NP-MRD: Showing NP-Card for Relhaniaic acid (NP0066118)

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Record Information

Version

2.0

Created at

2022-04-28 10:16:45 UTC

Updated at

2022-04-28 10:16:46 UTC

NP-MRD ID

NP0066118

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Relhaniaic acid

Description

Relhaniaic acid, also known as relhaniaate, belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms. Relhaniaic acid is found in Relhania acerosa. Based on a literature review very few articles have been published on Relhaniaic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 54  0  0  0  0  0  0  0  0999 V2000
    4.7585   -1.4888    0.7410 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6464   -0.7268    0.0158 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0072    0.4215   -0.4618 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3521    0.9436   -0.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6060    2.1073   -0.8297 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4151    0.3722    0.3153 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3885   -1.4237   -0.0122 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1209   -0.9425   -0.5125 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3361    0.1047    0.1831 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9298    1.4760    0.2072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9310    0.2690   -0.6359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7853    0.6516   -1.8819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0247    0.7851   -2.6806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1244    1.5885   -3.6218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1248   -0.1373   -2.2384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4276    0.2450   -0.8167 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5753   -0.6342   -0.3509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8137    1.7042   -0.8119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2117   -0.0303    0.0271 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2536    0.8380    1.2820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1026    0.5933    2.1819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0288   -0.2873    1.6009 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2850   -1.7361    1.8437 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1168   -0.9371    1.6000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3946   -2.4996    1.0557 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5859   -1.6976    0.0453 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2604    0.9863   -1.0337 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3319    0.4050   -0.0967 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6260   -2.4739   -0.4507 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2077   -1.7265    1.0950 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1865   -0.6082   -1.6092 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4448   -1.8542   -0.6452 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8168    1.6004    0.8478 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1861    2.2130    0.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1410    1.8915   -0.7969 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1534    0.8863   -2.3519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7264   -1.1669   -2.3043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0117   -0.0337   -2.9025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1766   -1.4893    0.2304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1463   -1.0671   -1.1929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2699   -0.0162    0.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4735    1.8751   -1.6900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2853    1.9646    0.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8868    2.2905   -0.9854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3134   -1.0865    0.3577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2399    1.8916    0.9093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2205    0.7205    1.8143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7055    1.5692    2.5322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4799    0.0717    3.1002 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9019   -0.0455    2.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4162   -2.1943    2.5812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2772   -1.7763    2.4071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4291   -2.3857    0.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
 19 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  1  1
 16 18  1  0
 11  9  1  0
  9 10  1  1
  9  8  1  0
  8  7  1  0
  7  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  6  1  0
  4  5  2  0
  9 22  1  0
 16 19  1  0
 23 51  1  0
 23 52  1  0
 23 53  1  0
 22 50  1  1
 21 48  1  0
 21 49  1  0
 20 46  1  0
 20 47  1  0
 19 45  1  1
 12 36  1  0
 15 37  1  0
 15 38  1  0
 17 39  1  0
 17 40  1  0
 17 41  1  0
 18 42  1  0
 18 43  1  0
 18 44  1  0
 10 33  1  0
 10 34  1  0
 10 35  1  0
  8 31  1  0
  8 32  1  0
  7 29  1  0
  7 30  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  6 28  1  0
M  END


  Mrv1652304282212162D          

 23 24  0  0  1  0            999 V2000
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   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
    0.0000   -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  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
    1.4289   -0.0000    0.0000 C   0  0  1  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
    1.0416    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788    1.4281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0915    2.1565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5287    2.8561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1414    3.5846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3169    3.6134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5785    4.2842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2670    2.1853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8163    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3873   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3873   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  6  7  2  0  0  0  0
  1  7  1  0  0  0  0
  6  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
  5 11  1  0  0  0  0
  9 12  1  6  0  0  0
  8 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 15 20  1  0  0  0  0
  8 21  1  1  0  0  0
  4 22  1  0  0  0  0
  4 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0066118

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC[C@@H]2C(=CC(=O)CC2(C)C)[C@]1(C)CC\C(C)=C\C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O3/c1-13(10-18(22)23)8-9-20(5)14(2)6-7-16-17(20)11-15(21)12-19(16,3)4/h10-11,14,16H,6-9,12H2,1-5H3,(H,22,23)/b13-10+/t14-,16-,20-/m1/s1

> <INCHI_KEY>
WLZMZARRLMIMRW-SSMFIEESSA-N

> <FORMULA>
C20H30O3

> <MOLECULAR_WEIGHT>
318.457

> <EXACT_MASS>
318.219494826

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
36.71058703393891

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-5-[(1R,2R,4aS)-1,2,5,5-tetramethyl-7-oxo-1,2,3,4,4a,5,6,7-octahydronaphthalen-1-yl]-3-methylpent-2-enoic acid

> <ALOGPS_LOGP>
4.61

> <JCHEM_LOGP>
4.602178735000001

> <ALOGPS_LOGS>
-4.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.607314185270456

> <JCHEM_PKA_STRONGEST_BASIC>
-4.980190744955018

> <JCHEM_POLAR_SURFACE_AREA>
54.370000000000005

> <JCHEM_REFRACTIVITY>
93.61179999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.63e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-5-[(1R,2R,4aS)-1,2,5,5-tetramethyl-7-oxo-3,4,4a,6-tetrahydro-2H-naphthalen-1-yl]-3-methylpent-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      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.944   1.360   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.760   2.666   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.037   4.025   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.854   5.331   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.131   6.691   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.591   6.745   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       2.947   7.997   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.498   4.079   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.390   1.360   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.723  -4.440   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.723  -4.440   0.000  0.00  0.00           C+0
CONECT    1    2    3    7                                                  
CONECT    2    1                                                            
CONECT    3    1    4                                                       
CONECT    4    3    5   22   23                                             
CONECT    5    4    6   11                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6    1                                                       
CONECT    8    6    9   13   21                                             
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10    5                                                       
CONECT   12    9                                                            
CONECT   13    8   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15                                                            
CONECT   21    8                                                            
CONECT   22    4                                                            
CONECT   23    4                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Value	Source
Relhaniaate	Generator

Chemical Formula

C₂₀H₃₀O₃

Average Mass

318.4570 Da

Monoisotopic Mass

318.21949 Da

IUPAC Name

(2E)-5-[(1R,2R,4aS)-1,2,5,5-tetramethyl-7-oxo-1,2,3,4,4a,5,6,7-octahydronaphthalen-1-yl]-3-methylpent-2-enoic acid

Traditional Name

(2E)-5-[(1R,2R,4aS)-1,2,5,5-tetramethyl-7-oxo-3,4,4a,6-tetrahydro-2H-naphthalen-1-yl]-3-methylpent-2-enoic acid

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@@H]2C(=CC(=O)CC2(C)C)[C@]1(C)CC\C(C)=C\C(O)=O

InChI Identifier

InChI=1S/C20H30O3/c1-13(10-18(22)23)8-9-20(5)14(2)6-7-16-17(20)11-15(21)12-19(16,3)4/h10-11,14,16H,6-9,12H2,1-5H3,(H,22,23)/b13-10+/t14-,16-,20-/m1/s1

InChI Key

WLZMZARRLMIMRW-SSMFIEESSA-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
Relhania acerosa	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Medium-chain fatty acids

Alternative Parents

Substituents

Medium-chain fatty acid
Branched fatty acid
Cyclohexenone
Methyl-branched fatty acid
Unsaturated fatty acid
Ketone
Cyclic ketone
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
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	4.61	ALOGPS
logP	4.6	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	4.61	ChemAxon
pKa (Strongest Basic)	-5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.37 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	93.61 m³·mol⁻¹	ChemAxon
Polarizability	36.71 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

C00023447

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

101967097

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Relhaniaic acid (NP0066118)

MOL for NP0066118 (Relhaniaic acid)

3D MOL for NP0066118 (Relhaniaic acid)

3D SDF for NP0066118 (Relhaniaic acid)

3D-SDF for NP0066118 (Relhaniaic acid)

PDB for NP0066118 (Relhaniaic acid)

3D PDB for NP0066118 (Relhaniaic acid)

SMILES for NP0066118 (Relhaniaic acid)

INCHI for NP0066118 (Relhaniaic acid)

Structure for NP0066118 (Relhaniaic acid)

3D Structure for NP0066118 (Relhaniaic acid)