NP-MRD: Showing NP-Card for [(1r,4s)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid (NP0217618)

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Record Information

Version

2.0

Created at

2022-09-05 18:01:40 UTC

Updated at

2022-09-05 18:01:41 UTC

NP-MRD ID

NP0217618

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1r,4s)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid

Description

[(1R,4S)-1,4-dihydroxy-1-methyl-7-(propan-2-yl)-1,2,3,3a,4,5,6,8a-octahydroazulen-4-yl]methanesulfonic 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. [(1r,4s)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid is found in Alisma plantago-aquatica. Based on a literature review very few articles have been published on [(1R,4S)-1,4-dihydroxy-1-methyl-7-(propan-2-yl)-1,2,3,3a,4,5,6,8a-octahydroazulen-4-yl]methanesulfonic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 48  0  0  0  0  0  0  0  0999 V2000
   -3.7589   -1.4009   -0.2284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5974   -1.4423    0.7511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1829   -2.8938    0.9460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4592   -0.6387    0.2746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0702    0.3775    1.0340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0167    1.3867    0.9231 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1200    1.0363    0.0256 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9322    1.7232   -1.2860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3129    2.5570   -1.1527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5103    2.6951    0.3428 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3367    3.8098    0.9155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8663    2.8938    0.5752 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4603   -0.4067   -0.0659 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5359   -0.8880    1.2511 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8893   -0.4551   -0.5823 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -2.0890   -0.7648 S   0  0  0  0  0  6  0  0  0  0  0  0
    2.8036   -2.8611   -1.8197 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9605   -1.9696   -1.1732 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4620   -2.8540    0.7295 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6257   -1.2913   -0.8734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8160   -1.0007   -1.0119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9321   -0.3235   -0.4962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6364   -1.8072    0.3122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5707   -1.9868   -1.1293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9631   -1.0202    1.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1082   -3.3580   -0.0485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9864   -3.3807    1.5587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2129   -2.9364    1.4841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6814    0.4662    1.9357 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3271    1.6320    1.9678 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0156    1.5081    0.4977 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7646    2.4475   -1.5326 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9106    1.0331   -2.1530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1965    2.1317   -1.6374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1756    3.5940   -1.5792 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8508    4.3597    0.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1306    3.4223    1.5900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3122    4.4812    1.5027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9674    2.9679    1.5674 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3035   -0.4893    1.7369 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8903    0.0827   -1.5653 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5520    0.0832    0.1401 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5942   -3.3169    0.7952 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0448   -1.3338   -1.9224 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7219   -2.3371   -0.5083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3197   -1.9481   -1.3511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0775   -0.2596   -1.7908 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  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  6
  7 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 19  1  0
 16 17  2  0
 16 18  2  0
 13 20  1  0
 20 21  1  0
 21  4  1  0
 10  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  5 29  1  0
  6 30  1  1
  7 31  1  1
  8 32  1  0
  8 33  1  0
  9 34  1  0
  9 35  1  0
 11 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 14 40  1  0
 15 41  1  0
 15 42  1  0
 19 43  1  0
 20 44  1  0
 20 45  1  0
 21 46  1  0
 21 47  1  0
M  END


  Mrv1652309052220012D          

 21 22  0  0  1  0            999 V2000
    2.1986   -0.6302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5000    0.1378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3158    0.2607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9856    0.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1813    0.5992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5363    1.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5363    1.9386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2483    2.1935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7333    1.5261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2483    0.8586    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8556    0.3002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0853    0.0499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1813    2.4530    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5363    2.9673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5392    3.1963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0745    3.8779    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.6098    4.5596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7561    4.3426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3929    3.4132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9856    2.2694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3436    1.5261    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  6  0  0  0
  7 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  2  0  0  0  0
 16 19  1  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  0  0  0  0
  4 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0217618

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=CC2C(CC[C@@]2(C)O)[C@](O)(CS(O)(=O)=O)CC1

> <INCHI_IDENTIFIER>
InChI=1S/C15H26O5S/c1-10(2)11-4-7-15(17,9-21(18,19)20)12-5-6-14(3,16)13(12)8-11/h8,10,12-13,16-17H,4-7,9H2,1-3H3,(H,18,19,20)/t12?,13?,14-,15-/m1/s1

> <INCHI_KEY>
ATJUNJLOOOPBEA-NEXFUWMNSA-N

> <FORMULA>
C15H26O5S

> <MOLECULAR_WEIGHT>
318.43

> <EXACT_MASS>
318.150095111

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
33.5493511754807

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1R,4S)-1,4-dihydroxy-1-methyl-7-(propan-2-yl)-1,2,3,3a,4,5,6,8a-octahydroazulen-4-yl]methanesulfonic acid

> <JCHEM_LOGP>
0.8869954796666663

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.896806004408411

> <JCHEM_PKA_STRONGEST_ACIDIC>
-0.545268751173059

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9238644508897575

> <JCHEM_POLAR_SURFACE_AREA>
94.83

> <JCHEM_REFRACTIVITY>
81.05029999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,4S)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic 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       4.104  -1.176   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.667   0.257   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.189   0.487   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.706   1.461   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.205   1.119   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.001   2.079   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.001   3.619   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.464   4.095   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.369   2.849   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.464   1.603   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.597   0.560   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.159   0.093   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.205   4.579   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.001   5.539   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.873   5.966   0.000  0.00  0.00           C+0
HETATM   16  S   UNK     0       2.006   7.239   0.000  0.00  0.00           S+0
HETATM   17  O   UNK     0       1.138   8.511   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       3.278   8.106   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       0.733   6.371   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.706   4.236   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.375   2.849   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   21                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    8   13                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    6   11   12                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    7   14   15   20                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16                                                            
CONECT   20   13   21                                                       
CONECT   21   20    4                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

View in JSmol

Synonyms

Value	Source
[(1R,4S)-1,4-Dihydroxy-1-methyl-7-(propan-2-yl)-1,2,3,3a,4,5,6,8a-octahydroazulen-4-yl]methanesulfonate	Generator
[(1R,4S)-1,4-Dihydroxy-1-methyl-7-(propan-2-yl)-1,2,3,3a,4,5,6,8a-octahydroazulen-4-yl]methanesulphonate	Generator
[(1R,4S)-1,4-Dihydroxy-1-methyl-7-(propan-2-yl)-1,2,3,3a,4,5,6,8a-octahydroazulen-4-yl]methanesulphonic acid	Generator

Chemical Formula

C₁₅H₂₆O₅S

Average Mass

318.4300 Da

Monoisotopic Mass

318.15010 Da

IUPAC Name

[(1R,4S)-1,4-dihydroxy-1-methyl-7-(propan-2-yl)-1,2,3,3a,4,5,6,8a-octahydroazulen-4-yl]methanesulfonic acid

Traditional Name

[(1R,4S)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid

CAS Registry Number

Not Available

SMILES

CC(C)C1=CC2C(CC[C@@]2(C)O)[C@](O)(CS(O)(=O)=O)CC1

InChI Identifier

InChI=1S/C15H26O5S/c1-10(2)11-4-7-15(17,9-21(18,19)20)12-5-6-14(3,16)13(12)8-11/h8,10,12-13,16-17H,4-7,9H2,1-3H3,(H,18,19,20)/t12?,13?,14-,15-/m1/s1

InChI Key

ATJUNJLOOOPBEA-NEXFUWMNSA-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
Alisma plantago-aquatica	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
Alkanesulfonic acid
Tertiary alcohol
Sulfonyl
Organosulfonic acid
Organosulfonic acid or derivatives
Organic sulfonic acid or derivatives
Cyclic alcohol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organosulfur compound
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	0.89	ChemAxon
pKa (Strongest Acidic)	-0.55	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	81.05 m³·mol⁻¹	ChemAxon
Polarizability	33.55 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

4479257

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5321551

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)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid (NP0217618)

MOL for NP0217618 ([(1r,4s)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid)

3D MOL for NP0217618 ([(1r,4s)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid)

3D SDF for NP0217618 ([(1r,4s)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid)

3D-SDF for NP0217618 ([(1r,4s)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid)

PDB for NP0217618 ([(1r,4s)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid)

3D PDB for NP0217618 ([(1r,4s)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid)

SMILES for NP0217618 ([(1r,4s)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid)

INCHI for NP0217618 ([(1r,4s)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid)

Structure for NP0217618 ([(1r,4s)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid)

3D Structure for NP0217618 ([(1r,4s)-1,4-dihydroxy-7-isopropyl-1-methyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]methanesulfonic acid)