NP-MRD: Showing NP-Card for (4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione (NP0188041)

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Record Information

Version

2.0

Created at

2022-09-04 04:18:11 UTC

Updated at

2022-09-04 04:18:11 UTC

NP-MRD ID

NP0188041

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione

Description

Picrodendrin A belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid. (4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione is found in Picrodendron baccatum. Based on a literature review very few articles have been published on Picrodendrin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042206182D          

 31 35  0  0  0  0            999 V2000
    5.4647   -2.5809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7940   -2.1004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8790   -1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6989   -1.4843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3001   -0.9194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3117   -0.4816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6511   -0.2212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5661    0.6256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3593    0.8524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8201    0.1681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6738    0.2527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5955    1.4501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4529    2.2627    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8205    1.7329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3121    1.0832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9373    1.9005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4897    1.1496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9251    0.5481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0968    0.8494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0434   -0.2684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7554   -0.6850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5251   -0.3881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070   -1.3638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2636   -2.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7729    0.3989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1780   -0.4387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3933    0.1991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9105    0.8052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9628   -0.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2649    0.3365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4768   -1.2190    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
  3  6  2  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
  6 10  1  0  0  0  0
 10 11  2  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  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
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
  8 25  1  0  0  0  0
 15 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 27  1  0  0  0  0
 17 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
M  END

     RDKit          3D

 59 63  0  0  0  0  0  0  0  0999 V2000
    5.8216    0.3577   -1.5208 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9274    0.9371   -0.5797 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5286    0.1151    0.4837 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5001   -0.2488    1.5385 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9272    0.9581    2.1273 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2797   -0.2975    0.4838 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2601    0.0224   -0.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0398   -0.7808   -0.2178 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4635   -1.6387    0.8105 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5912   -1.1450    1.4541 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9699   -1.3634    2.6304 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5893   -1.5509   -1.4605 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0117   -0.7287   -2.6553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2745   -0.7455   -2.1500 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7684    0.3221   -1.1952 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2751    1.5640   -1.6339 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2586    0.3697   -1.3206 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7459   -1.0053   -1.6433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2374   -1.4419   -2.7286 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5343   -1.7113   -0.4619 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5434   -0.7728    0.6244 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1077   -0.6554    1.1092 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5803   -1.8885    1.4541 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3838   -2.0483    2.8171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1929    0.0440    0.1511 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3445    1.2633    0.8816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9471    0.5344    0.0196 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4199    1.6360    0.6988 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4010    0.7768   -0.0531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2468   -0.1618   -0.8196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6589    2.2124   -0.5355 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7635    0.0444   -1.0216 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0989    1.0786   -2.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3939   -0.5398   -1.9976 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1089   -0.9413    2.2808 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3600   -0.7204    0.9922 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9501    1.6436    1.4150 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6957   -0.4178   -1.4853 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1200    1.0688   -0.7724 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9069   -2.5984   -1.5772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9857   -1.1307   -2.9395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9889    2.2498   -1.6415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6044    1.1108   -2.0609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1800   -1.0770    1.4442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2204   -0.1028    2.0927 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0393   -3.0641    2.9630 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2993   -1.3343    3.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3826   -2.0827    3.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0487    1.3285    1.9432 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2340    2.2028    0.3210 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4476    1.1839    1.1061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9591    1.9147    1.4546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8031    0.7831    1.0055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2957    0.1350   -1.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3320   -0.0800   -0.4906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0176   -1.2242   -0.6867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5164    2.3020   -1.6257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0401    2.9161    0.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7218    2.4229   -0.2735 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
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  8 25  1  0
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 25 15  1  0
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 22 45  1  1
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 17 43  1  6
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 31 57  1  0
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 31 59  1  0
 16 42  1  0
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  7 39  1  0
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  5 37  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
 26 49  1  0
 26 50  1  0
 26 51  1  0
M  END


  Mrv1652309042206182D          

 31 35  0  0  0  0            999 V2000
    5.4647   -2.5809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7940   -2.1004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8790   -1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6989   -1.4843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3001   -0.9194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3117   -0.4816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6511   -0.2212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5661    0.6256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3593    0.8524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8201    0.1681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6738    0.2527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5955    1.4501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4529    2.2627    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8205    1.7329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3121    1.0832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9373    1.9005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4897    1.1496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9251    0.5481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0968    0.8494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0434   -0.2684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7554   -0.6850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5251   -0.3881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070   -1.3638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2636   -2.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7729    0.3989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1780   -0.4387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3933    0.1991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9105    0.8052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9628   -0.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2649    0.3365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4768   -1.2190    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
  3  6  2  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
  6 10  1  0  0  0  0
 10 11  2  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  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
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
  8 25  1  0  0  0  0
 15 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 27  1  0  0  0  0
 17 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0188041

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1C2OC(=O)C(C2(O)C(C)C)C2(O)C3OC3C3(C\C(=C(\CO)OC)C(=O)O3)C12C

> <INCHI_IDENTIFIER>
InChI=1S/C21H28O10/c1-8(2)20(25)11-17(24)30-14(20)12(28-5)18(3)19(13-15(29-13)21(11,18)26)6-9(16(23)31-19)10(7-22)27-4/h8,11-15,22,25-26H,6-7H2,1-5H3/b10-9+

> <INCHI_KEY>
OZKNMGZZFOYTHQ-MDZDMXLPSA-N

> <FORMULA>
C21H28O10

> <MOLECULAR_WEIGHT>
440.445

> <EXACT_MASS>
440.168247102

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.65557273545473

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4E)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-8'-methoxy-7'-methyl-12'-(propan-2-yl)-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0^{2,7}.0^{3,5}]dodecane]-5,11'-dione

> <JCHEM_LOGP>
-1.0900664193333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.247485997922688

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.51215050296019

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0810512177740446

> <JCHEM_POLAR_SURFACE_AREA>
144.28

> <JCHEM_REFRACTIVITY>
101.3948

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4E)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0^{2,7}.0^{3,5}]dodecane]-5,11'-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      10.201  -4.818   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.949  -3.921   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       9.107  -2.309   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.638  -2.771   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      11.760  -1.716   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       8.048  -0.899   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.815  -0.413   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.657   1.168   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.137   1.591   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.997   0.314   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.591   0.472   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.712   2.707   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.445   4.224   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.265   3.235   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.316   2.022   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.616   3.548   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.781   2.146   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.727   1.023   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.181   1.586   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       1.948  -0.501   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.277  -1.279   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.714  -0.724   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.680  -2.546   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.225  -4.149   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.176   0.745   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.932  -0.819   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.601   0.372   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.566   1.503   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.664  -0.679   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.228   0.628   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.757  -2.276   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    6                                                  
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    3    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   12   25                                             
CONECT    9    8   10                                                       
CONECT   10    9    6   11                                                  
CONECT   11   10                                                            
CONECT   12    8   13   14                                                  
CONECT   13   12   14                                                       
CONECT   14   13   12   15                                                  
CONECT   15   14   16   17   25                                             
CONECT   16   15                                                            
CONECT   17   15   18   27                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22    8   15   26                                             
CONECT   26   25                                                            
CONECT   27   21   17   28   29                                             
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₈O₁₀

Average Mass

440.4450 Da

Monoisotopic Mass

440.16825 Da

IUPAC Name

(4E)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-8'-methoxy-7'-methyl-12'-(propan-2-yl)-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0^{2,7}.0^{3,5}]dodecane]-5,11'-dione

Traditional Name

(4E)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0^{2,7}.0^{3,5}]dodecane]-5,11'-dione

CAS Registry Number

Not Available

SMILES

COC1C2OC(=O)C(C2(O)C(C)C)C2(O)C3OC3C3(C\C(=C(\CO)OC)C(=O)O3)C12C

InChI Identifier

InChI=1S/C21H28O10/c1-8(2)20(25)11-17(24)30-14(20)12(28-5)18(3)19(13-15(29-13)21(11,18)26)6-9(16(23)31-19)10(7-22)27-4/h8,11-15,22,25-26H,6-7H2,1-5H3/b10-9+

InChI Key

OZKNMGZZFOYTHQ-MDZDMXLPSA-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
Picrodendron baccatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Eicosanoids

Direct Parent

Prostaglandins and related compounds

Alternative Parents

Substituents

Prostaglandin skeleton
Caprolactone
Oxepane
Dicarboxylic acid or derivatives
Gamma butyrolactone
Oxane
Cyclic alcohol
Vinylogous ester
Tertiary alcohol
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Primary alcohol
Organic oxygen compound
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	-1.1	ChemAxon
pKa (Strongest Acidic)	12.51	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	144.28 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	101.39 m³·mol⁻¹	ChemAxon
Polarizability	42.66 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

2274535

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3004155

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione (NP0188041)

MOL for NP0188041 ((4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

3D MOL for NP0188041 ((4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

3D SDF for NP0188041 ((4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

3D-SDF for NP0188041 ((4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

PDB for NP0188041 ((4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

3D PDB for NP0188041 ((4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

SMILES for NP0188041 ((4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

INCHI for NP0188041 ((4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

Structure for NP0188041 ((4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

3D Structure for NP0188041 ((4e)-2',12'-dihydroxy-4-(2-hydroxy-1-methoxyethylidene)-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)