NP-MRD: Showing NP-Card for (1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol (NP0244081)

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Record Information

Version

2.0

Created at

2022-09-07 04:46:56 UTC

Updated at

2022-09-07 04:46:56 UTC

NP-MRD ID

NP0244081

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol

Description

Cladiellisin belongs to the class of organic compounds known as eunicellane and asbestinane diterpenoids. These are diterpenoids with a structure based on either the eunicellane (5,14-cyclocembrane) or the asbestinane skeleton. (1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol is found in Cladiella pachyclados and Virgularia juncea. (1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol was first documented in 2009 (PMID: 19534538). Based on a literature review a small amount of articles have been published on cladiellisin (PMID: 20420415) (PMID: 21334794).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
    3.9499    1.3896    1.8812 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1639    1.4648    0.8102 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8934    2.2942    0.8504 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7538    1.4086    0.9755 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2192    0.0704    0.9191 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2586   -0.7227    0.3800 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9948    0.0528    0.5097 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2002   -0.3762   -0.1574 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3005   -0.6911    0.8750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4456   -1.4426    0.2552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7728   -1.5649    1.9977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7647    0.4496   -1.2543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2164    1.8084   -1.4237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7250    1.8519   -1.0754 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0293    2.2031   -2.0698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4981    1.4943    0.2842 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6804   -1.2745   -0.9084 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6696   -2.8194   -0.8602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1963   -1.0164   -1.9914 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0331   -0.9011   -1.4194 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1357   -0.7193   -0.4548 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5595    0.7256   -0.3989 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9603    0.8713   -0.5579 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8584    0.8086    1.8828 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6871    1.9198    2.7868 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0363    2.9555    1.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9932    2.9957    0.0264 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4968    1.4298    2.1042 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1777   -1.5937    1.1115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1828    0.0725    1.6366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0196   -1.4046   -0.6016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6613    0.2881    1.2362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1389   -2.2197   -0.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9793   -1.9671    1.0830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2259   -0.7473   -0.1745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4506   -0.9480    2.8403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6197   -2.1980    2.4077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0311   -2.2897    1.6591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7458   -0.0622   -2.2623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8742    0.5653   -1.0714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4269    2.2029   -2.4069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6771    2.5234   -0.6919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3483    2.4487   -3.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0967    2.2710   -1.9717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2071    2.1536    0.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0361   -3.1645    0.1166 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3177   -3.2258   -1.6665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3591   -3.1816   -1.0542 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2061   -1.5106   -2.7611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9058    0.0264   -2.0540 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2783   -1.6725   -2.2170 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0591   -1.2251    0.5162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0378   -1.2486   -0.9148 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1191    1.2419   -1.2751 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4490    0.1996   -0.0226 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9 11  1  0
  9  8  1  0
  8 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  3
 14 16  1  0
 16  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 22  1  0
 22 23  1  0
 22 21  1  0
 21 20  1  0
 20 17  1  0
 17 18  1  0
 17 19  1  6
 17  6  1  0
  6  5  1  0
  6  7  1  0
  7  8  1  0
  7 16  1  0
  5  4  1  0
 10 33  1  0
 10 34  1  0
 10 35  1  0
  9 32  1  0
 11 36  1  0
 11 37  1  0
 11 38  1  0
  8 31  1  6
 12 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  1
  4 28  1  1
  3 26  1  0
  3 27  1  0
  1 24  1  0
  1 25  1  0
 22 54  1  6
 23 55  1  0
 21 52  1  0
 21 53  1  0
 20 50  1  0
 20 51  1  0
 18 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  0
  6 29  1  1
  7 30  1  1
M  END


  Mrv1652309072206462D          

 23 25  0  0  1  0            999 V2000
    6.1282    0.9937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6433    0.3263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8587    0.5812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0740    0.3263    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3440   -0.7537    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0740   -1.8336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5891   -1.1662    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8746   -1.5787    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8746   -2.4037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602   -2.8162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891   -2.8162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602   -1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602   -0.3412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746    0.0713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746    0.8963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891   -0.3412    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8587   -2.0886    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3737   -2.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3436   -2.7560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6433   -1.8336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1282   -1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1282   -0.3412    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9128   -0.0862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  6  5  1  1  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16 14  1  6  0  0  0
  4 16  1  0  0  0  0
  7 16  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  6  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0244081

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@H]1CCC(=C)[C@@H]2[C@@H]3CC(=C)[C@@H](O)CC[C@](C)(O)[C@@H](O3)[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O3/c1-11(2)14-7-6-12(3)17-16-10-13(4)15(21)8-9-20(5,22)19(23-16)18(14)17/h11,14-19,21-22H,3-4,6-10H2,1-2,5H3/t14-,15+,16+,17-,18-,19+,20+/m1/s1

> <INCHI_KEY>
KIZAKRQUJAYYGA-SCDLFQHWSA-N

> <FORMULA>
C20H32O3

> <MOLECULAR_WEIGHT>
320.473

> <EXACT_MASS>
320.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
36.43827871213404

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,6R,7R,8S,9S,12S)-9-methyl-3,13-dimethylidene-6-(propan-2-yl)-15-oxatricyclo[6.6.1.0^{2,7}]pentadecane-9,12-diol

> <JCHEM_LOGP>
2.8615256710000008

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.73148573235467

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.9403574915439

> <JCHEM_PKA_STRONGEST_BASIC>
-2.962986204244732

> <JCHEM_POLAR_SURFACE_AREA>
49.69

> <JCHEM_REFRACTIVITY>
92.0475

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,6R,7R,8S,9S,12S)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0^{2,7}]pentadecane-9,12-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      11.439   1.855   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.534   0.609   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.070   1.085   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.605   0.609   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       8.109  -1.407   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       7.605  -3.423   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.700  -2.177   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.366  -2.947   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.366  -4.487   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.032  -5.257   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.700  -5.257   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.032  -2.177   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.032  -0.637   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.366   0.133   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.366   1.673   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.700  -0.637   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.070  -3.899   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.164  -5.145   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.975  -5.145   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      10.534  -3.423   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.439  -2.177   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.439  -0.637   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      12.904  -0.161   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   16                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8   16                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    4    7                                                  
CONECT   17    6   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    2   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂O₃

Average Mass

320.4730 Da

Monoisotopic Mass

320.23514 Da

IUPAC Name

(1S,2R,6R,7R,8S,9S,12S)-9-methyl-3,13-dimethylidene-6-(propan-2-yl)-15-oxatricyclo[6.6.1.0^{2,7}]pentadecane-9,12-diol

Traditional Name

(1S,2R,6R,7R,8S,9S,12S)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0^{2,7}]pentadecane-9,12-diol

CAS Registry Number

Not Available

SMILES

CC(C)[C@H]1CCC(=C)[C@@H]2[C@@H]3CC(=C)[C@@H](O)CC[C@](C)(O)[C@@H](O3)[C@H]12

InChI Identifier

InChI=1S/C20H32O3/c1-11(2)14-7-6-12(3)17-16-10-13(4)15(21)8-9-20(5,22)19(23-16)18(14)17/h11,14-19,21-22H,3-4,6-10H2,1-2,5H3/t14-,15+,16+,17-,18-,19+,20+/m1/s1

InChI Key

KIZAKRQUJAYYGA-SCDLFQHWSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Cladiella pachyclados	LOTUS Database	35616633
Virgularia juncea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eunicellane and asbestinane diterpenoids. These are diterpenoids with a structure based on either the eunicellane (5,14-cyclocembrane) or the asbestinane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Eunicellane and asbestinane diterpenoids

Alternative Parents

Substituents

Cladiellane diterpenoid
Eunicellane-type diterpenoid
Tertiary alcohol
Oxolane
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	2.86	ChemAxon
pKa (Strongest Acidic)	13.94	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	49.69 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	92.05 m³·mol⁻¹	ChemAxon
Polarizability	36.44 Å³	ChemAxon
Number of Rings	3	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

C00045780

Chemspider ID

23340079

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44567169

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Hassan HM, Khanfar MA, Elnagar AY, Mohammed R, Shaala LA, Youssef DT, Hifnawy MS, El Sayed KA: Pachycladins A-E, prostate cancer invasion and migration inhibitory Eunicellin-based diterpenoids from the red sea soft coral Cladiella pachyclados. J Nat Prod. 2010 May 28;73(5):848-53. doi: 10.1021/np900787p. [PubMed:20420415 ]
Hassan HM, Elnagar AY, Khanfar MA, Sallam AA, Mohammed R, Shaala LA, Youssef DT, Hifnawy MS, El Sayed KA: Design of semisynthetic analogues and 3D-QSAR study of eunicellin-based diterpenoids as prostate cancer migration and invasion inhibitors. Eur J Med Chem. 2011 Apr;46(4):1122-30. doi: 10.1016/j.ejmech.2011.01.028. Epub 2011 Jan 28. [PubMed:21334794 ]
Corminboeuf O, Overman LE, Pennington LD: A unified strategy for enantioselective total synthesis of cladiellin and briarellin diterpenes: total synthesis of briarellins E and F and the putative structure of alcyonin and revision of its structure assignment. J Org Chem. 2009 Aug 7;74(15):5458-70. doi: 10.1021/jo9010156. [PubMed:19534538 ]
LOTUS database [Link]

Showing NP-Card for (1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol (NP0244081)

MOL for NP0244081 ((1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol)

3D MOL for NP0244081 ((1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol)

3D SDF for NP0244081 ((1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol)

3D-SDF for NP0244081 ((1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol)

PDB for NP0244081 ((1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol)

3D PDB for NP0244081 ((1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol)

SMILES for NP0244081 ((1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol)

INCHI for NP0244081 ((1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol)

Structure for NP0244081 ((1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol)

3D Structure for NP0244081 ((1s,2r,6r,7r,8s,9s,12s)-6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol)