NP-MRD: Showing NP-Card for (2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol (NP0270900)

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Record Information

Version

2.0

Created at

2022-09-08 17:00:28 UTC

Updated at

2022-09-08 17:00:28 UTC

NP-MRD ID

NP0270900

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol

Description

(2S,3R,4R,5R,6S)-2-{[(4E,6Z,8Z,10E,12E,14E,16Z,18Z)-2-hydroxy-21-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol belongs to the class of organic compounds known as sesquaterpenoids. These are terpenoids with at least 7 consecutive isoprene units. (2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol is found in Ligia exotica and Oscillatoria limosa. Based on a literature review very few articles have been published on (2S,3R,4R,5R,6S)-2-{[(4E,6Z,8Z,10E,12E,14E,16Z,18Z)-2-hydroxy-21-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082219002D          

 48 49  0  0  1  0            999 V2000
   -9.2881  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2881  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2881  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0026   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7171  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0026   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2881   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2881   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0026   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  -10.7171   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4315   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.8592  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3895  -10.5055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.1447  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447  -12.3750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4302  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592  -12.7875    0.0000 C   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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
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 15 16  1  0  0  0  0
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 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
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 21 22  2  0  0  0  0
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 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 28 27  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 28 36  1  0  0  0  0
 36 37  1  1  0  0  0
 26 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 38 41  1  0  0  0  0
  3 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 42 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  6  0  0  0
 46 48  1  0  0  0  0
  2 48  1  0  0  0  0
M  END

     RDKit          3D

108109  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309082219002D          

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   -7.3289  -10.5055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447  -12.3750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -7.8592  -12.7875    0.0000 C   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
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  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
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 19 20  2  0  0  0  0
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  3 42  1  0  0  0  0
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 46 47  1  6  0  0  0
 46 48  1  0  0  0  0
  2 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0270900

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1O[C@@H](OC(\C=C\C(\C)=C/C=C\C(\C)=C\C=C\C=C(/C)\C=C/C=C(/C)\C=C\C2=C(C)C[C@@H](O)CC2(C)C)C(C)(C)O)[C@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C41H60O7/c1-27(17-13-19-29(3)21-23-34-31(5)25-33(42)26-40(34,7)8)15-11-12-16-28(2)18-14-20-30(4)22-24-35(41(9,10)46)48-39-38(45)37(44)36(43)32(6)47-39/h11-24,32-33,35-39,42-46H,25-26H2,1-10H3/b12-11+,17-13-,18-14-,23-21+,24-22+,27-15+,28-16+,29-19-,30-20-/t32-,33+,35?,36-,37+,38+,39-/m0/s1

> <INCHI_KEY>
QEATXFNUGGVKMK-ZNJSQPDCSA-N

> <FORMULA>
C41H60O7

> <MOLECULAR_WEIGHT>
664.924

> <EXACT_MASS>
664.433904272

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
108

> <JCHEM_AVERAGE_POLARIZABILITY>
78.84803231628152

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4R,5R,6S)-2-{[(4E,6Z,8Z,10E,12E,14E,16Z,18Z,20E)-2-hydroxy-21-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol

> <JCHEM_LOGP>
5.7730666280000005

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.233555946525552

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.219747726316115

> <JCHEM_PKA_STRONGEST_BASIC>
-1.0893500575428519

> <JCHEM_POLAR_SURFACE_AREA>
119.61000000000001

> <JCHEM_REFRACTIVITY>
205.6390000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4R,5R,6S)-2-{[(4E,6Z,8Z,10E,12E,14E,16Z,18Z,20E)-2-hydroxy-21-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0     -17.338 -23.870   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -16.004 -23.100   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -16.004 -21.560   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -17.338 -20.790   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -17.338 -19.250   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -18.672 -18.480   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -20.005 -19.250   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -18.672 -16.940   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -17.338 -16.170   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -17.338 -14.630   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -18.672 -13.860   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -18.672 -12.320   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -20.005 -11.550   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -20.005 -10.010   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -21.339  -9.240   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -21.339  -7.700   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -20.005  -6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -22.673  -6.930   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -22.673  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -21.339  -4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -21.339  -3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -20.005  -2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -22.673  -2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -22.673  -0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -24.006  -0.000   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0     -24.006   1.540   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0     -25.340   2.310   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0     -26.674   1.540   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0     -28.007   2.310   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0     -29.341   1.540   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -28.007   3.850   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0     -29.341   4.620   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0     -26.674   4.620   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0     -26.674   6.160   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0     -25.340   3.850   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0     -24.006   4.620   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0     -25.340  -0.770   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0     -26.674  -1.540   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -26.110   0.564   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0     -24.570  -2.104   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0     -14.670 -20.790   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0     -15.660 -19.610   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0     -13.681 -19.610   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0     -13.337 -21.560   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0     -13.337 -23.100   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0     -12.003 -23.870   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0     -14.670 -23.870   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   48                                                  
CONECT    3    2    4   42                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   38                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   36                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   28   37                                                  
CONECT   37   36                                                            
CONECT   38   26   39   40   41                                             
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   38                                                            
CONECT   42    3   43   44   45                                             
CONECT   43   42                                                            
CONECT   44   42                                                            
CONECT   45   42   46                                                       
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46    2                                                       
MASTER        0    0    0    0    0    0    0    0   48    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₁H₆₀O₇

Average Mass

664.9240 Da

Monoisotopic Mass

664.43390 Da

IUPAC Name

(2S,3R,4R,5R,6S)-2-{[(4E,6Z,8Z,10E,12E,14E,16Z,18Z,20E)-2-hydroxy-21-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H]1O[C@@H](OC(\C=C\C(\C)=C/C=C\C(\C)=C\C=C\C=C(/C)\C=C/C=C(/C)\C=C\C2=C(C)C[C@@H](O)CC2(C)C)C(C)(C)O)[C@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C41H60O7/c1-27(17-13-19-29(3)21-23-34-31(5)25-33(42)26-40(34,7)8)15-11-12-16-28(2)18-14-20-30(4)22-24-35(41(9,10)46)48-39-38(45)37(44)36(43)32(6)47-39/h11-24,32-33,35-39,42-46H,25-26H2,1-10H3/b12-11+,17-13-,18-14-,23-21+,24-22+,27-15+,28-16+,29-19-,30-20-/t32-,33+,35?,36-,37+,38+,39-/m0/s1

InChI Key

QEATXFNUGGVKMK-ZNJSQPDCSA-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
Ligia exotica	LOTUS Database	35616633
Oscillatoria limosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquaterpenoids. These are terpenoids with at least 7 consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquaterpenoids

Direct Parent

Sesquaterpenoids

Alternative Parents

Substituents

Sesquaterpenoid
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Fatty acyl
Monosaccharide
Oxane
Tertiary alcohol
Secondary alcohol
Polyol
Acetal
Organoheterocyclic compound
Oxacycle
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	5.77	ChemAxon
pKa (Strongest Acidic)	12.22	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	119.61 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	205.64 m³·mol⁻¹	ChemAxon
Polarizability	78.85 Å³	ChemAxon
Number of Rings	2	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

5319993

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol (NP0270900)

MOL for NP0270900 ((2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol)

3D MOL for NP0270900 ((2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol)

3D SDF for NP0270900 ((2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol)

3D-SDF for NP0270900 ((2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol)

PDB for NP0270900 ((2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol)

3D PDB for NP0270900 ((2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol)

SMILES for NP0270900 ((2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol)

INCHI for NP0270900 ((2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol)

Structure for NP0270900 ((2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol)

3D Structure for NP0270900 ((2s,3r,4r,5r,6s)-2-{[(4e,6z,8z,10e,12e,14e,16z,18z,20e)-2-hydroxy-21-[(4r)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-2,6,10,15,19-pentamethylhenicosa-4,6,8,10,12,14,16,18,20-nonaen-3-yl]oxy}-6-methyloxane-3,4,5-triol)