NP-MRD: Showing NP-Card for 3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate (NP0170169)

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Record Information

Version

2.0

Created at

2022-09-03 06:16:28 UTC

Updated at

2022-09-03 06:16:28 UTC

NP-MRD ID

NP0170169

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate

Description

3-[(7S,9R)-7-(2H-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]Nona-1(6),2,4-trien-3-yl]propyl (2R)-2-methylbutanoate belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms. 3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate is found in Styrax officinalis. Based on a literature review very few articles have been published on 3-[(7S,9R)-7-(2H-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]Nona-1(6),2,4-trien-3-yl]propyl (2R)-2-methylbutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032208162D          

 30 34  0  0  1  0            999 V2000
   -3.6565   -7.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9420   -7.3419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2275   -7.7544    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2275   -8.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5131   -7.3419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5131   -6.5169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7986   -7.7544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0841   -7.3419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6303   -7.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3448   -7.3419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0593   -7.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7737   -7.3419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4882   -7.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2027   -7.3419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2027   -6.5169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4882   -8.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7737   -8.9919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0593   -8.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1862   -9.7063    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9007  -10.1188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9007   -9.2938    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6976   -9.0803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9111   -8.2834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7080   -8.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2914   -8.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0779   -9.4502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2810   -9.6637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7698   -9.8995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4109   -9.3803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1153   -8.6101    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  6  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  2  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
 13 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 11 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 22 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
M  END

     RDKit          3D

 56 60  0  0  0  0  0  0  0  0999 V2000
   -6.5415    0.6408   -1.1509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7820   -0.1333    0.1107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7044   -1.1703    0.3514 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6258   -2.1674   -0.7601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3896   -0.4336    0.3687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6621   -0.4504    1.3836 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0099    0.2550   -0.7531 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8096    0.9644   -0.8184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7471    2.0621    0.2213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4355    2.7742    0.0797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2523    1.8950    0.2711 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3626    1.2293   -0.7684 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4539    0.4096   -0.6181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0797   -0.2644   -1.6546 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6380   -0.1643   -2.9970 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9650    0.2442    0.6554 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3901    0.8885    1.7477 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2998    1.6959    1.5343 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3941    0.2704    2.6518 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3957   -1.1212    2.5923 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9461   -0.3449    1.5883 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3282   -0.5776    1.1456 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1087    0.5085    0.8096 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4209    0.3445    0.3853 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9984   -0.9047    0.2817 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2172   -1.9942    0.6182 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9095   -1.8182    1.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0217   -3.1083    0.4299 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1460   -2.7844   -0.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2574   -1.3861   -0.1024 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1281    0.0394   -1.9785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5330    1.0167   -1.4983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9439    1.5509   -0.9311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7889   -0.5791    0.0956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7617    0.5806    0.9669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8394   -1.6345    1.3454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9549   -2.9997   -0.4273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1411   -1.7111   -1.6340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6051   -2.6241   -0.9892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6815    1.4664   -1.8058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9135    0.2908   -0.7278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8147    1.7061    1.2576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5354    2.8167   -0.0014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3287    3.2521   -0.9237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3672    3.5665    0.8791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0542    1.3741   -1.7641 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6011    0.9276   -3.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3404   -0.6195   -3.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6023   -0.5431   -3.0855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1984    2.2321    2.3551 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7224    0.7938    3.5476 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7235    1.5214    0.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0547    1.1854    0.1153 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3059   -2.6791    1.3015 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0423   -3.3369   -0.0944 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8238   -2.9527   -1.4356 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  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 13 16  2  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 30  1  0
 30 29  1  0
 29 28  1  0
 28 26  1  0
 26 27  2  0
 18 11  1  0
 21 19  1  0
 27 22  1  0
 21 16  1  0
 26 25  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  1
  4 37  1  0
  4 38  1  0
  4 39  1  0
  8 40  1  0
  8 41  1  0
  9 42  1  0
  9 43  1  0
 10 44  1  0
 10 45  1  0
 12 46  1  0
 15 47  1  0
 15 48  1  0
 15 49  1  0
 18 50  1  0
 19 51  1  1
 23 52  1  0
 24 53  1  0
 29 55  1  0
 29 56  1  0
 27 54  1  0
M  END


  Mrv1652309032208162D          

 30 34  0  0  1  0            999 V2000
   -3.6565   -7.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9420   -7.3419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2275   -7.7544    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2275   -8.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5131   -7.3419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5131   -6.5169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7986   -7.7544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0841   -7.3419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6303   -7.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3448   -7.3419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0593   -7.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7737   -7.3419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4882   -7.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2027   -7.3419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2027   -6.5169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4882   -8.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7737   -8.9919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0593   -8.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1862   -9.7063    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9007  -10.1188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9007   -9.2938    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6976   -9.0803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9111   -8.2834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7080   -8.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2914   -8.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0779   -9.4502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2810   -9.6637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7698   -9.8995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4109   -9.3803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1153   -8.6101    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  6  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  2  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
 13 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 11 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 22 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0170169

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H](C)C(=O)OCCCC1=CC(OC)=C2C(=C1)[C@H]1O[C@@]21C1=CC=C2OCOC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H26O6/c1-4-14(2)23(25)27-9-5-6-15-10-17-21(20(11-15)26-3)24(22(17)30-24)16-7-8-18-19(12-16)29-13-28-18/h7-8,10-12,14,22H,4-6,9,13H2,1-3H3/t14-,22-,24+/m1/s1

> <INCHI_KEY>
ZCBJMXAFTFFAMW-DXHOUVOYSA-N

> <FORMULA>
C24H26O6

> <MOLECULAR_WEIGHT>
410.466

> <EXACT_MASS>
410.172938557

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
45.50361416676325

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[(7S,9R)-7-(2H-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0^{7,9}]nona-1,3,5-trien-3-yl]propyl (2R)-2-methylbutanoate

> <ALOGPS_LOGP>
4.46

> <JCHEM_LOGP>
4.618439781333332

> <ALOGPS_LOGS>
-5.34

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.102914781304256

> <JCHEM_POLAR_SURFACE_AREA>
66.52000000000001

> <JCHEM_REFRACTIVITY>
109.61020000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.87e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[(7S,9R)-7-(2H-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0^{7,9}]nona-1,3,5-trien-3-yl]propyl (2R)-2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.825 -14.475   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.492 -13.705   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.158 -14.475   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.158 -16.015   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.824 -13.705   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.824 -12.165   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -1.491 -14.475   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.157 -13.705   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.177 -14.475   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.510 -13.705   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.844 -14.475   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.178 -13.705   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.511 -14.475   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.845 -13.705   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       7.845 -12.165   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.511 -16.015   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.178 -16.785   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.844 -16.015   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.948 -18.119   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.281 -18.889   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.281 -17.349   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.769 -16.950   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.167 -15.462   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.655 -15.064   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.744 -16.153   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.345 -17.640   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.858 -18.039   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      12.637 -18.479   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      13.834 -17.510   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      13.282 -16.072   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                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13   17   21                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   11                                                       
CONECT   19   17   20   21                                                  
CONECT   20   19   21                                                       
CONECT   21   20   16   19   22                                             
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   30                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26   22                                                       
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   25                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Value	Source
3-[(7S,9R)-7-(2H-1,3-Benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0,]nona-1(6),2,4-trien-3-yl]propyl (2R)-2-methylbutanoic acid	Generator

Chemical Formula

C₂₄H₂₆O₆

Average Mass

410.4660 Da

Monoisotopic Mass

410.17294 Da

IUPAC Name

3-[(7S,9R)-7-(2H-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0^{7,9}]nona-1,3,5-trien-3-yl]propyl (2R)-2-methylbutanoate

Traditional Name

3-[(7S,9R)-7-(2H-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0^{7,9}]nona-1,3,5-trien-3-yl]propyl (2R)-2-methylbutanoate

CAS Registry Number

Not Available

SMILES

CC[C@@H](C)C(=O)OCCCC1=CC(OC)=C2C(=C1)[C@H]1O[C@@]21C1=CC=C2OCOC2=C1

InChI Identifier

InChI=1S/C24H26O6/c1-4-14(2)23(25)27-9-5-6-15-10-17-21(20(11-15)26-3)24(22(17)30-24)16-7-8-18-19(12-16)29-13-28-18/h7-8,10-12,14,22H,4-6,9,13H2,1-3H3/t14-,22-,24+/m1/s1

InChI Key

ZCBJMXAFTFFAMW-DXHOUVOYSA-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
Styrax officinalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzodioxoles

Sub Class

Not Available

Direct Parent

Benzodioxoles

Alternative Parents

Substituents

Isocoumaran
Benzodioxole
Anisole
Alkyl aryl ether
Fatty acid ester
Fatty acyl
Benzenoid
Carboxylic acid ester
Acetal
Carboxylic acid derivative
Oxacycle
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic oxygen 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	4.46	ALOGPS
logP	4.62	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	66.52 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	109.61 m³·mol⁻¹	ChemAxon
Polarizability	45.5 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

162981490

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate (NP0170169)

MOL for NP0170169 (3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate)

3D MOL for NP0170169 (3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate)

3D SDF for NP0170169 (3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate)

3D-SDF for NP0170169 (3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate)

PDB for NP0170169 (3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate)

3D PDB for NP0170169 (3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate)

SMILES for NP0170169 (3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate)

INCHI for NP0170169 (3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate)

Structure for NP0170169 (3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate)

3D Structure for NP0170169 (3-[(7s,9r)-7-(2h-1,3-benzodioxol-5-yl)-5-methoxy-8-oxatricyclo[4.3.0.0⁷,⁹]nona-1,3,5-trien-3-yl]propyl (2r)-2-methylbutanoate)