NP-MRD: Showing NP-Card for 3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one (NP0191667)

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Record Information

Version

2.0

Created at

2022-09-04 08:42:11 UTC

Updated at

2022-09-04 08:42:11 UTC

NP-MRD ID

NP0191667

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one

Description

3,6-Dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]Icosa-1(20),2,4,9,12,15-hexaen-14-one belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring. 3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one is found in Penicillium chrysogenum. Based on a literature review very few articles have been published on 3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]Icosa-1(20),2,4,9,12,15-hexaen-14-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042210422D          

 29 33  0  0  0  0            999 V2000
    3.8364   -2.9081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2802   -2.2988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5298   -1.5124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9736   -0.9031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1678   -1.0802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6116   -0.4709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8058   -0.6479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2496   -0.0386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5562   -0.2157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1124    0.3936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8058   -1.0021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6116   -1.1791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2496   -1.6114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5562   -1.4343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1124   -2.0436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9182   -1.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4744   -2.4758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2249   -3.2622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8629   -2.8299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0571   -3.0070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1924   -3.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4991   -2.3977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3049   -2.5748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3811   -0.1859    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1893   -0.3519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7986    0.2044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2811   -1.1717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1061   -1.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7059   -1.8789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  2  0  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
  4 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
  3 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 53 57  0  0  0  0  0  0  0  0999 V2000
    3.0169    3.0279   -0.6413 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2829    1.7509   -0.3452 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9495    0.5515   -0.1998 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3227   -0.6455    0.0717 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9439   -0.6525    0.2079 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3215   -1.7744    0.4659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9807   -1.8781    0.6117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5950   -3.0740    0.8834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9538   -3.0933    1.0218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5650   -4.1802    1.2741 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7418   -1.9469    0.8980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1849   -2.0190    1.0711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1923   -0.7135    0.6250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8128   -0.6800    0.4824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1078    0.4771    0.2103 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2521    0.5456    0.0652 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9107    1.7277   -0.2068 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1592    2.8807   -0.3357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8540    1.6400    0.0789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1976    1.5615   -0.3048 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3050    1.3424   -1.7802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9524    0.4735    0.4871 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3098    0.5083   -0.0946 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2764   -1.6773    0.1594 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3535   -1.2253   -0.6766 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6271   -1.9531   -0.3968 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4017    0.2373   -0.2860 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0331    0.3133    1.0837 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0637    1.0101   -1.2194 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0607    2.9784   -0.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8633    3.3371   -1.6972 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5061    3.8142   -0.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0050   -3.9702    0.9826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4202   -3.0799    1.4263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5514   -1.4404    1.9664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8026   -1.9456    0.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5154    3.7891   -0.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6861    2.5271   -0.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4356    1.8286   -2.2855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2817    0.2521   -2.0067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2164    1.8290   -2.2074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0506    0.9557    1.5111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4879    1.6053   -0.3652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1602    0.3523    0.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4228    0.0214   -1.0859 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0446   -1.2624   -1.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9049   -2.5103   -1.3235 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4876   -1.2946   -0.1697 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5114   -2.7129    0.3930 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8502   -0.6194    1.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6236    1.1562    1.6846 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1241    0.4682    1.0213 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8668    1.3861   -0.7804 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 25  1  0
 25 24  1  0
 24  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 11 13  2  0
 13 22  1  0
 22 23  1  0
 22 20  1  0
 20 21  1  0
 20 19  1  0
 19 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17  2  1  0
  2  1  1  0
  2  3  2  0
  3 27  1  0
 27 28  1  0
 27 29  1  6
 15 14  2  0
 27 25  1  0
  3  4  1  0
 16  5  1  0
 14  7  1  0
 14 13  1  0
 26 47  1  0
 26 48  1  0
 26 49  1  0
 25 46  1  6
  8 33  1  0
 12 34  1  0
 12 35  1  0
 12 36  1  0
 22 42  1  1
 23 43  1  0
 23 44  1  0
 23 45  1  0
 20 38  1  6
 21 39  1  0
 21 40  1  0
 21 41  1  0
 18 37  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 28 50  1  0
 28 51  1  0
 28 52  1  0
 29 53  1  0
M  END


  Mrv1652309042210422D          

 29 33  0  0  0  0            999 V2000
    3.8364   -2.9081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2802   -2.2988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5298   -1.5124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9736   -0.9031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1678   -1.0802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6116   -0.4709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8058   -0.6479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2496   -0.0386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5562   -0.2157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1124    0.3936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8058   -1.0021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6116   -1.1791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2496   -1.6114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5562   -1.4343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1124   -2.0436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9182   -1.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4744   -2.4758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2249   -3.2622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8629   -2.8299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0571   -3.0070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1924   -3.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4991   -2.3977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3049   -2.5748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3811   -0.1859    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1893   -0.3519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7986    0.2044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2811   -1.1717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1061   -1.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7059   -1.8789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  2  0  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
  4 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
  3 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0191667

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC2=C3OC4=CC(=O)C(C)=C5C(C)C(C)OC(C3=C(O)C(C)=C2C1(C)O)=C45

> <INCHI_IDENTIFIER>
InChI=1S/C23H24O6/c1-8-11(4)27-20-16-14(7-13(24)9(2)15(8)16)29-21-17(20)19(25)10(3)18-22(21)28-12(5)23(18,6)26/h7-8,11-12,25-26H,1-6H3

> <INCHI_KEY>
CRSYXEQNEAGMIY-UHFFFAOYSA-N

> <FORMULA>
C23H24O6

> <MOLECULAR_WEIGHT>
396.439

> <EXACT_MASS>
396.157288493

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
43.19466833941243

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0^{2,10}.0^{5,9}.0^{16,20}]icosa-1(20),2,4,9,12,15-hexaen-14-one

> <JCHEM_LOGP>
2.4022160266666672

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.15171328721609

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.5097026706133905

> <JCHEM_PKA_STRONGEST_BASIC>
2.0744561979869567

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
110.12360000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0^{2,10}.0^{5,9}.0^{16,20}]icosa-1(20),2,4,9,12,15-hexaen-14-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       7.161  -5.428   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.123  -4.291   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.589  -2.823   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.551  -1.686   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.047  -2.016   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.008  -0.879   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.504  -1.210   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.466  -0.072   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.038  -0.403   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -2.077   0.735   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.504  -1.870   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.008  -2.201   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.466  -3.008   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.038  -2.677   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.077  -3.815   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.581  -3.484   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.619  -4.622   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.153  -6.089   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       1.611  -5.283   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.107  -5.613   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.359  -7.081   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.932  -4.476   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.436  -4.806   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.311  -0.347   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.820  -0.657   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.957   0.381   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.991  -2.187   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.531  -2.193   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.784  -3.507   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   17                                                  
CONECT    3    2    4   27                                                  
CONECT    4    3    5   24                                                  
CONECT    5    4    6   16                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   14                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   22                                                  
CONECT   14   13    7   15                                                  
CONECT   15   14   16   19                                                  
CONECT   16   15    5   17                                                  
CONECT   17   16    2   18                                                  
CONECT   18   17                                                            
CONECT   19   15   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   13   23                                                  
CONECT   23   22                                                            
CONECT   24    4   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25    3   28   29                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₄O₆

Average Mass

396.4390 Da

Monoisotopic Mass

396.15729 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1OC2=C3OC4=CC(=O)C(C)=C5C(C)C(C)OC(C3=C(O)C(C)=C2C1(C)O)=C45

InChI Identifier

InChI=1S/C23H24O6/c1-8-11(4)27-20-16-14(7-13(24)9(2)15(8)16)29-21-17(20)19(25)10(3)18-22(21)28-12(5)23(18,6)26/h7-8,11-12,25-26H,1-6H3

InChI Key

CRSYXEQNEAGMIY-UHFFFAOYSA-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
Penicillium chrysogenum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Xanthenes

Alternative Parents

Substituents

Xanthene
2-benzopyran
Coumaran
Alkyl aryl ether
Phenol
Benzenoid
Tertiary alcohol
Heteroaromatic compound
Cyclic ketone
Ether
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Alcohol
Organic oxide
Organooxygen 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

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

74830707

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one (NP0191667)

MOL for NP0191667 (3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one)

3D MOL for NP0191667 (3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one)

3D SDF for NP0191667 (3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one)

3D-SDF for NP0191667 (3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one)

PDB for NP0191667 (3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one)

3D PDB for NP0191667 (3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one)

SMILES for NP0191667 (3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one)

INCHI for NP0191667 (3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one)

Structure for NP0191667 (3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one)

3D Structure for NP0191667 (3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one)