NP-MRD: Showing NP-Card for (2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid (NP0192878)

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Record Information

Version

2.0

Created at

2022-09-04 10:11:24 UTC

Updated at

2022-09-04 10:11:24 UTC

NP-MRD ID

NP0192878

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid

Description

(2R,3S)-3-[(1R,2R,3S,7S,8R,10R)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]Tetradec-12-en-7-yl]-2-methylpentanedioic acid belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. (2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid is found in Ailanthus altissima. Based on a literature review very few articles have been published on (2R,3S)-3-[(1R,2R,3S,7S,8R,10R)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]Tetradec-12-en-7-yl]-2-methylpentanedioic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292206192D          

 29 32  0  0  1  0            999 V2000
    6.0559   -4.5864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3650   -3.7558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8668   -2.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6400   -2.5564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9211   -3.0920    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6448   -4.1082    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2244   -4.6524    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7224   -4.0122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2952   -2.9760    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7567   -3.4651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2277   -3.0933    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9266   -3.8614    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1031   -3.8125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4780   -4.4015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8951   -3.0141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5902   -2.5696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9356   -2.1876    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5309   -1.3503    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7173   -1.7832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1204   -0.5015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2773   -0.2460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4656    0.2943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4533   -1.3972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6093   -0.5015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1846    0.2748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4382   -0.2782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2509   -4.9051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4454   -2.1378    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1545   -5.4761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  5 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 11 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 17 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
  6 27  1  1  0  0  0
  5 28  1  1  0  0  0
  1 29  1  0  0  0  0
M  END

     RDKit          2D

 53 56  0  0  0  0  0  0  0  0999 V2000
   -2.6380    5.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9499    4.2246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3764    3.7611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6883    2.2939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1149    1.8303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5736    1.2902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8855   -0.1771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3288    2.1425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4086    3.6844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8351    3.2209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1470    1.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4589    0.2865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1293   -1.7730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3943   -1.2135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2760    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3943    1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8615    1.5254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3287    1.8373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7960    2.1491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7997    1.0344    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2595    3.5757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1734    0.0582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7062   -0.2537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4853   -1.4090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9118   -1.8726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3705   -2.4127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3261    7.1591    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1052    6.0037    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1389    5.7443    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4912    4.7648    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3120   -0.6406    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9782    3.4757    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7735    4.6079    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7714    5.1399    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5233    4.6881    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.9007   -0.1271    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4360   -0.8107    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9557   -0.4321    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6004    0.7041    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1147   -1.2436    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7308    3.0197    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8171    0.4190    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1980    3.3316    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7267    3.8876    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6677    0.1889    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5518   -1.0708    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2926   -1.6955    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0485    1.0945    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6824   -3.8800    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 25  1  0
 25 20  1  0
 20 21  1  0
 21 22  1  0
 22 24  1  0
 22 23  2  0
 20 19  1  0
 19 18  1  6
 18 17  1  0
 17 15  1  0
 15 16  2  0
 15 14  1  0
 14 12  1  0
 12 13  1  1
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  1  1
  6  4  1  0
  4  5  2  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
 25 27  1  0
 27 29  1  0
 27 28  2  0
 14 19  1  0
  6 12  1  0
  9 19  1  0
  2 11  1  0
 26 50  1  0
 26 51  1  0
 26 52  1  0
 25 49  1  1
 20 45  1  6
 21 46  1  0
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 18 44  1  0
 14 42  1  1
 13 39  1  0
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 11 38  1  6
 10 36  1  0
 10 37  1  0
  9 35  1  1
  7 34  1  0
  3 33  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 29 53  1  0
M  END


  Mrv1652304292206192D          

 29 32  0  0  1  0            999 V2000
    6.0559   -4.5864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3650   -3.7558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8668   -2.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6400   -2.5564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9211   -3.0920    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6448   -4.1082    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2244   -4.6524    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7224   -4.0122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2952   -2.9760    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7567   -3.4651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2277   -3.0933    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9266   -3.8614    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1031   -3.8125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4780   -4.4015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8951   -3.0141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5902   -2.5696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9356   -2.1876    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5309   -1.3503    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7173   -1.7832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1204   -0.5015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2773   -0.2460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4656    0.2943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4533   -1.3972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6093   -0.5015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1846    0.2748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4382   -0.2782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2509   -4.9051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4454   -2.1378    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1545   -5.4761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  5 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 11 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 17 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
  6 27  1  1  0  0  0
  5 28  1  1  0  0  0
  1 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0192878

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]([C@H](CC(O)=O)[C@@]12COC(=O)[C@@H]1[C@@]1(C)[C@@H]3C[C@H]2O[C@@]1(O)C(=O)C=C3C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H24O9/c1-8-4-12(21)20(27)18(3)10(8)5-13(29-20)19(7-28-17(26)15(18)19)11(6-14(22)23)9(2)16(24)25/h4,9-11,13,15,27H,5-7H2,1-3H3,(H,22,23)(H,24,25)/t9-,10-,11+,13-,15-,18-,19-,20+/m1/s1

> <INCHI_KEY>
DZBLDANEFRTEAG-OZHKUUMTSA-N

> <FORMULA>
C20H24O9

> <MOLECULAR_WEIGHT>
408.403

> <EXACT_MASS>
408.142032353

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
106.61971918274887

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3S)-3-[(1R,2R,3S,7S,8R,10R)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0^{2,10}.0^{3,7}]tetradec-12-en-7-yl]-2-methylpentanedioic acid

> <ALOGPS_LOGP>
0.69

> <JCHEM_LOGP>
0.9238535240000002

> <ALOGPS_LOGS>
-2.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.354466132592935

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.694263687297364

> <JCHEM_PKA_STRONGEST_BASIC>
-4.401601839577161

> <JCHEM_POLAR_SURFACE_AREA>
147.43000000000004

> <JCHEM_REFRACTIVITY>
95.28379999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.50e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S)-3-[(1R,2R,3S,7S,8R,10R)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0^{2,10}.0^{3,7}]tetradec-12-en-7-yl]-2-methylpentanedioic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      11.304  -8.561   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.881  -7.011   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.951  -5.581   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      12.395  -4.772   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       9.186  -5.772   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.670  -7.669   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.752  -8.684   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.682  -7.489   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.884  -5.555   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      10.746  -6.468   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       7.892  -5.774   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.330  -7.208   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.792  -7.117   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.626  -8.216   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       5.404  -5.626   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.702  -4.797   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.213  -4.084   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.458  -2.521   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.939  -3.329   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.691  -0.936   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.118  -0.459   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       8.336   0.549   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      10.179  -2.608   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.471  -0.936   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.678   0.513   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      12.018  -0.519   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       7.935  -9.156   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       8.298  -3.991   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      11.488 -10.222   0.000  0.00  0.00           C+0
CONECT    1    2    7   29                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   10   28                                             
CONECT    6    5    7   12   27                                             
CONECT    7    6    1    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9    5                                                       
CONECT   11    9   12   16   17                                             
CONECT   12   11    6   13                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   11                                                       
CONECT   17   11   18   23                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   17   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27    6                                                            
CONECT   28    5                                                            
CONECT   29    1                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Value	Source
(2R,3S)-3-[(1R,2R,3S,7S,8R,10R)-10-Hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0,.0,]tetradec-12-en-7-yl]-2-methylpentanedioate	Generator

Chemical Formula

C₂₀H₂₄O₉

Average Mass

408.4030 Da

Monoisotopic Mass

408.14203 Da

IUPAC Name

(2R,3S)-3-[(1R,2R,3S,7S,8R,10R)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0^{2,10}.0^{3,7}]tetradec-12-en-7-yl]-2-methylpentanedioic acid

Traditional Name

(2R,3S)-3-[(1R,2R,3S,7S,8R,10R)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0^{2,10}.0^{3,7}]tetradec-12-en-7-yl]-2-methylpentanedioic acid

CAS Registry Number

Not Available

SMILES

C[C@H]([C@H](CC(O)=O)[C@@]12COC(=O)[C@@H]1[C@@]1(C)[C@@H]3C[C@H]2O[C@@]1(O)C(=O)C=C3C)C(O)=O

InChI Identifier

InChI=1S/C20H24O9/c1-8-4-12(21)20(27)18(3)10(8)5-13(29-20)19(7-28-17(26)15(18)19)11(6-14(22)23)9(2)16(24)25/h4,9-11,13,15,27H,5-7H2,1-3H3,(H,22,23)(H,24,25)/t9-,10-,11+,13-,15-,18-,19-,20+/m1/s1

InChI Key

DZBLDANEFRTEAG-OZHKUUMTSA-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
Ailanthus altissima	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Sesquiterpenoid
Tricarboxylic acid or derivatives
Furopyran
Carbocyclic fatty acid
Cyclohexenone
Hydroxy fatty acid
Fatty acyl
Pyran
Oxane
Gamma butyrolactone
Tetrahydrofuran
Furan
Lactone
Ketone
Hemiacetal
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen 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	0.69	ALOGPS
logP	0.92	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	3.69	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	147.43 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	95.28 m³·mol⁻¹	ChemAxon
Polarizability	106.62 Å³	ChemAxon
Number of Rings	4	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

163103925

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid (NP0192878)

MOL for NP0192878 ((2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid)

3D MOL for NP0192878 ((2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid)

3D SDF for NP0192878 ((2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid)

3D-SDF for NP0192878 ((2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid)

PDB for NP0192878 ((2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid)

3D PDB for NP0192878 ((2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid)

SMILES for NP0192878 ((2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid)

INCHI for NP0192878 ((2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid)

Structure for NP0192878 ((2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid)

3D Structure for NP0192878 ((2r,3s)-3-[(1r,2s,3s,7s,8r,10r)-10-hydroxy-2,13-dimethyl-4,11-dioxo-5,9-dioxatetracyclo[6.5.1.0²,¹⁰.0³,⁷]tetradec-12-en-7-yl]-2-methylpentanedioic acid)