NP-MRD: Showing NP-Card for (2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid (NP0213215)

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Record Information

Version

2.0

Created at

2022-09-05 12:07:56 UTC

Updated at

2022-09-05 12:07:56 UTC

NP-MRD ID

NP0213215

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid

Description

[(2R)-2-[(3S,3aS,5R,8R,8aS)-8,8a-dihydroxy-3,8-dimethyl-decahydroazulen-5-yl]-2-hydroxypropoxy]sulfonic acid belongs to the class of organic compounds known as guaianes. These are sesquiterpenoids with a structure based on the guaiane skeleton. Guaiane is a bicyclic compound consisting of a decahydroazulene moiety, substituted with two methyl groups and a 1-methylethyl group at the 1-, 4-, and 7-position, respectively. (2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid is found in Cephalotaxus hainanensis. Based on a literature review very few articles have been published on [(2R)-2-[(3S,3aS,5R,8R,8aS)-8,8a-dihydroxy-3,8-dimethyl-decahydroazulen-5-yl]-2-hydroxypropoxy]sulfonic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 52  0  0  0  0  0  0  0  0999 V2000
   -1.8580    2.6598   -0.6034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0605    1.8892    0.6757 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5341    1.5096    0.7094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4744    0.1658   -0.0350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3212   -0.4698    0.7396 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7909   -0.5402    2.0747 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2953    0.5796    0.7089 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2433    0.4932   -0.3173 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8248   -0.5365    0.0380 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1489   -0.1883   -0.3658 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0740   -1.3998   -0.0276 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4269    0.1350   -1.6975 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7492    0.9791    0.4572 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0479    0.6034    0.7500 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2447    1.4911    0.0746 S   0  0  0  0  0  6  0  0  0  0  0  0
    4.9313    2.8945   -0.2475 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5363    0.8504   -1.3331 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6808    1.2724    0.8935 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3320   -1.8698   -0.4932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6587   -2.3611    0.5158 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0458   -1.8190    0.2732 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3658   -2.0963   -1.1884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8823   -2.7123    0.9803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2893    2.1580   -1.5020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4899    3.5890   -0.4791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8479    3.0232   -0.7856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8269    2.5447    1.5097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1310    2.2506    0.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8769    1.3933    1.7451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4142   -0.3776    0.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2153    0.3937   -1.0727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0442   -0.3632    2.6883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7546    0.5811    1.7013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5731    0.3698   -1.3686 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3399    1.4544   -0.3224 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7848   -0.5675    1.1775 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6082   -2.0732    0.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0548   -1.0880    0.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2233   -1.9490   -1.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3543    1.1440   -1.7846 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7516    1.9199   -0.0814 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1473    1.1049    1.3596 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9130    2.0417    1.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1065   -1.6583   -1.4921 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1802   -2.5749   -0.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3541   -2.1062    1.5456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7051   -3.4683    0.4027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2697   -1.2387   -1.8424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4168   -2.4700   -1.3081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7072   -2.9084   -1.5912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8014   -2.6549    0.6833 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
  4  5  1  0
  5  6  1  1
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  1
  9 10  1  0
 10 11  1  0
 10 12  1  6
 10 13  1  0
 13 14  1  0
 14 15  1  0
 15 18  1  0
 15 16  2  0
 15 17  2  0
  7  2  1  0
 21  5  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  1
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  6 32  1  0
  7 33  1  1
  8 34  1  0
  8 35  1  0
  9 36  1  1
 19 44  1  0
 19 45  1  0
 20 46  1  0
 20 47  1  0
 22 48  1  0
 22 49  1  0
 22 50  1  0
 23 51  1  0
 11 37  1  0
 11 38  1  0
 11 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 18 43  1  0
M  END


  Mrv1652309052214072D          

 23 24  0  0  1  0            999 V2000
   -0.5033    0.7510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2483   -0.0336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7333   -0.7011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2483   -1.3685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5363   -1.1136    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3890   -1.9253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5363   -0.2886    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1813    0.2258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9856    0.0422    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5000    0.6872    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1450    0.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8550    1.2016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0144    1.3322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8301    1.2093    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3445    1.8543    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.8589    2.4993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9895    1.3399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6995    2.3687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3436   -0.7011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9856   -1.4444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1813   -1.6280    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3829   -2.4280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6526   -2.2613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  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  1  0  0  0
  5  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  6  0  0  0
 10 12  1  6  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  2  0  0  0  0
 15 18  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0213215

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC[C@]2(O)[C@H]1C[C@@H](CC[C@@]2(C)O)[C@@](C)(O)COS(O)(=O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H28O7S/c1-10-4-7-15(18)12(10)8-11(5-6-14(15,3)17)13(2,16)9-22-23(19,20)21/h10-12,16-18H,4-9H2,1-3H3,(H,19,20,21)/t10-,11+,12-,13-,14+,15-/m0/s1

> <INCHI_KEY>
WGZJGSMZQTWTSO-HGPDSQILSA-N

> <FORMULA>
C15H28O7S

> <MOLECULAR_WEIGHT>
352.44

> <EXACT_MASS>
352.155574416

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
35.98237984720328

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R)-2-[(3S,3aS,5R,8R,8aS)-8,8a-dihydroxy-3,8-dimethyl-decahydroazulen-5-yl]-2-hydroxypropoxy]sulfonic acid

> <JCHEM_LOGP>
-0.7411065180526544

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.263936431225094

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.3121974477583347

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2557833309115543

> <JCHEM_POLAR_SURFACE_AREA>
124.28999999999999

> <JCHEM_REFRACTIVITY>
83.24919999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-[(3S,3aS,5R,8R,8aS)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.939   1.402   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.464  -0.063   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.369  -1.309   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.464  -2.555   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.001  -2.079   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.726  -3.594   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.001  -0.539   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.205   0.421   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.706   0.079   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.667   1.283   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.871   0.323   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.463   2.243   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.627   2.487   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.150   2.257   0.000  0.00  0.00           O+0
HETATM   15  S   UNK     0       8.110   3.461   0.000  0.00  0.00           S+0
HETATM   16  O   UNK     0       9.070   4.665   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       9.314   2.501   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       6.906   4.422   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.375  -1.309   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.706  -2.696   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.205  -3.039   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.581  -4.532   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.218  -4.221   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7   21                                             
CONECT    6    5                                                            
CONECT    7    5    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   19                                                  
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15                                                            
CONECT   19    9   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20    5   22   23                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Value	Source
[(2R)-2-[(3S,3AS,5R,8R,8as)-8,8a-dihydroxy-3,8-dimethyl-decahydroazulen-5-yl]-2-hydroxypropoxy]sulfonate	Generator
[(2R)-2-[(3S,3AS,5R,8R,8as)-8,8a-dihydroxy-3,8-dimethyl-decahydroazulen-5-yl]-2-hydroxypropoxy]sulphonate	Generator
[(2R)-2-[(3S,3AS,5R,8R,8as)-8,8a-dihydroxy-3,8-dimethyl-decahydroazulen-5-yl]-2-hydroxypropoxy]sulphonic acid	Generator

Chemical Formula

C₁₅H₂₈O₇S

Average Mass

352.4400 Da

Monoisotopic Mass

352.15557 Da

IUPAC Name

[(2R)-2-[(3S,3aS,5R,8R,8aS)-8,8a-dihydroxy-3,8-dimethyl-decahydroazulen-5-yl]-2-hydroxypropoxy]sulfonic acid

Traditional Name

(2R)-2-[(3S,3aS,5R,8R,8aS)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid

CAS Registry Number

Not Available

SMILES

C[C@H]1CC[C@]2(O)[C@H]1C[C@@H](CC[C@@]2(C)O)[C@@](C)(O)COS(O)(=O)=O

InChI Identifier

InChI=1S/C15H28O7S/c1-10-4-7-15(18)12(10)8-11(5-6-14(15,3)17)13(2,16)9-22-23(19,20)21/h10-12,16-18H,4-9H2,1-3H3,(H,19,20,21)/t10-,11+,12-,13-,14+,15-/m0/s1

InChI Key

WGZJGSMZQTWTSO-HGPDSQILSA-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
Cephalotaxus hainanensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as guaianes. These are sesquiterpenoids with a structure based on the guaiane skeleton. Guaiane is a bicyclic compound consisting of a decahydroazulene moiety, substituted with two methyl groups and a 1-methylethyl group at the 1-, 4-, and 7-position, respectively.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Guaianes

Alternative Parents

Substituents

Guaiane sesquiterpenoid
Sulfuric acid ester
Alkyl sulfate
Sulfate-ester
Sulfuric acid monoester
Tertiary alcohol
Organic sulfuric acid or derivatives
Cyclic alcohol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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	-0.74	ChemAxon
pKa (Strongest Acidic)	-1.3	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	124.29 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	83.25 m³·mol⁻¹	ChemAxon
Polarizability	35.98 Å³	ChemAxon
Number of Rings	2	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

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

163035820

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid (NP0213215)

MOL for NP0213215 ((2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid)

3D MOL for NP0213215 ((2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid)

3D SDF for NP0213215 ((2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid)

3D-SDF for NP0213215 ((2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid)

PDB for NP0213215 ((2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid)

3D PDB for NP0213215 ((2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid)

SMILES for NP0213215 ((2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid)

INCHI for NP0213215 ((2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid)

Structure for NP0213215 ((2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid)

3D Structure for NP0213215 ((2r)-2-[(3s,3as,5r,8r,8as)-8,8a-dihydroxy-3,8-dimethyl-octahydroazulen-5-yl]-2-hydroxypropoxysulfonic acid)