NP-MRD: Showing NP-Card for (-)-Stelliferin riboside (NP0078101)

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Record Information

Version

2.0

Created at

2022-04-28 23:14:03 UTC

Updated at

2022-04-28 23:14:03 UTC

NP-MRD ID

NP0078101

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Stelliferin riboside

Description

(3E,3aS,5aR,7R,9aR,9bS)-3-[(3E,5E,7S)-6,10-dimethyl-7-{[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}undeca-3,5,9-trien-2-ylidene]-3a,6,6,9a-tetramethyl-2-oxo-dodecahydro-1H-cyclopenta[a]naphthalen-7-yl acetate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (-)-Stelliferin riboside is found in Geodia globostellifera and Rhabdastrella globostellata. Based on a literature review very few articles have been published on (3E,3aS,5aR,7R,9aR,9bS)-3-[(3E,5E,7S)-6,10-dimethyl-7-{[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}undeca-3,5,9-trien-2-ylidene]-3a,6,6,9a-tetramethyl-2-oxo-dodecahydro-1H-cyclopenta[a]naphthalen-7-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292201142D          

 45 48  0  0  1  0            999 V2000
    2.3637    0.3610    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7983    1.0622    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4083    1.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837    1.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491    1.1137    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5391    0.3867    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1045   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.4383    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3245    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3612    1.5983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3215    1.9645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    0.4640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3247    1.1910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1493    1.2168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8901    1.8923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2295    1.3982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0833    2.2101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7133    2.7427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5671    3.5547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6896    8.4263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.9410    6.4971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.9734    3.8080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0058    1.1189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6601    0.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3613   -0.3918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8963   -0.2691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3038    1.7142    0.0000 C   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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  9 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
  6 17  1  6  0  0  0
  2 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
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 24 25  1  1  0  0  0
 26 25  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
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 26 31  1  0  0  0  0
 29 32  1  6  0  0  0
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 27 34  1  6  0  0  0
 24 35  1  0  0  0  0
 35 36  1  0  0  0  0
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 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 23 40  1  0  0  0  0
 19 41  1  0  0  0  0
 18 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
  1 44  1  1  0  0  0
  2 45  1  1  0  0  0
M  END

     RDKit          3D

101104  0  0  0  0  0  0  0  0999 V2000
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    6.4488    0.8020    1.5337 C   0  0  2  0  0  0  0  0  0  0  0  0
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 39 90  1  0
 40 91  1  0
 40 92  1  0
 41 93  1  0
 41 94  1  0
 42 95  1  6
 44 96  1  0
 44 97  1  0
 44 98  1  0
 45 99  1  0
 45100  1  0
 45101  1  0
  5 49  1  6
  6 50  1  0
  6 51  1  0
  7 52  1  0
  7 53  1  0
  9 54  1  0
  9 55  1  0
  9 56  1  0
  1 46  1  0
  1 47  1  0
  1 48  1  0
M  END


  Mrv1652304292201142D          

 45 48  0  0  1  0            999 V2000
    2.3637    0.3610    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7983    1.0622    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4083    1.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837    1.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491    1.1137    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5391    0.3867    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1045   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.4383    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3245    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3612    1.5983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3215    1.9645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    0.4640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3247    1.1910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1493    1.2168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8901    1.8923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9291   -0.3403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995    0.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2295    1.3982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0833    2.2101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7133    2.7427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5671    3.5547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1971    4.0873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0509    4.8992    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2746    5.1785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1283    5.9905    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3521    6.2698    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2058    7.0817    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8359    7.6144    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6121    7.3350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7584    6.5231    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6896    8.4263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4295    7.3610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7220    5.7372    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6809    5.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5347    6.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1647    6.7764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9410    6.4971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0185    7.5883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9734    3.8080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0058    1.1189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6601    0.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3613   -0.3918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8963   -0.2691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3038    1.7142    0.0000 C   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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  9 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
  6 17  1  6  0  0  0
  2 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 26 25  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 26 31  1  0  0  0  0
 29 32  1  6  0  0  0
 28 33  1  6  0  0  0
 27 34  1  6  0  0  0
 24 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 23 40  1  0  0  0  0
 19 41  1  0  0  0  0
 18 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
  1 44  1  1  0  0  0
  2 45  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0078101

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CC[C@H](O[C@H]1OC[C@@H](O)[C@@H](O)[C@H]1O)C(\C)=C\C=C\C(\C)=C1\C(=O)C[C@@H]2[C@]1(C)CC[C@H]1C(C)(C)[C@@H](CC[C@]21C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C37H56O8/c1-21(2)13-14-27(45-34-33(42)32(41)26(40)20-43-34)22(3)11-10-12-23(4)31-25(39)19-29-36(8)18-16-30(44-24(5)38)35(6,7)28(36)15-17-37(29,31)9/h10-13,26-30,32-34,40-42H,14-20H2,1-9H3/b12-10+,22-11+,31-23-/t26-,27+,28+,29+,30-,32-,33-,34-,36+,37+/m1/s1

> <INCHI_KEY>
DIFMBIWQHJHMSC-KITYKYSESA-N

> <FORMULA>
C37H56O8

> <MOLECULAR_WEIGHT>
628.847

> <EXACT_MASS>
628.397518763

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
101

> <JCHEM_AVERAGE_POLARIZABILITY>
71.97772617271215

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3E,3aS,5aR,7R,9aR,9bS)-3-[(3E,5E,7S)-6,10-dimethyl-7-{[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}undeca-3,5,9-trien-2-ylidene]-3a,6,6,9a-tetramethyl-2-oxo-dodecahydro-1H-cyclopenta[a]naphthalen-7-yl acetate

> <ALOGPS_LOGP>
5.64

> <JCHEM_LOGP>
5.1074986776666655

> <ALOGPS_LOGS>
-5.52

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.403064593844032

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.24575941127293

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5265808792916404

> <JCHEM_POLAR_SURFACE_AREA>
122.52000000000001

> <JCHEM_REFRACTIVITY>
176.30280000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.92e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3E,3aS,5aR,7R,9aR,9bS)-3-[(3E,5E,7S)-6,10-dimethyl-7-{[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}undeca-3,5,9-trien-2-ylidene]-3a,6,6,9a-tetramethyl-2-oxo-octahydrocyclopenta[a]naphthalen-7-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       4.412   0.674   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.223   1.983   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.495   3.340   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.956   3.388   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.145   2.079   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.873   0.722   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.062  -0.587   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.522  -0.539   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.206   0.818   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.606   2.127   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.674   2.984   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.600   3.667   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.745   0.866   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.473   2.223   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -4.012   2.271   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.662   3.532   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.601  -0.635   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.719   1.616   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.895   2.610   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.622   4.126   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.798   5.120   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.525   6.635   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.701   7.630   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.428   9.145   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       7.979   9.667   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.706  11.182   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.257  11.704   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.984  13.219   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.160  14.213   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.609  13.692   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       8.882  12.176   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       6.887  15.729   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       4.535  13.741   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       5.081  10.709   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      10.604  10.139   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.331  11.655   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      11.507  12.649   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      12.956  12.128   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      11.234  14.165   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      11.150   7.108   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       9.344   2.089   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       6.832   0.080   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       8.141  -0.731   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       5.406  -0.502   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       6.167   3.200   0.000  0.00  0.00           C+0
CONECT    1    2    6   44                                                  
CONECT    2    1    3   18   45                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    1    7   17                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   13                                                  
CONECT   10    9    5   11   12                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    9   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17    6                                                            
CONECT   18    2   19   42                                                  
CONECT   19   18   20   41                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   40                                                  
CONECT   24   23   25   35                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   31                                                  
CONECT   27   26   28   34                                                  
CONECT   28   27   29   33                                                  
CONECT   29   28   30   32                                                  
CONECT   30   29   31                                                       
CONECT   31   30   26                                                       
CONECT   32   29                                                            
CONECT   33   28                                                            
CONECT   34   27                                                            
CONECT   35   24   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   23                                                            
CONECT   41   19                                                            
CONECT   42   18   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42    1                                                       
CONECT   45    2                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   96    0
END

View in JSmol

Synonyms

Value	Source
(3E,3AS,5ar,7R,9ar,9BS)-3-[(3E,5E,7S)-6,10-dimethyl-7-{[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}undeca-3,5,9-trien-2-ylidene]-3a,6,6,9a-tetramethyl-2-oxo-dodecahydro-1H-cyclopenta[a]naphthalen-7-yl acetic acid	Generator

Chemical Formula

C₃₇H₅₆O₈

Average Mass

628.8470 Da

Monoisotopic Mass

628.39752 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(C)=CC[C@H](O[C@H]1OC[C@@H](O)[C@@H](O)[C@H]1O)C(\C)=C\C=C\C(\C)=C1\C(=O)C[C@@H]2[C@]1(C)CC[C@H]1C(C)(C)[C@@H](CC[C@]21C)OC(C)=O

InChI Identifier

InChI=1S/C37H56O8/c1-21(2)13-14-27(45-34-33(42)32(41)26(40)20-43-34)22(3)11-10-12-23(4)31-25(39)19-29-36(8)18-16-30(44-24(5)38)35(6,7)28(36)15-17-37(29,31)9/h10-13,26-30,32-34,40-42H,14-20H2,1-9H3/b12-10+,22-11+,31-23-/t26-,27+,28+,29+,30-,32-,33-,34-,36+,37+/m1/s1

InChI Key

DIFMBIWQHJHMSC-KITYKYSESA-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
Geodia globostellifera	Animalia	KNApSAcK
Rhabdastrella globostellata	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
O-glycosyl compound
Glycosyl compound
Oxane
Monosaccharide
Cyclic ketone
Secondary alcohol
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	5.64	ALOGPS
logP	5.11	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	12.25	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	122.52 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	176.3 m³·mol⁻¹	ChemAxon
Polarizability	71.98 Å³	ChemAxon
Number of Rings	4	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

162898627

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Stelliferin riboside (NP0078101)

MOL for NP0078101 ((-)-Stelliferin riboside)

3D MOL for NP0078101 ((-)-Stelliferin riboside)

3D SDF for NP0078101 ((-)-Stelliferin riboside)

3D-SDF for NP0078101 ((-)-Stelliferin riboside)

PDB for NP0078101 ((-)-Stelliferin riboside)

3D PDB for NP0078101 ((-)-Stelliferin riboside)

SMILES for NP0078101 ((-)-Stelliferin riboside)

INCHI for NP0078101 ((-)-Stelliferin riboside)

Structure for NP0078101 ((-)-Stelliferin riboside)

3D Structure for NP0078101 ((-)-Stelliferin riboside)