NP-MRD: Showing NP-Card for (3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one (NP0152102)

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Record Information

Version

2.0

Created at

2022-09-02 08:31:16 UTC

Updated at

2022-09-02 08:31:17 UTC

NP-MRD ID

NP0152102

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one

Description

(3E,4R,5R)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. (3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one is found in Picea jezoensis. Based on a literature review very few articles have been published on (3E,4R,5R)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022210312D          

 32 35  0  0  1  0            999 V2000
    3.9845    1.0837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4325    0.4706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6255    0.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0735    0.0291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2665    0.2006    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
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -1.7224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7376   -1.4675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.5070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.5070    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6119   -3.1745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2763   -3.9282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7613   -4.5956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5817   -4.5094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0667   -5.1768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9173   -3.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7378   -3.6695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4324   -3.0882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3819   -1.7224    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1665   -1.4675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3381   -0.6605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1227   -0.4056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7358    0.1465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7358   -0.9576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5642   -1.7646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1773   -2.3166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7796   -2.0195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0116    0.9852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5636    1.5983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3706    1.4268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9226    2.0399    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
  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  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  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
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 12 19  1  0  0  0  0
 11 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 21 28  1  0  0  0  0
  5 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
  3 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END

     RDKit          3D

 52 55  0  0  0  0  0  0  0  0999 V2000
   -1.8386    4.2960    0.6126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8861    3.4287    0.9068 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1306    2.2196    0.3094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3568    1.6690   -0.6932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6692    0.4551   -1.2380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8813   -0.1412   -2.2677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6344   -0.4557   -2.2907 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1336   -1.0604   -3.4213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3402   -1.1988   -4.5718 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3869   -1.4011   -2.9323 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1519   -1.6085   -1.5038 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4353   -1.7843   -0.9032 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7564   -1.5049    0.3936 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0575   -1.6894    0.8949 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0429   -2.1674    0.0566 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3359   -2.3578    0.5281 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7506   -2.4606   -1.2605 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7788   -2.9424   -2.0726 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4724   -2.2729   -1.7314 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4024   -0.3101   -1.2505 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0047   -0.0496    0.0982 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4913    1.1137    0.7270 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1837    1.4623    2.0038 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7310    2.6440    2.5386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6431    0.6629    2.7318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1545   -0.4884    2.1587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9999   -1.2742    2.9518 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8413   -0.8386    0.8656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7745   -0.2066   -0.7639 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5751    0.3111    0.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2493    1.5311    0.7772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0476    2.0570    1.7837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1828    5.3477    0.4419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1674    3.9899   -0.1967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1839    4.3449    1.5366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4912    2.2481   -1.0296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4339   -0.3777   -3.2162 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5016   -2.4689   -1.3515 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9849   -1.1547    1.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2396   -1.4447    1.9389 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0869   -2.6995   -0.0294 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5444   -3.1550   -3.0465 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2567   -2.5061   -2.7631 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1048    0.4886   -1.6292 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1497    1.7599    0.1629 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6186    2.6351    3.0239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8878    0.9416    3.7510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6487   -2.0240    3.5462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2333   -1.7332    0.4078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0419   -1.1667   -1.1785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4420   -0.2210    0.6024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8577    1.5580    2.1238 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
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7 20  1  0
 20 11  1  0
 11 10  1  0
 10  8  1  0
  8  9  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 25 26  1  0
 26 27  1  0
 26 28  2  0
  5 29  2  0
 29 30  1  0
 30 31  2  0
 31 32  1  0
 31  3  1  0
  8  7  1  0
 19 12  1  0
 28 21  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  4 36  1  0
  6 37  1  0
 20 44  1  6
 11 38  1  6
 13 39  1  0
 14 40  1  0
 16 41  1  0
 18 42  1  0
 19 43  1  0
 22 45  1  0
 24 46  1  0
 25 47  1  0
 27 48  1  0
 28 49  1  0
 29 50  1  0
 30 51  1  0
 32 52  1  0
M  END


  Mrv1652309022210312D          

 32 35  0  0  1  0            999 V2000
    3.9845    1.0837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4325    0.4706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6255    0.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0735    0.0291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2665    0.2006    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
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -1.7224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7376   -1.4675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.5070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.5070    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6119   -3.1745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2763   -3.9282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7613   -4.5956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5817   -4.5094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0667   -5.1768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9173   -3.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7378   -3.6695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4324   -3.0882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3819   -1.7224    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1665   -1.4675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3381   -0.6605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1227   -0.4056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7358    0.1465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7358   -0.9576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5642   -1.7646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1773   -2.3166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7796   -2.0195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0116    0.9852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5636    1.5983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3706    1.4268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9226    2.0399    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
  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  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  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
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 12 19  1  0  0  0  0
 11 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 21 28  1  0  0  0  0
  5 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
  3 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0152102

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(\C=C2/[C@H]([C@@H](OC2=O)C2=CC=C(O)C(O)=C2)C2=CC(O)=CC(O)=C2)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C24H20O8/c1-31-21-7-12(2-4-19(21)28)6-17-22(14-8-15(25)11-16(26)9-14)23(32-24(17)30)13-3-5-18(27)20(29)10-13/h2-11,22-23,25-29H,1H3/b17-6+/t22-,23+/m1/s1

> <INCHI_KEY>
IBZKQAXTWQRPIW-RNLXWWHBSA-N

> <FORMULA>
C24H20O8

> <MOLECULAR_WEIGHT>
436.416

> <EXACT_MASS>
436.115817604

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
42.91091551574269

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3E,4R,5R)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one

> <ALOGPS_LOGP>
3.57

> <JCHEM_LOGP>
4.0448503680000005

> <ALOGPS_LOGS>
-4.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.360379897702162

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.837421318451815

> <JCHEM_PKA_STRONGEST_BASIC>
-4.88993415342382

> <JCHEM_POLAR_SURFACE_AREA>
136.68

> <JCHEM_REFRACTIVITY>
115.67160000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.26e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3E,4R,5R)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       7.438   2.023   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.407   0.879   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.901   1.199   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.870   0.054   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.364   0.374   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.088  -3.215   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.377  -2.739   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       0.564  -4.680   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.104  -4.680   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.009  -5.926   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.382  -7.333   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.288  -8.578   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.819  -8.417   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.724  -9.663   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.446  -7.011   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.977  -6.850   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.540  -5.765   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.580  -3.215   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.044  -2.739   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.364  -1.233   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.829  -0.757   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.973   0.273   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.973  -1.788   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.653  -3.294   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.798  -4.324   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.189  -3.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.888   1.839   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.919   2.984   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.425   2.663   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       5.456   3.808   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   31                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   29                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   20                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   20                                                  
CONECT   12   11   13   19                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   12                                                       
CONECT   20   11    7   21                                                  
CONECT   21   20   22   28                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   21                                                       
CONECT   29    5   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30    3   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₀O₈

Average Mass

436.4160 Da

Monoisotopic Mass

436.11582 Da

IUPAC Name

(3E,4R,5R)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one

Traditional Name

(3E,4R,5R)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one

CAS Registry Number

Not Available

SMILES

COC1=CC(\C=C2/[C@H]([C@@H](OC2=O)C2=CC=C(O)C(O)=C2)C2=CC(O)=CC(O)=C2)=CC=C1O

InChI Identifier

InChI=1S/C24H20O8/c1-31-21-7-12(2-4-19(21)28)6-17-22(14-8-15(25)11-16(26)9-14)23(32-24(17)30)13-3-5-18(27)20(29)10-13/h2-11,22-23,25-29H,1H3/b17-6+/t22-,23+/m1/s1

InChI Key

IBZKQAXTWQRPIW-RNLXWWHBSA-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
Picea jezoensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Not Available

Direct Parent

Stilbenes

Alternative Parents

Substituents

Stilbene
Methoxyphenol
Phenoxy compound
Anisole
Catechol
Phenol ether
Resorcinol
Methoxybenzene
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Gamma butyrolactone
Tetrahydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Hydrocarbon derivative
Carbonyl group
Organic oxygen compound
Organooxygen compound
Organic oxide
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.57	ALOGPS
logP	4.04	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	8.84	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	136.68 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	115.67 m³·mol⁻¹	ChemAxon
Polarizability	42.91 Å³	ChemAxon
Number of Rings	4	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

163185584

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one (NP0152102)

MOL for NP0152102 ((3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one)

3D MOL for NP0152102 ((3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one)

3D SDF for NP0152102 ((3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one)

3D-SDF for NP0152102 ((3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one)

PDB for NP0152102 ((3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one)

3D PDB for NP0152102 ((3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one)

SMILES for NP0152102 ((3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one)

INCHI for NP0152102 ((3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one)

Structure for NP0152102 ((3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one)

3D Structure for NP0152102 ((3e,4r,5r)-5-(3,4-dihydroxyphenyl)-4-(3,5-dihydroxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one)