NP-MRD: Showing NP-Card for {5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate (NP0312012)

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Record Information

Version

2.0

Created at

2022-09-11 08:25:32 UTC

Updated at

2022-09-11 08:25:33 UTC

NP-MRD ID

NP0312012

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate

Description

{5-Hydroxy-6,9a-dimethyl-3-oxo-1H,3H,5H,5aH,6H,7H,8H,9H,9aH,9bH-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. {5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate is found in Aspergillus ochraceus. Based on a literature review very few articles have been published on {5-hydroxy-6,9a-dimethyl-3-oxo-1H,3H,5H,5aH,6H,7H,8H,9H,9aH,9bH-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112210252D          

 30 33  0  0  0  0            999 V2000
    0.2729   -1.8582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0390   -1.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2075   -2.3596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5924   -2.9094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1913   -2.6516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3598   -1.8440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8064   -3.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6378   -4.0089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2530   -4.5587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0366   -4.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6518   -4.8507    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -3.4354   -4.5928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4832   -5.6583    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -2.2052   -3.4933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5901   -2.9435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6043   -0.8508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9943   -0.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8189   -0.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2535   -0.7992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6435   -0.0722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0781   -0.7735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6108   -0.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3745   -0.4553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3140   -1.2781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9440   -1.8107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5127   -1.4747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1228   -2.2017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2982   -2.2275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9082   -2.9545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8636   -1.5262    0.0000 C   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
  5  6  2  0  0  0  0
  5  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
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 10 14  1  0  0  0  0
 14 15  2  0  0  0  0
  7 15  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 21 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
  2 30  1  0  0  0  0
 19 30  1  0  0  0  0
M  CHG  2  11   1  13  -1
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
   -2.7286   -2.0235   -0.2228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6847   -0.6786    0.5150 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1947   -1.0012    1.9095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7160   -1.3160    1.8105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0143   -0.0602    1.4044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4304    0.4313    0.0261 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0379    1.8917    0.0102 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3630   -0.3304   -0.9590 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7035   -0.3425   -0.7662 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7110    0.5256   -0.8743 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4889    1.6896   -1.2655 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1150    0.2160   -0.5597 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4607   -1.0417   -0.1205 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7724   -1.3463    0.1782 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7728   -0.4204    0.0514 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1094   -0.7589    0.3644 N   0  0  0  0  0  4  0  0  0  0  0  0
    8.3859   -1.9207    0.7634 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1083    0.1768    0.2344 O   0  0  0  0  0  1  0  0  0  0  0  0
    6.4576    0.8335   -0.3818 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1259    1.1406   -0.6844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9124    0.3792   -0.1590 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3763    0.4796   -1.5979 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6638    1.4416   -2.3273 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7583    1.0882   -1.4404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5138    0.7209   -0.4325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8484    1.1384    0.0739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7782    1.5665   -0.6340 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8522    0.9618    1.4583 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5358    0.4855    1.8361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1275   -0.2867    0.6119 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3181   -1.9722   -1.1577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7994   -2.5532   -0.2817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3988   -2.6581    0.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7148   -1.9030    2.2488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3294   -0.1904    2.6231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4833   -2.1713    1.1640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3586   -1.5507    2.8447 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0968   -0.2037    1.3510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2197    0.7215    2.1663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0048    2.3225   -0.9879 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8210    2.0579    0.6715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9075    2.4035    0.5709 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1804    0.0571   -2.0216 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0399   -1.4072   -1.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7011   -1.7794   -0.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0011   -2.3384    0.5178 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2253    1.5852   -0.4917 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8810    2.1373   -1.0279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2906    1.3596    0.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4100   -0.4845   -2.0982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6722    1.1091   -3.2804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1275    1.8088   -2.1371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6165   -0.1506    2.7200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9017    1.3432    2.0518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7947   -1.1831    0.5405 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 19  1  0
 19 20  2  0
 15 16  1  0
 16 18  1  0
 16 17  2  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  6
  2 30  1  0
 30 29  1  0
 29 28  1  0
 28 26  1  0
 26 27  2  0
 26 25  1  0
 25 24  2  0
 24 22  1  0
 22 23  1  0
 22 21  1  0
 21  6  1  0
 20 12  1  0
 21  2  1  0
 25 30  1  0
  7 40  1  0
  7 41  1  0
  7 42  1  0
  8 43  1  0
  8 44  1  0
 13 45  1  0
 14 46  1  0
 19 47  1  0
 20 48  1  0
  5 38  1  0
  5 39  1  0
  4 36  1  0
  4 37  1  0
  3 34  1  0
  3 35  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
 30 55  1  6
 29 53  1  0
 29 54  1  0
 24 52  1  0
 22 50  1  6
 23 51  1  0
 21 49  1  1
M  CHG  2  16   1  18  -1
M  END


  Mrv1652309112210252D          

 30 33  0  0  0  0            999 V2000
    0.2729   -1.8582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0390   -1.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2075   -2.3596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5924   -2.9094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1913   -2.6516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3598   -1.8440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8064   -3.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6378   -4.0089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2530   -4.5587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0366   -4.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6518   -4.8507    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -3.4354   -4.5928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4832   -5.6583    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -2.2052   -3.4933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5901   -2.9435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6043   -0.8508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9943   -0.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8189   -0.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2535   -0.7992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6435   -0.0722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0781   -0.7735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6108   -0.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3745   -0.4553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3140   -1.2781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9440   -1.8107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5127   -1.4747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1228   -2.2017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2982   -2.2275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9082   -2.9545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8636   -1.5262    0.0000 C   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
  5  6  2  0  0  0  0
  5  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
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 10 14  1  0  0  0  0
 14 15  2  0  0  0  0
  7 15  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 21 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
  2 30  1  0  0  0  0
 19 30  1  0  0  0  0
M  CHG  2  11   1  13  -1
M  END
> <DATABASE_ID>
NP0312012

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(COC(=O)C2=CC=C(C=C2)[N+]([O-])=O)CCCC2(C)C3COC(=O)C3=CC(O)C12

> <INCHI_IDENTIFIER>
InChI=1S/C22H25NO7/c1-21(12-30-19(25)13-4-6-14(7-5-13)23(27)28)8-3-9-22(2)16-11-29-20(26)15(16)10-17(24)18(21)22/h4-7,10,16-18,24H,3,8-9,11-12H2,1-2H3

> <INCHI_KEY>
OJYDAIRJVVQDEZ-UHFFFAOYSA-N

> <FORMULA>
C22H25NO7

> <MOLECULAR_WEIGHT>
415.442

> <EXACT_MASS>
415.163102149

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
42.45458038378705

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
{5-hydroxy-6,9a-dimethyl-3-oxo-1H,3H,5H,5aH,6H,7H,8H,9H,9aH,9bH-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate

> <JCHEM_LOGP>
3.4548613723333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.462003981679654

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0341194584133193

> <JCHEM_POLAR_SURFACE_AREA>
115.97000000000001

> <JCHEM_REFRACTIVITY>
106.98140000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
{5-hydroxy-6,9a-dimethyl-3-oxo-1H,5H,5aH,7H,8H,9H,9bH-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       0.509  -3.469   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.939  -2.897   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.254  -4.405   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.106  -5.431   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.357  -4.950   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.672  -3.442   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.505  -5.976   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.191  -7.483   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.339  -8.510   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.802  -8.028   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      -4.950  -9.055   0.000  0.00  0.00           N+1
HETATM   12  O   UNK     0      -6.413  -8.573   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -4.635 -10.562   0.000  0.00  0.00           O-1
HETATM   14  C   UNK     0      -4.116  -6.521   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.968  -5.495   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.128  -1.588   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.856  -0.231   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.395  -0.183   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.207  -1.492   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.935  -0.135   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.746  -1.444   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.740  -0.268   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.166  -0.850   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.053  -2.386   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.229  -3.380   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.557  -2.753   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.829  -4.110   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.290  -4.158   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       3.562  -5.515   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.479  -2.849   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   16   30                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   15                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   14                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   10   15                                                       
CONECT   15   14    7                                                       
CONECT   16    2   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21   30                                             
CONECT   20   19                                                            
CONECT   21   19   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   21   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28    2   19                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Value	Source
{5-hydroxy-6,9a-dimethyl-3-oxo-1H,3H,5H,5ah,6H,7H,8H,9H,9ah,9BH-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoic acid	Generator

Chemical Formula

C₂₂H₂₅NO₇

Average Mass

415.4420 Da

Monoisotopic Mass

415.16310 Da

IUPAC Name

{5-hydroxy-6,9a-dimethyl-3-oxo-1H,3H,5H,5aH,6H,7H,8H,9H,9aH,9bH-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate

Traditional Name

{5-hydroxy-6,9a-dimethyl-3-oxo-1H,5H,5aH,7H,8H,9H,9bH-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate

CAS Registry Number

Not Available

SMILES

CC1(COC(=O)C2=CC=C(C=C2)[N+]([O-])=O)CCCC2(C)C3COC(=O)C3=CC(O)C12

InChI Identifier

InChI=1S/C22H25NO7/c1-21(12-30-19(25)13-4-6-14(7-5-13)23(27)28)8-3-9-22(2)16-11-29-20(26)15(16)10-17(24)18(21)22/h4-7,10,16-18,24H,3,8-9,11-12H2,1-2H3

InChI Key

OJYDAIRJVVQDEZ-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
Aspergillus ochraceus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
Nitrobenzoate
Benzoate ester
Nitrobenzene
Benzoic acid or derivatives
Nitroaromatic compound
Benzoyl
Benzenoid
Gamma butyrolactone
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Organic nitro compound
Secondary alcohol
C-nitro compound
Lactone
Carboxylic acid ester
Oxacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Allyl-type 1,3-dipolar organic compound
Organic oxoazanium
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organic zwitterion
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
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	3.45	ChemAxon
pKa (Strongest Acidic)	14.46	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	115.97 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	106.98 m³·mol⁻¹	ChemAxon
Polarizability	42.45 Å³	ChemAxon
Number of Rings	4	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

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

163187271

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate (NP0312012)

MOL for NP0312012 ({5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate)

3D MOL for NP0312012 ({5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate)

3D SDF for NP0312012 ({5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate)

3D-SDF for NP0312012 ({5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate)

PDB for NP0312012 ({5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate)

3D PDB for NP0312012 ({5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate)

SMILES for NP0312012 ({5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate)

INCHI for NP0312012 ({5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate)

Structure for NP0312012 ({5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate)

3D Structure for NP0312012 ({5-hydroxy-6,9a-dimethyl-3-oxo-1h,5h,5ah,7h,8h,9h,9bh-naphtho[1,2-c]furan-6-yl}methyl 4-nitrobenzoate)