NP-MRD: Showing NP-Card for Gomisin K1 (NP0139069)

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Record Information

Version

1.0

Created at

2022-06-29 19:38:08 UTC

Updated at

2022-06-29 19:38:08 UTC

NP-MRD ID

NP0139069

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Gomisin K1

Description

3,4,14,15,16-Pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]Hexadeca-1(16),2,4,6,12,14-hexaen-5-ol belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit. Gomisin K1 is found in Schisandra chinensis and Schisandra lancifolia. 3,4,14,15,16-Pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]Hexadeca-1(16),2,4,6,12,14-hexaen-5-ol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171500332D          

 29 31  0  0  0  0            999 V2000
   -1.3985   -1.0775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6796   -1.5385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1990   -1.5114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2094   -0.5009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2094    0.3241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7928    0.9074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4582    1.7009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6178    0.9074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9554    1.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2011    0.3241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2011   -0.5009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9980   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2115   -1.5114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0697   -1.5766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6282   -2.0947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1775   -2.8190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9718   -3.1673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8313   -1.8812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5143   -2.8735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8130   -3.7163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6178   -1.0843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7928   -1.0843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5792   -1.8812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0650   -2.5844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8612   -3.5109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7823   -2.0947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2856   -2.8546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4756   -3.2834    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
 12 22  1  0  0  0  0
 22 23  1  0  0  0  0
  5 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 27  2  0  0  0  0
  3 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END

     RDKit          3D

 59 61  0  0  0  0  0  0  0  0999 V2000
   -0.3001    5.2859   -1.0583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1415    4.2724   -0.6047 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7647    2.9541   -0.4361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5518    2.6095   -0.7409 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9460    1.3158   -0.5863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0120    0.3918   -0.1244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2983    0.7047    0.1874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1098   -0.2949    0.6604 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2635   -0.5917    2.0388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6790    2.0164    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9816    2.4217    0.3116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3939    2.8772    1.5690 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0557   -1.0553    0.0583 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9779   -1.8964    0.7167 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7002   -3.2248    0.7871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4626   -3.7217    0.2186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7423   -5.0712    0.2958 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3373   -2.8581   -0.4243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5186   -3.3529   -1.0050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7274   -3.4471   -0.3132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0960   -1.5095   -0.5215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8903   -0.5859   -1.1618 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7726   -0.2689   -2.5352 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3060   -1.5951    1.3064 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1777   -0.9249    0.2108 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8786   -1.5622   -1.1216 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1427    0.5369    0.2305 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5662    1.1134    0.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3947    1.2374   -0.8954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1555    5.2391   -2.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6875    5.3043   -0.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8358    6.2625   -0.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2140    3.3962   -1.0920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3381   -0.5526    2.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9782   -1.6516    2.1693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6063    0.0261    2.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5414    2.8454    2.3014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1356    2.1313    1.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8570    3.8614    1.4962 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4111   -3.8930    1.3000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0940   -5.6755    0.7661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5451   -3.1088   -1.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9892   -4.5095   -0.0593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7881   -2.7790    0.5690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4008   -1.1660   -3.0834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6952    0.1598   -2.9521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9648    0.4795   -2.6348 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7681   -2.5106    1.6738 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1332   -0.8752    2.1331 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2192   -1.2660    0.4802 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0336   -1.1266   -1.6502 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6625   -2.6390   -0.9642 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7954   -1.4705   -1.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6839    0.9184    1.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2875    0.3829    0.6194 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8198    1.2371   -0.8793 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6206    2.0911    0.6780 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6188    0.8263   -1.8803 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7641    2.2862   -0.8868 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7 10  2  0
 10 11  1  0
 11 12  1  0
  6 13  1  0
 13 21  2  0
 21 22  1  0
 22 23  1  0
 21 18  1  0
 18 19  1  0
 19 20  1  0
 18 16  2  0
 16 17  1  0
 16 15  1  0
 15 14  2  0
 14 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 10  3  1  0
 14 13  1  0
 29  5  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  9 34  1  0
  9 35  1  0
  9 36  1  0
 12 37  1  0
 12 38  1  0
 12 39  1  0
 23 45  1  0
 23 46  1  0
 23 47  1  0
 20 42  1  0
 20 43  1  0
 20 44  1  0
 17 41  1  0
 15 40  1  0
 24 48  1  0
 24 49  1  0
 25 50  1  1
 26 51  1  0
 26 52  1  0
 26 53  1  0
 27 54  1  1
 28 55  1  0
 28 56  1  0
 28 57  1  0
 29 58  1  0
 29 59  1  0
M  END


  Mrv1533004171500332D          

 29 31  0  0  0  0            999 V2000
   -1.3985   -1.0775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6796   -1.5385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1990   -1.5114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2094   -0.5009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2094    0.3241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7928    0.9074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4582    1.7009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6178    0.9074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9554    1.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2011    0.3241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2011   -0.5009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9980   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2115   -1.5114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0697   -1.5766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6282   -2.0947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1775   -2.8190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9718   -3.1673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8313   -1.8812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5143   -2.8735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8130   -3.7163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6178   -1.0843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7928   -1.0843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5792   -1.8812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0650   -2.5844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8612   -3.5109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7823   -2.0947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2856   -2.8546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4756   -3.2834    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
 12 22  1  0  0  0  0
 22 23  1  0  0  0  0
  5 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 27  2  0  0  0  0
  3 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0139069

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C(OC)=C1OC)C1=C(OC)C(OC)=C(O)C=C1CC(C)C(C)C2

> <INCHI_IDENTIFIER>
InChI=1S/C23H30O6/c1-12-8-14-10-16(24)20(26-4)22(28-6)18(14)19-15(9-13(12)2)11-17(25-3)21(27-5)23(19)29-7/h10-13,24H,8-9H2,1-7H3

> <INCHI_KEY>
RCPUCQCVTDMJGJ-UHFFFAOYSA-N

> <FORMULA>
C23H30O6

> <MOLECULAR_WEIGHT>
402.487

> <EXACT_MASS>
402.204238686

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
44.00158322525995

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,4,14,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2,4,6,13,15-hexaen-5-ol

> <ALOGPS_LOGP>
4.10

> <JCHEM_LOGP>
4.554841926666667

> <ALOGPS_LOGS>
-4.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.001247979797945

> <JCHEM_PKA_STRONGEST_BASIC>
-4.2353046955977875

> <JCHEM_POLAR_SURFACE_AREA>
66.38000000000001

> <JCHEM_REFRACTIVITY>
112.07049999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.55e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,4,14,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2,4,6,13,15-hexaen-5-ol

> <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      -2.611  -2.011   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.269  -2.872   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.371  -2.821   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.770  -1.334   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.258  -0.935   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.258   0.605   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.346   1.694   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.722   3.175   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.886   1.694   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.517   3.172   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.975   0.605   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.975  -0.935   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.463  -1.334   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.862  -2.821   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.464  -2.943   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.773  -3.910   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.798  -5.262   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.281  -5.912   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.285  -3.512   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.693  -5.364   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.251  -6.937   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.886  -2.024   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.346  -2.024   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.948  -3.512   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.855  -4.824   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.474  -6.554   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.460  -3.910   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.533  -5.329   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -0.888  -6.129   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   27                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   22                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   12   23                                                  
CONECT   23   22    5   24                                                  
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24    3   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₀O₆

Average Mass

402.4870 Da

Monoisotopic Mass

402.20424 Da

IUPAC Name

3,4,14,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2,4,6,13,15-hexaen-5-ol

Traditional Name

3,4,14,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2,4,6,13,15-hexaen-5-ol

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C(OC)=C1OC)C1=C(OC)C(OC)=C(O)C=C1CC(C)C(C)C2

InChI Identifier

InChI=1S/C23H30O6/c1-12-8-14-10-16(24)20(26-4)22(28-6)18(14)19-15(9-13(12)2)11-17(25-3)21(27-5)23(19)29-7/h10-13,24H,8-9H2,1-7H3

InChI Key

RCPUCQCVTDMJGJ-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
Schisandra chinensis	LOTUS Database	35616633
Schisandra lancifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Hydrolyzable tannins

Direct Parent

Hydrolyzable tannins

Alternative Parents

Substituents

Hydrolyzable tannin
Dibenzocyclooctane lignan
Anisole
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	4.1	ALOGPS
logP	4.55	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	10	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	66.38 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	112.07 m³·mol⁻¹	ChemAxon
Polarizability	44 Å³	ChemAxon
Number of Rings	3	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

78385003

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Gomisin K1 (NP0139069)

MOL for NP0139069 (Gomisin K1)

3D MOL for NP0139069 (Gomisin K1)

3D SDF for NP0139069 (Gomisin K1)

3D-SDF for NP0139069 (Gomisin K1)

PDB for NP0139069 (Gomisin K1)

3D PDB for NP0139069 (Gomisin K1)

SMILES for NP0139069 (Gomisin K1)

INCHI for NP0139069 (Gomisin K1)

Structure for NP0139069 (Gomisin K1)

3D Structure for NP0139069 (Gomisin K1)