NP-MRD: Showing NP-Card for 2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione (NP0143992)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-01 22:51:52 UTC

Updated at

2022-09-01 22:51:52 UTC

NP-MRD ID

NP0143992

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione

Description

2'-(3,4-Dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2',4'-dihydro-3H-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione belongs to the class of organic compounds known as catechols. Catechols are compounds containing a 1,2-benzenediol moiety. 2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione is found in Hymenochaete xerantica, Phellinus igniarius, Sanghuangporus baumii and Tropicoporus linteus. 2'-(3,4-Dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2',4'-dihydro-3H-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161518312D          

 34 38  0  0  0  0            999 V2000
    4.4145    0.4626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5899    0.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1271   -0.2475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3346   -0.0184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6834   -0.5250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3075    0.8062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0834    1.0867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2804    1.6307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4879    1.8598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0251    1.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5317    0.5256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2210   -0.2387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7276   -0.8898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4038   -0.3518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1027    0.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2079    1.0637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9199    0.1863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4265    0.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1159    1.6017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6224    2.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3118    3.0172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4946    3.1303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1839    3.8946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0120    2.4791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8292    2.5922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2986    1.7148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9316    2.1373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6959    1.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3471    2.3332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2340    3.1504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8851    3.6569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4697    3.4610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3566    4.2782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8185    2.9545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 10 16  1  0  0  0  0
 17 15  1  4  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 19 26  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 27 34  1  0  0  0  0
M  END

     RDKit          3D

 52 56  0  0  0  0  0  0  0  0999 V2000
   -4.4395   -3.0062    2.4637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8198   -1.6351    2.3867 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4292   -0.9942    3.4761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8804    0.2955    3.0231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6794    1.2681    3.7649 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6603    0.1081    1.5635 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5793   -0.8850    1.2447 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2495   -0.3010    1.2964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5732    0.8158    0.8645 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7825    0.7127    0.5427 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3738   -0.5196    0.6782 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7749   -0.7353    0.3710 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5531    0.2264   -0.0508 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9627    0.0019   -0.3581 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5668   -1.2229   -0.2275 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9218   -1.3762   -0.5375 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6837   -0.2923   -0.9836 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0029   -0.5260   -1.2657 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1015    0.9202   -1.1169 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8024    2.0342   -1.5545 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7466    1.0343   -0.7979 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6675   -1.5722    1.1028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5862   -1.4987    1.4054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2597   -2.4972    1.8090 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4670    1.9037    0.8393 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7987    1.3688    0.7893 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2708    1.1940   -0.5927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5223    0.6427   -1.6001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0290    0.5042   -2.8936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3120    0.9316   -3.1655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7976    0.7829   -4.4670 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0900    1.4902   -2.1743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3734    1.9044   -2.4977 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5529    1.6071   -0.9185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6582   -3.3890    1.4475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2838   -3.0249    3.1517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6628   -3.7141    2.8769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4842   -1.3169    4.5097 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2971    1.5952    0.2065 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1874   -1.7232    0.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1684    1.2433   -0.1889 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0503   -2.0979    0.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3720   -2.3523   -0.4254 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5957    0.2056   -1.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7561    1.9753   -1.7840 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3146    2.0176   -0.9162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4480    2.0723    1.3328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5271    0.3081   -1.4011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4202    0.0654   -3.6756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7382    1.0909   -4.6867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9280    2.3146   -1.7445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1612    2.0453   -0.1380 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  6
  6 26  1  0
 26 25  1  0
 25  9  1  0
  9  8  2  0
  8 23  1  0
 23 24  2  0
 23 22  1  0
 22 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  2  0
 11 10  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 32 34  2  0
  7  2  1  0
 10  9  1  0
 34 27  1  0
  8  6  1  0
 21 14  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  3 38  1  0
 26 47  1  1
 12 40  1  0
 13 41  1  0
 15 42  1  0
 16 43  1  0
 18 44  1  0
 20 45  1  0
 21 46  1  0
 10 39  1  0
 28 48  1  0
 29 49  1  0
 31 50  1  0
 33 51  1  0
 34 52  1  0
M  END


  Mrv1533004161518312D          

 34 38  0  0  0  0            999 V2000
    4.4145    0.4626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5899    0.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1271   -0.2475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3346   -0.0184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6834   -0.5250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3075    0.8062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0834    1.0867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2804    1.6307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4879    1.8598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0251    1.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5317    0.5256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2210   -0.2387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7276   -0.8898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4038   -0.3518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1027    0.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2079    1.0637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9199    0.1863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4265    0.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1159    1.6017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6224    2.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3118    3.0172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4946    3.1303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1839    3.8946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0120    2.4791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8292    2.5922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2986    1.7148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9316    2.1373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6959    1.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3471    2.3332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2340    3.1504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8851    3.6569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4697    3.4610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3566    4.2782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8185    2.9545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 10 16  1  0  0  0  0
 17 15  1  4  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 19 26  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 27 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0143992

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(=O)C2(O1)C(OC1=C2C(=O)OC(C=CC2=CC=C(O)C(O)=C2)=C1)C1=CC=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H18O9/c1-12-8-21(30)25(34-12)22-20(33-23(25)14-4-7-17(27)19(29)10-14)11-15(32-24(22)31)5-2-13-3-6-16(26)18(28)9-13/h2-11,23,26-29H,1H3

> <INCHI_KEY>
ZGKUEJPXTILOCD-UHFFFAOYSA-N

> <FORMULA>
C25H18O9

> <MOLECULAR_WEIGHT>
462.41

> <EXACT_MASS>
462.09508216

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
46.61090365699722

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2',4'-dihydro-3H-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione

> <ALOGPS_LOGP>
4.12

> <JCHEM_LOGP>
3.117870585666666

> <ALOGPS_LOGS>
-4.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.525639667599304

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.923018676313786

> <JCHEM_PKA_STRONGEST_BASIC>
-4.607728483075193

> <JCHEM_POLAR_SURFACE_AREA>
142.75

> <JCHEM_REFRACTIVITY>
123.39

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.78e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'H-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       8.240   0.864   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.701   0.813   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.837  -0.462   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.358  -0.034   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       3.142  -0.980   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.307   1.505   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.756   2.028   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.257   3.044   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.777   3.472   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.914   2.197   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.859   0.981   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.279  -0.446   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.225  -1.661   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       0.754  -0.657   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -0.192   0.559   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.388   1.986   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.717   0.348   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.663   1.563   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.083   2.990   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.029   4.205   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.449   5.632   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.923   5.843   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.343   7.270   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.022   4.628   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.548   4.839   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -0.557   3.201   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.472   3.990   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.899   3.410   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.115   4.355   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.903   5.881   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       9.119   6.826   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       6.477   6.461   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       6.266   7.986   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.261   5.515   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8   11                                             
CONECT    7    6    2                                                       
CONECT    8    6    9   27                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10    6   12                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15   10                                                       
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   26                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   19                                                       
CONECT   27    8   28   34                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   27                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₁₈O₉

Average Mass

462.4100 Da

Monoisotopic Mass

462.09508 Da

IUPAC Name

2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2',4'-dihydro-3H-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione

Traditional Name

2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'H-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione

CAS Registry Number

Not Available

SMILES

CC1=CC(=O)C2(O1)C(OC1=C2C(=O)OC(C=CC2=CC=C(O)C(O)=C2)=C1)C1=CC=C(O)C(O)=C1

InChI Identifier

InChI=1S/C25H18O9/c1-12-8-21(30)25(34-12)22-20(33-23(25)14-4-7-17(27)19(29)10-14)11-15(32-24(22)31)5-2-13-3-6-16(26)18(28)9-13/h2-11,23,26-29H,1H3

InChI Key

ZGKUEJPXTILOCD-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
Hymenochaete xerantica	LOTUS Database	35616633
Phellinus igniarius	LOTUS Database	35616633
Sanghuangporus baumii	LOTUS Database	35616633
Tropicoporus linteus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as catechols. Catechols are compounds containing a 1,2-benzenediol moiety.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Catechol
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Monocyclic benzene moiety
3-furanone
Pyran
Dihydrofuran
Heteroaromatic compound
Vinylogous ester
Lactone
Ketone
Ether
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
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	4.12	ALOGPS
logP	3.12	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	8.92	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	142.75 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	123.39 m³·mol⁻¹	ChemAxon
Polarizability	46.61 Å³	ChemAxon
Number of Rings	5	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

85141893

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione (NP0143992)

MOL for NP0143992 (2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione)

3D MOL for NP0143992 (2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione)

3D SDF for NP0143992 (2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione)

3D-SDF for NP0143992 (2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione)

PDB for NP0143992 (2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione)

3D PDB for NP0143992 (2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione)

SMILES for NP0143992 (2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione)

INCHI for NP0143992 (2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione)

Structure for NP0143992 (2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione)

3D Structure for NP0143992 (2'-(3,4-dihydroxyphenyl)-6'-[2-(3,4-dihydroxyphenyl)ethenyl]-5-methyl-2'h-spiro[furan-2,3'-furo[3,2-c]pyran]-3,4'-dione)