NP-MRD: Showing NP-Card for 3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione (NP0248953)

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Record Information

Version

2.0

Created at

2022-09-07 11:23:01 UTC

Updated at

2022-09-07 11:23:01 UTC

NP-MRD ID

NP0248953

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

Description

3,6,9-Trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. 3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione is found in Taraxacum alpinum, Taraxacum obovatum and Taraxacum platycarpum. 3,6,9-Trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191523592D          

 30 33  0  0  0  0            999 V2000
    3.6754    3.7963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0304    3.2819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2140    2.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6996    1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8746    1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4201    1.1441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6248    1.3636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0202    0.8492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5878    2.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2280    2.0648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3803    2.9862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4150    3.2057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6226    4.0041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4178    4.2236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6254    5.0221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4207    5.2416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0056    3.6446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8008    3.8641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7980    2.8462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3857    2.2672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0027    2.6267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7952    1.8282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3602    2.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5438    3.2819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2871    3.6399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1541    1.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9493    1.3636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9864    2.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6749    2.6422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8642    0.3717    0.0000 C   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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
  9 23  1  0  0  0  0
  5 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  2 25  1  0  0  0  0
  4 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
  3 28  1  0  0  0  0
 28 29  2  0  0  0  0
 26 30  1  0  0  0  0
M  END

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
   -3.0664   -3.5052    1.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3746   -2.0416    1.0476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6049   -1.6115    1.1919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6905   -0.1718    1.0154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7588    0.5368    1.0981 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3316    0.2662    0.7330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0572    1.5453    0.4937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2517    2.4643    0.5424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8307    2.2142    0.1971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6457    1.3146   -0.0506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0971    0.2394   -0.9418 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4772   -1.0574   -0.2472 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7695   -1.8207   -1.4032 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8363   -1.4892   -2.3638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6356   -1.9502   -3.4738 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0094   -0.3276   -1.7729 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3083    0.6199   -2.9444 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0110   -0.7729   -1.1257 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9743   -0.4537   -0.3227 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2426   -0.4467   -1.0284 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0869    0.5010   -0.4844 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7797    1.9146   -0.8794 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8669    2.0528   -2.2834 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1833    0.3257    1.0221 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5814    1.3146    1.7507 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6507   -1.0505    1.3928 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5238   -2.0118    0.8963 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2482   -1.2910    0.8979 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3592   -0.9213    1.9029 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5037   -0.9241    0.7752 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0089   -3.6911    1.3391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4201   -4.0862    0.3135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6132   -3.8852    2.0761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5072   -2.2138    1.4191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6483    2.4977    1.5573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9649    2.2165   -0.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9283    3.5135    0.3177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5551    2.9531    1.0135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8753    2.8849   -0.7192 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1568    1.9622   -0.5245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2367    0.9097    0.8790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9631    0.5668   -1.6060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5447   -1.4747    0.1421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1004    0.2030   -3.5662 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4866    1.6021   -2.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6176    0.6618   -3.5549 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9247    0.6021    0.0022 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0962    0.2724   -0.9394 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8153    2.3021   -0.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6352    2.5550   -0.5082 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7586    1.1695   -2.6859 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2568    0.3178    1.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1285    2.1073    1.9186 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6991   -1.1084    2.4995 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4033   -1.5852    0.7306 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0782   -2.3747    0.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3728   -1.5422    2.6670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9231   -0.7979    1.7627 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 16 18  1  1
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 21 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 12 30  1  0
 30  2  1  0
 30  6  1  0
 16 11  1  0
 28 19  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  8 35  1  0
  8 36  1  0
  8 37  1  0
  9 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  6
 12 43  1  1
 17 44  1  0
 17 45  1  0
 17 46  1  0
 19 47  1  1
 21 48  1  6
 22 49  1  0
 22 50  1  0
 23 51  1  0
 24 52  1  1
 25 53  1  0
 26 54  1  1
 27 55  1  0
 28 56  1  6
 29 57  1  0
 30 58  1  1
M  END


  Mrv1533004191523592D          

 30 33  0  0  0  0            999 V2000
    3.6754    3.7963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0304    3.2819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2140    2.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6996    1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8746    1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4201    1.1441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6248    1.3636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0202    0.8492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5878    2.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2280    2.0648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3803    2.9862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4150    3.2057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6226    4.0041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4178    4.2236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6254    5.0221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4207    5.2416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0056    3.6446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8008    3.8641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7980    2.8462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3857    2.2672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0027    2.6267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7952    1.8282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3602    2.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5438    3.2819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2871    3.6399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1541    1.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9493    1.3636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9864    2.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6749    2.6422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8642    0.3717    0.0000 C   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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
  9 23  1  0  0  0  0
  5 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  2 25  1  0  0  0  0
  4 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
  3 28  1  0  0  0  0
 28 29  2  0  0  0  0
 26 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0248953

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(=O)C2=C(C)CCC3C(OC(=O)C3(C)OC3OC(CO)C(O)C(O)C3O)C12

> <INCHI_IDENTIFIER>
InChI=1S/C21H28O9/c1-8-4-5-10-18(14-9(2)6-11(23)13(8)14)29-20(27)21(10,3)30-19-17(26)16(25)15(24)12(7-22)28-19/h6,10,12,14-19,22,24-26H,4-5,7H2,1-3H3

> <INCHI_KEY>
FVSUVYLVYCAWSC-UHFFFAOYSA-N

> <FORMULA>
C21H28O9

> <MOLECULAR_WEIGHT>
424.446

> <EXACT_MASS>
424.173332482

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
43.37530357787681

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

> <ALOGPS_LOGP>
-0.20

> <JCHEM_LOGP>
-0.24402809899999967

> <ALOGPS_LOGS>
-1.92

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.194171623805396

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.20871119766913

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981083879796051

> <JCHEM_POLAR_SURFACE_AREA>
142.75000000000003

> <JCHEM_REFRACTIVITY>
102.6618

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.09e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3aH,4H,5H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       6.861   7.086   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.657   6.126   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.999   4.625   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.039   3.421   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.499   3.421   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.651   2.136   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.166   2.545   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.038   1.585   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.097   4.084   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.426   3.854   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.710   5.574   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.775   5.984   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.162   7.474   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.647   7.884   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.034   9.375   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -4.519   9.784   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.744   6.803   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -5.228   7.213   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -3.356   5.313   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -4.453   4.232   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.872   4.903   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -1.484   3.413   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.539   4.625   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.882   6.126   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.269   6.794   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.888   2.136   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.372   2.545   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.441   4.084   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.726   4.932   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.346   0.694   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4   28                                                  
CONECT    4    3    5   26                                                  
CONECT    5    4    6   23                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11   23                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   21                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   12   22                                                  
CONECT   22   21                                                            
CONECT   23    9    5   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24    2                                                       
CONECT   26    4   27   30                                                  
CONECT   27   26   28                                                       
CONECT   28   27    3   29                                                  
CONECT   29   28                                                            
CONECT   30   26                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₈O₉

Average Mass

424.4460 Da

Monoisotopic Mass

424.17333 Da

IUPAC Name

3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

Traditional Name

3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3aH,4H,5H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

CAS Registry Number

Not Available

SMILES

CC1=CC(=O)C2=C(C)CCC3C(OC(=O)C3(C)OC3OC(CO)C(O)C(O)C3O)C12

InChI Identifier

InChI=1S/C21H28O9/c1-8-4-5-10-18(14-9(2)6-11(23)13(8)14)29-20(27)21(10,3)30-19-17(26)16(25)15(24)12(7-22)28-19/h6,10,12,14-19,22,24-26H,4-5,7H2,1-3H3

InChI Key

FVSUVYLVYCAWSC-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Taraxacum alpinum	LOTUS Database	35616633
Taraxacum obovatum	LOTUS Database	35616633
Taraxacum platycarpum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Gamma butyrolactone
Monosaccharide
Oxane
Tetrahydrofuran
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Organoheterocyclic compound
Polyol
Oxacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Acetal
Primary alcohol
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Alcohol
Carbonyl group
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	-0.2	ALOGPS
logP	-0.24	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	142.75 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	102.66 m³·mol⁻¹	ChemAxon
Polarizability	43.38 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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione (NP0248953)

MOL for NP0248953 (3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D MOL for NP0248953 (3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D SDF for NP0248953 (3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D-SDF for NP0248953 (3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

PDB for NP0248953 (3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D PDB for NP0248953 (3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

SMILES for NP0248953 (3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

INCHI for NP0248953 (3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

Structure for NP0248953 (3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D Structure for NP0248953 (3,6,9-trimethyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)