NP-MRD: Showing NP-Card for {1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid (NP0158145)

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Record Information

Version

2.0

Created at

2022-09-02 15:40:54 UTC

Updated at

2022-09-02 15:40:55 UTC

NP-MRD ID

NP0158145

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid

Description

{14-[(3E)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-5,6,10,12-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan-8-yl}oxidanesulfonic acid belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. {1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid is found in Acodontaster conspicuus. Based on a literature review very few articles have been published on {14-[(3E)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-5,6,10,12-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan-8-yl}oxidanesulfonic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022217402D          

 57 62  0  0  0  0            999 V2000
   -3.6323    3.2431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9432    2.4789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7605    2.3660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0714    1.6019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5650    0.9505    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8759    0.1864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3695   -0.4650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5523   -0.3521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0459   -1.0035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2287   -0.8906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9178   -0.1264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7223   -1.5419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0332   -2.3061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9051   -1.4291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3987   -2.0804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4185   -1.9676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7294   -1.2034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9249   -2.6189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6955   -3.4114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3784   -3.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4052   -4.6989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0297   -3.3680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7494   -2.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3895   -1.8497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2812   -1.9614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0934   -2.1066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3737   -2.8825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1858   -3.0277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9055   -2.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7176   -2.3970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5297   -2.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8100   -3.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6221   -3.4634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2782   -3.9489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5585   -4.7248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4661   -3.8037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9343   -4.4344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2146   -5.2103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6827   -5.8410    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.0520   -5.3092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3134   -6.3728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1509   -6.4717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1221   -4.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -3.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3100   -4.1439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6804   -1.2292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4977   -1.3420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0040   -0.6907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8213   -0.8035    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6931    0.0735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1995    0.7248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8886    1.4890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3950    2.1403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0841    2.9045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5904    3.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.9559    3.7816    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
  7  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
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 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
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 28 36  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
 39 40  2  0  0  0  0
 39 41  2  0  0  0  0
 39 42  1  0  0  0  0
 37 43  1  0  0  0  0
 43 44  1  0  0  0  0
 27 44  1  0  0  0  0
 22 44  1  0  0  0  0
 44 45  1  0  0  0  0
  7 46  1  0  0  0  0
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 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
  6 50  1  0  0  0  0
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  4 52  1  0  0  0  0
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 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 54 56  1  0  0  0  0
  3 56  1  0  0  0  0
 56 57  1  0  0  0  0
M  END

     RDKit          3D

123128  0  0  0  0  0  0  0  0999 V2000
   11.8930   -0.6172    0.7342 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9133   -1.3883    0.1176 O   0  0  0  0  0  0  0  0  0  0  0  0
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   11.0276   -1.1133   -2.6256 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8438   -2.0220   -2.2071 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6523   -1.5792   -2.8057 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5456   -2.8328   -0.9880 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1504   -2.0947    0.0964 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6460   -0.8203    0.1591 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6766    0.0495   -0.3744 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1831    0.9074    0.6009 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6734    0.6335    0.6869 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0784    1.5543    1.5097 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5322    1.0453    2.6425 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3864    0.1428    2.4329 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9781   -0.3931    3.8432 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1490    0.8390    1.8964 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3791    1.4717    0.5936 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0100   -0.1301    1.8264 C   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.0453   -1.6124   -1.0194 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.5138    0.0075    0.6045 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.4606    1.2173    1.4766 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5161   -0.3803    1.1445 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


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M  END
> <DATABASE_ID>
NP0158145

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1C(O)C(O)COC1OC1C(O)C(O)COC1OCC(C)C(C)\C=C\C(C)C1CC(O)C2C1(C)CCC1C3(C)CCC(O)C(O)C3C(CC21O)OS(O)(=O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C39H66O17S/c1-18(20(3)15-52-35-33(31(46)25(43)16-53-35)55-36-32(51-6)30(45)24(42)17-54-36)7-8-19(2)21-13-23(41)34-37(21,4)12-10-27-38(5)11-9-22(40)29(44)28(38)26(14-39(27,34)47)56-57(48,49)50/h7-8,18-36,40-47H,9-17H2,1-6H3,(H,48,49,50)/b8-7+

> <INCHI_KEY>
SOSYNEHUFVEREI-BQYQJAHWSA-N

> <FORMULA>
C39H66O17S

> <MOLECULAR_WEIGHT>
839.0

> <EXACT_MASS>
838.402071839

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_ATOM_COUNT>
123

> <JCHEM_AVERAGE_POLARIZABILITY>
88.09687997234144

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{14-[(3E)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-5,6,10,12-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-8-yl}oxidanesulfonic acid

> <ALOGPS_LOGP>
-0.83

> <JCHEM_LOGP>
-1.787146468184404

> <ALOGPS_LOGS>
-2.93

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.48909902277147

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.3958092212354414

> <JCHEM_PKA_STRONGEST_BASIC>
-3.150901632461327

> <JCHEM_POLAR_SURFACE_AREA>
271.5899999999999

> <JCHEM_REFRACTIVITY>
200.83840000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.94e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{14-[(3E)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-5,6,10,12-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-8-yl}oxidanesulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.780   6.054   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -7.361   4.627   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -8.886   4.417   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.467   2.990   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -8.521   1.774   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -9.102   0.348   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.156  -0.868   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -6.631  -0.657   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -5.686  -1.873   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.160  -1.662   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.580  -0.236   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.215  -2.878   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.795  -4.305   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.690  -2.668   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.744  -3.883   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.781  -3.673   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.362  -2.246   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.726  -4.889   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.298  -6.368   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.573  -7.232   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.623  -8.771   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.789  -6.287   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.266  -4.839   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.594  -3.453   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.258  -3.661   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.774  -3.932   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.297  -5.381   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.813  -5.652   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.290  -4.203   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.806  -4.474   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.322  -4.746   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.845  -6.194   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      12.361  -6.465   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       9.853  -7.371   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      10.376  -8.820   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       8.337  -7.100   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.344  -8.277   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       7.867  -9.726   0.000  0.00  0.00           O+0
HETATM   39  S   UNK     0       6.874 -10.903   0.000  0.00  0.00           S+0
HETATM   40  O   UNK     0       5.697  -9.910   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       8.052 -11.896   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       5.882 -12.081   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       5.828  -8.006   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       5.305  -6.558   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       4.312  -7.735   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      -8.737  -2.294   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0     -10.262  -2.505   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0     -11.208  -1.289   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0     -12.733  -1.500   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0     -10.627   0.137   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0     -11.572   1.353   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0     -10.992   2.779   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0     -11.937   3.995   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0     -11.357   5.422   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0     -12.302   6.638   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0      -9.831   5.632   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0      -9.251   7.059   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   56                                                  
CONECT    4    3    5   52                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   50                                                  
CONECT    7    6    8   46                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   44                                                  
CONECT   23   22   18   24   25                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   44                                                  
CONECT   28   27   29   30   36                                             
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   28   37                                                  
CONECT   37   36   38   43                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41   42                                             
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   39                                                            
CONECT   43   37   44                                                       
CONECT   44   43   27   22   45                                             
CONECT   45   44                                                            
CONECT   46    7   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48    6   51                                                  
CONECT   51   50                                                            
CONECT   52    4   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55   56                                                  
CONECT   55   54                                                            
CONECT   56   54    3   57                                                  
CONECT   57   56                                                            
MASTER        0    0    0    0    0    0    0    0   57    0  124    0
END

View in JSmol

Synonyms

Value	Source
{14-[(3E)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-5,6,10,12-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0,.0,]heptadecan-8-yl}oxidanesulfonate	Generator
{14-[(3E)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-5,6,10,12-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0,.0,]heptadecan-8-yl}oxidanesulphonate	Generator
{14-[(3E)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-5,6,10,12-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0,.0,]heptadecan-8-yl}oxidanesulphonic acid	Generator

Chemical Formula

C₃₉H₆₆O₁₇S

Average Mass

839.0000 Da

Monoisotopic Mass

838.40207 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1C(O)C(O)COC1OC1C(O)C(O)COC1OCC(C)C(C)\C=C\C(C)C1CC(O)C2C1(C)CCC1C3(C)CCC(O)C(O)C3C(CC21O)OS(O)(=O)=O

InChI Identifier

InChI=1S/C39H66O17S/c1-18(20(3)15-52-35-33(31(46)25(43)16-53-35)55-36-32(51-6)30(45)24(42)17-54-36)7-8-19(2)21-13-23(41)34-37(21,4)12-10-27-38(5)11-9-22(40)29(44)28(38)26(14-39(27,34)47)56-57(48,49)50/h7-8,18-36,40-47H,9-17H2,1-6H3,(H,48,49,50)/b8-7+

InChI Key

SOSYNEHUFVEREI-BQYQJAHWSA-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
Acodontaster conspicuus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Ergostane steroids

Direct Parent

Ergosterols and derivatives

Alternative Parents

Substituents

Ergosterol-skeleton
Steroidal glycoside
Sulfated steroid skeleton
3-hydroxysteroid
4-hydroxysteroid
15-hydroxysteroid
Hydroxysteroid
Disaccharide
Glycosyl compound
O-glycosyl compound
Sulfuric acid ester
Alkyl sulfate
Oxane
Sulfate-ester
Sulfuric acid monoester
Organic sulfuric acid or derivatives
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Acetal
Organoheterocyclic compound
Oxacycle
Ether
Dialkyl ether
Polyol
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
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	-0.83	ALOGPS
logP	-1.8	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	-1.4	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	271.59 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	200.84 m³·mol⁻¹	ChemAxon
Polarizability	88.1 Å³	ChemAxon
Number of Rings	6	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

4946623

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6442553

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid (NP0158145)

MOL for NP0158145 ({1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid)

3D MOL for NP0158145 ({1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid)

3D SDF for NP0158145 ({1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid)

3D-SDF for NP0158145 ({1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid)

PDB for NP0158145 ({1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid)

3D PDB for NP0158145 ({1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid)

SMILES for NP0158145 ({1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid)

INCHI for NP0158145 ({1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid)

Structure for NP0158145 ({1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid)

3D Structure for NP0158145 ({1-[(3e)-7-({3-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-4,5-dihydroxyoxan-2-yl}oxy)-5,6-dimethylhept-3-en-2-yl]-3,3b,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-yl}oxidanesulfonic acid)