NP-MRD: Showing NP-Card for (2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate (NP0190291)

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Record Information

Version

2.0

Created at

2022-09-04 06:56:02 UTC

Updated at

2022-09-04 06:56:02 UTC

NP-MRD ID

NP0190291

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate

Description

Ancepsenolide acetate belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain. (2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate is found in Pterogorgia citrina. Based on a literature review very few articles have been published on ancepsenolide acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042208562D          

 30 31  0  0  1  0            999 V2000
    3.0388   -8.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2103   -7.2178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5973   -6.6657    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9950   -6.9628    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1665   -6.1559    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6145   -5.5428    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7940   -5.6290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0270   -4.8283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8339   -4.9998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4470   -4.4478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9202   -5.8203    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6346   -6.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3491   -5.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0636   -6.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7781   -5.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4925   -6.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2070   -5.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9215   -6.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6359   -5.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3504   -6.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0649   -5.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7794   -6.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4938   -5.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2083   -6.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9620   -5.8972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5140   -6.5103    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.3345   -6.4241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1015   -7.2248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2945   -7.0533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6814   -7.6053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  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  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  6  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  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  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  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  2  0  0  0  0
M  END

     RDKit          3D

 68 69  0  0  0  0  0  0  0  0999 V2000
   -6.5743   -1.1001    2.5140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9862   -0.1179    1.4910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1031    0.4581    1.4930 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1111    0.1914    0.4779 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3580    1.0950   -0.5541 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.2752    0.3035   -1.8551 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7179   -1.0777   -1.6448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5150    1.0897   -2.7185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8082    2.0622   -2.0568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8767    2.7838   -2.5028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3149    2.1551   -0.6722 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2589    2.1848    0.3587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3609    1.0324    0.5334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5239    0.6595   -0.6637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6277   -0.5235   -0.3928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6597   -0.2912    0.7262 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1726   -1.5443    0.8958 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9430   -1.8866   -0.3509 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8723   -0.7487   -0.6981 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8645   -0.4784    0.4160 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7405    0.6596   -0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7839    1.0374    0.9523 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8165    0.0778    1.3614 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7365   -0.4091    0.3091 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0749   -0.1995    0.2938 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7190   -0.8386   -0.8448 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.4243    0.1487   -1.7533 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6838   -1.4564   -1.5364 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4882   -1.2157   -0.8624 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3730   -1.6746   -1.2751 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8407   -2.1313    2.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1162   -0.9423    3.4679 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.3841    1.5565   -0.4612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3344    0.2084   -2.2463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1700   -1.1244   -0.6694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9797   -1.2933   -2.4533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5432   -1.7991   -1.6441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8842    3.1446   -0.5423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6099    3.1069    0.2858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7831    2.3341    1.3568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6804    1.3062    1.4106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9105    0.1564    0.9203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2107    0.3242   -1.4637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9237    1.5467   -0.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2286   -1.4113   -0.1607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0894   -0.7286   -1.3483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0338    0.6087    0.5967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2819   -0.2208    1.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7968   -1.5251    1.7957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5752   -2.3729    1.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6071   -2.7628   -0.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3134   -2.1949   -1.1849 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3657   -1.0007   -1.6446 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2596    0.1723   -0.9171 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3120   -0.2330    1.3611 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4731   -1.3812    0.5611 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0312    0.5381   -1.0561 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0053    1.5571   -0.0544 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2862    1.4922    1.8739 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3432    1.9520    0.5490 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4024   -0.7915    1.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4591    0.5951    2.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5770    0.3701    1.0384 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4598   -1.6307   -0.5351 H   0  0  0  0  0  0  0  0  0  0  0  0
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   10.5351    0.0059   -1.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
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 29 30  2  0
 29 24  1  0
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 11  5  1  0
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  4  2  1  0
  2  1  1  0
  2  3  2  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  2  0
 24 25  2  0
 25 26  1  0
  9 11  1  0
 27 66  1  0
 27 67  1  0
 27 68  1  0
 26 65  1  1
 23 62  1  0
 23 63  1  0
 22 60  1  0
 22 61  1  0
 21 58  1  0
 21 59  1  0
 20 56  1  0
 20 57  1  0
 19 54  1  0
 19 55  1  0
 18 52  1  0
 18 53  1  0
 17 50  1  0
 17 51  1  0
 16 48  1  0
 16 49  1  0
 15 46  1  0
 15 47  1  0
 14 44  1  0
 14 45  1  0
 13 42  1  0
 13 43  1  0
 12 40  1  0
 12 41  1  0
 11 39  1  6
  5 34  1  1
  1 31  1  0
  1 32  1  0
  1 33  1  0
  6 35  1  6
  7 36  1  0
  7 37  1  0
  7 38  1  0
 25 64  1  0
M  END


  Mrv1652309042208562D          

 30 31  0  0  1  0            999 V2000
    3.0388   -8.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2103   -7.2178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5973   -6.6657    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9950   -6.9628    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1665   -6.1559    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6145   -5.5428    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7940   -5.6290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0270   -4.8283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8339   -4.9998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4470   -4.4478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9202   -5.8203    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6346   -6.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3491   -5.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.7781   -5.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4925   -6.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2070   -5.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9215   -6.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6359   -5.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3504   -6.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0649   -5.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7794   -6.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4938   -5.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2083   -6.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9620   -5.8972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5140   -6.5103    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.3345   -6.4241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1015   -7.2248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2945   -7.0533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6814   -7.6053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  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  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  6  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  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
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 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0190291

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1OC(=O)C(CCCCCCCCCCCC[C@@H]2[C@H](OC(C)=O)[C@H](C)OC2=O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H38O6/c1-17-16-20(23(26)28-17)14-12-10-8-6-4-5-7-9-11-13-15-21-22(30-19(3)25)18(2)29-24(21)27/h16-18,21-22H,4-15H2,1-3H3/t17-,18-,21+,22+/m0/s1

> <INCHI_KEY>
FXNASNSEMIBZQX-MOXQZVSFSA-N

> <FORMULA>
C24H38O6

> <MOLECULAR_WEIGHT>
422.562

> <EXACT_MASS>
422.266838944

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
49.53549558726104

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,4R)-2-methyl-4-{12-[(5S)-5-methyl-2-oxo-2,5-dihydrofuran-3-yl]dodecyl}-5-oxooxolan-3-yl acetate

> <JCHEM_LOGP>
5.961943721999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.470827754881434

> <JCHEM_PKA_STRONGEST_BASIC>
-6.514040627354536

> <JCHEM_POLAR_SURFACE_AREA>
78.9

> <JCHEM_REFRACTIVITY>
113.89150000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,4R)-2-methyl-4-{12-[(5S)-5-methyl-2-oxo-5H-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       5.672 -14.980   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.993 -13.473   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.848 -12.443   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       7.457 -12.997   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.777 -11.491   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.747 -10.346   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.215 -10.507   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       7.517  -9.013   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.023  -9.333   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      10.168  -8.303   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       9.184 -10.865   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.518 -11.635   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.852 -10.865   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.185 -11.635   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.519 -10.865   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      15.853 -11.635   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.186 -10.865   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      18.520 -11.635   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      19.854 -10.865   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      21.187 -11.635   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      22.521 -10.865   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      23.855 -11.635   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      25.188 -10.865   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      26.522 -11.635   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      27.929 -11.008   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      28.959 -12.153   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      30.491 -11.992   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      28.189 -13.486   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      26.683 -13.166   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      25.539 -14.197   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    5   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   24   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   62    0
END

View in JSmol

Synonyms

Value	Source
Ancepsenolide acetic acid	Generator

Chemical Formula

C₂₄H₃₈O₆

Average Mass

422.5620 Da

Monoisotopic Mass

422.26684 Da

IUPAC Name

(2S,3S,4R)-2-methyl-4-{12-[(5S)-5-methyl-2-oxo-2,5-dihydrofuran-3-yl]dodecyl}-5-oxooxolan-3-yl acetate

Traditional Name

(2S,3S,4R)-2-methyl-4-{12-[(5S)-5-methyl-2-oxo-5H-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@@H]1OC(=O)C(CCCCCCCCCCCC[C@@H]2[C@H](OC(C)=O)[C@H](C)OC2=O)=C1

InChI Identifier

InChI=1S/C24H38O6/c1-17-16-20(23(26)28-17)14-12-10-8-6-4-5-7-9-11-13-15-21-22(30-19(3)25)18(2)29-24(21)27/h16-18,21-22H,4-15H2,1-3H3/t17-,18-,21+,22+/m0/s1

InChI Key

FXNASNSEMIBZQX-MOXQZVSFSA-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
Pterogorgia citrina	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Annonaceous acetogenins

Alternative Parents

Substituents

Annonaceae acetogenin skeleton
Tricarboxylic acid or derivatives
2-furanone
Gamma butyrolactone
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Carbonyl group
Organic oxygen compound
Organic oxide
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	5.96	ChemAxon
pKa (Strongest Acidic)	13.47	ChemAxon
pKa (Strongest Basic)	-6.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	78.9 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	113.89 m³·mol⁻¹	ChemAxon
Polarizability	49.54 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

10474274

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23427796

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate (NP0190291)

MOL for NP0190291 ((2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate)

3D MOL for NP0190291 ((2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate)

3D SDF for NP0190291 ((2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate)

3D-SDF for NP0190291 ((2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate)

PDB for NP0190291 ((2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate)

3D PDB for NP0190291 ((2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate)

SMILES for NP0190291 ((2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate)

INCHI for NP0190291 ((2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate)

Structure for NP0190291 ((2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate)

3D Structure for NP0190291 ((2s,3s,4r)-2-methyl-4-{12-[(5s)-5-methyl-2-oxo-5h-furan-3-yl]dodecyl}-5-oxooxolan-3-yl acetate)