NP-MRD: Showing NP-Card for (-)-leucothol c (NP0276113)

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Record Information

Version

2.0

Created at

2022-09-09 00:04:52 UTC

Updated at

2022-09-09 00:04:52 UTC

NP-MRD ID

NP0276113

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-leucothol c

Description

(-)-Leucothol c belongs to the class of organic compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ). Thus, (-)-leucothol c is considered to be an isoprenoid. Based on a literature review very few articles have been published on (-)-leucothol c.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -0.2966    3.0633   -0.3917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2576    1.7413   -0.5019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5329    1.0016   -0.6584 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6704    1.7389    0.0052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9156    0.9033    0.0668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7016   -0.5025    0.5077 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5437   -1.3546   -0.7057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5973   -2.2037   -1.3041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3069   -1.2332   -1.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4972   -0.4023   -0.1984 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1403   -1.0392   -0.0917 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8598   -0.0921    0.5349 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1951    0.5014    1.6325 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1278   -0.7284    0.9617 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0429   -2.1383    0.8914 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3542   -0.3005    0.2302 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5443   -0.7537    1.0975 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5315   -1.0269   -1.0895 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4775    1.1781    0.0989 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3975    1.4897   -0.9171 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1925    1.9212   -0.1111 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0471    1.0211   -0.4761 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2811   -0.6427    1.0766 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1257   -1.9675    1.4262 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6573    3.6143   -0.2811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2105    3.6128   -0.4054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7607    1.0525   -1.7668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3837    2.1683    0.9821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9189    2.6301   -0.6521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6777    1.4252    0.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3456    0.9069   -0.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4503   -0.8885    1.2137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1726   -2.6968   -0.4719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2210   -2.9570   -1.9943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3453   -1.5203   -1.7900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9622   -1.6687   -2.0912 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2111   -1.2497   -1.1215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2363   -1.9674    0.4912 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4617   -0.0239    2.4342 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2899   -0.5105    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7597   -2.4430    0.0129 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4520   -0.8882    0.4554 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7691   -0.0293    1.8850 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3117   -1.7307    1.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5701   -1.3134   -1.5571 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0614   -1.9839   -0.9043 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1709   -0.4225   -1.7475 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9478    1.5740    1.0340 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9543    1.7720   -1.7469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3577    2.6762   -0.9007 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9089    2.4753    0.8113 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2048    0.6489   -1.5094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0848    0.0682    1.8680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2220   -2.5051    0.5840 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  9  2  0
 10  9  1  6
 10 11  1  0
 11 12  1  0
 12 13  1  1
 12 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6 23  1  0
 23 24  1  0
  6  7  1  0
  3 10  1  0
 23 10  1  0
 22 12  1  0
  8 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
 11 37  1  0
 11 38  1  0
 13 39  1  0
 14 40  1  1
 15 41  1  0
 17 42  1  0
 17 43  1  0
 17 44  1  0
 18 45  1  0
 18 46  1  0
 18 47  1  0
 19 48  1  1
 20 49  1  0
 21 50  1  0
 21 51  1  0
 22 52  1  6
  1 25  1  0
  1 26  1  0
  3 27  1  6
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  1
 23 53  1  1
 24 54  1  0
M  END


  Mrv1652309092202042D          

 24 27  0  0  1  0            999 V2000
    3.6704   -1.1396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4720   -0.3387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6713   -0.1051    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1143   -0.7723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2839   -0.5673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0345    0.2636    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0092    1.1288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3282    1.5944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8326    1.4220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4183    0.7398    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0794    1.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8792    1.0419    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6883    1.8445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4801    1.6073    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2909    2.4103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2701    1.3696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3670    2.1889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0938    1.4165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4593    0.5666    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2493    0.3289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8585    0.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0684    0.2389    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7471    0.4672    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0160   -0.3127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
 10  9  1  1  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 22 21  1  6  0  0  0
  2 22  1  0  0  0  0
 12 22  1  0  0  0  0
 10 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0276113

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C[C@@]23C[C@@]4(O)[C@@H](O)C(C)(C)[C@@H](O)C[C@@H]4C(=C)[C@@H]2CC[C@@H]1[C@H]3O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O4/c1-10-8-19-9-20(24)14(7-15(21)18(3,4)17(20)23)11(2)13(19)6-5-12(10)16(19)22/h8,12-17,21-24H,2,5-7,9H2,1,3-4H3/t12-,13-,14+,15-,16+,17-,19+,20-/m0/s1

> <INCHI_KEY>
RPVINCFOPQZXJM-UIVPEWPISA-N

> <FORMULA>
C20H30O4

> <MOLECULAR_WEIGHT>
334.456

> <EXACT_MASS>
334.214409446

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
37.42568886477377

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3S,4S,6S,8R,10S,13S,16R)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0^{1,10}.0^{3,8}]hexadec-14-ene-3,4,6,16-tetrol

> <JCHEM_LOGP>
0.6576126143333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.070326842282004

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.175034482963177

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9687075194691683

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
92.33650000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3S,4S,6S,8R,10S,13S,16R)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0^{1,10}.0^{3,8}]hexadec-14-ene-3,4,6,16-tetrol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       6.851  -2.127   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.481  -0.632   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.986  -0.196   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.947  -1.442   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.397  -1.059   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.931   0.492   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.884   2.107   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.613   2.976   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.421   2.654   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.514   1.381   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.748   2.387   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.241   1.945   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.885   3.443   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.363   3.000   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.010   4.499   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.838   2.557   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.018   4.086   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.375   2.644   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.191   1.058   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      11.665   0.614   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       9.069   0.002   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.594   0.446   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.261   0.872   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.763  -0.584   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   23                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9    3   11   23                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   14   22                                             
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21    2   12                                                  
CONECT   23   10    6   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₄

Average Mass

334.4560 Da

Monoisotopic Mass

334.21441 Da

IUPAC Name

(1S,3S,4S,6S,8R,10S,13S,16R)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0^{1,10}.0^{3,8}]hexadec-14-ene-3,4,6,16-tetrol

Traditional Name

(1S,3S,4S,6S,8R,10S,13S,16R)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.0^{1,10}.0^{3,8}]hexadec-14-ene-3,4,6,16-tetrol

CAS Registry Number

Not Available

SMILES

CC1=C[C@@]23C[C@@]4(O)[C@@H](O)C(C)(C)[C@@H](O)C[C@@H]4C(=C)[C@@H]2CC[C@@H]1[C@H]3O

InChI Identifier

InChI=1S/C20H30O4/c1-10-8-19-9-20(24)14(7-15(21)18(3,4)17(20)23)11(2)13(19)6-5-12(10)16(19)22/h8,12-17,21-24H,2,5-7,9H2,1,3-4H3/t12-,13-,14+,15-,16+,17-,19+,20-/m0/s1

InChI Key

RPVINCFOPQZXJM-UIVPEWPISA-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 tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Tertiary alcohols

Alternative Parents

Substituents

Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Polyol
Hydrocarbon derivative
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Leucothol and grayanotoxane diterpenoids (LMPR0104180004 )

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	0.66	ChemAxon
pKa (Strongest Acidic)	13.18	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	80.92 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	92.34 m³·mol⁻¹	ChemAxon
Polarizability	37.43 Å³	ChemAxon
Number of Rings	4	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

24846790

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

42608227

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (-)-leucothol c (NP0276113)

MOL for NP0276113 ((-)-leucothol c)

3D MOL for NP0276113 ((-)-leucothol c)

3D SDF for NP0276113 ((-)-leucothol c)

3D-SDF for NP0276113 ((-)-leucothol c)

PDB for NP0276113 ((-)-leucothol c)

3D PDB for NP0276113 ((-)-leucothol c)

SMILES for NP0276113 ((-)-leucothol c)

INCHI for NP0276113 ((-)-leucothol c)

Structure for NP0276113 ((-)-leucothol c)

3D Structure for NP0276113 ((-)-leucothol c)