NP-MRD: Showing NP-Card for Artelasticinol (NP0078310)

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Record Information

Version

2.0

Created at

2022-04-28 23:24:36 UTC

Updated at

2022-04-28 23:24:36 UTC

NP-MRD ID

NP0078310

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Artelasticinol

Description

2-(2,5-Dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-[(1S)-1-hydroxy-3-methylbut-2-en-1-yl]-8-(3-methylbut-2-en-1-yl)-4H-chromen-4-one belongs to the class of organic compounds known as 8-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 8-position. Artelasticinol is found in Artocarpus elasticus . Based on a literature review very few articles have been published on 2-(2,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-[(1S)-1-hydroxy-3-methylbut-2-en-1-yl]-8-(3-methylbut-2-en-1-yl)-4H-chromen-4-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292201242D          

 34 36  0  0  1  0            999 V2000
   -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
    0.0000   -1.6500    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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    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
    1.4289   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    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
  1  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
  9 11  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
  4 15  1  0  0  0  0
 15 16  2  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 17 22  1  1  0  0  0
 13 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
 26 30  1  0  0  0  0
 30 31  1  0  0  0  0
 25 32  1  0  0  0  0
  3 33  1  0  0  0  0
  1 34  1  0  0  0  0
M  END

     RDKit          3D

 62 64  0  0  0  0  0  0  0  0999 V2000
   -1.2946    6.0834   -1.9340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6945    4.8471   -2.4881 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3533    3.6879   -1.8218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6417    3.7390   -0.6478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3022    2.5700    0.0190 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4047    2.7140    1.1814 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6458    1.3072   -0.4385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3393    0.0976    0.3042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8985   -0.0016    0.8384 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2804   -1.0390    1.5125 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5743   -1.0562    2.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4549    0.1145    1.7812 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4543   -0.2138    0.7414 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5527    0.4613   -0.3736 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6462    1.5996   -0.6323 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6053    0.0446   -1.3683 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0194   -2.1577    2.7577 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3098   -2.1426    3.2544 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2093   -3.2452    2.9910 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9292   -3.2352    2.4857 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0523   -4.2963    2.6798 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4737   -2.1286    1.7484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7883   -2.0850    1.2373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5830   -3.0397    1.4100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1718   -0.9272    0.5058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6084   -0.9080    0.1930 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2010    0.2434   -0.1743 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9328   -2.0433   -0.6974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1681   -2.4717   -0.9171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3270   -1.8353   -0.2779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4433   -3.6371   -1.8372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3540    1.2951   -1.6146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7048    2.4461   -2.2956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4236    2.3873   -3.4805 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7984    6.2681   -0.9651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2054    6.0936   -1.8941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6070    6.8948   -2.6260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3632    4.7195   -0.2738 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7384    2.0431    1.8112 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9238    0.4814    2.7188 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8335    0.9547    1.4130 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1092   -1.0570    0.9594 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0165    2.1079   -1.5681 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6569    2.3554    0.1955 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6139    1.3168   -0.8382 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5447    0.5619   -1.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3123    0.2924   -2.3903 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7908   -1.0455   -1.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6992   -2.8898    3.7842 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5832   -4.0816    3.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2890   -5.1223    3.1872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1705   -1.2393    1.1806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8941    0.1493   -0.8511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353   -2.5995   -1.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0939   -2.6101    0.0067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8482   -1.2175   -1.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1144   -1.2745    0.6365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4687   -3.9430   -2.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7711   -4.4934   -1.1862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1984   -3.3739   -2.5892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6318    0.3482   -2.0983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6984    3.1856   -4.0065 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 33  2  0
 33 34  1  0
 33 32  1  0
 32  7  2  0
  7  5  1  0
  5  6  1  0
  5  4  2  0
  7  8  1  0
  8 25  2  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  2  3
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 29 31  1  0
 25 23  1  0
 23 24  2  0
 23 22  1  0
 22 20  2  0
 20 21  1  0
 20 19  1  0
 19 17  2  0
 17 18  1  0
 17 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  3
 14 15  1  0
 14 16  1  0
 11 10  2  0
 10  9  1  0
  4  3  1  0
  9  8  1  0
 10 22  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
 34 62  1  0
 32 61  1  0
  6 39  1  0
  4 38  1  0
 26 52  1  1
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 30 57  1  0
 31 58  1  0
 31 59  1  0
 31 60  1  0
 21 51  1  0
 19 50  1  0
 18 49  1  0
 12 40  1  0
 12 41  1  0
 13 42  1  0
 15 43  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  0
 16 47  1  0
 16 48  1  0
M  END


  Mrv1652304292201242D          

 34 36  0  0  1  0            999 V2000
   -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
    0.0000   -1.6500    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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    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
    1.4289   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    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
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    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
  1  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
  9 11  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
  4 15  1  0  0  0  0
 15 16  2  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
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 17 22  1  1  0  0  0
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 23 24  2  0  0  0  0
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 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
 26 30  1  0  0  0  0
 30 31  1  0  0  0  0
 25 32  1  0  0  0  0
  3 33  1  0  0  0  0
  1 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0078310

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C=C(C(O)=C1)C1=C([C@@H](O)C=C(C)C)C(=O)C2=C(O)C=C(O)C(CC=C(C)C)=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C26H28O8/c1-12(2)6-7-14-16(27)10-20(31)23-24(32)22(19(30)8-13(3)4)26(34-25(14)23)15-9-18(29)21(33-5)11-17(15)28/h6,8-11,19,27-31H,7H2,1-5H3/t19-/m0/s1

> <INCHI_KEY>
KAWAJORUQDJNLV-IBGZPJMESA-N

> <FORMULA>
C26H28O8

> <MOLECULAR_WEIGHT>
468.502

> <EXACT_MASS>
468.178417862

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
48.73445902803977

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(2,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-[(1S)-1-hydroxy-3-methylbut-2-en-1-yl]-8-(3-methylbut-2-en-1-yl)-4H-chromen-4-one

> <ALOGPS_LOGP>
3.86

> <JCHEM_LOGP>
4.509812038000001

> <ALOGPS_LOGS>
-4.80

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.9683695941626675

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.3470512071154825

> <JCHEM_PKA_STRONGEST_BASIC>
-3.273361610888191

> <JCHEM_POLAR_SURFACE_AREA>
136.68

> <JCHEM_REFRACTIVITY>
130.52100000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.39e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(2,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-[(1S)-1-hydroxy-3-methylbut-2-en-1-yl]-8-(3-methylbut-2-en-1-yl)chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
CONECT    1    2    6   34                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   33                                                  
CONECT    4    3    5   15                                                  
CONECT    5    4    6   12                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    5   13                                                       
CONECT   13   12   14   23                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14    4   16                                                  
CONECT   16   15                                                            
CONECT   17   14   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17                                                            
CONECT   23   13   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   32                                                  
CONECT   26   25   27   30                                                  
CONECT   27   26   28                                                       
CONECT   28   27   23   29                                                  
CONECT   29   28                                                            
CONECT   30   26   31                                                       
CONECT   31   30                                                            
CONECT   32   25                                                            
CONECT   33    3                                                            
CONECT   34    1                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₂₈O₈

Average Mass

468.5020 Da

Monoisotopic Mass

468.17842 Da

IUPAC Name

2-(2,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-[(1S)-1-hydroxy-3-methylbut-2-en-1-yl]-8-(3-methylbut-2-en-1-yl)-4H-chromen-4-one

Traditional Name

2-(2,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-[(1S)-1-hydroxy-3-methylbut-2-en-1-yl]-8-(3-methylbut-2-en-1-yl)chromen-4-one

CAS Registry Number

Not Available

SMILES

COC1=C(O)C=C(C(O)=C1)C1=C([C@@H](O)C=C(C)C)C(=O)C2=C(O)C=C(O)C(CC=C(C)C)=C2O1

InChI Identifier

InChI=1S/C26H28O8/c1-12(2)6-7-14-16(27)10-20(31)23-24(32)22(19(30)8-13(3)4)26(34-25(14)23)15-9-18(29)21(33-5)11-17(15)28/h6,8-11,19,27-31H,7H2,1-5H3/t19-/m0/s1

InChI Key

KAWAJORUQDJNLV-IBGZPJMESA-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
Artocarpus elasticus	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 8-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 8-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavones

Direct Parent

8-prenylated flavones

Alternative Parents

Substituents

8-prenylated flavone
3-prenylated flavone
4p-methoxyflavonoid-skeleton
Hydroxyflavonoid
7-hydroxyflavonoid
5-hydroxyflavonoid
3'-hydroxyflavonoid
Chromone
1-benzopyran
Methoxyphenol
Benzopyran
Phenoxy compound
Methoxybenzene
Phenol ether
Hydroquinone
Anisole
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Phenol
Alkyl aryl ether
Benzenoid
Pyran
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous acid
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic alcohol
Organooxygen compound
Alcohol
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	3.86	ALOGPS
logP	4.51	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	6.35	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	136.68 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	130.52 m³·mol⁻¹	ChemAxon
Polarizability	48.73 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

162905075

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Artelasticinol (NP0078310)

MOL for NP0078310 (Artelasticinol)

3D MOL for NP0078310 (Artelasticinol)

3D SDF for NP0078310 (Artelasticinol)

3D-SDF for NP0078310 (Artelasticinol)

PDB for NP0078310 (Artelasticinol)

3D PDB for NP0078310 (Artelasticinol)

SMILES for NP0078310 (Artelasticinol)

INCHI for NP0078310 (Artelasticinol)

Structure for NP0078310 (Artelasticinol)

3D Structure for NP0078310 (Artelasticinol)