NP-MRD: Showing NP-Card for convalloside (NP0210134)

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Record Information

Version

2.0

Created at

2022-09-05 07:49:26 UTC

Updated at

2022-09-05 07:49:26 UTC

NP-MRD ID

NP0210134

Secondary Accession Numbers

None

Natural Product Identification

Common Name

convalloside

Description

Convalloside, also known as bogoroside, 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. Convalloside is an extremely weak basic (essentially neutral) compound (based on its pKa). Convalloside is a potentially toxic compound. Convalloside is a constituent of seeds of Convallaria majalis. convalloside is found in Antiaris toxicaria and Erysimum cheiranthoides. Constituent of seeds of Convallaria majalis.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02241216582D          

 50 56  0  0  0  0            999 V2000
    0.8979    0.5541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6113    0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6113   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8979   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1829   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1829   -1.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8979   -1.9207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6113   -1.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6113   -2.3332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3263   -1.9207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0413   -1.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0413   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3263   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3263    0.5541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0413    0.9665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7548    0.5541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8415    1.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5321   -1.9207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2456   -1.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2456   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5321   -0.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9605   -1.9207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6742   -1.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3892   -1.9207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9605    0.5541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9605   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6742   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3892   -0.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1041   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8177   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8177    0.5541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1041   -1.5083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8177   -1.9207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8177   -2.7457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5327   -3.1581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.5327   -1.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5327   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2462   -0.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8415   -1.0915    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7548   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5399   -0.5253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5399    0.8084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7943    1.5935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3103    2.2618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7943    2.9286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5794    1.8493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5794    2.6742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2462    3.1581    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  0  0  0  0
  3  8  1  0  0  0  0
  3 13  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6 18  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 41  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 41  1  0  0  0  0
 16 44  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 22  1  0  0  0  0
 20 21  1  0  0  0  0
 20 26  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 27  1  0  0  0  0
 25 26  1  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
 29 30  1  0  0  0  0
 29 32  1  0  0  0  0
 30 31  1  0  0  0  0
 30 38  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 37  1  0  0  0  0
 34 35  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 48  2  0  0  0  0
 46 47  1  0  0  0  0
 47 49  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
M  END

     RDKit          3D

102108  0  0  0  0  0  0  0  0999 V2000
    4.0101    1.6037   -1.2409 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4345    0.1326   -1.0912 C   0  0  2  0  0  0  0  0  0  0  0  0
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  1 51  1  0
  1 52  1  0
  1 53  1  0
  2 54  1  6
  4 55  1  1
  6 56  1  6
  7 57  1  0
  7 58  1  0
  8 59  1  0
  8 60  1  0
 10 61  1  0
 12 62  1  6
 13 63  1  0
 13 64  1  0
 14 65  1  0
 14 66  1  0
 16 67  1  0
 16 68  1  0
 16 69  1  0
 17 70  1  6
 24 74  1  0
 24 75  1  0
 25 76  1  0
 25 77  1  0
 27 78  1  0
 28 79  1  6
 29 80  1  0
 29 81  1  0
 30 82  1  0
 30 83  1  0
 32 84  1  0
 33 85  1  0
 33 86  1  0
 19 71  1  0
 23 72  1  0
 23 73  1  0
 34 87  1  1
 35 88  1  0
 36 89  1  6
 37 90  1  0
 38 91  1  1
 40 92  1  1
 42 93  1  6
 43 94  1  0
 43 95  1  0
 44 96  1  0
 45 97  1  1
 46 98  1  0
 47 99  1  1
 48100  1  0
 49101  1  6
 50102  1  0
M  END


  Mrv0541 02241216582D          

 50 56  0  0  0  0            999 V2000
    0.8979    0.5541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6113    0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6113   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8979   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1829   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1829   -1.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8979   -1.9207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6113   -1.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6113   -2.3332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3263   -1.9207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0413   -1.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0413   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3263   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3263    0.5541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0413    0.9665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7548    0.5541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8415    1.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5321   -1.9207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2456   -1.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2456   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5321   -0.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9605   -1.9207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6742   -1.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3892   -1.9207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9605    0.5541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9605   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6742   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3892   -0.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1041   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8177   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8177    0.5541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1041   -1.5083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8177   -1.9207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8177   -2.7457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5327   -3.1581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2462   -1.9207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5327   -1.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5327   -0.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2462   -0.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8415   -1.0915    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7548   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5399   -0.5253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0239    0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5399    0.8084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7943    1.5935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3103    2.2618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7943    2.9286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5794    1.8493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5794    2.6742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2462    3.1581    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  0  0  0  0
  3  8  1  0  0  0  0
  3 13  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6 18  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 41  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 41  1  0  0  0  0
 16 44  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 22  1  0  0  0  0
 20 21  1  0  0  0  0
 20 26  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 27  1  0  0  0  0
 25 26  1  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
 29 30  1  0  0  0  0
 29 32  1  0  0  0  0
 30 31  1  0  0  0  0
 30 38  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 37  1  0  0  0  0
 34 35  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 48  2  0  0  0  0
 46 47  1  0  0  0  0
 47 49  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0210134

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(OC2CCC3(C=O)C4CCC5(C)C(CCC5(O)C4CCC3(O)C2)C2=CC(=O)OC2)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C35H52O15/c1-16-29(50-31-27(42)25(40)24(39)22(13-36)49-31)26(41)28(43)30(47-16)48-18-3-8-33(15-37)20-4-7-32(2)19(17-11-23(38)46-14-17)6-10-35(32,45)21(20)5-9-34(33,44)12-18/h11,15-16,18-22,24-31,36,39-45H,3-10,12-14H2,1-2H3

> <INCHI_KEY>
CAYUJEAJKPLCAV-UHFFFAOYSA-N

> <FORMULA>
C35H52O15

> <MOLECULAR_WEIGHT>
712.7784

> <EXACT_MASS>
712.330620994

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_AVERAGE_POLARIZABILITY>
73.83242241362169

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-[(3,4-dihydroxy-6-methyl-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl)oxy]-7,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-2-carbaldehyde

> <ALOGPS_LOGP>
-0.77

> <JCHEM_LOGP>
-1.6264241620000017

> <ALOGPS_LOGS>
-2.77

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.939303206128804

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.182628582799383

> <JCHEM_PKA_STRONGEST_BASIC>
0.26896009723720427

> <JCHEM_POLAR_SURFACE_AREA>
242.12999999999997

> <JCHEM_REFRACTIVITY>
169.19980000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.20e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
convalloside

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  O   UNK     0       1.676   1.034   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.008   0.264   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.008  -1.275   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.676  -0.506   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.341  -1.275   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.341  -2.815   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.676  -3.585   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.008  -2.815   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.008  -4.355   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.342  -3.585   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.677  -2.815   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.677  -1.275   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.342  -0.506   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.342   1.034   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.677   1.804   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.009   1.034   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.171   2.567   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.993  -3.585   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.325  -2.815   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.325  -1.275   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.993  -0.506   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -3.660  -3.585   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -4.992  -2.815   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -6.327  -3.585   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -3.660   1.034   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -3.660  -0.506   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.992  -1.275   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -6.327  -0.506   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -7.661  -1.275   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -8.993  -0.506   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -8.993   1.034   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -7.661  -2.815   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -8.993  -3.585   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -8.993  -5.125   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0     -10.328  -5.895   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0     -11.660  -3.585   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0     -10.328  -2.815   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -10.328  -1.275   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0     -11.660  -0.506   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       7.171  -2.037   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       7.009  -0.506   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       8.474  -0.981   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       9.378   0.264   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       8.474   1.509   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       8.949   2.975   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       8.046   4.222   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       8.949   5.467   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      10.415   3.452   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      10.415   4.992   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      11.660   5.895   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8   13                                             
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   18                                                  
CONECT    7    6    8                                                       
CONECT    8    3    7    9   10                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   41                                                  
CONECT   13    3   12   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   41   44                                             
CONECT   17   16                                                            
CONECT   18    6   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21   26                                                  
CONECT   21   20                                                            
CONECT   22   19   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23                                                            
CONECT   25   26                                                            
CONECT   26   20   25   27                                                  
CONECT   27   23   26   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   32                                                  
CONECT   30   29   31   38                                                  
CONECT   31   30                                                            
CONECT   32   29   33                                                       
CONECT   33   32   34   37                                                  
CONECT   34   33   35                                                       
CONECT   35   34                                                            
CONECT   36   37                                                            
CONECT   37   33   36   38                                                  
CONECT   38   30   37   39                                                  
CONECT   39   38                                                            
CONECT   40   41                                                            
CONECT   41   12   16   40   42                                             
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   16   43   45                                                  
CONECT   45   44   46   48                                                  
CONECT   46   45   47                                                       
CONECT   47   46   49                                                       
CONECT   48   45   49                                                       
CONECT   49   47   48   50                                                  
CONECT   50   49                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  112    0
END

View in JSmol

Synonyms

Value	Source
Bogoroside	HMDB
Convalloside	MeSH
Neoconvalloside	MeSH

Chemical Formula

C₃₅H₅₂O₁₅

Average Mass

712.7784 Da

Monoisotopic Mass

712.33062 Da

IUPAC Name

5-[(3,4-dihydroxy-6-methyl-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl)oxy]-7,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-2-carbaldehyde

Traditional Name

convalloside

CAS Registry Number

Not Available

SMILES

CC1OC(OC2CCC3(C=O)C4CCC5(C)C(CCC5(O)C4CCC3(O)C2)C2=CC(=O)OC2)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O

InChI Identifier

InChI=1S/C35H52O15/c1-16-29(50-31-27(42)25(40)24(39)22(13-36)49-31)26(41)28(43)30(47-16)48-18-3-8-33(15-37)20-4-7-32(2)19(17-11-23(38)46-14-17)6-10-35(32,45)21(20)5-9-34(33,44)12-18/h11,15-16,18-22,24-31,36,39-45H,3-10,12-14H2,1-2H3

InChI Key

CAYUJEAJKPLCAV-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Antiaris toxicaria	LOTUS Database	35616633
Erysimum cheiranthoides	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
Steroidal glycoside
19-oxosteroid
14-hydroxysteroid
5-hydroxysteroid
Oxosteroid
Hydroxysteroid
Disaccharide
Glycosyl compound
O-glycosyl compound
2-furanone
Oxane
Cyclic alcohol
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Carboxylic acid ester
Secondary alcohol
Lactone
Polyol
Acetal
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Primary alcohol
Alcohol
Organic oxygen compound
Organic oxide
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Aldehyde
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	-0.77	ALOGPS
logP	-1.6	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	7.18	ChemAxon
pKa (Strongest Basic)	0.27	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	242.13 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	169.2 m³·mol⁻¹	ChemAxon
Polarizability	73.83 Å³	ChemAxon
Number of Rings	7	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

HMDB0034195

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB012491

KNApSAcK ID

Not Available

Chemspider ID

2681133

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3438253

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for convalloside (NP0210134)

MOL for NP0210134 (convalloside)

3D MOL for NP0210134 (convalloside)

3D SDF for NP0210134 (convalloside)

3D-SDF for NP0210134 (convalloside)

PDB for NP0210134 (convalloside)

3D PDB for NP0210134 (convalloside)

SMILES for NP0210134 (convalloside)

INCHI for NP0210134 (convalloside)

Structure for NP0210134 (convalloside)

3D Structure for NP0210134 (convalloside)