NP-MRD: Showing NP-Card for 7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1h,5h,6h,6ah,8h,9h,10h-naphtho[4,4a-c]furan-3-one (NP0157594)

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Record Information

Version

2.0

Created at

2022-09-02 15:00:48 UTC

Updated at

2022-09-02 15:00:48 UTC

NP-MRD ID

NP0157594

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1h,5h,6h,6ah,8h,9h,10h-naphtho[4,4a-c]furan-3-one

Description

AC1L7JWN belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. AC1L7JWN is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
   -0.4563    0.1568    2.6811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3610   -0.8324    1.5737 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5988   -1.6951    1.5383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8444   -1.0766    1.0639 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5827   -0.0922   -0.0506 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0112    1.2499    0.4325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3795    0.9284    0.8282 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8395    0.1246   -0.2280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0072   -0.2906   -0.4670 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6863   -0.1936   -1.0886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4856   -0.4473   -2.3453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1133   -0.6693   -2.9370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1318    0.1536   -2.0464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3215   -0.3663   -0.6761 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0625   -0.2674    0.1994 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9935   -1.1545   -0.4210 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4287    1.1255    0.2145 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6643    1.4859    0.9071 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9548    0.9208    0.3836 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6841    0.1327    1.1375 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9574   -0.5448    0.8838 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9462   -0.1189    1.8136 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3735    1.3516   -0.9572 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5751    0.8974   -1.4129 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3646    0.0363    3.4532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5706    1.2016    2.4223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3744   -0.0878    3.3026 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4744   -1.5154    1.8395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7671   -2.0805    2.5807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4214   -2.6347    0.9346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6241   -1.8218    0.7474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3187   -0.5397    1.9080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5893    1.6375    1.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1500    2.0003   -0.3842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3145   -0.5089   -3.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8796   -1.7298   -2.9166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1303   -0.2837   -3.9618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467   -0.0711   -2.4986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3988    1.2182   -2.1889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3519   -1.5098   -0.8490 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4792   -0.7710   -1.3105 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4103   -2.0619   -0.8345 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6605   -1.6365    0.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3875    1.8756    0.4253 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6459    1.3647   -0.8924 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7995    2.6074    0.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7164    1.3646    1.9990 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2978   -0.0930    2.1873 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8216   -1.6464    1.1918 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3584   -0.5812   -0.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4445    0.2623    2.5686 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5154    2.4864   -0.8590 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6288    1.1694   -1.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1110    1.5706   -1.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  5  4  1  1
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  6
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 23  1  0
 23 24  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 15  2  1  0
 10  5  1  0
 14  5  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  1
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  6 33  1  0
  6 34  1  0
 11 35  1  0
 12 36  1  0
 12 37  1  0
 13 38  1  0
 13 39  1  0
 14 40  1  6
 16 41  1  0
 16 42  1  0
 16 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  0
 18 47  1  0
 23 52  1  0
 23 53  1  0
 24 54  1  0
 20 48  1  0
 21 49  1  0
 21 50  1  0
 22 51  1  0
M  END


  Mrv0541 04121518142D          

 24 26  0  0  0  0            999 V2000
    0.0595   -1.6579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7768   -1.2503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7825   -0.4253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2739   -0.0766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2114   -0.4351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6021    0.1211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9428    0.8725    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7627    0.7806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3189    1.3899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9286   -0.0275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6403   -0.4449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6346   -1.2699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9173   -1.6775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2057   -1.2601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4884   -1.6677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8707   -2.3987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0961   -2.3934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2714   -2.4166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1209   -3.1423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9455   -3.1655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3379   -3.8912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9055   -4.5938    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3115   -3.8449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0808   -4.5707    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  4  0  0  0
 21 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0157594

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCC23COC(=O)C2=CCCC3C1(C)CCC(CO)=CCO

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O4/c1-14-6-10-20-13-24-18(23)16(20)4-3-5-17(20)19(14,2)9-7-15(12-22)8-11-21/h4,8,14,17,21-22H,3,5-7,9-13H2,1-2H3

> <INCHI_KEY>
BYASTQVSNAVAKL-UHFFFAOYSA-N

> <FORMULA>
C20H30O4

> <MOLECULAR_WEIGHT>
334.456

> <EXACT_MASS>
334.214409446

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
37.41194356078452

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1H,3H,5H,6H,6aH,7H,8H,9H,10H-naphtho[4,4a-c]furan-3-one

> <ALOGPS_LOGP>
3.11

> <JCHEM_LOGP>
2.6293315196666667

> <ALOGPS_LOGS>
-4.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.762103117695212

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.022491563704168

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5275413290012994

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
94.90069999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.22e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1H,5H,6H,6aH,8H,9H,10H-naphtho[4,4a-c]furan-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-APR-15         0                                  
HETATM    1  C   UNK     0       0.111  -3.095   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.450  -2.334   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.461  -0.794   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.378  -0.143   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.128  -0.812   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.991   0.226   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.627   1.629   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.157   1.457   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.195   2.594   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.467  -0.051   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.795  -0.831   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.785  -2.370   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.446  -3.131   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.117  -2.352   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.778  -3.113   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.492  -4.478   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.046  -4.468   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.507  -4.511   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.226  -5.866   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.765  -5.909   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.497  -7.264   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -1.690  -8.575   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.581  -7.177   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.151  -8.532   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   15                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10   14                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8    5   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    5   15                                                  
CONECT   15   14    2   16   17                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   19   24                                                       
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₄

Average Mass

334.4560 Da

Monoisotopic Mass

334.21441 Da

IUPAC Name

7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1H,3H,5H,6H,6aH,7H,8H,9H,10H-naphtho[4,4a-c]furan-3-one

Traditional Name

7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1H,5H,6H,6aH,8H,9H,10H-naphtho[4,4a-c]furan-3-one

CAS Registry Number

Not Available

SMILES

CC1CCC23COC(=O)C2=CCCC3C1(C)CCC(CO)=CCO

InChI Identifier

InChI=1S/C20H30O4/c1-14-6-10-20-13-24-18(23)16(20)4-3-5-17(20)19(14,2)9-7-15(12-22)8-11-21/h4,8,14,17,21-22H,3,5-7,9-13H2,1-2H3

InChI Key

BYASTQVSNAVAKL-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Clerodane diterpenoid
Naphthofuran
Fatty alcohol
Fatty acyl
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Primary alcohol
Alcohol
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	3.11	ALOGPS
logP	2.63	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	15.02	ChemAxon
pKa (Strongest Basic)	-2.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	94.9 m³·mol⁻¹	ChemAxon
Polarizability	37.41 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

362041

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1h,5h,6h,6ah,8h,9h,10h-naphtho[4,4a-c]furan-3-one (NP0157594)

MOL for NP0157594 (7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1h,5h,6h,6ah,8h,9h,10h-naphtho[4,4a-c]furan-3-one)

3D MOL for NP0157594 (7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1h,5h,6h,6ah,8h,9h,10h-naphtho[4,4a-c]furan-3-one)

3D SDF for NP0157594 (7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1h,5h,6h,6ah,8h,9h,10h-naphtho[4,4a-c]furan-3-one)

3D-SDF for NP0157594 (7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1h,5h,6h,6ah,8h,9h,10h-naphtho[4,4a-c]furan-3-one)

PDB for NP0157594 (7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1h,5h,6h,6ah,8h,9h,10h-naphtho[4,4a-c]furan-3-one)

3D PDB for NP0157594 (7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1h,5h,6h,6ah,8h,9h,10h-naphtho[4,4a-c]furan-3-one)

SMILES for NP0157594 (7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1h,5h,6h,6ah,8h,9h,10h-naphtho[4,4a-c]furan-3-one)

INCHI for NP0157594 (7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1h,5h,6h,6ah,8h,9h,10h-naphtho[4,4a-c]furan-3-one)

Structure for NP0157594 (7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1h,5h,6h,6ah,8h,9h,10h-naphtho[4,4a-c]furan-3-one)

3D Structure for NP0157594 (7-[5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-7,8-dimethyl-1h,5h,6h,6ah,8h,9h,10h-naphtho[4,4a-c]furan-3-one)