NP-MRD: Showing NP-Card for methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate (NP0283575)

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Record Information

Version

2.0

Created at

2022-09-09 10:53:40 UTC

Updated at

2022-09-09 10:53:40 UTC

NP-MRD ID

NP0283575

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate

Description

Methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-2,3-dihydro-1H-isoindol-5-yl]-4-methylhex-3-enoate belongs to the class of organic compounds known as isoindolones. These are aromatic polycyclic compounds that an isoindole bearing a ketone. methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate is found in Hericium erinaceus. Based on a literature review very few articles have been published on methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-2,3-dihydro-1H-isoindol-5-yl]-4-methylhex-3-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092212532D          

 25 26  0  0  0  0            999 V2000
    9.0681    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3536    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391    1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    2.2374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    0.0709    0.0000 O   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
  3  5  1  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 20 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END

     RDKit          3D

 48 49  0  0  0  0  0  0  0  0999 V2000
    7.5207    0.6498   -0.1030 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5218   -0.2804   -0.4337 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8746   -0.2959   -1.6574 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2465    0.6139   -2.4862 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8452   -1.2033   -2.1031 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4470   -0.9338   -1.7954 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8564   -0.0401   -1.0628 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5760    0.9949   -0.3099 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3426    0.0134   -0.9460 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0471   -0.2064    0.5208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3732   -0.1396    0.8933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7046    0.3521    2.1415 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2460    0.7324    3.0446 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0343    0.4903    2.5672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0440    0.1213    1.7052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7637   -0.3746    0.4532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4152   -0.4940    0.0763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1667   -0.9929   -1.1780 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9958   -0.7146   -0.2894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0741   -0.3156    0.6201 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4962   -0.3849    0.3603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0614    0.8653   -0.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8614    1.9232    0.6286 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5047    0.1589    1.8195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0740    0.5731    2.8782 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3309    1.6688   -0.4958 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5255    0.3630   -0.5005 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6021    0.6419    1.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9856   -1.4447   -3.2010 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0913   -2.2124   -1.6161 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7570   -1.6709   -2.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8531    0.5336    0.6873 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8761    1.8539   -0.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4045    1.4895   -0.8092 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9981   -0.8279   -1.5906 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9444    0.9905   -1.2375 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4363   -1.2027    0.8240 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6753    0.5476    1.0678 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2223    0.6970    2.9356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2398    0.8798    3.5634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8962   -1.2675   -1.8228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0618   -0.0994   -1.2105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0432   -1.8032   -0.4949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7426   -1.2934   -0.2537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0258   -0.5465    1.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1395    0.7064   -0.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6292    1.0761   -1.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8787    2.1073    0.7459 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  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
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 24  1  0
 24 25  2  0
 24 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 20 19  1  0
 19 16  1  0
 16 17  2  0
 17 18  1  0
 17 11  1  0
 16 15  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  8 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 13 39  1  0
 14 40  1  0
 21 44  1  0
 21 45  1  0
 22 46  1  0
 22 47  1  0
 23 48  1  0
 19 42  1  0
 19 43  1  0
 18 41  1  0
M  END


  Mrv1652309092212532D          

 25 26  0  0  0  0            999 V2000
    9.0681    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3536    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391    1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    2.2374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    0.0709    0.0000 O   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
  3  5  1  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 20 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0283575

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)CC=C(C)CCC1=C(O)C=C2C(=O)N(CCO)CC2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C18H23NO6/c1-11(4-6-16(22)25-2)3-5-12-15(21)9-13-14(17(12)23)10-19(7-8-20)18(13)24/h4,9,20-21,23H,3,5-8,10H2,1-2H3

> <INCHI_KEY>
KGNZYULDBJKXGC-UHFFFAOYSA-N

> <FORMULA>
C18H23NO6

> <MOLECULAR_WEIGHT>
349.383

> <EXACT_MASS>
349.152537465

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
37.371383661068755

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-2,3-dihydro-1H-isoindol-5-yl]-4-methylhex-3-enoate

> <JCHEM_LOGP>
1.1685895079999993

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.106655239585486

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.720197205792985

> <JCHEM_PKA_STRONGEST_BASIC>
-1.5981948648721067

> <JCHEM_POLAR_SURFACE_AREA>
107.30000000000001

> <JCHEM_REFRACTIVITY>
93.61779999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3H-isoindol-5-yl]-4-methylhex-3-enoate

> <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      16.927   3.613   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      15.593   4.383   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      14.260   3.613   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      14.260   2.073   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      12.926   4.383   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.592   3.613   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.259   4.383   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.259   5.923   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.925   3.613   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       7.591   1.303   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.924   5.923   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.126   4.089   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       1.220   2.843   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0      -0.320   2.843   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.090   4.177   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.630   4.177   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.126   1.597   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.650   0.132   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   17                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   24                                                  
CONECT   16   15   17   19                                                  
CONECT   17   16   11   18                                                  
CONECT   18   17                                                            
CONECT   19   16   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   20   15   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

View in JSmol

Synonyms

Value	Source
Methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-2,3-dihydro-1H-isoindol-5-yl]-4-methylhex-3-enoic acid	Generator

Chemical Formula

C₁₈H₂₃NO₆

Average Mass

349.3830 Da

Monoisotopic Mass

349.15254 Da

IUPAC Name

methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-2,3-dihydro-1H-isoindol-5-yl]-4-methylhex-3-enoate

Traditional Name

methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3H-isoindol-5-yl]-4-methylhex-3-enoate

CAS Registry Number

Not Available

SMILES

COC(=O)CC=C(C)CCC1=C(O)C=C2C(=O)N(CCO)CC2=C1O

InChI Identifier

InChI=1S/C18H23NO6/c1-11(4-6-16(22)25-2)3-5-12-15(21)9-13-14(17(12)23)10-19(7-8-20)18(13)24/h4,9,20-21,23H,3,5-8,10H2,1-2H3

InChI Key

KGNZYULDBJKXGC-UHFFFAOYSA-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

Species Name	Source	Reference
Hericium erinaceus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoindolones. These are aromatic polycyclic compounds that an isoindole bearing a ketone.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoindoles and derivatives

Sub Class

Isoindolines

Direct Parent

Isoindolones

Alternative Parents

Substituents

Isoindolone
Isoindole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Fatty acid methyl ester
Fatty acid ester
Fatty acyl
Benzenoid
Methyl ester
Tertiary carboxylic acid amide
Lactam
Carboxylic acid ester
Carboxamide group
Azacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Alkanolamine
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
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	1.17	ChemAxon
pKa (Strongest Acidic)	8.72	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	107.3 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	93.62 m³·mol⁻¹	ChemAxon
Polarizability	37.37 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

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

162880419

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate (NP0283575)

MOL for NP0283575 (methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate)

3D MOL for NP0283575 (methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate)

3D SDF for NP0283575 (methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate)

3D-SDF for NP0283575 (methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate)

PDB for NP0283575 (methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate)

3D PDB for NP0283575 (methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate)

SMILES for NP0283575 (methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate)

INCHI for NP0283575 (methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate)

Structure for NP0283575 (methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate)

3D Structure for NP0283575 (methyl 6-[4,6-dihydroxy-2-(2-hydroxyethyl)-1-oxo-3h-isoindol-5-yl]-4-methylhex-3-enoate)