NP-MRD: Showing NP-Card for Ilicic acid (NP0059324)

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Record Information

Version

2.0

Created at

2022-04-28 04:34:58 UTC

Updated at

2022-04-28 04:34:58 UTC

NP-MRD ID

NP0059324

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Ilicic acid

Description

Ilicic acid, also known as ilicate, belongs to the class of organic compounds known as eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids. These are sesquiterpenoids with a structure based on the eudesmane skeleton. Ilicic acid is found in Ambrosia ilicifolia, Artemisia scotina, Artemisia vachanica, Chiliadenus montanus, Dittrichia graveolens (L.) GREUTER , Inula viscosa , Flourensia oolepis, Heterocoma ekmaniana, Laggera alata , Laggera crispata, Ophryosporus floribundus, Pluchea sagittalis and Tessaria absinthioides. Ilicic acid was first documented in 2012 (PMID: 22986291). Based on a literature review a small amount of articles have been published on ilicic acid (PMID: 34915284) (PMID: 25190268) (PMID: 22347009) (PMID: 22259450).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 43  0  0  0  0  0  0  0  0999 V2000
    4.2011   -0.7560   -0.9718 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2620    0.0554   -0.5450 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6712    1.2479    0.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8828    1.4935    0.4028 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7086    2.1269    0.6505 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8385   -0.2460   -0.8093 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2079    0.7227   -1.7742 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0302    1.4543   -1.2835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9454    0.7024   -0.4514 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3668    1.5926    0.6915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2265    0.3826   -1.2343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1803   -0.3651   -0.3641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6296   -1.5355    0.3453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2541   -1.4017    0.9014 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2064   -0.9519    2.3276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7022   -2.7125    0.8882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4041   -0.6145   -0.0324 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0117   -0.4089    0.4517 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9394   -1.6425   -1.5148 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2326   -0.5447   -0.7846 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5675    2.3834    1.6037 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7944   -1.2448   -1.3059 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9621    0.2555   -2.7625 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0096    1.4786   -2.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3761    2.4022   -0.7775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5357    1.8368   -2.1848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4855    1.9633    1.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7794    2.5285    0.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1725    1.1967    1.3056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9228   -0.2915   -2.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7131    1.3059   -1.5843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7380    0.3359    0.3260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9989   -0.7403   -1.0515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3183   -1.7756    1.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7162   -2.4439   -0.3210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2651   -0.7689    2.6750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8415   -1.7534    3.0371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5485   -0.0895    2.5146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8600   -3.1463    1.7546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3479   -1.2483   -0.9700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0843    0.5154    1.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3787   -1.2987    1.0024 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 16  1  1
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  1  1
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6 18  1  0
 18 17  1  0
  6  2  1  0
  2  1  2  3
  2  3  1  0
  3  5  1  0
  3  4  2  0
 17 14  1  0
 17  9  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  0
 13 34  1  0
 13 35  1  0
 12 32  1  0
 12 33  1  0
 11 30  1  0
 11 31  1  0
 10 27  1  0
 10 28  1  0
 10 29  1  0
  8 25  1  0
  8 26  1  0
  7 23  1  0
  7 24  1  0
  6 22  1  6
 18 41  1  0
 18 42  1  0
 17 40  1  6
  1 19  1  0
  1 20  1  0
  5 21  1  0
M  END


  Mrv1652304282206342D          

 18 19  0  0  1  0            999 V2000
   -0.0000   -1.6500    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
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  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
    0.3873    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3873    0.7284    0.0000 O   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
    2.1434   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -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
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   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  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  4  7  1  6  0  0  0
  4  8  1  1  0  0  0
  3  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  2 12  1  0  0  0  0
 10 13  1  6  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
  2 18  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0059324

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]1(O)CCC[C@]2(C)CC[C@H](C[C@@H]12)C(=C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O3/c1-10(13(16)17)11-5-8-14(2)6-4-7-15(3,18)12(14)9-11/h11-12,18H,1,4-9H2,2-3H3,(H,16,17)/t11-,12-,14-,15-/m1/s1

> <INCHI_KEY>
FXKCXGBBUBCRPU-QHSBEEBCSA-N

> <FORMULA>
C15H24O3

> <MOLECULAR_WEIGHT>
252.354

> <EXACT_MASS>
252.172544633

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
28.48774555791887

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(2R,4aR,8R,8aR)-8-hydroxy-4a,8-dimethyl-decahydronaphthalen-2-yl]prop-2-enoic acid

> <ALOGPS_LOGP>
2.71

> <JCHEM_LOGP>
2.801374247

> <ALOGPS_LOGS>
-3.19

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.916438930100995

> <JCHEM_PKA_STRONGEST_BASIC>
-0.46154903947147863

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
70.0017

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.63e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(2R,4aR,8R,8aR)-8-hydroxy-4a,8-dimethyl-octahydronaphthalen-2-yl]prop-2-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.723   1.360   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.723   1.360   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.334  -3.850   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   12   18                                             
CONECT    3    2    4    9                                                  
CONECT    4    3    5    7    8                                             
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    4                                                            
CONECT    8    4                                                            
CONECT    9    3   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11    2                                                       
CONECT   13   10   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18    2                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   38    0
END

View in JSmol

Synonyms

Value	Source
Ilicate	Generator

Chemical Formula

C₁₅H₂₄O₃

Average Mass

252.3540 Da

Monoisotopic Mass

252.17254 Da

IUPAC Name

2-[(2R,4aR,8R,8aR)-8-hydroxy-4a,8-dimethyl-decahydronaphthalen-2-yl]prop-2-enoic acid

Traditional Name

2-[(2R,4aR,8R,8aR)-8-hydroxy-4a,8-dimethyl-octahydronaphthalen-2-yl]prop-2-enoic acid

CAS Registry Number

Not Available

SMILES

C[C@@]1(O)CCC[C@]2(C)CC[C@H](C[C@@H]12)C(=C)C(O)=O

InChI Identifier

InChI=1S/C15H24O3/c1-10(13(16)17)11-5-8-14(2)6-4-7-15(3,18)12(14)9-11/h11-12,18H,1,4-9H2,2-3H3,(H,16,17)/t11-,12-,14-,15-/m1/s1

InChI Key

FXKCXGBBUBCRPU-QHSBEEBCSA-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
Ambrosia ilicifolia	Plant	KNApSAcK
Artemisia scotina	LOTUS Database	35616633
Artemisia vachanica	LOTUS Database	35616633
Chiliadenus montanus	LOTUS Database	35616633
Dittrichia graveolens	Plant	KNApSAcK
Dittrichia viscosa	Plant	KNApSAcK
Flourensia oolepis	LOTUS Database	35616633
Heterocoma ekmaniana	LOTUS Database	35616633
Laggera alata	Plant	KNApSAcK
Laggera crispata	LOTUS Database	35616633
Ophryosporus floribundus	Plant	KNApSAcK
Pluchea sagittalis	LOTUS Database	35616633
Tessaria absinthioides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids. These are sesquiterpenoids with a structure based on the eudesmane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids

Alternative Parents

Substituents

Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoid
Tertiary alcohol
Cyclic alcohol
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	2.71	ALOGPS
logP	2.8	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	4.92	ChemAxon
pKa (Strongest Basic)	-0.46	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	70 m³·mol⁻¹	ChemAxon
Polarizability	28.49 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

C00012852

Chemspider ID

10050523

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11876195

PDB ID

Not Available

ChEBI ID

181639

Good Scents ID

Not Available

References

General References

Zhao G, Li X, Chen W, Xi Z, Sun L: Three new sesquiterpenes from Tithonia diversifolia and their anti-hyperglycemic activity. Fitoterapia. 2012 Dec;83(8):1590-7. doi: 10.1016/j.fitote.2012.09.007. Epub 2012 Sep 15. [PubMed:22986291 ]
Zeouk I, Sifaoui I, Ben Jalloul A, Bekhti K, Bazzocchi IL, Pinero JE, Jimenez IA, Lorenzo-Morales J: Isolation, identification, and activity evaluation of antioxidant components from Inula viscosa: A bioguided approach. Bioorg Chem. 2022 Feb;119:105551. doi: 10.1016/j.bioorg.2021.105551. Epub 2021 Dec 11. [PubMed:34915284 ]
Abu Irmaileh BE, Al-Aboudi AM, Abu Zarga MH, Awwadi F, Haddad SF: Selective phytotoxic activity of 2,3,11beta,13-tetrahydroaromaticin and ilicic acid isolated from Inula graveolens. Nat Prod Res. 2015;29(10):893-8. doi: 10.1080/14786419.2014.955489. Epub 2014 Sep 5. [PubMed:25190268 ]
Tebbaa M, Benharref A, Daran JC, Mellouki F, Berraho M: Methyl 2-(1a,4a-dimethyl-2,8-dioxo-2,3,4,4a,5,6,7,8-octa-hydro-1aH-1-oxacyclo-propa[d]na phthalen-7-yl)acrylate. Acta Crystallogr Sect E Struct Rep Online. 2012 Feb 1;68(Pt 2):o387. doi: 10.1107/S1600536812000086. Epub 2012 Jan 14. [PubMed:22347009 ]
Tebbaa M, Benharref A, Oudahmane A, Mellouki F, Berraho M: Methyl 2-(8a-hy-droxy-4a-methyl-8-methyl-enedeca-hydro-naphthalen-2-yl)acrylate. Acta Crystallogr Sect E Struct Rep Online. 2012 Jan;68(Pt 1):o165. doi: 10.1107/S1600536811053712. Epub 2011 Dec 17. [PubMed:22259450 ]

Showing NP-Card for Ilicic acid (NP0059324)

MOL for NP0059324 (Ilicic acid)

3D MOL for NP0059324 (Ilicic acid)

3D SDF for NP0059324 (Ilicic acid)

3D-SDF for NP0059324 (Ilicic acid)

PDB for NP0059324 (Ilicic acid)

3D PDB for NP0059324 (Ilicic acid)

SMILES for NP0059324 (Ilicic acid)

INCHI for NP0059324 (Ilicic acid)

Structure for NP0059324 (Ilicic acid)

3D Structure for NP0059324 (Ilicic acid)