NP-MRD: Showing NP-Card for 5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione (NP0284175)

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Record Information

Version

2.0

Created at

2022-09-09 11:46:07 UTC

Updated at

2022-09-09 11:46:07 UTC

NP-MRD ID

NP0284175

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione

Description

5,9,13-Trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]Pentadec-12-ene-4,10-dione belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton. 5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione is found in Artemisia herba-alba. 5,9,13-Trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]Pentadec-12-ene-4,10-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 04121512182D          

 28 31  0  0  0  0            999 V2000
    6.1596   -0.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3686   -0.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6097   -0.6335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3989   -1.3665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4481   -1.4812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8907   -0.8356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8232   -0.1356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0060   -1.1055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2441   -1.5683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3059   -0.4792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6494    0.3859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5169    0.7008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6502    1.5897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2037    0.0360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4500    0.1197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0158   -0.4600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5249   -1.3545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1718   -2.1857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4182   -1.1013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0498   -1.9077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1244   -2.8221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4459   -3.2913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5130   -4.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7002   -2.9383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0674   -0.0118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4911    0.6961    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2953    0.5119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9613    1.0949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 14 25  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
  2 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END

     RDKit          3D

 62 65  0  0  0  0  0  0  0  0999 V2000
    1.3434   -2.6142   -0.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7989   -1.3805   -0.2229 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2277   -1.1304    0.1649 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0053   -0.5481   -1.0110 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4284   -0.3078   -0.6012 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9387    0.9094   -0.6471 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0967    2.0590   -1.1098 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3358    1.1352   -0.2428 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9539   -0.2718   -0.6672 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3756   -0.5826   -1.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4870   -0.2974   -0.1736 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9137   -0.7497    1.1104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3638   -1.9012    1.9195 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1193   -0.0230    1.5550 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8317    0.7691    0.4726 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1844    1.7809    0.0740 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0605    2.9502   -0.0400 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5525    1.2397   -0.1797 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9995    1.7887   -1.4899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4243    1.6225    0.9710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7796    0.9889    0.8659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9708    0.0568   -0.2680 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0822   -0.9013    0.0826 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0663   -0.3094    1.0575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3320   -2.0394    0.6590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6914   -2.8047    1.6170 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1514   -2.0971   -0.0663 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7978   -0.8352   -0.5600 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3325   -2.8692   -0.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0460   -3.4003    0.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7092   -2.0932    0.4103 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3149   -0.4820    1.0578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9614   -1.2442   -1.8727 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5930    0.4403   -1.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0622   -1.1224   -0.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7098    2.9909   -1.1397 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2699    2.2651   -0.4069 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7518    1.8961   -2.1507 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4621    0.7663    0.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0791    0.6628   -0.9269 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5789    2.2311   -0.2537 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5692    0.2985   -1.4384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5337   -1.6127   -1.5430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5573    0.0434   -2.1214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2300   -1.6498    2.5773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5735   -2.1956    2.6838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4949   -2.8413    1.3447 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4533    0.0297    2.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7829    1.1578    0.7918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8798    2.4788   -1.3314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2877    1.0756   -2.2568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2338    2.4641   -1.9766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9346    1.2783    1.9038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4846    2.7432    1.0870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0471    0.5659    1.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5123    1.8379    0.7216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3560    0.5954   -1.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6030   -1.2789   -0.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2414    0.7694    0.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8284   -0.5536    2.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0563   -0.8035    0.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7900   -0.9510   -1.6871 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 22  1  0
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 18 19  1  6
 18 16  1  0
 16 17  2  0
 16 15  1  0
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 14 12  2  0
 12 13  1  0
 11 12  1  1
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 10  9  1  0
  9  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  3
  6  7  1  0
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 11 28  1  0
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 27 25  1  0
 25 26  2  0
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 28 22  1  0
 11 18  1  0
  9 15  1  0
 24 59  1  0
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 21 55  1  0
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 13 46  1  0
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  9 42  1  6
  1 29  1  0
  1 30  1  0
  3 31  1  0
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  5 35  1  0
  7 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
  8 41  1  0
 28 62  1  6
M  END


  Mrv0541 04121512182D          

 28 31  0  0  0  0            999 V2000
    6.1596   -0.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3686   -0.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6097   -0.6335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3989   -1.3665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4481   -1.4812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8907   -0.8356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8232   -0.1356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0060   -1.1055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2441   -1.5683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3059   -0.4792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6494    0.3859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5169    0.7008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6502    1.5897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2037    0.0360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4500    0.1197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0158   -0.4600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5249   -1.3545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1718   -2.1857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4182   -1.1013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0498   -1.9077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1244   -2.8221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4459   -3.2913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5130   -4.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7002   -2.9383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0674   -0.0118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4911    0.6961    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2953    0.5119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9613    1.0949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 14 25  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
  2 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0284175

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2CCC3(C)C(=O)C4C=C(C)C3(CC4C(=C)CCC=C(C)C)C2OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O3/c1-14(2)8-7-9-15(3)20-13-25-16(4)12-19(20)21(26)24(25,6)11-10-18-17(5)23(27)28-22(18)25/h8,12,17-20,22H,3,7,9-11,13H2,1-2,4-6H3

> <INCHI_KEY>
RENFBQSMEYXGMZ-UHFFFAOYSA-N

> <FORMULA>
C25H34O3

> <MOLECULAR_WEIGHT>
382.544

> <EXACT_MASS>
382.250794955

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
44.39266538434745

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione

> <ALOGPS_LOGP>
5.78

> <JCHEM_LOGP>
5.356993863333333

> <ALOGPS_LOGS>
-5.28

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.917431559932282

> <JCHEM_PKA_STRONGEST_BASIC>
-6.977831945106358

> <JCHEM_POLAR_SURFACE_AREA>
43.370000000000005

> <JCHEM_REFRACTIVITY>
112.53139999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.02e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-APR-15         0                                  
HETATM    1  C   UNK     0      11.498  -1.219   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.021  -0.578   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.605  -1.183   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.211  -2.551   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.436  -2.765   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.396  -1.560   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.270  -0.253   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.745  -2.064   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.322  -2.927   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.438  -0.894   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.079   0.720   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.698   1.308   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.947   2.967   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.980   0.067   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.573   0.224   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.763  -0.859   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.713  -2.528   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.054  -4.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.381  -2.056   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.560  -3.561   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.699  -5.268   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.432  -6.144   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.558  -7.679   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.040  -5.485   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.592  -0.022   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.383   1.299   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.884   0.955   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.128   2.044   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   27                                                  
CONECT    3    2    4   25                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   14                                             
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    6   15   25                                             
CONECT   15   14   16                                                       
CONECT   16   15   10   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   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   14    3   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26    2   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₄O₃

Average Mass

382.5440 Da

Monoisotopic Mass

382.25079 Da

IUPAC Name

5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione

Traditional Name

5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione

CAS Registry Number

Not Available

SMILES

CC1C2CCC3(C)C(=O)C4C=C(C)C3(CC4C(=C)CCC=C(C)C)C2OC1=O

InChI Identifier

InChI=1S/C25H34O3/c1-14(2)8-7-9-15(3)20-13-25-16(4)12-19(20)21(26)24(25,6)11-10-18-17(5)23(27)28-22(18)25/h8,12,17-20,22H,3,7,9-11,13H2,1-2,4-6H3

InChI Key

RENFBQSMEYXGMZ-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
Artemisia herba-alba	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Eudesmanolides, secoeudesmanolides, and derivatives

Alternative Parents

Substituents

Eudesmanolide
Bisabolane sesquiterpenoid
Sesquiterpenoid
Naphthofuran
Cyclohexenone
Gamma butyrolactone
Tetrahydrofuran
Carboxylic acid ester
Ketone
Lactone
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	5.78	ALOGPS
logP	5.36	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	16.92	ChemAxon
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	43.37 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	112.53 m³·mol⁻¹	ChemAxon
Polarizability	44.39 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

73827048

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione (NP0284175)

MOL for NP0284175 (5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione)

3D MOL for NP0284175 (5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione)

3D SDF for NP0284175 (5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione)

3D-SDF for NP0284175 (5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione)

PDB for NP0284175 (5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione)

3D PDB for NP0284175 (5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione)

SMILES for NP0284175 (5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione)

INCHI for NP0284175 (5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione)

Structure for NP0284175 (5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione)

3D Structure for NP0284175 (5,9,13-trimethyl-15-(6-methylhepta-1,5-dien-2-yl)-3-oxatetracyclo[9.2.2.0¹,⁹.0²,⁶]pentadec-12-ene-4,10-dione)