NP-MRD: Showing NP-Card for Rumphioside A (NP0331658)

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Record Information

Version

2.0

Created at

2023-05-31 12:00:50 UTC

Updated at

2024-09-03 04:16:24 UTC

NP-MRD ID

NP0331658

Natural Product DOI

https://doi.org/10.57994/0648

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Rumphioside A

Description

Rumphioside A belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated. Rumphioside A was first documented in 2023 (PMID: 37200063). Based on a literature review very few articles have been published on Rumphioside A.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305312314002D          

 42 46  0  0  1  0            999 V2000
    2.0329    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.6039    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    2.0329    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6829    2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    2.7474    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4454    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    3.4618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    3.4618    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2704    4.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    3.4618    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9204    4.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204    2.7474    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7454    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3329    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0954   -0.1105    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0329   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3684   -3.0076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7553   -3.5596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8416   -4.3801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0409   -3.1471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2124   -2.3402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6604   -1.7271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  6  0  0  0
  6 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 21 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 19 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
  3 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  1  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 35 40  1  0  0  0  0
 40 41  2  0  0  0  0
 34 42  1  0  0  0  0
  2 42  1  0  0  0  0
M  END


  Mrv1652305312314002D          

 42 46  0  0  1  0            999 V2000
    2.0329    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.6039    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    2.0329    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6829    2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    2.7474    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4454    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    3.4618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    3.4618    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2704    4.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    3.4618    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9204    4.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204    2.7474    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7454    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3329    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0954   -0.1105    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0329   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3684   -3.0076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7553   -3.5596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8416   -4.3801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0409   -3.1471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2124   -2.3402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6604   -1.7271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  6  0  0  0
  6 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 21 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 19 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
  3 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  1  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 35 40  1  0  0  0  0
 40 41  2  0  0  0  0
 34 42  1  0  0  0  0
  2 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0331658

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12CC(O[C@H]3O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]3O)[C@@]3(C)C(=CCC[C@@]3([H])[C@]1(C)C[C@H](OC2=O)C1=CC(O)OC1=O)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C27H36O13/c1-26-9-14(11-7-18(29)40-22(11)33)37-24(35)13(26)8-17(27(2)12(23(34)36-3)5-4-6-16(26)27)39-25-21(32)20(31)19(30)15(10-28)38-25/h5,7,13-21,25,28-32H,4,6,8-10H2,1-3H3/t13-,14-,15-,16-,17?,18?,19-,20+,21-,25+,26+,27-/m0/s1

> <INCHI_KEY>
AWJJHUWOCLBMBI-ODIZXGNZSA-N

> <FORMULA>
C27H36O13

> <MOLECULAR_WEIGHT>
568.572

> <EXACT_MASS>
568.215591219

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
56.02418742099495

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2S,4aR,6aR,10aS,10bS)-2-(5-hydroxy-2-oxo-2,5-dihydrofuran-3-yl)-6a,10b-dimethyl-4-oxo-6-{[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,2H,4H,4aH,5H,6H,6aH,9H,10H,10aH,10bH-naphtho[2,1-c]pyran-7-carboxylate

> <JCHEM_LOGP>
-0.2346913583333353

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.331298054790476

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.643560895870266

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835454156583

> <JCHEM_POLAR_SURFACE_AREA>
198.51

> <JCHEM_REFRACTIVITY>
132.5109

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2S,4aR,6aR,10aS,10bS)-2-(5-hydroxy-2-oxo-5H-furan-3-yl)-6a,10b-dimethyl-4-oxo-6-{[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,2H,4aH,5H,6H,9H,10H,10aH-naphtho[2,1-c]pyran-7-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 31-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   31-MAY-23         0                                  
HETATM    1  O   UNK     0       3.795   1.127   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.105  -0.206   0.000  0.00  0.00           C+0
HETATM    4  H   UNK     0       5.335   1.127   0.000  0.00  0.00           H+0
HETATM    5  C   UNK     0       6.875   1.127   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.415   1.127   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.185   2.461   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.415   3.795   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.875   3.795   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.105   5.128   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.565   5.128   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.795   6.462   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.875   6.462   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.105   7.796   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.415   6.462   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.185   7.796   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.185   5.128   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      10.725   5.128   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.955   1.127   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.495   1.127   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.725   2.461   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      11.495   3.795   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.035   1.127   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.185  -2.874   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   30  H   UNK     0       7.645  -0.206   0.000  0.00  0.00           H+0
HETATM   31  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.645  -2.874   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.105  -2.874   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.795  -4.207   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.421  -5.614   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.277  -6.645   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       3.438  -8.176   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       1.943  -5.875   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       2.263  -4.368   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       1.233  -3.224   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       3.795  -1.540   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   42                                                  
CONECT    3    2    4    5   31                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   19                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   17                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    8   18                                                  
CONECT   18   17                                                            
CONECT   19    6   20   21   29                                             
CONECT   20   19                                                            
CONECT   21   19   22   26                                                  
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22                                                            
CONECT   26   21   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   19   30   31                                             
CONECT   30   29                                                            
CONECT   31   29    3   32   33                                             
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   42                                                  
CONECT   35   34   36   40                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   35   41                                                  
CONECT   41   40                                                            
CONECT   42   34    2                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₆O₁₃

Average Mass

568.5720 Da

Monoisotopic Mass

568.21559 Da

IUPAC Name

methyl (2S,4aR,6aR,10aS,10bS)-2-(5-hydroxy-2-oxo-2,5-dihydrofuran-3-yl)-6a,10b-dimethyl-4-oxo-6-{[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,2H,4H,4aH,5H,6H,6aH,9H,10H,10aH,10bH-naphtho[2,1-c]pyran-7-carboxylate

Traditional Name

methyl (2S,4aR,6aR,10aS,10bS)-2-(5-hydroxy-2-oxo-5H-furan-3-yl)-6a,10b-dimethyl-4-oxo-6-{[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,2H,4aH,5H,6H,9H,10H,10aH-naphtho[2,1-c]pyran-7-carboxylate

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC(O[C@H]3O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]3O)[C@@]3(C)C(=CCC[C@@]3([H])[C@]1(C)C[C@H](OC2=O)C1=CC(O)OC1=O)C(=O)OC

InChI Identifier

InChI=1S/C27H36O13/c1-26-9-14(11-7-18(29)40-22(11)33)37-24(35)13(26)8-17(27(2)12(23(34)36-3)5-4-6-16(26)27)39-25-21(32)20(31)19(30)15(10-28)38-25/h5,7,13-21,25,28-32H,4,6,8-10H2,1-3H3/t13-,14-,15-,16-,17?,18?,19-,20+,21-,25+,26+,27-/m0/s1

InChI Key

AWJJHUWOCLBMBI-ODIZXGNZSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View

Predicted Spectra

Not Available

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 400, CD₃OD, simulated)	Not Available	Not Available	Not Available	2024-05-11	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
crispa		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Diterpene glycosides

Alternative Parents

Substituents

Diterpene glycoside
Clerodane diterpenoid
Diterpenoid
Diterpene lactone
Fatty acyl glycoside of mono- or disaccharide
Fatty acyl glycoside
Naphthopyran
Fatty alcohol ester
Alkyl glycoside
Naphthalene
Tricarboxylic acid or derivatives
Fatty alcohol
Delta_valerolactone
Fatty acid ester
Delta valerolactone
Fatty acyl
Pyran
Oxane
Monosaccharide
2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Dihydrofuran
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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	-0.23	ChemAxon
pKa (Strongest Acidic)	11.64	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	198.51 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	132.51 m³·mol⁻¹	ChemAxon
Polarizability	56.02 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Rumphioside A (NP0331658)

MOL for NP0331658 (Rumphioside A)

3D MOL for NP0331658 (Rumphioside A)

3D SDF for NP0331658 (Rumphioside A)

3D-SDF for NP0331658 (Rumphioside A)

PDB for NP0331658 (Rumphioside A)

3D PDB for NP0331658 (Rumphioside A)

SMILES for NP0331658 (Rumphioside A)

INCHI for NP0331658 (Rumphioside A)

Structure for NP0331658 (Rumphioside A)

3D Structure for NP0331658 (Rumphioside A)