NP-MRD: Showing NP-Card for fuscol (NP0207646)

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Record Information

Version

2.0

Created at

2022-09-05 04:20:23 UTC

Updated at

2022-09-05 04:20:23 UTC

NP-MRD ID

NP0207646

Secondary Accession Numbers

None

Natural Product Identification

Common Name

fuscol

Description

Fuscol belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. fuscol is found in Eunicea fusca and Lobophytum pauciflorum. fuscol was first documented in 2011 (PMID: 21865038). Based on a literature review a small amount of articles have been published on Fuscol (PMID: 31588327) (PMID: 25240256) (PMID: 22734800) (PMID: 22209732).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 53  0  0  0  0  0  0  0  0999 V2000
   -4.2602    2.2107    1.8481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3727    1.2756    1.5956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0704    0.8110    0.1975 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3188    1.0033   -0.6786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0336    1.7231   -0.3493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6160    1.4348    0.0728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3958    0.0105    0.4439 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9792   -0.4614    0.4495 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3408   -1.8755    0.7861 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9701    0.3514    0.1540 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3496   -0.1539    0.1673 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3557    0.6466   -0.1263 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7755    0.1665   -0.1231 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9005   -1.2527   -0.5764 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5363    1.1035   -1.0541 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2360    0.2943    1.1850 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3540   -0.8268   -0.3864 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7199   -0.6353    0.2520 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7458   -1.5180   -0.3403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4294   -2.2706   -1.3625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1036   -1.5508    0.2271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4540    2.5219    2.8651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8242    2.6995    1.0630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8177    0.7971    2.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2248    1.0498   -0.0716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2702    1.9988   -1.2109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3407    0.2587   -1.5000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2702    2.7588    0.0354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1299    1.8362   -1.4671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2488    2.1594    0.8277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0095    1.6283   -0.8522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7726   -0.0866    1.5125 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0688   -1.9263    1.6104 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8330   -2.3708   -0.0949 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4442   -2.4455    1.1082 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8239    1.3834   -0.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5607   -1.1986    0.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1162    1.6907   -0.3767 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9851   -1.9549    0.2634 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8390   -1.3715   -1.1907 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0731   -1.5849   -1.2366 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8538    1.3039   -1.9054 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6862    2.0647   -0.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5016    0.6652   -1.3684 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6864    0.9238    1.7000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3814   -0.4403   -1.4207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1136   -1.9080   -0.3126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5595   -0.9448    1.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4272   -2.2701   -1.8094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1835   -2.9221   -1.7884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9039   -1.2166   -0.4515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1723   -0.9836    1.1874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4106   -2.6021    0.5152 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 19  1  0
 19 20  2  3
 19 18  1  0
 18 17  1  0
 17  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  0
  3  2  1  1
  2  1  2  3
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 13 16  1  0
  3 18  1  0
 21 51  1  0
 21 52  1  0
 21 53  1  0
 20 49  1  0
 20 50  1  0
 18 48  1  1
 17 46  1  0
 17 47  1  0
  7 32  1  1
  6 30  1  0
  6 31  1  0
  5 28  1  0
  5 29  1  0
  4 25  1  0
  4 26  1  0
  4 27  1  0
  2 24  1  0
  1 22  1  0
  1 23  1  0
  9 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 11 37  1  0
 12 38  1  0
 14 39  1  0
 14 40  1  0
 14 41  1  0
 15 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
M  END


  Mrv1652309052206202D          

 21 21  0  0  1  0            999 V2000
    2.0572    1.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2448    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1842    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    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
    0.7145   -0.4125    0.0000 C   0  0  2  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
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    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
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5395   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  2  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
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  6  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  6  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 13 16  1  0  0  0  0
  7 17  1  0  0  0  0
 17 18  1  0  0  0  0
  3 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0207646

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)[C@H]1C[C@H](CC[C@]1(C)C=C)C(\C)=C\C=C\C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O/c1-8-20(7)13-11-17(14-18(20)15(2)3)16(4)10-9-12-19(5,6)21/h8-10,12,17-18,21H,1-2,11,13-14H2,3-7H3/b12-9+,16-10+/t17-,18+,20-/m0/s1

> <INCHI_KEY>
PGZCBHXBAUSEPY-VHSBKHBUSA-N

> <FORMULA>
C20H32O

> <MOLECULAR_WEIGHT>
288.475

> <EXACT_MASS>
288.24531565

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
36.56867325978672

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3E,5E)-6-[(1S,3R,4R)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]-2-methylhepta-3,5-dien-2-ol

> <JCHEM_LOGP>
5.067212182666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.91153564552257

> <JCHEM_PKA_STRONGEST_BASIC>
-1.5252943086484274

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
95.05

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
fuscol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       3.840   3.222   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.324   3.490   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.344   3.490   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.000  -4.620   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      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.874  -6.930   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.206  -6.930   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   18                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   17                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   13                                                            
CONECT   17    7   18                                                       
CONECT   18   17    3   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂O

Average Mass

288.4750 Da

Monoisotopic Mass

288.24532 Da

IUPAC Name

(3E,5E)-6-[(1S,3R,4R)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]-2-methylhepta-3,5-dien-2-ol

Traditional Name

fuscol

CAS Registry Number

Not Available

SMILES

CC(=C)[C@H]1C[C@H](CC[C@]1(C)C=C)C(\C)=C\C=C\C(C)(C)O

InChI Identifier

InChI=1S/C20H32O/c1-8-20(7)13-11-17(14-18(20)15(2)3)16(4)10-9-12-19(5,6)21/h8-10,12,17-18,21H,1-2,11,13-14H2,3-7H3/b12-9+,16-10+/t17-,18+,20-/m0/s1

InChI Key

PGZCBHXBAUSEPY-VHSBKHBUSA-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
Eunicea fusca	LOTUS Database	35616633
Lobophytum pauciflorum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Lobane diterpenoid
Diterpenoid
Tertiary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	5.07	ChemAxon
pKa (Strongest Acidic)	17.91	ChemAxon
pKa (Strongest Basic)	-1.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	95.05 m³·mol⁻¹	ChemAxon
Polarizability	36.57 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

9066802

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10891538

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Rovira AR, Muller N, Deng W, Ndubaku C, Sarpong R: Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol. Chem Sci. 2019 Jul 3;10(33):7788-7791. doi: 10.1039/c9sc02572c. eCollection 2019 Sep 7. [PubMed:31588327 ]
Kerr RG, Brophy S, Derksen DJ: Synthesis and evaluation of anti-inflammatory activity of derivatives of the marine natural products fuscol and eunicol. Bioorg Med Chem Lett. 2014 Oct 15;24(20):4804-6. doi: 10.1016/j.bmcl.2014.09.008. Epub 2014 Sep 15. [PubMed:25240256 ]
Marchbank DH, Berrue F, Kerr RG: Eunicidiol, an anti-inflammatory dilophol diterpene from Eunicea fusca. J Nat Prod. 2012 Jul 27;75(7):1289-93. doi: 10.1021/np300149y. Epub 2012 Jun 26. [PubMed:22734800 ]
Govindam SV, Yoshioka Y, Kanamoto A, Fujiwara T, Okamoto T, Ojika M: Cyclolobatriene, a novel prenylated germacrene diterpene, from the soft coral Lobophytum pauciflorum. Bioorg Med Chem. 2012 Jan 15;20(2):687-92. doi: 10.1016/j.bmc.2011.12.012. Epub 2011 Dec 14. [PubMed:22209732 ]
Reina E, Puentes C, Rojas J, Garcia J, Ramos FA, Castellanos L, Aragon M, Ospina LF: Fuscoside E: a strong anti-inflammatory diterpene from Caribbean octocoral Eunicea fusca. Bioorg Med Chem Lett. 2011 Oct 1;21(19):5888-91. doi: 10.1016/j.bmcl.2011.07.092. Epub 2011 Aug 4. [PubMed:21865038 ]
LOTUS database [Link]

Showing NP-Card for fuscol (NP0207646)

MOL for NP0207646 (fuscol)

3D MOL for NP0207646 (fuscol)

3D SDF for NP0207646 (fuscol)

3D-SDF for NP0207646 (fuscol)

PDB for NP0207646 (fuscol)

3D PDB for NP0207646 (fuscol)

SMILES for NP0207646 (fuscol)

INCHI for NP0207646 (fuscol)

Structure for NP0207646 (fuscol)

3D Structure for NP0207646 (fuscol)