NP-MRD: Showing NP-Card for (1r,4s,6s)-1,7,7-trimethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one (NP0263371)

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Record Information

Version

2.0

Created at

2022-09-08 06:32:17 UTC

Updated at

2022-09-08 06:32:17 UTC

NP-MRD ID

NP0263371

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,4s,6s)-1,7,7-trimethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one

Description

(1R,4S,6S)-6-(beta-D-Glucopyranosyloxy)bornane-2-one belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. Based on a literature review very few articles have been published on (1R,4S,6S)-6-(beta-D-Glucopyranosyloxy)bornane-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 51  0  0  0  0  0  0  0  0999 V2000
    3.1705    1.7828   -0.8946 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2945    0.4071   -0.3333 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5244   -0.2882   -0.8119 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2007    0.4255    1.2023 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1733   -1.0614    1.4754 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3733   -1.5813    0.3408 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0589   -2.7263    0.1579 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0313   -0.4349   -0.5268 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7788   -0.7644   -1.9484 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0019    0.3694    0.1799 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0414   -0.5076    0.6950 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2587   -0.1667    0.4050 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9608    0.2278    1.5643 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1319    0.8219    1.1132 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8566    1.5758    2.1967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2271    0.7886    3.2574 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0515   -0.1957    0.4589 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2164    0.4532    0.1124 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3356   -0.6673   -0.7875 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0394   -1.6284   -1.4757 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9918   -1.2415   -0.3332 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2916   -1.5544   -1.4913 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8125    0.9565    1.3587 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3053    1.7440   -1.9828 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2607    2.2931   -0.5849 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0244    2.3775   -0.4865 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3297   -1.2695   -1.2982 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0024    0.3480   -1.5967 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2923   -0.4137    0.0019 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9826    0.9791    1.6751 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7090   -1.2510    2.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2264   -1.4428    1.4096 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7247   -0.6526   -2.5122 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4269   -1.7973   -2.0256 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9872   -0.1025   -2.3357 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5657    1.1803   -0.4018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2451    0.7463   -0.2245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8487    1.5493    0.3256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2980    2.4856    2.4911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8059    1.9557    1.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4500    1.3776    4.0140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2027   -1.0204    1.1763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9978   -0.1613    0.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1381    0.2224   -1.4182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0485   -2.4571   -0.9558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1955   -2.1367    0.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8124   -2.1711   -2.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3622    0.5688    2.2924 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7428    2.0574    1.3730 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4 23  1  0
 23 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 10  8  1  0
  8  9  1  6
  8  6  1  0
  6  7  2  0
  6  5  1  0
  8  2  1  0
  5  4  1  0
 21 12  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  1
 23 48  1  0
 23 49  1  0
 10 36  1  6
 12 37  1  6
 14 38  1  6
 15 39  1  0
 15 40  1  0
 16 41  1  0
 17 42  1  1
 18 43  1  0
 19 44  1  6
 20 45  1  0
 21 46  1  1
 22 47  1  0
  9 33  1  0
  9 34  1  0
  9 35  1  0
  5 31  1  0
  5 32  1  0
M  END


  Mrv1652309082208322D          

 23 25  0  0  1  0            999 V2000
    0.2085   -0.1075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9988    0.1293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2085    0.3661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2050    0.9543    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4906    0.5418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4906   -0.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2239   -0.6957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2050   -0.6957    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2050   -1.5207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9195   -0.2832    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6340   -0.6957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3484   -0.2832    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3484    0.5418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0629    0.9543    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0629    1.7793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3484    2.1918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7774    0.5418    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4919    0.9543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7774   -0.2832    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4919   -0.6957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0629   -0.6957    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0629   -1.5207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9195    0.5418    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
  2  4  1  0  0  0  0
  4  5  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  1  0  0  0
 10 23  1  0  0  0  0
  4 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0263371

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)[C@H]2C[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@]1(C)C(=O)C2

> <INCHI_IDENTIFIER>
InChI=1S/C16H26O7/c1-15(2)7-4-9(18)16(15,3)10(5-7)23-14-13(21)12(20)11(19)8(6-17)22-14/h7-8,10-14,17,19-21H,4-6H2,1-3H3/t7-,8-,10+,11-,12+,13-,14+,16+/m1/s1

> <INCHI_KEY>
XBXUOFIJMNLOGI-RFJIILTISA-N

> <FORMULA>
C16H26O7

> <MOLECULAR_WEIGHT>
330.377

> <EXACT_MASS>
330.167853177

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
34.000939752818006

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,4S,6S)-1,7,7-trimethyl-6-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one

> <JCHEM_LOGP>
-0.4486611226666663

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.20007804245185

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.210530784210896

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835454571354

> <JCHEM_POLAR_SURFACE_AREA>
116.45000000000002

> <JCHEM_REFRACTIVITY>
78.4208

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4S,6S)-1,7,7-trimethyl-6-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one

> <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       0.389  -0.201   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.864   0.241   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.389   0.683   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.249   1.781   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.916   1.011   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.916  -0.529   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.418  -1.299   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.249  -1.299   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.249  -2.839   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.583  -0.529   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.917  -1.299   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.250  -0.529   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.250   1.011   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.584   1.781   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.584   3.321   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.250   4.091   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.918   1.011   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      10.251   1.781   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.918  -0.529   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      10.251  -1.299   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.584  -1.299   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.584  -2.839   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       3.583   1.011   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    8                                             
CONECT    3    2                                                            
CONECT    4    2    5   23                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    2    9   10                                             
CONECT    9    8                                                            
CONECT   10    8   11   23                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   21                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   12   22                                                  
CONECT   22   21                                                            
CONECT   23   10    4                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Value	Source
(1R,4S,6S)-6-(b-D-Glucopyranosyloxy)bornane-2-one	Generator
(1R,4S,6S)-6-(Β-D-glucopyranosyloxy)bornane-2-one	Generator

Chemical Formula

C₁₆H₂₆O₇

Average Mass

330.3770 Da

Monoisotopic Mass

330.16785 Da

IUPAC Name

(1R,4S,6S)-1,7,7-trimethyl-6-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one

Traditional Name

(1R,4S,6S)-1,7,7-trimethyl-6-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one

CAS Registry Number

Not Available

SMILES

CC1(C)[C@H]2C[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@]1(C)C(=O)C2

InChI Identifier

InChI=1S/C16H26O7/c1-15(2)7-4-9(18)16(15,3)10(5-7)23-14-13(21)12(20)11(19)8(6-17)22-14/h7-8,10-14,17,19-21H,4-6H2,1-3H3/t7-,8-,10+,11-,12+,13-,14+,16+/m1/s1

InChI Key

XBXUOFIJMNLOGI-RFJIILTISA-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 terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Terpene glycosides

Alternative Parents

Substituents

Terpene glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Norbornane monoterpenoid
Bornane monoterpenoid
Bicyclic monoterpenoid
Monoterpenoid
Monosaccharide
Oxane
Secondary alcohol
Ketone
Oxacycle
Acetal
Organoheterocyclic compound
Polyol
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organic oxide
Aldehyde
Primary alcohol
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	-0.45	ChemAxon
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	116.45 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	78.42 m³·mol⁻¹	ChemAxon
Polarizability	34 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

10260931

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21631088

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,4s,6s)-1,7,7-trimethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one (NP0263371)

MOL for NP0263371 ((1r,4s,6s)-1,7,7-trimethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one)

3D MOL for NP0263371 ((1r,4s,6s)-1,7,7-trimethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one)

3D SDF for NP0263371 ((1r,4s,6s)-1,7,7-trimethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one)

3D-SDF for NP0263371 ((1r,4s,6s)-1,7,7-trimethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one)

PDB for NP0263371 ((1r,4s,6s)-1,7,7-trimethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one)

3D PDB for NP0263371 ((1r,4s,6s)-1,7,7-trimethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one)

SMILES for NP0263371 ((1r,4s,6s)-1,7,7-trimethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one)

INCHI for NP0263371 ((1r,4s,6s)-1,7,7-trimethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one)

Structure for NP0263371 ((1r,4s,6s)-1,7,7-trimethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one)

3D Structure for NP0263371 ((1r,4s,6s)-1,7,7-trimethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}bicyclo[2.2.1]heptan-2-one)