NP-MRD: Showing NP-Card for Parvifoliol D (NP0085966)

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Record Information

Version

2.0

Created at

2022-04-29 06:22:47 UTC

Updated at

2022-04-29 06:22:47 UTC

NP-MRD ID

NP0085966

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Parvifoliol D

Description

(2S,3S)-2-Methyl-2-(4-methyl-3-pentenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-6-carboxylic acid methyl ester belongs to the class of organic compounds known as salicylic acid and derivatives. Salicylic acid and derivatives are compounds containing a 2-hydroxybenzoic acid moiety or a derivative thereof. Parvifoliol D is found in Garcinia parvifolia . Based on a literature review very few articles have been published on (2S,3S)-2-Methyl-2-(4-methyl-3-pentenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-6-carboxylic acid methyl ester.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 49  0  0  0  0  0  0  0  0999 V2000
   -7.0763   -0.8852    1.1327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7278   -0.6555    0.7516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3188    0.6209    0.3553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1763    1.5166    0.3553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9334    0.8525   -0.0353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4672    2.0864   -0.4358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2572    3.2051   -0.5042 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1251    2.2546   -0.8009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2651    1.1824   -0.7606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7362   -0.0404   -0.3621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0625   -0.2451    0.0085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5519   -1.4764    0.4154 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8260   -1.2167   -0.3179 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3437   -0.9925   -1.2122 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2448   -2.0227   -1.1083 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0353    0.3193   -0.9656 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0619    0.5307   -2.0536 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5470    0.4738    0.4230 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5359   -0.5104    0.9170 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8078   -0.6111    0.1854 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9546   -0.3115    0.7941 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2695   -0.3973    0.0977 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9476    0.1251    2.2136 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0819    1.3992   -1.1370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0897   -1.9072    1.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3474   -0.1025    1.8470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7317   -0.8486    0.2517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1928    3.3634   -0.3139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7467    3.2120   -1.1155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9239   -2.2559    0.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3658   -2.1122   -0.7462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5117   -1.4631    0.7131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0473   -0.9502   -2.2602 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9235   -2.7947   -1.6426 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9744    1.0535   -1.7074 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6550    1.2311   -2.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3660   -0.4105   -2.5530 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9141    1.5377    0.5203 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6269    0.4738    1.0872 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0753   -1.5405    1.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7276   -0.2406    2.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8685   -0.9353   -0.8356 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3210    0.4617   -0.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0906   -0.4053    0.8151 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2920   -1.3239   -0.5403 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3434    1.0678    2.2441 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9490    0.3489    2.5808 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5235   -0.6608    2.8805 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  9 24  1  0
 24 16  1  0
 16 17  1  6
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  3
 21 22  1  0
 21 23  1  0
 16 14  1  0
 14 15  1  0
 14 13  1  0
 13 10  1  0
 10 11  2  0
 11 12  1  0
 11  5  1  0
 10  9  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  7 28  1  0
  8 29  1  0
 17 35  1  0
 17 36  1  0
 17 37  1  0
 18 38  1  0
 18 39  1  0
 19 40  1  0
 19 41  1  0
 20 42  1  0
 22 43  1  0
 22 44  1  0
 22 45  1  0
 23 46  1  0
 23 47  1  0
 23 48  1  0
 14 33  1  6
 15 34  1  0
 13 31  1  0
 13 32  1  0
 12 30  1  0
M  END


  Mrv1652304292208222D          

 24 25  0  0  1  0            999 V2000
   -1.8431   -4.3385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5610   -3.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0913   -2.9313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7485   -3.4200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4663   -2.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966   -2.0127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5269   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    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
    0.7145   -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
   -0.7145   -0.4125    0.0000 C   0  0  2  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
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    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
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   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
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  1  0  0  0
 11 15  2  0  0  0  0
 15 16  1  0  0  0  0
 10 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 24  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0085966

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=C(O)C=C2O[C@@](C)(CCC=C(C)C)[C@@H](O)CC2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C18H24O6/c1-10(2)6-5-7-18(3)14(20)8-11-13(24-18)9-12(19)15(16(11)21)17(22)23-4/h6,9,14,19-21H,5,7-8H2,1-4H3/t14-,18-/m0/s1

> <INCHI_KEY>
IYHBOJQFFYKDII-KSSFIOAISA-N

> <FORMULA>
C18H24O6

> <MOLECULAR_WEIGHT>
336.384

> <EXACT_MASS>
336.157288493

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
36.50943926342236

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2S,3S)-3,5,7-trihydroxy-2-methyl-2-(4-methylpent-3-en-1-yl)-3,4-dihydro-2H-1-benzopyran-6-carboxylate

> <ALOGPS_LOGP>
2.49

> <JCHEM_LOGP>
4.356294133333333

> <ALOGPS_LOGS>
-3.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.92271483199405

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.704438194590045

> <JCHEM_PKA_STRONGEST_BASIC>
-3.338931279133387

> <JCHEM_POLAR_SURFACE_AREA>
96.22

> <JCHEM_REFRACTIVITY>
90.56299999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.32e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2S,3S)-3,5,7-trihydroxy-2-methyl-2-(4-methylpent-3-en-1-yl)-3,4-dihydro-1-benzopyran-6-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      -3.441  -8.099   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.914  -6.651   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.904  -5.472   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.397  -6.384   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.870  -4.937   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.860  -3.757   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.850  -2.043   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   13                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12    7   14                                                  
CONECT   14   13                                                            
CONECT   15   11   16   20                                                  
CONECT   16   15                                                            
CONECT   17   10   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   15   21                                                  
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Value	Source
(2S,3S)-2-Methyl-2-(4-methyl-3-pentenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-6-carboxylate methyl ester	Generator

Chemical Formula

C₁₈H₂₄O₆

Average Mass

336.3840 Da

Monoisotopic Mass

336.15729 Da

IUPAC Name

methyl (2S,3S)-3,5,7-trihydroxy-2-methyl-2-(4-methylpent-3-en-1-yl)-3,4-dihydro-2H-1-benzopyran-6-carboxylate

Traditional Name

methyl (2S,3S)-3,5,7-trihydroxy-2-methyl-2-(4-methylpent-3-en-1-yl)-3,4-dihydro-1-benzopyran-6-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=C(O)C=C2O[C@@](C)(CCC=C(C)C)[C@@H](O)CC2=C1O

InChI Identifier

InChI=1S/C18H24O6/c1-10(2)6-5-7-18(3)14(20)8-11-13(24-18)9-12(19)15(16(11)21)17(22)23-4/h6,9,14,19-21H,5,7-8H2,1-4H3/t14-,18-/m0/s1

InChI Key

IYHBOJQFFYKDII-KSSFIOAISA-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
Garcinia parvifolia	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as salicylic acid and derivatives. Salicylic acid and derivatives are compounds containing a 2-hydroxybenzoic acid moiety or a derivative thereof.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Salicylic acid and derivatives

Alternative Parents

Substituents

Chromane
Benzopyran
1-benzopyran
Salicylic acid or derivatives
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Vinylogous acid
Methyl ester
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Oxacycle
Ether
Organoheterocyclic compound
Polyol
Alcohol
Organic oxygen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	2.49	ALOGPS
logP	4.36	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	9.7	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	90.56 m³·mol⁻¹	ChemAxon
Polarizability	36.51 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

C00056048

Chemspider ID

17243939

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16085271

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Parvifoliol D (NP0085966)

MOL for NP0085966 (Parvifoliol D)

3D MOL for NP0085966 (Parvifoliol D)

3D SDF for NP0085966 (Parvifoliol D)

3D-SDF for NP0085966 (Parvifoliol D)

PDB for NP0085966 (Parvifoliol D)

3D PDB for NP0085966 (Parvifoliol D)

SMILES for NP0085966 (Parvifoliol D)

INCHI for NP0085966 (Parvifoliol D)

Structure for NP0085966 (Parvifoliol D)

3D Structure for NP0085966 (Parvifoliol D)