NP-MRD: Showing NP-Card for 2-[(1r,2s,4ar,5s,6r,8s,8ar)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(furan-3-yl)ethyl acetate (NP0228505)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 08:11:45 UTC

Updated at

2022-09-06 08:11:45 UTC

NP-MRD ID

NP0228505

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(1r,2s,4ar,5s,6r,8s,8ar)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(furan-3-yl)ethyl acetate

Description

Teugracilin C belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups. Based on a literature review very few articles have been published on Teugracilin C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062210112D          

 32 35  0  0  1  0            999 V2000
    1.2753    1.8883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0308    1.5570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6955    2.0457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1217    0.7370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8773    0.4057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9681   -0.4142    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2186    0.3718    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6632    0.9818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0246    0.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5801   -0.0621    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3861    0.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3296   -0.8481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3631   -1.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1472   -0.9583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4606   -1.7215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2782   -1.8317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5916   -2.5949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4092   -2.7051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0873   -3.2478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9564   -2.3745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1882   -3.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5069   -3.6314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8539   -3.1272    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1317   -2.3503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5236   -1.0242    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2731   -1.8103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4671   -1.9863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9116   -1.3764    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1057   -1.5525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1622   -0.5903    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3761   -0.3398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9861    0.2157    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
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  6  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
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  2  0  0  0  0
 12 25  1  0  0  0  0
  6 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
  6 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 30 32  1  1  0  0  0
M  END

     RDKit          3D

 66 69  0  0  0  0  0  0  0  0999 V2000
   -3.2752   -1.1245    3.8095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5681   -1.0531    2.3651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6330   -1.5806    1.9518 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7261   -0.4345    1.4539 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0271   -0.3795    0.0830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0381    0.3128   -0.7774 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8311    1.7665   -0.3793 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0253    2.4544   -0.1893 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0562    1.8650    0.8849 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1137    0.9955    1.0479 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2400    0.7738    2.5693 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2690   -0.2341    0.2529 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1181   -1.5028    1.0885 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5909   -0.4033   -0.4608 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8607   -0.4449    0.2637 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9145   -0.6853   -0.7351 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7706   -1.7496   -0.6285 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8467   -1.9846   -1.6596 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6219   -2.5072    0.3487 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3427    0.8614    0.8371 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5052    1.1207    2.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9976    2.4117    2.2405 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1086    2.8609    1.0327 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7234    1.9578    0.1389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6931   -0.2595   -0.9239 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8297   -1.5440   -1.6403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9322   -1.2152   -3.1406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6915    0.0620   -3.2854 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8894    1.1518   -3.7032 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6328    0.3972   -2.1882 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8896    1.0175   -2.3750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8664   -0.4581   -2.3424 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2170   -1.0797    4.0640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8495   -0.2946    4.3029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7342   -2.0702    4.2168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3586   -1.3627   -0.2928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9941    0.2229    0.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2862    2.2588   -1.1996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4528    2.2460    0.6878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7893    1.6826    1.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7810    2.9377    1.0282 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0098    1.6444    0.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7267    0.4931    3.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4775    1.7696    3.0582 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9584    0.0050    2.8351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2836   -1.3534    2.0804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4868   -2.2245    0.4681 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1127   -1.9819    1.1768 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6920    0.3691   -1.2796 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5574   -1.3991   -1.0094 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0129   -1.2785    0.9635 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5701   -1.5309   -2.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7807   -1.6304   -1.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9279   -3.0977   -1.7389 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193    0.5163    3.0335 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2431    2.9445    3.1417 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7381    2.1334   -0.9202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1614    0.4573   -1.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8297   -2.0109   -1.4180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0989   -2.3158   -1.5304 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1212   -1.0138   -3.4605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3764   -2.0698   -3.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3262   -0.0928   -4.2159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4582    1.9532   -3.5861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2008    1.3859   -3.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5287    1.3390   -1.5507 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
 10  9  1  0
  9  7  1  0
  7  8  1  0
  7  6  1  0
  6  5  1  1
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  6 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 31 32  1  0
 25 12  1  0
 12 13  1  1
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 15 20  1  0
 20 24  2  0
 24 23  1  0
 23 22  1  0
 22 21  2  0
 12 10  1  0
 21 20  1  0
 30  6  1  0
 30 32  1  1
 11 43  1  0
 11 44  1  0
 11 45  1  0
 10 42  1  6
  9 40  1  0
  9 41  1  0
  7 38  1  6
  8 39  1  0
  5 36  1  0
  5 37  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
 25 58  1  6
 26 59  1  0
 26 60  1  0
 27 61  1  0
 27 62  1  0
 28 63  1  6
 29 64  1  0
 31 65  1  0
 31 66  1  0
 13 46  1  0
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 15 51  1  1
 18 52  1  0
 18 53  1  0
 18 54  1  0
 24 57  1  0
 22 56  1  0
 21 55  1  0
M  END


  Mrv1652309062210112D          

 32 35  0  0  1  0            999 V2000
    1.2753    1.8883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0308    1.5570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6955    2.0457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1217    0.7370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8773    0.4057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9681   -0.4142    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2186    0.3718    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6632    0.9818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0246    0.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5801   -0.0621    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3861    0.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3296   -0.8481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3631   -1.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1472   -0.9583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4606   -1.7215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2782   -1.8317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5916   -2.5949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4092   -2.7051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0873   -3.2478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9564   -2.3745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1882   -3.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5069   -3.6314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8539   -3.1272    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1317   -2.3503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5236   -1.0242    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2731   -1.8103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4671   -1.9863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9116   -1.3764    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1057   -1.5525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1622   -0.5903    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3761   -0.3398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9861    0.2157    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
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  6  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
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  2  0  0  0  0
 12 25  1  0  0  0  0
  6 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
  6 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 30 32  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0228505

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@H](O)[C@]2(COC(C)=O)[C@H](CC[C@H](O)[C@]22CO2)[C@@]1(C)CC(OC(C)=O)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H34O8/c1-14-9-21(28)23(12-30-15(2)25)19(5-6-20(27)24(23)13-31-24)22(14,4)10-18(32-16(3)26)17-7-8-29-11-17/h7-8,11,14,18-21,27-28H,5-6,9-10,12-13H2,1-4H3/t14-,18?,19-,20+,21+,22+,23+,24-/m1/s1

> <INCHI_KEY>
DXKNBOULLLBFAY-UWTWJMKQSA-N

> <FORMULA>
C24H34O8

> <MOLECULAR_WEIGHT>
450.528

> <EXACT_MASS>
450.225368055

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
46.62674155729549

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(1R,2S,4aR,5S,6R,8S,8aR)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]-1-(furan-3-yl)ethyl acetate

> <JCHEM_LOGP>
1.233693995666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.615712408659618

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.802358447201648

> <JCHEM_PKA_STRONGEST_BASIC>
-2.869089209792662

> <JCHEM_POLAR_SURFACE_AREA>
118.73000000000002

> <JCHEM_REFRACTIVITY>
112.61829999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1R,2S,4aR,5S,6R,8S,8aR)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]-1-(furan-3-yl)ethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       2.381   3.525   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.791   2.906   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.032   3.819   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.961   1.376   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.371   0.757   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.541  -0.773   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.008   0.694   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.971   1.833   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       7.513   1.023   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.550  -0.116   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.054   0.213   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.082  -1.583   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.144  -3.122   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.608  -1.789   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.193  -3.213   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      11.719  -3.419   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      12.304  -4.844   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.830  -5.049   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      11.363  -6.063   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.252  -4.432   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.685  -5.910   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.413  -6.779   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.194  -5.837   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       7.713  -4.387   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.577  -1.912   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.110  -3.379   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.605  -3.708   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.568  -2.569   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       2.064  -2.898   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.036  -1.102   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.569  -0.634   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       3.707   0.403   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                                                       
CONECT    6    5    7   25   30                                             
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14   25                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   20                                                       
CONECT   25   12    6   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28    6   31   32                                             
CONECT   31   30   32                                                       
CONECT   32   31   30                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₄O₈

Average Mass

450.5280 Da

Monoisotopic Mass

450.22537 Da

IUPAC Name

2-[(1R,2S,4aR,5S,6R,8S,8aR)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]-1-(furan-3-yl)ethyl acetate

Traditional Name

2-[(1R,2S,4aR,5S,6R,8S,8aR)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2H-spiro[naphthalene-1,2'-oxirane]-5-yl]-1-(furan-3-yl)ethyl acetate

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@H](O)[C@]2(COC(C)=O)[C@H](CC[C@H](O)[C@]22CO2)[C@@]1(C)CC(OC(C)=O)C1=COC=C1

InChI Identifier

InChI=1S/C24H34O8/c1-14-9-21(28)23(12-30-15(2)25)19(5-6-20(27)24(23)13-31-24)22(14,4)10-18(32-16(3)26)17-7-8-29-11-17/h7-8,11,14,18-21,27-28H,5-6,9-10,12-13H2,1-4H3/t14-,18?,19-,20+,21+,22+,23+,24-/m1/s1

InChI Key

DXKNBOULLLBFAY-UWTWJMKQSA-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 dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Dicarboxylic acids and derivatives

Direct Parent

Dicarboxylic acids and derivatives

Alternative Parents

Substituents

Dicarboxylic acid or derivatives
Heteroaromatic compound
Furan
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	1.23	ChemAxon
pKa (Strongest Acidic)	13.8	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	118.73 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	112.62 m³·mol⁻¹	ChemAxon
Polarizability	46.63 Å³	ChemAxon
Number of Rings	4	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

15109174

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(1r,2s,4ar,5s,6r,8s,8ar)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(furan-3-yl)ethyl acetate (NP0228505)

MOL for NP0228505 (2-[(1r,2s,4ar,5s,6r,8s,8ar)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(furan-3-yl)ethyl acetate)

3D MOL for NP0228505 (2-[(1r,2s,4ar,5s,6r,8s,8ar)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(furan-3-yl)ethyl acetate)

3D SDF for NP0228505 (2-[(1r,2s,4ar,5s,6r,8s,8ar)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(furan-3-yl)ethyl acetate)

3D-SDF for NP0228505 (2-[(1r,2s,4ar,5s,6r,8s,8ar)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(furan-3-yl)ethyl acetate)

PDB for NP0228505 (2-[(1r,2s,4ar,5s,6r,8s,8ar)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(furan-3-yl)ethyl acetate)

3D PDB for NP0228505 (2-[(1r,2s,4ar,5s,6r,8s,8ar)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(furan-3-yl)ethyl acetate)

SMILES for NP0228505 (2-[(1r,2s,4ar,5s,6r,8s,8ar)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(furan-3-yl)ethyl acetate)

INCHI for NP0228505 (2-[(1r,2s,4ar,5s,6r,8s,8ar)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(furan-3-yl)ethyl acetate)

Structure for NP0228505 (2-[(1r,2s,4ar,5s,6r,8s,8ar)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(furan-3-yl)ethyl acetate)

3D Structure for NP0228505 (2-[(1r,2s,4ar,5s,6r,8s,8ar)-8a-[(acetyloxy)methyl]-2,8-dihydroxy-5,6-dimethyl-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-5-yl]-1-(furan-3-yl)ethyl acetate)