NP-MRD: Showing NP-Card for Melophlin F (NP0080005)

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Record Information

Version

2.0

Created at

2022-04-29 01:03:35 UTC

Updated at

2022-04-29 01:03:35 UTC

NP-MRD ID

NP0080005

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Melophlin F

Description

(3Z)-3-[(13S)-1-hydroxy-13-methylpentadecylidene]-1-methylpyrrolidine-2,4-dione belongs to the class of organic compounds known as n-alkylpyrrolidines. N-alkylpyrrolidines are compounds containing a pyrrolidine moiety that is substituted at the N1-position with an alkyl group. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms. Melophlin F is found in Melophlus sarassinorum. Based on a literature review very few articles have been published on (3Z)-3-[(13S)-1-hydroxy-13-methylpentadecylidene]-1-methylpyrrolidine-2,4-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 62 62  0  0  0  0  0  0  0  0999 V2000
    8.3598    0.8115    0.3450 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9900   -0.1982    1.3954 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4710   -0.5143    1.1591 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4467   -1.0510   -0.2386 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7945    0.7830    1.3868 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3177    0.7483    1.2776 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8242    0.3252   -0.0561 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2382    0.3889   -0.0493 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8596   -0.0495   -1.3994 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4812   -0.0707   -1.8712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5520   -0.8821   -1.2179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8743   -0.4727    0.1703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9729   -1.3888    0.6951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2360   -1.3584   -0.0809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8326    0.0576   -0.0986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0715   -0.0275   -0.8742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0758   -0.4453   -2.2219 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2409    0.2817   -0.3520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5205    0.7414    1.0134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7175    1.3171    1.7985 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9422    0.3850    1.2683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5328    0.6665   -0.0338 N   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8388    1.2544   -0.2892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5635    0.2456   -0.9985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8131   -0.0904   -2.1786 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6817    0.8304   -0.5212 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3550    1.8484    0.7764 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3726    0.5920   -0.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5454   -1.1525    1.2849 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0742    0.1812    2.4261 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2031   -1.2861    1.8767 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8874   -2.0210   -0.2979 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1009   -0.3581   -1.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4980   -1.3306   -0.5773 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0506    1.2188    2.3998 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1476    1.5500    0.6152 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8574    1.7508    1.5154 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8878    0.0524    2.0696 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9757   -0.7644   -0.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1090    0.9288   -0.9079 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0287   -0.3051    0.7910 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9710    1.3944    0.2486 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3063   -1.0863   -1.5484 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4606    0.6199   -2.1209 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5405   -0.3327   -2.9978 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1349    1.0344   -1.9319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2247   -1.9771   -1.2289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5001   -0.9422   -1.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0874   -0.5050    0.9067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3299    0.5629    0.2099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6170   -2.4185    0.8068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1994   -1.0201    1.7240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9867   -2.0501    0.4163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1897   -1.7074   -1.1130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1158    0.7044   -0.6938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8714    0.4881    0.8826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1930   -0.5237   -2.7085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3905    1.0062    2.0640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9743   -0.6961    1.4905 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5959    0.5390    0.0967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9477    1.5086   -1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9638    2.2092    0.2839 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
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 24 18  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  1
  4 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  6 38  1  0
  7 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  9 43  1  0
  9 44  1  0
 10 45  1  0
 10 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  0
 12 50  1  0
 13 51  1  0
 13 52  1  0
 14 53  1  0
 14 54  1  0
 15 55  1  0
 15 56  1  0
 17 57  1  0
 21 58  1  0
 21 59  1  0
 23 60  1  0
 23 61  1  0
 23 62  1  0
M  END


  Mrv1652304292203032D          

 25 25  0  0  1  0            999 V2000
   -3.7433    1.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9363    1.7948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3232    2.3469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8501    0.9744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1356    0.5619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1356   -0.2631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4211    0.9744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7066    0.5619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0078    0.9744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7223    0.5619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4368    0.9744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1512    0.5619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8657    0.9744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5802    0.5619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2947    0.9744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0091    0.5619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7236    0.9744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4381    0.5619    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1525    0.9744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8670    0.5619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4381   -0.2631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6037    0.6388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7753   -0.1682    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1558    1.2519    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9762    1.1657    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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  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  0  0  0  0
 10 11  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
 18 21  1  6  0  0  0
  4 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  1 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0080005

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)CCCCCCCCCCC\C(O)=C1/C(=O)CN(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H37NO3/c1-4-17(2)14-12-10-8-6-5-7-9-11-13-15-18(23)20-19(24)16-22(3)21(20)25/h17,23H,4-16H2,1-3H3/b20-18-/t17-/m0/s1

> <INCHI_KEY>
RXRWOJMGCVBNQH-VGVBMJIYSA-N

> <FORMULA>
C21H37NO3

> <MOLECULAR_WEIGHT>
351.531

> <EXACT_MASS>
351.277344055

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
44.43142627015357

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3Z)-3-[(13S)-1-hydroxy-13-methylpentadecylidene]-1-methylpyrrolidine-2,4-dione

> <ALOGPS_LOGP>
6.09

> <JCHEM_LOGP>
5.4178468209999995

> <ALOGPS_LOGS>
-5.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.84444509427934

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.273158935990117

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3943846712635568

> <JCHEM_POLAR_SURFACE_AREA>
57.61

> <JCHEM_REFRACTIVITY>
104.05469999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.45e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3Z)-3-[(13S)-1-hydroxy-13-methylpentadecylidene]-1-methylpyrrolidine-2,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      -6.987   3.671   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.481   3.350   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -4.337   4.381   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -5.320   1.819   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.986   1.049   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -3.986  -0.491   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -2.653   1.819   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.319   1.049   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.015   1.819   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.348   1.049   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.682   1.819   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.016   1.049   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.349   1.819   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.683   1.049   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.017   1.819   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.350   1.049   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.684   1.819   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.018   1.049   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.351   1.819   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.685   1.049   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.018  -0.491   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.727   1.192   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -7.047  -0.314   0.000  0.00  0.00           O+0
HETATM   24  N   UNK     0      -7.757   2.337   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0      -9.289   2.176   0.000  0.00  0.00           C+0
CONECT    1    2   24                                                       
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   22                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   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   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18                                                            
CONECT   22    4   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22    1   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₇NO₃

Average Mass

351.5310 Da

Monoisotopic Mass

351.27734 Da

IUPAC Name

(3Z)-3-[(13S)-1-hydroxy-13-methylpentadecylidene]-1-methylpyrrolidine-2,4-dione

Traditional Name

(3Z)-3-[(13S)-1-hydroxy-13-methylpentadecylidene]-1-methylpyrrolidine-2,4-dione

CAS Registry Number

Not Available

SMILES

CC[C@H](C)CCCCCCCCCCC\C(O)=C1/C(=O)CN(C)C1=O

InChI Identifier

InChI=1S/C21H37NO3/c1-4-17(2)14-12-10-8-6-5-7-9-11-13-15-18(23)20-19(24)16-22(3)21(20)25/h17,23H,4-16H2,1-3H3/b20-18-/t17-/m0/s1

InChI Key

RXRWOJMGCVBNQH-VGVBMJIYSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Melophlus sarassinorum	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-alkylpyrrolidines. N-alkylpyrrolidines are compounds containing a pyrrolidine moiety that is substituted at the N1-position with an alkyl group. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolidines

Sub Class

N-alkylpyrrolidines

Direct Parent

N-alkylpyrrolidines

Alternative Parents

Substituents

Pyrrolidone
2-pyrrolidone
3-pyrrolidone
N-alkylpyrrolidine
Tertiary carboxylic acid amide
Vinylogous acid
Carboxamide group
Ketone
Lactam
Cyclic ketone
Enol
Carboxylic acid derivative
Azacycle
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
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	6.09	ALOGPS
logP	5.42	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	5.27	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	57.61 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	104.05 m³·mol⁻¹	ChemAxon
Polarizability	44.43 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	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

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

163037838

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Melophlin F (NP0080005)

MOL for NP0080005 (Melophlin F)

3D MOL for NP0080005 (Melophlin F)

3D SDF for NP0080005 (Melophlin F)

3D-SDF for NP0080005 (Melophlin F)

PDB for NP0080005 (Melophlin F)

3D PDB for NP0080005 (Melophlin F)

SMILES for NP0080005 (Melophlin F)

INCHI for NP0080005 (Melophlin F)

Structure for NP0080005 (Melophlin F)

3D Structure for NP0080005 (Melophlin F)