NP-MRD: Showing NP-Card for 5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid (NP0146428)

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Record Information

Version

2.0

Created at

2022-09-02 01:49:31 UTC

Updated at

2022-09-02 01:49:31 UTC

NP-MRD ID

NP0146428

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid

Description

5-[2-(Furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-1,2,3,4,4a,5,8,8a-octahydronaphthalene-1-carboxylic acid belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations. 5-[2-(Furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-1,2,3,4,4a,5,8,8a-octahydronaphthalene-1-carboxylic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171503512D          

 30 32  0  0  0  0            999 V2000
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  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
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   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 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    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    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
    1.4760    2.5474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309    3.3320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559    3.3320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8109    2.5474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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
    1.9592   -2.2820    0.0000 C   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
    0.8986   -2.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0862   -2.1387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1808   -3.0572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  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
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 15 19  1  0  0  0  0
 12 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
  8 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 20 30  1  0  0  0  0
M  END

     RDKit          3D

 64 66  0  0  0  0  0  0  0  0999 V2000
    4.8414    3.3581   -1.2958 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9553    3.0988    0.1587 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2429    2.1986    0.8042 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4363    2.0196    2.2646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2818    1.4055    0.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1330    1.5716   -1.1862 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4821    0.4322    0.6278 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5353   -0.3470   -0.1261 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7748   -1.7853    0.0258 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6282   -2.7063    0.1122 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8589   -3.6236    1.3372 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5711   -3.6710   -1.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4170   -3.9649   -1.6858 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7805   -4.2986   -1.3369 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7043   -2.0386    0.3705 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8535   -2.9501    0.3312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7864   -2.6338   -0.7669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9824   -1.3849   -1.1102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9181   -1.0571   -2.2085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2472   -0.2949   -0.3753 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9522    0.2045    0.7940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5484    1.5030    1.4205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7838    2.6698    0.5536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9332    3.2803   -0.3034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6360    4.3443   -0.8740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8173    4.3339   -0.3661 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9945    3.3752    0.4904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8367   -0.7072   -0.3437 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3888   -0.7777   -1.7890 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1724    0.1475    0.3612 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5609    4.1648   -1.5732 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8492    3.7438   -1.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1428    2.4861   -1.9129 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6658    3.6780    0.7459 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5405    1.8871    2.4587 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1540    2.9675    2.7559 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9449    1.1298    2.6588 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6289    0.0185   -1.1654 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4200   -2.1246   -0.8429 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4907   -1.9172    0.8962 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6167   -2.9870    2.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9433   -3.9014    1.3949 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2044   -4.4965    1.2629 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1436   -5.0629   -0.7680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6224   -1.7345    1.4694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5752   -4.0353    0.3430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5090   -2.8853    1.2629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3116   -3.4250   -1.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9525   -1.2967   -1.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6983   -1.6539   -3.1358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8066    0.0092   -2.5226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2450    0.6131   -1.1201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9814   -0.5268    1.6586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0403    0.3410    0.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2443    1.6429    2.3094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5214    1.5172    1.7778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9031    3.0726   -0.5633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1766    5.0046   -1.6065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8939    3.1520    1.0526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1585    0.2633   -2.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4618   -1.3997   -2.0032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2448   -1.0876   -2.4583 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1499   -0.0319    1.4794 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0731    1.1727    0.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
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 25 24  2  0
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 18 17  2  0
 17 16  1  0
 16 15  1  0
 15 10  1  0
 10 11  1  0
 10  9  1  0
 10 12  1  6
 12 14  1  0
 12 13  2  0
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 15 28  1  0
 24 23  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  4 35  1  0
  4 36  1  0
  4 37  1  0
  8 38  1  6
 30 63  1  0
 30 64  1  0
 29 60  1  0
 29 61  1  0
 29 62  1  0
 20 52  1  6
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 27 59  1  0
 25 58  1  0
 24 57  1  0
 19 49  1  0
 19 50  1  0
 19 51  1  0
 17 48  1  0
 16 46  1  0
 16 47  1  0
 15 45  1  1
 11 41  1  0
 11 42  1  0
 11 43  1  0
  9 39  1  0
  9 40  1  0
 14 44  1  0
M  END


  Mrv1533004171503512D          

 30 32  0  0  0  0            999 V2000
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  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
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   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 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    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    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
    1.4760    2.5474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309    3.3320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559    3.3320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8109    2.5474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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
    1.9592   -2.2820    0.0000 C   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
    0.8986   -2.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0862   -2.1387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1808   -3.0572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  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
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 15 19  1  0  0  0  0
 12 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
  8 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 20 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0146428

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C(C)C(=O)OC1CC2(C)C(CCC3=COC=C3)C(C)=CCC2C(C)(C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O5/c1-6-16(2)22(26)30-19-13-24(4)20(9-8-18-11-12-29-15-18)17(3)7-10-21(24)25(5,14-19)23(27)28/h6-7,11-12,15,19-21H,8-10,13-14H2,1-5H3,(H,27,28)

> <INCHI_KEY>
XTFVHRXNAYKKTD-UHFFFAOYSA-N

> <FORMULA>
C25H34O5

> <MOLECULAR_WEIGHT>
414.542

> <EXACT_MASS>
414.240624195

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
45.88800691653922

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-1,2,3,4,4a,5,8,8a-octahydronaphthalene-1-carboxylic acid

> <ALOGPS_LOGP>
5.47

> <JCHEM_LOGP>
5.903531787333334

> <ALOGPS_LOGS>
-4.63

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.9002519338152055

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7841541990964096

> <JCHEM_POLAR_SURFACE_AREA>
76.74

> <JCHEM_REFRACTIVITY>
116.57589999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.80e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         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   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.334  -2.310   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+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   0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.755   4.755   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.231   6.220   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.771   6.220   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.247   4.755   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.657  -4.260   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.677  -4.260   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.161  -3.992   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       2.204  -5.707   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+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   26                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12   23                                             
CONECT   11   10                                                            
CONECT   12   10   13   20                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   15                                                       
CONECT   20   12   21   30                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   10   24                                                  
CONECT   24   23   25   26   27                                             
CONECT   25   24                                                            
CONECT   26   24    8                                                       
CONECT   27   24   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   20                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Value	Source
5-[2-(Furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-1,2,3,4,4a,5,8,8a-octahydronaphthalene-1-carboxylate	Generator

Chemical Formula

C₂₅H₃₄O₅

Average Mass

414.5420 Da

Monoisotopic Mass

414.24062 Da

IUPAC Name

5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-1,2,3,4,4a,5,8,8a-octahydronaphthalene-1-carboxylic acid

Traditional Name

5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC=C(C)C(=O)OC1CC2(C)C(CCC3=COC=C3)C(C)=CCC2C(C)(C1)C(O)=O

InChI Identifier

InChI=1S/C25H34O5/c1-6-16(2)22(26)30-19-13-24(4)20(9-8-18-11-12-29-15-18)17(3)7-10-21(24)25(5,14-19)23(27)28/h6-7,11-12,15,19-21H,8-10,13-14H2,1-5H3,(H,27,28)

InChI Key

XTFVHRXNAYKKTD-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Colensane and clerodane diterpenoids

Alternative Parents

Substituents

Clerodane diterpenoid
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Furan
Heteroaromatic compound
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid
Carboxylic acid derivative
Carbonyl group
Organic oxide
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
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	5.47	ALOGPS
logP	5.9	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	4.9	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	76.74 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	116.58 m³·mol⁻¹	ChemAxon
Polarizability	45.89 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid (NP0146428)

MOL for NP0146428 (5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid)

3D MOL for NP0146428 (5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid)

3D SDF for NP0146428 (5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid)

3D-SDF for NP0146428 (5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid)

PDB for NP0146428 (5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid)

3D PDB for NP0146428 (5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid)

SMILES for NP0146428 (5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid)

INCHI for NP0146428 (5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid)

Structure for NP0146428 (5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid)

3D Structure for NP0146428 (5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid)