NP-MRD: Showing NP-Card for (1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one (NP0251162)

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Record Information

Version

2.0

Created at

2022-09-07 14:16:42 UTC

Updated at

2022-09-07 14:16:42 UTC

NP-MRD ID

NP0251162

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one

Description

(1'S,2S,5S,6R,10'Z,14'R,16'E,19'S)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]Tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one belongs to the class of organic compounds known as aryl alkyl ketones. These are ketones have the generic structure RC(=O)R', where R = aryl group and R'=alkyl group. (1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one is found in Streptomyces bingchenggensis. Based on a literature review very few articles have been published on (1'S,2S,5S,6R,10'Z,14'R,16'E,19'S)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]Tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072216162D          

 39 42  0  0  1  0            999 V2000
    7.4300    4.9682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6150    4.8399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5037    3.9416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.7260    2.5301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5410    2.6584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8373    3.4283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4297    1.7601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6147    1.6318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3183    0.8619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  3  4  2  0  0  0  0
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 23 39  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309072216162D          

 39 42  0  0  1  0            999 V2000
    7.4300    4.9682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4297    1.7601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6147    1.6318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3183    0.8619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9483    1.1185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6519    0.3486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8370    0.2203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5406   -0.5497    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0592   -1.1913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7256   -0.6780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2070   -0.0364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5034    0.7335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3921   -0.1647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8735    0.4769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1698    1.2468    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9848    1.3752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2811    2.1451    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0961    2.2734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3924    3.0434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8738    3.6850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7625    2.7867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9476    2.6584    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1326    2.5301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6140    3.1717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9103    3.9416    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3917    4.5832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7253    4.0699    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0216    4.8399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8366    4.9682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2439    3.4283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6512    1.8884    0.0000 C   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 25 24  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
  5 27  1  0  0  0  0
 27 28  2  0  0  0  0
 25 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  1  0  0  0
 36 37  1  0  0  0  0
 35 38  1  0  0  0  0
 30 38  1  6  0  0  0
 30 39  1  0  0  0  0
 23 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0251162

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H]1O[C@@]2(CC[C@@H]1C)C[C@H]1C[C@@H](C2)CC(=O)C2=C(C=C(O)C(CC)=C2)\C(CO)=C\C=C\[C@H](C)C\C(C)=C\C1

> <INCHI_IDENTIFIER>
InChI=1S/C35H50O4/c1-6-28-18-31-30(19-32(28)37)29(22-36)10-8-9-23(3)15-24(4)11-12-26-16-27(17-33(31)38)21-35(20-26)14-13-25(5)34(7-2)39-35/h8-11,18-19,23,25-27,34,36-37H,6-7,12-17,20-22H2,1-5H3/b9-8+,24-11+,29-10+/t23-,25-,26+,27+,34+,35-/m0/s1

> <INCHI_KEY>
WBCISIGINBDRFM-CIZNTZCXSA-N

> <FORMULA>
C35H50O4

> <MOLECULAR_WEIGHT>
534.781

> <EXACT_MASS>
534.37091009

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
63.20896488117583

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'S,2S,5S,6R,10'Z,12'E,14'R,16'E,19'S)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0^{4,9}]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one

> <JCHEM_LOGP>
7.816668920333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.995574212956338

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.942917296283397

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8159226456523756

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
163.9596

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2S,5S,6R,10'Z,12'E,14'R,16'E,19'S)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0^{4,9}]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      13.869   9.274   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.348   9.034   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.795   7.597   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.274   7.358   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.720   5.920   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.689   4.723   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.210   4.962   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.763   6.400   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      14.284   6.639   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      10.135   3.286   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.614   3.046   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.061   1.609   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      11.103   2.088   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.550   0.651   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.029   0.411   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.476  -1.026   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.444  -2.224   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.955  -1.266   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.986  -0.068   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.540   1.369   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.465  -0.307   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.497   0.890   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.050   2.327   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.572   2.567   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.125   4.004   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.646   4.244   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.199   5.681   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       7.231   6.879   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.157   5.202   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.635   4.962   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.114   4.723   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.146   5.920   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.699   7.358   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.731   8.555   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.221   7.597   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.774   9.034   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.295   9.274   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       4.189   6.400   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       3.082   3.525   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   27                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8                                                            
CONECT   10    6   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   39                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   29                                                  
CONECT   26   25   27                                                       
CONECT   27   26    5   28                                                  
CONECT   28   27                                                            
CONECT   29   25   30                                                       
CONECT   30   29   31   38   39                                             
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   38                                                  
CONECT   36   35   37                                                       
CONECT   37   36                                                            
CONECT   38   35   30                                                       
CONECT   39   30   23                                                       
MASTER        0    0    0    0    0    0    0    0   39    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₅₀O₄

Average Mass

534.7810 Da

Monoisotopic Mass

534.37091 Da

IUPAC Name

(1'S,2S,5S,6R,10'Z,12'E,14'R,16'E,19'S)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0^{4,9}]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one

Traditional Name

(1'S,2S,5S,6R,10'Z,12'E,14'R,16'E,19'S)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0^{4,9}]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one

CAS Registry Number

Not Available

SMILES

CC[C@H]1O[C@@]2(CC[C@@H]1C)C[C@H]1C[C@@H](C2)CC(=O)C2=C(C=C(O)C(CC)=C2)\C(CO)=C\C=C\[C@H](C)C\C(C)=C\C1

InChI Identifier

InChI=1S/C35H50O4/c1-6-28-18-31-30(19-32(28)37)29(22-36)10-8-9-23(3)15-24(4)11-12-26-16-27(17-33(31)38)21-35(20-26)14-13-25(5)34(7-2)39-35/h8-11,18-19,23,25-27,34,36-37H,6-7,12-17,20-22H2,1-5H3/b9-8+,24-11+,29-10+/t23-,25-,26+,27+,34+,35-/m0/s1

InChI Key

WBCISIGINBDRFM-CIZNTZCXSA-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
Streptomyces bingchenggensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aryl alkyl ketones. These are ketones have the generic structure RC(=O)R', where R = aryl group and R'=alkyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Aryl alkyl ketones

Alternative Parents

Substituents

Aryl alkyl ketone
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Oxane
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Organic oxide
Hydrocarbon derivative
Primary alcohol
Alcohol
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	7.82	ChemAxon
pKa (Strongest Acidic)	7.94	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	163.96 m³·mol⁻¹	ChemAxon
Polarizability	63.21 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

163191291

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one (NP0251162)

MOL for NP0251162 ((1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one)

3D MOL for NP0251162 ((1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one)

3D SDF for NP0251162 ((1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one)

3D-SDF for NP0251162 ((1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one)

PDB for NP0251162 ((1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one)

3D PDB for NP0251162 ((1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one)

SMILES for NP0251162 ((1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one)

INCHI for NP0251162 ((1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one)

Structure for NP0251162 ((1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one)

3D Structure for NP0251162 ((1's,2s,5s,6r,10'z,12'e,14'r,16'e,19's)-6,6'-diethyl-7'-hydroxy-10'-(hydroxymethyl)-5,14',16'-trimethylspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one)