NP-MRD: Showing NP-Card for 12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate (NP0174633)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 11:55:05 UTC

Updated at

2022-09-03 11:55:05 UTC

NP-MRD ID

NP0174633

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate

Description

12-Hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]Dodecan-11-yl acetate belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety. 12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate is found in Botrytis cinerea. 12-Hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]Dodecan-11-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
    4.7113    1.7737    0.6052 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4373    1.7579    0.0087 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8971    0.5070   -0.0473 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8454    0.0518   -1.4140 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2712   -1.1817   -1.7218 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6547   -1.9279   -2.6454 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1372   -1.5886   -0.8706 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5203   -2.6110    0.1652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0944   -2.0305   -1.5695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2817   -1.4043   -0.8126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0879   -2.5462   -0.2284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1621   -0.6313   -1.7263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6795   -0.6420    0.3246 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2961    0.6696    0.6703 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6155    0.5625    1.0915 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6867    1.2280    0.5719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0847    1.0766    1.0563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4513    2.0096   -0.3717 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4067    1.3228    1.7146 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9852    1.5566    1.2295 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0078    2.7449    0.3338 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6234    0.3177    0.6776 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6485   -0.2949   -0.2623 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4092    0.5745   -1.3410 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4403    1.1612    0.0784 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0839    2.7866    0.7435 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6067    1.3194    1.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6552   -0.1944    0.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5919   -2.9140    0.6920 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8730   -3.5120   -0.3748 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2310   -2.2585    0.9122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1403   -3.1384   -1.5335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1326   -1.7555   -2.6411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1630   -2.4852    0.8777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1212   -2.5747   -0.6117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6419   -3.5407   -0.4733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0752   -1.1264   -2.7420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2248   -0.7700   -1.4561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8519    0.4060   -1.8993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5008   -1.2761    1.2224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2649    1.3649   -0.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7618    0.6870    0.2841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4651    2.0816    1.3364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1393    0.3974    1.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3709    0.6970    2.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8517    2.3234    1.9189 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5909    1.8304    2.1461 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6148    3.6013    0.7542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0250    3.1928    0.2294 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3700    2.5919   -0.6777 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7209   -0.3913    1.5526 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6497    0.2014   -2.2016 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  1
  7  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 10 13  1  0
 13 14  1  0
 14 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  6
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 22  3  1  0
 23  7  1  0
 23 13  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  1
  8 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
  9 33  1  0
 11 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  1
 14 41  1  6
 19 45  1  0
 19 46  1  0
 20 47  1  1
 21 48  1  0
 21 49  1  0
 21 50  1  0
 22 51  1  1
 24 52  1  0
 17 42  1  0
 17 43  1  0
 17 44  1  0
M  END


  Mrv1533004171516182D          

 24 26  0  0  0  0            999 V2000
    0.6790   -2.3177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4326   -1.9821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5189   -1.1617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -0.6767    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9377    0.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2702    0.6287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6913    0.4793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0782    1.0313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9463    1.2639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7713    1.2639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6850    2.0844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5782    1.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0262    0.4793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7799    0.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8661   -0.6767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1987   -1.1617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3141   -1.9785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2725   -0.8261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3588   -0.0056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0732   -0.4181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4473    0.6287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2010    0.2931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8684    0.7780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2872   -0.5274    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  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 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
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
  3 18  1  0  0  0  0
 18 19  1  0  0  0  0
  7 19  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0174633

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1OC(=O)C2(C)CC(C)(C)C3C(CC(C)C1C23O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H28O6/c1-9-7-11(23-10(2)19)13-16(3,4)8-17(5)15(20)24-14(22-6)12(9)18(13,17)21/h9,11-14,21H,7-8H2,1-6H3

> <INCHI_KEY>
GOGNSPHNRCZEML-UHFFFAOYSA-N

> <FORMULA>
C18H28O6

> <MOLECULAR_WEIGHT>
340.416

> <EXACT_MASS>
340.188588622

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
36.08467499056617

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate

> <ALOGPS_LOGP>
1.96

> <JCHEM_LOGP>
1.9081509626666666

> <ALOGPS_LOGS>
-2.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.506596548447956

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4520146697088636

> <JCHEM_POLAR_SURFACE_AREA>
82.06

> <JCHEM_REFRACTIVITY>
84.3721

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.28e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       1.267  -4.326   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.674  -3.700   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.835  -2.168   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.589  -1.263   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.750   0.268   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.504   1.174   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.157   0.895   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.013   1.925   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.633   2.359   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.173   2.359   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.012   3.891   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.679   2.680   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.649   0.895   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.056   0.268   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.217  -1.263   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.971  -2.168   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.186  -3.693   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.242  -1.542   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.403  -0.010   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.737  -0.780   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       8.302   1.174   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.709   0.547   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.954   1.452   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       9.870  -0.984   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   18                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9   19                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10   14   19                                                  
CONECT   14   13   15   21                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16    3   19                                                  
CONECT   19   18    7   13   20                                             
CONECT   20   19                                                            
CONECT   21   14   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
12-Hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0,]dodecan-11-yl acetic acid	Generator
12-Hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetic acid	Generator

Chemical Formula

C₁₈H₂₈O₆

Average Mass

340.4160 Da

Monoisotopic Mass

340.18859 Da

IUPAC Name

12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate

Traditional Name

12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate

CAS Registry Number

Not Available

SMILES

COC1OC(=O)C2(C)CC(C)(C)C3C(CC(C)C1C23O)OC(C)=O

InChI Identifier

InChI=1S/C18H28O6/c1-9-7-11(23-10(2)19)13-16(3,4)8-17(5)15(20)24-14(22-6)12(9)18(13,17)21/h9,11-14,21H,7-8H2,1-6H3

InChI Key

GOGNSPHNRCZEML-UHFFFAOYSA-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
Botrytis cinerea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Delta valerolactones

Direct Parent

Delta valerolactones

Alternative Parents

Substituents

Delta valerolactone
Delta_valerolactone
Dicarboxylic acid or derivatives
Oxane
Cyclic alcohol
Tertiary alcohol
Carboxylic acid ester
Acetal
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
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	1.96	ALOGPS
logP	1.91	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	13.51	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	82.06 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	84.37 m³·mol⁻¹	ChemAxon
Polarizability	36.08 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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate (NP0174633)

MOL for NP0174633 (12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate)

3D MOL for NP0174633 (12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate)

3D SDF for NP0174633 (12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate)

3D-SDF for NP0174633 (12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate)

PDB for NP0174633 (12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate)

3D PDB for NP0174633 (12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate)

SMILES for NP0174633 (12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate)

INCHI for NP0174633 (12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate)

Structure for NP0174633 (12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate)

3D Structure for NP0174633 (12-hydroxy-7-methoxy-2,2,4,9-tetramethyl-5-oxo-6-oxatricyclo[6.3.1.0⁴,¹²]dodecan-11-yl acetate)