NP-MRD: Showing NP-Card for (3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one (NP0153360)

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Record Information

Version

2.0

Created at

2022-09-02 10:00:26 UTC

Updated at

2022-09-02 10:00:26 UTC

NP-MRD ID

NP0153360

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one

Description

Pilosanone A belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. (3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one is found in Portulaca pilosa. Based on a literature review very few articles have been published on Pilosanone A.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 55 56  0  0  0  0  0  0  0  0999 V2000
   -5.5139   -0.4262    0.4938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0331   -0.3816    0.6082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3931   -1.4572    1.0794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9702   -1.6969    1.2980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0455   -1.2318    0.2058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1191    0.2032   -0.1531 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0038    0.9450    0.7572 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4241    0.8937    0.1709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7104    2.3551    1.0106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4991    3.0305    1.6267 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4562    3.0180    0.5353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0768    2.2870   -0.7083 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0658    2.9994   -1.3512 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3014    0.8281   -0.2997 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9165    0.8020    1.0305 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    0.3090   -1.4887 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5714   -0.9912   -1.6414 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7917   -1.4291   -0.9401 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5782   -0.7278   -0.1854 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7708   -1.2311    0.4874 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5543   -1.0288    1.8842 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1272   -2.8923   -1.2019 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1190   -3.7254   -0.7563 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8938   -1.4792    0.4583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9038    0.1920   -0.3146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9155   -0.0099    1.4642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0817   -2.2553    1.3262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8326   -2.8272    1.3148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5647   -1.3857    2.2800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2909   -1.8803   -0.6784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0218   -1.5388    0.5519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5076    0.2720   -1.2138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1178    0.4644    1.7737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0126    1.7803    0.4690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3183    0.8470   -0.9306 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3337    3.0397    1.2836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6747    4.0791    0.2489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9261    2.2388   -1.4014 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8798    4.1029   -1.1840 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0483    2.8195   -0.8677 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1003    2.9027   -2.4593 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2707   -0.1903    1.3269 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7408    1.5368    1.1844 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1696    1.0658    1.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7667    1.0738   -1.8707 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2161    0.4269   -2.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8924   -1.0653   -2.7586 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8508   -1.8546   -1.6017 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3139    0.3603   -0.1001 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7017   -0.6849    0.2088 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0064   -2.2904    0.4096 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7644   -0.0934    2.1195 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1232   -3.0318   -2.3376 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0797   -3.2173   -0.8782 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2679   -3.8493    0.2256 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  2  0
  9  7  1  0
  7  8  1  0
  8  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6 14  1  0
 14 15  1  1
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 22  1  0
 22 23  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 14 12  1  0
  6  7  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
 12 38  1  6
 11 36  1  0
 11 37  1  0
  7 33  1  1
  8 34  1  0
  8 35  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  6
 15 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 22 53  1  0
 22 54  1  0
 23 55  1  0
 19 49  1  0
 20 50  1  0
 20 51  1  0
 21 52  1  0
M  END


  Mrv1652309022212002D          

 23 24  0  0  1  0            999 V2000
    4.9502    2.4825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4358    1.8374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7938    1.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4358    0.3508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6315    0.1673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9865    0.6816    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9865    1.5066    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6315    2.0210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2720    1.9191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2720    2.7441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5575    1.5066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5575    0.6816    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8431    0.2691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2720    0.2691    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8847   -0.4593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6593   -0.4593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2222   -1.1589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6095   -1.8874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1723   -2.5870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5596   -3.3154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3841   -3.3442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4340   -1.9161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8213   -2.6446    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  2  8  1  0  0  0  0
  7  9  1  1  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 18 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0153360

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O3/c1-14-5-4-6-18-17(11-14)19(23)12-15(2)20(18,3)9-7-16(13-22)8-10-21/h5,8,15,17-18,21-22H,4,6-7,9-13H2,1-3H3/b16-8-/t15-,17+,18+,20+/m1/s1

> <INCHI_KEY>
SQKQROXBIUWNIQ-UVJHWCRFSA-N

> <FORMULA>
C20H32O3

> <MOLECULAR_WEIGHT>
320.473

> <EXACT_MASS>
320.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
37.87240470513487

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,4S,4aS,9aS)-4-[(3Z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-2,3,4,4a,5,6,9,9a-octahydro-1H-benzo[7]annulen-1-one

> <ALOGPS_LOGP>
3.60

> <JCHEM_LOGP>
3.041876621000001

> <ALOGPS_LOGS>
-3.97

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.762103117644319

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.022491563633245

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5275413290194884

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
95.6942

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.43e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4S,4aS,9aS)-4-[(3Z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2H-benzo[7]annulen-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       9.240   4.634   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.280   3.430   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.948   2.042   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.280   0.655   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.779   0.312   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.575   1.272   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.575   2.812   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.779   3.773   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.241   3.582   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.241   5.122   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.907   2.812   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.907   1.272   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.574   0.502   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.241   0.502   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.518  -0.857   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.964  -0.857   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.148  -2.163   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.871  -3.523   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.055  -4.829   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.778  -6.189   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.317  -6.243   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.410  -3.577   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.133  -4.937   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   14                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7    2                                                       
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    6   15   16                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   18   23                                                       
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂O₃

Average Mass

320.4730 Da

Monoisotopic Mass

320.23514 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C20H32O3/c1-14-5-4-6-18-17(11-14)19(23)12-15(2)20(18,3)9-7-16(13-22)8-10-21/h5,8,15,17-18,21-22H,4,6-7,9-13H2,1-3H3/b16-8-/t15-,17+,18+,20+/m1/s1

InChI Key

SQKQROXBIUWNIQ-UVJHWCRFSA-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
Portulaca pilosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Fatty alcohols

Alternative Parents

Substituents

Fatty alcohol
Ketone
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	3.6	ALOGPS
logS	-4	ALOGPS

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

26647560

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44143718

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one (NP0153360)

MOL for NP0153360 ((3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one)

3D MOL for NP0153360 ((3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one)

3D SDF for NP0153360 ((3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one)

3D-SDF for NP0153360 ((3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one)

PDB for NP0153360 ((3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one)

3D PDB for NP0153360 ((3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one)

SMILES for NP0153360 ((3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one)

INCHI for NP0153360 ((3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one)

Structure for NP0153360 ((3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one)

3D Structure for NP0153360 ((3r,4s,4as,9as)-4-[(3z)-5-hydroxy-3-(hydroxymethyl)pent-3-en-1-yl]-3,4,8-trimethyl-3,4a,5,6,9,9a-hexahydro-2h-benzo[7]annulen-1-one)