NP-MRD: Showing NP-Card for Botryomaman (NP0007257)

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Record Information

Version

2.0

Created at

2020-12-09 04:05:48 UTC

Updated at

2021-07-15 16:57:06 UTC

NP-MRD ID

NP0007257

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Botryomaman

Provided By

NPAtlas

Description

(2E)-3-[(2S,3S)-5-hydroxy-6-methoxy-2-methyl-4-pentyl-2,3-dihydro-1-benzofuran-3-yl]prop-2-enoic acid belongs to the class of organic compounds known as coumarans. Coumarans are compounds containing the coumaran skeleton, which consists of a benzene ring fused to a 2,3-dihydrofuran ring. Botryomaman is found in Botryosphaeria and Cophinforma mamane. Botryomaman was first documented in 2007 (PMID: 17827773). Based on a literature review very few articles have been published on (2E)-3-[(2S,3S)-5-hydroxy-6-methoxy-2-methyl-4-pentyl-2,3-dihydro-1-benzofuran-3-yl]prop-2-enoic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118383D          

 47 48  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652306242118383D          

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  3 30  1  0  0  0  0
  4 31  1  0  0  0  0
  4 32  1  0  0  0  0
  5 33  1  0  0  0  0
  5 34  1  0  0  0  0
  8 35  1  0  0  0  0
 11 36  1  0  0  0  0
 11 37  1  0  0  0  0
 11 38  1  0  0  0  0
 12 39  1  0  0  0  0
 15 40  1  1  0  0  0
 16 41  1  0  0  0  0
 17 42  1  0  0  0  0
 20 43  1  0  0  0  0
 21 44  1  1  0  0  0
 22 45  1  0  0  0  0
 22 46  1  0  0  0  0
 22 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007257

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C(\[H])=C(/[H])[C@@]1([H])C2=C(O[C@@]1([H])C([H])([H])[H])C([H])=C(OC([H])([H])[H])C(O[H])=C2C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H24O5/c1-4-5-6-7-13-17-12(8-9-16(19)20)11(2)23-14(17)10-15(22-3)18(13)21/h8-12,21H,4-7H2,1-3H3,(H,19,20)/b9-8+/t11-,12+/m0/s1

> <INCHI_KEY>
UBYLMNDNGLUBCF-VDTGWRSZSA-N

> <FORMULA>
C18H24O5

> <MOLECULAR_WEIGHT>
320.385

> <EXACT_MASS>
320.162373873

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
35.127237447494394

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-3-[(2S,3S)-5-hydroxy-6-methoxy-2-methyl-4-pentyl-2,3-dihydro-1-benzofuran-3-yl]prop-2-enoic acid

> <ALOGPS_LOGP>
3.98

> <JCHEM_LOGP>
4.034189424333333

> <ALOGPS_LOGS>
-3.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
10.608522022847803

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.945907649101726

> <JCHEM_PKA_STRONGEST_BASIC>
-4.584809808308344

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
88.5712

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.34e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-3-[(2S,3S)-5-hydroxy-6-methoxy-2-methyl-4-pentyl-2,3-dihydro-1-benzofuran-3-yl]prop-2-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 47 48  0  0  0  0  0  0  0  0999 V2000
    4.8269   -0.7640   -1.4295 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8005   -1.2633   -0.4534 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4037   -1.2744   -1.0730 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3637   -1.7397   -0.1143 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0851   -0.9226    1.0838 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5027    0.4143    0.8691 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2028    1.5326    0.5374 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5648    1.5347    0.3942 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5696    2.7689    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3251    3.8958   -0.0194 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6179    5.1030   -0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7950    2.8206    0.4572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5599    1.7248    0.7919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9008    0.5421    0.9920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9134   -0.4742    1.3356 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2978   -1.3235    0.1856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2127   -2.6632    0.2107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5965   -3.4714   -0.9324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4949   -4.7158   -0.8503 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0675   -2.9079   -2.1001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1286    0.3466    1.7123 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4216   -0.2746    1.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9462    1.5685    0.9786 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3499   -1.6068   -1.9708 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3664   -0.1584   -2.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6521   -0.2041   -0.9340 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1080   -2.3426   -0.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8706   -0.7504    0.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2016   -0.2980   -1.5536 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4764   -2.0822   -1.8688 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6884   -2.7702    0.2218 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4371   -1.9430   -0.7254 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4595   -1.5056    1.8332 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0754   -0.8066    1.6287 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0682    2.3573    0.1515 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0310    5.2749    0.7121 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2754    5.9467   -0.4666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1382    4.8977   -1.0214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2838    3.7718    0.2913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5419   -1.1024    2.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6713   -0.9002   -0.7453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8467   -3.1006    1.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0412   -2.5696   -2.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1434    0.5221    2.8001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6886    0.1430    0.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4059   -1.3667    1.2328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2266    0.1368    1.9162 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  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 15 21  1  0
 21 22  1  0
 21 23  1  0
 14  6  1  0
 23 13  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  8 35  1  0
 11 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 15 40  1  1
 16 41  1  0
 17 42  1  0
 20 43  1  0
 21 44  1  1
 22 45  1  0
 22 46  1  0
 22 47  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       4.827  -0.764  -1.430  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.801  -1.263  -0.453  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.404  -1.274  -1.073  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.364  -1.740  -0.114  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.085  -0.923   1.084  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.503   0.414   0.869  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.203   1.533   0.537  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.565   1.535   0.394  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.570   2.769   0.322  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.325   3.896  -0.019  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.618   5.103  -0.221  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.795   2.821   0.457  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.560   1.725   0.792  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.901   0.542   0.992  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.913  -0.474   1.336  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.298  -1.323   0.186  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.213  -2.663   0.211  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.596  -3.471  -0.932  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.495  -4.716  -0.850  0.00  0.00           O+0
HETATM   20  O   UNK     0      -3.067  -2.908  -2.100  0.00  0.00           O+0
HETATM   21  C   UNK     0      -3.129   0.347   1.712  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.422  -0.275   1.240  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.946   1.569   0.979  0.00  0.00           O+0
HETATM   24  H   UNK     0       5.350  -1.607  -1.971  0.00  0.00           H+0
HETATM   25  H   UNK     0       4.366  -0.158  -2.246  0.00  0.00           H+0
HETATM   26  H   UNK     0       5.652  -0.204  -0.934  0.00  0.00           H+0
HETATM   27  H   UNK     0       4.108  -2.343  -0.239  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.871  -0.750   0.495  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.202  -0.298  -1.554  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.476  -2.082  -1.869  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.688  -2.770   0.222  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.437  -1.943  -0.725  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.460  -1.506   1.833  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.075  -0.807   1.629  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.068   2.357   0.152  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.031   5.275   0.712  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.275   5.947  -0.467  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.138   4.898  -1.021  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.284   3.772   0.291  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.542  -1.102   2.142  0.00  0.00           H+0
HETATM   41  H   UNK     0      -2.671  -0.900  -0.745  0.00  0.00           H+0
HETATM   42  H   UNK     0      -1.847  -3.101   1.118  0.00  0.00           H+0
HETATM   43  H   UNK     0      -4.041  -2.570  -2.095  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.143   0.522   2.800  0.00  0.00           H+0
HETATM   45  H   UNK     0      -4.689   0.143   0.228  0.00  0.00           H+0
HETATM   46  H   UNK     0      -4.406  -1.367   1.233  0.00  0.00           H+0
HETATM   47  H   UNK     0      -5.227   0.137   1.916  0.00  0.00           H+0
CONECT    1    2   24   25   26                                             
CONECT    2    1    3   27   28                                             
CONECT    3    2    4   29   30                                             
CONECT    4    3    5   31   32                                             
CONECT    5    4    6   33   34                                             
CONECT    6    5    7   14                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7   35                                                       
CONECT    9    7   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10   36   37   38                                             
CONECT   12    9   13   39                                                  
CONECT   13   12   14   23                                                  
CONECT   14   13   15    6                                                  
CONECT   15   14   16   21   40                                             
CONECT   16   15   17   41                                                  
CONECT   17   16   18   42                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   43                                                       
CONECT   21   15   22   23   44                                             
CONECT   22   21   45   46   47                                             
CONECT   23   21   13                                                       
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    2                                                            
CONECT   28    2                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
CONECT   31    4                                                            
CONECT   32    4                                                            
CONECT   33    5                                                            
CONECT   34    5                                                            
CONECT   35    8                                                            
CONECT   36   11                                                            
CONECT   37   11                                                            
CONECT   38   11                                                            
CONECT   39   12                                                            
CONECT   40   15                                                            
CONECT   41   16                                                            
CONECT   42   17                                                            
CONECT   43   20                                                            
CONECT   44   21                                                            
CONECT   45   22                                                            
CONECT   46   22                                                            
CONECT   47   22                                                            
MASTER        0    0    0    0    0    0    0    0   47    0   96    0
END

RDKit          3D

47 48  0  0  0  0  0  0  0  0999 V2000
    4.8269   -0.7640   -1.4295 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8005   -1.2633   -0.4534 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4037   -1.2744   -1.0730 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3637   -1.7397   -0.1143 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0851   -0.9226    1.0838 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5027    0.4143    0.8691 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2028    1.5326    0.5374 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5648    1.5347    0.3942 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5696    2.7689    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3251    3.8958   -0.0194 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6179    5.1030   -0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7950    2.8206    0.4572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5599    1.7248    0.7919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9008    0.5421    0.9920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9134   -0.4742    1.3356 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2978   -1.3235    0.1856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2127   -2.6632    0.2107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5965   -3.4714   -0.9324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4949   -4.7158   -0.8503 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0675   -2.9079   -2.1001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1286    0.3466    1.7123 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4216   -0.2746    1.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9462    1.5685    0.9786 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3499   -1.6068   -1.9708 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3664   -0.1584   -2.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6521   -0.2041   -0.9340 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1080   -2.3426   -0.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8706   -0.7504    0.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2016   -0.2980   -1.5536 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4764   -2.0822   -1.8688 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6884   -2.7702    0.2218 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4371   -1.9430   -0.7254 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4595   -1.5056    1.8332 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0754   -0.8066    1.6287 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0682    2.3573    0.1515 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0310    5.2749    0.7121 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2754    5.9467   -0.4666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1382    4.8977   -1.0214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2838    3.7718    0.2913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5419   -1.1024    2.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6713   -0.9002   -0.7453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8467   -3.1006    1.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0412   -2.5696   -2.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1434    0.5221    2.8001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6886    0.1430    0.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4059   -1.3667    1.2328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2266    0.1368    1.9162 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  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 15 21  1  0
 21 22  1  0
 21 23  1  0
 14  6  1  0
 23 13  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  8 35  1  0
 11 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 15 40  1  1
 16 41  1  0
 17 42  1  0
 20 43  1  0
 21 44  1  1
 22 45  1  0
 22 46  1  0
 22 47  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(2E)-3-[(2S,3S)-5-Hydroxy-6-methoxy-2-methyl-4-pentyl-2,3-dihydro-1-benzofuran-3-yl]prop-2-enoate	Generator

Chemical Formula

C₁₈H₂₄O₅

Average Mass

320.3850 Da

Monoisotopic Mass

320.16237 Da

IUPAC Name

(2E)-3-[(2S,3S)-5-hydroxy-6-methoxy-2-methyl-4-pentyl-2,3-dihydro-1-benzofuran-3-yl]prop-2-enoic acid

Traditional Name

(2E)-3-[(2S,3S)-5-hydroxy-6-methoxy-2-methyl-4-pentyl-2,3-dihydro-1-benzofuran-3-yl]prop-2-enoic acid

CAS Registry Number

Not Available

SMILES

CCCCCC1=C2[C@H](\C=C\C(O)=O)[C@H](C)OC2=CC(OC)=C1O

InChI Identifier

InChI=1S/C18H24O5/c1-4-5-6-7-13-17-12(8-9-16(19)20)11(2)23-14(17)10-15(22-3)18(13)21/h8-12,21H,4-7H2,1-3H3,(H,19,20)/b9-8+/t11-,12+/m0/s1

InChI Key

UBYLMNDNGLUBCF-VDTGWRSZSA-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
Botryosphaeria	NPAtlas	17827773
Cophinforma mamane	LOTUS Database	35616633

Species Where Detected

Species Name	Source	Reference
Botryosphaeria mamane PSU-M76	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumarans. Coumarans are compounds containing the coumaran skeleton, which consists of a benzene ring fused to a 2,3-dihydrofuran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Coumarans

Sub Class

Not Available

Direct Parent

Coumarans

Alternative Parents

Substituents

Coumaran
Anisole
Phenol ether
Alkyl aryl ether
Phenol
Benzenoid
Carboxylic acid derivative
Carboxylic acid
Ether
Monocarboxylic acid or derivatives
Oxacycle
Organic oxide
Carbonyl group
Organooxygen compound
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	3.98	ALOGPS
logP	4.03	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	3.95	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	88.57 m³·mol⁻¹	ChemAxon
Polarizability	35.13 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

NPAtlas ID

NPA018678

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28284452

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23651318

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Pongcharoen W, Rukachaisirikul V, Phongpaichit S, Sakayaroj J: A new dihydrobenzofuran derivative from the endophytic fungus Botryosphaeria mamane PSU-M76. Chem Pharm Bull (Tokyo). 2007 Sep;55(9):1404-5. doi: 10.1248/cpb.55.1404. [PubMed:17827773 ]

Showing NP-Card for Botryomaman (NP0007257)

MOL for NP0007257 (Botryomaman)

3D MOL for NP0007257 (Botryomaman)

3D SDF for NP0007257 (Botryomaman)

3D-SDF for NP0007257 (Botryomaman)

PDB for NP0007257 (Botryomaman)

3D PDB for NP0007257 (Botryomaman)

SMILES for NP0007257 (Botryomaman)

INCHI for NP0007257 (Botryomaman)

Structure for NP0007257 (Botryomaman)

3D Structure for NP0007257 (Botryomaman)