NP-MRD: Showing NP-Card for Alternaric acid (NP0066329)

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Record Information

Version

2.0

Created at

2022-04-28 10:36:49 UTC

Updated at

2022-04-28 10:36:49 UTC

NP-MRD ID

NP0066329

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Alternaric acid

Description

Alternaric acid is found in Alternaria solani and Alternaria sp..

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282212362D          

 29 29  0  0  1  0            999 V2000
   -1.4289    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5888   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7638   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4138    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    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
  1  2  1  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
  5  7  1  0  0  0  0
  1  7  1  0  0  0  0
  4  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 17 16  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  1  0  0  0
 21 26  1  1  0  0  0
 17 27  1  1  0  0  0
  3 28  1  0  0  0  0
  1 29  1  6  0  0  0
M  END

     RDKit          3D

 59 59  0  0  0  0  0  0  0  0999 V2000
    0.8713    1.7352    4.3269 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9053    0.5987    3.5930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3607   -0.1287    3.4544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0059   -0.0982    2.1298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2408    0.4120    1.9718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9487    0.4722    0.6596 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0908    1.2786    0.8216 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0564    1.1607   -0.2946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9669    0.6905   -0.6874 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3978    2.4094   -0.8190 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3039   -0.9296    0.2889 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1382   -1.6701    0.1347 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1760   -1.0909   -0.9063 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.5178   -0.3899   -0.7412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5990   -0.6603   -2.2099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6078   -1.0945   -3.2887 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2253    0.2058    3.0733 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3472    0.0765    1.5810 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7546   -0.2808    1.1985 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5768   -0.3971    2.1574 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1988   -0.4888   -0.1483 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3613   -0.3758   -1.1451 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0225   -0.0563   -0.9765 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8454   -0.5958   -2.5251 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3143   -0.2672   -2.6655 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5994    1.1852   -2.4174 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0204   -1.0208   -1.6826 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6240   -0.8293   -0.3672 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4206   -0.9341    0.6198 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0496    2.0343    4.7547 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7857    2.2829    4.4406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1012    0.2765    4.1982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2351   -1.1990    3.7658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4997   -0.4869    1.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7174    0.7903    2.8664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8342    1.9907    1.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1032    3.0029   -0.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9107   -1.3530    1.1566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6826   -1.5315   -0.7072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4424   -2.1907   -0.9460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2719   -0.9468   -1.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7815   -0.4679    0.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4677    0.6576   -1.0999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5987   -1.0383   -2.4441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5545    0.4435   -2.3116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8400   -2.1495   -3.1100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1192   -0.9320   -4.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4997   -0.4492   -3.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6154   -0.7146    3.5872 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9727    1.0088    3.3582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0147    1.0106    1.1166 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7599   -0.8260    1.2304 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3245   -0.5141   -1.5526 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2360   -0.0521   -3.2742 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7546   -1.7019   -2.7148 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6038   -0.5841   -3.6936 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6243    1.6788   -2.1676 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2560    1.3677   -1.5485 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0854    1.6762   -3.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 13  1  0
 13 14  1  0
 13 11  1  0
 11 12  1  0
 11  6  1  0
  6  7  1  1
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 28 29  2  0
  6  8  1  0
  8 10  1  0
  8  9  2  0
 28 21  1  0
 16 46  1  0
 16 47  1  0
 16 48  1  0
 15 44  1  0
 15 45  1  0
 13 40  1  6
 14 41  1  0
 14 42  1  0
 14 43  1  0
 11 38  1  1
 12 39  1  0
  7 36  1  0
  5 35  1  0
  4 34  1  0
  3 32  1  0
  3 33  1  0
  1 30  1  0
  1 31  1  0
 17 49  1  0
 17 50  1  0
 18 51  1  0
 18 52  1  0
 23 53  1  0
 24 54  1  0
 24 55  1  0
 25 56  1  6
 26 57  1  0
 26 58  1  0
 26 59  1  0
 10 37  1  0
M  END


  Mrv1652304282212362D          

 29 29  0  0  1  0            999 V2000
   -1.4289    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5888   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7638   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4138    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    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
  1  2  1  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
  5  7  1  0  0  0  0
  1  7  1  0  0  0  0
  4  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 17 16  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  1  0  0  0
 21 26  1  1  0  0  0
 17 27  1  1  0  0  0
  3 28  1  0  0  0  0
  1 29  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0066329

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)[C@@H](O)[C@@](O)(\C=C\CC(=C)CCC(=O)C1=C(O)C[C@@H](C)OC1=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O8/c1-5-13(3)18(24)21(28,20(26)27)10-6-7-12(2)8-9-15(22)17-16(23)11-14(4)29-19(17)25/h6,10,13-14,18,23-24,28H,2,5,7-9,11H2,1,3-4H3,(H,26,27)/b10-6+/t13-,14+,18+,21-/m0/s1

> <INCHI_KEY>
KMEVEPGHUURWPL-KBUHGEJUSA-N

> <FORMULA>
C21H30O8

> <MOLECULAR_WEIGHT>
410.463

> <EXACT_MASS>
410.194067926

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
43.16888057222495

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3E)-2-hydroxy-2-[(1R,2S)-1-hydroxy-2-methylbutyl]-9-[(6R)-4-hydroxy-6-methyl-2-oxo-5,6-dihydro-2H-pyran-3-yl]-6-methylidene-9-oxonon-3-enoic acid

> <ALOGPS_LOGP>
1.76

> <JCHEM_LOGP>
2.303666134666667

> <ALOGPS_LOGS>
-2.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.25313419999096

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6510154339889667

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4614347631116162

> <JCHEM_POLAR_SURFACE_AREA>
141.36

> <JCHEM_REFRACTIVITY>
107.00089999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.20e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3E)-2-hydroxy-2-[(1R,2S)-1-hydroxy-2-methylbutyl]-9-[(6R)-4-hydroxy-6-methyl-2-oxo-5,6-dihydropyran-3-yl]-6-methylidene-9-oxonon-3-enoic 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      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667   3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.334   0.770   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -1.334   0.770   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.334   5.390   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667   3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002   3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.336   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.566  -0.564   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.336  -1.897   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       7.026  -0.564   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.003   0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.337   0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.337  -1.540   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.003   2.310   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      10.669  -1.540   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      10.106   2.104   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -1.334   5.390   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -4.001   0.770   0.000  0.00  0.00           C+0
CONECT    1    2    7   29                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   28                                                  
CONECT    4    3    5    8                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    1                                                       
CONECT    8    4    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   21   27                                             
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   17   22   26                                                  
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22                                                            
CONECT   26   21                                                            
CONECT   27   17                                                            
CONECT   28    3                                                            
CONECT   29    1                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₀O₈

Average Mass

410.4630 Da

Monoisotopic Mass

410.19407 Da

IUPAC Name

(2S,3E)-2-hydroxy-2-[(1R,2S)-1-hydroxy-2-methylbutyl]-9-[(6R)-4-hydroxy-6-methyl-2-oxo-5,6-dihydro-2H-pyran-3-yl]-6-methylidene-9-oxonon-3-enoic acid

Traditional Name

(2S,3E)-2-hydroxy-2-[(1R,2S)-1-hydroxy-2-methylbutyl]-9-[(6R)-4-hydroxy-6-methyl-2-oxo-5,6-dihydropyran-3-yl]-6-methylidene-9-oxonon-3-enoic acid

CAS Registry Number

Not Available

SMILES

CC[C@H](C)[C@@H](O)[C@@](O)(\C=C\CC(=C)CCC(=O)C1=C(O)C[C@@H](C)OC1=O)C(O)=O

InChI Identifier

InChI=1S/C21H30O8/c1-5-13(3)18(24)21(28,20(26)27)10-6-7-12(2)8-9-15(22)17-16(23)11-14(4)29-19(17)25/h6,10,13-14,18,23-24,28H,2,5,7-9,11H2,1,3-4H3,(H,26,27)/b10-6+/t13-,14+,18+,21-/m0/s1

InChI Key

KMEVEPGHUURWPL-KBUHGEJUSA-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
Alternaria solani	Fungi	KNApSAcK
Alternaria sp.	Fungi	KNApSAcK

Chemical Taxonomy

Classification

Not classified

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	1.76	ALOGPS
logP	2.3	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	3.65	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	141.36 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	107 m³·mol⁻¹	ChemAxon
Polarizability	43.17 Å³	ChemAxon
Number of Rings	1	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

Not Available

References

General References

Not Available

Showing NP-Card for Alternaric acid (NP0066329)

MOL for NP0066329 (Alternaric acid)

3D MOL for NP0066329 (Alternaric acid)

3D SDF for NP0066329 (Alternaric acid)

3D-SDF for NP0066329 (Alternaric acid)

PDB for NP0066329 (Alternaric acid)

3D PDB for NP0066329 (Alternaric acid)

SMILES for NP0066329 (Alternaric acid)

INCHI for NP0066329 (Alternaric acid)

Structure for NP0066329 (Alternaric acid)

3D Structure for NP0066329 (Alternaric acid)