NP-MRD: Showing NP-Card for 1-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol (NP0242775)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 03:09:58 UTC

Updated at

2022-09-07 03:09:58 UTC

NP-MRD ID

NP0242775

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol

Description

14-{5-[({4-Hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-5,8,12-triol 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-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol is found in Certonardoa semiregularis. 14-{5-[({4-Hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-5,8,12-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241507482D          

 52 57  0  0  0  0            999 V2000
   -5.9886   -0.2545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3579    0.2773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5819   -0.0030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9512    0.5288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1753    0.2485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0301   -0.5636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2542   -0.8439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6235   -0.3121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6830    0.5108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3837    0.9463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9188    0.8217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7212    1.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0713    1.8519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3870    0.1910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8225   -0.5097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5116   -1.2739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3056   -1.3868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165   -2.1509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4338   -2.2638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7447   -3.0280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5619   -3.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8728   -3.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0683   -2.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390   -1.6970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5218   -1.2340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5486   -0.4095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1731   -1.7404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9853   -1.5952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2655   -0.8192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0777   -0.6740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3580    0.1019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6095   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4216   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9534   -1.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7655   -1.6450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6731   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8610   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3292   -2.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0489   -2.8566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5171   -2.2259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2368   -3.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4247   -3.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8928   -2.5163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5330   -3.2587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1102   -2.8023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4211   -3.5665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7071   -2.6894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6608   -1.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5156   -1.9075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1463   -2.4394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4367   -0.8151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0674   -1.3469    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
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 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
 25 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
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 32 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 28 40  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
 23 43  1  0  0  0  0
 27 43  1  0  0  0  0
 43 44  1  0  0  0  0
 18 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
  6 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 48 51  1  0  0  0  0
  3 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END

     RDKit          3D

120125  0  0  0  0  0  0  0  0999 V2000
   10.4030    3.0389   -2.2087 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3808    2.1824   -1.1204 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1003    1.6737   -0.8716 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.7121    2.1001    0.5099 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5339    1.5634    0.9669 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3810    0.2103    0.7116 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5038    0.0999   -0.3699 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3140   -0.5183    0.0125 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9364   -1.6740   -0.8843 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5008   -2.7846   -0.1751 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8772   -1.0662   -1.7543 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0525   -1.5024   -3.2020 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3289   -1.1130   -3.6351 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0010    0.3157   -1.6291 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2058    0.4712   -0.2656 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0703    0.0306    0.3951 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6114    1.0075    1.2293 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4002    0.7180    2.0266 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1675    0.4254    1.2428 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1076    0.2292   -0.0581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0880   -0.0608   -0.8795 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7898   -1.3607   -1.5911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3163   -0.0553   -0.0854 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5289    1.3238    0.5128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6348    1.8647   -0.3779 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0857    3.0846   -0.0094 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5833    0.7406   -0.4904 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3264    0.3649    0.7414 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.0649    1.5031    1.3983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2219    1.9030    0.5798 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.9885    2.2882   -0.7050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2203    0.7682    0.5563 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.3099    1.2458   -0.3781 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2048    0.1664   -0.8731 C   0  0  2  0  0  0  0  0  0  0  0  0
  -11.0549   -0.3334    0.1168 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3954   -0.8784   -1.5510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9382   -0.8847   -1.2119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6571   -0.5567    0.2595 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.4846   -1.5878    1.0495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2280   -0.7899    0.5645 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6172   -1.6830   -0.5280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1097   -1.6864   -0.2286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5859   -0.3929   -0.8103 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4655   -0.4402   -2.3039 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6279   -0.3419    3.0913 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7022    0.1211    4.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9855   -1.6727    2.5510 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6634   -0.4802    0.3347 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.6034   -0.3947    1.3615 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9383   -1.6846    1.7565 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1775    0.1766   -0.9344 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.4822   -0.2627   -1.1598 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0648    2.5036   -3.1408 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4418    3.3464   -2.3774 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7623    3.9179   -2.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3844    2.0756   -1.6097 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5321    1.9430    1.2363 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5699    3.2176    0.4715 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9119   -0.2284    1.6238 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3230   -0.7912    1.0915 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7857   -2.0059   -1.5164 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6044   -2.6123    0.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8890   -1.4123   -1.3864 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2527   -1.1276   -3.8410 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0326   -2.6075   -3.2256 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9789   -1.8592   -3.5777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4896    1.5047    0.0128 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3931    1.9606    0.6555 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4911    1.3138    1.8683 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1637    1.6535    2.6143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7968    0.3396    1.7846 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0908    0.2990   -0.6053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0738    0.7401   -1.6890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9096   -1.2626   -2.6900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4171   -2.1952   -1.2702 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2684   -1.7026   -1.4572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1526   -0.7482    0.7933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6577    2.0025    0.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9186    1.3322    1.5261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1482    1.9812   -1.3935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0245    3.7845   -0.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2684    0.8491   -1.3544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5216    0.0909    1.4946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4080    2.3178    1.7480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4818    1.0624    2.3570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7413    2.7601    1.1016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3928    3.1727   -0.9378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6950    0.7703    1.5832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8444    2.0727    0.1333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7892    1.6818   -1.2700 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9005    0.6596   -1.6163 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0939    0.3188    0.8676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8778   -1.8931   -1.4275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4574   -0.7080   -2.6681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6132   -1.9607   -1.3384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4173   -0.1903   -1.8668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0697   -1.0745    1.8659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0909   -2.2321    0.4197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7992   -2.2800    1.6251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1387   -1.4399    1.4904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9473   -2.7176   -0.4182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7189   -1.2593   -1.5256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8940   -1.7305    0.8384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7229   -2.5825   -0.7524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2921   -1.5025   -2.5954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4551   -0.1875   -2.7933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7544    0.2668   -2.7282 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6793   -0.3700    3.6877 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6627    0.0959    3.4966 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7546   -0.6534    4.8545 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4737    1.1240    4.4517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9737   -1.7460    1.4451 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2074   -2.4093    2.8971 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9475   -2.0892    2.9721 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4214   -1.5262    0.0939 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3607   -2.1915    0.8599 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0216   -2.2614    2.0472 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6796   -1.6948    2.5736 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5688   -0.1653   -1.7932 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4347   -1.1521   -1.5751 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  1
 38 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  6
 18 45  1  0
 45 46  1  0
 45 47  1  0
 15 14  1  0
 14 11  1  0
 11 12  1  0
 12 13  1  0
 11  9  1  0
  9 10  1  0
  6 48  1  0
 48 49  1  0
 49 50  1  0
 48 51  1  0
 51 52  1  0
 51  3  1  0
  9  8  1  0
 43 23  1  0
 43 27  1  0
 40 28  1  0
 38 32  1  0
  1 53  1  0
  1 54  1  0
  1 55  1  0
  3 56  1  6
  4 57  1  0
  4 58  1  0
  6 59  1  1
  8 60  1  1
 15 67  1  6
 17 68  1  0
 17 69  1  0
 18 70  1  1
 19 71  1  0
 20 72  1  0
 21 73  1  6
 22 74  1  0
 22 75  1  0
 22 76  1  0
 23 77  1  1
 24 78  1  0
 24 79  1  0
 25 80  1  6
 26 81  1  0
 27 82  1  6
 28 83  1  1
 29 84  1  0
 29 85  1  0
 30 86  1  1
 31 87  1  0
 32 88  1  1
 33 89  1  0
 33 90  1  0
 34 91  1  6
 35 92  1  0
 36 93  1  0
 36 94  1  0
 37 95  1  0
 37 96  1  0
 39 97  1  0
 39 98  1  0
 39 99  1  0
 40100  1  1
 41101  1  0
 41102  1  0
 42103  1  0
 42104  1  0
 44105  1  0
 44106  1  0
 44107  1  0
 45108  1  0
 46109  1  0
 46110  1  0
 46111  1  0
 47112  1  0
 47113  1  0
 47114  1  0
 11 63  1  1
 12 64  1  0
 12 65  1  0
 13 66  1  0
  9 61  1  6
 10 62  1  0
 48115  1  6
 50116  1  0
 50117  1  0
 50118  1  0
 51119  1  6
 52120  1  0
M  END


  Mrv1533004241507482D          

 52 57  0  0  0  0            999 V2000
   -5.9886   -0.2545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3579    0.2773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5819   -0.0030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9512    0.5288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1753    0.2485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0301   -0.5636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2542   -0.8439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6235   -0.3121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6830    0.5108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3837    0.9463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9188    0.8217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7212    1.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0713    1.8519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3870    0.1910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8225   -0.5097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5116   -1.2739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3056   -1.3868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165   -2.1509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4338   -2.2638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7447   -3.0280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5619   -3.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8728   -3.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0683   -2.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390   -1.6970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5218   -1.2340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5486   -0.4095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1731   -1.7404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9853   -1.5952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2655   -0.8192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0777   -0.6740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3580    0.1019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6095   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4216   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9534   -1.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7655   -1.6450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6731   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8610   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3292   -2.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0489   -2.8566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5171   -2.2259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2368   -3.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4247   -3.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8928   -2.5163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5330   -3.2587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1102   -2.8023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4211   -3.5665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7071   -2.6894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6608   -1.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5156   -1.9075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1463   -2.4394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4367   -0.8151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0674   -1.3469    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
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 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
 25 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
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 32 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 28 40  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
 23 43  1  0  0  0  0
 27 43  1  0  0  0  0
 43 44  1  0  0  0  0
 18 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
  6 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 48 51  1  0  0  0  0
  3 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0242775

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1COC(OC2C(OCC(C=CC(C)C3CC(O)C4C5CC(O)C6CC(O)CCC6(C)C5CCC34C)C(C)C)OC(CO)C2O)C(OC)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C40H68O12/c1-20(2)22(18-49-38-36(33(45)30(17-41)51-38)52-37-35(48-7)34(46)31(47-6)19-50-37)9-8-21(3)26-16-29(44)32-24-15-28(43)27-14-23(42)10-12-39(27,4)25(24)11-13-40(26,32)5/h8-9,20-38,41-46H,10-19H2,1-7H3

> <INCHI_KEY>
HYHAOXIXQYQVNQ-UHFFFAOYSA-N

> <FORMULA>
C40H68O12

> <MOLECULAR_WEIGHT>
740.972

> <EXACT_MASS>
740.47107763

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
120

> <JCHEM_AVERAGE_POLARIZABILITY>
83.8307312787654

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,8,12-triol

> <ALOGPS_LOGP>
2.36

> <JCHEM_LOGP>
2.472563070999998

> <ALOGPS_LOGS>
-4.54

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.254922016039227

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.667730065721557

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6487339942708864

> <JCHEM_POLAR_SURFACE_AREA>
176.76

> <JCHEM_REFRACTIVITY>
192.87240000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.12e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,8,12-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0     -11.179  -0.475   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0     -10.001   0.518   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -8.553  -0.006   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.376   0.987   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -5.927   0.464   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -5.656  -1.052   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -4.208  -1.575   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.030  -0.583   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.142   0.953   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -4.450   1.766   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.715   1.534   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.346   3.029   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.133   3.457   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      -0.722   0.356   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.535  -0.952   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -0.955  -2.378   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       0.571  -2.589   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.151  -4.015   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.676  -4.226   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.257  -5.652   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.782  -5.863   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.363  -7.289   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.727  -4.647   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.299  -3.168   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.574  -2.304   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.624  -0.764   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       7.790  -3.249   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.306  -2.978   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.829  -1.529   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.345  -1.258   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      11.868   0.190   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      12.338  -2.436   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      13.854  -2.164   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      14.846  -3.342   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      16.362  -3.071   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      14.323  -4.790   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      12.807  -5.061   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      11.814  -3.884   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      11.291  -5.332   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      10.299  -4.155   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       9.775  -5.603   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       8.259  -5.874   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       7.267  -4.697   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       6.595  -6.083   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       0.206  -5.231   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       0.786  -6.657   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -1.320  -5.020   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -6.834  -2.045   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      -6.562  -3.561   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      -7.740  -4.553   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -8.282  -1.522   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      -9.459  -2.514   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   51                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   48                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   15                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15                                                       
CONECT   15   14    8   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   45                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   43                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   43                                                  
CONECT   28   27   29   40                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   38                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   32   39   40                                             
CONECT   39   38                                                            
CONECT   40   38   28   41                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   23   27   44                                             
CONECT   44   43                                                            
CONECT   45   18   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45                                                            
CONECT   48    6   49   51                                                  
CONECT   49   48   50                                                       
CONECT   50   49                                                            
CONECT   51   48    3   52                                                  
CONECT   52   51                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  114    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₆₈O₁₂

Average Mass

740.9720 Da

Monoisotopic Mass

740.47108 Da

IUPAC Name

14-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,8,12-triol

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1COC(OC2C(OCC(C=CC(C)C3CC(O)C4C5CC(O)C6CC(O)CCC6(C)C5CCC34C)C(C)C)OC(CO)C2O)C(OC)C1O

InChI Identifier

InChI=1S/C40H68O12/c1-20(2)22(18-49-38-36(33(45)30(17-41)51-38)52-37-35(48-7)34(46)31(47-6)19-50-37)9-8-21(3)26-16-29(44)32-24-15-28(43)27-14-23(42)10-12-39(27,4)25(24)11-13-40(26,32)5/h8-9,20-38,41-46H,10-19H2,1-7H3

InChI Key

HYHAOXIXQYQVNQ-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
Certonardoa semiregularis	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
3-hydroxysteroid
6-hydroxysteroid
15-hydroxysteroid
Hydroxysteroid
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Disaccharide
Glycosyl compound
O-glycosyl compound
Oxane
Fatty acyl
Cyclic alcohol
Tetrahydrofuran
Secondary alcohol
Polyol
Dialkyl ether
Oxacycle
Ether
Acetal
Organoheterocyclic compound
Alcohol
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Primary 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	2.36	ALOGPS
logP	2.47	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	12.67	ChemAxon
pKa (Strongest Basic)	-0.65	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	176.76 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	192.87 m³·mol⁻¹	ChemAxon
Polarizability	83.83 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

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 1-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol (NP0242775)

MOL for NP0242775 (1-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol)

3D MOL for NP0242775 (1-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol)

3D SDF for NP0242775 (1-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol)

3D-SDF for NP0242775 (1-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol)

PDB for NP0242775 (1-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol)

3D PDB for NP0242775 (1-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol)

SMILES for NP0242775 (1-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol)

INCHI for NP0242775 (1-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol)

Structure for NP0242775 (1-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol)

3D Structure for NP0242775 (1-{5-[({4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyoxan-2-yl)oxy]-5-(hydroxymethyl)oxolan-2-yl}oxy)methyl]-6-methylhept-3-en-2-yl}-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthrene-3,5,7-triol)