NP-MRD: Showing NP-Card for (5z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one (NP0206737)

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Record Information

Version

2.0

Created at

2022-09-05 03:06:02 UTC

Updated at

2022-09-05 03:06:02 UTC

NP-MRD ID

NP0206737

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one

Description

Aspulvinone C belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position. Based on a literature review very few articles have been published on Aspulvinone C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052205062D          

 33 37  0  0  0  0            999 V2000
    0.6025   -7.0772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4150   -7.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1328   -7.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4150   -6.3955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1294   -5.9830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8439   -6.3955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5584   -5.9830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2728   -6.3955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9873   -5.9830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0735   -5.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4605   -4.6105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8805   -4.9910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2161   -4.2373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0366   -4.1511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5215   -4.8185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3420   -4.7323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6775   -3.9786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1926   -3.3111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3721   -3.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8872   -2.7299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4980   -3.8923    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9829   -4.5598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5560   -3.9663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6669   -5.0211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6474   -5.3135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8269   -5.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2930   -5.7054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7410   -6.3185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9125   -7.1255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2728   -7.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5584   -7.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8439   -7.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1294   -7.6330    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 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
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 19 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
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 16 26  1  0  0  0  0
 12 27  1  0  0  0  0
 27 28  1  0  0  0  0
  9 28  1  0  0  0  0
 28 29  2  0  0  0  0
  8 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
  6 32  1  0  0  0  0
 32 33  1  0  0  0  0
  2 33  1  0  0  0  0
M  END

     RDKit          3D

 61 65  0  0  0  0  0  0  0  0999 V2000
    9.2426    0.7145    0.4223 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9438    0.1180   -0.1134 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3888   -0.9706   -1.1034 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2244    1.1621   -0.9090 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0718    1.7919   -0.1520 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1757    0.7196    0.3157 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8057    0.8120    0.2388 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9843   -0.1999    0.6637 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5324   -0.1415    0.6403 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7405   -1.1092    0.1645 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1871   -2.2869   -0.3735 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6670   -0.6793    0.3336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7263   -1.3833   -0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1134   -1.0143    0.1277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6443    0.2248   -0.1335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0063    0.4647    0.0926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8246   -0.5328    0.5764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2509   -1.7573    0.8218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9327   -2.0435    0.6187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3963   -3.2682    0.8696 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1685   -0.2749    0.7973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8994    0.6406   -0.0146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6461   -0.2711   -1.0094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9559    1.3771    0.7698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0028    1.5342   -0.8063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6448    1.7752   -0.1703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6929    0.5659    0.9199 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6624    0.9068    1.1130 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0166    1.9942    1.6332 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6131   -1.3408    1.1827 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9690   -1.4353    1.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7604   -0.4088    0.8311 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1519   -0.4600    0.8959 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0402    0.6155   -0.3491 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1606    1.7695    0.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5944    0.1060    1.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8899   -1.8101   -0.5489 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2159   -0.4981   -1.6995 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5503   -1.2986   -1.7312 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7781    0.6776   -1.8217 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9193    1.9512   -1.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5362    2.4380   -0.8808 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4479    2.4480    0.6335 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3347    1.7140   -0.1704 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4776   -2.9783   -0.6461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4962   -2.3547   -0.4931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0113    1.0232   -0.5099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9138   -2.5430    1.1976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4416   -3.5622    0.7433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1284   -1.0563   -0.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4333    0.2900   -1.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9325   -0.7577   -1.6988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2477    2.2446    0.1579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8873    0.7930    0.9182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5582    1.7247    1.7516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5075    2.5241   -1.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8133    1.1221   -1.8217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8384    2.2932    0.7986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0673    2.3949   -0.8929 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9972   -2.1534    1.5251 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4364   -2.3411    1.6747 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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 33  2  1  0
 28  9  1  0
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 26 16  1  0
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 31 61  1  0
 11 45  1  0
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 23 50  1  0
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 26 58  1  0
 26 59  1  0
 18 48  1  0
 20 49  1  0
M  END


  Mrv1652309052205062D          

 33 37  0  0  0  0            999 V2000
    0.6025   -7.0772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4150   -7.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1328   -7.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4150   -6.3955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1294   -5.9830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8439   -6.3955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5584   -5.9830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2728   -6.3955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9873   -5.9830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0735   -5.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4605   -4.6105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8805   -4.9910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2161   -4.2373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0366   -4.1511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5215   -4.8185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3420   -4.7323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6775   -3.9786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1926   -3.3111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3721   -3.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8872   -2.7299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4980   -3.8923    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9829   -4.5598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5560   -3.9663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6669   -5.0211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6474   -5.3135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8269   -5.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2930   -5.7054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7410   -6.3185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9125   -7.1255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2728   -7.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5584   -7.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8439   -7.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1294   -7.6330    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  2 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0206737

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CCC2=CC(=CC=C2O1)C1=C(O)\C(OC1=O)=C\C1=CC2=C(OC(C)(C)CC2)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H28O6/c1-26(2)9-7-15-11-17(5-6-20(15)32-26)23-24(29)22(31-25(23)30)13-18-12-16-8-10-27(3,4)33-21(16)14-19(18)28/h5-6,11-14,28-29H,7-10H2,1-4H3/b22-13-

> <INCHI_KEY>
XLEVGQVQFXMEHD-XKZIYDEJSA-N

> <FORMULA>
C27H28O6

> <MOLECULAR_WEIGHT>
448.515

> <EXACT_MASS>
448.188588622

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
50.63095395709431

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5Z)-3-(2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl)methylidene]-2,5-dihydrofuran-2-one

> <JCHEM_LOGP>
5.1015111499999986

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.392757818287404

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.730542181799907

> <JCHEM_PKA_STRONGEST_BASIC>
-4.577336757079347

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
126.96549999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(5Z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       1.125 -13.211   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.641 -13.478   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.115 -14.925   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.641 -11.938   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.975 -11.168   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.309 -11.938   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.642 -11.168   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.976 -11.938   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.310 -11.168   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.471  -9.637   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.326  -8.606   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      10.977  -9.316   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.603  -7.910   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.135  -7.749   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.040  -8.995   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      15.572  -8.834   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      16.198  -7.427   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      15.293  -6.181   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.761  -6.342   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      12.856  -5.096   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      17.730  -7.266   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      18.635  -8.512   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      19.705  -7.404   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      19.912  -9.373   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.008  -9.918   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      16.477 -10.079   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      11.747 -10.650   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      10.717 -11.795   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      11.037 -13.301   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       7.976 -13.478   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.642 -14.248   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.309 -13.478   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       3.975 -14.248   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   33                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   32                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   30                                                  
CONECT    9    8   10   28                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   27                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   26                                                  
CONECT   17   16   18   21                                                  
CONECT   18   17   19                                                       
CONECT   19   18   14   20                                                  
CONECT   20   19                                                            
CONECT   21   17   22                                                       
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   26                                                       
CONECT   26   25   16                                                       
CONECT   27   12   28                                                       
CONECT   28   27    9   29                                                  
CONECT   29   28                                                            
CONECT   30    8   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31    6   33                                                  
CONECT   33   32    2                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₂₈O₆

Average Mass

448.5150 Da

Monoisotopic Mass

448.18859 Da

IUPAC Name

(5Z)-3-(2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl)methylidene]-2,5-dihydrofuran-2-one

Traditional Name

(5Z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one

CAS Registry Number

Not Available

SMILES

CC1(C)CCC2=CC(=CC=C2O1)C1=C(O)\C(OC1=O)=C\C1=CC2=C(OC(C)(C)CC2)C=C1O

InChI Identifier

InChI=1S/C27H28O6/c1-26(2)9-7-15-11-17(5-6-20(15)32-26)23-24(29)22(31-25(23)30)13-18-12-16-8-10-27(3,4)33-21(16)14-19(18)28/h5-6,11-14,28-29H,7-10H2,1-4H3/b22-13-

InChI Key

XLEVGQVQFXMEHD-XKZIYDEJSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

2,2-dimethyl-1-benzopyrans

Alternative Parents

Substituents

2,2-dimethyl-1-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
2-furanone
Benzenoid
Dihydrofuran
Enol ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Vinylogous acid
Lactone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Ether
Enol
Oxacycle
Carboxylic acid derivative
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
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	5.1	ChemAxon
pKa (Strongest Acidic)	6.73	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	126.97 m³·mol⁻¹	ChemAxon
Polarizability	50.63 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

62976256

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

90473410

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one (NP0206737)

MOL for NP0206737 ((5z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one)

3D MOL for NP0206737 ((5z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one)

3D SDF for NP0206737 ((5z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one)

3D-SDF for NP0206737 ((5z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one)

PDB for NP0206737 ((5z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one)

3D PDB for NP0206737 ((5z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one)

SMILES for NP0206737 ((5z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one)

INCHI for NP0206737 ((5z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one)

Structure for NP0206737 ((5z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one)

3D Structure for NP0206737 ((5z)-3-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-4-hydroxy-5-[(7-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methylidene]furan-2-one)