NP-MRD: Showing NP-Card for ferruginene c (NP0253981)

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Record Information

Version

2.0

Created at

2022-09-07 18:00:44 UTC

Updated at

2022-09-07 18:00:44 UTC

NP-MRD ID

NP0253981

Secondary Accession Numbers

None

Natural Product Identification

Common Name

ferruginene c

Description

Ferruginene C belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. ferruginene c is found in Rhododendron ferrugineum. ferruginene c was first documented in 2011 (PMID: 21443171). Based on a literature review very few articles have been published on Ferruginene C.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 55 56  0  0  0  0  0  0  0  0999 V2000
    6.2168    0.1367    0.3721 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2956   -0.6012    0.9871 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6447   -1.8740    1.6325 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8780   -0.1052    1.0058 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4699   -0.1970    2.3795 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0552   -1.1089    0.2818 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6057   -0.8873    0.1123 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1368    0.2235   -0.7339 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0348    1.0354   -1.3587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2768    0.3650   -1.0746 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4388    0.9215   -2.4788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9646    2.2965   -2.5436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9921    2.6538   -1.5597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8876    3.8479   -1.8497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1218    1.9643   -0.4629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2828    0.8174   -0.1370 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2156   -0.2241    0.4111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3355   -0.5094   -0.3717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5283    0.0675   -1.6143 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2589   -1.3873    0.1220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1187   -1.9881    1.3472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1633   -2.9292    1.8185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0188   -1.7174    2.1351 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0604   -0.8076    1.6331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0301   -0.5935    2.5190 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2406   -0.2603    0.3769 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0040    1.0667   -0.1113 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9727   -1.7180    2.6982 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4962   -2.3817    1.0761 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8256   -2.5950    1.6541 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8168    0.9317    0.7151 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8424    0.5778    2.5010 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1605   -2.0883    0.8676 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5352   -1.3191   -0.7168 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1345   -0.8850    1.1227 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1972   -1.8268   -0.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7409    1.8648   -1.9838 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0955    0.8669   -1.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5740   -0.7666   -1.2734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1532    0.2803   -3.0869 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4987    0.8392   -3.0313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1845    3.1086   -2.4730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4242    2.5007   -3.5568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6655    3.9355   -1.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2400    4.7390   -1.7786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4085    3.7674   -2.8062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8970    2.2233    0.2881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7377    1.1547    0.8282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3392   -0.1611   -2.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1410   -1.6173   -0.4915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0837   -2.8648    1.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7529   -3.9570    1.8132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4149   -2.6353    2.8665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9154   -2.1979    3.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2726    0.0184    2.4945 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  3
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  3
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
 16 10  1  0
 24 17  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  1 26  1  0
  1 27  1  0
  4 31  1  6
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  6
 11 40  1  0
 11 41  1  0
 12 42  1  0
 12 43  1  0
 14 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 16 48  1  1
 19 49  1  0
 20 50  1  0
 22 51  1  0
 22 52  1  0
 22 53  1  0
 23 54  1  0
 25 55  1  0
M  END


  Mrv1652309072220002D          

 25 26  0  0  1  0            999 V2000
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5737    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2881   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7532   -2.5612    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
 10  8  1  6  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
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  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
 17 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0253981

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)C(O)CCC(=C)[C@@H]1CCC(C)=C[C@H]1C1=C(O)C=C(C)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O3/c1-13(2)19(23)9-7-16(5)17-8-6-14(3)10-18(17)22-20(24)11-15(4)12-21(22)25/h10-12,17-19,23-25H,1,5-9H2,2-4H3/t17-,18+,19?/m0/s1

> <INCHI_KEY>
LQECQNLKIZLVSL-PAMZHZACSA-N

> <FORMULA>
C22H30O3

> <MOLECULAR_WEIGHT>
342.479

> <EXACT_MASS>
342.219494826

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
39.99186142852497

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(1R,6R)-6-(5-hydroxy-6-methylhepta-1,6-dien-2-yl)-3-methylcyclohex-2-en-1-yl]-5-methylbenzene-1,3-diol

> <JCHEM_LOGP>
5.0337633450000006

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.612662215169385

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.1578180770875

> <JCHEM_PKA_STRONGEST_BASIC>
-1.443328923876349

> <JCHEM_POLAR_SURFACE_AREA>
60.69

> <JCHEM_REFRACTIVITY>
104.37249999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1R,6R)-6-(5-hydroxy-6-methylhepta-1,6-dien-2-yl)-3-methylcyclohex-2-en-1-yl]-5-methylbenzene-1,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       8.002  -1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336  -3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.669  -1.540   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      10.669  -0.000   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.337  -1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.670  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.670  -3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.004  -1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.004   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.338   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      18.672   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      20.005   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      18.672  -1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      17.338  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.338  -3.850   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      20.005  -3.850   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      18.672  -6.160   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      17.338  -6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      17.338  -8.470   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      16.004  -6.160   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      14.473  -4.781   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   10   17                                                  
CONECT   17   16   18   24                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   17   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₃

Average Mass

342.4790 Da

Monoisotopic Mass

342.21949 Da

IUPAC Name

2-[(1R,6R)-6-(5-hydroxy-6-methylhepta-1,6-dien-2-yl)-3-methylcyclohex-2-en-1-yl]-5-methylbenzene-1,3-diol

Traditional Name

2-[(1R,6R)-6-(5-hydroxy-6-methylhepta-1,6-dien-2-yl)-3-methylcyclohex-2-en-1-yl]-5-methylbenzene-1,3-diol

CAS Registry Number

Not Available

SMILES

CC(=C)C(O)CCC(=C)[C@@H]1CCC(C)=C[C@H]1C1=C(O)C=C(C)C=C1O

InChI Identifier

InChI=1S/C22H30O3/c1-13(2)19(23)9-7-16(5)17-8-6-14(3)10-18(17)22-20(24)11-15(4)12-21(22)25/h10-12,17-19,23-25H,1,5-9H2,2-4H3/t17-,18+,19?/m0/s1

InChI Key

LQECQNLKIZLVSL-PAMZHZACSA-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
Rhododendron ferrugineum	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

Bisabolane sesquiterpenoid
Sesquiterpenoid
M-cresol
Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Toluene
Phenol
Monocyclic benzene moiety
Benzenoid
Secondary alcohol
Alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

sesquiterpenoid (CHEBI:67893 )

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	5.03	ChemAxon
pKa (Strongest Acidic)	9.16	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	60.69 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	104.37 m³·mol⁻¹	ChemAxon
Polarizability	39.99 Å³	ChemAxon
Number of Rings	2	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

26344488

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

52951888

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Seephonkai P, Popescu R, Zehl M, Krupitza G, Urban E, Kopp B: Ferruginenes A-C from Rhododendron ferrugineum and their cytotoxic evaluation. J Nat Prod. 2011 Apr 25;74(4):712-7. doi: 10.1021/np100778k. Epub 2011 Mar 28. [PubMed:21443171 ]
LOTUS database [Link]

Showing NP-Card for ferruginene c (NP0253981)

MOL for NP0253981 (ferruginene c)

3D MOL for NP0253981 (ferruginene c)

3D SDF for NP0253981 (ferruginene c)

3D-SDF for NP0253981 (ferruginene c)

PDB for NP0253981 (ferruginene c)

3D PDB for NP0253981 (ferruginene c)

SMILES for NP0253981 (ferruginene c)

INCHI for NP0253981 (ferruginene c)

Structure for NP0253981 (ferruginene c)

3D Structure for NP0253981 (ferruginene c)