NP-MRD: Showing NP-Card for 9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one (NP0270764)

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Record Information

Version

2.0

Created at

2022-09-08 16:49:06 UTC

Updated at

2022-09-08 16:49:06 UTC

NP-MRD ID

NP0270764

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one

Description

17-({4,5-Dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-4,7-dihydroxy-6-(2-hydroxypropan-2-yl)-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosan-20-one belongs to the class of organic compounds known as hopanoids. These are terpenoids containing hopane skeleton(A'-Neogammacerane), a pentacyclic structure with four cyclohexane rings and one cyclopentane ring (and often, a side chain emerging from C30). 9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one is found in Glinus lotoides. 17-({4,5-Dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-4,7-dihydroxy-6-(2-hydroxypropan-2-yl)-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosan-20-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241515522D          

 54 60  0  0  0  0            999 V2000
   -2.2237   -0.7216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8004   -1.4297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9755   -1.4171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5522   -2.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2727   -2.1127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6743   -1.3920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2510   -0.6839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5739   -0.6965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6526    0.0368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2293    0.7449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4775    0.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9008   -0.6588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4992   -1.3795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9225   -2.0876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7475   -2.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1490   -1.3544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9739   -1.3418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3973   -2.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7988   -1.3293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2222   -2.0374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6238   -1.3167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4487   -1.3042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8720   -2.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6969   -1.9998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3499   -1.2513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2395   -1.3783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9982   -1.7024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.1202   -2.7079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7186   -3.4285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1419   -4.1367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8937   -3.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4704   -2.7330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.6455   -2.7455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4190   -3.4787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0174   -4.1994    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9957   -2.7706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1708   -2.7832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1545   -3.6080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4779   -3.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5459   -3.0667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1673   -3.6094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0885   -2.4453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0032   -3.6882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9538   -2.8459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5304   -3.5540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7787   -2.8584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1802   -3.5791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2020   -2.1503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0269   -2.1629    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
  7  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
  6 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 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
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 23 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 20 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 18 41  1  0  0  0  0
 41 42  1  0  0  0  0
 15 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 29 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 45 48  1  0  0  0  0
  4 49  1  0  0  0  0
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 51 52  1  0  0  0  0
 51 53  1  0  0  0  0
  2 53  1  0  0  0  0
 53 54  1  0  0  0  0
M  END

     RDKit          3D

122128  0  0  0  0  0  0  0  0999 V2000
    8.2383    1.2675    3.5835 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1394    1.6424    2.1415 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.7711   -0.2162    0.9440 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0014   -0.4415   -0.3425 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5633   -1.6965   -0.9744 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2835    0.7572   -1.2109 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7454    1.7532   -0.7878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4996    2.7856   -0.1930 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1721    1.4012   -1.1496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4278   -0.0822   -1.0051 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2683   -0.7036   -2.3848 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.8229   -0.0265    1.3463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1643   -0.6936    1.7074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1820    0.0154    0.8085 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5708   -0.1874    1.2198 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7301   -1.4234    2.1214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9909    0.9889    2.0861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2640    1.5640    1.4469 C   0  0  1  0  0  0  0  0  0  0  0  0
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    1.6643    1.2367   -1.2868 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1330    1.1955   -2.7586 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3253   -0.1353   -2.5365 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9408   -2.4842   -2.3191 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4422   -3.5110   -3.1213 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9847   -2.2540   -1.2287 C   0  0  1  0  0  0  0  0  0  0  0  0
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 53121  1  6
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M  END


  Mrv1533004241515522D          

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 53 54  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0270764

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(OC2C(O)C(O)COC2OC2CCC3(C)C4CCC5C6(C)CC(O)C(C6C(O)CC5(C)C4(C)CC(=O)C3C2(C)C)C(C)(C)O)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C41H68O13/c1-18-28(46)30(48)31(49)34(52-18)54-32-29(47)22(45)17-51-35(32)53-25-12-13-38(6)23-10-11-24-39(7)14-19(42)26(37(4,5)50)27(39)20(43)15-40(24,8)41(23,9)16-21(44)33(38)36(25,2)3/h18-20,22-35,42-43,45-50H,10-17H2,1-9H3

> <INCHI_KEY>
PMIQHWRFLIHWFG-UHFFFAOYSA-N

> <FORMULA>
C41H68O13

> <MOLECULAR_WEIGHT>
768.982

> <EXACT_MASS>
768.46599225

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
122

> <JCHEM_AVERAGE_POLARIZABILITY>
85.09347288139959

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
17-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-4,7-dihydroxy-6-(2-hydroxypropan-2-yl)-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-20-one

> <ALOGPS_LOGP>
1.33

> <JCHEM_LOGP>
0.960927813999999

> <ALOGPS_LOGS>
-3.83

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.779687092833687

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.124785784809063

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8104472730958

> <JCHEM_POLAR_SURFACE_AREA>
215.82999999999998

> <JCHEM_REFRACTIVITY>
194.0408000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.14e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
17-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-4,7-dihydroxy-6-(2-hydroxypropan-2-yl)-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-20-one

> <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      -4.151  -1.347   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.361  -2.669   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.821  -2.645   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -1.031  -3.967   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.509  -3.944   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.259  -2.598   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.469  -1.277   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.071  -1.300   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.218   0.069   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.428   1.390   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.758   0.092   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.548  -1.230   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.799  -2.575   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.589  -3.897   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.129  -3.873   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.878  -2.528   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.418  -2.505   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.208  -3.827   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.958  -2.481   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.748  -3.803   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.498  -2.458   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.037  -2.435   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.828  -3.756   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.368  -3.733   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.720  -2.336   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.380  -2.573   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      16.797  -3.178   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      18.118  -2.388   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      16.659  -4.712   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      15.158  -5.055   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      14.408  -6.400   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      15.198  -7.722   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      12.868  -6.423   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      12.078  -5.102   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      11.328  -6.447   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.538  -5.125   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      10.401  -6.659   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.789  -6.470   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       8.249  -6.494   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       7.499  -7.839   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       7.459  -5.172   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.919  -5.195   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       5.888  -6.735   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       4.625  -6.031   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      17.819  -5.725   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      18.979  -6.738   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      18.832  -4.565   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      16.806  -6.885   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      -1.780  -5.312   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      -0.990  -6.634   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      -3.320  -5.336   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      -4.070  -6.681   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      -4.110  -4.014   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      -5.650  -4.037   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   53                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   49                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   13                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    6   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   42                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   41                                             
CONECT   19   18                                                            
CONECT   20   18   21   36                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   34                                                  
CONECT   24   23   25   26   30                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   45                                                  
CONECT   30   29   24   31                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   23   35   36                                             
CONECT   35   34                                                            
CONECT   36   34   20   37   38                                             
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   18   42                                                  
CONECT   42   41   15   43   44                                             
CONECT   43   42                                                            
CONECT   44   42                                                            
CONECT   45   29   46   47   48                                             
CONECT   46   45                                                            
CONECT   47   45                                                            
CONECT   48   45                                                            
CONECT   49    4   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49   52   53                                                  
CONECT   52   51                                                            
CONECT   53   51    2   54                                                  
CONECT   54   53                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  120    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₁H₆₈O₁₃

Average Mass

768.9820 Da

Monoisotopic Mass

768.46599 Da

IUPAC Name

17-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-4,7-dihydroxy-6-(2-hydroxypropan-2-yl)-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-20-one

Traditional Name

CAS Registry Number

Not Available

SMILES

CC1OC(OC2C(O)C(O)COC2OC2CCC3(C)C4CCC5C6(C)CC(O)C(C6C(O)CC5(C)C4(C)CC(=O)C3C2(C)C)C(C)(C)O)C(O)C(O)C1O

InChI Identifier

InChI=1S/C41H68O13/c1-18-28(46)30(48)31(49)34(52-18)54-32-29(47)22(45)17-51-35(32)53-25-12-13-38(6)23-10-11-24-39(7)14-19(42)26(37(4,5)50)27(39)20(43)15-40(24,8)41(23,9)16-21(44)33(38)36(25,2)3/h18-20,22-35,42-43,45-50H,10-17H2,1-9H3

InChI Key

PMIQHWRFLIHWFG-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
Glinus lotoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hopanoids. These are terpenoids containing hopane skeleton(A'-Neogammacerane), a pentacyclic structure with four cyclohexane rings and one cyclopentane ring (and often, a side chain emerging from C30).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Hopanoids

Direct Parent

Hopanoids

Alternative Parents

Substituents

Hopane-skeleton
Triterpenoid
20-hydroxysteroid
12-hydroxysteroid
Hydroxysteroid
16-hydroxysteroid
Oxosteroid
2-oxosteroid
Steroid
Disaccharide
Glycosyl compound
O-glycosyl compound
Oxane
Cyclic alcohol
Tertiary alcohol
Ketone
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Polyol
Alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.33	ALOGPS
logP	0.96	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	12.12	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	215.83 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	194.04 m³·mol⁻¹	ChemAxon
Polarizability	85.09 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

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 9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one (NP0270764)

MOL for NP0270764 (9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one)

3D MOL for NP0270764 (9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one)

3D SDF for NP0270764 (9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one)

3D-SDF for NP0270764 (9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one)

PDB for NP0270764 (9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one)

3D PDB for NP0270764 (9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one)

SMILES for NP0270764 (9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one)

INCHI for NP0270764 (9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one)

Structure for NP0270764 (9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one)

3D Structure for NP0270764 (9-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-2,4-dihydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-tetradecahydro-1h-cyclopenta[a]chrysen-7-one)