NP-MRD: Showing NP-Card for (-)-Fortuneanoside K (NP0071251)

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Record Information

Version

2.0

Created at

2022-04-28 16:38:41 UTC

Updated at

2022-04-28 16:38:41 UTC

NP-MRD ID

NP0071251

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Fortuneanoside K

Description

Fortuneanoside K belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. (-)-Fortuneanoside K is found in Pyracantha fortuneana and Pyracantha fortuneana (MAXIM) LI . Based on a literature review very few articles have been published on Fortuneanoside K.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282218382D          

 30 33  0  0  1  0            999 V2000
    1.2101    0.5213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9552    1.3059    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1482    1.4774    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4038    0.8644    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1489    0.0797    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6581   -0.0918    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9130   -0.8764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7200   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2720   -0.4349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0790   -0.6064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7464   -0.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4139   -0.6064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2208   -0.4349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7729   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5179   -1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7110   -2.0041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1589   -1.3910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3339   -1.3910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7819   -2.0041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9749   -1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4229   -2.4457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6159   -2.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4560   -2.7887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0171    0.3498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5691    0.9629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7009   -0.5334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2108    1.0359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1067    2.2621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5072    1.9190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2523    2.7036    0.0000 O   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  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  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 12 17  2  0  0  0  0
 17 18  1  0  0  0  0
 10 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
  8 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 16 23  1  0  0  0  0
  9 24  1  0  0  0  0
 24 25  1  0  0  0  0
  5 26  1  6  0  0  0
  4 27  1  1  0  0  0
  3 28  1  6  0  0  0
  2 29  1  1  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 52 55  0  0  0  0  0  0  0  0999 V2000
    1.2931   -2.0321    3.1084 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5431   -1.1626    2.2868 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1373   -0.4776    1.2179 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4771   -0.6284    0.9302 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0915    0.0355   -0.1194 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3583    0.8898   -0.9279 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1534    1.4026   -1.8526 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3757    0.9467   -1.7166 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5387    1.1856   -2.4293 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7049    0.5553   -2.0552 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7181   -0.3160   -0.9693 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5370   -0.5451   -0.2625 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4910   -1.4005    0.8245 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3679    0.0797   -0.6287 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0190    1.0342   -0.6323 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2790    1.8980   -1.4503 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1987    3.2609   -1.0769 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4110    0.3718    0.4131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9308    0.5516    0.6652 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9520   -0.2659    0.0693 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6779    0.5537   -0.7486 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9056    0.0818   -1.1327 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4998    1.0712   -2.1252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7457    0.6845   -2.5760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7658    0.0267    0.1364 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.0814   -0.2384   -0.1340 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1635   -1.0316    1.0070 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7982   -0.9289    2.2665 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6933   -0.9231    1.1706 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1877   -2.2384    1.2958 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5710   -2.6580    3.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9398   -1.4896    3.8274 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9629   -2.7012    2.5219 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0701   -1.2903    1.5476 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5740    1.8505   -3.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6432    0.6957   -2.5647 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5970   -0.8294   -0.6394 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2832   -1.8978    1.1652 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0734    3.5838   -0.4825 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1266    3.9273   -1.9720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7172    3.4033   -0.4426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4010   -1.0068   -0.5811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8928   -0.9028   -1.6072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5414    2.0942   -1.7113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8089    1.0869   -2.9919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9048   -0.2874   -2.4644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5950    1.0087    0.6410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6239    0.1792    0.6043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4524   -2.0611    0.6424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8283   -1.8048    2.7240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4901   -0.4266    2.1641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8785   -2.9149    1.1636 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 14  2  0
 14 12  1  0
 12 13  1  0
 12 11  2  0
 11 10  1  0
 10  9  2  0
  6 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 18  3  1  0
 29 20  1  0
 14  5  1  0
  9  8  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
 13 38  1  0
 11 37  1  0
 10 36  1  0
  9 35  1  0
 17 39  1  0
 17 40  1  0
 17 41  1  0
 20 42  1  6
 22 43  1  6
 23 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  1
 26 48  1  0
 27 49  1  6
 28 50  1  0
 29 51  1  1
 30 52  1  0
M  END


  Mrv1652304282218382D          

 30 33  0  0  1  0            999 V2000
    1.2101    0.5213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9552    1.3059    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1482    1.4774    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4038    0.8644    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1489    0.0797    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6581   -0.0918    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9130   -0.8764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7200   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2720   -0.4349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0790   -0.6064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7464   -0.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4139   -0.6064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2208   -0.4349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7729   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5179   -1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7110   -2.0041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1589   -1.3910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3339   -1.3910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7819   -2.0041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9749   -1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4229   -2.4457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6159   -2.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4560   -2.7887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0171    0.3498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5691    0.9629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7009   -0.5334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2108    1.0359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1067    2.2621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5072    1.9190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2523    2.7036    0.0000 O   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  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  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 12 17  2  0  0  0  0
 17 18  1  0  0  0  0
 10 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
  8 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 16 23  1  0  0  0  0
  9 24  1  0  0  0  0
 24 25  1  0  0  0  0
  5 26  1  6  0  0  0
  4 27  1  1  0  0  0
  3 28  1  6  0  0  0
  2 29  1  1  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0071251

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(OC3=C2C(O)=CC=C3)C(OC)=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H22O10/c1-26-11-6-8-13-9(22)4-3-5-10(13)28-17(8)19(27-2)18(11)30-20-16(25)15(24)14(23)12(7-21)29-20/h3-6,12,14-16,20-25H,7H2,1-2H3/t12-,14-,15+,16-,20+/m1/s1

> <INCHI_KEY>
DAOOAXHBKMQZRM-CTXHMNPMSA-N

> <FORMULA>
C20H22O10

> <MOLECULAR_WEIGHT>
422.386

> <EXACT_MASS>
422.121296908

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
41.46225911281586

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3R,4S,5S,6R)-2-({13-hydroxy-4,6-dimethoxy-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2(7),3,5,10,12-hexaen-5-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
0.30

> <JCHEM_LOGP>
-0.03929417100000007

> <ALOGPS_LOGS>
-2.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.200419833955804

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.336081914367682

> <JCHEM_PKA_STRONGEST_BASIC>
-2.916495944479445

> <JCHEM_POLAR_SURFACE_AREA>
151.21

> <JCHEM_REFRACTIVITY>
100.2594

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.54e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5S,6R)-2-({13-hydroxy-4,6-dimethoxy-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2(7),3,5,10,12-hexaen-5-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

> <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       2.259   0.973   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.783   2.438   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.277   2.758   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.754   1.613   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.278   0.149   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.228  -0.171   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.704  -1.636   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.211  -1.956   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.241  -0.812   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.747  -1.132   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.993  -0.227   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       8.239  -1.132   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.746  -0.812   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.776  -1.956   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.300  -3.421   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.794  -3.741   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.763  -2.597   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.223  -2.597   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.193  -3.741   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.687  -3.421   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.656  -4.565   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.150  -4.245   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.318  -5.206   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       3.765   0.653   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       4.796   1.797   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.308  -0.996   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -2.260   1.934   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -0.199   4.223   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.813   3.582   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.338   5.047   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   29                                                  
CONECT    3    2    4   28                                                  
CONECT    4    3    5   27                                                  
CONECT    5    4    6   26                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   20                                                  
CONECT    9    8   10   24                                                  
CONECT   10    9   11   18                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   12   18                                                  
CONECT   18   17   10   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19    8   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   16                                                            
CONECT   24    9   25                                                       
CONECT   25   24                                                            
CONECT   26    5                                                            
CONECT   27    4                                                            
CONECT   28    3                                                            
CONECT   29    2   30                                                       
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₂O₁₀

Average Mass

422.3860 Da

Monoisotopic Mass

422.12130 Da

IUPAC Name

(2S,3R,4S,5S,6R)-2-({13-hydroxy-4,6-dimethoxy-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2(7),3,5,10,12-hexaen-5-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

(2S,3R,4S,5S,6R)-2-({13-hydroxy-4,6-dimethoxy-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2(7),3,5,10,12-hexaen-5-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(OC3=C2C(O)=CC=C3)C(OC)=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C20H22O10/c1-26-11-6-8-13-9(22)4-3-5-10(13)28-17(8)19(27-2)18(11)30-20-16(25)15(24)14(23)12(7-21)29-20/h3-6,12,14-16,20-25H,7H2,1-2H3/t12-,14-,15+,16-,20+/m1/s1

InChI Key

DAOOAXHBKMQZRM-CTXHMNPMSA-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
Pyracantha fortuneana	LOTUS Database	35616633
Pyracantha fortuneana (MAXIM) LI	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Dibenzofuran
Hexose monosaccharide
O-glycosyl compound
Benzofuran
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Monosaccharide
Oxane
Furan
Heteroaromatic compound
Secondary alcohol
Acetal
Ether
Organoheterocyclic compound
Oxacycle
Polyol
Alcohol
Hydrocarbon derivative
Primary 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	0.3	ALOGPS
logP	-0.039	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	9.34	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	151.21 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	100.26 m³·mol⁻¹	ChemAxon
Polarizability	41.46 Å³	ChemAxon
Number of Rings	4	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

C00030327

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

24864266

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Fortuneanoside K (NP0071251)

MOL for NP0071251 ((-)-Fortuneanoside K)

3D MOL for NP0071251 ((-)-Fortuneanoside K)

3D SDF for NP0071251 ((-)-Fortuneanoside K)

3D-SDF for NP0071251 ((-)-Fortuneanoside K)

PDB for NP0071251 ((-)-Fortuneanoside K)

3D PDB for NP0071251 ((-)-Fortuneanoside K)

SMILES for NP0071251 ((-)-Fortuneanoside K)

INCHI for NP0071251 ((-)-Fortuneanoside K)

Structure for NP0071251 ((-)-Fortuneanoside K)

3D Structure for NP0071251 ((-)-Fortuneanoside K)