9333    0.0980    0.4282 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5527    0.0447    0.4816 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7878   -0.3495   -0.5958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6701   -0.4125   -0.5561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3692   -1.3508   -1.2938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7380   -1.4456   -1.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4511   -2.3836   -2.0218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4702   -0.5673   -0.5062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8105    0.3822    0.2434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4211    0.4522    0.2130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5899    1.3015    1.0589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8911    1.2070    1.0622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6557    0.2189    0.2867 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4853   -0.6039    1.2726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6696    0.9204   -0.6161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8453   -0.6455   -0.4835 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4690   -0.6930   -1.7452 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8452   -0.6506   -1.8311 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6158   -0.2495   -0.7332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9686   -0.1882   -0.7589 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7683    1.3124   -1.2447 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8708    2.3127   -0.0104 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4579    1.4890    0.4347 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8397   -0.3508    0.7109 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5981   -1.3224    1.5479 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9319   -1.5709   -0.2578 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6478    0.8796    2.3773 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2495    0.7924    2.4865 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0324    0.3173    1.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7931   -2.0340   -1.9003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8854   -3.0258   -2.5928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8951    1.1982    0.8011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0473    2.0382    1.6397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4703    1.8937    1.6708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3796   -0.0006    1.5119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7945   -1.5623    0.8312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8207   -0.7431    2.1741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7001    0.7787   -0.2938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4422    2.0109   -0.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5394    0.5568   -1.6690 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8841   -1.0072   -2.6087 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3812   -0.9213   -2.7383 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2 25  1  0
 25 24  1  0
 24 23  2  0
 23 22  1  0
 22  8  2  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 21  1  0
 21 18  1  0
 18 19  1  0
 18 20  1  0
 18 17  1  0
 17 16  2  0
 16 14  1  0
 14 15  2  0
  4  2  1  0
 15  9  1  0
  6 24  1  0
 14 13  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  3 31  1  0
 23 47  1  0
 22 46  1  0
  7 34  1  0
  5 33  1  0
  4 32  1  0
 10 35  1  0
 12 36  1  0
 19 40  1  0
 19 41  1  0
 19 42  1  0
 20 43  1  0
 20 44  1  0
 20 45  1  0
 17 39  1  0
 16 38  1  0
 15 37  1  0
M  END


  Mrv1533004161502112D          

 25 28  0  0  0  0            999 V2000
   -2.9559   -3.5692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4256   -4.4877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8545    0.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -0.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  2 12  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  2  0  0  0  0
 13 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0085948

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)OC2=CC=C(C=C2C=C1)C1=CC(O)=C2OC(C)(C)C=CC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H22O3/c1-21(2)9-7-15-11-14(5-6-19(15)24-21)17-12-16-8-10-22(3,4)25-20(16)18(23)13-17/h5-13,23H,1-4H3

> <INCHI_KEY>
MCFNMYNIZCFNFK-UHFFFAOYSA-N

> <FORMULA>
C22H22O3

> <MOLECULAR_WEIGHT>
334.415

> <EXACT_MASS>
334.156894568

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
38.578263189726016

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-(2,2-dimethyl-2H-chromen-6-yl)-2,2-dimethyl-2H-chromen-8-ol

> <ALOGPS_LOGP>
5.32

> <JCHEM_LOGP>
5.118152660333333

> <ALOGPS_LOGS>
-5.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.679869970520752

> <JCHEM_PKA_STRONGEST_BASIC>
-4.635007130195795

> <JCHEM_POLAR_SURFACE_AREA>
38.69

> <JCHEM_REFRACTIVITY>
101.96190000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.34e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-(2,2-dimethylchromen-6-yl)-2,2-dimethylchromen-8-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -5.518  -6.663   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.528  -8.377   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.195   0.677   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.185  -1.037   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   12                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11    2                                                       
CONECT   13    8   14   25                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   24                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   19   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   17   25                                                  
CONECT   25   24   13                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₂O₃

Average Mass

334.4150 Da

Monoisotopic Mass

334.15689 Da

IUPAC Name

6-(2,2-dimethyl-2H-chromen-6-yl)-2,2-dimethyl-2H-chromen-8-ol

Traditional Name

6-(2,2-dimethylchromen-6-yl)-2,2-dimethylchromen-8-ol

CAS Registry Number

Not Available

SMILES

CC1(C)OC2=CC=C(C=C2C=C1)C1=CC(O)=C2OC(C)(C)C=CC2=C1

InChI Identifier

InChI=1S/C22H22O3/c1-21(2)9-7-15-11-14(5-6-19(15)24-21)17-12-16-8-10-22(3,4)25-20(16)18(23)13-17/h5-13,23H,1-4H3

InChI Key

MCFNMYNIZCFNFK-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Garcinia oblongifolia	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

2,2-dimethyl-1-benzopyrans

Alternative Parents

Substituents

2,2-dimethyl-1-benzopyran
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Benzenoid
Oxacycle
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen 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	5.32	ALOGPS
logP	5.12	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	9.68	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	38.69 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	101.96 m³·mol⁻¹	ChemAxon
Polarizability	38.58 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

24882249

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Oblongifoliagarcinine C (NP0085948)

MOL for NP0085948 (Oblongifoliagarcinine C)

3D MOL for NP0085948 (Oblongifoliagarcinine C)

3D SDF for NP0085948 (Oblongifoliagarcinine C)

3D-SDF for NP0085948 (Oblongifoliagarcinine C)

PDB for NP0085948 (Oblongifoliagarcinine C)

3D PDB for NP0085948 (Oblongifoliagarcinine C)

SMILES for NP0085948 (Oblongifoliagarcinine C)

INCHI for NP0085948 (Oblongifoliagarcinine C)

Structure for NP0085948 (Oblongifoliagarcinine C)

3D Structure for NP0085948 (Oblongifoliagarcinine C)