NP-MRD: Showing NP-Card for 6-epi-gomisin (NP0032265)

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Record Information

Version

2.0

Created at

2021-06-19 23:06:45 UTC

Updated at

2021-06-30 00:01:20 UTC

NP-MRD ID

NP0032265

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-epi-gomisin

Provided By

JEOL Database JEOL Logo

Description

Gomisin R 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. 6-epi-gomisin is found in Kadsura angustifolia, Kadsura coccinea, Kadsura philippinensis, Schisandra chinensis Baill. and Schisandra rubriflora. 6-epi-gomisin was first documented in 2006 (Shen, Y. -C., et al.). Based on a literature review very few articles have been published on Gomisin R.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202101063D          

 53 57  0  0  0  0            999 V2000
    0.1977    1.5060    4.1879 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0158    0.4794    3.2187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6847    0.8609    2.1013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8211    1.6530    2.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5145    1.9461    0.9845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1383    1.4532   -0.2450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0088    0.6157   -0.3255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2515    0.3390    0.8514 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9937   -0.4650    0.7795 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9358   -1.8559    0.4758 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1286   -2.6035    0.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3250   -1.9679    0.6526 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3992   -0.6245    0.9377 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2568    0.1599    1.0049 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2260    1.5141    1.2263 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3954    2.1278    1.7470 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6951   -0.2298    1.1015 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4063   -1.4648    0.9041 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5424   -2.5747    0.6116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3815   -2.5432    0.1384 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3490   -3.8601    0.7023 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5908   -2.6002   -1.4001 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2715   -3.9069   -1.8435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3158   -1.3541   -2.0071 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8318   -1.3540   -1.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6608    0.0142   -1.6757 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6027    2.7321    1.2069 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5293    2.8954    2.6344 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4105    2.2119    3.2285 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0925    1.2584    4.7675 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3623    2.4886    3.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6472    1.5297    4.8822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7258    1.6977   -1.1245 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1172   -3.6608    0.1612 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7546    1.6172    2.6466 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1732    2.1998    0.9809 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1301    3.1493    2.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1088   -1.3361    0.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9764   -1.6910    1.8125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2293   -2.0565    0.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1212   -3.7493    1.6424 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3998   -2.6262   -1.8784 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2157   -4.0716   -1.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6229   -4.7682   -1.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.4533    2.5100    3.0805 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 14  2  0  0  0  0
 14 13  1  0  0  0  0
 27 28  1  0  0  0  0
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 11 10  2  0  0  0  0
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 14 15  1  0  0  0  0
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 15 16  1  0  0  0  0
  7  8  2  0  0  0  0
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 10 20  1  0  0  0  0
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 11 34  1  0  0  0  0
 16 35  1  0  0  0  0
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 24 46  1  6  0  0  0
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  1 30  1  0  0  0  0
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  1 32  1  0  0  0  0
 18 38  1  0  0  0  0
 18 39  1  0  0  0  0
 21 41  1  0  0  0  0
M  END

     RDKit          3D

 53 57  0  0  0  0  0  0  0  0999 V2000
    0.1977    1.5060    4.1879 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0158    0.4794    3.2187 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1383    1.4532   -0.2450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0088    0.6157   -0.3255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2515    0.3390    0.8514 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9937   -0.4650    0.7795 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9358   -1.8559    0.4758 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1286   -2.6035    0.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3250   -1.9679    0.6526 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3992   -0.6245    0.9377 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2568    0.1599    1.0049 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2260    1.5141    1.2263 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3954    2.1278    1.7470 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6951   -0.2298    1.1015 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4063   -1.4648    0.9041 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5424   -2.5747    0.6116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3815   -2.5432    0.1384 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3490   -3.8601    0.7023 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5908   -2.6002   -1.4001 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -2.8318   -1.3540   -1.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2157   -4.0716   -1.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
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 21 41  1  0
M  END


  Mrv1652306202101063D          

 53 57  0  0  0  0            999 V2000
    0.1977    1.5060    4.1879 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0158    0.4794    3.2187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6847    0.8609    2.1013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8211    1.6530    2.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5145    1.9461    0.9845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1383    1.4532   -0.2450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0088    0.6157   -0.3255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2515    0.3390    0.8514 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9937   -0.4650    0.7795 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9358   -1.8559    0.4758 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1286   -2.6035    0.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3992   -0.6245    0.9377 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2568    0.1599    1.0049 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2260    1.5141    1.2263 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3954    2.1278    1.7470 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6951   -0.2298    1.1015 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4063   -1.4648    0.9041 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5424   -2.5747    0.6116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3815   -2.5432    0.1384 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3490   -3.8601    0.7023 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5908   -2.6002   -1.4001 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2715   -3.9069   -1.8435 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6608    0.0142   -1.6757 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -3.5293    2.8954    2.6344 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4105    2.2119    3.2285 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0925    1.2584    4.7675 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3623    2.4886    3.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6472    1.5297    4.8822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7258    1.6977   -1.1245 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1172   -3.6608    0.1612 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7546    1.6172    2.6466 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1732    2.1998    0.9809 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1301    3.1493    2.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1088   -1.3361    0.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9764   -1.6910    1.8125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2293   -2.0565    0.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1212   -3.7493    1.6424 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3998   -2.6262   -1.8784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4756   -3.8968   -2.9195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2157   -4.0716   -1.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6229   -4.7682   -1.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1975   -1.4618   -3.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3104   -2.2197   -2.2297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2972   -0.4682   -2.2061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0754   -1.3762   -0.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4268   -0.0460   -1.8034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9757    0.7324   -2.4467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4493    3.9644    2.8627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4533    2.5100    3.0805 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 14  2  0  0  0  0
 14 13  1  0  0  0  0
 27 28  1  0  0  0  0
 12 11  1  0  0  0  0
 11 10  2  0  0  0  0
 28 29  1  0  0  0  0
 14 15  1  0  0  0  0
 29  4  1  0  0  0  0
 15 16  1  0  0  0  0
  7  8  2  0  0  0  0
 26 24  1  0  0  0  0
  4  5  1  0  0  0  0
 24 22  1  0  0  0  0
 20 22  1  0  0  0  0
  4  3  2  0  0  0  0
 24 25  1  0  0  0  0
  3  8  1  0  0  0  0
 22 23  1  0  0  0  0
  3  2  1  0  0  0  0
  7 26  1  0  0  0  0
  2  1  1  0  0  0  0
 12 13  2  0  0  0  0
  8  9  1  0  0  0  0
 10 20  1  0  0  0  0
  7  6  1  0  0  0  0
  6  5  2  0  0  0  0
 10  9  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 12  1  0  0  0  0
  5 27  1  0  0  0  0
 20 21  1  0  0  0  0
  6 33  1  0  0  0  0
 28 52  1  0  0  0  0
 28 53  1  0  0  0  0
 20 40  1  1  0  0  0
 26 50  1  0  0  0  0
 26 51  1  0  0  0  0
 11 34  1  0  0  0  0
 16 35  1  0  0  0  0
 16 36  1  0  0  0  0
 16 37  1  0  0  0  0
 24 46  1  6  0  0  0
 22 42  1  6  0  0  0
 25 47  1  0  0  0  0
 25 48  1  0  0  0  0
 25 49  1  0  0  0  0
 23 43  1  0  0  0  0
 23 44  1  0  0  0  0
 23 45  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
  1 32  1  0  0  0  0
 18 38  1  0  0  0  0
 18 39  1  0  0  0  0
 21 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0032265

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1([H])C2=C([H])C3=C(OC([H])([H])O3)C(OC([H])([H])[H])=C2C2=C(C([H])=C3OC([H])([H])OC3=C2OC([H])([H])[H])C([H])([H])[C@]([H])(C([H])([H])[H])[C@]1([H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C22H24O7/c1-10-5-12-6-14-19(28-8-26-14)21(24-3)16(12)17-13(18(23)11(10)2)7-15-20(22(17)25-4)29-9-27-15/h6-7,10-11,18,23H,5,8-9H2,1-4H3/t10-,11-,18+/m0/s1

> <INCHI_KEY>
HOPDFAWBFXSPSA-LDLUMPKVSA-N

> <FORMULA>
C22H24O7

> <MOLECULAR_WEIGHT>
400.427

> <EXACT_MASS>
400.152203113

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
41.961592510737205

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(11R,12S,13S)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0^{2,10}.0^{4,8}.0^{17,21}]docosa-1(15),2,4(8),9,16,21-hexaen-11-ol

> <ALOGPS_LOGP>
2.95

> <JCHEM_LOGP>
3.4250306436666658

> <ALOGPS_LOGS>
-3.91

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.23380555848641

> <JCHEM_PKA_STRONGEST_BASIC>
-3.133933448718044

> <JCHEM_POLAR_SURFACE_AREA>
75.61000000000001

> <JCHEM_REFRACTIVITY>
103.67230000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.93e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(11R,12S,13S)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0^{2,10}.0^{4,8}.0^{17,21}]docosa-1(15),2,4(8),9,16,21-hexaen-11-ol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 53 57  0  0  0  0  0  0  0  0999 V2000
    0.1977    1.5060    4.1879 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0158    0.4794    3.2187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6847    0.8609    2.1013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8211    1.6530    2.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5145    1.9461    0.9845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1383    1.4532   -0.2450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0088    0.6157   -0.3255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2515    0.3390    0.8514 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9937   -0.4650    0.7795 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9358   -1.8559    0.4758 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1286   -2.6035    0.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3250   -1.9679    0.6526 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3992   -0.6245    0.9377 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2568    0.1599    1.0049 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2260    1.5141    1.2263 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3954    2.1278    1.7470 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6951   -0.2298    1.1015 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4063   -1.4648    0.9041 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5424   -2.5747    0.6116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3815   -2.5432    0.1384 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3490   -3.8601    0.7023 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5908   -2.6002   -1.4001 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2715   -3.9069   -1.8435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3158   -1.3541   -2.0071 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8318   -1.3540   -1.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6608    0.0142   -1.6757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6027    2.7321    1.2069 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5293    2.8954    2.6344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4105    2.2119    3.2285 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0925    1.2584    4.7675 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3623    2.4886    3.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6472    1.5297    4.8822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7258    1.6977   -1.1245 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1172   -3.6608    0.1612 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7546    1.6172    2.6466 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1732    2.1998    0.9809 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1301    3.1493    2.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1088   -1.3361    0.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9764   -1.6910    1.8125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2293   -2.0565    0.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1212   -3.7493    1.6424 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3998   -2.6262   -1.8784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4756   -3.8968   -2.9195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2157   -4.0716   -1.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6229   -4.7682   -1.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1975   -1.4618   -3.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3104   -2.2197   -2.2297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2972   -0.4682   -2.2061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0754   -1.3762   -0.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4268   -0.0460   -1.8034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9757    0.7324   -2.4467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4493    3.9644    2.8627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4533    2.5100    3.0805 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 14  2  0
 14 13  1  0
 27 28  1  0
 12 11  1  0
 11 10  2  0
 28 29  1  0
 14 15  1  0
 29  4  1  0
 15 16  1  0
  7  8  2  0
 26 24  1  0
  4  5  1  0
 24 22  1  0
 20 22  1  0
  4  3  2  0
 24 25  1  0
  3  8  1  0
 22 23  1  0
  3  2  1  0
  7 26  1  0
  2  1  1  0
 12 13  2  0
  8  9  1  0
 10 20  1  0
  7  6  1  0
  6  5  2  0
 10  9  1  0
 13 17  1  0
 17 18  1  0
 18 19  1  0
 19 12  1  0
  5 27  1  0
 20 21  1  0
  6 33  1  0
 28 52  1  0
 28 53  1  0
 20 40  1  1
 26 50  1  0
 26 51  1  0
 11 34  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
 24 46  1  6
 22 42  1  6
 25 47  1  0
 25 48  1  0
 25 49  1  0
 23 43  1  0
 23 44  1  0
 23 45  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 18 38  1  0
 18 39  1  0
 21 41  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       0.198   1.506   4.188  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.016   0.479   3.219  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.685   0.861   2.101  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.821   1.653   2.133  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.515   1.946   0.985  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.138   1.453  -0.245  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.009   0.616  -0.326  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.252   0.339   0.851  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.994  -0.465   0.780  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.936  -1.856   0.476  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.129  -2.603   0.412  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.325  -1.968   0.653  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.399  -0.625   0.938  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.257   0.160   1.005  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.226   1.514   1.226  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.395   2.128   1.747  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.695  -0.230   1.101  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.406  -1.465   0.904  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.542  -2.575   0.612  0.00  0.00           O+0
HETATM   20  C   UNK     0      -0.382  -2.543   0.138  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.349  -3.860   0.702  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.591  -2.600  -1.400  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.272  -3.907  -1.843  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.316  -1.354  -2.007  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.832  -1.354  -1.761  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.661   0.014  -1.676  0.00  0.00           C+0
HETATM   27  O   UNK     0      -3.603   2.732   1.207  0.00  0.00           O+0
HETATM   28  C   UNK     0      -3.529   2.895   2.634  0.00  0.00           C+0
HETATM   29  O   UNK     0      -2.410   2.212   3.228  0.00  0.00           O+0
HETATM   30  H   UNK     0       1.093   1.258   4.768  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.362   2.489   3.731  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.647   1.530   4.882  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.726   1.698  -1.125  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.117  -3.661   0.161  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.755   1.617   2.647  0.00  0.00           H+0
HETATM   36  H   UNK     0       4.173   2.200   0.981  0.00  0.00           H+0
HETATM   37  H   UNK     0       3.130   3.149   2.037  0.00  0.00           H+0
HETATM   38  H   UNK     0       6.109  -1.336   0.073  0.00  0.00           H+0
HETATM   39  H   UNK     0       5.976  -1.691   1.813  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.229  -2.057   0.628  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.121  -3.749   1.642  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.400  -2.626  -1.878  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.476  -3.897  -2.920  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.216  -4.072  -1.314  0.00  0.00           H+0
HETATM   45  H   UNK     0      -0.623  -4.768  -1.649  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.198  -1.462  -3.096  0.00  0.00           H+0
HETATM   47  H   UNK     0      -3.310  -2.220  -2.230  0.00  0.00           H+0
HETATM   48  H   UNK     0      -3.297  -0.468  -2.206  0.00  0.00           H+0
HETATM   49  H   UNK     0      -3.075  -1.376  -0.695  0.00  0.00           H+0
HETATM   50  H   UNK     0       0.427  -0.046  -1.803  0.00  0.00           H+0
HETATM   51  H   UNK     0      -0.976   0.732  -2.447  0.00  0.00           H+0
HETATM   52  H   UNK     0      -3.449   3.964   2.863  0.00  0.00           H+0
HETATM   53  H   UNK     0      -4.453   2.510   3.080  0.00  0.00           H+0
CONECT    1    2   30   31   32                                             
CONECT    2    3    1                                                       
CONECT    3    4    8    2                                                  
CONECT    4   29    5    3                                                  
CONECT    5    4    6   27                                                  
CONECT    6    7    5   33                                                  
CONECT    7    8   26    6                                                  
CONECT    8    7    3    9                                                  
CONECT    9   14    8   10                                                  
CONECT   10   11   20    9                                                  
CONECT   11   12   10   34                                                  
CONECT   12   11   13   19                                                  
CONECT   13   14   12   17                                                  
CONECT   14    9   13   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   35   36   37                                             
CONECT   17   13   18                                                       
CONECT   18   17   19   38   39                                             
CONECT   19   18   12                                                       
CONECT   20   22   10   21   40                                             
CONECT   21   20   41                                                       
CONECT   22   24   20   23   42                                             
CONECT   23   22   43   44   45                                             
CONECT   24   26   22   25   46                                             
CONECT   25   24   47   48   49                                             
CONECT   26   24    7   50   51                                             
CONECT   27   28    5                                                       
CONECT   28   27   29   52   53                                             
CONECT   29   28    4                                                       
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    1                                                            
CONECT   33    6                                                            
CONECT   34   11                                                            
CONECT   35   16                                                            
CONECT   36   16                                                            
CONECT   37   16                                                            
CONECT   38   18                                                            
CONECT   39   18                                                            
CONECT   40   20                                                            
CONECT   41   21                                                            
CONECT   42   22                                                            
CONECT   43   23                                                            
CONECT   44   23                                                            
CONECT   45   23                                                            
CONECT   46   24                                                            
CONECT   47   25                                                            
CONECT   48   25                                                            
CONECT   49   25                                                            
CONECT   50   26                                                            
CONECT   51   26                                                            
CONECT   52   28                                                            
CONECT   53   28                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  114    0
END

RDKit          3D

53 57  0  0  0  0  0  0  0  0999 V2000
    0.1977    1.5060    4.1879 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0158    0.4794    3.2187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6847    0.8609    2.1013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8211    1.6530    2.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5145    1.9461    0.9845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1383    1.4532   -0.2450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0088    0.6157   -0.3255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2515    0.3390    0.8514 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9937   -0.4650    0.7795 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9358   -1.8559    0.4758 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1286   -2.6035    0.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3250   -1.9679    0.6526 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3992   -0.6245    0.9377 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2568    0.1599    1.0049 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2260    1.5141    1.2263 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3954    2.1278    1.7470 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6951   -0.2298    1.1015 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4063   -1.4648    0.9041 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5424   -2.5747    0.6116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3815   -2.5432    0.1384 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3490   -3.8601    0.7023 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5908   -2.6002   -1.4001 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2715   -3.9069   -1.8435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3158   -1.3541   -2.0071 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8318   -1.3540   -1.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6608    0.0142   -1.6757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6027    2.7321    1.2069 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5293    2.8954    2.6344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4105    2.2119    3.2285 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0925    1.2584    4.7675 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3623    2.4886    3.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6472    1.5297    4.8822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7258    1.6977   -1.1245 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1172   -3.6608    0.1612 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7546    1.6172    2.6466 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1732    2.1998    0.9809 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1301    3.1493    2.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1088   -1.3361    0.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9764   -1.6910    1.8125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2293   -2.0565    0.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1212   -3.7493    1.6424 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3998   -2.6262   -1.8784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4756   -3.8968   -2.9195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2157   -4.0716   -1.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6229   -4.7682   -1.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1975   -1.4618   -3.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3104   -2.2197   -2.2297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2972   -0.4682   -2.2061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0754   -1.3762   -0.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4268   -0.0460   -1.8034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9757    0.7324   -2.4467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4493    3.9644    2.8627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4533    2.5100    3.0805 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 14  2  0
 14 13  1  0
 27 28  1  0
 12 11  1  0
 11 10  2  0
 28 29  1  0
 14 15  1  0
 29  4  1  0
 15 16  1  0
  7  8  2  0
 26 24  1  0
  4  5  1  0
 24 22  1  0
 20 22  1  0
  4  3  2  0
 24 25  1  0
  3  8  1  0
 22 23  1  0
  3  2  1  0
  7 26  1  0
  2  1  1  0
 12 13  2  0
  8  9  1  0
 10 20  1  0
  7  6  1  0
  6  5  2  0
 10  9  1  0
 13 17  1  0
 17 18  1  0
 18 19  1  0
 19 12  1  0
  5 27  1  0
 20 21  1  0
  6 33  1  0
 28 52  1  0
 28 53  1  0
 20 40  1  1
 26 50  1  0
 26 51  1  0
 11 34  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
 24 46  1  6
 22 42  1  6
 25 47  1  0
 25 48  1  0
 25 49  1  0
 23 43  1  0
 23 44  1  0
 23 45  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 18 38  1  0
 18 39  1  0
 21 41  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₂₂H₂₄O₇

Average Mass

400.4270 Da

Monoisotopic Mass

400.15220 Da

IUPAC Name

(11R,12S,13S)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0^{2,10}.0^{4,8}.0^{17,21}]docosa-1(15),2,4(8),9,16,21-hexaen-11-ol

Traditional Name

(11R,12S,13S)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0^{2,10}.0^{4,8}.0^{17,21}]docosa-1(15),2,4(8),9,16,21-hexaen-11-ol

CAS Registry Number

Not Available

SMILES

[H]O[C@@]1([H])C2=C([H])C3=C(OC([H])([H])O3)C(OC([H])([H])[H])=C2C2=C(C([H])=C3OC([H])([H])OC3=C2OC([H])([H])[H])C([H])([H])[C@]([H])(C([H])([H])[H])[C@]1([H])C([H])([H])[H]

InChI Identifier

InChI=1S/C22H24O7/c1-10-5-12-6-14-19(28-8-26-14)21(24-3)16(12)17-13(18(23)11(10)2)7-15-20(22(17)25-4)29-9-27-15/h6-7,10-11,18,23H,5,8-9H2,1-4H3/t10-,11-,18+/m0/s1

InChI Key

HOPDFAWBFXSPSA-LDLUMPKVSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Kadsura angustifolia	Plant	KNApSAcK
Kadsura coccinea	Plant	KNApSAcK
Kadsura philippinensis	JEOL database	Shen, Y. -C., et al, J. Nat. Prod. 69, 963 (2006)
Schisandra chinensis Baill.	Plant	KNApSAcK
Schisandra rubriflora	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
Benzodioxole
Anisole
Alkyl aryl ether
Benzenoid
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Ether
Alcohol
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	2.95	ALOGPS
logP	3.43	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	14.23	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	75.61 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	103.67 m³·mol⁻¹	ChemAxon
Polarizability	41.96 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9669821

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11495015

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Shen, Y. -C., et al. (2006). Shen, Y. -C., et al, J. Nat. Prod. 69, 963 (2006) . J. Nat. Prod..

Showing NP-Card for 6-epi-gomisin (NP0032265)

MOL for NP0032265 (6-epi-gomisin)

3D MOL for NP0032265 (6-epi-gomisin)

3D SDF for NP0032265 (6-epi-gomisin)

3D-SDF for NP0032265 (6-epi-gomisin)

PDB for NP0032265 (6-epi-gomisin)

3D PDB for NP0032265 (6-epi-gomisin)

SMILES for NP0032265 (6-epi-gomisin)

INCHI for NP0032265 (6-epi-gomisin)

Structure for NP0032265 (6-epi-gomisin)

3D Structure for NP0032265 (6-epi-gomisin)