NP-MRD: Showing NP-Card for 5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one (NP0197521)

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Record Information

Version

2.0

Created at

2022-09-04 15:48:07 UTC

Updated at

2022-09-04 15:48:07 UTC

NP-MRD ID

NP0197521

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one

Description

5-Chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-7,8-dihydro-6H-isochromen-6-one belongs to the class of organic compounds known as cyclohexenones. Cyclohexenones are compounds containing a cylohexenone moiety, which is a six-membered aliphatic ring that carries a ketone and has one endocyclic double bond. 5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one is found in Arcopilus cupreus. 5-Chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-7,8-dihydro-6H-isochromen-6-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241505222D          

 27 28  0  0  0  0            999 V2000
   -2.8579    2.4750    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
   -2.1434    1.2375    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
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   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
   -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  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
    1.4289    0.0000    0.0000 C   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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 O   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
    4.3848   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8545   -2.0127    0.0000 O   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   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   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
    0.7145   -1.2375    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  1  0  0  0  0
  5  3  1  4  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  8  6  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 20 25  1  0  0  0  0
 12 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 10 27  1  0  0  0  0
M  END

     RDKit          3D

 54 55  0  0  0  0  0  0  0  0999 V2000
   -6.3145    2.5011    0.3952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6938    1.0539    0.3410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9464    0.2935   -0.7448 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2379    0.8861   -2.1152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4886    0.4040   -0.5370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6807   -0.6025   -0.3360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0684   -2.0121   -0.2804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2488   -0.3208   -0.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3643   -1.2523    0.0605 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0533   -1.0145    0.2535 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9008   -2.0010    0.4552 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3429   -1.7931    0.6547 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1385   -2.8337    0.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4246   -4.4290    0.8131 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.5555   -2.5994    0.9166 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3096   -3.3849    1.4809 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0448   -1.3489    0.2878 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5153   -1.2102    0.5571 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8367   -1.4120   -1.0720 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2705   -0.1595    0.9187 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8074    1.0527    0.2609 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3586    2.3553    0.7724 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4466    3.6113   -0.0518 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8916    2.4646    1.9012 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8328   -0.4003    0.6273 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9668    0.5270    0.4233 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5820    0.2569    0.2348 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6134    3.0907   -0.4783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8793    2.9416    1.2657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2444    2.5864    0.6661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7893    1.0084    0.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4858    0.5997    1.3081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3455   -0.7325   -0.7154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2014    0.5592   -2.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4458    0.4550   -2.7943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0787    1.9737   -2.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1028    1.4300   -0.5628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1227   -2.2469   -0.2704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5962   -2.5867   -1.1321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6479   -2.4148    0.6904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8972    0.6990   -0.1721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7094   -2.2914    0.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5166   -3.0068    0.4743 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0121   -0.6969   -0.3182 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9772   -2.2056    0.6205 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7113   -0.6281    1.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0216   -2.3319   -1.3749 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5198   -0.1657    1.9889 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6018    0.9985   -0.8491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9427    1.0726    0.3056 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4625    4.0440    0.0835 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6295    4.2610    0.2585 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3666    3.3602   -1.1390 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1630    1.5951    0.3653 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 17 19  1  6
 17 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  2  0
 20 25  1  0
 25 26  2  0
 26 27  1  0
 27 10  1  0
 25 12  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  6
  4 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  7 38  1  0
  7 39  1  0
  7 40  1  0
  8 41  1  0
  9 42  1  0
 11 43  1  0
 18 44  1  0
 18 45  1  0
 18 46  1  0
 19 47  1  0
 20 48  1  1
 21 49  1  0
 21 50  1  0
 23 51  1  0
 23 52  1  0
 23 53  1  0
 26 54  1  0
M  END


  Mrv1533004241505222D          

 27 28  0  0  0  0            999 V2000
   -2.8579    2.4750    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
   -2.1434    1.2375    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
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   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
   -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  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
    1.4289    0.0000    0.0000 C   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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 O   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
    4.3848   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8545   -2.0127    0.0000 O   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   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   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
    0.7145   -1.2375    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  1  0  0  0  0
  5  3  1  4  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  8  6  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 20 25  1  0  0  0  0
 12 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 10 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0197521

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C=C(C)C=CC1=CC2=C(Cl)C(=O)C(C)(O)C(CC(C)=O)C2=CO1

> <INCHI_IDENTIFIER>
InChI=1S/C22H27ClO4/c1-6-13(2)9-14(3)7-8-16-11-17-18(12-27-16)19(10-15(4)24)22(5,26)21(25)20(17)23/h7-9,11-13,19,26H,6,10H2,1-5H3

> <INCHI_KEY>
QEPMTPAOVMUVBT-UHFFFAOYSA-N

> <FORMULA>
C22H27ClO4

> <MOLECULAR_WEIGHT>
390.9

> <EXACT_MASS>
390.159787

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
42.76343136911392

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-7,8-dihydro-6H-isochromen-6-one

> <ALOGPS_LOGP>
4.37

> <JCHEM_LOGP>
3.2793405339999997

> <ALOGPS_LOGS>
-5.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.54194513342063

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.874990609940205

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7282598731293843

> <JCHEM_POLAR_SURFACE_AREA>
63.599999999999994

> <JCHEM_REFRACTIVITY>
112.58299999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.28e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8H-isochromen-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   14 Cl   UNK     0       5.335   1.540   0.000  0.00  0.00          Cl+0
HETATM   15  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.185  -2.043   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.195  -3.757   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       1.334  -2.310   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    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   27                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   25                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   20   12   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   10                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₇ClO₄

Average Mass

390.9000 Da

Monoisotopic Mass

390.15979 Da

IUPAC Name

5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-7,8-dihydro-6H-isochromen-6-one

Traditional Name

5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8H-isochromen-6-one

CAS Registry Number

Not Available

SMILES

CCC(C)C=C(C)C=CC1=CC2=C(Cl)C(=O)C(C)(O)C(CC(C)=O)C2=CO1

InChI Identifier

InChI=1S/C22H27ClO4/c1-6-13(2)9-14(3)7-8-16-11-17-18(12-27-16)19(10-15(4)24)22(5,26)21(25)20(17)23/h7-9,11-13,19,26H,6,10H2,1-5H3

InChI Key

QEPMTPAOVMUVBT-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
Arcopilus cupreus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclohexenones. Cyclohexenones are compounds containing a cylohexenone moiety, which is a six-membered aliphatic ring that carries a ketone and has one endocyclic double bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Cyclohexenones

Alternative Parents

Substituents

Cyclohexenone
Acyloin
Pyran
Alpha-haloketone
Alpha-chloroketone
Tertiary alcohol
Oxacycle
Chloroalkene
Haloalkene
Organoheterocyclic compound
Vinyl halide
Vinyl chloride
Organic oxide
Hydrocarbon derivative
Organochloride
Organohalogen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	4.37	ALOGPS
logP	3.28	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	12.87	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	112.58 m³·mol⁻¹	ChemAxon
Polarizability	42.76 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

73045720

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one (NP0197521)

MOL for NP0197521 (5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one)

3D MOL for NP0197521 (5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one)

3D SDF for NP0197521 (5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one)

3D-SDF for NP0197521 (5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one)

PDB for NP0197521 (5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one)

3D PDB for NP0197521 (5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one)

SMILES for NP0197521 (5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one)

INCHI for NP0197521 (5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one)

Structure for NP0197521 (5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one)

3D Structure for NP0197521 (5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one)