NP-MRD: Showing NP-Card for 6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid (NP0155852)

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Record Information

Version

2.0

Created at

2022-09-02 12:58:54 UTC

Updated at

2022-09-02 12:58:54 UTC

NP-MRD ID

NP0155852

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid

Description

6-Hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2,5-dihydrofuran-2-yl)pent-3-en-1-yl]-decahydronaphthalene-1-carboxylic acid belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. 6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid is found in Salvia mirzayanii. Based on a literature review very few articles have been published on 6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2,5-dihydrofuran-2-yl)pent-3-en-1-yl]-decahydronaphthalene-1-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022214582D          

 30 32  0  0  0  0            999 V2000
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8007   -6.1830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6077   -6.3545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9432   -7.1082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0202   -5.6400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4681   -5.0269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6397   -4.2200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4323   -2.0127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980   -1.0942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3276    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3882    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1060    1.4072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2007    0.4887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    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  4  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 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
 15 18  1  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 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
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 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 14 29  1  0  0  0  0
 20 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 68 70  0  0  0  0  0  0  0  0999 V2000
    4.2743    1.3291   -2.0246 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6256   -0.0319   -1.6212 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0888   -1.1383   -2.0908 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993   -2.3129   -1.4517 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4036   -3.4986   -1.6847 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7389   -0.1403    1.2008 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -2.1849    0.6146   -2.2165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6053    0.8202   -1.8875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0813    0.5384   -0.5169 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2514   -0.4761   -0.6535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7711    1.7373    0.0792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6906    2.8291   -0.5068 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4751    1.6299    1.2464 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0811   -0.0870    0.3751 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0612   -1.5716    0.1097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9849   -2.3147    0.7875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7671   -1.6172    1.2402 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5599   -2.0437    2.7044 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3693   -2.1424    0.5531 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6194    2.0801   -1.2599 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3186   -1.2234   -2.8275 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6291   -0.0336   -0.9442 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.3426    1.2967    0.5749 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8468   -1.3383    1.3110 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7920    2.2923    0.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0197    2.4594    1.6508 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7825   -1.1234    2.0455 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5055    0.4398    2.8934 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9271   -0.0627   -0.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7336    1.4599    0.8057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9838    0.2495    2.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9650    2.2408    1.4312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7986    2.7140   -0.0525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7813    2.1582    1.3288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3805    1.2944   -1.2655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6550   -0.4416   -1.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8897    1.4995   -2.8732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0258   -0.2447   -2.9465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9552    1.8780   -2.1384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2101    0.2170   -2.6403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0569    0.1286   -1.1660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6607   -0.7516    0.3120 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.4312    0.0256    1.4340 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1 32  1  0
  1 33  1  0
M  END


  Mrv1652309022214582D          

 30 32  0  0  0  0            999 V2000
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3276    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1060    1.4072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2007    0.4887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0155852

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CCC1C(C)(O)CCC2C1(C)CCCC2(C)C(O)=O)=CCC1OC(=O)C=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C25H38O5/c1-16(7-9-18-17(2)15-21(26)30-18)8-10-20-23(3)12-6-13-24(4,22(27)28)19(23)11-14-25(20,5)29/h7,15,18-20,29H,6,8-14H2,1-5H3,(H,27,28)

> <INCHI_KEY>
IYKWRWFFFLJWCZ-UHFFFAOYSA-N

> <FORMULA>
C25H38O5

> <MOLECULAR_WEIGHT>
418.574

> <EXACT_MASS>
418.271924324

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
47.54691920369362

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2,5-dihydrofuran-2-yl)pent-3-en-1-yl]-decahydronaphthalene-1-carboxylic acid

> <ALOGPS_LOGP>
4.40

> <JCHEM_LOGP>
5.030423835333333

> <ALOGPS_LOGS>
-4.83

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.392424121213423

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.7548762731560545

> <JCHEM_PKA_STRONGEST_BASIC>
-0.4354582986024501

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
117.36889999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.13e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2H-furan-2-yl)pent-3-en-1-yl]-hexahydro-2H-naphthalene-1-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.495 -11.542   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -3.001 -11.862   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -3.627 -13.269   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -3.771 -10.528   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.741  -9.384   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.061  -7.877   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.807  -3.757   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.183  -2.043   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.345   1.180   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.325   1.180   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.798   2.627   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       7.841   0.912   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10                                                            
CONECT   12    2   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   29                                                  
CONECT   15   14   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   29                                                  
CONECT   21   20   22   23   26                                             
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   21   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   14   20   30                                             
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Value	Source
6-Hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2,5-dihydrofuran-2-yl)pent-3-en-1-yl]-decahydronaphthalene-1-carboxylate	Generator

Chemical Formula

C₂₅H₃₈O₅

Average Mass

418.5740 Da

Monoisotopic Mass

418.27192 Da

IUPAC Name

6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2,5-dihydrofuran-2-yl)pent-3-en-1-yl]-decahydronaphthalene-1-carboxylic acid

Traditional Name

6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2H-furan-2-yl)pent-3-en-1-yl]-hexahydro-2H-naphthalene-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC(CCC1C(C)(O)CCC2C1(C)CCCC2(C)C(O)=O)=CCC1OC(=O)C=C1C

InChI Identifier

InChI=1S/C25H38O5/c1-16(7-9-18-17(2)15-21(26)30-18)8-10-20-23(3)12-6-13-24(4,22(27)28)19(23)11-14-25(20,5)29/h7,15,18-20,29H,6,8-14H2,1-5H3,(H,27,28)

InChI Key

IYKWRWFFFLJWCZ-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
Salvia mirzayanii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Labdane diterpenoid
Diterpenoid
2-furanone
Dicarboxylic acid or derivatives
Cyclic alcohol
Dihydrofuran
Tertiary alcohol
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Lactone
Organoheterocyclic compound
Oxacycle
Carboxylic acid
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Alcohol
Organooxygen compound
Organic oxygen compound
Carbonyl group
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	4.4	ALOGPS
logP	5.03	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	4.75	ChemAxon
pKa (Strongest Basic)	-0.44	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	117.37 m³·mol⁻¹	ChemAxon
Polarizability	47.55 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	Yes	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

73799282

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid (NP0155852)

MOL for NP0155852 (6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid)

3D MOL for NP0155852 (6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid)

3D SDF for NP0155852 (6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid)

3D-SDF for NP0155852 (6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid)

PDB for NP0155852 (6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid)

3D PDB for NP0155852 (6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid)

SMILES for NP0155852 (6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid)

INCHI for NP0155852 (6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid)

Structure for NP0155852 (6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid)

3D Structure for NP0155852 (6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2h-furan-2-yl)pent-3-en-1-yl]-hexahydro-2h-naphthalene-1-carboxylic acid)