NP-MRD: Showing NP-Card for (1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate (NP0307870)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 01:18:04 UTC

Updated at

2022-09-11 01:18:05 UTC

NP-MRD ID

NP0307870

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate

Description

(1R,2R,4aS,5R,7R,8aR)-1,8a-dimethyl-5-[(3-methylbut-2-enoyl)oxy]-6-oxo-7-(prop-1-en-2-yl)-decahydronaphthalen-2-yl 3-methylbut-2-enoate belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5. (1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate is found in Senecio provincialis and Senecio sandersonii. Based on a literature review very few articles have been published on (1R,2R,4aS,5R,7R,8aR)-1,8a-dimethyl-5-[(3-methylbut-2-enoyl)oxy]-6-oxo-7-(prop-1-en-2-yl)-decahydronaphthalen-2-yl 3-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112203182D          

 30 31  0  0  1  0            999 V2000
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 11 19  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  1  6  0  0  0
  8 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  2  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
 26 28  1  0  0  0  0
 21 29  1  0  0  0  0
  4 29  1  0  0  0  0
 29 30  2  0  0  0  0
M  END

     RDKit          3D

 66 67  0  0  0  0  0  0  0  0999 V2000
   -3.0572    1.2383   -3.5649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2977    0.1593   -3.6406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7356   -0.2133   -4.9687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9753   -0.7107   -2.5015 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5403   -0.8358   -2.1480 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0197    0.2739   -1.2902 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1378    1.4846   -2.2206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8638    0.5888   -0.1035 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0435    0.5016    1.1928 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2030    1.3385    1.0860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0841    0.8123   -0.0018 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3193    0.3205    0.5056 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5416    0.8367    0.2298 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6265    1.8335   -0.5345 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7569    0.2750    0.7891 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7683   -0.7672    1.5978 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0237   -1.3171    2.1522 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4825   -1.3989    1.9547 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3948   -0.1863   -0.8654 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2112   -0.5300   -2.0910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9405   -0.4066    0.0112 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7876   -0.3176    1.1082 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9702   -1.2689    2.0845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2679   -2.3039    1.9082 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8689   -1.0857    3.1802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5787    0.0157    3.3159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5198    0.2003    4.4689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4960    1.1395    2.3453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7359   -0.4313   -1.2582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9469   -0.2280   -1.2316 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2453    1.8199   -4.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4966    1.5531   -2.6239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7374   -0.6535   -4.8185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7090    0.6490   -5.6598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3830   -1.0447   -5.3589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3393   -1.7482   -2.8212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3869   -1.7921   -1.5781 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1383   -0.9200   -3.0182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7892    2.0934   -1.9984 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1119    1.2167   -3.2743 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9690    2.1475   -1.9732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1685    1.6330   -0.2166 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2188   -0.5710    1.3434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6789    0.8642    1.9972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8761    2.3750    0.8666 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6924    1.3647    2.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3839    1.6809   -0.6458 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7377    0.7027    0.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9586   -2.4051    2.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9026   -1.0516    1.4973 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2767   -0.8961    3.1527 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6950   -2.2252    2.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9545   -1.8260    1.0645 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8128   -0.7028    2.5189 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2239   -1.1657   -0.3273 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9473    0.0774   -2.9760 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0309   -1.6050   -2.3888 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2948   -0.4285   -1.9243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4497   -1.4154    0.1077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9782   -1.8618    3.9221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4915    1.2684    4.8113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5424    0.0271    4.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3149   -0.4851    5.2967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2150    1.9532    2.6292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4538    1.5329    2.3366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7887    0.8217    1.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  2  3
 26 27  1  0
 26 28  1  0
 21 29  1  0
 29 30  2  0
 29  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  4  2  1  0
  2  3  1  0
  2  1  2  3
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  3
 16 17  1  0
 16 18  1  0
  6 19  1  0
  6  8  1  0
 20 56  1  0
 20 57  1  0
 20 58  1  0
 19 55  1  1
 11 47  1  6
 10 45  1  0
 10 46  1  0
  9 43  1  0
  9 44  1  0
  8 42  1  6
 21 59  1  1
 25 60  1  0
 27 61  1  0
 27 62  1  0
 27 63  1  0
 28 64  1  0
 28 65  1  0
 28 66  1  0
  4 36  1  6
  5 37  1  0
  5 38  1  0
  7 39  1  0
  7 40  1  0
  7 41  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  1 31  1  0
  1 32  1  0
 15 48  1  0
 17 49  1  0
 17 50  1  0
 17 51  1  0
 18 52  1  0
 18 53  1  0
 18 54  1  0
M  END


  Mrv1652309112203182D          

 30 31  0  0  1  0            999 V2000
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 11 19  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  1  6  0  0  0
  8 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  2  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
 26 28  1  0  0  0  0
 21 29  1  0  0  0  0
  4 29  1  0  0  0  0
 29 30  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0307870

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@@H](CC[C@@H]2[C@@H](OC(=O)C=C(C)C)C(=O)[C@H](C[C@]12C)C(C)=C)OC(=O)C=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C25H36O5/c1-14(2)11-21(26)29-20-10-9-19-24(30-22(27)12-15(3)4)23(28)18(16(5)6)13-25(19,8)17(20)7/h11-12,17-20,24H,5,9-10,13H2,1-4,6-8H3/t17-,18+,19+,20+,24+,25+/m0/s1

> <INCHI_KEY>
LMKIKXBJEVOGLH-HDQBBZGBSA-N

> <FORMULA>
C25H36O5

> <MOLECULAR_WEIGHT>
416.558

> <EXACT_MASS>
416.256274259

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
46.72774434651119

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,3R,4aR,5R,6R,8aS)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-decahydronaphthalen-1-yl 3-methylbut-2-enoate

> <JCHEM_LOGP>
6.021257375999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.835853412520805

> <JCHEM_PKA_STRONGEST_BASIC>
-6.504845215802173

> <JCHEM_POLAR_SURFACE_AREA>
69.67

> <JCHEM_REFRACTIVITY>
117.78679999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3R,4aR,5R,6R,8aS)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate

> <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      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   29                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8   19                                             
CONECT    7    6                                                            
CONECT    8    6    9   21                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   11    6   20                                                  
CONECT   20   19                                                            
CONECT   21    8   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   21    4   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   62    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,4AS,5R,7R,8ar)-1,8a-dimethyl-5-[(3-methylbut-2-enoyl)oxy]-6-oxo-7-(prop-1-en-2-yl)-decahydronaphthalen-2-yl 3-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₅H₃₆O₅

Average Mass

416.5580 Da

Monoisotopic Mass

416.25627 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@@H](CC[C@@H]2[C@@H](OC(=O)C=C(C)C)C(=O)[C@H](C[C@]12C)C(C)=C)OC(=O)C=C(C)C

InChI Identifier

InChI=1S/C25H36O5/c1-14(2)11-21(26)29-20-10-9-19-24(30-22(27)12-15(3)4)23(28)18(16(5)6)13-25(19,8)17(20)7/h11-12,17-20,24H,5,9-10,13H2,1-4,6-8H3/t17-,18+,19+,20+,24+,25+/m0/s1

InChI Key

LMKIKXBJEVOGLH-HDQBBZGBSA-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
Senecio provincialis	LOTUS Database	35616633
Senecio sandersonii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids

Alternative Parents

Substituents

Eremophilane sesquiterpenoid
Fatty acid ester
Alpha-acyloxy ketone
Dicarboxylic acid or derivatives
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Cyclic ketone
Ketone
Carboxylic acid ester
Carboxylic acid derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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

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

162991496

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate (NP0307870)

MOL for NP0307870 ((1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate)

3D MOL for NP0307870 ((1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate)

3D SDF for NP0307870 ((1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate)

3D-SDF for NP0307870 ((1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate)

PDB for NP0307870 ((1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate)

3D PDB for NP0307870 ((1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate)

SMILES for NP0307870 ((1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate)

INCHI for NP0307870 ((1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate)

Structure for NP0307870 ((1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate)

3D Structure for NP0307870 ((1r,3r,4ar,5r,6r,8as)-4a,5-dimethyl-6-[(3-methylbut-2-enoyl)oxy]-2-oxo-3-(prop-1-en-2-yl)-octahydronaphthalen-1-yl 3-methylbut-2-enoate)