NP-MRD: Showing NP-Card for 4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate (NP0215745)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 15:27:46 UTC

Updated at

2022-09-05 15:27:46 UTC

NP-MRD ID

NP0215745

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate

Description

4',5'-Dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]Nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate belongs to the class of organic compounds known as quassinoids. These are a group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring. 4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate is found in Ailanthus excelsa. 4',5'-Dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]Nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251507142D          

 33 38  0  0  0  0            999 V2000
   -1.3947    0.7316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5697    0.7316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1572    0.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5697   -0.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6678    0.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0803    0.7316    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0803   -0.6974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9053   -0.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1528   -1.2468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9053   -2.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1908   -2.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1908   -1.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3178   -2.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9053   -3.5553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1428   -2.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9465   -3.0268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2495   -2.4039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3358   -1.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1428   -1.4118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5553   -0.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3803   -0.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7928   -1.4118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6178   -1.4118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0303   -0.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0303   -2.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6178   -2.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7928   -2.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3803   -3.5553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3803   -2.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5553   -2.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1428    0.0171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3178    0.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9053    0.7316    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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  9 19  1  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
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  0  0  0  0
 15 30  1  0  0  0  0
 19 30  1  0  0  0  0
 20 31  1  0  0  0  0
 31 32  1  0  0  0  0
  8 32  1  0  0  0  0
 32 33  2  0  0  0  0
M  END

     RDKit          3D

 65 70  0  0  0  0  0  0  0  0999 V2000
    6.3394   -0.1674   -0.2742 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8871    0.0276    1.1485 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5743    0.7794    1.1176 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8382    2.1050    0.4338 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6574   -0.0098    0.2234 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0260   -1.0780   -0.3369 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3606    0.4009   -0.0275 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4487   -0.2886   -0.8535 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2277    0.4082   -2.1352 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    1.3954   -2.3853 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2341   -0.0581   -2.9425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9823   -0.3990   -2.3037 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6574    0.9353   -2.0560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7708    0.8246   -1.0751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5410    1.9659   -0.9912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1713    3.1811   -1.8090 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6385    1.9955   -0.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9109    0.8511    0.5447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1463   -0.3110    0.4735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6301   -1.4730    1.2622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0571   -0.3157   -0.3505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2024   -1.4550   -0.4664 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8226   -1.1923   -1.1018 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6031   -2.7075   -1.3128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5872   -2.9898    0.0798 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6471   -2.2086    0.6531 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3843   -3.1832    1.2802 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1592   -1.2462    1.6835 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3883   -1.9725    2.6047 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2365   -0.1561    1.0815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4304    1.2504    1.3155 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5745    0.4670    2.1264 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2661   -0.8278   -0.1495 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3460   -1.2268   -0.5916 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3970    0.1934   -0.4259 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7204    0.3876   -1.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7854   -0.9554    1.6430 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6140    0.6789    1.6841 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1357    0.9029    2.1241 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5025    2.0916   -0.6381 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9372    2.3336    0.3808 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3690    2.9497    0.9696 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0684   -1.1931   -1.2037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5836   -0.9525   -3.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9531    1.6846   -1.6440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0089    1.3399   -3.0283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5506    2.9983   -2.8338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6752    4.0786   -1.4232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0850    3.3762   -1.7694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2701    2.8529   -0.0616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7929    0.8728    1.2113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7469   -2.3949    0.6758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2076   -1.5602    2.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7309   -1.2415    1.5062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7409   -2.1846   -1.1609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4489   -3.1672   -1.8199 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3857   -2.9051   -1.7168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2487   -3.1695    2.2774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9889   -0.7833    2.1959 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1593   -2.6750    2.1361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0604    1.9646    0.5517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3527    1.6566    1.8183 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2571    0.3887    3.2114 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5769    0.8650    2.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7321   -1.7545    0.3627 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8 33  1  0
 33 30  1  0
 30 31  1  0
 31 32  1  0
 30 28  1  0
 28 29  1  0
 28 26  1  0
 26 27  1  1
 26 25  1  0
 25 24  1  0
 23 24  1  6
 23 22  1  0
 22 21  1  0
 21 19  2  0
 19 20  1  0
 19 18  1  0
 18 17  2  0
 17 15  1  0
 15 16  1  0
 15 14  2  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  2  0
  9  8  1  0
 23 33  1  0
 12 23  1  0
 32 30  1  0
 22 26  1  0
 14 21  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  0
  2 38  1  0
  3 39  1  1
  4 40  1  0
  4 41  1  0
  4 42  1  0
  8 43  1  6
 33 65  1  1
 31 61  1  0
 31 62  1  0
 32 63  1  0
 32 64  1  0
 28 59  1  1
 29 60  1  0
 27 58  1  0
 24 56  1  0
 24 57  1  0
 22 55  1  6
 20 52  1  0
 20 53  1  0
 20 54  1  0
 18 51  1  0
 17 50  1  0
 16 47  1  0
 16 48  1  0
 16 49  1  0
 13 45  1  0
 13 46  1  0
 12 44  1  6
M  END


  Mrv1533004251507142D          

 33 38  0  0  0  0            999 V2000
   -1.3947    0.7316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5697    0.7316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1572    0.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5697   -0.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6678    0.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0803    0.7316    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0803   -0.6974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9053   -0.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1528   -1.2468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9053   -2.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1908   -2.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1908   -1.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3178   -2.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9053   -3.5553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1428   -2.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9465   -3.0268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2495   -2.4039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3358   -1.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1428   -1.4118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5553   -0.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3803   -0.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7928   -1.4118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6178   -1.4118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0303   -0.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0303   -2.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6178   -2.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7928   -2.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3803   -3.5553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3803   -2.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5553   -2.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1428    0.0171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3178    0.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9053    0.7316    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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  9 19  1  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
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  0  0  0  0
 15 30  1  0  0  0  0
 19 30  1  0  0  0  0
 20 31  1  0  0  0  0
 31 32  1  0  0  0  0
  8 32  1  0  0  0  0
 32 33  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0215745

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(=O)OC1C2C3(CC3)C(O)C3(O)OCC22C3C3=C(C)C=CC(C)=C3CC2OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H32O7/c1-5-12(2)21(27)33-18-20-24(8-9-24)23(29)26(30)19-17-14(4)7-6-13(3)15(17)10-16(32-22(18)28)25(19,20)11-31-26/h6-7,12,16,18-20,23,29-30H,5,8-11H2,1-4H3

> <INCHI_KEY>
STRRLWSZGQUEPP-UHFFFAOYSA-N

> <FORMULA>
C26H32O7

> <MOLECULAR_WEIGHT>
456.535

> <EXACT_MASS>
456.21480337

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.799887275832305

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate

> <ALOGPS_LOGP>
2.48

> <JCHEM_LOGP>
3.405426615333333

> <ALOGPS_LOGS>
-3.92

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.66449011014176

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.812166442285076

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7369362445538767

> <JCHEM_POLAR_SURFACE_AREA>
102.29000000000002

> <JCHEM_REFRACTIVITY>
117.6107

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.50e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      -2.604   1.366   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.064   1.366   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.294   0.032   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.064  -1.302   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.246   0.032   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.016   1.366   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       2.016  -1.302   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.556  -1.302   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.018  -2.327   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.556  -3.969   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.223  -4.739   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.223  -3.199   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.326  -5.303   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.556  -6.636   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.866  -5.303   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.367  -5.650   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       4.199  -4.487   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.360  -2.956   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.866  -2.635   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.636  -1.302   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.176  -1.302   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.946  -2.635   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.486  -2.635   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.256  -1.302   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.256  -3.969   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.486  -5.303   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.946  -5.303   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.176  -6.636   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.176  -3.969   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.636  -3.969   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       5.866   0.032   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.326   0.032   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       3.556   1.366   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   32                                                  
CONECT    9    8   10   19                                                  
CONECT   10    9   11   12   13                                             
CONECT   11   10   12                                                       
CONECT   12   11   10                                                       
CONECT   13   10   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17   30                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18    9   20   30                                             
CONECT   20   19   21   31                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   29                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   22   30                                                  
CONECT   30   29   15   19                                                  
CONECT   31   20   32                                                       
CONECT   32   31    8   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   76    0
END

View in JSmol

Synonyms

Value	Source
4',5'-Dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0,.0,.0,]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoic acid	Generator
4',5'-Dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoic acid	Generator

Chemical Formula

C₂₆H₃₂O₇

Average Mass

456.5350 Da

Monoisotopic Mass

456.21480 Da

IUPAC Name

4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate

Traditional Name

4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate

CAS Registry Number

Not Available

SMILES

CCC(C)C(=O)OC1C2C3(CC3)C(O)C3(O)OCC22C3C3=C(C)C=CC(C)=C3CC2OC1=O

InChI Identifier

InChI=1S/C26H32O7/c1-5-12(2)21(27)33-18-20-24(8-9-24)23(29)26(30)19-17-14(4)7-6-13(3)15(17)10-16(32-22(18)28)25(19,20)11-31-26/h6-7,12,16,18-20,23,29-30H,5,8-11H2,1-4H3

InChI Key

STRRLWSZGQUEPP-UHFFFAOYSA-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
Ailanthus excelsa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quassinoids. These are a group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Quassinoids

Alternative Parents

Substituents

Quassinoid
Naphthopyranone
Naphthopyran
Phenanthrene
Naphthofuran
Naphthalene
Tetralin
Delta valerolactone
Oxepane
Pyranone
Fatty acid ester
Delta_valerolactone
Pyran
Dicarboxylic acid or derivatives
Oxane
Fatty acyl
Benzenoid
Cyclic alcohol
Tetrahydrofuran
Lactone
Hemiacetal
Carboxylic acid ester
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
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	2.48	ALOGPS
logP	3.41	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	10.81	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	102.29 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	117.61 m³·mol⁻¹	ChemAxon
Polarizability	47.8 Å³	ChemAxon
Number of Rings	6	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

78385432

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate (NP0215745)

MOL for NP0215745 (4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate)

3D MOL for NP0215745 (4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate)

3D SDF for NP0215745 (4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate)

3D-SDF for NP0215745 (4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate)

PDB for NP0215745 (4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate)

3D PDB for NP0215745 (4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate)

SMILES for NP0215745 (4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate)

INCHI for NP0215745 (4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate)

Structure for NP0215745 (4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate)

3D Structure for NP0215745 (4',5'-dihydroxy-14',17'-dimethyl-9'-oxo-3',10'-dioxaspiro[cyclopropane-1,6'-pentacyclo[9.8.0.0¹,⁷.0⁴,¹⁹.0¹³,¹⁸]nonadecane]-13',15',17'-trien-8'-yl 2-methylbutanoate)