NP-MRD: Showing NP-Card for 1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid (NP0223351)

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Record Information

Version

2.0

Created at

2022-09-06 01:25:15 UTC

Updated at

2022-09-06 01:25:15 UTC

NP-MRD ID

NP0223351

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid

Description

Diplodiatoxin belongs to the class of organic compounds known as gamma-keto acids and derivatives. These are organic compounds containing an aldehyde substituted with a keto group on the C4 carbon atom. Diplodiatoxin is an extremely weak basic (essentially neutral) compound (based on its pKa). Diplodiatoxin is a metabolite of Diplodia maydis (parasite of sweet corn). Metabolite of Diplodia maydis (parasite of sweet corn). 1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid is found in Stenocarpella maydis. Toxin causing diplodiosis disease of cattle and sheep.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 50 51  0  0  0  0  0  0  0  0999 V2000
    1.1438   -2.4765    2.4610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4982   -1.6478    1.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5312   -0.8835    1.7627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2600   -0.0042    0.7939 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6960   -0.5102    0.7199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4981    0.1382   -0.3377 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2091    1.3376    0.2807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8294    0.4315   -1.6152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3486    0.8194   -1.5061 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3143    2.2695   -1.1974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7059   -0.1281   -0.6116 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7924   -0.2924   -0.6137 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2778   -0.3573   -2.0285 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5165    0.7630    0.0729 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9133    1.6601    0.6089 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9868    0.7842    0.1432 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4948    2.0243    0.9032 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8617    2.0463    0.9699 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0044   -1.6778    0.0319 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2667   -2.3120   -0.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9563   -2.7335    0.7730 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8263   -2.5133   -1.4348 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1277   -2.0739    2.8123 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3234   -3.5316    2.1754 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4881   -2.5663    3.3840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8905   -0.8705    2.7831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2478    0.9999    1.1966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2075   -0.3466    1.6999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6219   -1.6082    0.5530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3366   -0.5856   -0.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9971    0.8938    0.9586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7289    1.9437   -0.4580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5520    1.9028    0.9729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3369    1.3039   -2.0992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9389   -0.3980   -2.3744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9670    0.6780   -2.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5537    2.5480   -0.1737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3577    2.7223   -1.5815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0904    2.8157   -1.8211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0618   -1.1419   -0.9480 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7916   -1.1819   -2.5672 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3943   -0.3833   -2.0589 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9903    0.6125   -2.5429 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4647    0.8741   -0.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3744   -0.0551    0.7258 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0593    2.9514    0.4789 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0590    1.9431    1.9385 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2466    1.5630    1.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2233   -2.3136   -0.5089 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1997   -3.4331   -1.6890 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11  4  1  0
  4  5  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 19  1  0
 19 20  1  0
 20 22  1  0
 20 21  2  0
 19 12  1  0
 12 13  1  0
 12 14  1  1
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
  5  6  1  0
 12 11  1  0
  7 31  1  0
  7 32  1  0
  7 33  1  0
  6 30  1  6
  8 34  1  0
  8 35  1  0
  9 36  1  6
 10 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  6
  4 27  1  1
  5 28  1  0
  5 29  1  0
  3 26  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
 19 49  1  6
 22 50  1  0
 13 41  1  0
 13 42  1  0
 13 43  1  0
 16 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
M  END


  Mrv0541 05061305572D          

 22 23  0  0  0  0            999 V2000
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    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
    0.8986    3.1070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7717    2.9637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3020    3.5957    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
    0.0000    0.8250    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
   -0.7145    1.2375    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
    2.1434    1.2375    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
    1.9592    3.1070    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
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1145    3.4525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6771    3.8822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3428    3.1424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
 10  1  1  0  0  0  0
 10  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  2  1  0  0  0  0
 11  7  1  0  0  0  0
 12  3  1  0  0  0  0
 12  9  2  0  0  0  0
 13  8  1  0  0  0  0
 13  9  1  0  0  0  0
 14  5  1  0  0  0  0
 15 11  1  0  0  0  0
 15 13  1  0  0  0  0
 16 12  1  0  0  0  0
 17 16  1  0  0  0  0
 18  4  1  0  0  0  0
 18 14  1  0  0  0  0
 18 15  1  0  0  0  0
 18 16  1  0  0  0  0
 19  6  1  0  0  0  0
 20 14  2  0  0  0  0
 21 17  2  0  0  0  0
 22 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0223351

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC(C)C2C(C1)C=C(C)C(C(O)=O)C2(C)C(=O)CCO

> <INCHI_IDENTIFIER>
InChI=1S/C18H28O4/c1-10-7-11(2)15-13(8-10)9-12(3)16(17(21)22)18(15,4)14(20)5-6-19/h9-11,13,15-16,19H,5-8H2,1-4H3,(H,21,22)

> <INCHI_KEY>
SFTQDPVLDKOILY-UHFFFAOYSA-N

> <FORMULA>
C18H28O4

> <MOLECULAR_WEIGHT>
308.4125

> <EXACT_MASS>
308.198759384

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
34.406996269363304

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalene-2-carboxylic acid

> <ALOGPS_LOGP>
2.82

> <JCHEM_LOGP>
2.873232959333332

> <ALOGPS_LOGS>
-3.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
15.74414127943545

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.595082629661371

> <JCHEM_PKA_STRONGEST_BASIC>
-2.4411054596780364

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
85.53229999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.30e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2H-naphthalene-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.677   5.800   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.174   5.532   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.164   6.712   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.334   2.310   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       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.657   5.800   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.680   6.445   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       3.131   7.247   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       6.240   5.866   0.000  0.00  0.00           O+0
CONECT    1   10                                                            
CONECT    2   11                                                            
CONECT    3   12                                                            
CONECT    4   18                                                            
CONECT    5    6   14                                                       
CONECT    6    5   19                                                       
CONECT    7   10   11                                                       
CONECT    8   10   13                                                       
CONECT    9   12   13                                                       
CONECT   10    1    7    8                                                  
CONECT   11    2    7   15                                                  
CONECT   12    3    9   16                                                  
CONECT   13    8    9   15                                                  
CONECT   14    5   18   20                                                  
CONECT   15   11   13   18                                                  
CONECT   16   12   17   18                                                  
CONECT   17   16   21   22                                                  
CONECT   18    4   14   15   16                                             
CONECT   19    6                                                            
CONECT   20   14                                                            
CONECT   21   17                                                            
CONECT   22   17                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Value	Source
1,2,4a,5,6,7,8,8a-Octahydro-1-(3-hydroxy-1-oxopropyl)-1,3,6,8-tetramethyl-2-naphthalenecarboxylic acid, 9ci	HMDB
1-(3-Hydroxypropanoyl)-1,3,6,8-tetramethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalene-2-carboxylate	Generator
Diplodiatoxin	MeSH

Chemical Formula

C₁₈H₂₈O₄

Average Mass

308.4125 Da

Monoisotopic Mass

308.19876 Da

IUPAC Name

1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalene-2-carboxylic acid

Traditional Name

1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2H-naphthalene-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC1CC(C)C2C(C1)C=C(C)C(C(O)=O)C2(C)C(=O)CCO

InChI Identifier

InChI=1S/C18H28O4/c1-10-7-11(2)15-13(8-10)9-12(3)16(17(21)22)18(15,4)14(20)5-6-19/h9-11,13,15-16,19H,5-8H2,1-4H3,(H,21,22)

InChI Key

SFTQDPVLDKOILY-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
Diplodia maydis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gamma-keto acids and derivatives. These are organic compounds containing an aldehyde substituted with a keto group on the C4 carbon atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Keto acids and derivatives

Sub Class

Gamma-keto acids and derivatives

Direct Parent

Gamma-keto acids and derivatives

Alternative Parents

Substituents

Gamma-keto acid
Beta-hydroxy ketone
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
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	2.82	ALOGPS
logP	2.87	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	4.6	ChemAxon
pKa (Strongest Basic)	-2.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	85.53 m³·mol⁻¹	ChemAxon
Polarizability	34.41 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

HMDB0031471

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB008044

KNApSAcK ID

Not Available

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

12309246

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid (NP0223351)

MOL for NP0223351 (1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid)

3D MOL for NP0223351 (1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid)

3D SDF for NP0223351 (1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid)

3D-SDF for NP0223351 (1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid)

PDB for NP0223351 (1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid)

3D PDB for NP0223351 (1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid)

SMILES for NP0223351 (1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid)

INCHI for NP0223351 (1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid)

Structure for NP0223351 (1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid)

3D Structure for NP0223351 (1-(3-hydroxypropanoyl)-1,3,6,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-2h-naphthalene-2-carboxylic acid)