NP-MRD: Showing NP-Card for picrasin e (NP0312224)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 08:49:37 UTC

Updated at

2022-09-11 08:49:37 UTC

NP-MRD ID

NP0312224

Secondary Accession Numbers

None

Natural Product Identification

Common Name

picrasin e

Description

Picrasin E 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. picrasin e is found in Picrasma quassioides. Based on a literature review very few articles have been published on Picrasin E.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112210492D          

 29 33  0  0  1  0            999 V2000
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 O   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  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  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
    0.0000   -1.6500    0.0000 O   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
    1.4289   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  1  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
    2.1434    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3149    2.0445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1354    2.1307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4710    1.3770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  1  0  0  0
 18 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
  3 26  1  0  0  0  0
 26 27  2  0  0  0  0
 23 28  1  0  0  0  0
  9 28  1  0  0  0  0
 14 28  1  0  0  0  0
 28 29  1  6  0  0  0
M  END

     RDKit          3D

 59 63  0  0  0  0  0  0  0  0999 V2000
    4.7963    1.5648    2.2074 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8153    0.5495    2.3665 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1489    0.1151    1.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4741   -1.1137    0.7914 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7749   -1.6400   -0.4425 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7807   -3.1537   -0.4287 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3792   -1.1957   -0.2797 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3023   -1.9276   -0.9770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8183   -1.1851   -1.6007 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8954   -2.1402   -1.7258 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1559   -1.9449   -1.2784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9093   -2.8850   -0.9227 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6531   -0.5772   -1.2099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6255    0.2967   -0.5761 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0823    1.6235   -0.8532 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8136    0.2206    0.9166 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8060   -1.1558    1.4879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9626    1.2076    1.5620 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4111    2.4038    1.9612 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2141    3.0993    2.2585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1561    2.3191    1.7337 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7637    1.6878    0.6947 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2257    0.5253    0.0321 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1843    0.3371   -0.3363 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6317    0.7631   -1.7110 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1622    0.9395    0.5664 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1708    2.1612    0.7774 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2174    0.1279   -1.0758 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1708    1.1200   -2.2557 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2770    2.4503    1.7809 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5666    1.2711    1.4601 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2756    1.7486    3.1735 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1906   -1.7471    1.2472 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2874   -1.3265   -1.3563 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7100   -3.5593   -1.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8096   -3.4563   -0.0791 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9933   -3.5805    0.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1629   -1.3845    0.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1518   -2.7396   -0.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8160   -2.5641   -1.7634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5384   -1.0966   -2.7072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5930   -0.4503   -0.6665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8392   -0.1674   -2.2438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7539    1.6645   -1.5425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8829    0.5735    1.0812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1823   -1.8983    0.9894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8338   -1.6008    1.5069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5321   -1.0573    2.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4822    0.7035    2.4578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0669    3.1572    3.3562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2364    4.0854    1.7630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1357    2.5192    0.0259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4079   -0.3214    0.7864 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5677   -0.0404   -2.4736 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7647    0.9175   -1.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2938    1.7543   -2.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5701    0.7504   -3.1009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2032    1.1022   -2.7380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0450    2.1499   -1.9556 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  6
 14 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  6
 24 26  1  0
 26 27  2  0
 23 28  1  0
 28 29  1  6
 26  3  1  0
 24  7  1  0
 28  9  1  0
 28 14  1  0
 22 18  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  5 34  1  6
  6 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  1
  8 39  1  0
  8 40  1  0
  9 41  1  6
 13 42  1  0
 13 43  1  0
 15 44  1  0
 16 45  1  6
 17 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  1
 20 50  1  0
 20 51  1  0
 22 52  1  6
 23 53  1  1
 25 54  1  0
 25 55  1  0
 25 56  1  0
 29 57  1  0
 29 58  1  0
 29 59  1  0
M  END


  Mrv1652309112210492D          

 29 33  0  0  1  0            999 V2000
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 O   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  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  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
    0.0000   -1.6500    0.0000 O   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
    1.4289   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  1  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
    2.1434    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3149    2.0445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1354    2.1307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4710    1.3770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  1  0  0  0
 18 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
  3 26  1  0  0  0  0
 26 27  2  0  0  0  0
 23 28  1  0  0  0  0
  9 28  1  0  0  0  0
 14 28  1  0  0  0  0
 28 29  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0312224

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C[C@@H](C)[C@@H]2C[C@H]3OC(=O)C[C@@]4(O)[C@@H](C)[C@@H]5OCO[C@H]5[C@H]([C@@]2(C)C1=O)[C@@]34C

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O7/c1-10-6-13(26-5)19(24)20(3)12(10)7-14-21(4)18(20)17-16(27-9-28-17)11(2)22(21,25)8-15(23)29-14/h6,10-12,14,16-18,25H,7-9H2,1-5H3/t10-,11+,12+,14-,16+,17-,18-,20+,21-,22-/m1/s1

> <INCHI_KEY>
MPKJVOULXZBGDT-ATNJLCLCSA-N

> <FORMULA>
C22H30O7

> <MOLECULAR_WEIGHT>
406.475

> <EXACT_MASS>
406.199153306

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.2849650496547

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,6S,7S,8R,12R,14S,15S,19S,20S)-8-hydroxy-17-methoxy-7,15,19,20-tetramethyl-3,5,11-trioxapentacyclo[10.7.1.0^{2,6}.0^{8,20}.0^{14,19}]icos-16-ene-10,18-dione

> <JCHEM_LOGP>
1.5674383073333336

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.7414514032987

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3492891561971474

> <JCHEM_POLAR_SURFACE_AREA>
91.29000000000002

> <JCHEM_REFRACTIVITY>
102.48599999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,6S,7S,8R,12R,14S,15S,19S,20S)-8-hydroxy-17-methoxy-7,15,19,20-tetramethyl-3,5,11-trioxapentacyclo[10.7.1.0^{2,6}.0^{8,20}.0^{14,19}]icos-16-ene-10,18-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.669   0.000   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.334   0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.321   3.816   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.853   3.977   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.479   2.570   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.668   0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.002   1.540   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.335  -1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   26                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   24                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   28                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16   28                                             
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   18   23                                                  
CONECT   23   22   24   28                                                  
CONECT   24   23    7   25   26                                             
CONECT   25   24                                                            
CONECT   26   24    3   27                                                  
CONECT   27   26                                                            
CONECT   28   23    9   14   29                                             
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

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

COC1=C[C@@H](C)[C@@H]2C[C@H]3OC(=O)C[C@@]4(O)[C@@H](C)[C@@H]5OCO[C@H]5[C@H]([C@@]2(C)C1=O)[C@@]34C

InChI Identifier

InChI=1S/C22H30O7/c1-10-6-13(26-5)19(24)20(3)12(10)7-14-21(4)18(20)17-16(27-9-28-17)11(2)22(21,25)8-15(23)29-14/h6,10-12,14,16-18,25H,7-9H2,1-5H3/t10-,11+,12+,14-,16+,17-,18-,20+,21-,22-/m1/s1

InChI Key

MPKJVOULXZBGDT-ATNJLCLCSA-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
Picrasma quassioides	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

Triterpenoid
Polycyclic triterpenoid
C-20 quassinoid skeleton
Quassinoid
Naphthopyran
Naphthalene
Cyclohexenone
Delta valerolactone
Delta_valerolactone
Pyran
Oxane
Cyclic alcohol
Tertiary alcohol
Meta-dioxolane
Carboxylic acid ester
Ketone
Lactone
Oxacycle
Acetal
Carboxylic acid derivative
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

triterpenoid (CHEBI:80892 )
Dammarenes (C17052 )

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

C00058673

Chemspider ID

158397

KEGG Compound ID

C17052

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

182116

PDB ID

Not Available

ChEBI ID

80892

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for picrasin e (NP0312224)

MOL for NP0312224 (picrasin e)

3D MOL for NP0312224 (picrasin e)

3D SDF for NP0312224 (picrasin e)

3D-SDF for NP0312224 (picrasin e)

PDB for NP0312224 (picrasin e)

3D PDB for NP0312224 (picrasin e)

SMILES for NP0312224 (picrasin e)

INCHI for NP0312224 (picrasin e)

Structure for NP0312224 (picrasin e)

3D Structure for NP0312224 (picrasin e)