NP-MRD: Showing NP-Card for Cliviahaksine (NP0066747)

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Record Information

Version

2.0

Created at

2022-04-28 10:59:27 UTC

Updated at

2022-04-28 10:59:28 UTC

NP-MRD ID

NP0066747

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cliviahaksine

Description

6-[(5S,7R,7aR)-5-hydroxy-1-methyl-2,3,5,6,7,7a-hexahydro-1H-indol-7-yl]-2H-1,3-benzodioxole-5-carboxylic acid belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms. Cliviahaksine is found in Clivia miniata Regel . Based on a literature review very few articles have been published on 6-[(5S,7R,7aR)-5-hydroxy-1-methyl-2,3,5,6,7,7a-hexahydro-1H-indol-7-yl]-2H-1,3-benzodioxole-5-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 45  0  0  0  0  0  0  0  0999 V2000
   -1.1217    0.4830   -2.2290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6893   -0.4946   -1.2883 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1263   -0.4156   -1.4711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7358   -0.5935   -0.1021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6726   -0.0899    0.7993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6307    0.3453    2.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2390    0.7500    2.5048 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2135    0.9987    3.8678 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4206   -0.4971    2.2559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3518   -0.8659    0.7789 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0069   -0.4982    0.3009 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7102    0.4981    0.9606 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9524    0.9366    0.4931 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5116    0.3900   -0.6376 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8029   -0.5942   -1.2766 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5546   -1.0506   -0.8236 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9985   -2.1474   -1.5840 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1151   -2.8907   -1.1276 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4446   -2.4169   -2.8919 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7459    1.0131   -0.8726 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7702    2.1906   -0.1012 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8585    1.8920    0.9388 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4050   -0.0660    0.0373 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8762    1.3138   -2.3635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2409    0.9917   -1.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9550    0.0533   -3.2242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4947   -1.1514   -2.1954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4074    0.6172   -1.8123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7017   -0.0678    0.0203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8821   -1.7070    0.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4983    0.3866    2.6523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9531    1.6155    1.9179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3210    0.7147    4.2413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9938   -1.3279    2.7962 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5558   -0.5057    2.7580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5716   -1.9195    0.6950 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3602    1.0046    1.8486 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2581   -1.0128   -2.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7179   -2.3630   -3.6148 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7821    2.4402    0.2802 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3430    3.0480   -0.6816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9863    0.9928    0.0317 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  2  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 23  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 20  1  0
 20 21  1  0
 21 22  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 19  1  0
 17 18  2  0
 23  2  1  0
 16 11  1  0
 23  5  1  0
 22 13  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  6 31  1  0
  7 32  1  6
  8 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  1
 23 42  1  6
 12 37  1  0
 21 40  1  0
 21 41  1  0
 15 38  1  0
 19 39  1  0
M  END


  Mrv1652304282212592D          

 23 26  0  0  1  0            999 V2000
    3.2789    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249    1.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9514    3.8520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2869    4.6057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1074    4.5195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
 10  4  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 14 18  1  0  0  0  0
 16 19  1  0  0  0  0
 12 20  1  6  0  0  0
  2 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  1 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0066747

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1CCC2=C[C@@H](O)C[C@@H]([C@@H]12)C1=CC2=C(OCO2)C=C1C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H19NO5/c1-18-3-2-9-4-10(19)5-12(16(9)18)11-6-14-15(23-8-22-14)7-13(11)17(20)21/h4,6-7,10,12,16,19H,2-3,5,8H2,1H3,(H,20,21)/t10-,12-,16+/m1/s1

> <INCHI_KEY>
AOQKBSQBUASZKT-SIVJFFJCSA-N

> <FORMULA>
C17H19NO5

> <MOLECULAR_WEIGHT>
317.341

> <EXACT_MASS>
317.126322716

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
32.56895144265516

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-[(5S,7R,7aR)-5-hydroxy-1-methyl-2,3,5,6,7,7a-hexahydro-1H-indol-7-yl]-2H-1,3-benzodioxole-5-carboxylic acid

> <ALOGPS_LOGP>
0.54

> <JCHEM_LOGP>
-1.6109624557576236

> <ALOGPS_LOGS>
-2.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.85800876646461

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.640155538817437

> <JCHEM_PKA_STRONGEST_BASIC>
8.023747743151324

> <JCHEM_POLAR_SURFACE_AREA>
79.23

> <JCHEM_REFRACTIVITY>
83.6205

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.88e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-[(5S,7R,7aR)-5-hydroxy-1-methyl-2,3,5,6,7,7a-hexahydroindol-7-yl]-2H-1,3-benzodioxole-5-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       6.121   6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.787   6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.787   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.121   3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.454   4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.454   6.160   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.788   3.850   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.122   4.620   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       8.788   2.310   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.454   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       3.322   2.016   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.846   3.481   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.788  -0.770   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       3.643   7.190   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.269   8.597   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.800   8.436   0.000  0.00  0.00           O+0
CONECT    1    2    6   23                                                  
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    4   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   18                                                  
CONECT   15   14   10   16                                                  
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17   14                                                       
CONECT   19   16                                                            
CONECT   20   12                                                            
CONECT   21    2   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    1                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Value	Source
6-[(5S,7R,7AR)-5-hydroxy-1-methyl-2,3,5,6,7,7a-hexahydro-1H-indol-7-yl]-2H-1,3-benzodioxole-5-carboxylate	Generator

Chemical Formula

C₁₇H₁₉NO₅

Average Mass

317.3410 Da

Monoisotopic Mass

317.12632 Da

IUPAC Name

6-[(5S,7R,7aR)-5-hydroxy-1-methyl-2,3,5,6,7,7a-hexahydro-1H-indol-7-yl]-2H-1,3-benzodioxole-5-carboxylic acid

Traditional Name

6-[(5S,7R,7aR)-5-hydroxy-1-methyl-2,3,5,6,7,7a-hexahydroindol-7-yl]-2H-1,3-benzodioxole-5-carboxylic acid

CAS Registry Number

Not Available

SMILES

CN1CCC2=C[C@@H](O)C[C@@H]([C@@H]12)C1=CC2=C(OCO2)C=C1C(O)=O

InChI Identifier

InChI=1S/C17H19NO5/c1-18-3-2-9-4-10(19)5-12(16(9)18)11-6-14-15(23-8-22-14)7-13(11)17(20)21/h4,6-7,10,12,16,19H,2-3,5,8H2,1H3,(H,20,21)/t10-,12-,16+/m1/s1

InChI Key

AOQKBSQBUASZKT-SIVJFFJCSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Clivia miniata Regel	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzodioxoles

Sub Class

Not Available

Direct Parent

Benzodioxoles

Alternative Parents

Substituents

Benzodioxole
Indole or derivatives
Aralkylamine
Benzenoid
N-alkylpyrrolidine
Pyrrolidine
Amino acid or derivatives
Amino acid
Secondary alcohol
Tertiary amine
Tertiary aliphatic amine
Acetal
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Oxacycle
Azacycle
Organic nitrogen compound
Organopnictogen compound
Amine
Alcohol
Organonitrogen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
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	0.54	ALOGPS
logP	-1.6	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	3.64	ChemAxon
pKa (Strongest Basic)	8.02	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	79.23 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	83.62 m³·mol⁻¹	ChemAxon
Polarizability	32.57 Å³	ChemAxon
Number of Rings	4	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

163016972

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Cliviahaksine (NP0066747)

MOL for NP0066747 (Cliviahaksine)

3D MOL for NP0066747 (Cliviahaksine)

3D SDF for NP0066747 (Cliviahaksine)

3D-SDF for NP0066747 (Cliviahaksine)

PDB for NP0066747 (Cliviahaksine)

3D PDB for NP0066747 (Cliviahaksine)

SMILES for NP0066747 (Cliviahaksine)

INCHI for NP0066747 (Cliviahaksine)

Structure for NP0066747 (Cliviahaksine)

3D Structure for NP0066747 (Cliviahaksine)