NP-MRD: Showing NP-Card for 6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one (NP0192097)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 09:13:40 UTC

Updated at

2022-09-04 09:13:40 UTC

NP-MRD ID

NP0192097

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one

Description

6-(3,4-Dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one belongs to the class of organic compounds known as linear diarylheptanoids. These are diarylheptanoids with an open heptane chain. The two aromatic rings are linked only by the heptane chain. 6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one is found in Cyperus longus. 6-(3,4-Dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201506272D          

 32 35  0  0  0  0            999 V2000
    0.2779   -0.4730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2779   -1.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9923   -1.7105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9923   -2.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7068   -2.9480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2779   -2.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4366   -2.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4366   -1.7105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1511   -2.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0894   -3.7707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6942   -4.3318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5100   -4.2089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9225   -3.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7452   -3.5561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6211   -2.7264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8327   -2.4833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7098   -1.6675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9418   -1.3661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8188   -0.5503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4639   -0.0359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3409    0.7799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2318   -0.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8768    0.1771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3548   -1.1531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4510   -5.1202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0122   -5.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8165   -5.5414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3776   -6.1461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1819   -5.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4251   -5.1742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8640   -4.5695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0597   -4.7530    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  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  2  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  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
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 17 24  1  0  0  0  0
 25 11  1  4  0  0  0
 25 26  2  0  0  0  0
 26 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
 31 32  2  0  0  0  0
 27 32  1  0  0  0  0
M  END

     RDKit          3D

 56 59  0  0  0  0  0  0  0  0999 V2000
    2.3578   -2.9478   -3.2490 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3605   -2.4455   -2.6571 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6699   -3.2045   -1.6338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0626   -2.8139   -0.5599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5293   -3.8392    0.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2552   -3.9415    1.3160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0270   -3.1472    2.2172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6066   -1.9419    1.9989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2388   -1.2456    2.9848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3360   -1.7176    4.2712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7624   -2.9339    4.5222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1235   -3.6451    3.5456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2373   -1.3553   -0.3112 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0178   -0.5703   -0.5818 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1411    0.5967    0.3262 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0314    1.3389    0.6313 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1405    2.4261    1.4588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9981    3.1486    1.7426 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3886    2.7772    1.9927 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4921    2.0397    1.6904 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7056    2.4251    2.2421 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3664    0.9419    0.8512 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2874   -0.1037   -1.9505 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7448    1.2331   -2.2798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5918    1.4091   -2.5788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0596    2.6593   -2.8642 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2294    3.7578   -2.8617 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7580    4.9901   -3.1564 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1311    3.5875   -2.5584 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9291    4.7231   -2.5674 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5957    2.3349   -2.2740 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9298   -1.0531   -3.0543 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7438   -4.2844   -1.7387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1304   -4.8776   -0.0600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3299   -5.0884    1.6070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6111   -1.5285    0.9923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7044   -0.2667    2.7899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8407   -1.1565    5.0544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8482   -3.3005    5.5516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6917   -4.5942    3.8080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1379   -0.9932   -0.7750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3300   -1.2924    0.8073 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8770   -1.2547   -0.2962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9057    1.0398    0.2158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371    2.8468    2.5668 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4493    3.6362    2.6390 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3578    3.0635    1.8304 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2652    0.3861    0.6365 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4227    0.0105   -2.0511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2685    0.5617   -2.5899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1266    2.7522   -3.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1181    5.7901   -3.1478 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9154    4.7018   -2.3607 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6651    2.1835   -2.0354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1279   -1.0233   -3.3447 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5379   -0.7948   -3.9393 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 16  2  0
 16 15  1  0
 15 22  2  0
 22 20  1  0
 20 21  1  0
 20 19  2  0
 15 14  1  0
 14 13  1  0
 13  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
  4  3  2  0
  3  2  1  0
  2  1  2  0
  2 32  1  0
 32 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  2  0
 19 17  1  0
 23 14  1  0
 31 24  1  0
 12  7  1  0
 18 45  1  0
 16 44  1  0
 22 48  1  0
 21 47  1  0
 19 46  1  0
 14 43  1  1
 13 41  1  0
 13 42  1  0
  5 34  1  0
  6 35  1  0
  8 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
  3 33  1  0
 32 55  1  0
 32 56  1  0
 23 49  1  1
 25 50  1  0
 26 51  1  0
 28 52  1  0
 30 53  1  0
 31 54  1  0
M  END


  Mrv1533004201506272D          

 32 35  0  0  0  0            999 V2000
    0.2779   -0.4730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2779   -1.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9923   -1.7105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9923   -2.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7068   -2.9480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2779   -2.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4366   -2.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4366   -1.7105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1511   -2.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0894   -3.7707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6942   -4.3318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5100   -4.2089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9225   -3.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7452   -3.5561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6211   -2.7264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8327   -2.4833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7098   -1.6675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9418   -1.3661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8188   -0.5503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4639   -0.0359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3409    0.7799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2318   -0.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8768    0.1771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3548   -1.1531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4510   -5.1202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0122   -5.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8165   -5.5414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3776   -6.1461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1819   -5.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4251   -5.1742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8640   -4.5695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0597   -4.7530    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  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  2  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  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
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 17 24  1  0  0  0  0
 25 11  1  4  0  0  0
 25 26  2  0  0  0  0
 26 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
 31 32  2  0  0  0  0
 27 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0192097

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC(=CC(O)=C1)C1CC(C=CC2=CC=CC=C2)=CC(=O)CC1C1=CC=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C27H24O5/c28-21-10-18(7-6-17-4-2-1-3-5-17)11-24(20-12-22(29)15-23(30)13-20)25(16-21)19-8-9-26(31)27(32)14-19/h1-10,12-15,24-25,29-32H,11,16H2

> <INCHI_KEY>
YWRWOKCDBFSFCZ-UHFFFAOYSA-N

> <FORMULA>
C27H24O5

> <MOLECULAR_WEIGHT>
428.484

> <EXACT_MASS>
428.162373873

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
46.23474903061956

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one

> <ALOGPS_LOGP>
4.46

> <JCHEM_LOGP>
5.545052188333333

> <ALOGPS_LOGS>
-4.93

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.58018801752264

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.991981656319963

> <JCHEM_PKA_STRONGEST_BASIC>
-4.720080576512401

> <JCHEM_POLAR_SURFACE_AREA>
97.99000000000001

> <JCHEM_REFRACTIVITY>
125.84810000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.06e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  O   UNK     0       0.519  -0.883   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       0.519  -2.423   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.852  -3.193   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.852  -4.733   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       3.186  -5.503   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.519  -5.503   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.815  -4.733   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.815  -3.193   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.149  -5.503   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.034  -7.039   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.163  -8.086   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.685  -7.857   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.455  -6.523   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -6.991  -6.638   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -4.893  -5.089   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.421  -4.635   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.192  -3.113   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.758  -2.550   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.529  -1.027   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.733  -0.067   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.503   1.456   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -4.166  -0.630   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -5.370   0.331   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -4.396  -2.152   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.709  -9.558   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.756 -10.687   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.257 -10.344   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -6.305 -11.473   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -7.806 -11.130   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -8.260  -9.659   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -7.213  -8.530   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -5.711  -8.872   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7    2                                                       
CONECT    9    7   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   25                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15    9   17                                                  
CONECT   17   16   18   24                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   17                                                       
CONECT   25   11   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   27                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₂₄O₅

Average Mass

428.4840 Da

Monoisotopic Mass

428.16237 Da

IUPAC Name

6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one

Traditional Name

6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one

CAS Registry Number

Not Available

SMILES

OC1=CC(=CC(O)=C1)C1CC(C=CC2=CC=CC=C2)=CC(=O)CC1C1=CC=C(O)C(O)=C1

InChI Identifier

InChI=1S/C27H24O5/c28-21-10-18(7-6-17-4-2-1-3-5-17)11-24(20-12-22(29)15-23(30)13-20)25(16-21)19-8-9-26(31)27(32)14-19/h1-10,12-15,24-25,29-32H,11,16H2

InChI Key

YWRWOKCDBFSFCZ-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
Cyperus longus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as linear diarylheptanoids. These are diarylheptanoids with an open heptane chain. The two aromatic rings are linked only by the heptane chain.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Diarylheptanoids

Sub Class

Linear diarylheptanoids

Direct Parent

Linear diarylheptanoids

Alternative Parents

Substituents

Linear 1,7-diphenylheptane skeleton
Stilbene
Catechol
Styrene
Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Ketone
Cyclic ketone
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organooxygen compound
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	4.46	ALOGPS
logP	5.55	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	8.99	ChemAxon
pKa (Strongest Basic)	-4.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	97.99 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	125.85 m³·mol⁻¹	ChemAxon
Polarizability	46.23 Å³	ChemAxon
Number of Rings	4	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one (NP0192097)

MOL for NP0192097 (6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one)

3D MOL for NP0192097 (6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one)

3D SDF for NP0192097 (6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one)

3D-SDF for NP0192097 (6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one)

PDB for NP0192097 (6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one)

3D PDB for NP0192097 (6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one)

SMILES for NP0192097 (6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one)

INCHI for NP0192097 (6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one)

Structure for NP0192097 (6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one)

3D Structure for NP0192097 (6-(3,4-dihydroxyphenyl)-5-(3,5-dihydroxyphenyl)-3-(2-phenylethenyl)cyclohept-2-en-1-one)