NP-MRD: Showing NP-Card for 2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate (NP0305845)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 21:58:28 UTC

Updated at

2022-09-10 21:58:29 UTC

NP-MRD ID

NP0305845

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate

Description

2,5,10,11,19-Pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]Nonadecan-14-yl acetate belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms. 2,5,10,11,19-Pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]Nonadecan-14-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201505312D          

 32 36  0  0  0  0            999 V2000
    4.5720   -2.9334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6998   -2.1183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4696   -1.8216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0579   -1.6001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1858   -0.7851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9555   -0.4883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0834    0.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6016    0.9687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9597    1.4869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4415    0.8450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9556    1.5117    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6717    0.5482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0271    1.1195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1508    1.9352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1310    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6263   -0.2710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8050   -0.3940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2957   -1.0430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7355    0.3649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0577    0.1381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3732    1.0856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0020    1.6094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6989    1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2219    1.7976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7304    0.3147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5373    0.4868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0928   -0.5851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5563   -1.2119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9051   -0.7736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0862   -1.5785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5438   -0.2668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5404   -1.0918    0.0000 C   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
  5  6  1  0  0  0  0
  6  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
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 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  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
  5 31  1  0  0  0  0
 12 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END

     RDKit          3D

 64 68  0  0  0  0  0  0  0  0999 V2000
    3.9404   -2.2349    2.2207 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6655   -1.8450    0.8217 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0341   -2.6236   -0.0916 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0200   -0.6569    0.5072 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7349   -0.2443   -0.8141 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6184    0.9753   -1.0480 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4163    1.7765    0.2224 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8326    3.0904    0.1691 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5280    3.4292   -0.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0137    2.1011    0.4280 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6889    2.3436    1.7555 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9732    1.4021   -0.4087 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3194    1.7184    0.3253 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7741    3.0337    0.0205 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4427    0.8225    0.0609 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8010    1.3723   -0.2509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5193    0.1869   -0.9177 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8955    0.4523   -0.7334 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2342   -1.1301   -0.3201 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9538   -2.1868   -1.0779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8391   -1.0412    0.9665 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9608   -0.3241    1.7374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6041   -0.3012    1.0266 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5888   -0.4850    2.0702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8519   -1.4845    0.1083 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9917   -2.5838    0.9969 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8358   -1.7302   -0.9131 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2189   -1.4480   -2.2271 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5032   -1.1306   -0.5841 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0511   -1.9022    0.1830 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2580    0.0974   -0.9560 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1402    0.0857   -2.5143 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9954   -2.0046    2.5205 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7998   -3.3212    2.4052 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2317   -1.7281    2.9355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0621   -1.0426   -1.5131 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6491    0.6250   -1.0643 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3127    1.6127   -1.8672 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8754    1.2576    1.0986 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4063    3.3608   -1.2675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1122    4.3192    0.3138 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4154    2.9068    2.1219 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8733    2.0935   -1.3197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1543    1.8168    1.4414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4609    3.2674    0.6797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1803    0.5009   -1.0030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7026    2.1435   -1.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3550    1.8477    0.5279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2587    0.1727   -1.9937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3115   -0.2020   -0.1175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4827   -3.1789   -1.0689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9966   -2.3083   -0.6693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1153   -1.8914   -2.1552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8275   -0.9662    2.6653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2866    0.6278    2.1226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9889   -0.0252    3.0349 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3895   -0.0408    1.9706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5707   -1.5827    2.3483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8558   -3.0426    0.8672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7270   -2.8689   -0.9618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9357   -2.0901   -2.8903 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0305    0.5547   -2.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2793    0.6327   -2.8696 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1902   -0.9810   -2.8500 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  1
 10 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  6
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  1
 23 25  1  0
 25 26  1  1
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 29 31  1  0
 31 32  1  6
 31  5  1  0
 10  7  1  0
 31 12  1  0
 23 15  1  0
 25 19  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  5 36  1  6
  6 37  1  0
  6 38  1  0
  7 39  1  1
  9 40  1  0
  9 41  1  0
 11 42  1  0
 12 43  1  6
 13 44  1  1
 14 45  1  0
 15 46  1  6
 16 47  1  0
 16 48  1  0
 17 49  1  6
 18 50  1  0
 20 51  1  0
 20 52  1  0
 20 53  1  0
 22 54  1  0
 22 55  1  0
 24 56  1  0
 24 57  1  0
 24 58  1  0
 26 59  1  0
 27 60  1  6
 28 61  1  0
 32 62  1  0
 32 63  1  0
 32 64  1  0
M  END


  Mrv1533004201505312D          

 32 36  0  0  0  0            999 V2000
    4.5720   -2.9334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6998   -2.1183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4696   -1.8216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0579   -1.6001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1858   -0.7851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9555   -0.4883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0834    0.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6016    0.9687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9597    1.4869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4415    0.8450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9556    1.5117    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6717    0.5482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0271    1.1195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1508    1.9352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1310    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6263   -0.2710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8050   -0.3940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2957   -1.0430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7355    0.3649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0577    0.1381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3732    1.0856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0020    1.6094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6989    1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2219    1.7976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7304    0.3147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5373    0.4868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0928   -0.5851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5563   -1.2119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9051   -0.7736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0862   -1.5785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5438   -0.2668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5404   -1.0918    0.0000 C   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
  5  6  1  0  0  0  0
  6  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
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 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  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
  5 31  1  0  0  0  0
 12 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0305845

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1CC2OCC2(O)C2C(O)C3CC(O)C4(C)OCC3(C)C4(O)C(O)C(=O)C12C

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O10/c1-9(23)32-12-6-13-21(28,8-30-13)15-14(25)10-5-11(24)20(4)22(29,18(10,2)7-31-20)17(27)16(26)19(12,15)3/h10-15,17,24-25,27-29H,5-8H2,1-4H3

> <INCHI_KEY>
PPOAAMJIUQKYNN-UHFFFAOYSA-N

> <FORMULA>
C22H32O10

> <MOLECULAR_WEIGHT>
456.488

> <EXACT_MASS>
456.19954723

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
44.36963203500508

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate

> <ALOGPS_LOGP>
-1.00

> <JCHEM_LOGP>
-2.4941248883333333

> <ALOGPS_LOGS>
-1.33

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.824322956580158

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.20451552653347

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0057725632279064

> <JCHEM_POLAR_SURFACE_AREA>
162.98000000000002

> <JCHEM_REFRACTIVITY>
105.47399999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.13e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0       8.534  -5.476   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.773  -3.954   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      10.210  -3.400   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       7.575  -2.987   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.813  -1.465   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.250  -0.911   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.489   0.610   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.456   1.808   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.258   2.776   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.291   1.577   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       7.384   2.822   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.854   1.023   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.651   2.090   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.881   3.612   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.978   1.334   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.036  -0.506   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.503  -0.735   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.552  -1.947   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.373   0.681   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.108   0.258   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.697   2.026   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.870   3.004   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.171   2.164   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.148   3.355   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.230   0.587   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.736   0.909   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.907  -1.092   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.905  -2.262   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.423  -1.444   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       5.761  -2.947   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.615  -0.498   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.609  -2.038   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   31                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    7   11   12                                             
CONECT   11   10                                                            
CONECT   12   10   13   31                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21   25                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   15   24   25                                             
CONECT   24   23                                                            
CONECT   25   23   19   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29    5   12   32                                             
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Value	Source
2,5,10,11,19-Pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0,.0,.0,]nonadecan-14-yl acetic acid	Generator
2,5,10,11,19-Pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetic acid	Generator

Chemical Formula

C₂₂H₃₂O₁₀

Average Mass

456.4880 Da

Monoisotopic Mass

456.19955 Da

IUPAC Name

2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate

Traditional Name

2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1CC2OCC2(O)C2C(O)C3CC(O)C4(C)OCC3(C)C4(O)C(O)C(=O)C12C

InChI Identifier

InChI=1S/C22H32O10/c1-9(23)32-12-6-13-21(28,8-30-13)15-14(25)10-5-11(24)20(4)22(29,18(10,2)7-31-20)17(27)16(26)19(12,15)3/h10-15,17,24-25,27-29H,5-8H2,1-4H3

InChI Key

PPOAAMJIUQKYNN-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxepanes

Sub Class

Not Available

Direct Parent

Oxepanes

Alternative Parents

Substituents

Oxepane
Cyclic alcohol
Tertiary alcohol
Tetrahydrofuran
Carboxylic acid ester
Ketone
Oxetane
Secondary alcohol
Oxacycle
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Polyol
Carboxylic acid derivative
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Alcohol
Organic oxide
Carbonyl group
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	ALOGPS
logP	-2.5	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	10.2	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	162.98 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	105.47 m³·mol⁻¹	ChemAxon
Polarizability	44.37 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

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

14866185

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate (NP0305845)

MOL for NP0305845 (2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate)

3D MOL for NP0305845 (2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate)

3D SDF for NP0305845 (2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate)

3D-SDF for NP0305845 (2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate)

PDB for NP0305845 (2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate)

3D PDB for NP0305845 (2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate)

SMILES for NP0305845 (2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate)

INCHI for NP0305845 (2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate)

Structure for NP0305845 (2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate)

3D Structure for NP0305845 (2,5,10,11,19-pentahydroxy-6,9,13-trimethyl-12-oxo-7,17-dioxapentacyclo[11.6.0.0³,⁹.0⁶,¹⁰.0¹⁶,¹⁹]nonadecan-14-yl acetate)