NP-MRD: Showing NP-Card for Camelliatannin G (NP0056454)

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Record Information

Version

2.0

Created at

2022-04-28 02:14:02 UTC

Updated at

2022-04-28 02:14:02 UTC

NP-MRD ID

NP0056454

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Camelliatannin G

Description

(1S,4R,14R,15S,16R,20R,21R)-20-(3,4-dihydroxyphenyl)-14-[(10R,11R)-3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]Nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-4,7,8,9,21,24-hexahydroxy-2,12,29-trioxo-3,13,19,27,30-pentaoxaheptacyclo[13.12.3.0¹,¹⁶.0⁵,²⁸.0⁶,¹¹.0¹⁷,²⁶.0¹⁸,²³]Triaconta-5(28),6,8,10,17(26),18(23),24-heptaene-4-carboxylic acid belongs to the class of organic compounds known as complex tannins. These are tannins made of a catechin bound to a gallotannin or elagitannin. Camelliatannin G is found in Camellia japonica . Based on a literature review very few articles have been published on (1S,4R,14R,15S,16R,20R,21R)-20-(3,4-dihydroxyphenyl)-14-[(10R,11R)-3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]Nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-4,7,8,9,21,24-hexahydroxy-2,12,29-trioxo-3,13,19,27,30-pentaoxaheptacyclo[13.12.3.0¹,¹⁶.0⁵,²⁸.0⁶,¹¹.0¹⁷,²⁶.0¹⁸,²³]Triaconta-5(28),6,8,10,17(26),18(23),24-heptaene-4-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282204142D          

 78 88  0  0  1  0            999 V2000
    7.8616    1.0269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6904    1.8339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3037    2.3857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0882    2.1305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2594    1.3234    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.6461    0.7716    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.8173   -0.0354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6018   -0.2906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7731   -1.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1598   -1.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3752   -1.3942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2040   -0.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5248   -2.4015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6142   -1.4215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1203    1.4023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1324    3.1927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3479    3.4480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7346    2.8962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9058    2.0892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1912    1.6769    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    5.5147    0.2142    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9543   -0.4839    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    6.2062   -1.4060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    9.2369   -0.9055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8637   -1.8607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4287   -2.7230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.7077    0.0430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.3726    3.6324    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1373    3.5884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3526    3.3337    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4679    3.5614    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1527    4.2705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4361    5.1066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.9142    2.9827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    8.7800    3.7620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
 10 13  1  0  0  0  0
  9 14  1  0  0  0  0
  5 15  1  1  0  0  0
  3 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
  2 19  1  0  0  0  0
 20 19  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 30 35  1  0  0  0  0
 34 36  1  0  0  0  0
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 31 39  1  0  0  0  0
 39 40  2  0  0  0  0
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 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
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 39 44  1  0  0  0  0
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 40 48  1  0  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
 23 50  1  6  0  0  0
 22 51  1  0  0  0  0
 51 52  1  0  0  0  0
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 54 55  2  0  0  0  0
 55 56  1  0  0  0  0
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 62 71  1  1  0  0  0
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 21 74  1  6  0  0  0
 58 75  1  0  0  0  0
 57 76  1  0  0  0  0
 56 77  1  0  0  0  0
 16 78  1  0  0  0  0
M  END

     RDKit          3D

112122  0  0  0  0  0  0  0  0999 V2000
    2.3569    1.9511   -3.2948 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0053    1.2718   -0.5630 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -1.7390   -0.5585   -3.3193 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.6533    0.7314   -2.9538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1490    1.8793   -3.5844 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.9108   -2.2690   -1.3564 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2724   -2.8561   -1.0821 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4099    6.6500    0.4716 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652304282204142D          

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M  END
> <DATABASE_ID>
NP0056454

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1CC2=C(O[C@@H]1C1=CC(O)=C(O)C=C1)C1=C(O[C@@]34[C@H]1[C@@H]1OC(=O)C3=C(C3=C(O)C(O)=C(O)C=C3C(=O)O[C@H]1[C@@H]1OC(=O)C3=C(C(O)=C(O)C(O)=C3)C3=C(C=C(O)C(O)=C3O)C(=O)OC[C@H]1O)[C@@](O)(OC4=O)C(O)=O)C=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C49H34O29/c50-15-2-1-10(3-17(15)52)37-21(56)4-11-16(51)8-23-27(38(11)73-37)29-40-41(39-22(57)9-72-42(64)12-5-18(53)31(58)34(61)24(12)25-13(43(65)74-39)6-19(54)32(59)35(25)62)76-44(66)14-7-20(55)33(60)36(63)26(14)28-30(45(67)75-40)48(29,77-23)47(70)78-49(28,71)46(68)69/h1-3,5-8,21-22,29,37,39-41,50-63,71H,4,9H2,(H,68,69)/t21-,22-,29-,37-,39-,40+,41+,48+,49-/m1/s1

> <INCHI_KEY>
MMIYRWRTSJNIBU-JRTAIVKMSA-N

> <FORMULA>
C49H34O29

> <MOLECULAR_WEIGHT>
1086.782

> <EXACT_MASS>
1086.118575075

> <JCHEM_ACCEPTOR_COUNT>
24

> <JCHEM_ATOM_COUNT>
112

> <JCHEM_AVERAGE_POLARIZABILITY>
95.10699223864262

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
16

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4R,14R,15S,16R,20R,21R)-20-(3,4-dihydroxyphenyl)-14-[(10R,11R)-3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0^{2,7}]nonadeca-1(15),2(7),3,5,16,18-hexaen-10-yl]-4,7,8,9,21,24-hexahydroxy-2,12,29-trioxo-3,13,19,27,30-pentaoxaheptacyclo[13.12.3.0^{1,16}.0^{5,28}.0^{6,11}.0^{17,26}.0^{18,23}]triaconta-5(28),6,8,10,17(26),18(23),24-heptaene-4-carboxylic acid

> <ALOGPS_LOGP>
2.57

> <JCHEM_LOGP>
2.0526301189999994

> <ALOGPS_LOGS>
-2.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
11

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
7.356774734925396

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.9277887510056915

> <JCHEM_PKA_STRONGEST_BASIC>
-6.059800237954929

> <JCHEM_POLAR_SURFACE_AREA>
490.7100000000001

> <JCHEM_REFRACTIVITY>
245.42700000000013

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.92e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4R,14R,15S,16R,20R,21R)-20-(3,4-dihydroxyphenyl)-14-[(10R,11R)-3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0^{2,7}]nonadeca-1(15),2(7),3,5,16,18-hexaen-10-yl]-4,7,8,9,21,24-hexahydroxy-2,12,29-trioxo-3,13,19,27,30-pentaoxaheptacyclo[13.12.3.0^{1,16}.0^{5,28}.0^{6,11}.0^{17,26}.0^{18,23}]triaconta-5(28),6,8,10,17(26),18(23),24-heptaene-4-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  O   UNK     0      14.675   1.917   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      14.355   3.423   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.500   4.453   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.965   3.977   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.284   2.470   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.139   1.440   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.459  -0.066   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.923  -0.543   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      18.243  -2.049   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.098  -3.079   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      15.634  -2.603   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.314  -1.096   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      17.780  -4.483   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      19.813  -2.653   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      18.891   2.618   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      15.181   5.960   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.716   6.436   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.571   5.406   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.891   3.900   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.557   3.130   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.236   1.624   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.294   0.400   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.115  -0.903   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.297  -2.377   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      11.585  -2.625   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.863  -2.939   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.956  -4.477   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      10.446  -4.864   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      10.929  -3.324   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      11.435  -6.228   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.972  -6.136   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.821  -7.421   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      13.133  -8.798   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.595  -8.891   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.747  -7.606   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      10.859 -10.318   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      13.815 -10.288   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      15.640  -7.828   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      13.661  -4.758   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      13.568  -3.221   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      14.853  -2.372   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      16.231  -3.061   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      16.323  -4.598   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      15.038  -5.447   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      14.997  -7.013   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      18.060  -5.364   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0      17.242  -1.690   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      12.812  -3.473   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      12.000  -5.083   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      12.652  -0.811   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0       8.788   0.080   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0       7.381   0.707   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0       6.509  -0.773   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0       6.612   2.041   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       5.204   1.415   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       3.959   2.321   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0       4.120   3.853   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0       5.528   4.478   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0       6.773   3.573   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0       7.804   4.717   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0       8.948   3.686   0.000  0.00  0.00           C+0
HETATM   62  C   UNK     0      10.413   4.161   0.000  0.00  0.00           C+0
HETATM   63  C   UNK     0      10.516   5.656   0.000  0.00  0.00           C+0
HETATM   64  O   UNK     0      11.896   6.780   0.000  0.00  0.00           O+0
HETATM   65  O   UNK     0       9.590   6.698   0.000  0.00  0.00           O+0
HETATM   66  C   UNK     0       8.125   6.223   0.000  0.00  0.00           C+0
HETATM   67  O   UNK     0       6.473   6.648   0.000  0.00  0.00           O+0
HETATM   68  C   UNK     0       7.752   7.972   0.000  0.00  0.00           C+0
HETATM   69  O   UNK     0       8.281   9.532   0.000  0.00  0.00           O+0
HETATM   70  O   UNK     0       6.625   9.182   0.000  0.00  0.00           O+0
HETATM   71  O   UNK     0      11.040   5.568   0.000  0.00  0.00           O+0
HETATM   72  C   UNK     0       8.627   2.180   0.000  0.00  0.00           C+0
HETATM   73  O   UNK     0       7.437   1.648   0.000  0.00  0.00           O+0
HETATM   74  O   UNK     0       9.771   1.149   0.000  0.00  0.00           O+0
HETATM   75  O   UNK     0       5.345   5.994   0.000  0.00  0.00           O+0
HETATM   76  O   UNK     0       2.669   4.540   0.000  0.00  0.00           O+0
HETATM   77  O   UNK     0       2.435   1.821   0.000  0.00  0.00           O+0
HETATM   78  O   UNK     0      16.389   7.022   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   19                                                  
CONECT    3    2    4   16                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   15                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11    7                                                       
CONECT   13   10                                                            
CONECT   14    9                                                            
CONECT   15    5                                                            
CONECT   16    3   17   78                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   71                                                  
CONECT   19   18    2   20                                                  
CONECT   20   19   21   62                                                  
CONECT   21   20   22   74                                                  
CONECT   22   21   23   51                                                  
CONECT   23   22   24   50                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   35                                                  
CONECT   31   30   32   39                                                  
CONECT   32   31   33   38                                                  
CONECT   33   32   34   37                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34   30                                                       
CONECT   36   34                                                            
CONECT   37   33                                                            
CONECT   38   32                                                            
CONECT   39   31   40   44                                                  
CONECT   40   39   41   48                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43   47                                                  
CONECT   43   42   44   46                                                  
CONECT   44   43   39   45                                                  
CONECT   45   44                                                            
CONECT   46   43                                                            
CONECT   47   42                                                            
CONECT   48   40   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   23                                                       
CONECT   51   22   52                                                       
CONECT   52   51   53   54                                                  
CONECT   53   52                                                            
CONECT   54   52   55   59                                                  
CONECT   55   54   56                                                       
CONECT   56   55   57   77                                                  
CONECT   57   56   58   76                                                  
CONECT   58   57   59   75                                                  
CONECT   59   58   54   60                                                  
CONECT   60   59   61   66                                                  
CONECT   61   60   62   72                                                  
CONECT   62   61   20   63   71                                             
CONECT   63   62   64   65                                                  
CONECT   64   63                                                            
CONECT   65   63   66                                                       
CONECT   66   65   60   67   68                                             
CONECT   67   66                                                            
CONECT   68   66   69   70                                                  
CONECT   69   68                                                            
CONECT   70   68                                                            
CONECT   71   62   18                                                       
CONECT   72   61   73   74                                                  
CONECT   73   72                                                            
CONECT   74   72   21                                                       
CONECT   75   58                                                            
CONECT   76   57                                                            
CONECT   77   56                                                            
CONECT   78   16                                                            
MASTER        0    0    0    0    0    0    0    0   78    0  176    0
END

View in JSmol

Synonyms

Value	Source
(1S,4R,14R,15S,16R,20R,21R)-20-(3,4-Dihydroxyphenyl)-14-[(10R,11R)-3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0,]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-4,7,8,9,21,24-hexahydroxy-2,12,29-trioxo-3,13,19,27,30-pentaoxaheptacyclo[13.12.3.0,.0,.0,.0,.0,]triaconta-5(28),6,8,10,17(26),18(23),24-heptaene-4-carboxylate	Generator

Chemical Formula

C₄₉H₃₄O₂₉

Average Mass

1086.7820 Da

Monoisotopic Mass

1086.11858 Da

IUPAC Name

(1S,4R,14R,15S,16R,20R,21R)-20-(3,4-dihydroxyphenyl)-14-[(10R,11R)-3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0^{2,7}]nonadeca-1(15),2(7),3,5,16,18-hexaen-10-yl]-4,7,8,9,21,24-hexahydroxy-2,12,29-trioxo-3,13,19,27,30-pentaoxaheptacyclo[13.12.3.0^{1,16}.0^{5,28}.0^{6,11}.0^{17,26}.0^{18,23}]triaconta-5(28),6,8,10,17(26),18(23),24-heptaene-4-carboxylic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

O[C@@H]1CC2=C(O[C@@H]1C1=CC(O)=C(O)C=C1)C1=C(O[C@@]34[C@H]1[C@@H]1OC(=O)C3=C(C3=C(O)C(O)=C(O)C=C3C(=O)O[C@H]1[C@@H]1OC(=O)C3=C(C(O)=C(O)C(O)=C3)C3=C(C=C(O)C(O)=C3O)C(=O)OC[C@H]1O)[C@@](O)(OC4=O)C(O)=O)C=C2O

InChI Identifier

InChI=1S/C49H34O29/c50-15-2-1-10(3-17(15)52)37-21(56)4-11-16(51)8-23-27(38(11)73-37)29-40-41(39-22(57)9-72-42(64)12-5-18(53)31(58)34(61)24(12)25-13(43(65)74-39)6-19(54)32(59)35(25)62)76-44(66)14-7-20(55)33(60)36(63)26(14)28-30(45(67)75-40)48(29,77-23)47(70)78-49(28,71)46(68)69/h1-3,5-8,21-22,29,37,39-41,50-63,71H,4,9H2,(H,68,69)/t21-,22-,29-,37-,39-,40+,41+,48+,49-/m1/s1

InChI Key

MMIYRWRTSJNIBU-JRTAIVKMSA-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
Camellia japonica	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as complex tannins. These are tannins made of a catechin bound to a gallotannin or elagitannin.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Complex tannins

Direct Parent

Complex tannins

Alternative Parents

Substituents

Complex tannin
Catechin
8-prenylated flavan
Hexacarboxylic acid or derivatives
Hydroxyflavonoid
Flavan-3-ol
5-hydroxyflavonoid
4'-hydroxyflavonoid
3-hydroxyflavonoid
3'-hydroxyflavonoid
Flavan
Gallic acid or derivatives
1-benzopyran
Benzopyran
Chromane
Coumaran
Catechol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Delta_valerolactone
Dihydropyranone
Delta valerolactone
Alkyl aryl ether
Benzenoid
Pyran
Oxane
Hydroxy acid
Monocyclic benzene moiety
Alpha-hydroxy acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Secondary alcohol
Lactone
Hemiacetal
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Ether
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.57	ALOGPS
logP	2.05	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	1.93	ChemAxon
pKa (Strongest Basic)	-6.1	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	24	ChemAxon
Hydrogen Donor Count	16	ChemAxon
Polar Surface Area	490.71 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	245.43 m³·mol⁻¹	ChemAxon
Polarizability	95.11 Å³	ChemAxon
Number of Rings	11	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

163072008

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Camelliatannin G (NP0056454)

MOL for NP0056454 (Camelliatannin G)

3D MOL for NP0056454 (Camelliatannin G)

3D SDF for NP0056454 (Camelliatannin G)

3D-SDF for NP0056454 (Camelliatannin G)

PDB for NP0056454 (Camelliatannin G)

3D PDB for NP0056454 (Camelliatannin G)

SMILES for NP0056454 (Camelliatannin G)

INCHI for NP0056454 (Camelliatannin G)

Structure for NP0056454 (Camelliatannin G)

3D Structure for NP0056454 (Camelliatannin G)