NP-MRD: Showing NP-Card for Suspensolide F (NP0057596)

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Record Information

Version

2.0

Created at

2022-04-28 03:00:39 UTC

Updated at

2022-04-28 03:00:39 UTC

NP-MRD ID

NP0057596

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Suspensolide F

Description

(1S,4aS,6S,7R,7aS)-6,7-dihydroxy-7-(hydroxymethyl)-4-({[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-1-yl 3-methylbutanoate belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. Suspensolide F is found in Viburnum suspensum. Based on a literature review very few articles have been published on (1S,4aS,6S,7R,7aS)-6,7-dihydroxy-7-(hydroxymethyl)-4-({[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-1-yl 3-methylbutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282205002D          

 33 35  0  0  1  0            999 V2000
   -3.5724    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0294    3.2820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8499    3.3682    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1854    2.6145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2624    4.0827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2475    3.5451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8494    4.0871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4567    4.6455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.4302   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4302   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7158    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  1  0  0  0
  4  6  1  6  0  0  0
  3  7  1  1  0  0  0
  3  8  1  6  0  0  0
  8  9  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  1 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  6  0  0  0
 20 23  1  1  0  0  0
 19 24  1  1  0  0  0
 18 25  1  6  0  0  0
 25 26  1  0  0  0  0
 10 27  1  6  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  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
M  END

     RDKit          3D

 67 69  0  0  0  0  0  0  0  0999 V2000
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   -1.8202   -0.3554    0.4850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4644    0.8613    0.3616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8260    0.6240    0.2901 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2627    1.0289   -0.9485 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5485    0.8326   -1.2947 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9423    1.5634   -2.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2727    1.3005   -2.8413 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4925    1.0542   -0.1876 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.8017   -0.1955    0.4017 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8865    1.8728    0.9127 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.8373    1.9660    1.9292 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5948    1.2677    1.4159 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8194    2.2827    1.9450 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4363   -1.4766    0.7037 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5579   -2.2599   -0.5813 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6316   -3.2649   -0.2293 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0016   -4.2415    0.5754 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5743   -2.4921    0.6646 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7697   -2.3113   -0.0100 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9077   -3.2732    1.9230 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4646   -4.4765    1.5455 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8916   -1.1929    1.0059 C   0  0  1  0  0  0  0  0  0  0  0  0
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    5.3826    3.1606   -1.9221 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.3700    0.2328    0.8150 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7876   -0.0551   -0.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1427   -0.1634   -0.8784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3730    1.8362    0.4281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2474   -0.8557    1.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1337   -1.0126   -0.3610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9858   -0.4649    0.3564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6270   -0.2634   -1.5998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7527    2.6318   -2.5399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3404    1.1122   -3.3798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4841    0.3415   -2.7523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4445    1.5494   -0.4812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5356   -0.1004    1.0573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7338    2.9016    0.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5361    1.3376    2.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8386    0.5669    2.2240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0068    1.9595    2.3951 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4012   -2.7504   -0.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
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  7  8  1  0
  8  9  1  0
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 10 11  2  0
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 33  8  1  0
 23 14  1  0
 33 25  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  1
  3 38  1  0
  3 39  1  0
  3 40  1  0
  4 41  1  0
  4 42  1  0
  8 43  1  6
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 27 61  1  6
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 30 63  1  0
 31 64  1  0
 31 65  1  0
 32 66  1  0
 33 67  1  1
M  END


  Mrv1652304282205002D          

 33 35  0  0  1  0            999 V2000
   -3.5724    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0294    3.2820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8499    3.3682    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1854    2.6145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2624    4.0827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.8494    4.0871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.4302   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4302   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7158    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
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  1  5  1  1  0  0  0
  4  6  1  6  0  0  0
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  2 10  1  0  0  0  0
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 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  6  0  0  0
 20 23  1  1  0  0  0
 19 24  1  1  0  0  0
 18 25  1  6  0  0  0
 25 26  1  0  0  0  0
 10 27  1  6  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  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0057596

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC(=O)O[C@@H]1OC=C(CO[C@@H]2O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]2O)[C@H]2C[C@H](O)[C@](O)(CO)[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C21H34O12/c1-9(2)3-14(25)33-19-15-11(4-13(24)21(15,29)8-23)10(6-30-19)7-31-20-18(28)17(27)16(26)12(5-22)32-20/h6,9,11-13,15-20,22-24,26-29H,3-5,7-8H2,1-2H3/t11-,12-,13+,15-,16-,17-,18+,19+,20-,21-/m1/s1

> <INCHI_KEY>
HOCKGUMMVOPFFC-VMJZJKJGSA-N

> <FORMULA>
C21H34O12

> <MOLECULAR_WEIGHT>
478.491

> <EXACT_MASS>
478.205026535

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
47.8042168781824

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4aS,6S,7R,7aS)-6,7-dihydroxy-7-(hydroxymethyl)-4-({[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-1-yl 3-methylbutanoate

> <ALOGPS_LOGP>
-1.54

> <JCHEM_LOGP>
-2.7607181713333357

> <ALOGPS_LOGS>
-1.50

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.692963879359223

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.084749281221928

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835523452752

> <JCHEM_POLAR_SURFACE_AREA>
195.59999999999997

> <JCHEM_REFRACTIVITY>
108.40179999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.51e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4aS,6S,7R,7aS)-6,7-dihydroxy-7-(hydroxymethyl)-4-({[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-1H,4aH,5H,6H,7aH-cyclopenta[c]pyran-1-yl 3-methylbutanoate

> <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  C   UNK     0      -6.668   3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.655   6.126   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.186   6.287   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.813   4.880   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -7.956   7.621   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -4.195   6.618   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -5.319   7.629   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -6.453   8.672   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -8.002   1.540   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -8.002   0.000   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -9.336  -2.310   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0     -10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -10.669   0.000   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0     -10.669   1.540   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0     -13.337   0.000   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0     -13.337  -3.080   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0     -10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0     -12.003  -5.390   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -2.667   4.620   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -0.000   4.620   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
CONECT    1    2    5   13                                                  
CONECT    2    1    3   10                                                  
CONECT    3    2    4    7    8                                             
CONECT    4    3    5    6                                                  
CONECT    5    4    1                                                       
CONECT    6    4                                                            
CONECT    7    3                                                            
CONECT    8    3    9                                                       
CONECT    9    8                                                            
CONECT   10    2   11   27                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    1   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   25                                                  
CONECT   19   18   20   24                                                  
CONECT   20   19   21   23                                                  
CONECT   21   20   16   22                                                  
CONECT   22   21                                                            
CONECT   23   20                                                            
CONECT   24   19                                                            
CONECT   25   18   26                                                       
CONECT   26   25                                                            
CONECT   27   10   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

View in JSmol

Synonyms

Value	Source
(1S,4AS,6S,7R,7as)-6,7-dihydroxy-7-(hydroxymethyl)-4-({[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-1H,4ah,5H,6H,7H,7ah-cyclopenta[c]pyran-1-yl 3-methylbutanoic acid	Generator

Chemical Formula

C₂₁H₃₄O₁₂

Average Mass

478.4910 Da

Monoisotopic Mass

478.20503 Da

IUPAC Name

(1S,4aS,6S,7R,7aS)-6,7-dihydroxy-7-(hydroxymethyl)-4-({[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-1-yl 3-methylbutanoate

Traditional Name

(1S,4aS,6S,7R,7aS)-6,7-dihydroxy-7-(hydroxymethyl)-4-({[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-1H,4aH,5H,6H,7aH-cyclopenta[c]pyran-1-yl 3-methylbutanoate

CAS Registry Number

Not Available

SMILES

CC(C)CC(=O)O[C@@H]1OC=C(CO[C@@H]2O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]2O)[C@H]2C[C@H](O)[C@](O)(CO)[C@@H]12

InChI Identifier

InChI=1S/C21H34O12/c1-9(2)3-14(25)33-19-15-11(4-13(24)21(15,29)8-23)10(6-30-19)7-31-20-18(28)17(27)16(26)12(5-22)32-20/h6,9,11-13,15-20,22-24,26-29H,3-5,7-8H2,1-2H3/t11-,12-,13+,15-,16-,17-,18+,19+,20-,21-/m1/s1

InChI Key

HOCKGUMMVOPFFC-VMJZJKJGSA-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
Viburnum suspensum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Terpene glycosides

Alternative Parents

Substituents

Terpene glycoside
Hexose monosaccharide
O-glycosyl compound
Iridoid-skeleton
Glycosyl compound
Monoterpenoid
Bicyclic monoterpenoid
Fatty acid ester
Fatty acyl
Oxane
Monosaccharide
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
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	-1.5	ALOGPS
logP	-2.8	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	12.08	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	195.6 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	108.4 m³·mol⁻¹	ChemAxon
Polarizability	47.8 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

162956839

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Suspensolide F (NP0057596)

MOL for NP0057596 (Suspensolide F)

3D MOL for NP0057596 (Suspensolide F)

3D SDF for NP0057596 (Suspensolide F)

3D-SDF for NP0057596 (Suspensolide F)

PDB for NP0057596 (Suspensolide F)

3D PDB for NP0057596 (Suspensolide F)

SMILES for NP0057596 (Suspensolide F)

INCHI for NP0057596 (Suspensolide F)

Structure for NP0057596 (Suspensolide F)

3D Structure for NP0057596 (Suspensolide F)