NP-MRD: Showing NP-Card for (1r,2s,3r,11r,14s,16s)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1e,3z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0¹,¹⁴.0²,¹¹.0⁴,⁹]icosa-4(9),6-dien-5-one (NP0256979)

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Record Information

Version

2.0

Created at

2022-09-07 21:58:41 UTC

Updated at

2022-09-07 21:58:41 UTC

NP-MRD ID

NP0256979

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,3r,11r,14s,16s)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1e,3z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0¹,¹⁴.0²,¹¹.0⁴,⁹]icosa-4(9),6-dien-5-one

Description

Hesseltin A photoisomer C belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. Based on a literature review very few articles have been published on Hesseltin A photoisomer C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072223582D          

 32 36  0  0  1  0            999 V2000
    9.1490    2.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4063    1.2214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8561    0.6067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0486    0.7758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4984    0.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6909    0.3301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4336    1.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6261    1.2831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3688    2.0670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0759    0.6683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3332   -0.1155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1407   -0.2846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7830   -0.7303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9756   -0.5611    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2137   -1.3510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3797   -1.1652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5754   -0.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3137   -0.0776    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0223    0.6943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3937    0.0185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4576   -0.8040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5962   -0.1929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9929    0.8681    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1796    1.0066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6462    1.5310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5679    1.4830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9415    0.6032    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2799    0.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6542    0.6092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7183    0.2227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2685    0.8375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0112    1.6213    0.0000 O   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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 26  1  6  0  0  0
 18 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 23 29  1  0  0  0  0
 30 27  1  1  0  0  0
 14 30  1  0  0  0  0
 30 31  1  0  0  0  0
 10 31  1  0  0  0  0
 31 32  1  1  0  0  0
M  END

     RDKit          3D

 64 68  0  0  0  0  0  0  0  0999 V2000
    8.6339    1.2595   -1.0021 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7012   -0.1896   -1.2739 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6286   -0.9334   -1.1034 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3682   -0.3137   -0.6422 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3110   -1.0770   -0.4794 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0113   -0.5467   -0.0229 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8554    0.7889    0.2537 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6249    1.2729    0.6827 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4348    2.4849    0.9474 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6076    0.3561    0.8078 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7975   -0.9777    0.5219 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9839   -1.3490    0.1249 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7517   -1.9119    0.6520 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6057   -1.5355    0.7598 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1048   -2.0040    2.0805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3198   -2.2738   -0.3795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7395   -1.8200   -0.4920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8747   -0.3492   -0.6312 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4148    0.0212   -1.8925 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3509    0.0289   -0.5868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1766   -0.9905    0.1365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9063    0.1147   -2.0042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3847    1.3934    0.0852 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.6385    1.9814    0.0043 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4033    2.2859   -0.6312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9899    1.8736   -0.2263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1085    0.4607    0.3806 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8311    0.6673    1.6582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0466    1.2750    1.4017 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7285   -0.0798    0.4702 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2385    0.7716    1.2621 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0768    0.7347    2.6148 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6389    1.7323   -1.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1909    1.5005   -0.0139 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9983    1.7238   -1.7678 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6518   -0.6239   -1.6159 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6989   -1.9903   -1.3076 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3552    0.7288   -0.4566 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4300   -2.1338   -0.6972 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6526    1.5093    0.1560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1545   -2.4168    1.9902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9909   -1.3141    2.9135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5137   -2.9246    2.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2419   -3.3539   -0.2890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7779   -1.9505   -1.3068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3246   -2.2609    0.3300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1403   -2.2729   -1.4468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2072   -0.7544   -2.4707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9018   -1.1718    1.1716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1743   -1.9108   -0.4916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2241   -0.6266    0.1280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2173   -0.4575   -2.6729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8908   -0.3893   -2.0896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0611    1.1558   -2.3326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5669    2.9411    0.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6327    3.3271   -0.3283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4482    2.2380   -1.7136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2776    1.9122   -1.0451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7371    2.5699    0.6274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0117   -0.2000    2.2775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2405    1.3906    2.2695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3258    0.0180   -0.5929 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1276    1.8173    0.9221 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9159    0.7687    3.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
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 13 14  1  0
 14 15  1  1
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 18 19  1  6
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 23 24  1  1
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 27 26  1  6
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 30 31  1  0
 31 32  1  0
 12  6  1  0
 30 14  1  0
 31 10  1  0
 27 18  1  0
 29 23  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
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  3 37  1  0
  4 38  1  0
  5 39  1  0
  7 40  1  0
 15 41  1  0
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 19 48  1  0
 21 49  1  0
 21 50  1  0
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 22 52  1  0
 22 53  1  0
 22 54  1  0
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 25 56  1  0
 25 57  1  0
 26 58  1  0
 26 59  1  0
 28 60  1  0
 28 61  1  0
 30 62  1  6
 31 63  1  6
 32 64  1  0
M  END


  Mrv1652309072223582D          

 32 36  0  0  1  0            999 V2000
    9.1490    2.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4063    1.2214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8561    0.6067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0486    0.7758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4984    0.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6909    0.3301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4336    1.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6261    1.2831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3688    2.0670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0759    0.6683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3332   -0.1155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1407   -0.2846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7830   -0.7303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9756   -0.5611    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2137   -1.3510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3797   -1.1652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5754   -0.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3137   -0.0776    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0223    0.6943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3937    0.0185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4576   -0.8040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5962   -0.1929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9929    0.8681    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1796    1.0066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6462    1.5310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5679    1.4830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9415    0.6032    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2799    0.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6542    0.6092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7183    0.2227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2685    0.8375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0112    1.6213    0.0000 O   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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
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 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
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 20 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
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 18 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 23 29  1  0  0  0  0
 30 27  1  1  0  0  0
 14 30  1  0  0  0  0
 30 31  1  0  0  0  0
 10 31  1  0  0  0  0
 31 32  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0256979

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C/C=C/C1=CC(=O)C2=C(O1)O[C@]1(C)CC[C@@]3(O)C(C)(C)[C@]4(O)CC[C@]3(CO4)[C@H]1[C@H]2O

> <INCHI_IDENTIFIER>
InChI=1S/C25H32O7/c1-5-6-7-8-15-13-16(26)17-18(27)19-22(4,32-20(17)31-15)9-11-24(28)21(2,3)25(29)12-10-23(19,24)14-30-25/h5-8,13,18-19,27-29H,9-12,14H2,1-4H3/b6-5-,8-7+/t18-,19-,22+,23-,24+,25-/m0/s1

> <INCHI_KEY>
LFPBILWIIIPSMS-OUEPJCAYSA-N

> <FORMULA>
C25H32O7

> <MOLECULAR_WEIGHT>
444.524

> <EXACT_MASS>
444.21480337

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
47.89370775427949

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,3R,11R,14S,16S)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1E,3Z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0^{1,14}.0^{2,11}.0^{4,9}]icosa-4(9),6-dien-5-one

> <JCHEM_LOGP>
2.188081860999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.56855406830977

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.60071916510894

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3068514029940133

> <JCHEM_POLAR_SURFACE_AREA>
105.45000000000002

> <JCHEM_REFRACTIVITY>
130.4128

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3R,11R,14S,16S)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1E,3Z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0^{1,14}.0^{2,11}.0^{4,9}]icosa-4(9),6-dien-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      17.078   3.743   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.558   2.280   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      16.531   1.132   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.024   1.448   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.997   0.301   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.490   0.616   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.009   2.079   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.502   2.395   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      10.022   3.858   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.475   1.248   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.955  -0.216   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      11.463  -0.531   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       8.928  -1.363   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.421  -1.047   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.866  -2.522   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.309  -2.175   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.808  -1.660   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.319  -0.145   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.775   1.296   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.602   0.035   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.721  -1.501   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.113  -0.360   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.853   1.620   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.335   1.879   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.073   2.858   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.793   2.768   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.491   1.126   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.256   1.818   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       3.088   1.137   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.941   0.416   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.968   1.563   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       7.488   3.026   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   31                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11    6                                                       
CONECT   13   11   14                                                       
CONECT   14   13   15   16   30                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   27                                             
CONECT   19   18                                                            
CONECT   20   18   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20   24   25   29                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   18   28   30                                             
CONECT   28   27   29                                                       
CONECT   29   28   23                                                       
CONECT   30   27   14   31                                                  
CONECT   31   30   10   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₂O₇

Average Mass

444.5240 Da

Monoisotopic Mass

444.21480 Da

IUPAC Name

(1R,2S,3R,11R,14S,16S)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1E,3Z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0^{1,14}.0^{2,11}.0^{4,9}]icosa-4(9),6-dien-5-one

Traditional Name

(1R,2S,3R,11R,14S,16S)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1E,3Z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0^{1,14}.0^{2,11}.0^{4,9}]icosa-4(9),6-dien-5-one

CAS Registry Number

Not Available

SMILES

C\C=C/C=C/C1=CC(=O)C2=C(O1)O[C@]1(C)CC[C@@]3(O)C(C)(C)[C@]4(O)CC[C@]3(CO4)[C@H]1[C@H]2O

InChI Identifier

InChI=1S/C25H32O7/c1-5-6-7-8-15-13-16(26)17-18(27)19-22(4,32-20(17)31-15)9-11-24(28)21(2,3)25(29)12-10-23(19,24)14-30-25/h5-8,13,18-19,27-29H,9-12,14H2,1-4H3/b6-5-,8-7+/t18-,19-,22+,23-,24+,25-/m0/s1

InChI Key

LFPBILWIIIPSMS-OUEPJCAYSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
Alkyl aryl ether
Pyranone
Oxane
Pyran
Cyclic alcohol
Heteroaromatic compound
Vinylogous ester
Tertiary alcohol
Hemiacetal
Secondary alcohol
Oxacycle
Ether
Polyol
Organooxygen compound
Hydrocarbon derivative
Alcohol
Organic oxide
Organic oxygen 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	2.19	ChemAxon
pKa (Strongest Acidic)	11.6	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	105.45 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	130.41 m³·mol⁻¹	ChemAxon
Polarizability	47.89 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

139587241

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,3r,11r,14s,16s)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1e,3z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0¹,¹⁴.0²,¹¹.0⁴,⁹]icosa-4(9),6-dien-5-one (NP0256979)

MOL for NP0256979 ((1r,2s,3r,11r,14s,16s)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1e,3z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0¹,¹⁴.0²,¹¹.0⁴,⁹]icosa-4(9),6-dien-5-one)

3D MOL for NP0256979 ((1r,2s,3r,11r,14s,16s)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1e,3z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0¹,¹⁴.0²,¹¹.0⁴,⁹]icosa-4(9),6-dien-5-one)

3D SDF for NP0256979 ((1r,2s,3r,11r,14s,16s)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1e,3z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0¹,¹⁴.0²,¹¹.0⁴,⁹]icosa-4(9),6-dien-5-one)

3D-SDF for NP0256979 ((1r,2s,3r,11r,14s,16s)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1e,3z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0¹,¹⁴.0²,¹¹.0⁴,⁹]icosa-4(9),6-dien-5-one)

PDB for NP0256979 ((1r,2s,3r,11r,14s,16s)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1e,3z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0¹,¹⁴.0²,¹¹.0⁴,⁹]icosa-4(9),6-dien-5-one)

3D PDB for NP0256979 ((1r,2s,3r,11r,14s,16s)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1e,3z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0¹,¹⁴.0²,¹¹.0⁴,⁹]icosa-4(9),6-dien-5-one)

SMILES for NP0256979 ((1r,2s,3r,11r,14s,16s)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1e,3z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0¹,¹⁴.0²,¹¹.0⁴,⁹]icosa-4(9),6-dien-5-one)

INCHI for NP0256979 ((1r,2s,3r,11r,14s,16s)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1e,3z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0¹,¹⁴.0²,¹¹.0⁴,⁹]icosa-4(9),6-dien-5-one)

Structure for NP0256979 ((1r,2s,3r,11r,14s,16s)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1e,3z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0¹,¹⁴.0²,¹¹.0⁴,⁹]icosa-4(9),6-dien-5-one)

3D Structure for NP0256979 ((1r,2s,3r,11r,14s,16s)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1e,3z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0¹,¹⁴.0²,¹¹.0⁴,⁹]icosa-4(9),6-dien-5-one)