NP-MRD: Showing NP-Card for (3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate (NP0303763)

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Record Information

Version

2.0

Created at

2022-09-10 18:23:36 UTC

Updated at

2022-09-10 18:23:36 UTC

NP-MRD ID

NP0303763

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

Description

CHEMBL465264 belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. (3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate is found in Ferula communis. Based on a literature review very few articles have been published on CHEMBL465264.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102220232D          

 28 30  0  0  1  0            999 V2000
    4.3735    1.8011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5485    1.8011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1906    1.0578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3863    0.8742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7413    1.3886    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5940    0.5769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9566    1.1337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4717    1.8011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9566    2.4686    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2922    3.2222    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2422    2.8811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4723    2.4686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2422    3.7061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7413    2.2136    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3863    2.7280    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2027    3.5323    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4143    3.7755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8096    3.2143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2308    4.5798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4424    4.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2588    5.6273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5295    5.8705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7131    6.6748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1083    7.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2919    8.0402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6800    6.9927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8636    6.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1906    2.5444    0.0000 C   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
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  1  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 14  9  1  6  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 21 27  1  0  0  0  0
 15 28  1  0  0  0  0
  2 28  1  0  0  0  0
M  END

     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
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   -0.6912   -1.4233   -2.4475 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.0994   -0.4630   -1.6126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9097   -1.5752    0.5368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2643   -0.8876    1.6851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6393    0.3254    0.9668 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6988    1.1652    0.6702 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1245    1.8289   -0.3622 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7677    0.7286   -0.1041 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1736    0.6696    0.2797 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9791    1.7766    0.4119 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3078    1.6768    0.7779 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8866    0.4611    1.0274 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2272    0.3613    1.3967 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1082   -0.6661    0.9041 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7902   -0.5585    0.5404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2440   -0.0557   -2.5882 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1551   -0.6960   -3.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6466   -2.2747   -3.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2665   -2.1531   -2.1683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7514   -3.3637   -1.8813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7015   -3.3449   -0.5828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3633   -2.7817   -2.1345 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6334    2.7711   -0.2973 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2182   -0.2261   -0.1789 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5703    2.7609    0.2260 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.5921   -1.6165    1.1076 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1913   -1.4549    0.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
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 27 58  1  0
 14 50  1  1
M  END


  Mrv1652309102220232D          

 28 30  0  0  1  0            999 V2000
    4.3735    1.8011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5485    1.8011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1906    1.0578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3863    0.8742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7413    1.3886    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5940    0.5769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9566    1.1337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4717    1.8011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9566    2.4686    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2922    3.2222    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2422    2.8811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4723    2.4686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2422    3.7061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7413    2.2136    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3863    2.7280    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2027    3.5323    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4143    3.7755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8096    3.2143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2308    4.5798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4424    4.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2588    5.6273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5295    5.8705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1083    7.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2919    8.0402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1906    2.5444    0.0000 C   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
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  1  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 14  9  1  6  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
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 26 27  2  0  0  0  0
 21 27  1  0  0  0  0
 15 28  1  0  0  0  0
  2 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0303763

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O4/c1-16(2)24(27)14-13-23(4)12-11-17(3)15-20(22(23)24)28-21(26)10-7-18-5-8-19(25)9-6-18/h5-11,16,20,22,25,27H,12-15H2,1-4H3/b10-7+/t20-,22+,23-,24+/m0/s1

> <INCHI_KEY>
GXBJQSIDGYHXDO-WMOIQOFXSA-N

> <FORMULA>
C24H32O4

> <MOLECULAR_WEIGHT>
384.516

> <EXACT_MASS>
384.23005951

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
43.403227272760674

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,3aS,4S,8aR)-3-hydroxy-6,8a-dimethyl-3-(propan-2-yl)-1,2,3,3a,4,5,8,8a-octahydroazulen-4-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
5.092819034

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.269335157937991

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.398607749241897

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1183953601765904

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
112.32229999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R,3aS,4S,8aR)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       8.164   3.362   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.624   3.362   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.956   1.975   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.454   1.632   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.250   2.592   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.975   1.077   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.786   2.116   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.881   3.362   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.786   4.608   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.412   6.015   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.452   5.378   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.882   4.608   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.452   6.918   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.250   4.132   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.454   5.092   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.112   6.594   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.640   7.048   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.511   6.000   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.297   8.549   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.826   9.003   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.483  10.504   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.988  10.958   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.331  12.460   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.202  13.507   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -0.545  15.008   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.269  13.053   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.612  11.552   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.956   4.750   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   28                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7   14                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   14                                             
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    9    5   15                                                  
CONECT   15   14   16   28                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   21                                                       
CONECT   28   15    2                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₂O₄

Average Mass

384.5160 Da

Monoisotopic Mass

384.23006 Da

IUPAC Name

(3R,3aS,4S,8aR)-3-hydroxy-6,8a-dimethyl-3-(propan-2-yl)-1,2,3,3a,4,5,8,8a-octahydroazulen-4-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

Traditional Name

(3R,3aS,4S,8aR)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

CC(C)[C@]1(O)CC[C@]2(C)CC=C(C)C[C@H](OC(=O)\C=C\C3=CC=C(O)C=C3)[C@@H]12

InChI Identifier

InChI=1S/C24H32O4/c1-16(2)24(27)14-13-23(4)12-11-17(3)15-20(22(23)24)28-21(26)10-7-18-5-8-19(25)9-6-18/h5-11,16,20,22,25,27H,12-15H2,1-4H3/b10-7+/t20-,22+,23-,24+/m0/s1

InChI Key

GXBJQSIDGYHXDO-WMOIQOFXSA-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
Ferula communis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Daucane sesquiterpenoid
Coumaric acid ester
Cinnamic acid or derivatives
Coumaric acid or derivatives
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Styrene
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Phenol
Benzenoid
Fatty acyl
Monocyclic benzene moiety
Enoate ester
Tertiary alcohol
Alpha,beta-unsaturated carboxylic ester
Cyclic alcohol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Alcohol
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
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	5.09	ChemAxon
pKa (Strongest Acidic)	9.4	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	112.32 m³·mol⁻¹	ChemAxon
Polarizability	43.4 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

23340052

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14466059

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate (NP0303763)

MOL for NP0303763 ((3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D MOL for NP0303763 ((3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D SDF for NP0303763 ((3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D-SDF for NP0303763 ((3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

PDB for NP0303763 ((3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D PDB for NP0303763 ((3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

SMILES for NP0303763 ((3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

INCHI for NP0303763 ((3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

Structure for NP0303763 ((3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D Structure for NP0303763 ((3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)