NP-MRD: Showing NP-Card for 10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid (NP0273785)

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Record Information

Version

2.0

Created at

2022-09-08 20:56:33 UTC

Updated at

2022-09-08 20:56:34 UTC

NP-MRD ID

NP0273785

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid

Description

10-{1,4-Dimethyl-2,8-dioxabicyclo[3.2.1]Octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid is found in Salinispora arenicola. 10-{1,4-Dimethyl-2,8-dioxabicyclo[3.2.1]Octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251508032D          

 29 30  0  0  0  0            999 V2000
   -3.5932   -0.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5932   -0.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    1.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0221    1.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0221    2.3306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7366    2.7431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7366    3.5681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    2.7431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    3.5681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5932    2.3306    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8787    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8787    1.0931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1643   -0.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1643   -0.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4498    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4498    1.0931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7353   -0.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7353   -0.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0208    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6608   -0.1966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4492    0.0465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0103   -0.5582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7506    0.8145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3381    1.5290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5223    1.6520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1864    0.9651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0825    1.0908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8505    1.3922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  4  0  0  0
  3  4  2  0  0  0  0
  5  4  1  4  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 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
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 27  1  0  0  0  0
 26 28  1  0  0  0  0
 20 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END

     RDKit          3D

 66 67  0  0  0  0  0  0  0  0999 V2000
   -2.4286    1.3147   -1.9393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2206    0.3019   -0.8322 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9357    0.5108   -0.1330 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9446    1.8382    0.3555 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2854    0.4006   -1.0238 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4255   -0.9302   -1.6632 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4466    0.7029   -0.1454 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2057    1.8724    0.6115 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8035    0.8084   -0.7151 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9209    2.0553   -1.6259 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3808   -0.3301   -1.4127 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4382   -1.0298   -1.1298 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2716   -0.7687    0.0092 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3489   -1.4065    0.3814 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8776   -2.5481   -0.3700 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1907   -2.2189   -0.7922 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0613   -0.9717    1.5931 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5940    0.1310    2.3626 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.0906   -1.5508    1.9832 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3397    0.5305    0.1704 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6016    0.3604   -0.3889 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5204    0.8814    0.5159 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1691    2.0907   -0.0696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5157   -0.2161    0.8425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6529   -1.1070    1.7466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5511   -0.1811    2.1425 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9604    1.1205    1.7717 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2599   -0.4198    1.3462 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1801   -1.8563    0.9518 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4423    1.1028   -2.3746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6381    1.3011   -2.6901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5513    2.3108   -1.4339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3633   -0.6928   -1.2885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7676   -0.1361    0.7414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8258    2.4946   -0.3622 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1964    1.2245   -1.8030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5410   -1.5185   -1.6453 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6213   -0.8123   -2.7446 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1557   -1.5505   -1.1494 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4931   -0.1029    0.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8425    1.9192    1.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4661    1.1108    0.1574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3033    1.8878   -2.5055 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6466    2.9159   -1.0056 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9849    2.0789   -1.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8686   -0.6313   -2.3481 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7100   -1.8552   -1.7852 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9707    0.0747    0.6582 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2657   -2.8553   -1.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0227   -3.4372    0.2985 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7522   -3.0201   -0.8302 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1844    0.9845    2.4629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6668    0.0770    2.8192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2779    1.5590    0.5788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2520    2.0689    0.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9633    2.1416   -1.1382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6791    2.9886    0.4056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7738   -0.7140   -0.0998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3845    0.1835    1.3984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3085   -1.3806    2.6148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3620   -1.9697    1.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3889   -0.2672    3.2212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4051   -0.1461    1.9857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5093   -2.4839    1.8178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6775   -2.1109    0.0093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1006   -2.1241    0.8119 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 17 19  2  0
  9  7  1  0
  7  8  1  0
  7  5  1  0
  5  6  1  0
  5  3  1  0
  3  4  1  0
  3  2  1  0
  2  1  1  0
  2 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 20  1  0
 27 22  1  0
 10 43  1  0
 10 44  1  0
 10 45  1  0
  9 42  1  1
 11 46  1  0
 12 47  1  0
 13 48  1  0
 15 49  1  0
 15 50  1  0
 16 51  1  0
 18 52  1  0
 18 53  1  0
  7 40  1  1
  8 41  1  0
  5 36  1  6
  6 37  1  0
  6 38  1  0
  6 39  1  0
  3 34  1  1
  4 35  1  0
  2 33  1  6
  1 30  1  0
  1 31  1  0
  1 32  1  0
 20 54  1  1
 23 55  1  0
 23 56  1  0
 23 57  1  0
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 24 59  1  0
 25 60  1  0
 25 61  1  0
 26 62  1  1
 28 63  1  1
 29 64  1  0
 29 65  1  0
 29 66  1  0
M  END


  Mrv1533004251508032D          

 29 30  0  0  0  0            999 V2000
   -3.5932   -0.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5932   -0.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    1.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0221    1.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0221    2.3306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7366    2.7431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7366    3.5681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    2.7431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    3.5681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5932    2.3306    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8787    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8787    1.0931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1643   -0.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1643   -0.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4498    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4498    1.0931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7353   -0.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7353   -0.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0208    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6608   -0.1966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4492    0.0465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0103   -0.5582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7506    0.8145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3381    1.5290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5223    1.6520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1864    0.9651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0825    1.0908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8505    1.3922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  4  0  0  0
  3  4  2  0  0  0  0
  5  4  1  4  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 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
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 27  1  0  0  0  0
 26 28  1  0  0  0  0
 20 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0273785

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C=CC=C(CO)C(N)=O)C(O)C(C)C(O)C(C)C1OC2(C)CCC(O2)C1C

> <INCHI_IDENTIFIER>
InChI=1S/C22H37NO6/c1-12(7-6-8-16(11-24)21(23)27)18(25)14(3)19(26)15(4)20-13(2)17-9-10-22(5,28-17)29-20/h6-8,12-15,17-20,24-26H,9-11H2,1-5H3,(H2,23,27)

> <INCHI_KEY>
QWSYKJZSJYRUSS-UHFFFAOYSA-N

> <FORMULA>
C22H37NO6

> <MOLECULAR_WEIGHT>
411.539

> <EXACT_MASS>
411.262087915

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
45.47045076905426

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienamide

> <ALOGPS_LOGP>
1.25

> <JCHEM_LOGP>
0.7798745540000012

> <ALOGPS_LOGS>
-3.33

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.720068579316646

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.170698533635342

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3239003048012904

> <JCHEM_POLAR_SURFACE_AREA>
122.24000000000001

> <JCHEM_REFRACTIVITY>
112.58610000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.91e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienamide

> <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      -6.707  -1.810   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.707  -0.270   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.041   0.500   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.041   2.040   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.375   2.810   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.375   4.350   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -10.708   5.120   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0     -10.708   6.660   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -8.041   5.120   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -8.041   6.660   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0      -6.707   4.350   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -5.374   0.500   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -5.374   2.040   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -4.040  -0.270   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.040  -1.810   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.706   0.500   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.706   2.040   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.373  -0.270   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.373  -1.810   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.039   0.500   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.234  -0.367   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.705   0.087   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.753  -1.042   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.268   1.520   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.498   2.854   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.975   3.084   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.215   1.802   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -0.154   2.036   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.588   2.599   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    2   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   28                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24   27                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26   22                                                       
CONECT   28   26   20   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

View in JSmol

Synonyms

Value	Source
10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidate	Generator

Chemical Formula

C₂₂H₃₇NO₆

Average Mass

411.5390 Da

Monoisotopic Mass

411.26209 Da

IUPAC Name

10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienamide

Traditional Name

10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienamide

CAS Registry Number

Not Available

SMILES

CC(C=CC=C(CO)C(N)=O)C(O)C(C)C(O)C(C)C1OC2(C)CCC(O2)C1C

InChI Identifier

InChI=1S/C22H37NO6/c1-12(7-6-8-16(11-24)21(23)27)18(25)14(3)19(26)15(4)20-13(2)17-9-10-22(5,28-17)29-20/h6-8,12-15,17-20,24-26H,9-11H2,1-5H3,(H2,23,27)

InChI Key

QWSYKJZSJYRUSS-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
Salinispora arenicola	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Ketal
Oxepane
Meta-dioxane
Oxolane
Secondary alcohol
Acetal
Carboximidic acid
Carboximidic acid derivative
Oxacycle
Organoheterocyclic compound
Organic nitrogen compound
Primary alcohol
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Alcohol
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	1.25	ALOGPS
logP	0.78	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	14.17	ChemAxon
pKa (Strongest Basic)	-0.32	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	122.24 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	112.59 m³·mol⁻¹	ChemAxon
Polarizability	45.47 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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid (NP0273785)

MOL for NP0273785 (10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

3D MOL for NP0273785 (10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

3D SDF for NP0273785 (10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

3D-SDF for NP0273785 (10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

PDB for NP0273785 (10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

3D PDB for NP0273785 (10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

SMILES for NP0273785 (10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

INCHI for NP0273785 (10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

Structure for NP0273785 (10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

3D Structure for NP0273785 (10-{1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)