NP-MRD: Showing NP-Card for amarolide 11-acetate (NP0181411)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 19:55:43 UTC

Updated at

2022-09-03 19:55:43 UTC

NP-MRD ID

NP0181411

Secondary Accession Numbers

None

Natural Product Identification

Common Name

amarolide 11-acetate

Description

Amarolide 11-acetate belongs to the class of organic compounds known as quassinoids. These are a group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring. amarolide 11-acetate is found in Ailanthus altissima and Simarouba versicolor. Based on a literature review very few articles have been published on Amarolide 11-acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032221552D          

 29 32  0  0  1  0            999 V2000
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 15 14  1  6  0  0  0
 15 16  1  0  0  0  0
 17 16  1  1  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  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  1  0  0  0
 27 25  1  1  0  0  0
  5 27  1  0  0  0  0
 27 28  1  0  0  0  0
 10 28  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END

     RDKit          3D

 59 62  0  0  0  0  0  0  0  0999 V2000
   -2.1935    4.2816   -0.0744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7880    3.1604   -0.9466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5395    3.3690   -2.1504 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6879    1.9136   -0.4365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2997    0.7318   -1.1615 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6226    0.0028   -1.3042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3432    0.3897   -2.2057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0620   -1.0982   -0.4482 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3854   -0.8092    0.2487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0622   -1.4206    0.6105 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1449   -0.6230    1.8499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9228   -0.7632    2.6544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9422   -0.5232    3.8800 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2425   -1.1577    2.0632 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2371   -2.0527    0.9388 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6838   -2.0221    0.4353 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9565   -0.5582    0.2071 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3955   -0.2740    0.1279 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1190   -0.9888    1.2492 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7443    1.1895    0.1646 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5365    2.0684   -0.0908 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8628    2.3766    1.0878 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5932    1.4202   -1.0530 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2101    2.0994   -1.9771 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1261    0.0209   -0.9226 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3576   -0.6570   -2.2264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2990   -0.0532   -0.3996 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7059   -1.4570   -0.0673 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8522   -2.3890   -1.2327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4623    5.1395   -0.1305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2316    4.6179   -0.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1548    3.9728    1.0092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0236    0.9597   -2.2108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2426   -2.0258   -1.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4430   -1.5227    1.1050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2512   -1.0072   -0.4048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3999    0.2060    0.7042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2473   -2.4981    0.9085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4649    0.4349    1.7284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9733   -1.0681    2.4826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0613   -3.0312    1.3045 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8339   -2.6674   -0.4246 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3115   -2.3203    1.3161 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5608   -0.0423    1.1366 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8022   -0.6958   -0.8269 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5172   -0.9373    2.1961 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0817   -0.4714    1.4458 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3098   -2.0470    1.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5775    1.4005   -0.5319 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1044    1.4251    1.1845 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9352    3.0223   -0.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2483    3.1301    1.5795 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0269   -1.5611   -2.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4564   -0.8619   -2.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9822   -0.0060   -2.9131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2064    0.4362    0.6248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4714   -2.0214   -2.0494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4348   -3.2748   -0.8249 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1063   -2.8619   -1.5539 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  6
 25 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 12  1  0
 12 13  2  0
 12 11  1  0
 11 10  1  0
 10  8  1  0
  8  9  1  0
  8  6  1  0
  6  7  2  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 27  1  0
 27 28  1  0
 28 29  1  6
 17 18  1  0
 28 15  1  0
 27 25  1  0
 28 10  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
 18 45  1  6
 20 49  1  0
 20 50  1  0
 21 51  1  6
 22 52  1  0
 26 53  1  0
 26 54  1  0
 26 55  1  0
 17 44  1  1
 16 42  1  0
 16 43  1  0
 15 41  1  1
 11 39  1  0
 11 40  1  0
 10 38  1  1
  8 34  1  6
  9 35  1  0
  9 36  1  0
  9 37  1  0
  5 33  1  6
  1 30  1  0
  1 31  1  0
  1 32  1  0
 27 56  1  1
 29 57  1  0
 29 58  1  0
 29 59  1  0
M  END


  Mrv1652309032221552D          

 29 32  0  0  1  0            999 V2000
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 15 14  1  6  0  0  0
 15 16  1  0  0  0  0
 17 16  1  1  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  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  1  0  0  0
 27 25  1  1  0  0  0
  5 27  1  0  0  0  0
 27 28  1  0  0  0  0
 10 28  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0181411

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@H](O)C(=O)[C@@]2(C)[C@H]1C[C@H]1OC(=O)C[C@H]3[C@@H](C)C(=O)[C@@H](OC(C)=O)[C@H]2[C@@]13C

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O7/c1-9-6-14(24)20(27)22(5)12(9)7-15-21(4)13(8-16(25)29-15)10(2)17(26)18(19(21)22)28-11(3)23/h9-10,12-15,18-19,24H,6-8H2,1-5H3/t9-,10-,12+,13+,14+,15-,18-,19+,21-,22+/m1/s1

> <INCHI_KEY>
HTUPNZUADSZJNJ-WGRRCHGUSA-N

> <FORMULA>
C22H30O7

> <MOLECULAR_WEIGHT>
406.475

> <EXACT_MASS>
406.199153306

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.05224679773395

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,4S,6R,7S,9R,13S,14R,16S,17S)-4-hydroxy-2,6,14,17-tetramethyl-3,11,15-trioxo-10-oxatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadecan-16-yl acetate

> <JCHEM_LOGP>
1.8718631109999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.951586299699233

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.38253115844056

> <JCHEM_PKA_STRONGEST_BASIC>
-3.505710666442284

> <JCHEM_POLAR_SURFACE_AREA>
106.97

> <JCHEM_REFRACTIVITY>
100.90510000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4S,6R,7S,9R,13S,14R,16S,17S)-4-hydroxy-2,6,14,17-tetramethyl-3,11,15-trioxo-10-oxatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadecan-16-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      10.669  -3.080   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.668  -3.850   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   27                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   28                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   28                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   25                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   17   26   27                                             
CONECT   26   25                                                            
CONECT   27   25    5   28                                                  
CONECT   28   27   10   15   29                                             
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Value	Source
Amarolide 11-acetic acid	Generator

Chemical Formula

C₂₂H₃₀O₇

Average Mass

406.4750 Da

Monoisotopic Mass

406.19915 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@H](O)C(=O)[C@@]2(C)[C@H]1C[C@H]1OC(=O)C[C@H]3[C@@H](C)C(=O)[C@@H](OC(C)=O)[C@H]2[C@@]13C

InChI Identifier

InChI=1S/C22H30O7/c1-9-6-14(24)20(27)22(5)12(9)7-15-21(4)13(8-16(25)29-15)10(2)17(26)18(19(21)22)28-11(3)23/h9-10,12-15,18-19,24H,6-8H2,1-5H3/t9-,10-,12+,13+,14+,15-,18-,19+,21-,22+/m1/s1

InChI Key

HTUPNZUADSZJNJ-WGRRCHGUSA-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
Simarouba versicolor	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quassinoids. These are a group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Quassinoids

Alternative Parents

Substituents

Polycyclic triterpenoid
Triterpenoid
C-20 quassinoid skeleton
Quassinoid
Naphthopyran
Naphthalene
Delta valerolactone
Delta_valerolactone
Alpha-acyloxy ketone
Dicarboxylic acid or derivatives
Oxane
Pyran
Cyclic alcohol
Lactone
Ketone
Carboxylic acid ester
Cyclic ketone
Secondary alcohol
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
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

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

405273

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

460540

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for amarolide 11-acetate (NP0181411)

MOL for NP0181411 (amarolide 11-acetate)

3D MOL for NP0181411 (amarolide 11-acetate)

3D SDF for NP0181411 (amarolide 11-acetate)

3D-SDF for NP0181411 (amarolide 11-acetate)

PDB for NP0181411 (amarolide 11-acetate)

3D PDB for NP0181411 (amarolide 11-acetate)

SMILES for NP0181411 (amarolide 11-acetate)

INCHI for NP0181411 (amarolide 11-acetate)

Structure for NP0181411 (amarolide 11-acetate)

3D Structure for NP0181411 (amarolide 11-acetate)