NP-MRD: Showing NP-Card for (7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one (NP0264564)

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Record Information

Version

2.0

Created at

2022-09-08 08:08:05 UTC

Updated at

2022-09-08 08:08:06 UTC

NP-MRD ID

NP0264564

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one

Description

CHEMBL3357565 belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system. (7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one is found in Maclura tricuspidata. Based on a literature review very few articles have been published on CHEMBL3357565.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082210082D          

 29 33  0  0  1  0            999 V2000
    0.5906   -4.7876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3900   -4.5838    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0248   -5.1108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7221   -4.6699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5163   -4.8931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1068   -4.3169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9010   -4.5402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4914   -3.9640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2857   -4.1872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8761   -3.6110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6723   -2.8116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2627   -2.2354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8781   -2.5883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2876   -3.1645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4934   -2.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2896   -2.1419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9030   -3.5175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1088   -3.2943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9050   -2.4948    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5183   -3.8705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6950   -3.8173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6533   -2.9933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9686   -3.4261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6703   -3.8342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8741   -4.6337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6260   -4.2942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3390   -5.3152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2837   -5.2099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4894   -4.9866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
  4 20  2  0  0  0  0
 20 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 10 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  2  0  0  0  0
  9 29  1  0  0  0  0
M  END

     RDKit          3D

 51 55  0  0  0  0  0  0  0  0999 V2000
   -6.3681    1.6946   -1.0293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0355    1.6002   -0.3181 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9602    1.9618   -1.1147 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8668    1.2077   -0.7087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4923    1.3703   -0.8924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5685    0.4806   -0.3938 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7341    0.6299   -0.5647 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6138   -0.2190   -0.0889 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9697   -0.0028   -0.3045 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8707   -0.9104    0.2065 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4772   -2.0364    0.9309 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4279   -2.9199    1.4240 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1296   -2.2237    1.1281 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2024   -1.3380    0.6322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1451   -1.5359    0.8360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5540   -2.5302    1.4793 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0199   -0.6168    0.3162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3911   -0.8079    0.5174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7861   -1.9177    1.2288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2775    0.0920    0.0112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7390    0.1690    0.0640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3330   -0.1512    1.4217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3309   -0.7490   -1.0117 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2068   -0.7067   -0.0002 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7226    0.3683   -0.7001 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6208   -0.1720   -1.8045 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6389    1.1691    0.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7316    1.3185   -1.2323 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4544    1.1429   -1.0466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3447    1.3221   -2.0569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0846    1.0616   -0.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7809    2.7317   -0.9499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0524    2.2718    0.5671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1544    2.2338   -1.4504 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4022   -2.7348    1.2505 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8104   -3.0919    1.6876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7339   -2.1388    1.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0829    0.6629    1.6263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8674   -1.1177    1.4173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5975   -0.0887    2.2223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8119   -1.7263   -0.9345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0664   -0.2660   -1.9868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4119   -0.8163   -0.8681 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1144   -1.0056   -2.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5614   -0.4991   -1.3114 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8730    0.5846   -2.5498 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2939    0.5439    0.8202 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0096    1.7729    0.8984 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2252    1.8956   -0.4054 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0581    2.2006   -1.8008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7084    1.8366   -1.4338 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 20  2  0
 20 18  1  0
 18 19  1  0
 18 17  2  0
 17  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 29  1  0
 29 28  2  0
 28 25  1  0
 25 26  1  0
 25 27  1  0
 25 24  1  0
 24 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  6  5  2  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 21  2  1  0
  5  4  1  0
 15 17  1  0
 14  8  1  0
 10  9  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  1
 19 37  1  0
 29 51  1  0
 28 50  1  0
 26 44  1  0
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 27 48  1  0
 27 49  1  0
 12 35  1  0
 13 36  1  0
  5 34  1  0
 22 38  1  0
 22 39  1  0
 22 40  1  0
 23 41  1  0
 23 42  1  0
 23 43  1  0
M  END


  Mrv1652309082210082D          

 29 33  0  0  1  0            999 V2000
    0.5906   -4.7876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3900   -4.5838    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0248   -5.1108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7221   -4.6699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5163   -4.8931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1068   -4.3169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9010   -4.5402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4914   -3.9640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2857   -4.1872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8761   -3.6110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6723   -2.8116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2627   -2.2354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8781   -2.5883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2876   -3.1645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4934   -2.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2896   -2.1419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9030   -3.5175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1088   -3.2943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9050   -2.4948    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5183   -3.8705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6950   -3.8173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6533   -2.9933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9686   -3.4261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6703   -3.8342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8741   -4.6337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6260   -4.2942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3390   -5.3152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2837   -5.2099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4894   -4.9866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
  4 20  2  0  0  0  0
 20 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 10 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  2  0  0  0  0
  9 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0264564

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1OC2=C(C(O)=C3C(OC4=C5C=CC(C)(C)OC5=C(O)C=C4C3=O)=C2)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C23H22O6/c1-10-23(4,5)17-15(27-10)9-14-16(19(17)26)18(25)12-8-13(24)21-11(20(12)28-14)6-7-22(2,3)29-21/h6-10,24,26H,1-5H3/t10-/m0/s1

> <INCHI_KEY>
UNAGKSRBZSVESZ-JTQLQIEISA-N

> <FORMULA>
C23H22O6

> <MOLECULAR_WEIGHT>
394.423

> <EXACT_MASS>
394.141638428

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
42.71882819864665

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(7S)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0^{3,11}.0^{5,9}.0^{14,19}]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one

> <JCHEM_LOGP>
4.944898920666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.606391037727168

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.767648629127079

> <JCHEM_PKA_STRONGEST_BASIC>
-3.716110503864529

> <JCHEM_POLAR_SURFACE_AREA>
85.22

> <JCHEM_REFRACTIVITY>
108.23280000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(7S)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0^{3,11}.0^{5,9}.0^{14,19}]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       1.102  -8.937   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.595  -8.556   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.780  -9.540   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       5.081  -8.717   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.564  -9.134   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.666  -8.058   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.149  -8.475   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.251  -7.399   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.733  -7.816   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.835  -6.741   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.455  -5.248   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      13.557  -4.173   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.972  -4.832   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.870  -5.907   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.388  -5.490   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.007  -3.998   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.286  -6.566   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.803  -6.149   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.423  -4.657   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.701  -7.225   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.164  -7.126   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.086  -5.588   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.808  -6.395   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      14.318  -7.157   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      14.698  -8.650   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      16.102  -8.016   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.566  -9.922   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.596  -9.725   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.114  -9.308   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   20                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10   29                                                  
CONECT   10    9   11   24                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13    8   15                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    6   18                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    4   21                                                  
CONECT   21   20    2   22   23                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   10   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   29                                                       
CONECT   29   28    9                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₂O₆

Average Mass

394.4230 Da

Monoisotopic Mass

394.14164 Da

IUPAC Name

(7S)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0^{3,11}.0^{5,9}.0^{14,19}]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one

Traditional Name

(7S)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0^{3,11}.0^{5,9}.0^{14,19}]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one

CAS Registry Number

Not Available

SMILES

C[C@@H]1OC2=C(C(O)=C3C(OC4=C5C=CC(C)(C)OC5=C(O)C=C4C3=O)=C2)C1(C)C

InChI Identifier

InChI=1S/C23H22O6/c1-10-23(4,5)17-15(27-10)9-14-16(19(17)26)18(25)12-8-13(24)21-11(20(12)28-14)6-7-22(2,3)29-21/h6-10,24,26H,1-5H3/t10-/m0/s1

InChI Key

UNAGKSRBZSVESZ-JTQLQIEISA-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
Maclura tricuspidata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Pyranoxanthones

Alternative Parents

Substituents

Pyranoxanthone
Pyranochromene
Furanochromone
2,2-dimethyl-1-benzopyran
Chromone
Coumaran
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Heteroaromatic compound
Vinylogous acid
Ether
Oxacycle
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
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	4.94	ChemAxon
pKa (Strongest Acidic)	8.77	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	108.23 m³·mol⁻¹	ChemAxon
Polarizability	42.72 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

58132703

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

118722299

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one (NP0264564)

MOL for NP0264564 ((7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one)

3D MOL for NP0264564 ((7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one)

3D SDF for NP0264564 ((7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one)

3D-SDF for NP0264564 ((7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one)

PDB for NP0264564 ((7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one)

3D PDB for NP0264564 ((7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one)

SMILES for NP0264564 ((7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one)

INCHI for NP0264564 ((7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one)

Structure for NP0264564 ((7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one)

3D Structure for NP0264564 ((7s)-4,20-dihydroxy-6,6,7,17,17-pentamethyl-8,12,18-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-1(21),3,5(9),10,13,15,19-heptaen-2-one)