NP-MRD: Showing NP-Card for 11-hydroxyhainanolidol (NP0033434)

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Record Information

Version

2.0

Created at

2021-06-19 23:58:49 UTC

Updated at

2021-06-30 00:03:12 UTC

NP-MRD ID

NP0033434

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-hydroxyhainanolidol

Provided By

JEOL Database JEOL Logo

Description

11-hydroxyhainanolidol is found in Cephalotaxus koreana. 11-hydroxyhainanolidol was first documented in 2007 (Yoon, K. D., et al.). Based on a literature review very few articles have been published on 11-Hydroxyhainanolidol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202101583D          

 44 48  0  0  0  0            999 V2000
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   -0.8341   -2.7633   -1.6093 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4291   -6.1415   -0.5468 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2383   -4.5054    1.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0932   -3.2594    1.4519 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0915   -2.1988    0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3230   -1.9492   -0.6577 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7594    0.6669    2.7520 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9463    1.1925    4.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2607    1.7346    1.7089 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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   -0.5404   -4.9492   -0.3281 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652306202101583D          

 44 48  0  0  0  0            999 V2000
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   -0.8341   -2.7633   -1.6093 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0033434

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]1([H])[C@]2([H])OC(=O)[C@]3(C([H])([H])C([H])([H])C4=C([H])C(=O)C([H])=C(C5=C4[C@@]3(O[H])[C@]2([H])C5([H])[H])C([H])([H])[H])[C@]1([H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H20O5/c1-8-5-11(20)6-10-3-4-18-9(2)15(21)16(24-17(18)22)13-7-12(8)14(10)19(13,18)23/h5-6,9,13,15-16,21,23H,3-4,7H2,1-2H3/t9-,13-,15+,16-,18+,19+/m1/s1

> <INCHI_KEY>
GUYXSLDVVLPJSY-RLZVLGHRSA-N

> <FORMULA>
C19H20O5

> <MOLECULAR_WEIGHT>
328.364

> <EXACT_MASS>
328.131073744

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
33.84348634153473

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,11S,12R,13R,16S,17S)-11,17-dihydroxy-8,16-dimethyl-14-oxapentacyclo[11.2.2.1^{9,12}.0^{1,11}.0^{4,10}]octadeca-4,7,9-triene-6,15-dione

> <ALOGPS_LOGP>
0.86

> <JCHEM_LOGP>
0.2870319363333337

> <ALOGPS_LOGS>
-2.37

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.976886791410507

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.123199377236134

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2882846481156927

> <JCHEM_POLAR_SURFACE_AREA>
83.83000000000001

> <JCHEM_REFRACTIVITY>
86.7228

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.39e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,11S,12R,13R,16S,17S)-11,17-dihydroxy-8,16-dimethyl-14-oxapentacyclo[11.2.2.1^{9,12}.0^{1,11}.0^{4,10}]octadeca-4,7,9-triene-6,15-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 44 48  0  0  0  0  0  0  0  0999 V2000
   -1.2775   -2.1743   -2.9410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8341   -2.7633   -1.6093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9658   -4.0950   -1.4986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5404   -4.9492   -0.3281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4291   -6.1415   -0.5468 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2383   -4.5054    1.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0932   -3.2594    1.4519 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0915   -2.1988    0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3230   -1.9492   -0.6577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2735   -0.3829   -0.9020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3715    0.0443    0.5409 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1740    1.3815    1.2369 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9095    1.1609    2.5043 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5430    0.0039    3.1717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1907   -0.4574    4.0981 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7793   -0.5628    2.6454 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2637   -1.8262    3.3503 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4609   -3.0810    2.9389 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7594    0.6669    2.7520 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9463    1.1925    4.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2607    1.7346    1.7089 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2651    3.0462    2.2710 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6228   -0.9040    1.1638 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9289   -0.7522    0.5502 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4471   -2.9428   -3.7044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5132   -1.5054   -3.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2162   -1.6225   -2.8217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3893   -4.6644   -2.3219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2421   -5.3043    1.8202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1380   -0.0096   -1.4589 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6489   -0.0807   -1.4081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4070   -0.2415    0.8164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6693    2.2072    0.7184 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2134   -1.7173    4.4400 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3190   -2.0009    3.1023 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0327   -3.9532    3.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4797   -3.0832    3.5068 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7645    0.3523    2.4383 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3015    0.3983    4.8451 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0217    1.5968    4.6037 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6980    1.9891    4.1998 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9335    1.7655    0.8453 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5081    3.1115    2.8827 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3394   -1.6356    0.4920 H   0  0  0  0  0  0  0  0  0  0  0  0
  8 23  1  0
  7 18  1  0
 18 17  1  0
 16 17  1  0
 16 23  1  0
  4  3  1  0
 16 19  1  0
 23 11  1  0
 11 12  1  0
 11 10  1  0
 12 21  1  0
 19 21  1  0
 10  9  1  0
  4  5  2  0
  8  7  1  0
 16 14  1  1
 14 13  1  0
 12 13  1  0
  3  2  2  0
 14 15  2  0
  9  2  1  0
 21 22  1  0
  9  8  2  0
 19 20  1  0
  6  4  1  0
 23 24  1  6
  7  6  2  0
  2  1  1  0
  6 29  1  0
  3 28  1  0
 11 32  1  1
 10 30  1  0
 10 31  1  0
 18 36  1  0
 18 37  1  0
 17 34  1  0
 17 35  1  0
 19 38  1  6
 12 33  1  6
 21 42  1  6
 22 43  1  0
 20 39  1  0
 20 40  1  0
 20 41  1  0
 24 44  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -1.278  -2.174  -2.941  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.834  -2.763  -1.609  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.966  -4.095  -1.499  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.540  -4.949  -0.328  0.00  0.00           C+0
HETATM    5  O   UNK     0      -0.429  -6.141  -0.547  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.238  -4.505   1.083  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.093  -3.259   1.452  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.092  -2.199   0.622  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.323  -1.949  -0.658  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.274  -0.383  -0.902  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.372   0.044   0.541  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.174   1.381   1.237  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.910   1.161   2.504  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.543   0.004   3.172  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.191  -0.457   4.098  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.779  -0.563   2.645  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.264  -1.826   3.350  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.461  -3.081   2.939  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.759   0.667   2.752  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.946   1.192   4.181  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.261   1.735   1.709  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.265   3.046   2.271  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.623  -0.904   1.164  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.929  -0.752   0.550  0.00  0.00           O+0
HETATM   25  H   UNK     0      -1.447  -2.943  -3.704  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.513  -1.505  -3.352  0.00  0.00           H+0
HETATM   27  H   UNK     0      -2.216  -1.623  -2.822  0.00  0.00           H+0
HETATM   28  H   UNK     0      -1.389  -4.664  -2.322  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.242  -5.304   1.820  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.138  -0.010  -1.459  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.649  -0.081  -1.408  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.407  -0.242   0.816  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.669   2.207   0.718  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.213  -1.717   4.440  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.319  -2.001   3.102  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.033  -3.953   3.284  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.480  -3.083   3.507  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.765   0.352   2.438  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.301   0.398   4.845  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.022   1.597   4.604  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.698   1.989   4.200  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.934   1.766   0.845  0.00  0.00           H+0
HETATM   43  H   UNK     0       0.508   3.111   2.883  0.00  0.00           H+0
HETATM   44  H   UNK     0       2.339  -1.636   0.492  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    3    9    1                                                  
CONECT    3    4    2   28                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   29                                                  
CONECT    7   18    8    6                                                  
CONECT    8   23    7    9                                                  
CONECT    9   10    2    8                                                  
CONECT   10   11    9   30   31                                             
CONECT   11   23   12   10   32                                             
CONECT   12   11   21   13   33                                             
CONECT   13   14   12                                                       
CONECT   14   16   13   15                                                  
CONECT   15   14                                                            
CONECT   16   17   23   19   14                                             
CONECT   17   18   16   34   35                                             
CONECT   18    7   17   36   37                                             
CONECT   19   16   21   20   38                                             
CONECT   20   19   39   40   41                                             
CONECT   21   12   19   22   42                                             
CONECT   22   21   43                                                       
CONECT   23    8   16   11   24                                             
CONECT   24   23   44                                                       
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    3                                                            
CONECT   29    6                                                            
CONECT   30   10                                                            
CONECT   31   10                                                            
CONECT   32   11                                                            
CONECT   33   12                                                            
CONECT   34   17                                                            
CONECT   35   17                                                            
CONECT   36   18                                                            
CONECT   37   18                                                            
CONECT   38   19                                                            
CONECT   39   20                                                            
CONECT   40   20                                                            
CONECT   41   20                                                            
CONECT   42   21                                                            
CONECT   43   22                                                            
CONECT   44   24                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   96    0
END

RDKit          3D

44 48  0  0  0  0  0  0  0  0999 V2000
   -1.2775   -2.1743   -2.9410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8341   -2.7633   -1.6093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9658   -4.0950   -1.4986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5404   -4.9492   -0.3281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4291   -6.1415   -0.5468 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2383   -4.5054    1.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0932   -3.2594    1.4519 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0915   -2.1988    0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3230   -1.9492   -0.6577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2735   -0.3829   -0.9020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3715    0.0443    0.5409 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1740    1.3815    1.2369 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9095    1.1609    2.5043 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5430    0.0039    3.1717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1907   -0.4574    4.0981 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7793   -0.5628    2.6454 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2637   -1.8262    3.3503 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4609   -3.0810    2.9389 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7594    0.6669    2.7520 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9463    1.1925    4.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2607    1.7346    1.7089 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2651    3.0462    2.2710 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6693    2.2072    0.7184 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2134   -1.7173    4.4400 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3190   -2.0009    3.1023 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0327   -3.9532    3.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4797   -3.0832    3.5068 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3015    0.3983    4.8451 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0217    1.5968    4.6037 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6980    1.9891    4.1998 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9335    1.7655    0.8453 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5081    3.1115    2.8827 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3394   -1.6356    0.4920 H   0  0  0  0  0  0  0  0  0  0  0  0
  8 23  1  0
  7 18  1  0
 18 17  1  0
 16 17  1  0
 16 23  1  0
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 23 11  1  0
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 10  9  1  0
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  3  2  2  0
 14 15  2  0
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 21 22  1  0
  9  8  2  0
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  1 25  1  0
  1 26  1  0
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M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₀O₅

Average Mass

328.3640 Da

Monoisotopic Mass

328.13107 Da

IUPAC Name

(1R,11S,12R,13R,16S,17S)-11,17-dihydroxy-8,16-dimethyl-14-oxapentacyclo[11.2.2.1^{9,12}.0^{1,11}.0^{4,10}]octadeca-4,7,9-triene-6,15-dione

Traditional Name

(1R,11S,12R,13R,16S,17S)-11,17-dihydroxy-8,16-dimethyl-14-oxapentacyclo[11.2.2.1^{9,12}.0^{1,11}.0^{4,10}]octadeca-4,7,9-triene-6,15-dione

CAS Registry Number

Not Available

SMILES

[H]O[C@]1([H])[C@]2([H])OC(=O)[C@]3(C([H])([H])C([H])([H])C4=C([H])C(=O)C([H])=C(C5=C4[C@@]3(O[H])[C@]2([H])C5([H])[H])C([H])([H])[H])[C@]1([H])C([H])([H])[H]

InChI Identifier

InChI=1S/C19H20O5/c1-8-5-11(20)6-10-3-4-18-9(2)15(21)16(24-17(18)22)13-7-12(8)14(10)19(13,18)23/h5-6,9,13,15-16,21,23H,3-4,7H2,1-2H3/t9-,13-,15+,16-,18+,19+/m1/s1

InChI Key

GUYXSLDVVLPJSY-RLZVLGHRSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CD₃OD, 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
Cephalotaxus koreana	JEOL database	Yoon, K. D., et al, J. Nat. Prod. 70, 2029 (2007)

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	0.86	ALOGPS
logP	0.29	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	13.12	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	86.72 m³·mol⁻¹	ChemAxon
Polarizability	33.84 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

101838330

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yoon, K. D., et al. (2007). Yoon, K. D., et al, J. Nat. Prod. 70, 2029 (2007). J. Nat. Prod..

Showing NP-Card for 11-hydroxyhainanolidol (NP0033434)

MOL for NP0033434 (11-hydroxyhainanolidol)

3D MOL for NP0033434 (11-hydroxyhainanolidol)

3D SDF for NP0033434 (11-hydroxyhainanolidol)

3D-SDF for NP0033434 (11-hydroxyhainanolidol)

PDB for NP0033434 (11-hydroxyhainanolidol)

3D PDB for NP0033434 (11-hydroxyhainanolidol)

SMILES for NP0033434 (11-hydroxyhainanolidol)

INCHI for NP0033434 (11-hydroxyhainanolidol)

Structure for NP0033434 (11-hydroxyhainanolidol)

3D Structure for NP0033434 (11-hydroxyhainanolidol)