NP-MRD: Showing NP-Card for Erinacol (NP0005462)

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Record Information

Version

1.0

Created at

2020-12-09 02:41:40 UTC

Updated at

2021-07-15 16:52:04 UTC

NP-MRD ID

NP0005462

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Erinacol

Provided By

NPAtlas

Description

Erinacol belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Erinacol is found in Hericium and Hericium erinaceus. It was first documented in 2004 (PMID: 15322365). Based on a literature review very few articles have been published on Erinacol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118193D          

 53 55  0  0  0  0            999 V2000
    4.4948    1.4362   -1.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1432    0.7910   -1.0440 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0982   -0.5039   -1.3036 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9821   -1.4848   -1.3661 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1639   -1.2201   -2.4459 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1016   -1.3382   -0.0983 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1223   -1.3533    1.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0218   -0.1375    0.4334 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
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M  END

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652306242118193D          

 53 55  0  0  0  0            999 V2000
    4.4948    1.4362   -1.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2012    1.4651   -0.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9578    3.2568   -0.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3559    3.3107   -0.4639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    2.0507   -1.6197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7762    3.5785   -1.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1910    0.1154   -1.2969 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9681    0.6619    1.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6257    1.7507    0.9130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4487    2.0237   -1.5800 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4400    2.6326   -0.2437 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 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
 15 17  1  0  0  0  0
 14 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21  2  1  0  0  0  0
 19  6  1  0  0  0  0
 18 10  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  3 25  1  0  0  0  0
  4 26  1  6  0  0  0
  5 27  1  0  0  0  0
  7 28  1  0  0  0  0
  7 29  1  0  0  0  0
  7 30  1  0  0  0  0
  8 31  1  0  0  0  0
  8 32  1  0  0  0  0
  9 33  1  0  0  0  0
  9 34  1  0  0  0  0
 11 35  1  0  0  0  0
 11 36  1  0  0  0  0
 11 37  1  0  0  0  0
 12 38  1  0  0  0  0
 12 39  1  0  0  0  0
 13 40  1  0  0  0  0
 13 41  1  0  0  0  0
 15 42  1  1  0  0  0
 16 43  1  0  0  0  0
 16 44  1  0  0  0  0
 16 45  1  0  0  0  0
 17 46  1  0  0  0  0
 17 47  1  0  0  0  0
 17 48  1  0  0  0  0
 19 49  1  6  0  0  0
 20 50  1  0  0  0  0
 20 51  1  0  0  0  0
 21 52  1  0  0  0  0
 21 53  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005462

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1([H])C([H])=C(C([H])([H])[H])C([H])([H])C([H])([H])[C@]2([H])C3=C(C([H])([H])C([H])([H])[C@]3(C([H])([H])[H])C([H])([H])C([H])([H])[C@@]12C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O/c1-13(2)15-8-9-19(4)10-11-20(5)16(18(15)19)7-6-14(3)12-17(20)21/h12-13,16-17,21H,6-11H2,1-5H3/t16-,17+,19-,20-/m1/s1

> <INCHI_KEY>
ZTGGPQBJLZKPHO-PIKOESSRSA-N

> <FORMULA>
C20H32O

> <MOLECULAR_WEIGHT>
288.475

> <EXACT_MASS>
288.24531565

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
35.57545313890171

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aR,5aR,6S,10aR)-3a,5a,8-trimethyl-1-(propan-2-yl)-2H,3H,3aH,4H,5H,5aH,6H,9H,10H,10aH-cyclohepta[e]inden-6-ol

> <ALOGPS_LOGP>
5.34

> <JCHEM_LOGP>
4.642311029666668

> <ALOGPS_LOGS>
-4.07

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.752717218419736

> <JCHEM_PKA_STRONGEST_BASIC>
-0.7199614886632072

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
90.59189999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.47e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aR,5aR,6S,10aR)-1-isopropyl-3a,5a,8-trimethyl-2H,3H,4H,5H,6H,9H,10H,10aH-cyclohepta[e]inden-6-ol

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
    4.4948    1.4362   -1.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1432    0.7910   -1.0440 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0982   -0.5039   -1.3036 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9821   -1.4848   -1.3661 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1639   -1.2201   -2.4459 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1016   -1.3382   -0.0983 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1223   -1.3533    1.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3089   -2.5945    0.0687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4787   -2.4052    1.3711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5133   -1.3948    1.0880 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6019   -2.0106    0.1718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2860   -0.8485    2.2499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1091    0.1692    1.4513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9456    0.7839    0.6184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1445    2.1645    0.1307 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5632    2.2205   -0.5059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2440    2.7705   -0.8449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0218   -0.1375    0.4334 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3227   -0.0696   -0.1933 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2129    1.0202    0.3502 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0176    1.6963   -0.7148 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2961    0.6764   -1.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6403    2.1164   -0.2141 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5721    2.0739   -1.9851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1112   -0.8976   -1.5100 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4037   -2.5002   -1.4134 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6356   -0.7898   -3.2063 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0765   -0.8902    0.7503 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3916   -2.4602    1.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7160   -1.0344    2.0027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3519   -2.8352   -0.7449 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0476   -3.4045    0.2935 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1447   -2.2797    2.2472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0123   -3.3932    1.5069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8581   -1.2870   -0.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2393   -2.9437   -0.3090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5183   -2.2439    0.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9209   -1.5779    2.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5859   -0.3263    2.9466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4945    0.9216    2.1488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8202   -0.3303    0.8424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2694    2.8785    1.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4721    1.9904   -1.5929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2012    1.4651   -0.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9578    3.2568   -0.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3559    3.3107   -0.4639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    2.0507   -1.6197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7762    3.5785   -1.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1910    0.1154   -1.2969 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9681    0.6619    1.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6257    1.7507    0.9130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4487    2.0237   -1.5800 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4400    2.6326   -0.2437 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  6
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 14 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21  2  1  0
 19  6  1  0
 18 10  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  4 26  1  6
  5 27  1  0
  7 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 15 42  1  1
 16 43  1  0
 16 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 17 48  1  0
 19 49  1  6
 20 50  1  0
 20 51  1  0
 21 52  1  0
 21 53  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       4.495   1.436  -1.080  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.143   0.791  -1.044  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.098  -0.504  -1.304  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.982  -1.485  -1.366  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.164  -1.220  -2.446  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.102  -1.338  -0.098  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.122  -1.353   1.040  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.309  -2.595   0.069  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.479  -2.405   1.371  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.513  -1.395   1.088  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.602  -2.011   0.172  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.286  -0.849   2.250  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.109   0.169   1.451  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.946   0.784   0.618  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.144   2.164   0.131  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.563   2.220  -0.506  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.244   2.771  -0.845  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.022  -0.138   0.433  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.323  -0.070  -0.193  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.213   1.020   0.350  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.018   1.696  -0.715  0.00  0.00           C+0
HETATM   22  H   UNK     0       5.296   0.676  -1.036  0.00  0.00           H+0
HETATM   23  H   UNK     0       4.640   2.116  -0.214  0.00  0.00           H+0
HETATM   24  H   UNK     0       4.572   2.074  -1.985  0.00  0.00           H+0
HETATM   25  H   UNK     0       4.111  -0.898  -1.510  0.00  0.00           H+0
HETATM   26  H   UNK     0       2.404  -2.500  -1.413  0.00  0.00           H+0
HETATM   27  H   UNK     0       1.636  -0.790  -3.206  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.076  -0.890   0.750  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.392  -2.460   1.168  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.716  -1.034   2.003  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.352  -2.835  -0.745  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.048  -3.405   0.294  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.145  -2.280   2.247  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.012  -3.393   1.507  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.858  -1.287  -0.613  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.239  -2.944  -0.309  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.518  -2.244   0.751  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.921  -1.578   2.747  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.586  -0.326   2.947  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.494   0.922   2.149  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.820  -0.330   0.842  0.00  0.00           H+0
HETATM   42  H   UNK     0      -2.269   2.878   1.002  0.00  0.00           H+0
HETATM   43  H   UNK     0      -3.472   1.990  -1.593  0.00  0.00           H+0
HETATM   44  H   UNK     0      -4.201   1.465  -0.048  0.00  0.00           H+0
HETATM   45  H   UNK     0      -3.958   3.257  -0.448  0.00  0.00           H+0
HETATM   46  H   UNK     0      -0.356   3.311  -0.464  0.00  0.00           H+0
HETATM   47  H   UNK     0      -0.935   2.051  -1.620  0.00  0.00           H+0
HETATM   48  H   UNK     0      -1.776   3.579  -1.465  0.00  0.00           H+0
HETATM   49  H   UNK     0       0.191   0.115  -1.297  0.00  0.00           H+0
HETATM   50  H   UNK     0       1.968   0.662   1.093  0.00  0.00           H+0
HETATM   51  H   UNK     0       0.626   1.751   0.913  0.00  0.00           H+0
HETATM   52  H   UNK     0       1.449   2.024  -1.580  0.00  0.00           H+0
HETATM   53  H   UNK     0       2.440   2.633  -0.244  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    1    3   21                                                  
CONECT    3    2    4   25                                                  
CONECT    4    3    5    6   26                                             
CONECT    5    4   27                                                       
CONECT    6    4    7    8   19                                             
CONECT    7    6   28   29   30                                             
CONECT    8    6    9   31   32                                             
CONECT    9    8   10   33   34                                             
CONECT   10    9   11   12   18                                             
CONECT   11   10   35   36   37                                             
CONECT   12   10   13   38   39                                             
CONECT   13   12   14   40   41                                             
CONECT   14   13   15   18                                                  
CONECT   15   14   16   17   42                                             
CONECT   16   15   43   44   45                                             
CONECT   17   15   46   47   48                                             
CONECT   18   14   19   10                                                  
CONECT   19   18   20    6   49                                             
CONECT   20   19   21   50   51                                             
CONECT   21   20    2   52   53                                             
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    3                                                            
CONECT   26    4                                                            
CONECT   27    5                                                            
CONECT   28    7                                                            
CONECT   29    7                                                            
CONECT   30    7                                                            
CONECT   31    8                                                            
CONECT   32    8                                                            
CONECT   33    9                                                            
CONECT   34    9                                                            
CONECT   35   11                                                            
CONECT   36   11                                                            
CONECT   37   11                                                            
CONECT   38   12                                                            
CONECT   39   12                                                            
CONECT   40   13                                                            
CONECT   41   13                                                            
CONECT   42   15                                                            
CONECT   43   16                                                            
CONECT   44   16                                                            
CONECT   45   16                                                            
CONECT   46   17                                                            
CONECT   47   17                                                            
CONECT   48   17                                                            
CONECT   49   19                                                            
CONECT   50   20                                                            
CONECT   51   20                                                            
CONECT   52   21                                                            
CONECT   53   21                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  110    0
END

RDKit          3D

53 55  0  0  0  0  0  0  0  0999 V2000
    4.4948    1.4362   -1.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1432    0.7910   -1.0440 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0982   -0.5039   -1.3036 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9821   -1.4848   -1.3661 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1639   -1.2201   -2.4459 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1016   -1.3382   -0.0983 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1223   -1.3533    1.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3089   -2.5945    0.0687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4787   -2.4052    1.3711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5133   -1.3948    1.0880 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6019   -2.0106    0.1718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2860   -0.8485    2.2499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1091    0.1692    1.4513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9456    0.7839    0.6184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1445    2.1645    0.1307 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5632    2.2205   -0.5059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2440    2.7705   -0.8449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0218   -0.1375    0.4334 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3227   -0.0696   -0.1933 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2129    1.0202    0.3502 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0176    1.6963   -0.7148 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2961    0.6764   -1.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6403    2.1164   -0.2141 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5721    2.0739   -1.9851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1112   -0.8976   -1.5100 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4037   -2.5002   -1.4134 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6356   -0.7898   -3.2063 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0765   -0.8902    0.7503 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3916   -2.4602    1.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7160   -1.0344    2.0027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3519   -2.8352   -0.7449 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0476   -3.4045    0.2935 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1447   -2.2797    2.2472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0123   -3.3932    1.5069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8581   -1.2870   -0.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2393   -2.9437   -0.3090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5183   -2.2439    0.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9209   -1.5779    2.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5859   -0.3263    2.9466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4945    0.9216    2.1488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8202   -0.3303    0.8424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2694    2.8785    1.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4721    1.9904   -1.5929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2012    1.4651   -0.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9578    3.2568   -0.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3559    3.3107   -0.4639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    2.0507   -1.6197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7762    3.5785   -1.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1910    0.1154   -1.2969 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9681    0.6619    1.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6257    1.7507    0.9130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4487    2.0237   -1.5800 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4400    2.6326   -0.2437 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
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  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  4 26  1  6
  5 27  1  0
  7 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
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 21 53  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Cyatha-3,12-dien-14beta-ol	MeSH

Chemical Formula

C₂₀H₃₂O

Average Mass

288.4750 Da

Monoisotopic Mass

288.24532 Da

IUPAC Name

(3aR,5aR,6S,10aR)-3a,5a,8-trimethyl-1-(propan-2-yl)-2H,3H,3aH,4H,5H,5aH,6H,9H,10H,10aH-cyclohepta[e]inden-6-ol

Traditional Name

(3aR,5aR,6S,10aR)-1-isopropyl-3a,5a,8-trimethyl-2H,3H,4H,5H,6H,9H,10H,10aH-cyclohepta[e]inden-6-ol

CAS Registry Number

Not Available

SMILES

CC(C)C1=C2[C@H]3CCC(C)=C[C@H](O)[C@]3(C)CC[C@@]2(C)CC1

InChI Identifier

InChI=1S/C20H32O/c1-13(2)15-8-9-19(4)10-11-20(5)16(18(15)19)7-6-14(3)12-17(20)21/h12-13,16-17,21H,6-11H2,1-5H3/t16-,17+,19-,20-/m1/s1

InChI Key

ZTGGPQBJLZKPHO-PIKOESSRSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Hericium	NPAtlas	15322365
Hericium erinaceus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	5.34	ALOGPS
logP	4.64	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	19.75	ChemAxon
pKa (Strongest Basic)	-0.72	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	90.59 m³·mol⁻¹	ChemAxon
Polarizability	35.58 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA007542

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28282186

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101348970

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kenmoku H, Tanaka K, Okada K, Kato N, Sassa T: Erinacol (cyatha-3,12-dien-14beta-ol) and 11-O-acetylcyathin A3, new cyathane metabolites from an erinacine Q-producing Hericium erinaceum. Biosci Biotechnol Biochem. 2004 Aug;68(8):1786-9. doi: 10.1271/bbb.68.1786. [PubMed:15322365 ]

Showing NP-Card for Erinacol (NP0005462)

MOL for NP0005462 (Erinacol)

3D MOL for NP0005462 (Erinacol)

3D SDF for NP0005462 (Erinacol)

3D-SDF for NP0005462 (Erinacol)

PDB for NP0005462 (Erinacol)

3D PDB for NP0005462 (Erinacol)

SMILES for NP0005462 (Erinacol)

INCHI for NP0005462 (Erinacol)

Structure for NP0005462 (Erinacol)

3D Structure for NP0005462 (Erinacol)