NP-MRD: Showing NP-Card for 5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one (NP0223843)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 02:03:28 UTC

Updated at

2022-09-06 02:03:28 UTC

NP-MRD ID

NP0223843

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one

Description

Muricin H belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain. Muricin H is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Muricin H has been detected, but not quantified in, fruits. 5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one is found in Annona muricata. This could make muricin H a potential biomarker for the consumption of these foods.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02241210552D          

 41 42  0  0  0  0            999 V2000
   -5.3121    0.4941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3121   -0.3305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5288   -0.5847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0464    0.0818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5288    0.7455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5288    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5288   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8142    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2434   -1.8215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8142   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0996    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3849    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6703    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9558    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2412    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4733    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1880    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9026    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6172    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3318    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0464    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0464    0.7455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8297    0.4913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3121    1.1577    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8297    1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8297    2.6460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0854   -0.2920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0996   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3849   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6703   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9558   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2412   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9558   -2.6460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4733   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2412   -0.5847    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1880   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9026   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6172   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3318   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0464   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7610   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  5  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  7  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
  8 11  1  0  0  0  0
 10 28  1  0  0  0  0
 11 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
 16 17  1  0  0  0  0
 17 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  2  0  0  0  0
 21 25  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 27  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 32 34  1  0  0  0  0
 32 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
M  END


  Mrv0541 02241210552D          

 41 42  0  0  0  0            999 V2000
   -5.3121    0.4941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3121   -0.3305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5288   -0.5847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0464    0.0818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5288    0.7455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5288    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5288   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8142    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2434   -1.8215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8142   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0996    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3849    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6703    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9558    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2412    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4733    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1880    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9026    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6172    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3318    1.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0464    1.5700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0464    0.7455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8297    0.4913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3121    1.1577    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8297    1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8297    2.6460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0854   -0.2920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0996   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3849   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6703   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9558   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2412   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9558   -2.6460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4733   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2412   -0.5847    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1880   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9026   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6172   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3318   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0464   -1.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7610   -1.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  5  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  7  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
  8 11  1  0  0  0  0
 10 28  1  0  0  0  0
 11 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
 16 17  1  0  0  0  0
 17 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  2  0  0  0  0
 21 25  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 27  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 32 34  1  0  0  0  0
 32 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0223843

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC(O)C(O)CCCCC(O)C1CCC(CCCCCCCCCCCCC2=CC(C)OC2=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C35H64O6/c1-3-4-5-12-17-22-31(36)32(37)23-18-19-24-33(38)34-26-25-30(41-34)21-16-14-11-9-7-6-8-10-13-15-20-29-27-28(2)40-35(29)39/h27-28,30-34,36-38H,3-26H2,1-2H3

> <INCHI_KEY>
LZWAOCORLSBLAU-UHFFFAOYSA-N

> <FORMULA>
C35H64O6

> <MOLECULAR_WEIGHT>
580.8791

> <EXACT_MASS>
580.47028978

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
74.01257350494863

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
7.61

> <JCHEM_LOGP>
9.092973164999997

> <ALOGPS_LOGS>
-6.06

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.29876433983458

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.71258809512586

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1440192629383388

> <JCHEM_POLAR_SURFACE_AREA>
96.22

> <JCHEM_REFRACTIVITY>
167.6737

> <JCHEM_ROTATABLE_BOND_COUNT>
26

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.01e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5H-furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -9.916   0.922   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -9.916  -0.617   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.454  -1.091   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -7.553   0.153   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -8.454   1.392   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.454   2.931   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.454  -2.631   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -7.120   3.700   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -9.788  -3.400   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -7.120  -3.400   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.786   2.931   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.452   3.700   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.118   2.931   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.784   3.700   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.450   2.931   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.883   3.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.218   2.931   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.552   3.700   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.885   2.931   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.219   3.700   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.553   2.931   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.553   1.392   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.015   0.917   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.916   2.161   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       9.015   3.400   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.015   4.939   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.493  -0.545   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -5.786  -2.631   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -4.452  -3.400   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.118  -2.631   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.784  -3.400   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.450  -2.631   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -1.784  -4.939   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       0.883  -3.400   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -0.450  -1.091   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       2.218  -2.631   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.552  -3.400   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.885  -2.631   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.219  -3.400   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       7.553  -2.631   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       8.887  -3.400   0.000  0.00  0.00           C+0
CONECT    1    2    5                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4    7                                                  
CONECT    4    3    5                                                       
CONECT    5    1    4    6                                                  
CONECT    6    5    8                                                       
CONECT    7    3    9   10                                                  
CONECT    8    6   11                                                       
CONECT    9    7                                                            
CONECT   10    7   28                                                       
CONECT   11    8   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   21   24   26                                                  
CONECT   26   25                                                            
CONECT   27   23                                                            
CONECT   28   10   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31   34   35                                                  
CONECT   33   31                                                            
CONECT   34   32   36                                                       
CONECT   35   32                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   84    0
END

View in JSmol

Synonyms

Value	Source
Muricin H	MeSH

Chemical Formula

C₃₅H₆₄O₆

Average Mass

580.8791 Da

Monoisotopic Mass

580.47029 Da

IUPAC Name

5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-2,5-dihydrofuran-2-one

Traditional Name

5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

CCCCCCCC(O)C(O)CCCCC(O)C1CCC(CCCCCCCCCCCCC2=CC(C)OC2=O)O1

InChI Identifier

InChI=1S/C35H64O6/c1-3-4-5-12-17-22-31(36)32(37)23-18-19-24-33(38)34-26-25-30(41-34)21-16-14-11-9-7-6-8-10-13-15-20-29-27-28(2)40-35(29)39/h27-28,30-34,36-38H,3-26H2,1-2H3

InChI Key

LZWAOCORLSBLAU-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Annona muricata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Annonaceous acetogenins

Alternative Parents

Substituents

Annonaceae acetogenin skeleton
Long chain fatty alcohol
2-furanone
Dihydrofuran
Tetrahydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Lactone
Secondary alcohol
Monocarboxylic acid or derivatives
Oxacycle
Ether
Dialkyl ether
Carboxylic acid derivative
Polyol
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxide
Organic oxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	7.61	ALOGPS
logP	9.09	ChemAxon
logS	-6.1	ALOGPS
pKa (Strongest Acidic)	13.71	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	26	ChemAxon
Refractivity	167.67 m³·mol⁻¹	ChemAxon
Polarizability	74.01 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0039453

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB019052

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

75072253

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one (NP0223843)

MOL for NP0223843 (5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one)

3D MOL for NP0223843 (5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one)

3D SDF for NP0223843 (5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one)

3D-SDF for NP0223843 (5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one)

PDB for NP0223843 (5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one)

3D PDB for NP0223843 (5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one)

SMILES for NP0223843 (5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one)

INCHI for NP0223843 (5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one)

Structure for NP0223843 (5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one)

3D Structure for NP0223843 (5-methyl-3-{12-[5-(1,6,7-trihydroxytetradecyl)oxolan-2-yl]dodecyl}-5h-furan-2-one)