NP-MRD: Showing NP-Card for (5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one (NP0157573)

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Record Information

Version

2.0

Created at

2022-09-02 14:59:15 UTC

Updated at

2022-09-02 14:59:15 UTC

NP-MRD ID

NP0157573

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one

Description

SCHEMBL19665245 belongs to the class of organic compounds known as 6-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 6-position. (5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one is found in Helminthostachys zeylanica. Based on a literature review very few articles have been published on SCHEMBL19665245.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022216592D          

 32 36  0  0  1  0            999 V2000
    2.0647   -2.2380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748   -2.0821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449   -1.3025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -1.1466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1154    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3854    1.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1955    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7356    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5458    1.1921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4656    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0057   -0.3671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6555    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7386   -1.1378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2635   -0.7906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7946    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    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  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  8 15  1  0  0  0  0
  7 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
  3 21  2  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 20 32  1  0  0  0  0
M  END

     RDKit          3D

 60 64  0  0  0  0  0  0  0  0999 V2000
   -0.4638   -4.4819    1.2897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0063   -3.3028    0.7831 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2861   -2.1764    0.4526 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0975   -2.1027    0.5967 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7652   -0.9245    0.2404 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0473   -0.9049    0.3921 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7328    0.1656    0.0782 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1924    0.1092    0.2802 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7668   -1.0475    0.7822 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1243   -1.1317    0.9820 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9437   -0.0627    0.6855 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3077   -0.1711    0.8951 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4017    1.0959    0.1868 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2298    2.1493   -0.1028 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0293    1.1423   -0.0008 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1318    1.2963   -0.4177 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7588    1.2826   -0.5828 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1253    2.2739   -1.0308 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0749    0.1582   -0.2486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2881    0.0968   -0.3947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9255   -1.0665   -0.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3950   -1.1177   -0.2033 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9377    0.2116    0.3060 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4282    0.1748    0.3503 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8790   -0.2689    1.7319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0444   -0.7793   -0.6408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0399    1.5354    0.1055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5965    2.1554   -1.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2356    1.7296   -1.6307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3750    1.3796   -0.4378 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3217    2.6276    0.4478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0507    1.1498   -0.8817 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5694   -4.6982    0.9019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0553   -5.3865    1.0423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4660   -4.4094    2.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6221   -2.9541    0.9791 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1464   -1.8892    1.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5255   -2.0506    1.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7105   -1.0190    1.2609 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8265    3.0015   -0.4703 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6247    2.0669   -0.3954 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6616    2.1826   -0.6823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5902   -1.2530   -1.2886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8605   -1.9047    0.4231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5542    0.2910    1.3660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9868   -1.3688    1.7899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0679   -0.0153    2.4760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7848    0.2699    2.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5073   -1.7151   -0.7651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0786   -1.0558   -0.2794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2168   -0.2743   -1.6226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8776    2.1503    0.9939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1543    1.3598    0.0539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3189    1.8668   -1.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6841    3.2614   -1.0883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2785    0.9238   -2.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7631    2.6039   -2.1437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0350    3.4036    0.1038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3259    3.0931    0.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5366    2.3240    1.4920 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
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 27 28  1  0
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 29 30  1  0
 30 31  1  1
 30 32  1  0
 32 20  1  0
 20 19  2  0
 19 17  1  0
 17 18  2  0
 17 16  1  0
 16  7  2  0
  7  6  1  0
  6  5  1  0
  5  4  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  2  0
  4  3  1  0
 15  8  1  0
 20 21  1  0
  5 19  1  0
 30 23  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
 22 43  1  0
 22 44  1  0
 23 45  1  1
 25 46  1  0
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 29 56  1  0
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 31 58  1  0
 31 59  1  0
 31 60  1  0
 16 42  1  0
  4 36  1  0
  9 37  1  0
 10 38  1  0
 12 39  1  0
 14 40  1  0
 15 41  1  0
M  END


  Mrv1652309022216592D          

 32 36  0  0  1  0            999 V2000
    2.0647   -2.2380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748   -2.0821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449   -1.3025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -1.1466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1154    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3854    1.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1955    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7356    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5458    1.1921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4656    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0057   -0.3671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6555    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7386   -1.1378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2635   -0.7906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7946    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    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  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  8 15  1  0  0  0  0
  7 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
  3 21  2  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 20 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0157573

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2C[C@@H]3C(C)(C)CCC[C@]3(C)OC2=C2C(=O)C=C(OC2=C1)C1=CC=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C26H28O6/c1-25(2)8-5-9-26(3)22(25)11-15-20(30-4)13-21-23(24(15)32-26)18(29)12-19(31-21)14-6-7-16(27)17(28)10-14/h6-7,10,12-13,22,27-28H,5,8-9,11H2,1-4H3/t22-,26+/m1/s1

> <INCHI_KEY>
DVUORASKJFBCTF-GJZUVCINSA-N

> <FORMULA>
C26H28O6

> <MOLECULAR_WEIGHT>
436.504

> <EXACT_MASS>
436.188588622

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
48.249625983709144

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5aS,9aR)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-4,5a,6,7,8,9,9a,10-octahydro-1,5-dioxatetraphen-4-one

> <ALOGPS_LOGP>
5.42

> <JCHEM_LOGP>
4.681924988333333

> <ALOGPS_LOGS>
-5.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.158988338909243

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.703191031971462

> <JCHEM_PKA_STRONGEST_BASIC>
-4.531092193386513

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
121.64509999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.62e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5aS,9aR)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6H-1,5-dioxatetraphen-4-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       3.854  -4.178   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.366  -3.887   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.870  -2.431   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.383  -2.140   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.887  -0.685   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       9.399  -0.394   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       9.903   1.061   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.415   1.352   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.919   2.807   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.432   3.098   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.440   1.934   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      15.952   2.225   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      13.936   0.479   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      14.944  -0.685   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      12.424   0.188   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.895   2.225   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.383   1.934   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.375   3.098   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.879   0.479   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.366   0.188   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.862  -1.267   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.350  -1.558   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.342  -0.394   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.830  -0.685   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.379  -2.124   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.492  -1.476   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.179   0.479   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.326   1.934   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.838   2.225   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.846   1.061   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.350   2.516   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       4.358   1.352   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   19                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   16                                                  
CONECT    8    7    9   15                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    8                                                       
CONECT   16    7   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17    5   20                                                  
CONECT   20   19   21   32                                                  
CONECT   21   20    3   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   30                                                  
CONECT   24   23   25   26   27                                             
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   24   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   23   31   32                                             
CONECT   31   30                                                            
CONECT   32   30   20                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₂₈O₆

Average Mass

436.5040 Da

Monoisotopic Mass

436.18859 Da

IUPAC Name

(5aS,9aR)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-4,5a,6,7,8,9,9a,10-octahydro-1,5-dioxatetraphen-4-one

Traditional Name

(5aS,9aR)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6H-1,5-dioxatetraphen-4-one

CAS Registry Number

Not Available

SMILES

COC1=C2C[C@@H]3C(C)(C)CCC[C@]3(C)OC2=C2C(=O)C=C(OC2=C1)C1=CC=C(O)C(O)=C1

InChI Identifier

InChI=1S/C26H28O6/c1-25(2)8-5-9-26(3)22(25)11-15-20(30-4)13-21-23(24(15)32-26)18(29)12-19(31-21)14-6-7-16(27)17(28)10-14/h6-7,10,12-13,22,27-28H,5,8-9,11H2,1-4H3/t22-,26+/m1/s1

InChI Key

DVUORASKJFBCTF-GJZUVCINSA-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
Helminthostachys zeylanica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 6-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 6-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavones

Direct Parent

6-prenylated flavones

Alternative Parents

Substituents

6-prenylated flavone
Pyranoflavonoid
7-methoxyflavonoid-skeleton
Hydroxyflavonoid
4'-hydroxyflavonoid
3'-hydroxyflavonoid
Xanthene
Dibenzopyran
Chromone
1-benzopyran
Benzopyran
Chromane
Catechol
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Phenol
Alkyl aryl ether
Benzenoid
Pyran
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous ester
Oxacycle
Organoheterocyclic compound
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	5.42	ALOGPS
logP	4.68	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	8.7	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	121.65 m³·mol⁻¹	ChemAxon
Polarizability	48.25 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

132188474

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one (NP0157573)

MOL for NP0157573 ((5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one)

3D MOL for NP0157573 ((5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one)

3D SDF for NP0157573 ((5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one)

3D-SDF for NP0157573 ((5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one)

PDB for NP0157573 ((5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one)

3D PDB for NP0157573 ((5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one)

SMILES for NP0157573 ((5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one)

INCHI for NP0157573 ((5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one)

Structure for NP0157573 ((5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one)

3D Structure for NP0157573 ((5as,9ar)-2-(3,4-dihydroxyphenyl)-11-methoxy-5a,9,9-trimethyl-7,8,9a,10-tetrahydro-6h-1,5-dioxatetraphen-4-one)