NP-MRD: Showing NP-Card for soulattrolide (NP0147146)

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Record Information

Version

2.0

Created at

2022-09-02 02:41:29 UTC

Updated at

2022-09-02 02:41:30 UTC

NP-MRD ID

NP0147146

Secondary Accession Numbers

None

Natural Product Identification

Common Name

soulattrolide

Description

Soulattrolide belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone. Soulattrolide is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. soulattrolide is found in Calophyllum brasiliense, Calophyllum soulattri and Calophyllum teysmannii. soulattrolide was first documented in 2004 (PMID: 15340243). Based on a literature review very few articles have been published on soulattrolide (PMID: 30244493).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022204412D          

 30 34  0  0  1  0            999 V2000
    2.0329    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3954   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -4.3974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0329   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7899   -1.3553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7899   -0.2947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
  8 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
  7 19  1  0  0  0  0
 19 20  2  0  0  0  0
  4 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
  2 23  1  0  0  0  0
 23 24  1  1  0  0  0
  6 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  2  0  0  0  0
  5 30  1  0  0  0  0
M  END

     RDKit          3D

 54 58  0  0  0  0  0  0  0  0999 V2000
    4.4935    1.5729    0.8544 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2321    0.5666   -0.2743 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9926    0.9025   -0.8303 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8028    0.2342   -0.5235 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5828    0.8532   -0.5501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6152    0.1881   -0.2422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4817   -1.1650    0.0999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6124   -1.8703    0.4084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9042   -1.2160    0.4597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2708   -0.3163    1.4333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5081    0.2788    1.4403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4214   -0.0118    0.4652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0878   -0.9069   -0.5233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8262   -1.5075   -0.5221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5129   -3.2243    0.7434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2608   -3.7700    0.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1525   -4.9923    1.0449 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8039   -3.0703    0.4463 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7657   -1.7893    0.1213 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8879   -1.0855   -0.1879 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2171   -1.7257   -0.1687 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5270   -2.1295   -1.4677 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2964   -0.8071    0.3036 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6486   -1.4565   -0.0006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8147    0.8527   -0.2882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9132    2.1980   -0.6346 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9292    2.4339   -1.7405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4896    2.9635    0.5758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6461    2.8765   -0.9535 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5097    2.2669   -0.9178 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4824    1.3941    1.3128 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4046    2.5962    0.4485 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7307    1.3890    1.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0004    0.6789   -1.0672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5527   -0.0631    2.2332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7785    0.9905    2.2229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4229    0.4506    0.4449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8302   -1.1169   -1.2807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6308   -2.2010   -1.3283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4239   -3.7352    0.9752 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2405   -2.6399    0.4667 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9134   -2.9022   -1.6833 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2385   -0.7733    1.4290 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7709   -1.5734   -1.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6310   -2.4558    0.4544 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4903   -0.8344    0.3387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6242    1.9822   -2.6906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9001    2.1017   -1.3590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9713    3.5319   -1.8978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1206    2.4394    1.4718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1355    4.0265    0.5524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5779    2.8762    0.5479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7042    3.9202   -1.2246 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4564    2.7747   -1.1564 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  2  0
  5 30  1  0
 30 29  2  0
 29 26  1  0
 26 27  1  0
 26 28  1  0
 26 25  1  0
 25  6  1  0
  6  7  2  0
  7 19  1  0
 19 18  1  0
 18 16  1  0
 16 17  2  0
 16 15  1  0
 15  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23  2  1  0
 20  4  1  0
  6  5  1  0
  8  7  1  0
 14  9  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  6
 30 54  1  0
 29 53  1  0
 27 47  1  0
 27 48  1  0
 27 49  1  0
 28 50  1  0
 28 51  1  0
 28 52  1  0
 15 40  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 13 38  1  0
 14 39  1  0
 21 41  1  1
 22 42  1  0
 23 43  1  1
 24 44  1  0
 24 45  1  0
 24 46  1  0
M  END


  Mrv1652309022204412D          

 30 34  0  0  1  0            999 V2000
    2.0329    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3954   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -4.3974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0329   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7899   -1.3553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7899   -0.2947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
  8 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
  7 19  1  0  0  0  0
 19 20  2  0  0  0  0
  4 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
  2 23  1  0  0  0  0
 23 24  1  1  0  0  0
  6 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  2  0  0  0  0
  5 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0147146

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1OC2=C3C=CC(C)(C)OC3=C3C(OC(=O)C=C3C3=CC=CC=C3)=C2[C@@H](O)[C@H]1C

> <INCHI_IDENTIFIER>
InChI=1S/C25H24O5/c1-13-14(2)28-22-16-10-11-25(3,4)30-23(16)19-17(15-8-6-5-7-9-15)12-18(26)29-24(19)20(22)21(13)27/h5-14,21,27H,1-4H3/t13-,14-,21-/m0/s1

> <INCHI_KEY>
BXENDTPSKAICGV-RXSFTSLZSA-N

> <FORMULA>
C25H24O5

> <MOLECULAR_WEIGHT>
404.462

> <EXACT_MASS>
404.162373873

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
43.53022501527937

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(10S,11R,12S)-12-hydroxy-6,6,10,11-tetramethyl-4-phenyl-6,10,11,12-tetrahydro-2H-1,5,9-trioxatriphenylen-2-one

> <ALOGPS_LOGP>
4.56

> <JCHEM_LOGP>
4.036261011666666

> <ALOGPS_LOGS>
-4.97

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.616036057033043

> <JCHEM_PKA_STRONGEST_BASIC>
-3.404145828653747

> <JCHEM_POLAR_SURFACE_AREA>
64.99000000000001

> <JCHEM_REFRACTIVITY>
124.17559999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.36e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(10S,11R,12S)-12-hydroxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10H-1,5,9-trioxatriphenylen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       3.795   1.127   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       6.105  -0.206   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.185  -2.874   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.415  -4.207   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.185  -5.541   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.725  -5.541   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.495  -4.207   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.035  -4.207   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.805  -5.541   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.035  -6.875   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.495  -6.875   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.415  -6.875   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.875  -6.875   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.105  -8.208   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       6.105  -5.541   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.875  -4.207   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.105  -2.874   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.795  -4.207   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.255  -1.540   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.725  -2.874   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.674  -2.530   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.674  -0.550   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   20                                                  
CONECT    5    4    6   30                                                  
CONECT    6    5    7   25                                                  
CONECT    7    6    8   19                                                  
CONECT    8    7    9   15                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15    8   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18    7   20                                                  
CONECT   20   19    4   21                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    2   24                                                  
CONECT   24   23                                                            
CONECT   25    6   26                                                       
CONECT   26   25   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26   30                                                       
CONECT   30   29    5                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Value	Source
(10alpha,11beta,12beta)-(-)-11,12-Dihydro-12-hydroxy-6,6,10,11-tetramethyl-4-phenyl-2H,6H,10H-benzo(1,2-b:3,4-b':5,6-b'')tripyran-2-one	ChEBI
(10a,11b,12b)-(-)-11,12-Dihydro-12-hydroxy-6,6,10,11-tetramethyl-4-phenyl-2H,6H,10H-benzo(1,2-b:3,4-b':5,6-b'')tripyran-2-one	Generator
(10Α,11β,12β)-(-)-11,12-dihydro-12-hydroxy-6,6,10,11-tetramethyl-4-phenyl-2H,6H,10H-benzo(1,2-b:3,4-b':5,6-b'')tripyran-2-one	Generator
11,12-Dihydro-12-hydroxy-6,6,10,11-tetramethyl-4-phenyl-2,6,10-benzotripyran-2-one	MeSH

Chemical Formula

C₂₅H₂₄O₅

Average Mass

404.4620 Da

Monoisotopic Mass

404.16237 Da

IUPAC Name

(10S,11R,12S)-12-hydroxy-6,6,10,11-tetramethyl-4-phenyl-6,10,11,12-tetrahydro-2H-1,5,9-trioxatriphenylen-2-one

Traditional Name

(10S,11R,12S)-12-hydroxy-6,6,10,11-tetramethyl-4-phenyl-11,12-dihydro-10H-1,5,9-trioxatriphenylen-2-one

CAS Registry Number

Not Available

SMILES

C[C@@H]1OC2=C3C=CC(C)(C)OC3=C3C(OC(=O)C=C3C3=CC=CC=C3)=C2[C@@H](O)[C@H]1C

InChI Identifier

InChI=1S/C25H24O5/c1-13-14(2)28-22-16-10-11-25(3,4)30-23(16)19-17(15-8-6-5-7-9-15)12-18(26)29-24(19)20(22)21(13)27/h5-14,21,27H,1-4H3/t13-,14-,21-/m0/s1

InChI Key

BXENDTPSKAICGV-RXSFTSLZSA-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
Calophyllum brasiliense	LOTUS Database	35616633
Calophyllum soulattri	LOTUS Database	35616633
Calophyllum teysmannii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Neoflavonoids

Sub Class

Prenylated neoflavonoids

Direct Parent

Prenylated neoflavonoids

Alternative Parents

Substituents

Prenylated neoflavonoid
Pyranoneoflavonoid
4-phenylcoumarin
Angular pyranocoumarin
Pyranocoumarin
Pyranochromene
2,2-dimethyl-1-benzopyran
Coumarin
Chromane
Benzopyran
1-benzopyran
Alkyl aryl ether
Pyranone
Monocyclic benzene moiety
Pyran
Benzenoid
Heteroaromatic compound
Lactone
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Ether
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

secondary alcohol (CHEBI:66516 )
coumarins (CHEBI:66516 )

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	4.56	ALOGPS
logP	4.04	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	13.62	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	64.99 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	124.18 m³·mol⁻¹	ChemAxon
Polarizability	43.53 Å³	ChemAxon
Number of Rings	5	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

65791

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

72978

PDB ID

Not Available

ChEBI ID

66516

Good Scents ID

rw1531911

References

General References

Huerta-Reyes M, Basualdo Mdel C, Abe F, Jimenez-Estrada M, Soler C, Reyes-Chilpa R: HIV-1 inhibitory compounds from Calophyllum brasiliense leaves. Biol Pharm Bull. 2004 Sep;27(9):1471-5. doi: 10.1248/bpb.27.1471. [PubMed:15340243 ]
Alonso-Castro AJ, Guzman-Gutierrez SL, Betancourt CA, Gasca-Martinez D, Alvarez-Martinez KL, Perez-Nicolas M, Espitia-Pinzon CI, Reyes-Chilpa R: Antinociceptive, anti-inflammatory, and central nervous system (CNS) effects of the natural coumarin soulattrolide. Drug Dev Res. 2018 Nov;79(7):332-338. doi: 10.1002/ddr.21471. Epub 2018 Sep 23. [PubMed:30244493 ]
LOTUS database [Link]

Showing NP-Card for soulattrolide (NP0147146)

MOL for NP0147146 (soulattrolide)

3D MOL for NP0147146 (soulattrolide)

3D SDF for NP0147146 (soulattrolide)

3D-SDF for NP0147146 (soulattrolide)

PDB for NP0147146 (soulattrolide)

3D PDB for NP0147146 (soulattrolide)

SMILES for NP0147146 (soulattrolide)

INCHI for NP0147146 (soulattrolide)

Structure for NP0147146 (soulattrolide)

3D Structure for NP0147146 (soulattrolide)