NP-MRD: Showing NP-Card for (2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate (NP0314343)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 12:23:58 UTC

Updated at

2022-09-11 12:23:58 UTC

NP-MRD ID

NP0314343

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate

Description

CHEMBL457830 belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. (2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate is found in Botrytis cinerea. Based on a literature review very few articles have been published on CHEMBL457830.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112214232D          

 30 31  0  0  1  0            999 V2000
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5737   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.8605   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.8605   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.2894   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0039   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0039   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4315   -3.3000    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  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 28 27  1  1  0  0  0
 16 28  1  0  0  0  0
 28 29  1  0  0  0  0
 12 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END

     RDKit          3D

 66 67  0  0  0  0  0  0  0  0999 V2000
    7.8796    1.4196   -1.5097 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7421    0.4232   -0.3787 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4331    0.7030    0.4092 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3224   -0.2843    1.5099 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1540   -0.2131    2.4052 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4611   -1.2562    3.4158 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8254   -0.6481    1.8628 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3621    0.1032    0.6772 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9527   -0.4030    0.3888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7877   -1.6253    0.2016 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8601    0.4386    0.3302 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4480   -0.0242    0.0703 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3584    0.1600    1.2536 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1916   -0.9999    2.2466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6551    0.3457    1.0332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2112    0.3179   -0.1993 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4651    1.7846   -0.5946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5877   -0.3507   -0.2195 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6281    0.5734   -0.4695 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6563    0.8204    0.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7355    1.7973    0.1387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6172    0.1546    1.5158 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6548   -1.3760   -1.3319 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.0375   -1.9428   -1.4467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2717   -0.6332   -2.5842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0479   -0.5600   -3.5557 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0037   -0.0579   -2.5413 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3496   -0.2431   -1.3057 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0540    0.5312   -1.2003 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1499    0.3495   -2.3733 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4709    2.3914   -1.1758 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9692    1.5261   -1.7692 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3326    1.0031   -2.4016 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6038    0.4580    0.3177 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6998   -0.5895   -0.8041 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6147    1.7462    0.8382 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6266    0.8116   -0.2870 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3002   -0.2243    2.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3121   -1.3111    1.0104 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0759    0.7011    3.0181 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7224   -1.1603    4.1042 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8652   -1.7722    1.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0649   -0.6249    2.7086 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9099   -0.3838   -0.2150 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4536    1.1657    0.6561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3948   -1.1234   -0.0883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9495    1.0536    1.8152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0846   -1.1012    2.8988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3019   -0.8776    2.8762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1534   -1.9519    1.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7709    2.4651   -0.0370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4864    2.1061   -0.2959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4087    1.9278   -1.6871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7103   -0.8387    0.7719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4019    2.8473    0.3247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1007    1.7645   -0.9019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6347    1.5571    0.7800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9639   -2.2441   -1.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1353   -2.9034   -0.8930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8232   -1.2758   -1.0870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1844   -2.2122   -2.5346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1373   -1.3131   -1.2028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2219    1.6180   -1.0555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1263   -0.6866   -2.7603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5355    0.9713   -3.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8470    0.7374   -2.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  6
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 18 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 29 12  1  0
 28 16  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  5 40  1  1
  6 41  1  0
  7 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
 12 46  1  6
 13 47  1  1
 14 48  1  0
 14 49  1  0
 14 50  1  0
 17 51  1  0
 17 52  1  0
 17 53  1  0
 18 54  1  1
 21 55  1  0
 21 56  1  0
 21 57  1  0
 23 58  1  1
 24 59  1  0
 24 60  1  0
 24 61  1  0
 28 62  1  1
 29 63  1  1
 30 64  1  0
 30 65  1  0
 30 66  1  0
M  END


  Mrv1652309112214232D          

 30 31  0  0  1  0            999 V2000
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5737   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.8605   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.8605   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.2894   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0039   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0039   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4315   -3.3000    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  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 28 27  1  1  0  0  0
 16 28  1  0  0  0  0
 28 29  1  0  0  0  0
 12 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0314343

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC[C@H](O)CCC(=O)O[C@H]1[C@H](C)O[C@]2(C)[C@@H](OC(C)=O)[C@@H](C)C(=O)O[C@H]2[C@@H]1C

> <INCHI_IDENTIFIER>
InChI=1S/C22H36O8/c1-7-8-9-16(24)10-11-17(25)28-18-12(2)19-22(6,30-14(18)4)20(27-15(5)23)13(3)21(26)29-19/h12-14,16,18-20,24H,7-11H2,1-6H3/t12-,13-,14+,16+,18-,19+,20+,22+/m1/s1

> <INCHI_KEY>
IYTJBDCGCIESLE-SPVCLDLCSA-N

> <FORMULA>
C22H36O8

> <MOLECULAR_WEIGHT>
428.522

> <EXACT_MASS>
428.241018119

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
47.28758795089085

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3R,4R,4aS,7R,8S,8aS)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-octahydropyrano[3,2-b]pyran-3-yl (4S)-4-hydroxyoctanoate

> <JCHEM_LOGP>
2.699586640333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.240912112812975

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6934250418556047

> <JCHEM_POLAR_SURFACE_AREA>
108.36

> <JCHEM_REFRACTIVITY>
106.41069999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4R,4aS,7R,8S,8aS)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4S)-4-hydroxyoctanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.003  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.337  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.670  -3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      16.004  -3.080   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      16.004  -1.540   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      17.338  -3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      18.672  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.005  -3.850   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      20.005  -5.390   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      21.339  -3.080   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      22.673  -3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      24.006  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      24.006  -1.540   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      25.340  -3.850   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      25.340  -5.390   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      26.674  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      26.674  -6.160   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      28.007  -5.390   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      29.341  -6.160   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      30.675  -5.390   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      29.341  -7.700   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      26.674  -7.700   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      28.007  -8.470   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      25.340  -8.470   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      25.340 -10.010   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      24.006  -7.700   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      24.006  -6.160   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      22.673  -5.390   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      21.339  -6.160   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   29                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18   28                                             
CONECT   17   16                                                            
CONECT   18   16   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   16   29                                                  
CONECT   29   28   12   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₆O₈

Average Mass

428.5220 Da

Monoisotopic Mass

428.24102 Da

IUPAC Name

(2S,3R,4R,4aS,7R,8S,8aS)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-octahydropyrano[3,2-b]pyran-3-yl (4S)-4-hydroxyoctanoate

Traditional Name

(2S,3R,4R,4aS,7R,8S,8aS)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4S)-4-hydroxyoctanoate

CAS Registry Number

Not Available

SMILES

CCCC[C@H](O)CCC(=O)O[C@H]1[C@H](C)O[C@]2(C)[C@@H](OC(C)=O)[C@@H](C)C(=O)O[C@H]2[C@@H]1C

InChI Identifier

InChI=1S/C22H36O8/c1-7-8-9-16(24)10-11-17(25)28-18-12(2)19-22(6,30-14(18)4)20(27-15(5)23)13(3)21(26)29-19/h12-14,16,18-20,24H,7-11H2,1-6H3/t12-,13-,14+,16+,18-,19+,20+,22+/m1/s1

InChI Key

IYTJBDCGCIESLE-SPVCLDLCSA-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
Botrytis cinerea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Delta valerolactone
Fatty acid ester
Delta_valerolactone
Fatty acyl
Oxane
Carboxylic acid ester
Lactone
Secondary alcohol
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Alcohol
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organic oxygen compound
Organooxygen 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	2.7	ChemAxon
pKa (Strongest Acidic)	15.24	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	108.36 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	106.41 m³·mol⁻¹	ChemAxon
Polarizability	47.29 Å³	ChemAxon
Number of Rings	2	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

9886344

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11711622

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate (NP0314343)

MOL for NP0314343 ((2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate)

3D MOL for NP0314343 ((2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate)

3D SDF for NP0314343 ((2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate)

3D-SDF for NP0314343 ((2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate)

PDB for NP0314343 ((2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate)

3D PDB for NP0314343 ((2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate)

SMILES for NP0314343 ((2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate)

INCHI for NP0314343 ((2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate)

Structure for NP0314343 ((2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate)

3D Structure for NP0314343 ((2s,3r,4r,4as,7r,8s,8as)-8-(acetyloxy)-2,4,7,8a-tetramethyl-6-oxo-hexahydropyrano[3,2-b]pyran-3-yl (4s)-4-hydroxyoctanoate)