NP-MRD: Showing NP-Card for Helihumulone (NP0055347)

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Record Information

Version

2.0

Created at

2022-04-28 01:25:44 UTC

Updated at

2022-04-28 01:25:44 UTC

NP-MRD ID

NP0055347

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Helihumulone

Description

(6S)-3,5-dihydroxy-6-methoxy-4,6-bis(3-methylbut-2-en-1-yl)-2-(3-phenylpropanoyl)cyclohexa-2,4-dien-1-one belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene. Helihumulone is found in Helichrysum cymosum, Helichrysum forskahlii , Helichrysum polycladum, Helichrysum subglomeratum and Metalasia cymbifolia. Based on a literature review very few articles have been published on (6S)-3,5-dihydroxy-6-methoxy-4,6-bis(3-methylbut-2-en-1-yl)-2-(3-phenylpropanoyl)cyclohexa-2,4-dien-1-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282203252D          

 31 32  0  0  1  0            999 V2000
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4706   -1.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6461   -1.7178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2588   -0.9893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4343   -0.9606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6959   -0.2897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2452   -1.7466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0697   -1.7178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  5  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  1  6  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
  7 13  1  1  0  0  0
 13 14  1  0  0  0  0
  4 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 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
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
  3 25  1  0  0  0  0
  2 26  1  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
 28 30  1  0  0  0  0
  1 31  1  0  0  0  0
M  END

     RDKit          3D

 63 64  0  0  0  0  0  0  0  0999 V2000
   -1.9647   -0.4101    3.0957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9631    0.3634    2.0070 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9900   -0.0817    0.7478 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1238   -0.9144    0.2541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3933   -2.1887    0.8749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3133   -3.3316    0.1564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5948   -4.6253    0.8184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9508   -3.3201   -1.2765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7054   -0.7786    0.4566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4426   -1.8695    1.0698 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2860   -0.3091   -0.4829 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5399   -1.0975   -0.6844 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6783   -2.1584   -0.0180 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5898   -0.6889   -1.6092 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7666   -1.6153   -1.6935 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4518   -1.7577   -0.4064 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3092   -2.8535    0.3750 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9454   -2.9318    1.6061 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7323   -1.8941    2.0487 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8757   -0.7812    1.2495 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2494   -0.6999    0.0348 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0818    0.8014   -1.1526 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0318    1.2809   -2.0772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1495    1.5564   -0.9400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3704    2.8235   -1.7132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3077    3.8071   -1.4272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6242    4.9736   -0.9103 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4314    6.0023   -0.6049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    5.3192   -0.6084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0366    1.1575   -0.1121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2242    1.9047    0.0779 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1423   -1.1570    3.1812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9512   -0.7498    3.4234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6761    0.3074    3.9635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8948   -1.0972   -0.8400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0452   -0.2563    0.1858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6704   -2.2851    1.8994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4621   -4.4348    1.5155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7534   -4.9077    1.4742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9188   -5.4096    0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9217   -2.9568   -1.4562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0863   -4.3330   -1.7014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7141   -2.6856   -1.8164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1665   -0.6098   -2.6621 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9486    0.3600   -1.3425 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5040   -1.2682   -2.4618 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4161   -2.6343   -2.0484 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7331   -3.7091    0.0725 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8392   -3.7948    2.2349 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2376   -1.9394    3.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4979    0.0554    1.5827 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3537    0.1704   -0.6044 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7008    1.4873   -3.0123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3624    3.2360   -1.4986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3357    2.5995   -2.8016 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7314    3.5779   -1.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5147    6.6897   -1.4595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4008    5.4572   -0.4635 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2163    6.5096    0.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4765    4.5804    0.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6151    5.2590   -1.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1291    6.3532   -0.2265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8839    1.9031   -0.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  1
  3  4  1  0
  4  5  1  0
  5  6  2  3
  6  7  1  0
  6  8  1  0
  3 30  1  0
 30 31  1  0
 30 24  2  0
 24 25  1  0
 25 26  1  0
 26 27  2  3
 27 28  1  0
 27 29  1  0
 24 22  1  0
 22 23  1  0
 22 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 11  9  1  0
  9 10  2  0
  9  3  1  0
 21 16  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  7 38  1  0
  7 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  8 43  1  0
 31 63  1  0
 25 54  1  0
 25 55  1  0
 26 56  1  0
 28 57  1  0
 28 58  1  0
 28 59  1  0
 29 60  1  0
 29 61  1  0
 29 62  1  0
 23 53  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
 17 48  1  0
 18 49  1  0
 19 50  1  0
 20 51  1  0
 21 52  1  0
M  END


  Mrv1652304282203252D          

 31 32  0  0  1  0            999 V2000
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4706   -1.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6461   -1.7178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2588   -0.9893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4343   -0.9606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6959   -0.2897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2452   -1.7466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0697   -1.7178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  5  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  1  6  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
  7 13  1  1  0  0  0
 13 14  1  0  0  0  0
  4 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 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
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
  3 25  1  0  0  0  0
  2 26  1  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
 28 30  1  0  0  0  0
  1 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0055347

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@]1(CC=C(C)C)C(O)=C(CC=C(C)C)C(O)=C(C(=O)CCC2=CC=CC=C2)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H32O5/c1-17(2)11-13-20-23(28)22(21(27)14-12-19-9-7-6-8-10-19)25(30)26(31-5,24(20)29)16-15-18(3)4/h6-11,15,28-29H,12-14,16H2,1-5H3/t26-/m0/s1

> <INCHI_KEY>
IRPIRROHIISGKY-SANMLTNESA-N

> <FORMULA>
C26H32O5

> <MOLECULAR_WEIGHT>
424.537

> <EXACT_MASS>
424.22497413

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
47.22257971884034

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6S)-3,5-dihydroxy-6-methoxy-4,6-bis(3-methylbut-2-en-1-yl)-2-(3-phenylpropanoyl)cyclohexa-2,4-dien-1-one

> <ALOGPS_LOGP>
3.49

> <JCHEM_LOGP>
5.090519546

> <ALOGPS_LOGS>
-4.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.092063084231587

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.098672815054949

> <JCHEM_PKA_STRONGEST_BASIC>
-4.248121863978186

> <JCHEM_POLAR_SURFACE_AREA>
83.83000000000001

> <JCHEM_REFRACTIVITY>
126.60110000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.09e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6S)-3,5-dihydroxy-6-methoxy-4,6-bis(3-methylbut-2-en-1-yl)-2-(3-phenylpropanoyl)cyclohexa-2,4-dien-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.612  -3.260   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.073  -3.207   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.350  -1.847   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.811  -1.793   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.166  -0.541   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.058  -3.260   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.597  -3.207   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2    7   31                                                  
CONECT    2    1    3   26                                                  
CONECT    3    2    4   25                                                  
CONECT    4    3    5   15                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    1    8   13                                             
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    7   14                                                       
CONECT   14   13                                                            
CONECT   15    4   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19                                                       
CONECT   25    3                                                            
CONECT   26    2   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31    1                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₂O₅

Average Mass

424.5370 Da

Monoisotopic Mass

424.22497 Da

IUPAC Name

(6S)-3,5-dihydroxy-6-methoxy-4,6-bis(3-methylbut-2-en-1-yl)-2-(3-phenylpropanoyl)cyclohexa-2,4-dien-1-one

Traditional Name

(6S)-3,5-dihydroxy-6-methoxy-4,6-bis(3-methylbut-2-en-1-yl)-2-(3-phenylpropanoyl)cyclohexa-2,4-dien-1-one

CAS Registry Number

Not Available

SMILES

CO[C@@]1(CC=C(C)C)C(O)=C(CC=C(C)C)C(O)=C(C(=O)CCC2=CC=CC=C2)C1=O

InChI Identifier

InChI=1S/C26H32O5/c1-17(2)11-13-20-23(28)22(21(27)14-12-19-9-7-6-8-10-19)25(30)26(31-5,24(20)29)16-15-18(3)4/h6-11,15,28-29H,12-14,16H2,1-5H3/t26-/m0/s1

InChI Key

IRPIRROHIISGKY-SANMLTNESA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Helichrysum cymosum	Plant	KNApSAcK
Helichrysum forskahlii	Plant	KNApSAcK
Helichrysum polycladum	Plant	KNApSAcK
Helichrysum subglomeratum	Plant	KNApSAcK
Metalasia cymbifolia	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Not Available

Direct Parent

Benzene and substituted derivatives

Alternative Parents

Substituents

Monocyclic benzene moiety
Vinylogous acid
Cyclic ketone
Ketone
Ether
Enol
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	3.49	ALOGPS
logP	5.09	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	4.1	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	126.6 m³·mol⁻¹	ChemAxon
Polarizability	47.22 Å³	ChemAxon
Number of Rings	2	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

163039081

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Helihumulone (NP0055347)

MOL for NP0055347 (Helihumulone)

3D MOL for NP0055347 (Helihumulone)

3D SDF for NP0055347 (Helihumulone)

3D-SDF for NP0055347 (Helihumulone)

PDB for NP0055347 (Helihumulone)

3D PDB for NP0055347 (Helihumulone)

SMILES for NP0055347 (Helihumulone)

INCHI for NP0055347 (Helihumulone)

Structure for NP0055347 (Helihumulone)

3D Structure for NP0055347 (Helihumulone)