NP-MRD: Showing NP-Card for (4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one (NP0281038)

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Record Information

Version

2.0

Created at

2022-09-09 07:08:59 UTC

Updated at

2022-09-09 07:08:59 UTC

NP-MRD ID

NP0281038

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one

Description

Austocystin A belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring. (4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one is found in Aspergillus ustus. Based on a literature review very few articles have been published on Austocystin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092209092D          

 26 30  0  0  1  0            999 V2000
    5.7332    4.7905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0788    4.2881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1867    3.4701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9490    3.1546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6034    3.6571    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    6.0569    2.3367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4026    1.8343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6403    2.1498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9859    1.6474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2236    1.9629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5692    1.4605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8069    1.7760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990    2.5939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3534    3.0963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2455    3.9142    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8999    4.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1157    2.7808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7701    3.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6622    4.1011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5324    2.9677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8878    2.7440    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3197    3.3423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4248    2.9869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3169    2.1690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944    2.0189    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0624    1.4206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  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
 14 17  2  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  3 20  2  0  0  0  0
  8 20  1  0  0  0  0
 21 13  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  1  0  0  0
 21 25  1  0  0  0  0
 25 26  1  0  0  0  0
 12 26  1  0  0  0  0
M  END

     RDKit          3D

 39 43  0  0  0  0  0  0  0  0999 V2000
   -3.8657   -1.4837    1.5456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7999   -1.1859    0.1671 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6567    0.1417   -0.1913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7374    0.9686   -0.4027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3812    0.3439   -0.2182 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -4.5036    2.2819   -0.7580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2278    2.7855   -0.9062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1387    1.9551   -0.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9047    2.3780   -0.8207 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1260    1.5803   -0.6172 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4169    2.0498   -0.7567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5313    1.2313   -0.5485 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3535   -0.0889   -0.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0776   -0.5673   -0.0506 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -1.8659    0.3004 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7045   -2.9450   -0.5971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0344    0.2598   -0.2610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3160   -0.2192   -0.1189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4567   -1.4269    0.2065 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3779    0.6302   -0.3357 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6614   -0.7341   -0.0348 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2182   -0.6229    1.3205 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4340   -0.1178    1.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7775    0.1385   -0.0975 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5705    0.2183   -0.8233 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8995    1.4464   -0.6202 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4791   -2.4948    1.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9330   -1.3641    1.8415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3098   -0.6953    2.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3505    2.9441   -0.9275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0521    3.8321   -1.1892 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5501    3.0733   -1.0329 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7071   -3.4636   -0.6285 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3650   -2.6542   -1.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0005   -3.7228   -0.2163 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7090   -1.7595   -0.4308 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7711   -0.8891    2.2822 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1434    0.1030    2.0459 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6567   -0.0610   -1.8719 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 14  1  0
 14 17  2  0
 17 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  4  2  0
  4  5  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  3 20  2  0
 20 18  1  0
 18 19  2  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 13 14  1  0
 25 21  1  0
 18 17  1  0
 26 12  1  0
 20  8  1  0
 16 33  1  0
 16 34  1  0
 16 35  1  0
  7 31  1  0
  6 30  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
 11 32  1  0
 21 36  1  6
 22 37  1  0
 23 38  1  0
 25 39  1  6
M  END


  Mrv1652309092209092D          

 26 30  0  0  1  0            999 V2000
    5.7332    4.7905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0788    4.2881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1867    3.4701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9490    3.1546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6034    3.6571    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    6.0569    2.3367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4026    1.8343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6403    2.1498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9859    1.6474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2236    1.9629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5692    1.4605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8069    1.7760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990    2.5939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3534    3.0963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2455    3.9142    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8999    4.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1157    2.7808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7701    3.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6622    4.1011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5324    2.9677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8878    2.7440    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3197    3.3423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4248    2.9869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3169    2.1690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944    2.0189    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0624    1.4206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  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
 14 17  2  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  3 20  2  0  0  0  0
  8 20  1  0  0  0  0
 21 13  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  1  0  0  0
 21 25  1  0  0  0  0
 25 26  1  0  0  0  0
 12 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0281038

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2C(OC3=CC=C(Cl)C(OC)=C3C2=O)=CC2=C1[C@@H]1C=CO[C@@H]1O2

> <INCHI_IDENTIFIER>
InChI=1S/C19H13ClO6/c1-22-17-9(20)3-4-10-14(17)16(21)15-12(25-10)7-11-13(18(15)23-2)8-5-6-24-19(8)26-11/h3-8,19H,1-2H3/t8-,19+/m0/s1

> <INCHI_KEY>
POXKBPUNCDMQMW-WPCRTTGESA-N

> <FORMULA>
C19H13ClO6

> <MOLECULAR_WEIGHT>
372.76

> <EXACT_MASS>
372.0400658

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
36.044268559565424

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4S,8R)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0^{3,10}.0^{4,8}.0^{14,19}]icosa-1,3(10),5,11,14,16,18-heptaen-20-one

> <JCHEM_LOGP>
3.198530423333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.671090166241363

> <JCHEM_POLAR_SURFACE_AREA>
63.22000000000001

> <JCHEM_REFRACTIVITY>
92.9897

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4S,8R)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0^{3,10}.0^{4,8}.0^{14,19}]icosa-1,3(10),5,11,14,16,18-heptaen-20-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      10.702   8.942   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.480   8.004   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       9.682   6.478   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.105   5.889   0.000  0.00  0.00           C+0
HETATM    5 Cl   UNK     0      12.326   6.827   0.000  0.00  0.00          Cl+0
HETATM    6  C   UNK     0      11.306   4.362   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.085   3.424   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.662   4.013   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.440   3.075   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.017   3.664   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.796   2.726   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.373   3.315   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.172   4.842   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.393   5.780   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.192   7.307   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.413   8.244   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.816   5.191   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.037   6.129   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.836   7.655   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.460   5.540   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.657   5.122   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.597   6.239   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.793   5.576   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.591   4.049   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.923   3.769   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.983   2.652   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   20                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   26                                                  
CONECT   13   12   14   21                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   10   18                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    3    8                                                  
CONECT   21   13   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   21   26                                                  
CONECT   26   25   12                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₃ClO₆

Average Mass

372.7600 Da

Monoisotopic Mass

372.04007 Da

IUPAC Name

(4S,8R)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0^{3,10}.0^{4,8}.0^{14,19}]icosa-1,3(10),5,11,14,16,18-heptaen-20-one

Traditional Name

(4S,8R)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0^{3,10}.0^{4,8}.0^{14,19}]icosa-1,3(10),5,11,14,16,18-heptaen-20-one

CAS Registry Number

Not Available

SMILES

COC1=C2C(OC3=CC=C(Cl)C(OC)=C3C2=O)=CC2=C1[C@@H]1C=CO[C@@H]1O2

InChI Identifier

InChI=1S/C19H13ClO6/c1-22-17-9(20)3-4-10-14(17)16(21)15-12(25-10)7-11-13(18(15)23-2)8-5-6-24-19(8)26-11/h3-8,19H,1-2H3/t8-,19+/m0/s1

InChI Key

POXKBPUNCDMQMW-WPCRTTGESA-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
Aspergillus ustus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Xanthones

Alternative Parents

Substituents

Xanthone
Furanochromone
Chromone
Coumaran
Anisole
Alkyl aryl ether
Pyranone
Aryl chloride
Aryl halide
Benzenoid
Pyran
Heteroaromatic compound
Vinylogous ester
Dihydrofuran
Acetal
Oxacycle
Ether
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organochloride
Organic oxide
Organohalogen 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	3.2	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	63.22 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	92.99 m³·mol⁻¹	ChemAxon
Polarizability	36.04 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

19978634

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21119330

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one (NP0281038)

MOL for NP0281038 ((4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one)

3D MOL for NP0281038 ((4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one)

3D SDF for NP0281038 ((4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one)

3D-SDF for NP0281038 ((4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one)

PDB for NP0281038 ((4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one)

3D PDB for NP0281038 ((4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one)

SMILES for NP0281038 ((4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one)

INCHI for NP0281038 ((4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one)

Structure for NP0281038 ((4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one)

3D Structure for NP0281038 ((4s,8r)-17-chloro-2,18-dimethoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one)