NP-MRD: Showing NP-Card for (+)-Eucalmaidin A (NP0081589)

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Record Information

Version

2.0

Created at

2022-04-29 02:35:33 UTC

Updated at

2022-04-29 02:35:33 UTC

NP-MRD ID

NP0081589

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Eucalmaidin A

Description

(2R,3R,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexyl (4R)-4-(2-hydroxypropan-2-yl)cyclohex-1-ene-1-carboxylate belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. Based on a literature review very few articles have been published on (2R,3R,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexyl (4R)-4-(2-hydroxypropan-2-yl)cyclohex-1-ene-1-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 50 50  0  0  0  0  0  0  0  0999 V2000
   -6.4482    1.3959   -0.4256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5940    0.1796   -0.2425 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7686   -0.4644    1.1136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0185   -0.7705   -1.1916 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1282    0.4434   -0.5364 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5588    1.5290    0.3196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1634    1.2649    0.7431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4091    0.3049    0.3050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0385    0.1010    0.7664 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4126    0.8947    1.6208 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7402   -0.9133    0.2950 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0500   -1.1898    0.6566 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9826   -0.1037    0.2649 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7726    1.1321    0.8021 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4397   -0.5394    0.5083 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6620   -1.7836   -0.0292 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3021    0.5367   -0.0653 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0614    0.6259   -1.4427 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7768    0.3025    0.1984 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9692    0.2202    1.5707 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2932   -0.8720   -0.5234 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1830   -0.9152   -1.7272 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9477   -0.6321   -0.7066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4022   -0.8818   -0.3055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4259    2.0905    0.4301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1740    1.8640   -1.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5111    1.0469   -0.5295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8059   -0.3373    1.4627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5868   -1.5733    1.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0125   -0.1274    1.8515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0961   -1.6752   -0.7975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0490    0.7240   -1.6021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1506    1.7189    1.2476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5594    2.4895   -0.2429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7488    1.9422    1.4859 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3463   -2.1616    0.1701 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0566   -1.3642    1.7618 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9085    0.0298   -0.8601 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2009    1.1964    1.6988 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5406   -0.5591    1.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6388   -2.4855    0.6801 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9814    1.5086    0.3607 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9210   -0.2925   -1.7673 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2974    1.2449   -0.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9015    1.0990    1.9973 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7666   -1.6786    0.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8864   -0.2244   -1.7371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4402   -1.6169   -0.7010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4131   -1.0555    0.7852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8681   -1.6678   -0.9009 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  6
  2  5  1  0
  5 24  1  0
 24 23  1  0
 23  8  1  0
  8  7  2  0
  7  6  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
  6  5  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  5 32  1  6
 24 49  1  0
 24 50  1  0
 23 47  1  0
 23 48  1  0
  7 35  1  0
  6 33  1  0
  6 34  1  0
 12 36  1  0
 12 37  1  0
 13 38  1  6
 14 39  1  0
 15 40  1  1
 16 41  1  0
 17 42  1  1
 18 43  1  0
 19 44  1  6
 20 45  1  0
 21 46  1  0
M  END


  Mrv1652304292204352D          

 24 24  0  0  1  0            999 V2000
   -3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5888   -1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4138   -0.5230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.8250    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  1  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 18 21  1  1  0  0  0
 17 22  1  1  0  0  0
 16 23  1  1  0  0  0
 15 24  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0081589

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(O)[C@@H]1CCC(=CC1)C(=O)OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H26O8/c1-16(2,23)10-5-3-9(4-6-10)15(22)24-8-12(19)14(21)13(20)11(18)7-17/h3,7,10-14,18-21,23H,4-6,8H2,1-2H3/t10-,11-,12+,13+,14+/m0/s1

> <INCHI_KEY>
LXDQFZXPMQXZJM-ODXJTPSBSA-N

> <FORMULA>
C16H26O8

> <MOLECULAR_WEIGHT>
346.376

> <EXACT_MASS>
346.162767797

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
35.65302822002373

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexyl (4R)-4-(2-hydroxypropan-2-yl)cyclohex-1-ene-1-carboxylate

> <ALOGPS_LOGP>
-0.07

> <JCHEM_LOGP>
-1.304565998333334

> <ALOGPS_LOGS>
-1.60

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.072348531588805

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.255242937561377

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8732545127334189

> <JCHEM_POLAR_SURFACE_AREA>
144.52

> <JCHEM_REFRACTIVITY>
84.03249999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.73e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexyl (4R)-4-(2-hydroxypropan-2-yl)cyclohex-1-ene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      -6.668   0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.335   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.335  -1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.002  -1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.002  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -8.566  -3.644   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0     -10.106  -0.976   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -4.001   0.770   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.334   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001   0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.668   0.770   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       2.667  -1.540   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       0.000  -1.540   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7                                                            
CONECT   11    2   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   24                                                  
CONECT   16   15   17   23                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18                                                            
CONECT   22   17                                                            
CONECT   23   16                                                            
CONECT   24   15                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   48    0
END

View in JSmol

Synonyms

Value	Source
(2R,3R,4S,5R)-2,3,4,5-Tetrahydroxy-6-oxohexyl (4R)-4-(2-hydroxypropan-2-yl)cyclohex-1-ene-1-carboxylic acid	Generator

Chemical Formula

C₁₆H₂₆O₈

Average Mass

346.3760 Da

Monoisotopic Mass

346.16277 Da

IUPAC Name

(2R,3R,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexyl (4R)-4-(2-hydroxypropan-2-yl)cyclohex-1-ene-1-carboxylate

Traditional Name

(2R,3R,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexyl (4R)-4-(2-hydroxypropan-2-yl)cyclohex-1-ene-1-carboxylate

CAS Registry Number

Not Available

SMILES

CC(C)(O)[C@@H]1CCC(=CC1)C(=O)OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O

InChI Identifier

InChI=1S/C16H26O8/c1-16(2,23)10-5-3-9(4-6-10)15(22)24-8-12(19)14(21)13(20)11(18)7-17/h3,7,10-14,18-21,23H,4-6,8H2,1-2H3/t10-,11-,12+,13+,14+/m0/s1

InChI Key

LXDQFZXPMQXZJM-ODXJTPSBSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Menthane monoterpenoids

Alternative Parents

Substituents

P-menthane monoterpenoid
Monocyclic monoterpenoid
Monosaccharide
Beta-hydroxy aldehyde
Alpha-hydroxyaldehyde
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	-0.07	ALOGPS
logP	-1.3	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Acidic)	12.26	ChemAxon
pKa (Strongest Basic)	-0.87	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	144.52 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	84.03 m³·mol⁻¹	ChemAxon
Polarizability	35.65 Å³	ChemAxon
Number of Rings	1	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

162901290

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Eucalmaidin A (NP0081589)

MOL for NP0081589 ((+)-Eucalmaidin A)

3D MOL for NP0081589 ((+)-Eucalmaidin A)

3D SDF for NP0081589 ((+)-Eucalmaidin A)

3D-SDF for NP0081589 ((+)-Eucalmaidin A)

PDB for NP0081589 ((+)-Eucalmaidin A)

3D PDB for NP0081589 ((+)-Eucalmaidin A)

SMILES for NP0081589 ((+)-Eucalmaidin A)

INCHI for NP0081589 ((+)-Eucalmaidin A)

Structure for NP0081589 ((+)-Eucalmaidin A)

3D Structure for NP0081589 ((+)-Eucalmaidin A)