NP-MRD: Showing NP-Card for (2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate (NP0312717)

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Record Information

Version

2.0

Created at

2022-09-11 09:44:44 UTC

Updated at

2022-09-11 09:44:44 UTC

NP-MRD ID

NP0312717

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate

Description

(2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate is found in Ferula assa-foetida.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112211442D          

 32 33  0  0  1  0            999 V2000
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -4.5375    0.0000 C   0  0  2  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
    5.7158   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4302   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    0.4125    0.0000 C   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
    5.7158    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 25 31  1  0  0  0  0
 31 32  2  0  0  0  0
 22 32  1  0  0  0  0
M  END

     RDKit          3D

 64 65  0  0  0  0  0  0  0  0999 V2000
    0.3826   -4.1365   -0.5359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1644   -2.9568    0.1762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0477   -2.8047    1.4184 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8487   -1.9380   -0.5118 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3733   -0.8165    0.1518 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8614   -0.7846   -0.1447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7467   -1.4010    0.6093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2174   -2.1992    1.7738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2288   -1.3807    0.3350 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.4958   -2.6718   -0.1749 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5812   -0.4181   -0.7472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3541    0.9708   -0.2644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3785    1.8109   -0.2629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1938    3.2081    0.2119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6943    1.3576   -0.7310 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8203    0.4895   -0.3599 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6370    0.6527   -0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6004   -0.2574   -0.8119 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0608    1.6493    0.5802 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4675    1.9144    0.8471 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3922    1.0548    0.2735 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7503    1.1280    0.3989 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4100    2.0910    1.1317 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7839    2.0803    1.1971 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5553    1.1398    0.5568 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9387    1.1377    0.6289 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6628    0.1658   -0.0368 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9288   -0.7635   -0.7491 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5371   -1.6713   -1.3745 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6219   -0.7246   -0.7905 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8922    0.1742   -0.1781 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5110    0.1802   -0.2473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3808   -4.9252   -0.7027 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1871   -4.5822    0.0705 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7403   -3.8453   -1.5634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1811   -0.8375    1.2444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1977   -0.2327   -1.0384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1263   -2.4810    2.3828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7627   -3.1350    1.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5969   -1.6072    2.4549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7694   -1.2691    1.2695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2305   -2.6476   -1.1271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0325   -0.6565   -1.6659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6664   -0.5633   -0.9988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4123    1.3570    0.0975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1433    3.5322    0.1391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5003    3.2507    1.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8124    3.8508   -0.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1258    0.5366   -0.0986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6509    1.0368   -1.7865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4323    2.1981   -0.6815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3951    1.3298    0.1048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0626    0.5811   -1.4571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461   -0.9827   -1.4881 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1294   -0.8649   -0.0846 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2603    0.2844   -1.5464 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3066    2.3264    1.0324 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6967    2.9403    0.4250 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6259    2.0520    1.9527 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8097    2.8258    1.6322 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3231    2.8388    1.7754 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4593    1.8938    1.2045 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7427    0.1084   -0.0208 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0264   -0.5930   -0.8334 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 15  1  0
 13 12  2  3
 12 11  1  0
 11  9  1  0
  9 10  1  0
  9  7  1  0
  7  8  1  0
  7  6  2  0
  6  5  1  0
  5 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 28 30  1  0
 30 31  1  0
 31 32  2  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
 32 22  1  0
 31 25  1  0
 14 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  0
 15 50  1  0
 15 51  1  0
 12 45  1  0
 11 43  1  0
 11 44  1  0
  9 41  1  1
 10 42  1  0
  8 38  1  0
  8 39  1  0
  8 40  1  0
  6 37  1  0
  5 36  1  1
 16 52  1  0
 16 53  1  0
 18 54  1  0
 18 55  1  0
 18 56  1  0
 19 57  1  0
 20 58  1  0
 20 59  1  0
 23 60  1  0
 24 61  1  0
 26 62  1  0
 27 63  1  0
 32 64  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
M  END


  Mrv1652309112211442D          

 32 33  0  0  1  0            999 V2000
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -4.5375    0.0000 C   0  0  2  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
    5.7158   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4302   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    0.4125    0.0000 C   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
    5.7158    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 25 31  1  0  0  0  0
 31 32  2  0  0  0  0
 22 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0312717

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C26H32O6/c1-17(2)6-10-24(28)19(4)15-23(31-20(5)27)14-18(3)12-13-30-22-9-7-21-8-11-26(29)32-25(21)16-22/h6-9,11-12,15-16,23-24,28H,10,13-14H2,1-5H3/b18-12+,19-15+/t23-,24+/m0/s1

> <INCHI_KEY>
DVSVJMWULNKUJW-TUCXABMJSA-N

> <FORMULA>
C26H32O6

> <MOLECULAR_WEIGHT>
440.536

> <EXACT_MASS>
440.21988875

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
48.94445063865973

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,5S,6E,8R)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxo-2H-chromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate

> <JCHEM_LOGP>
4.285866265666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.554963934444913

> <JCHEM_PKA_STRONGEST_BASIC>
-2.993458775073794

> <JCHEM_POLAR_SURFACE_AREA>
82.06000000000002

> <JCHEM_REFRACTIVITY>
126.91769999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2E,5S,6E,8R)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  -8.470   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       6.668 -10.010   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       9.336  -8.470   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.669 -10.780   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      12.003 -13.090   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       9.336 -13.090   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336 -14.630   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002 -15.400   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002 -16.940   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.669  -6.160   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.003  -3.850   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      10.669  -3.080   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.669  -1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.336   0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.669   3.080   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.003   3.850   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.337   3.080   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      14.670   3.850   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      13.337   1.540   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      12.003   0.770   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   16                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    5   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   32                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   25   32                                                  
CONECT   32   31   22                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₂O₆

Average Mass

440.5360 Da

Monoisotopic Mass

440.21989 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)=CC[C@@H](O)C(\C)=C\[C@H](C\C(C)=C\COC1=CC=C2C=CC(=O)OC2=C1)OC(C)=O

InChI Identifier

InChI=1S/C26H32O6/c1-17(2)6-10-24(28)19(4)15-23(31-20(5)27)14-18(3)12-13-30-22-9-7-21-8-11-26(29)32-25(21)16-22/h6-9,11-12,15-16,23-24,28H,10,13-14H2,1-5H3/b18-12+,19-15+/t23-,24+/m0/s1

InChI Key

DVSVJMWULNKUJW-TUCXABMJSA-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
Ferula assa-foetida	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate (NP0312717)

MOL for NP0312717 ((2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate)

3D MOL for NP0312717 ((2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate)

3D SDF for NP0312717 ((2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate)

3D-SDF for NP0312717 ((2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate)

PDB for NP0312717 ((2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate)

3D PDB for NP0312717 ((2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate)

SMILES for NP0312717 ((2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate)

INCHI for NP0312717 ((2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate)

Structure for NP0312717 ((2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate)

3D Structure for NP0312717 ((2e,5s,6e,8r)-8-hydroxy-3,7,11-trimethyl-1-[(2-oxochromen-7-yl)oxy]dodeca-2,6,10-trien-5-yl acetate)