NP-MRD: Showing NP-Card for 7beta-Methoxydeoxocryptojaponol (NP0070803)

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Record Information

Version

2.0

Created at

2022-04-28 16:13:58 UTC

Updated at

2022-04-28 16:13:58 UTC

NP-MRD ID

NP0070803

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7beta-Methoxydeoxocryptojaponol

Description

(4BS,8aS,10S)-3,10-dimethoxy-4b,8,8-trimethyl-2-(propan-2-yl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-4-ol belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 7beta-Methoxydeoxocryptojaponol is found in Cryptomeria japonica and Cryptomeria japonica D.DON.. Based on a literature review very few articles have been published on (4bS,8aS,10S)-3,10-dimethoxy-4b,8,8-trimethyl-2-(propan-2-yl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-4-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 59 61  0  0  0  0  0  0  0  0999 V2000
   -3.8646   -2.8575   -0.2085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3321   -2.0852    0.8746 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4114   -1.0643    0.5064 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9115    0.1850    0.2883 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2376    0.6481    0.6594 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3512    0.6113   -0.3037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5953    0.2725    2.0620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9739    1.1470   -0.0884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6340    0.8157   -0.2106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1312   -0.4487    0.0145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0784   -1.3856    0.3795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7551   -2.7266    0.6450 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2851   -0.8408   -0.0782 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6616   -1.5849    1.1782 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6577   -1.7219   -1.2314 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0679   -2.1956   -0.9686 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0576   -1.1750   -0.5799 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5845    0.1575   -0.1122 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2997    1.2017   -0.9978 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0026    0.4976    1.2957 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1286    0.3976   -0.3326 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5604    1.5903    0.3256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3082    1.9410   -0.5288 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1940    3.1496   -0.1404 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1449    4.0223   -1.2421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6888   -2.2887   -0.6705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0590   -3.0117   -0.9651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2939   -3.7754    0.1975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1236    1.8631    0.7943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1143    0.8556   -1.3519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9468   -0.3464   -0.1898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1220    1.3929    0.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3101   -0.7693    2.2919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0422    0.9789    2.7648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6986    0.3387    2.2283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2740    2.1908   -0.2929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4115   -3.4295    0.9185 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4558   -2.6848    0.9705 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9942   -1.3267    2.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076   -1.5555    1.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5951   -1.0976   -2.1644 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0200   -2.5759   -1.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3771   -2.7342   -1.9211 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0116   -3.0262   -0.2332 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7100   -1.6116    0.2285 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7959   -1.0769   -1.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0688    2.2049   -0.5267 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7847    1.2265   -1.9682 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3681    0.9870   -1.0559 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6261    1.4311    1.3525 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1594    0.7016    1.9652 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6954   -0.3077    1.6721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0303    0.5779   -1.4579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2368    2.4384    0.4174 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1299    1.3801    1.3441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6197    1.8336   -1.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5513    5.0298   -1.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9144    4.0923   -1.5376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6635    3.5435   -2.0908 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21 18  1  0
 18 19  1  6
 18 20  1  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 13  1  0
 13 14  1  1
 13 10  1  0
 10  9  2  0
  9  8  1  0
  8  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  3 11  2  0
 11 12  1  0
  9 23  1  0
 13 21  1  0
 11 10  1  0
 25 57  1  0
 25 58  1  0
 25 59  1  0
 23 56  1  6
 22 54  1  0
 22 55  1  0
 21 53  1  6
 19 47  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  0
 20 51  1  0
 20 52  1  0
 17 45  1  0
 17 46  1  0
 16 43  1  0
 16 44  1  0
 15 41  1  0
 15 42  1  0
 14 38  1  0
 14 39  1  0
 14 40  1  0
  8 36  1  0
  5 29  1  1
  6 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  7 35  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
 12 37  1  0
M  END


  Mrv1652304282218132D          

 25 27  0  0  1  0            999 V2000
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3016   -0.7392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6308   -1.1265    0.0000 C   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
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  6  0  0  0
  9 11  1  6  0  0  0
 11 12  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
  5 23  1  6  0  0  0
  3 24  1  0  0  0  0
  3 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0070803

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1C[C@H]2C(C)(C)CCC[C@]2(C)C2=C1C=C(C(C)C)C(OC)=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O3/c1-13(2)14-11-15-16(24-6)12-17-21(3,4)9-8-10-22(17,5)18(15)19(23)20(14)25-7/h11,13,16-17,23H,8-10,12H2,1-7H3/t16-,17-,22-/m0/s1

> <INCHI_KEY>
KEQVPNIOSICVBG-HOIFWPIMSA-N

> <FORMULA>
C22H34O3

> <MOLECULAR_WEIGHT>
346.511

> <EXACT_MASS>
346.250794955

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
41.37167637222146

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4bS,8aS,10S)-3,10-dimethoxy-4b,8,8-trimethyl-2-(propan-2-yl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-4-ol

> <ALOGPS_LOGP>
6.24

> <JCHEM_LOGP>
5.508150978333333

> <ALOGPS_LOGS>
-5.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.519830624692487

> <JCHEM_PKA_STRONGEST_BASIC>
-4.0814402455204855

> <JCHEM_POLAR_SURFACE_AREA>
38.69

> <JCHEM_REFRACTIVITY>
102.4376

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.69e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4bS,8aS,10S)-2-isopropyl-3,10-dimethoxy-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-4-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.104  -3.231   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.874  -4.565   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.874   3.437   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -0.206   3.437   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.564   4.771   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.746   0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.516  -0.564   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.516   2.104   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.030  -1.380   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.777  -2.103   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   24   25                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   23                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   16                                                  
CONECT    8    7    9   13                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9    4                                                       
CONECT   11    9   12                                                       
CONECT   12   11                                                            
CONECT   13    8   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16   18                                                  
CONECT   16   15    7   17                                                  
CONECT   17   16                                                            
CONECT   18   15   19                                                       
CONECT   19   18                                                            
CONECT   20   14   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23    5                                                            
CONECT   24    3                                                            
CONECT   25    3                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₄O₃

Average Mass

346.5110 Da

Monoisotopic Mass

346.25079 Da

IUPAC Name

(4bS,8aS,10S)-3,10-dimethoxy-4b,8,8-trimethyl-2-(propan-2-yl)-4b,5,6,7,8,8a,9,10-octahydrophenanthren-4-ol

Traditional Name

(4bS,8aS,10S)-2-isopropyl-3,10-dimethoxy-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-4-ol

CAS Registry Number

Not Available

SMILES

CO[C@H]1C[C@H]2C(C)(C)CCC[C@]2(C)C2=C1C=C(C(C)C)C(OC)=C2O

InChI Identifier

InChI=1S/C22H34O3/c1-13(2)14-11-15-16(24-6)12-17-21(3,4)9-8-10-22(17,5)18(15)19(23)20(14)25-7/h11,13,16-17,23H,8-10,12H2,1-7H3/t16-,17-,22-/m0/s1

InChI Key

KEQVPNIOSICVBG-HOIFWPIMSA-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
Cryptomeria japonica	LOTUS Database	35616633
Cryptomeria japonica D.DON.	Plant	KNApSAcK

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

Abietane diterpenoid
Diterpenoid
Phenanthrene
Hydrophenanthrene
Tetralin
Cumene
Anisole
Phenol ether
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Benzenoid
Dialkyl ether
Ether
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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	6.24	ALOGPS
logP	5.51	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	10.52	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	38.69 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	102.44 m³·mol⁻¹	ChemAxon
Polarizability	41.37 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

20120006

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21159045

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 7beta-Methoxydeoxocryptojaponol (NP0070803)

MOL for NP0070803 (7beta-Methoxydeoxocryptojaponol)

3D MOL for NP0070803 (7beta-Methoxydeoxocryptojaponol)

3D SDF for NP0070803 (7beta-Methoxydeoxocryptojaponol)

3D-SDF for NP0070803 (7beta-Methoxydeoxocryptojaponol)

PDB for NP0070803 (7beta-Methoxydeoxocryptojaponol)

3D PDB for NP0070803 (7beta-Methoxydeoxocryptojaponol)

SMILES for NP0070803 (7beta-Methoxydeoxocryptojaponol)

INCHI for NP0070803 (7beta-Methoxydeoxocryptojaponol)

Structure for NP0070803 (7beta-Methoxydeoxocryptojaponol)

3D Structure for NP0070803 (7beta-Methoxydeoxocryptojaponol)