NP-MRD: Showing NP-Card for {4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate (NP0213364)

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Record Information

Version

2.0

Created at

2022-09-05 12:20:03 UTC

Updated at

2022-09-05 12:20:03 UTC

NP-MRD ID

NP0213364

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate

Description

{4,6-Dihydroxy-5a,9-dimethyl-2-oxo-2H,4H,5H,5aH,6H,7H,9aH,9bH-naphtho[1,2-b]furan-3-yl}methyl acetate belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. {4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate is found in Cotula cinerea. {4,6-Dihydroxy-5a,9-dimethyl-2-oxo-2H,4H,5H,5aH,6H,7H,9aH,9bH-naphtho[1,2-b]furan-3-yl}methyl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 47  0  0  0  0  0  0  0  0999 V2000
    4.6933    0.5584    2.2653 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8883    0.2936    1.0317 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8955   -0.4695    1.1113 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1920    0.8520   -0.1843 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4084    0.5755   -1.3177 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9891    0.9988   -1.1154 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9242    0.2349   -1.1598 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6583   -1.1995   -1.4159 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1250   -1.3665   -2.5630 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0403   -1.7418   -0.2259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1303   -0.9495    0.3807 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0705   -1.2437    1.8952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4454   -1.6239   -0.0397 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4508   -2.9487    0.3956 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6359   -0.9467    0.5600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6348    0.4694    0.1001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4977    1.0899   -0.0512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5211    2.5282   -0.5174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1414    0.5083    0.1974 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2652    1.0393   -0.9088 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1828    2.3296   -0.7061 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5576    2.3692   -0.8236 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3056    3.3798   -0.7052 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1461    1.2628    2.9315 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7860   -0.3903    2.8309 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7101    0.9055    2.0345 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4029   -0.4984   -1.5718 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8638    1.1213   -2.1829 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6333   -1.7383   -1.5216 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3173   -0.9007   -3.3165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3930   -2.7790   -0.5511 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7638   -2.0261    0.5192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0543   -0.9509    2.2877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2410   -2.3258    2.0349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7856   -0.6029    2.4312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5370   -1.6136   -1.1281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2710   -3.5921   -0.3121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5369   -1.4181    0.1271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6386   -0.9850    1.6678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5537    1.0114   -0.1166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3001    2.5949   -1.6055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8672    3.1586    0.0976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5585    2.9524   -0.3979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7941    1.0293    1.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8293    1.0480   -1.8946 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 20 19  1  0
 19 17  1  0
 17 18  1  0
 17 16  2  0
 16 15  1  0
 15 13  1  0
 13 14  1  0
 13 11  1  0
 11 12  1  1
 11 10  1  0
 10  8  1  0
  8  9  1  0
 22  6  1  0
 11 19  1  0
  8  7  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  5 27  1  0
  5 28  1  0
 20 45  1  6
 19 44  1  1
 18 41  1  0
 18 42  1  0
 18 43  1  0
 16 40  1  0
 15 38  1  0
 15 39  1  0
 13 36  1  6
 14 37  1  0
 12 33  1  0
 12 34  1  0
 12 35  1  0
 10 31  1  0
 10 32  1  0
  8 29  1  6
  9 30  1  0
M  END


  Mrv1533004171515132D          

 23 25  0  0  0  0            999 V2000
   -0.6374    0.1347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1389    0.4140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2851    1.2259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7689   -0.1186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5452    0.1607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1752   -0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9765   -0.1753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3664    0.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9318    1.2530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1910    0.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6256   -0.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0156    0.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4502   -0.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8402    0.6290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8849   -0.7992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4949   -1.5262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6703   -1.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2803   -2.2790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2357   -0.8508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4111   -0.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8784   -1.5066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1147   -1.1947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4134   -1.6293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0213364

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1=C2C(OC1=O)C1C(C)=CCC(O)C1(C)CC2O

> <INCHI_IDENTIFIER>
InChI=1S/C17H22O6/c1-8-4-5-12(20)17(3)6-11(19)13-10(7-22-9(2)18)16(21)23-15(13)14(8)17/h4,11-12,14-15,19-20H,5-7H2,1-3H3

> <INCHI_KEY>
YLZRFDXWFCVDAG-UHFFFAOYSA-N

> <FORMULA>
C17H22O6

> <MOLECULAR_WEIGHT>
322.357

> <EXACT_MASS>
322.141638428

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
33.33959683122997

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
{4,6-dihydroxy-5a,9-dimethyl-2-oxo-2H,4H,5H,5aH,6H,7H,9aH,9bH-naphtho[1,2-b]furan-3-yl}methyl acetate

> <ALOGPS_LOGP>
1.04

> <JCHEM_LOGP>
0.05308973633333372

> <ALOGPS_LOGS>
-2.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.509663839984857

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.19316412344064

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9649009575764973

> <JCHEM_POLAR_SURFACE_AREA>
93.06

> <JCHEM_REFRACTIVITY>
81.87899999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.59e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{4,6-dihydroxy-5a,9-dimethyl-2-oxo-4H,5H,6H,7H,9aH,9bH-naphtho[1,2-b]furan-3-yl}methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -1.190   0.251   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.259   0.773   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.532   2.288   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       1.435  -0.221   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.884   0.300   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.060  -0.694   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.556  -0.327   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.284   1.030   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.473   2.339   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.823   1.078   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.635  -0.231   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.363   1.126   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.174  -0.183   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      10.902   1.174   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      10.985  -1.492   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.257  -2.849   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.718  -2.897   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.990  -4.254   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.907  -1.588   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.367  -1.636   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.373  -2.812   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.947  -2.230   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.638  -3.041   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   22                                                  
CONECT    7    6    8   20                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13   19                                             
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   11   20                                                  
CONECT   20   19    7   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21    6   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Value	Source
{4,6-dihydroxy-5a,9-dimethyl-2-oxo-2H,4H,5H,5ah,6H,7H,9ah,9BH-naphtho[1,2-b]furan-3-yl}methyl acetic acid	Generator

Chemical Formula

C₁₇H₂₂O₆

Average Mass

322.3570 Da

Monoisotopic Mass

322.14164 Da

IUPAC Name

{4,6-dihydroxy-5a,9-dimethyl-2-oxo-2H,4H,5H,5aH,6H,7H,9aH,9bH-naphtho[1,2-b]furan-3-yl}methyl acetate

Traditional Name

{4,6-dihydroxy-5a,9-dimethyl-2-oxo-4H,5H,6H,7H,9aH,9bH-naphtho[1,2-b]furan-3-yl}methyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1=C2C(OC1=O)C1C(C)=CCC(O)C1(C)CC2O

InChI Identifier

InChI=1S/C17H22O6/c1-8-4-5-12(20)17(3)6-11(19)13-10(7-22-9(2)18)16(21)23-15(13)14(8)17/h4,11-12,14-15,19-20H,5-7H2,1-3H3

InChI Key

YLZRFDXWFCVDAG-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
Cotula cinerea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
2-furanone
Dicarboxylic acid or derivatives
Cyclic alcohol
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Lactone
Secondary alcohol
Oxacycle
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	1.04	ALOGPS
logP	0.053	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	12.19	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	93.06 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	81.88 m³·mol⁻¹	ChemAxon
Polarizability	33.34 Å³	ChemAxon
Number of Rings	3	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

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

14137562

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate (NP0213364)

MOL for NP0213364 ({4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate)

3D MOL for NP0213364 ({4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate)

3D SDF for NP0213364 ({4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate)

3D-SDF for NP0213364 ({4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate)

PDB for NP0213364 ({4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate)

3D PDB for NP0213364 ({4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate)

SMILES for NP0213364 ({4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate)

INCHI for NP0213364 ({4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate)

Structure for NP0213364 ({4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate)

3D Structure for NP0213364 ({4,6-dihydroxy-5a,9-dimethyl-2-oxo-4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-3-yl}methyl acetate)