NP-MRD: Showing NP-Card for Blancoic acid (NP0078341)

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Record Information

Version

2.0

Created at

2022-04-28 23:26:24 UTC

Updated at

2022-04-28 23:26:24 UTC

NP-MRD ID

NP0078341

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Blancoic acid

Description

(3R)-3-[(2S,3R)-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-10-yl]octanoic 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. Blancoic acid is found in Calophyllum blancoi, Calophyllum membranaceum and Calophyllum polyanthum. 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[3,2-g]chromen-10-yl]octanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292201262D          

 30 32  0  0  1  0            999 V2000
    0.0169    3.1084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2870    3.8880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2531    4.5116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0632    4.3557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3333    3.5762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7932    2.9525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0632    2.1730    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8734    2.0171    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
   -1.6033    0.6139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9535    1.0816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5231    1.5493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2870    1.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8271    1.0816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6372    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1773    0.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.4202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6835    4.0439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4135    4.8234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6033    4.9793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3256    3.5259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4720    4.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0169    5.2912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971    4.0439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3672    4.8234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6372    3.4202    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3672    2.6407    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5570    2.4848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9073    2.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4473    3.5762    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  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
  4 20  1  0  0  0  0
 18 21  1  0  0  0  0
 18 22  1  0  0  0  0
  3 23  1  0  0  0  0
  2 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  1 28  1  0  0  0  0
 27 29  1  6  0  0  0
 26 30  1  6  0  0  0
M  END

     RDKit          3D

 62 64  0  0  0  0  0  0  0  0999 V2000
    6.3707   -2.0493   -0.2799 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3304   -0.9740   -0.0317 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9098   -1.5434   -0.1499 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9987   -0.3655    0.1240 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5272   -0.7346    0.0256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7552    0.5277    0.2996 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0077    1.0796    1.6607 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6606    0.1907    2.7883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8668    0.5275    3.9755 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0975   -1.0363    2.5513 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6448    0.5088   -0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2919    1.7322   -0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6007    1.8113   -0.6656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3467    0.6666   -0.9641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6258    0.7805   -1.3551 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6874   -0.5502   -0.8308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3766   -0.6262   -0.4302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7326   -1.8181   -0.3020 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2258   -3.0423   -0.6958 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9865   -4.0854    0.3989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462   -3.0883   -1.1269 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4688   -4.0654   -0.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3634   -1.8117   -1.1012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5921   -1.8392   -1.3223 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1915    3.1318   -0.8087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5219    4.2443   -0.5711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1210    4.2055   -0.1432 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9170    4.9331    1.1854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2186    4.8883   -1.1573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6315    2.9039    0.0097 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1947   -2.9286    0.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3485   -1.5719   -0.0368 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4100   -2.2626   -1.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4868   -0.4312    0.9018 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4890   -0.2085   -0.8540 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8236   -2.3015    0.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7416   -1.9666   -1.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1944    0.3869   -0.6648 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3023    0.0475    1.0834 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3133   -1.5641    0.7151 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3723   -1.0558   -1.0271 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2469    1.2895   -0.4094 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0714    1.4537    1.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4074    2.0268    1.7845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4837   -1.5758    3.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3449    0.1866   -1.6158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5757   -3.4007   -1.5514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4726   -5.0173    0.1105 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1053   -4.2715    0.4112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2465   -3.7085    1.4046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7350   -3.4934   -2.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4589   -5.0806   -0.7264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1585   -4.0763    0.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5466   -3.7516   -0.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2202    3.1941   -1.1202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9996    5.2303   -0.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5703    4.4840    1.9709 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1490    4.8447    1.4369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2659    5.9774    1.0309 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8357    4.8069   -0.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4915    5.9358   -1.3462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2559    4.3001   -2.0958 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  7  1  0
  7  8  1  0
  8 10  1  0
  8  9  2  0
  6 11  1  0
 11 12  2  0
 12 30  1  0
 30 27  1  0
 27 28  1  1
 27 29  1  0
 27 26  1  0
 26 25  2  0
 25 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
 17 11  1  0
 13 12  1  0
 23 16  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  6 42  1  6
  7 43  1  0
  7 44  1  0
 10 45  1  0
 28 57  1  0
 28 58  1  0
 28 59  1  0
 29 60  1  0
 29 61  1  0
 29 62  1  0
 26 56  1  0
 25 55  1  0
 15 46  1  0
 19 47  1  6
 20 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  6
 22 52  1  0
 22 53  1  0
 22 54  1  0
M  END


  Mrv1652304292201262D          

 30 32  0  0  1  0            999 V2000
    0.0169    3.1084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2870    3.8880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2531    4.5116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0632    4.3557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3333    3.5762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7932    2.9525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0632    2.1730    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8734    2.0171    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
   -1.6033    0.6139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9535    1.0816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5231    1.5493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2870    1.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8271    1.0816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6372    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1773    0.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.4202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6835    4.0439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4135    4.8234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6033    4.9793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3256    3.5259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4720    4.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0169    5.2912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971    4.0439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3672    4.8234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6372    3.4202    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3672    2.6407    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5570    2.4848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9073    2.0171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4473    3.5762    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  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
  4 20  1  0  0  0  0
 18 21  1  0  0  0  0
 18 22  1  0  0  0  0
  3 23  1  0  0  0  0
  2 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  1 28  1  0  0  0  0
 27 29  1  6  0  0  0
 26 30  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0078341

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC[C@H](CC(O)=O)C1=C2OC(C)(C)C=CC2=C(O)C2=C1O[C@@H](C)[C@@H](C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O6/c1-6-7-8-9-15(12-17(25)26)18-22-16(10-11-24(4,5)30-22)21(28)19-20(27)13(2)14(3)29-23(18)19/h10-11,13-15,28H,6-9,12H2,1-5H3,(H,25,26)/t13-,14+,15-/m1/s1

> <INCHI_KEY>
ZZCZMGFDYJQMIS-QLFBSQMISA-N

> <FORMULA>
C24H32O6

> <MOLECULAR_WEIGHT>
416.514

> <EXACT_MASS>
416.21988875

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
45.54371264069067

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R)-3-[(5S,6R)-9-hydroxy-5,6,13,13-tetramethyl-7-oxo-4,14-dioxatricyclo[8.4.0.0^{3,8}]tetradeca-1,3(8),9,11-tetraen-2-yl]octanoic acid

> <ALOGPS_LOGP>
4.81

> <JCHEM_LOGP>
5.665793922000001

> <ALOGPS_LOGS>
-4.27

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.556546105244697

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.092254804265887

> <JCHEM_PKA_STRONGEST_BASIC>
-4.638539111831608

> <JCHEM_POLAR_SURFACE_AREA>
93.06000000000002

> <JCHEM_REFRACTIVITY>
115.2931

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.24e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R)-3-[(5S,6R)-9-hydroxy-5,6,13,13-tetramethyl-7-oxo-4,14-dioxatricyclo[8.4.0.0^{3,8}]tetradeca-1,3(8),9,11-tetraen-2-yl]octanoic 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       0.032   5.802   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.536   7.258   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.472   8.422   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.985   8.131   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.489   6.675   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.481   5.511   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.985   4.056   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.497   3.765   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      -2.993   1.146   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      -5.513   2.019   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.977   2.892   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.536   3.183   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.544   2.019   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.056   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.064   1.146   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -4.001   6.384   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -5.009   7.549   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.505   9.004   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.993   9.295   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.208   6.582   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.481   8.002   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.032   9.877   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.048   7.549   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.552   9.004   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.056   6.384   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.552   4.929   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.040   4.638   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.560   3.765   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.568   6.675   0.000  0.00  0.00           C+0
CONECT    1    2    6   28                                                  
CONECT    2    1    3   24                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5   20                                                  
CONECT    5    4    6   17                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17    5   18                                                       
CONECT   18   17   19   21   22                                             
CONECT   19   18   20                                                       
CONECT   20   19    4                                                       
CONECT   21   18                                                            
CONECT   22   18                                                            
CONECT   23    3                                                            
CONECT   24    2   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   30                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27    1                                                       
CONECT   29   27                                                            
CONECT   30   26                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    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[3,2-g]chromen-10-yl]octanoate	Generator

Chemical Formula

C₂₄H₃₂O₆

Average Mass

416.5140 Da

Monoisotopic Mass

416.21989 Da

IUPAC Name

(3R)-3-[(5S,6R)-9-hydroxy-5,6,13,13-tetramethyl-7-oxo-4,14-dioxatricyclo[8.4.0.0^{3,8}]tetradeca-1,3(8),9,11-tetraen-2-yl]octanoic acid

Traditional Name

(3R)-3-[(5S,6R)-9-hydroxy-5,6,13,13-tetramethyl-7-oxo-4,14-dioxatricyclo[8.4.0.0^{3,8}]tetradeca-1,3(8),9,11-tetraen-2-yl]octanoic acid

CAS Registry Number

Not Available

SMILES

CCCCC[C@H](CC(O)=O)C1=C2OC(C)(C)C=CC2=C(O)C2=C1O[C@@H](C)[C@@H](C)C2=O

InChI Identifier

InChI=1S/C24H32O6/c1-6-7-8-9-15(12-17(25)26)18-22-16(10-11-24(4,5)30-22)21(28)19-20(27)13(2)14(3)29-23(18)19/h10-11,13-15,28H,6-9,12H2,1-5H3,(H,25,26)/t13-,14+,15-/m1/s1

InChI Key

ZZCZMGFDYJQMIS-QLFBSQMISA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
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 blancoi	Plant	KNApSAcK
Calophyllum membranaceum	Plant	KNApSAcK
Calophyllum polyanthum	LOTUS Database	35616633

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	4.81	ALOGPS
logP	5.67	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	4.09	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	7	ChemAxon
Refractivity	115.29 m³·mol⁻¹	ChemAxon
Polarizability	45.54 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

163030896

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Blancoic acid (NP0078341)

MOL for NP0078341 (Blancoic acid)

3D MOL for NP0078341 (Blancoic acid)

3D SDF for NP0078341 (Blancoic acid)

3D-SDF for NP0078341 (Blancoic acid)

PDB for NP0078341 (Blancoic acid)

3D PDB for NP0078341 (Blancoic acid)

SMILES for NP0078341 (Blancoic acid)

INCHI for NP0078341 (Blancoic acid)

Structure for NP0078341 (Blancoic acid)

3D Structure for NP0078341 (Blancoic acid)