NP-MRD: Showing NP-Card for c25:2 highly branched isoprenoid (NP0317384)

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Record Information

Version

2.0

Created at

2022-09-11 17:14:45 UTC

Updated at

2022-09-11 17:14:46 UTC

NP-MRD ID

NP0317384

Secondary Accession Numbers

None

Natural Product Identification

Common Name

c25:2 highly branched isoprenoid

Description

C25:2 Highly branched isoprenoid belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units. Thus, C25:2 Highly branched isoprenoid is considered to be an isoprenoid. c25:2 highly branched isoprenoid is found in Haslea ostrearia. Based on a literature review very few articles have been published on C25:2 Highly branched isoprenoid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 73 72  0  0  0  0  0  0  0  0999 V2000
    1.8488    6.2988   -0.8537 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0980    5.1437   -0.2794 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4831    4.8074    1.0152 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6157    5.9640    1.4856 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6003    3.5320    0.9305 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4818    2.4349    0.4765 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9232    1.0642    0.3629 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1890    0.7943   -0.5517 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4878    1.4685   -0.4097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1613    1.2744    0.9215 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4300    2.0840    1.0304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4616   -0.1482    1.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4923   -0.7899    0.3597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6881   -2.2112    0.8267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6971   -2.9683    0.0065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3526   -3.0834   -1.4385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0880   -2.4197    0.1527 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0695    0.1651   -0.1046 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2562    0.6805   -0.3364 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8456   -1.2874   -0.2741 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1575   -1.9672   -0.6447 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9395   -3.4657   -0.8197 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2845   -4.0579   -1.1840 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1137   -5.5593   -1.3687 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7876   -3.4974   -2.5054 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2007    7.0474   -0.4279 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3029    6.5425   -1.8057 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7650    4.4488   -0.7650 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2821    4.6686    1.7599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2390    6.8600    1.5820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1694    6.1447    0.7471 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1730    5.7201    2.4822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2002    3.8464    0.2513 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2282    3.4034    1.9757 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8403    2.7117   -0.5576 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3777    2.4078    1.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7382    0.6578    1.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4077   -0.3283   -0.6287 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1817    1.0238   -1.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6056    2.4922   -0.7414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1901    0.8818   -1.1327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4627    1.6516    1.7006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9897    2.0239    0.0610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1217    1.6880    1.7961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2369    3.1506    1.3015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5562   -0.7777    1.3686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9249   -0.1344    2.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1878   -0.8365   -0.6940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4494   -0.2663    0.4272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0738   -2.1853    1.8698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7251   -2.7556    0.8724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7259   -4.0058    0.4538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8320   -3.9871   -1.8886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7213   -2.2010   -2.0365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2736   -3.1544   -1.6499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1504   -1.3284    0.0679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4889   -2.7456    1.1445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7151   -2.9102   -0.6366 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0560    0.0204   -0.6679 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5492    1.7136   -0.2411 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4623   -1.7523    0.6367 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1232   -1.4469   -1.1188 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4529   -1.6004   -1.6483 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9255   -1.8041    0.1209 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2290   -3.6369   -1.6401 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6151   -3.9246    0.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0425   -3.8124   -0.4180 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7119   -5.7018   -2.3899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4244   -5.9329   -0.5887 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1183   -6.0032   -1.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9340   -3.5470   -3.2072 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6177   -4.1104   -2.8794 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1604   -2.4717   -2.3444 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 17  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 10  1  0
 10 11  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  0
  3  2  1  0
  2  1  2  3
  7 18  1  0
 18 19  2  3
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 16 53  1  0
 16 54  1  0
 16 55  1  0
 15 52  1  0
 17 56  1  0
 17 57  1  0
 17 58  1  0
 14 50  1  0
 14 51  1  0
 13 48  1  0
 13 49  1  0
 12 46  1  0
 12 47  1  0
 10 42  1  1
 11 43  1  0
 11 44  1  0
 11 45  1  0
  9 40  1  0
  9 41  1  0
  8 38  1  0
  8 39  1  0
  7 37  1  1
  6 35  1  0
  6 36  1  0
  5 33  1  0
  5 34  1  0
  3 29  1  1
  4 30  1  0
  4 31  1  0
  4 32  1  0
  2 28  1  0
  1 26  1  0
  1 27  1  0
 19 59  1  0
 19 60  1  0
 20 61  1  0
 20 62  1  0
 21 63  1  0
 21 64  1  0
 22 65  1  0
 22 66  1  0
 23 67  1  0
 24 68  1  0
 24 69  1  0
 24 70  1  0
 25 71  1  0
 25 72  1  0
 25 73  1  0
M  END


  Mrv1652309112219142D          

 25 24  0  0  0  0            999 V2000
   10.9974    7.9993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9974    7.1743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7118    6.7618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4263    7.1743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7118    5.9368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4263    5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4263    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7118    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9974    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2829    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2829    3.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5684    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8539    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1395    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7105    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    3.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1408    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1408    3.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8552    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5697    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2842    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9987    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7131    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9987    3.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  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
 10 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
  7 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0317384

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCCC(C)CCC(CCC(C)C=C)C(=C)CCCC(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C25H48/c1-9-22(6)16-18-25(24(8)15-11-13-21(4)5)19-17-23(7)14-10-12-20(2)3/h9,20-23,25H,1,8,10-19H2,2-7H3

> <INCHI_KEY>
RNCKFEUHFHLLAW-UHFFFAOYSA-N

> <FORMULA>
C25H48

> <MOLECULAR_WEIGHT>
348.659

> <EXACT_MASS>
348.375601546

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
47.71850555345749

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,10,14-trimethyl-6-methylidene-7-(3-methylpent-4-en-1-yl)pentadecane

> <JCHEM_LOGP>
9.981011318333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
116.33439999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2,10,14-trimethyl-6-methylidene-7-(3-methylpent-4-en-1-yl)pentadecane

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      20.528  14.932   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      20.528  13.392   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      21.862  12.622   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      23.196  13.392   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      21.862  11.082   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      23.196  10.312   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      23.196   8.772   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.862   8.002   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.528   8.772   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.195   8.002   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      19.195   6.462   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.861   8.772   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.527   8.002   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      15.194   8.772   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.860   8.002   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.526   8.772   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.860   6.462   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      24.529   8.002   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      24.529   6.462   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      25.863   8.772   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      27.197   8.002   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      28.530   8.772   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      29.864   8.002   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      31.198   8.772   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      29.864   6.462   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   18                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18    7   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₄₈

Average Mass

348.6590 Da

Monoisotopic Mass

348.37560 Da

IUPAC Name

2,10,14-trimethyl-6-methylidene-7-(3-methylpent-4-en-1-yl)pentadecane

Traditional Name

2,10,14-trimethyl-6-methylidene-7-(3-methylpent-4-en-1-yl)pentadecane

CAS Registry Number

Not Available

SMILES

CC(C)CCCC(C)CCC(CCC(C)C=C)C(=C)CCCC(C)C

InChI Identifier

InChI=1S/C25H48/c1-9-22(6)16-18-25(24(8)15-11-13-21(4)5)19-17-23(7)14-10-12-20(2)3/h9,20-23,25H,1,8,10-19H2,2-7H3

InChI Key

RNCKFEUHFHLLAW-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
Haslea ostrearia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Sesterterpenoids

Alternative Parents

Substituents

Sesterterpenoid
Branched unsaturated hydrocarbon
Alkadiene
Unsaturated aliphatic hydrocarbon
Unsaturated hydrocarbon
Olefin
Acyclic olefin
Hydrocarbon
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Acyclic sesterterpenoids (LMPR0105010011 )

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	9.98	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	116.33 m³·mol⁻¹	ChemAxon
Polarizability	47.72 Å³	ChemAxon
Number of Rings	0	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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

24823125

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

12067128

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for c25:2 highly branched isoprenoid (NP0317384)

MOL for NP0317384 (c25:2 highly branched isoprenoid)

3D MOL for NP0317384 (c25:2 highly branched isoprenoid)

3D SDF for NP0317384 (c25:2 highly branched isoprenoid)

3D-SDF for NP0317384 (c25:2 highly branched isoprenoid)

PDB for NP0317384 (c25:2 highly branched isoprenoid)

3D PDB for NP0317384 (c25:2 highly branched isoprenoid)

SMILES for NP0317384 (c25:2 highly branched isoprenoid)

INCHI for NP0317384 (c25:2 highly branched isoprenoid)

Structure for NP0317384 (c25:2 highly branched isoprenoid)

3D Structure for NP0317384 (c25:2 highly branched isoprenoid)