NP-MRD: Showing NP-Card for 1beta-hydroxybufotalin (NP0040767)

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Record Information

Version

2.0

Created at

2021-06-20 22:50:46 UTC

Updated at

2021-06-30 00:14:51 UTC

NP-MRD ID

NP0040767

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1beta-hydroxybufotalin

Provided By

JEOL Database JEOL Logo

Description

1beta-hydroxybufotalin is found in Saussurea involucrata. 1beta-hydroxybufotalin was first documented in 2011 (Zhang, X., et al.). Based on a literature review very few articles have been published on (1S,2S,3R,5R,7R,10R,11S,13S,14S,15R)-3,5,11-trihydroxy-2,15-dimethyl-14-(2-oxo-2H-pyran-5-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan-13-yl acetate.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212100503D          

 69 73  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652306212100503D          

 69 73  0  0  0  0            999 V2000
   -0.7276   -5.6387   -3.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0629   -4.5494   -2.3482 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2319   -4.6508   -2.0038 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7123   -3.4402   -2.1923 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0801   -2.3439   -1.5208 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8872   -1.0489   -1.7187 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9878   -0.3511   -0.3428 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2983   -0.6620    0.1542 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8906    1.2044   -0.3885 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9436    1.8074   -1.3388 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8670    3.3273   -1.4138 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4610    3.8406   -1.7581 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1199    3.5165   -3.2334 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2696    3.9973   -3.6399 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3013    5.4263   -3.6079 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3433    3.4613   -2.6957 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0317    3.8020   -1.2338 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1508    5.2193   -1.0538 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6201    3.3088   -0.7577 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3606    3.9301    0.6439 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5404    1.7290   -0.6894 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5202    1.1096    0.3253 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4966   -0.4144    0.2637 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0967   -1.0408    0.5348 C   0  0  1  0  0  0  0  0  0  0  0  0
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    0.1087   -2.5241    0.0104 C   0  0  1  0  0  0  0  0  0  0  0  0
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    0.6967    5.7444   -4.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4449    2.3782   -2.8214 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3047    3.9173   -2.9640 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8153    3.3748   -0.6026 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8408    5.6457   -1.8821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2385    5.0176    0.5823 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1985    3.7394    1.3234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5419    3.5422    1.1220 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8246    1.3439   -1.6755 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5458    1.4273    0.1159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2910    1.4407    1.3432 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2238   -0.8116    0.9839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8770   -0.7062   -0.7219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1416   -1.4033    2.3270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2278    0.0943    2.3848 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5957   -1.4509    2.6236 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1308   -2.9104    0.1475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6655   -2.9860   -0.3081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0334   -4.6459    0.8534 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7425   -4.4906    1.8821 H   0  0  0  0  0  0  0  0  0  0  0  0
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 14 13  1  0  0  0  0
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  7  6  1  0  0  0  0
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 26 24  1  0  0  0  0
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 12 11  1  0  0  0  0
 11 10  1  0  0  0  0
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 18 54  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0040767

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1([H])C([H])([H])[C@@]([H])(O[H])[C@@]2(C([H])([H])[H])[C@]([H])(C([H])([H])C([H])([H])[C@]3([H])[C@]2([H])C([H])([H])C([H])([H])[C@]2(C([H])([H])[H])[C@@]([H])(C4=C([H])OC(=O)C([H])=C4[H])[C@@]([H])(OC(=O)C([H])([H])[H])C([H])([H])[C@]32O[H])C1([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C26H36O7/c1-14(27)33-20-12-26(31)19-6-5-16-10-17(28)11-21(29)25(16,3)18(19)8-9-24(26,2)23(20)15-4-7-22(30)32-13-15/h4,7,13,16-21,23,28-29,31H,5-6,8-12H2,1-3H3/t16-,17-,18+,19-,20+,21-,23+,24-,25+,26+/m1/s1

> <INCHI_KEY>
CNWMEPYBSNWPLG-CNYMZALTSA-N

> <FORMULA>
C26H36O7

> <MOLECULAR_WEIGHT>
460.567

> <EXACT_MASS>
460.246103499

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
49.10888810527305

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,3R,5R,7R,10R,11S,13S,14S,15R)-3,5,11-trihydroxy-2,15-dimethyl-14-(2-oxo-2H-pyran-5-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-13-yl acetate

> <ALOGPS_LOGP>
1.64

> <JCHEM_LOGP>
1.0327230379999999

> <ALOGPS_LOGS>
-3.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.620024681015078

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.936233449994845

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7257466965749453

> <JCHEM_POLAR_SURFACE_AREA>
113.29

> <JCHEM_REFRACTIVITY>
120.66099999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.17e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3R,5R,7R,10R,11S,13S,14S,15R)-3,5,11-trihydroxy-2,15-dimethyl-14-(6-oxopyran-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-13-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 69 73  0  0  0  0  0  0  0  0999 V2000
   -0.7276   -5.6387   -3.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0629   -4.5494   -2.3482 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2319   -4.6508   -2.0038 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7123   -3.4402   -2.1923 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0801   -2.3439   -1.5208 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8872   -1.0489   -1.7187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9878   -0.3511   -0.3428 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2983   -0.6620    0.1542 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8906    1.2044   -0.3885 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9436    1.8074   -1.3388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8670    3.3273   -1.4138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4610    3.8406   -1.7581 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1199    3.5165   -3.2334 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2696    3.9973   -3.6399 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3013    5.4263   -3.6079 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3433    3.4613   -2.6957 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0317    3.8020   -1.2338 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1508    5.2193   -1.0538 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6201    3.3088   -0.7577 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3606    3.9301    0.6439 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5404    1.7290   -0.6894 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5202    1.1096    0.3253 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4966   -0.4144    0.2637 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0967   -1.0408    0.5348 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1877   -0.9460    2.0471 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1087   -2.5241    0.0104 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7990   -3.5387    0.7038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2117   -3.6427    0.4262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9732   -4.5500    1.0469 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3969   -5.4817    2.0311 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.1650    1.5541    0.6162 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.5879    3.6874   -2.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8685    3.9972   -3.8761 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4945    3.6856   -4.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6967    5.7444   -4.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4449    2.3782   -2.8214 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3047    3.9173   -2.9640 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8153    3.3748   -0.6026 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8408    5.6457   -1.8821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2385    5.0176    0.5823 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1985    3.7394    1.3234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5419    3.5422    1.1220 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8246    1.3439   -1.6755 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5458    1.4273    0.1159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2910    1.4407    1.3432 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2238   -0.8116    0.9839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8770   -0.7062   -0.7219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1416   -1.4033    2.3270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2278    0.0943    2.3848 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5957   -1.4509    2.6236 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1308   -2.9104    0.1475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6655   -2.9860   -0.3081 H   0  0  0  0  0  0  0  0  0  0  0  0
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 14 13  1  0
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M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.728  -5.639  -3.005  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.063  -4.549  -2.348  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.232  -4.651  -2.004  0.00  0.00           O+0
HETATM    4  O   UNK     0      -0.712  -3.440  -2.192  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.080  -2.344  -1.521  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.887  -1.049  -1.719  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.988  -0.351  -0.343  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.298  -0.662   0.154  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.891   1.204  -0.389  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.944   1.807  -1.339  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.867   3.327  -1.414  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.461   3.841  -1.758  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.120   3.517  -3.233  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.270   3.997  -3.640  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.301   5.426  -3.608  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.343   3.461  -2.696  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.032   3.802  -1.234  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.151   5.219  -1.054  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.620   3.309  -0.758  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.361   3.930   0.644  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.540   1.729  -0.689  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.520   1.110   0.325  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.497  -0.414   0.264  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.097  -1.041   0.535  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.188  -0.946   2.047  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.109  -2.524   0.010  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.799  -3.539   0.704  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.212  -3.643   0.426  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.973  -4.550   1.047  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.397  -5.482   2.031  0.00  0.00           C+0
HETATM   31  O   UNK     0      -3.109  -6.301   2.601  0.00  0.00           O+0
HETATM   32  O   UNK     0      -1.052  -5.388   2.258  0.00  0.00           O+0
HETATM   33  C   UNK     0      -0.295  -4.420   1.582  0.00  0.00           C+0
HETATM   34  H   UNK     0      -1.577  -5.911  -2.373  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.092  -6.519  -3.135  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.069  -5.308  -3.988  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.898  -2.183  -1.996  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.352  -0.430  -2.447  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.876  -1.260  -2.143  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.444  -0.172   0.983  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.165   1.554   0.616  0.00  0.00           H+0
HETATM   42  H   UNK     0      -2.951   1.531  -1.004  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.836   1.392  -2.346  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.192   3.751  -0.456  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.588   3.687  -2.158  0.00  0.00           H+0
HETATM   46  H   UNK     0      -0.500   4.936  -1.676  0.00  0.00           H+0
HETATM   47  H   UNK     0      -0.184   2.440  -3.424  0.00  0.00           H+0
HETATM   48  H   UNK     0      -0.869   3.997  -3.876  0.00  0.00           H+0
HETATM   49  H   UNK     0       1.494   3.686  -4.666  0.00  0.00           H+0
HETATM   50  H   UNK     0       0.697   5.744  -4.303  0.00  0.00           H+0
HETATM   51  H   UNK     0       2.445   2.378  -2.821  0.00  0.00           H+0
HETATM   52  H   UNK     0       3.305   3.917  -2.964  0.00  0.00           H+0
HETATM   53  H   UNK     0       2.815   3.375  -0.603  0.00  0.00           H+0
HETATM   54  H   UNK     0       1.841   5.646  -1.882  0.00  0.00           H+0
HETATM   55  H   UNK     0       0.239   5.018   0.582  0.00  0.00           H+0
HETATM   56  H   UNK     0       1.198   3.739   1.323  0.00  0.00           H+0
HETATM   57  H   UNK     0      -0.542   3.542   1.122  0.00  0.00           H+0
HETATM   58  H   UNK     0       0.825   1.344  -1.676  0.00  0.00           H+0
HETATM   59  H   UNK     0       2.546   1.427   0.116  0.00  0.00           H+0
HETATM   60  H   UNK     0       1.291   1.441   1.343  0.00  0.00           H+0
HETATM   61  H   UNK     0       2.224  -0.812   0.984  0.00  0.00           H+0
HETATM   62  H   UNK     0       1.877  -0.706  -0.722  0.00  0.00           H+0
HETATM   63  H   UNK     0      -1.142  -1.403   2.327  0.00  0.00           H+0
HETATM   64  H   UNK     0      -0.228   0.094   2.385  0.00  0.00           H+0
HETATM   65  H   UNK     0       0.596  -1.451   2.624  0.00  0.00           H+0
HETATM   66  H   UNK     0       1.131  -2.910   0.148  0.00  0.00           H+0
HETATM   67  H   UNK     0      -2.666  -2.986  -0.308  0.00  0.00           H+0
HETATM   68  H   UNK     0      -4.033  -4.646   0.853  0.00  0.00           H+0
HETATM   69  H   UNK     0       0.743  -4.491   1.882  0.00  0.00           H+0
CONECT    1    2   34   35   36                                             
CONECT    2    4    1    3                                                  
CONECT    3    2                                                            
CONECT    4    5    2                                                       
CONECT    5    6   26    4   37                                             
CONECT    6    7    5   38   39                                             
CONECT    7    6    8    9   24                                             
CONECT    8    7   40                                                       
CONECT    9   10   21    7   41                                             
CONECT   10   11    9   42   43                                             
CONECT   11   12   10   44   45                                             
CONECT   12   11   13   19   46                                             
CONECT   13   14   12   47   48                                             
CONECT   14   13   15   16   49                                             
CONECT   15   14   50                                                       
CONECT   16   17   14   51   52                                             
CONECT   17   16   19   18   53                                             
CONECT   18   17   54                                                       
CONECT   19   21   17   12   20                                             
CONECT   20   19   55   56   57                                             
CONECT   21   19    9   22   58                                             
CONECT   22   21   23   59   60                                             
CONECT   23   24   22   61   62                                             
CONECT   24   26   25   23    7                                             
CONECT   25   24   63   64   65                                             
CONECT   26   24    5   27   66                                             
CONECT   27   26   28   33                                                  
CONECT   28   27   29   67                                                  
CONECT   29   28   30   68                                                  
CONECT   30   29   32   31                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   27   32   69                                                  
CONECT   34    1                                                            
CONECT   35    1                                                            
CONECT   36    1                                                            
CONECT   37    5                                                            
CONECT   38    6                                                            
CONECT   39    6                                                            
CONECT   40    8                                                            
CONECT   41    9                                                            
CONECT   42   10                                                            
CONECT   43   10                                                            
CONECT   44   11                                                            
CONECT   45   11                                                            
CONECT   46   12                                                            
CONECT   47   13                                                            
CONECT   48   13                                                            
CONECT   49   14                                                            
CONECT   50   15                                                            
CONECT   51   16                                                            
CONECT   52   16                                                            
CONECT   53   17                                                            
CONECT   54   18                                                            
CONECT   55   20                                                            
CONECT   56   20                                                            
CONECT   57   20                                                            
CONECT   58   21                                                            
CONECT   59   22                                                            
CONECT   60   22                                                            
CONECT   61   23                                                            
CONECT   62   23                                                            
CONECT   63   25                                                            
CONECT   64   25                                                            
CONECT   65   25                                                            
CONECT   66   26                                                            
CONECT   67   28                                                            
CONECT   68   29                                                            
CONECT   69   33                                                            
MASTER        0    0    0    0    0    0    0    0   69    0  146    0
END

RDKit          3D

69 73  0  0  0  0  0  0  0  0999 V2000
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 26 66  1  6
  5 37  1  6
 25 63  1  0
 25 64  1  0
 25 65  1  0
  8 40  1  0
 28 67  1  0
 29 68  1  0
 33 69  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
 18 54  1  0
M  END

View in JSmol

Synonyms

Value	Source
(1S,2S,3R,5R,7R,10R,11S,13S,14S,15R)-3,5,11-Trihydroxy-2,15-dimethyl-14-(2-oxo-2H-pyran-5-yl)tetracyclo[8.7.0.0,.0,]heptadecan-13-yl acetic acid	Generator

Chemical Formula

C₂₆H₃₆O₇

Average Mass

460.5670 Da

Monoisotopic Mass

460.24610 Da

IUPAC Name

(1S,2S,3R,5R,7R,10R,11S,13S,14S,15R)-3,5,11-trihydroxy-2,15-dimethyl-14-(2-oxo-2H-pyran-5-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-13-yl acetate

Traditional Name

(1S,2S,3R,5R,7R,10R,11S,13S,14S,15R)-3,5,11-trihydroxy-2,15-dimethyl-14-(6-oxopyran-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-13-yl acetate

CAS Registry Number

Not Available

SMILES

[H]O[C@@]1([H])C([H])([H])[C@@]([H])(O[H])[C@@]2(C([H])([H])[H])[C@]([H])(C([H])([H])C([H])([H])[C@]3([H])[C@]2([H])C([H])([H])C([H])([H])[C@]2(C([H])([H])[H])[C@@]([H])(C4=C([H])OC(=O)C([H])=C4[H])[C@@]([H])(OC(=O)C([H])([H])[H])C([H])([H])[C@]32O[H])C1([H])[H]

InChI Identifier

InChI=1S/C26H36O7/c1-14(27)33-20-12-26(31)19-6-5-16-10-17(28)11-21(29)25(16,3)18(19)8-9-24(26,2)23(20)15-4-7-22(30)32-13-15/h4,7,13,16-21,23,28-29,31H,5-6,8-12H2,1-3H3/t16-,17-,18+,19-,20+,21-,23+,24-,25+,26+/m1/s1

InChI Key

CNWMEPYBSNWPLG-CNYMZALTSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Saussurea involucrata	JEOL database	Zhang, X., et al, Phytochem. 72, 1779 (2011)

Chemical Taxonomy

Classification

Not classified

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	1.64	ALOGPS
logP	1.03	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	13.94	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	120.66 m³·mol⁻¹	ChemAxon
Polarizability	49.11 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

54589500

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhang, X., et al. (2011). Zhang, X., et al, Phytochem. 72, 1779 (2011). Phytochem..

Showing NP-Card for 1beta-hydroxybufotalin (NP0040767)

MOL for NP0040767 (1beta-hydroxybufotalin)

3D MOL for NP0040767 (1beta-hydroxybufotalin)

3D SDF for NP0040767 (1beta-hydroxybufotalin)

3D-SDF for NP0040767 (1beta-hydroxybufotalin)

PDB for NP0040767 (1beta-hydroxybufotalin)

3D PDB for NP0040767 (1beta-hydroxybufotalin)

SMILES for NP0040767 (1beta-hydroxybufotalin)

INCHI for NP0040767 (1beta-hydroxybufotalin)

Structure for NP0040767 (1beta-hydroxybufotalin)

3D Structure for NP0040767 (1beta-hydroxybufotalin)