NP-MRD: Showing NP-Card for 14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate (NP0264184)

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Record Information

Version

2.0

Created at

2022-09-08 07:37:23 UTC

Updated at

2022-09-08 07:37:23 UTC

NP-MRD ID

NP0264184

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate

Description

14,15-Dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]Octadecan-4-yl acetate belongs to the class of organic compounds known as lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. 14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate is found in Briareum asbestinum. 14,15-Dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]Octadecan-4-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251507382D          

 29 32  0  0  0  0            999 V2000
    1.3710   -2.4959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0775   -2.0698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9782   -1.2064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2211   -0.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1145   -0.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7818    0.5012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1616    1.0453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1909    1.2177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7749    1.9301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1840    2.6466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9499    1.9262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5632    0.2445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4180    0.6191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2827    0.8586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1205    0.5806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1523    1.4050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9212    0.7794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5521   -0.1642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3662   -0.0303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3871   -0.9830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7127   -1.4902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8689   -1.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3240   -2.1622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5497   -2.2663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7671   -2.5415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6594   -3.3594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3543   -0.8201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5208   -0.0294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5909   -0.6365    0.0000 C   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  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  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
  6 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  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 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
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  2  0  0  0  0
 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
 13 28  1  0  0  0  0
 27 29  1  0  0  0  0
  3 29  1  0  0  0  0
 12 29  1  0  0  0  0
M  END

     RDKit          3D

 63 66  0  0  0  0  0  0  0  0999 V2000
    4.8979    1.1921   -2.1409 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3472    0.5266   -0.9077 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0663    0.0313   -0.0253 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9916    0.4851   -0.7893 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3018   -0.1108    0.3213 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6957    0.6710    1.5375 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6547   -1.5734    0.4293 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5836   -2.4864   -0.0981 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3479   -2.3647    0.8295 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0251   -0.9765    0.8941 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8343   -0.0322   -0.0250 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1874    1.2502    0.4259 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1027    2.2424   -0.6484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2943    3.1050   -0.2069 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2272    3.4529    1.2479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0368    4.3296   -0.8925 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6094    2.6424   -0.6795 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4602    2.2333   -2.0271 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3337    1.5721    0.0450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3159    0.2139   -0.6069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2148   -0.7193   -0.3089 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6137   -1.0929   -1.6702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7802   -2.0101    0.0601 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0233   -3.1278    0.4027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8312   -4.0813    0.6971 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6104   -3.4322    0.4939 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4868   -4.6476    1.4459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3122   -0.4074    0.7799 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0232    0.9529    0.9911 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848    0.7130   -2.9986 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9819    1.1215   -2.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5186    2.2477   -2.0825 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9140    1.7259    1.2755 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6996    0.2571    1.8555 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0484    0.5322    2.4096 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7694   -1.8106    1.5247 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5977   -1.8347   -0.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3423   -2.3443   -1.1431 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9578   -3.5273    0.0551 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8278   -2.7001    1.8135 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3860   -0.5575    1.9030 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7442   -0.2744   -1.0656 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8842    1.6787    1.2055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3091    1.8098   -1.6204 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8080    2.8682   -0.7632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9147    2.9089    1.8965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2098    3.3334    1.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4713    4.5458    1.4120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4127    4.8917   -0.3730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2451    3.5805   -0.7969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2529    2.4502   -2.5642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4354    1.8806   -0.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2368    1.5562    1.1456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4352    0.4626   -1.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3082   -0.3017   -0.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9417   -1.9308   -1.6354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3188   -0.2374   -2.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5211   -1.4931   -2.2352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3157   -3.9161   -0.4893 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5898   -4.7458    1.6861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8149   -5.5668    0.9631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1127   -4.4959    2.3456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8562   -0.6657    1.7502 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
 26  9  1  0
  9  8  1  0
  8  7  1  0
  7  5  1  0
  5  6  1  0
  5  4  1  6
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  6
 14 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  1  0
 24 25  2  0
 21 28  1  0
 28 29  1  0
 28 10  1  0
 24 26  1  0
 10  9  1  0
 10 11  1  0
 29 12  1  0
 27 60  1  0
 27 61  1  0
 27 62  1  0
 26 59  1  6
  9 40  1  1
  8 38  1  0
  8 39  1  0
  7 36  1  0
  7 37  1  0
  6 33  1  0
  6 34  1  0
  6 35  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 11 42  1  6
 12 43  1  1
 13 44  1  0
 13 45  1  0
 15 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  6
 18 51  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  0
 20 55  1  0
 22 56  1  0
 22 57  1  0
 22 58  1  0
 28 63  1  1
 10 41  1  1
M  END


  Mrv1533004251507382D          

 29 32  0  0  0  0            999 V2000
    1.3710   -2.4959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0775   -2.0698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9782   -1.2064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2211   -0.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1145   -0.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7818    0.5012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1616    1.0453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1909    1.2177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7749    1.9301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1840    2.6466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9499    1.9262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5632    0.2445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4180    0.6191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2827    0.8586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1205    0.5806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1523    1.4050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9212    0.7794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5521   -0.1642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3662   -0.0303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3871   -0.9830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7127   -1.4902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8689   -1.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3240   -2.1622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5497   -2.2663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7671   -2.5415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6594   -3.3594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3543   -0.8201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5208   -0.0294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5909   -0.6365    0.0000 C   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  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  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
  6 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  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 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
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  2  0  0  0  0
 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
 13 28  1  0  0  0  0
 27 29  1  0  0  0  0
  3 29  1  0  0  0  0
 12 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0264184

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2CCC(C)(OC(C)=O)C3C4CC(C)(O)C(O)CCC(C)(OC1=O)C(O4)C23

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O7/c1-11-13-6-8-21(4,28-12(2)23)17-14-10-20(3,26)15(24)7-9-22(5,29-19(11)25)18(27-14)16(13)17/h11,13-18,24,26H,6-10H2,1-5H3

> <INCHI_KEY>
MATSVTSXOGSXAL-UHFFFAOYSA-N

> <FORMULA>
C22H34O7

> <MOLECULAR_WEIGHT>
410.507

> <EXACT_MASS>
410.230453435

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
43.519379220598196

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate

> <ALOGPS_LOGP>
1.77

> <JCHEM_LOGP>
0.9364875159999994

> <ALOGPS_LOGS>
-2.92

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.079034078168196

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.691344624944211

> <JCHEM_PKA_STRONGEST_BASIC>
-3.234910709082574

> <JCHEM_POLAR_SURFACE_AREA>
102.29

> <JCHEM_REFRACTIVITY>
103.06489999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.98e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       2.559  -4.659   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.878  -3.864   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.693  -2.252   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.279  -1.554   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.080  -0.010   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.326   0.936   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.168   1.951   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.090   2.273   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.313   3.603   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.077   4.940   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.773   3.596   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.785   0.456   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.380   1.156   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.994   1.603   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.558   1.084   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.618   2.623   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      11.053   1.455   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.364  -0.307   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      11.884  -0.056   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      10.056  -1.835   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.797  -2.782   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.222  -2.752   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.071  -4.036   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.626  -4.230   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.165  -4.744   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.964  -6.271   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.261  -1.531   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.572  -0.055   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.836  -1.188   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4   29                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   12                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    6   13   29                                                  
CONECT   13   12   14   28                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   27                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24    2   26                                                  
CONECT   26   25                                                            
CONECT   27   22   28   29                                                  
CONECT   28   27   13                                                       
CONECT   29   27    3   12                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Value	Source
14,15-Dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0,.0,]octadecan-4-yl acetic acid	Generator
14,15-Dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetic acid	Generator

Chemical Formula

C₂₂H₃₄O₇

Average Mass

410.5070 Da

Monoisotopic Mass

410.23045 Da

IUPAC Name

14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate

Traditional Name

14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate

CAS Registry Number

Not Available

SMILES

CC1C2CCC(C)(OC(C)=O)C3C4CC(C)(O)C(O)CCC(C)(OC1=O)C(O4)C23

InChI Identifier

InChI=1S/C22H34O7/c1-11-13-6-8-21(4,28-12(2)23)17-14-10-20(3,26)15(24)7-9-22(5,29-19(11)25)18(27-14)16(13)17/h11,13-18,24,26H,6-10H2,1-5H3

InChI Key

MATSVTSXOGSXAL-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

Species Name	Source	Reference
Briareum asbestinum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Not Available

Direct Parent

Lactones

Alternative Parents

Substituents

Caprolactone
Oxepane
Dicarboxylic acid or derivatives
Tertiary alcohol
Tetrahydrofuran
1,2-diol
Carboxylic acid ester
Lactone
Secondary alcohol
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organic oxide
Alcohol
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	1.77	ALOGPS
logP	0.94	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	13.69	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	102.29 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	103.06 m³·mol⁻¹	ChemAxon
Polarizability	43.52 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	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

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

73837520

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate (NP0264184)

MOL for NP0264184 (14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

3D MOL for NP0264184 (14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

3D SDF for NP0264184 (14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

3D-SDF for NP0264184 (14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

PDB for NP0264184 (14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

3D PDB for NP0264184 (14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

SMILES for NP0264184 (14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

INCHI for NP0264184 (14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

Structure for NP0264184 (14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

3D Structure for NP0264184 (14,15-dihydroxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)