NP-MRD: Showing NP-Card for (4r,6r,7s,8s,13s,17s)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1⁴,⁷]octadeca-1(16),9-diene-11,15-dione (NP0144664)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-01 23:41:54 UTC

Updated at

2022-09-01 23:41:54 UTC

NP-MRD ID

NP0144664

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4r,6r,7s,8s,13s,17s)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1⁴,⁷]octadeca-1(16),9-diene-11,15-dione

Description

Mangromicin B belongs to the class of organic compounds known as dihydropyranones. Dihydropyranones are compounds containing a hydrogenated pyran ring which bears a ketone, and contains one double bond. Based on a literature review very few articles have been published on Mangromicin B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022201412D          

 28 30  0  0  1  0            999 V2000
   -1.1357   -1.7947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3110   -1.7753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0846   -1.0513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9094   -1.0319    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3022   -0.2886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8541    0.4041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1488   -0.2345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8990    0.2029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7626    0.2550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4539   -0.2648    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2788   -0.2797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7765   -0.7367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9672   -1.5332    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4219   -2.1522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7904   -1.6230    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0953   -0.8262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5626   -2.4606    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2667   -2.8906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9263   -3.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0966   -3.2688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1280   -4.0932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2590   -3.1065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9275   -3.8620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5708   -2.5988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3410   -1.7632    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1677   -1.6962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5437   -0.9663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3687   -0.9585    0.0000 O   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
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  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
 10 11  1  6  0  0  0
 10 12  1  0  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  6  0  0  0
 10 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  4  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
  4 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END

     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
   -3.3955   -0.2312    3.1099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4972   -0.6638    1.6462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5061    0.1976    0.8665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4881   -0.1056   -0.5798 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2457   -1.5791   -0.8630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5278   -2.1980   -0.6777 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0497   -2.0607   -1.2149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3421   -3.1326   -0.5232 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1412   -3.1222   -0.3520 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8772   -1.8734   -0.1125 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0530   -1.8576   -1.1238 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5811   -1.8279    1.2470 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7852   -0.3266    1.4178 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0529    0.1732    0.8053 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5876    0.2186    0.7334 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2831   -0.6833   -0.2161 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7686    1.5786    0.0738 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1511    1.5329   -1.2333 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5546    2.4228    0.3339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1028    3.2575   -0.4397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0787    4.7124    0.0458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8402    3.0409   -1.6612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5934    3.7634   -2.6983 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9348    2.0192   -1.9166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5555    0.6821   -1.4341 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3974   -0.1797   -2.6181 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4677   -1.2813   -2.3115 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5082   -1.2135   -3.0833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3282    0.8907    3.1631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2874   -0.5048    3.6858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4539   -0.6073    3.5668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5456   -0.4587    1.3446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2489   -1.7354    1.5956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5200    0.0405    1.2938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7988    1.2437    1.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5099    0.1862   -0.9751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2639   -2.0654   -1.3228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6986   -3.3657    0.5287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4905   -4.1758   -0.9895 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5575   -3.6580   -1.2707 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4399   -3.8328    0.4645 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0239   -1.9082   -0.6481 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0029   -2.7751   -1.7871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9605   -1.0186   -1.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9618   -2.2457    2.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5635   -2.3367    1.2116 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7984   -0.0889    2.5187 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9286   -0.4864    1.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9566    0.4531   -0.2535 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3356    1.1391    1.3276 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8019    0.3398    1.5274 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6572    2.0203    0.6269 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5884    0.9346   -1.7750 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2207    2.2556    1.3895 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7878    5.2587   -0.3888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9584    5.2855   -0.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0892    4.7441    1.1730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8802    2.3065   -1.3996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2199    2.0421   -2.9901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6128    0.8606   -0.9051 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 25  1  0
 25 24  1  0
 24 22  1  0
 22 23  2  0
 22 20  1  0
 20 21  1  0
 20 19  2  0
 19 17  1  0
 17 18  1  0
 17 15  1  0
 15 16  1  0
 16 10  1  0
 10 11  1  6
 10 12  1  0
 12 13  1  0
 13 14  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7 27  1  0
 27 28  2  0
 27 26  1  0
  7  5  2  0
  5  6  1  0
  5  4  1  0
 26 25  1  0
 13 15  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  2 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  6
 25 60  1  1
 24 58  1  0
 24 59  1  0
 21 55  1  0
 21 56  1  0
 21 57  1  0
 19 54  1  0
 17 52  1  1
 18 53  1  0
 15 51  1  1
 11 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 13 47  1  1
 14 48  1  0
 14 49  1  0
 14 50  1  0
  9 40  1  0
  9 41  1  0
  8 38  1  0
  8 39  1  0
  6 37  1  0
M  END


  Mrv1652309022201412D          

 28 30  0  0  1  0            999 V2000
   -1.1357   -1.7947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3110   -1.7753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0846   -1.0513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9094   -1.0319    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3022   -0.2886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8541    0.4041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1488   -0.2345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8990    0.2029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7626    0.2550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4539   -0.2648    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2788   -0.2797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7765   -0.7367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9672   -1.5332    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4219   -2.1522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7904   -1.6230    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0953   -0.8262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5626   -2.4606    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2667   -2.8906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9263   -3.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0966   -3.2688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1280   -4.0932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2590   -3.1065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9275   -3.8620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5708   -2.5988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3410   -1.7632    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1677   -1.6962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5437   -0.9663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3687   -0.9585    0.0000 O   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
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  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
 10 11  1  6  0  0  0
 10 12  1  0  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  6  0  0  0
 10 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  4  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
  4 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0144664

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC[C@H]1[C@@H]2CC(=O)C(C)=C[C@H](O)[C@H]3O[C@@](C)(C[C@H]3C)CCC(C(=O)O2)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O6/c1-5-6-14-18-10-16(23)12(2)9-17(24)20-13(3)11-22(4,28-20)8-7-15(19(14)25)21(26)27-18/h9,13-14,17-18,20,24-25H,5-8,10-11H2,1-4H3/t13-,14+,17+,18+,20+,22-/m1/s1

> <INCHI_KEY>
AFAXFXGTXQUJRU-GIZGSCRPSA-N

> <FORMULA>
C22H32O6

> <MOLECULAR_WEIGHT>
392.492

> <EXACT_MASS>
392.21988875

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
41.89821764199193

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R,6R,7S,8S,13S,17S)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1^{4,7}]octadeca-1(16),9-diene-11,15-dione

> <ALOGPS_LOGP>
1.82

> <JCHEM_LOGP>
3.2065442239999995

> <ALOGPS_LOGS>
-3.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.763497651444393

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.727890143246867

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3396406297451176

> <JCHEM_POLAR_SURFACE_AREA>
93.06

> <JCHEM_REFRACTIVITY>
106.01319999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.93e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4R,6R,7S,8S,13S,17S)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1^{4,7}]octadeca-1(16),9-diene-11,15-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.120  -3.350   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.580  -3.314   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.158  -1.962   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.698  -1.926   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.431  -0.539   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.594   0.754   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.011  -0.438   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.411   0.379   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.024   0.476   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.314  -0.494   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.854  -0.522   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.050  -1.375   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.406  -2.862   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.387  -4.017   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.942  -3.030   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.511  -1.542   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.517  -4.593   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.831  -5.396   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.329  -5.677   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.780  -6.102   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.839  -7.641   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.217  -5.799   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.598  -7.209   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.932  -4.851   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.503  -3.291   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.046  -3.166   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.748  -1.804   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.288  -1.789   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   25                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   27                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   16                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15   10                                                       
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24    4   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26    7   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₂O₆

Average Mass

392.4920 Da

Monoisotopic Mass

392.21989 Da

IUPAC Name

(4R,6R,7S,8S,13S,17S)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1^{4,7}]octadeca-1(16),9-diene-11,15-dione

Traditional Name

(4R,6R,7S,8S,13S,17S)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1^{4,7}]octadeca-1(16),9-diene-11,15-dione

CAS Registry Number

Not Available

SMILES

CCC[C@H]1[C@@H]2CC(=O)C(C)=C[C@H](O)[C@H]3O[C@@](C)(C[C@H]3C)CCC(C(=O)O2)=C1O

InChI Identifier

InChI=1S/C22H32O6/c1-5-6-14-18-10-16(23)12(2)9-17(24)20-13(3)11-22(4,28-20)8-7-15(19(14)25)21(26)27-18/h9,13-14,17-18,20,24-25H,5-8,10-11H2,1-4H3/t13-,14+,17+,18+,20+,22-/m1/s1

InChI Key

AFAXFXGTXQUJRU-GIZGSCRPSA-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 dihydropyranones. Dihydropyranones are compounds containing a hydrogenated pyran ring which bears a ketone, and contains one double bond.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrans

Sub Class

Pyranones and derivatives

Direct Parent

Dihydropyranones

Alternative Parents

Substituents

Dihydropyranone
Vinylogous acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Ketone
Lactone
Cyclic ketone
Secondary alcohol
Carboxylic acid derivative
Dialkyl ether
Enol
Ether
Oxacycle
Monocarboxylic acid or derivatives
Organic oxide
Carbonyl group
Alcohol
Hydrocarbon derivative
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	1.82	ALOGPS
logP	3.21	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	4.73	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	93.06 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	106.01 m³·mol⁻¹	ChemAxon
Polarizability	41.9 Å³	ChemAxon
Number of Rings	3	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

139585918

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4r,6r,7s,8s,13s,17s)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1⁴,⁷]octadeca-1(16),9-diene-11,15-dione (NP0144664)

MOL for NP0144664 ((4r,6r,7s,8s,13s,17s)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1⁴,⁷]octadeca-1(16),9-diene-11,15-dione)

3D MOL for NP0144664 ((4r,6r,7s,8s,13s,17s)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1⁴,⁷]octadeca-1(16),9-diene-11,15-dione)

3D SDF for NP0144664 ((4r,6r,7s,8s,13s,17s)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1⁴,⁷]octadeca-1(16),9-diene-11,15-dione)

3D-SDF for NP0144664 ((4r,6r,7s,8s,13s,17s)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1⁴,⁷]octadeca-1(16),9-diene-11,15-dione)

PDB for NP0144664 ((4r,6r,7s,8s,13s,17s)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1⁴,⁷]octadeca-1(16),9-diene-11,15-dione)

3D PDB for NP0144664 ((4r,6r,7s,8s,13s,17s)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1⁴,⁷]octadeca-1(16),9-diene-11,15-dione)

SMILES for NP0144664 ((4r,6r,7s,8s,13s,17s)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1⁴,⁷]octadeca-1(16),9-diene-11,15-dione)

INCHI for NP0144664 ((4r,6r,7s,8s,13s,17s)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1⁴,⁷]octadeca-1(16),9-diene-11,15-dione)

Structure for NP0144664 ((4r,6r,7s,8s,13s,17s)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1⁴,⁷]octadeca-1(16),9-diene-11,15-dione)

3D Structure for NP0144664 ((4r,6r,7s,8s,13s,17s)-8,16-dihydroxy-4,6,10-trimethyl-17-propyl-14,18-dioxatricyclo[11.2.2.1⁴,⁷]octadeca-1(16),9-diene-11,15-dione)