NP-MRD: Showing NP-Card for Isocalolongic acid (NP0078529)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 23:35:52 UTC

Updated at

2022-04-28 23:35:52 UTC

NP-MRD ID

NP0078529

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Isocalolongic acid

Description

(3R)-3-[(2S,3R)-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2H,3H,4H,8H-pyrano[2,3-f]chromen-6-yl]hexanoic acid belongs to the class of organic compounds known as pyranochromenes. These are organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety. Isocalolongic acid is found in Calophyllum membranaceum and Calophyllum recedens. Based on a literature review very few articles have been published on (3R)-3-[(2S,3R)-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2H,3H,4H,8H-pyrano[2,3-f]chromen-6-yl]hexanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292201352D          

 28 30  0  0  1  0            999 V2000
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -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
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    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
    0.6044   -4.0962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9918   -3.4254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  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  0  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
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
  4 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 13 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
  3 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  1 26  1  0  0  0  0
 25 27  1  6  0  0  0
 24 28  1  6  0  0  0
M  END

     RDKit          3D

 56 58  0  0  0  0  0  0  0  0999 V2000
   -4.3447   -2.3955   -0.6945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1408   -0.9587   -1.2126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7452   -0.5427   -1.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0315   -0.5224    0.2483 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5920    0.4486    1.2278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9664    0.1545    1.6471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3029   -0.8359    2.3617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9825    1.0484    1.2241 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5918   -0.3169   -0.0681 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2211   -1.4653    0.1681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2712   -2.6335    0.5514 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6017   -1.3381   -0.0218 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1934   -0.1370   -0.4230 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3660    0.9536   -0.6315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0013    0.8298   -0.4511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7464    1.9557   -0.6915 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2708    3.2497   -0.5873 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9399    4.1392   -1.6498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6131    3.8279    0.8012 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1791    3.3445   -0.8212 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9335    2.2739   -0.8322 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5610   -0.0658   -0.5957 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4779   -1.0651   -0.2519 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9387   -0.7289    1.1708 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8864   -2.4589   -0.3340 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6699   -3.3619    0.5950 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4811   -2.4668    0.1110 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0151   -3.5378    0.6509 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5590   -2.4930    0.3440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3395   -2.8947   -0.8639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0310   -2.9826   -1.3520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9612   -0.3035   -0.9991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3207   -1.1435   -2.3564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6899    0.4964   -1.5396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1221   -1.1564   -1.8112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1282   -1.5080    0.7300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5173    1.5105    0.8380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0419    0.4785    2.1880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9227    0.7279    1.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4399   -3.4800    0.8126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1888    4.7189   -2.2326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6091    4.8917   -1.1874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5276    3.5397   -2.3673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4849    4.5240    0.6840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8434    3.0193    1.5186 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2574    4.3660    1.1501 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6328    4.3541   -0.9771 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0122    2.3772   -0.9925 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3570   -0.9812   -0.9090 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2817    0.3207    1.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7033   -1.4431    1.5290 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0098   -0.7510    1.7830 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0001   -2.8285   -1.3753 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7691   -3.2052    0.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3775   -4.4009    0.3848 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3421   -3.1481    1.6251 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  8  1  0
  6  7  2  0
  4  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  6
 17 19  1  0
 17 20  1  0
 20 21  2  0
 15  9  1  0
 27 12  1  0
 21 14  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  2 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  1
  5 37  1  0
  5 38  1  0
  8 39  1  0
 11 40  1  0
 23 49  1  6
 24 50  1  0
 24 51  1  0
 24 52  1  0
 25 53  1  6
 26 54  1  0
 26 55  1  0
 26 56  1  0
 18 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 19 45  1  0
 19 46  1  0
 20 47  1  0
 21 48  1  0
M  END


  Mrv1652304292201352D          

 28 30  0  0  1  0            999 V2000
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -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
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    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
    0.6044   -4.0962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9918   -3.4254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  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  0  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
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
  4 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 13 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
  3 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  1 26  1  0  0  0  0
 25 27  1  6  0  0  0
 24 28  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0078529

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC[C@H](CC(O)=O)C1=C(O)C2=C(O[C@@H](C)[C@@H](C)C2=O)C2=C1OC(C)(C)C=C2

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O6/c1-6-7-13(10-15(23)24)16-19(26)17-18(25)11(2)12(3)27-20(17)14-8-9-22(4,5)28-21(14)16/h8-9,11-13,26H,6-7,10H2,1-5H3,(H,23,24)/t11-,12+,13-/m1/s1

> <INCHI_KEY>
MXFUJXIOAUPXPT-FRRDWIJNSA-N

> <FORMULA>
C22H28O6

> <MOLECULAR_WEIGHT>
388.46

> <EXACT_MASS>
388.188588622

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
41.58156840718058

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R)-3-[(4S,5R)-8-hydroxy-4,5,12,12-tetramethyl-6-oxo-3,11-dioxatricyclo[8.4.0.0^{2,7}]tetradeca-1(10),2(7),8,13-tetraen-9-yl]hexanoic acid

> <ALOGPS_LOGP>
4.28

> <JCHEM_LOGP>
4.776656592

> <ALOGPS_LOGS>
-3.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.725637149933641

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.8697654246763014

> <JCHEM_PKA_STRONGEST_BASIC>
-4.643917261818343

> <JCHEM_POLAR_SURFACE_AREA>
93.06000000000002

> <JCHEM_REFRACTIVITY>
106.0911

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.26e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R)-3-[(4S,5R)-8-hydroxy-4,5,12,12-tetramethyl-6-oxo-3,11-dioxatricyclo[8.4.0.0^{2,7}]tetradeca-1(10),2(7),8,13-tetraen-9-yl]hexanoic 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       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.128  -7.646   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.851  -6.394   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       9.336  -2.310   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       9.336  -6.930   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.669  -9.240   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.668 -11.550   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       8.002 -13.860   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
CONECT    1    2    6   26                                                  
CONECT    2    1    3   22                                                  
CONECT    3    2    4   21                                                  
CONECT    4    3    5   13                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   12                                             
CONECT   10    9    5                                                       
CONECT   11    9                                                            
CONECT   12    9                                                            
CONECT   13    4   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   13   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21    3                                                            
CONECT   22    2   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   28                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25    1                                                       
CONECT   27   25                                                            
CONECT   28   24                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Value	Source
(3R)-3-[(2S,3R)-5-Hydroxy-2,3,8,8-tetramethyl-4-oxo-2H,3H,4H,8H-pyrano[2,3-F]chromen-6-yl]hexanoate	Generator

Chemical Formula

C₂₂H₂₈O₆

Average Mass

388.4600 Da

Monoisotopic Mass

388.18859 Da

IUPAC Name

(3R)-3-[(4S,5R)-8-hydroxy-4,5,12,12-tetramethyl-6-oxo-3,11-dioxatricyclo[8.4.0.0^{2,7}]tetradeca-1(10),2(7),8,13-tetraen-9-yl]hexanoic acid

Traditional Name

(3R)-3-[(4S,5R)-8-hydroxy-4,5,12,12-tetramethyl-6-oxo-3,11-dioxatricyclo[8.4.0.0^{2,7}]tetradeca-1(10),2(7),8,13-tetraen-9-yl]hexanoic acid

CAS Registry Number

Not Available

SMILES

CCC[C@H](CC(O)=O)C1=C(O)C2=C(O[C@@H](C)[C@@H](C)C2=O)C2=C1OC(C)(C)C=C2

InChI Identifier

InChI=1S/C22H28O6/c1-6-7-13(10-15(23)24)16-19(26)17-18(25)11(2)12(3)27-20(17)14-8-9-22(4,5)28-21(14)16/h8-9,11-13,26H,6-7,10H2,1-5H3,(H,23,24)/t11-,12+,13-/m1/s1

InChI Key

MXFUJXIOAUPXPT-FRRDWIJNSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Calophyllum membranaceum	Plant	KNApSAcK
Calophyllum recedens	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranochromenes. These are organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Pyranochromenes

Alternative Parents

Substituents

Pyranochromene
2,2-dimethyl-1-benzopyran
Chromone
Medium-chain fatty acid
Aryl alkyl ketone
Aryl ketone
Alkyl aryl ether
Heterocyclic fatty acid
Hydroxy fatty acid
Fatty acyl
Benzenoid
Vinylogous acid
Ketone
Monocarboxylic acid or derivatives
Oxacycle
Ether
Carboxylic acid
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	4.28	ALOGPS
logP	4.78	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	3.87	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	93.06 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	106.09 m³·mol⁻¹	ChemAxon
Polarizability	41.58 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162932865

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Isocalolongic acid (NP0078529)

MOL for NP0078529 (Isocalolongic acid)

3D MOL for NP0078529 (Isocalolongic acid)

3D SDF for NP0078529 (Isocalolongic acid)

3D-SDF for NP0078529 (Isocalolongic acid)

PDB for NP0078529 (Isocalolongic acid)

3D PDB for NP0078529 (Isocalolongic acid)

SMILES for NP0078529 (Isocalolongic acid)

INCHI for NP0078529 (Isocalolongic acid)

Structure for NP0078529 (Isocalolongic acid)

3D Structure for NP0078529 (Isocalolongic acid)