NP-MRD: Showing NP-Card for 2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol (NP0183239)

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Record Information

Version

2.0

Created at

2022-09-03 22:06:34 UTC

Updated at

2022-09-03 22:06:34 UTC

NP-MRD ID

NP0183239

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol

Description

2-(Hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]Icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol belongs to the class of organic compounds known as steroidal saponins. These are saponins in which the aglycone moiety is a steroid. The steroidal aglycone is usually a spirostane, furostane, spirosolane, solanidane, or curcubitacin derivative. 2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol is found in Agave utahensis. 2-(Hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]Icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261502592D          

 66 73  0  0  0  0            999 V2000
    3.1293   -1.3136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1339   -2.1386    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8507   -2.5471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3696   -3.2172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5486   -3.1356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0675   -3.8058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4073   -4.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2465   -3.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7654   -4.3943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0556   -4.3127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5367   -4.9829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3577   -4.9013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8389   -5.5714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6598   -5.4898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6975   -4.1495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5185   -4.0679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2163   -3.4793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5562   -2.7276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3954   -3.5610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0858   -2.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1820   -1.7915    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0030   -1.8731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7151   -1.4566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3313   -2.0052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1513   -1.9143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4826   -1.1588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3026   -1.0679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6339   -0.3124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4539   -0.2215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9425   -0.8862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7625   -0.7953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2512   -1.4600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0712   -1.3692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0938   -0.0398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9138    0.0511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6052    0.6249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9365    1.3805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    9.2965    1.1988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7913   -1.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6112   -1.6417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0999   -2.3064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7686   -3.0620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9486   -3.1529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4600   -2.4882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1286   -3.2437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6400   -2.5790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3087   -3.3346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4887   -3.4254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0000   -2.7607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5915   -3.4775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1791   -2.6791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4669   -3.0956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3853   -3.9166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9199   -2.2156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4086   -2.8803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2286   -2.7894    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7172   -3.4541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5372   -3.3633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8685   -2.6077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3859   -4.2097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8746   -4.8744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5659   -4.3005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2346   -5.0561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0773   -3.6358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2573   -3.7267    0.0000 O   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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 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
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
  3 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
 24 25  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
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 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 34  1  0  0  0  0
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 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 29 38  1  0  0  0  0
 38 39  1  0  0  0  0
 27 40  1  0  0  0  0
 40 41  1  0  0  0  0
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 43 44  1  0  0  0  0
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 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 24 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
 22 52  1  0  0  0  0
 52 53  1  0  0  0  0
  3 53  1  0  0  0  0
 53 54  1  0  0  0  0
 42 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 60  1  0  0  0  0
 58 61  1  0  0  0  0
 61 62  1  0  0  0  0
 61 63  1  0  0  0  0
 63 64  1  0  0  0  0
 63 65  1  0  0  0  0
 56 65  1  0  0  0  0
 65 66  1  0  0  0  0
M  END

     RDKit          3D

144151  0  0  0  0  0  0  0  0999 V2000
    5.5300    1.3478   -2.7702 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9503    0.3866   -1.9912 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0666    0.8149   -1.0372 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5854    1.6233    0.0893 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6049    0.9776    0.9138 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9350    0.6621    0.3559 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7187    1.8758   -0.0815 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8103   -0.0370    1.4070 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0596   -0.3082    0.8490 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9124   -0.9446    1.7142 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.9721   -0.0653    2.0352 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4989    0.4660    0.8838 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.6001    1.4479    1.2351 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6239    0.8548    1.9368 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.1557   -0.0251   -1.0915 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -7.3219    3.4431    2.9916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6708    4.3888    3.9869 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7015    1.9027    0.7544 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004261502592D          

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> <DATABASE_ID>
NP0183239

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1(CCC(C)COC2OC(CO)C(O)C(O)C2O)OC2CC3C4CC(OC5OC(CO)C(O)C(O)C5O)C5CC(CCC5(C)C4CCC3(C)C2C1C)OC1OC(CO)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C46H78O20/c1-19(18-60-41-38(56)35(53)32(50)28(15-47)63-41)6-11-46(59-5)20(2)31-27(66-46)14-24-22-13-26(62-43-40(58)37(55)34(52)30(17-49)65-43)25-12-21(7-9-44(25,3)23(22)8-10-45(24,31)4)61-42-39(57)36(54)33(51)29(16-48)64-42/h19-43,47-58H,6-18H2,1-5H3

> <INCHI_KEY>
XZFHDNHLVGUNKU-UHFFFAOYSA-N

> <FORMULA>
C46H78O20

> <MOLECULAR_WEIGHT>
951.11

> <EXACT_MASS>
950.508644912

> <JCHEM_ACCEPTOR_COUNT>
20

> <JCHEM_ATOM_COUNT>
144

> <JCHEM_AVERAGE_POLARIZABILITY>
101.65590883194325

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
12

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol

> <ALOGPS_LOGP>
-0.91

> <JCHEM_LOGP>
-1.8069638673333315

> <ALOGPS_LOGS>
-3.15

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.201608046638711

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.756616793392858

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6483775322989924

> <JCHEM_POLAR_SURFACE_AREA>
316.59999999999997

> <JCHEM_REFRACTIVITY>
226.50960000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.72e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0       5.841  -2.452   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.850  -3.992   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.188  -4.755   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.290  -6.006   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.757  -5.853   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.859  -7.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.494  -8.507   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.327  -6.952   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.429  -8.203   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.104  -8.050   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.002  -9.301   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.534  -9.149   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.433 -10.400   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -4.965 -10.248   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -3.169  -7.746   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -4.701  -7.593   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.271  -6.495   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.905  -5.091   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.738  -6.647   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.160  -5.396   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       7.806  -3.344   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.339  -3.497   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.668  -2.719   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.818  -3.743   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.349  -3.573   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      13.968  -2.163   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.498  -1.993   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      16.117  -0.583   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      17.647  -0.413   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      18.559  -1.654   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      20.090  -1.485   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      21.002  -2.725   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      22.533  -2.556   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      20.708  -0.074   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      22.239   0.095   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      19.796   1.167   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      20.415   2.577   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      18.266   0.997   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      17.353   2.238   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      16.410  -3.234   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      17.941  -3.065   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      18.853  -4.305   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      18.235  -5.716   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      16.704  -5.885   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      15.792  -4.645   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      15.173  -6.055   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      14.261  -4.814   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      13.643  -6.225   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      12.112  -6.394   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      11.200  -5.153   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      10.438  -6.491   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       9.668  -5.001   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       8.338  -5.779   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       8.186  -7.311   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      20.384  -4.136   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0      21.296  -5.377   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0      22.827  -5.207   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0      23.739  -6.448   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      25.269  -6.278   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0      25.888  -4.868   0.000  0.00  0.00           O+0
HETATM   61  C   UNK     0      23.120  -7.858   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0      24.033  -9.099   0.000  0.00  0.00           O+0
HETATM   63  C   UNK     0      21.590  -8.028   0.000  0.00  0.00           C+0
HETATM   64  O   UNK     0      20.971  -9.438   0.000  0.00  0.00           O+0
HETATM   65  C   UNK     0      20.678  -6.787   0.000  0.00  0.00           C+0
HETATM   66  O   UNK     0      19.147  -6.956   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21   53                                             
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   19                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   10   20                                                  
CONECT   20   19                                                            
CONECT   21    3   22                                                       
CONECT   22   21   23   52                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   50                                                  
CONECT   25   24   26   47                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   40                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   38                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   34                                                  
CONECT   32   31   33                                                       
CONECT   33   32                                                            
CONECT   34   31   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   29   39                                                  
CONECT   39   38                                                            
CONECT   40   27   41   45                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43   55                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   40   46   47                                             
CONECT   46   45                                                            
CONECT   47   45   25   48                                                  
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   24   51   52                                             
CONECT   51   50                                                            
CONECT   52   50   22   53                                                  
CONECT   53   52    3   54                                                  
CONECT   54   53                                                            
CONECT   55   42   56                                                       
CONECT   56   55   57   65                                                  
CONECT   57   56   58                                                       
CONECT   58   57   59   61                                                  
CONECT   59   58   60                                                       
CONECT   60   59                                                            
CONECT   61   58   62   63                                                  
CONECT   62   61                                                            
CONECT   63   61   64   65                                                  
CONECT   64   63                                                            
CONECT   65   63   56   66                                                  
CONECT   66   65                                                            
MASTER        0    0    0    0    0    0    0    0   66    0  146    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₆H₇₈O₂₀

Average Mass

951.1100 Da

Monoisotopic Mass

950.50864 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1(CCC(C)COC2OC(CO)C(O)C(O)C2O)OC2CC3C4CC(OC5OC(CO)C(O)C(O)C5O)C5CC(CCC5(C)C4CCC3(C)C2C1C)OC1OC(CO)C(O)C(O)C1O

InChI Identifier

InChI=1S/C46H78O20/c1-19(18-60-41-38(56)35(53)32(50)28(15-47)63-41)6-11-46(59-5)20(2)31-27(66-46)14-24-22-13-26(62-43-40(58)37(55)34(52)30(17-49)65-43)25-12-21(7-9-44(25,3)23(22)8-10-45(24,31)4)61-42-39(57)36(54)33(51)29(16-48)64-42/h19-43,47-58H,6-18H2,1-5H3

InChI Key

XZFHDNHLVGUNKU-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
Agave utahensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroidal saponins. These are saponins in which the aglycone moiety is a steroid. The steroidal aglycone is usually a spirostane, furostane, spirosolane, solanidane, or curcubitacin derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Steroidal saponins

Alternative Parents

Substituents

Steroidal saponin
Diterpene glycoside
Furostane-skeleton
Diterpenoid
Terpene glycoside
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Glycosyl compound
O-glycosyl compound
Ketal
Fatty acyl
Monosaccharide
Oxane
Tetrahydrofuran
Secondary alcohol
Organoheterocyclic compound
Acetal
Oxacycle
Polyol
Primary alcohol
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
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	-0.91	ALOGPS
logP	-1.8	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	11.76	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	20	ChemAxon
Hydrogen Donor Count	12	ChemAxon
Polar Surface Area	316.6 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	226.51 m³·mol⁻¹	ChemAxon
Polarizability	101.66 Å³	ChemAxon
Number of Rings	8	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol (NP0183239)

MOL for NP0183239 (2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol)

3D MOL for NP0183239 (2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol)

3D SDF for NP0183239 (2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol)

3D-SDF for NP0183239 (2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol)

PDB for NP0183239 (2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol)

3D PDB for NP0183239 (2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol)

SMILES for NP0183239 (2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol)

INCHI for NP0183239 (2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol)

Structure for NP0183239 (2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol)

3D Structure for NP0183239 (2-(hydroxymethyl)-6-{4-[6-methoxy-7,9,13-trimethyl-16,19-bis({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-6-yl]-2-methylbutoxy}oxane-3,4,5-triol)