NP-MRD: Showing NP-Card for (1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one (NP0252669)

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Record Information

Version

2.0

Created at

2022-09-07 16:15:21 UTC

Updated at

2022-09-07 16:15:21 UTC

NP-MRD ID

NP0252669

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one

Description

(1R,3R,5S,7R,8S,9R,10S,12R,14S,15R,17R,18S,19R,22S,23S)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2,5-dihydrofuran-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]Pentacosan-16-one belongs to the class of organic compounds known as cardenolide glycosides and derivatives. Cardenolide glycosides and derivatives are compounds containing a carbohydrate glycosidically bound to the cardenolide moiety. (1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one is found in Anodendron affine. Based on a literature review very few articles have been published on (1R,3R,5S,7R,8S,9R,10S,12R,14S,15R,17R,18S,19R,22S,23S)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2,5-dihydrofuran-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]Pentacosan-16-one.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309072218152D          

 41 47  0  0  1  0            999 V2000
   -3.1873    1.0606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9680    0.7939    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1274   -0.0155    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9081   -0.2822    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.5294    0.2606    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0675   -1.0917    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8483   -1.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4462   -1.6345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6655   -1.3678    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0442   -1.9106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2635   -1.6439    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6422   -2.1867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8615   -1.9200    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2402   -2.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5405   -2.1961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6999   -1.3867    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0786   -0.8439    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2380   -0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3833    0.5083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0188    0.2322    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1782    1.0417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6401   -0.3106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8832    0.4778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4591   -0.2120    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8609    0.5085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5141    1.2571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1188    1.8182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0203    2.6373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8394    1.4165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6800    0.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8060   -0.9606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2012   -1.5218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4806   -1.1200    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4067   -1.9417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7021   -1.1106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5427   -0.3011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3234   -0.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1041   -0.8344    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7254   -0.2917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5061   -0.5583    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3467    0.2511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
 24 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 16 33  1  0  0  0  0
 22 33  1  0  0  0  0
 33 34  1  1  0  0  0
 17 35  1  0  0  0  0
 13 35  1  0  0  0  0
 35 36  1  1  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 11 38  1  0  0  0  0
 38 39  1  6  0  0  0
 39 40  1  0  0  0  0
  9 40  1  0  0  0  0
  3 40  1  0  0  0  0
 40 41  1  1  0  0  0
M  END


  Mrv1652309072218152D          

 41 47  0  0  1  0            999 V2000
   -3.1873    1.0606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9680    0.7939    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1274   -0.0155    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9081   -0.2822    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.5294    0.2606    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0675   -1.0917    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8483   -1.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4462   -1.6345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6655   -1.3678    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0442   -1.9106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2635   -1.6439    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6422   -2.1867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8615   -1.9200    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2402   -2.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5405   -2.1961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6999   -1.3867    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0786   -0.8439    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2380   -0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3833    0.5083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0188    0.2322    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1782    1.0417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6401   -0.3106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8832    0.4778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4591   -0.2120    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8609    0.5085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5141    1.2571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1188    1.8182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0203    2.6373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8394    1.4165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6800    0.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8060   -0.9606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2012   -1.5218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4806   -1.1200    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4067   -1.9417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7021   -1.1106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5427   -0.3011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3234   -0.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1041   -0.8344    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7254   -0.2917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5061   -0.5583    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3467    0.2511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
 24 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 16 33  1  0  0  0  0
 22 33  1  0  0  0  0
 33 34  1  1  0  0  0
 17 35  1  0  0  0  0
 13 35  1  0  0  0  0
 35 36  1  1  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 11 38  1  0  0  0  0
 38 39  1  6  0  0  0
 39 40  1  0  0  0  0
  9 40  1  0  0  0  0
  3 40  1  0  0  0  0
 40 41  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0252669

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1[C@@H](O)[C@@H](C)O[C@H]2O[C@@H]3C[C@H]4CC[C@H]5[C@@H](C(=O)[C@H](O)[C@]6(C)[C@H](CC[C@]56O)C5=CC(=O)OC5)[C@@]4(C)C[C@H]3O[C@@]12O

> <INCHI_IDENTIFIER>
InChI=1S/C30H42O11/c1-13-22(32)25(37-4)30(36)26(39-13)40-18-10-15-5-6-17-21(27(15,2)11-19(18)41-30)23(33)24(34)28(3)16(7-8-29(17,28)35)14-9-20(31)38-12-14/h9,13,15-19,21-22,24-26,32,34-36H,5-8,10-12H2,1-4H3/t13-,15-,16-,17+,18-,19-,21+,22+,24+,25-,26+,27+,28+,29+,30+/m1/s1

> <INCHI_KEY>
GUJNEGVSJKEOLL-ODBBJSKOSA-N

> <FORMULA>
C30H42O11

> <MOLECULAR_WEIGHT>
578.655

> <EXACT_MASS>
578.272712172

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
59.89570574838067

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,3R,5S,7R,8S,9R,10S,12R,14S,15R,17R,18S,19R,22S,23S)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2,5-dihydrofuran-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0^{3,12}.0^{5,10}.0^{15,23}.0^{18,22}]pentacosan-16-one

> <JCHEM_LOGP>
1.245262331333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.36941825151227

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.142811908298031

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2133653681271923

> <JCHEM_POLAR_SURFACE_AREA>
161.21

> <JCHEM_REFRACTIVITY>
140.58559999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3R,5S,7R,8S,9R,10S,12R,14S,15R,17R,18S,19R,22S,23S)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2H-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0^{3,12}.0^{5,10}.0^{15,23}.0^{18,22}]pentacosan-16-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.950   1.980   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -7.407   1.482   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -7.704  -0.029   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.162  -0.527   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0     -10.322   0.486   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -9.459  -2.038   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -10.917  -2.536   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -8.300  -3.051   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -6.842  -2.553   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -5.683  -3.566   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -4.225  -3.069   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.065  -4.082   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.608  -3.584   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.448  -4.597   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.009  -4.099   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.307  -2.588   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.147  -1.575   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.444  -0.064   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.715   0.949   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.902   0.433   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.199   1.944   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.061  -0.580   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.515   0.892   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.590  -0.396   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.340   0.949   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.693   2.347   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.822   3.394   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.638   4.923   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       7.167   2.644   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.869   1.133   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.238  -1.793   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.109  -2.841   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.764  -2.091   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       2.626  -3.625   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -1.311  -2.073   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -1.013  -0.562   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -2.470  -1.060   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -3.928  -1.558   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -5.087  -0.544   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -6.545  -1.042   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -6.247   0.469   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   40                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   40                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   38                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   35                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   33                                                  
CONECT   17   16   18   35                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24   33                                             
CONECT   23   22                                                            
CONECT   24   22   25   31                                                  
CONECT   25   24   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   25                                                       
CONECT   31   24   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   16   22   34                                             
CONECT   34   33                                                            
CONECT   35   17   13   36   37                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   11   39                                                  
CONECT   39   38   40                                                       
CONECT   40   39    9    3   41                                             
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   94    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₂O₁₁

Average Mass

578.6550 Da

Monoisotopic Mass

578.27271 Da

IUPAC Name

Traditional Name

(1R,3R,5S,7R,8S,9R,10S,12R,14S,15R,17R,18S,19R,22S,23S)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2H-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0^{3,12}.0^{5,10}.0^{15,23}.0^{18,22}]pentacosan-16-one

CAS Registry Number

Not Available

SMILES

CO[C@@H]1[C@@H](O)[C@@H](C)O[C@H]2O[C@@H]3C[C@H]4CC[C@H]5[C@@H](C(=O)[C@H](O)[C@]6(C)[C@H](CC[C@]56O)C5=CC(=O)OC5)[C@@]4(C)C[C@H]3O[C@@]12O

InChI Identifier

InChI=1S/C30H42O11/c1-13-22(32)25(37-4)30(36)26(39-13)40-18-10-15-5-6-17-21(27(15,2)11-19(18)41-30)23(33)24(34)28(3)16(7-8-29(17,28)35)14-9-20(31)38-12-14/h9,13,15-19,21-22,24-26,32,34-36H,5-8,10-12H2,1-4H3/t13-,15-,16-,17+,18-,19-,21+,22+,24+,25-,26+,27+,28+,29+,30+/m1/s1

InChI Key

GUJNEGVSJKEOLL-ODBBJSKOSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Anodendron affine	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cardenolide glycosides and derivatives. Cardenolide glycosides and derivatives are compounds containing a carbohydrate glycosidically bound to the cardenolide moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Cardenolide glycosides and derivatives

Alternative Parents

Substituents

Cardanolide-glycoside
12-hydroxysteroid
14-hydroxysteroid
Oxosteroid
11-oxosteroid
Hydroxysteroid
Para-dioxane
2-furanone
Oxane
Monosaccharide
Cyclic alcohol
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Carboxylic acid ester
Hemiacetal
Secondary alcohol
Ketone
Lactone
Acetal
Ether
Organoheterocyclic compound
Dialkyl ether
Oxacycle
Carboxylic acid derivative
Polyol
Monocarboxylic acid or derivatives
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organooxygen compound
Organic oxide
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	1.25	ChemAxon
pKa (Strongest Acidic)	7.14	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	161.21 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	140.59 m³·mol⁻¹	ChemAxon
Polarizability	59.9 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

163004541

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one (NP0252669)

MOL for NP0252669 ((1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one)

3D MOL for NP0252669 ((1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one)

3D SDF for NP0252669 ((1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one)

3D-SDF for NP0252669 ((1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one)

PDB for NP0252669 ((1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one)

3D PDB for NP0252669 ((1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one)

SMILES for NP0252669 ((1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one)

INCHI for NP0252669 ((1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one)

Structure for NP0252669 ((1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one)

3D Structure for NP0252669 ((1r,3r,5s,7r,8s,9r,10s,12r,14s,15r,17r,18s,19r,22s,23s)-8,10,17,22-tetrahydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosan-16-one)