NP-MRD: Showing NP-Card for 5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+ (NP0037020)

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Record Information

Version

2.0

Created at

2021-06-20 20:02:37 UTC

Updated at

2021-06-30 00:08:59 UTC

NP-MRD ID

NP0037020

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+

Provided By

JEOL Database JEOL Logo

Description

CHEMBL2152650 belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings. 5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+ is found in Streptomyces spinoverrucosus. 5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+ was first documented in 2012 (Hu, Y., et al.). Based on a literature review very few articles have been published on CHEMBL2152650.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202122023D          

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  Mrv1652306202122023D          

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    1.2195   -2.6006   -3.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1810   -2.5579   -4.8990 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5243   -1.4122   -3.5923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2549    4.4892    2.7487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8528    4.4732    3.8458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7268    2.9770    3.4752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4262    5.5861    2.0182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3139    4.8419    0.4170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8250    5.5890    0.9157 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3835    2.2285    4.1015 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4251    1.0875    4.8991 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6548   -0.4577    3.3899 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6410   -1.0445    0.0787 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 11  1  0  0  0  0
 22 23  2  0  0  0  0
  6  7  1  0  0  0  0
 23 24  1  0  0  0  0
 24 26  2  0  0  0  0
 12 11  2  0  0  0  0
 24 25  1  0  0  0  0
  8  9  1  0  0  0  0
 27 28  2  0  0  0  0
 11  5  1  0  0  0  0
  3  4  1  0  0  0  0
  5  6  1  0  0  0  0
  5  3  2  0  0  0  0
 13  2  2  0  0  0  0
  2  1  1  0  0  0  0
 12 13  1  0  0  0  0
  3  2  1  0  0  0  0
  8 10  1  0  0  0  0
  7  8  1  0  0  0  0
 26 20  1  0  0  0  0
 20 19  1  0  0  0  0
 20 21  2  0  0  0  0
 12 19  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  2  0  0  0  0
 26 27  1  0  0  0  0
 15 16  1  0  0  0  0
 21 22  1  0  0  0  0
 15 17  1  0  0  0  0
  6 33  1  0  0  0  0
  6 34  1  0  0  0  0
  7 35  1  0  0  0  0
  7 36  1  0  0  0  0
  8 37  1  0  0  0  0
  9 38  1  0  0  0  0
  9 39  1  0  0  0  0
  9 40  1  0  0  0  0
 10 41  1  0  0  0  0
 10 42  1  0  0  0  0
 10 43  1  0  0  0  0
 21 50  1  0  0  0  0
 22 51  1  0  0  0  0
 23 52  1  0  0  0  0
 25 53  1  0  0  0  0
  4 32  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
 16 44  1  0  0  0  0
 16 45  1  0  0  0  0
 16 46  1  0  0  0  0
 17 47  1  0  0  0  0
 17 48  1  0  0  0  0
 17 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0037020

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)C3=C4C(OC(N=C4C2=C([H])C([H])=C1[H])(C([H])([H])[H])C([H])([H])[H])=C(C(O[H])=C3C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H25NO4/c1-11(2)9-10-14-17-18-19(13-7-6-8-15(25)16(13)21(17)27)24-23(4,5)28-22(18)12(3)20(14)26/h6-8,11,25-26H,9-10H2,1-5H3

> <INCHI_KEY>
WMURTDFNFBXFFU-UHFFFAOYSA-N

> <FORMULA>
C23H25NO4

> <MOLECULAR_WEIGHT>
379.456

> <EXACT_MASS>
379.178358289

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
42.469554924264216

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6,11-dihydroxy-12,15,15-trimethyl-10-(3-methylbutyl)-14-oxa-16-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2,4,6,9(17),10,12-heptaen-8-one

> <ALOGPS_LOGP>
4.33

> <JCHEM_LOGP>
6.103981223000002

> <ALOGPS_LOGS>
-4.60

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.451483701812148

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.395500451707028

> <JCHEM_PKA_STRONGEST_BASIC>
0.21279448983099003

> <JCHEM_POLAR_SURFACE_AREA>
79.12

> <JCHEM_REFRACTIVITY>
109.66839999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.45e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6,11-dihydroxy-12,15,15-trimethyl-10-(3-methylbutyl)-14-oxa-16-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2,4,6,9(17),10,12-heptaen-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 53 56  0  0  0  0  0  0  0  0999 V2000
   -4.6151    2.3488   -1.4856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2630    1.7806   -1.1426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6100    0.8833   -2.0018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1773    0.5127   -3.1947 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3515    0.3208   -1.6918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7423   -0.6692   -2.6716 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1432    0.0290   -3.7113 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7401   -0.9369   -4.7517 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4449   -0.1414   -5.8536 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7215   -1.9303   -4.1277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7174    0.7125   -0.4885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3616    1.6164    0.3658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6111    2.1474    0.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2680    3.0117    0.8722 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4464    3.6551    1.8542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3671    3.9220    3.0509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9763    4.9970    1.2764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2761    2.9549    2.3830 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7749    2.0183    1.6536 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4362    1.3171    2.1331 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9098    1.5477    3.4348 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0628    0.9070    3.8899 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7522    0.0409    3.0456 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2859   -0.1818    1.7519 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0298   -1.0381    0.9835 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1196    0.4483    1.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6231    0.2090   -0.0792 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3587   -0.4088   -0.8429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3223    1.5392   -1.6951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5348    2.9984   -2.3633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0504    2.9419   -0.6762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9887    1.0160   -3.3612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5390   -1.2201   -3.1883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2108   -1.4551   -2.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4584    0.7832   -4.2361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9508    0.5821   -3.2158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0761   -1.5039   -5.2169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8457   -0.8111   -6.6219 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7480    0.5467   -6.3437 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2756    0.4473   -5.4496 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2195   -2.6006   -3.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1810   -2.5579   -4.8990 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5243   -1.4122   -3.5923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2549    4.4892    2.7487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8528    4.4732    3.8458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7268    2.9770    3.4752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4262    5.5861    2.0182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3139    4.8419    0.4170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8250    5.5890    0.9157 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3835    2.2285    4.1015 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4251    1.0875    4.8991 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6548   -0.4577    3.3899 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6410   -1.0445    0.0787 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 11  1  0
 22 23  2  0
  6  7  1  0
 23 24  1  0
 24 26  2  0
 12 11  2  0
 24 25  1  0
  8  9  1  0
 27 28  2  0
 11  5  1  0
  3  4  1  0
  5  6  1  0
  5  3  2  0
 13  2  2  0
  2  1  1  0
 12 13  1  0
  3  2  1  0
  8 10  1  0
  7  8  1  0
 26 20  1  0
 20 19  1  0
 20 21  2  0
 12 19  1  0
 13 14  1  0
 14 15  1  0
 15 18  1  0
 18 19  2  0
 26 27  1  0
 15 16  1  0
 21 22  1  0
 15 17  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  8 37  1  0
  9 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 10 43  1  0
 21 50  1  0
 22 51  1  0
 23 52  1  0
 25 53  1  0
  4 32  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 16 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 17 49  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -4.615   2.349  -1.486  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.263   1.781  -1.143  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.610   0.883  -2.002  0.00  0.00           C+0
HETATM    4  O   UNK     0      -3.177   0.513  -3.195  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.351   0.321  -1.692  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.742  -0.669  -2.672  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.143   0.029  -3.711  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.740  -0.937  -4.752  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.445  -0.141  -5.854  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.722  -1.930  -4.128  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.717   0.713  -0.489  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.362   1.616   0.366  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.611   2.147   0.043  0.00  0.00           C+0
HETATM   14  O   UNK     0      -3.268   3.012   0.872  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.446   3.655   1.854  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.367   3.922   3.051  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.976   4.997   1.276  0.00  0.00           C+0
HETATM   18  N   UNK     0      -1.276   2.955   2.383  0.00  0.00           N+0
HETATM   19  C   UNK     0      -0.775   2.018   1.654  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.436   1.317   2.133  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.910   1.548   3.435  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.063   0.907   3.890  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.752   0.041   3.046  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.286  -0.182   1.752  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.030  -1.038   0.984  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.120   0.448   1.289  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.623   0.209  -0.079  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.359  -0.409  -0.843  0.00  0.00           O+0
HETATM   29  H   UNK     0      -5.322   1.539  -1.695  0.00  0.00           H+0
HETATM   30  H   UNK     0      -4.535   2.998  -2.363  0.00  0.00           H+0
HETATM   31  H   UNK     0      -5.050   2.942  -0.676  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.989   1.016  -3.361  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.539  -1.220  -3.188  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.211  -1.455  -2.129  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.458   0.783  -4.236  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.951   0.582  -3.216  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.076  -1.504  -5.217  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.846  -0.811  -6.622  0.00  0.00           H+0
HETATM   39  H   UNK     0       0.748   0.547  -6.344  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.276   0.447  -5.450  0.00  0.00           H+0
HETATM   41  H   UNK     0       1.220  -2.601  -3.424  0.00  0.00           H+0
HETATM   42  H   UNK     0       2.181  -2.558  -4.899  0.00  0.00           H+0
HETATM   43  H   UNK     0       2.524  -1.412  -3.592  0.00  0.00           H+0
HETATM   44  H   UNK     0      -4.255   4.489   2.749  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.853   4.473   3.846  0.00  0.00           H+0
HETATM   46  H   UNK     0      -3.727   2.977   3.475  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.426   5.586   2.018  0.00  0.00           H+0
HETATM   48  H   UNK     0      -1.314   4.842   0.417  0.00  0.00           H+0
HETATM   49  H   UNK     0      -2.825   5.589   0.916  0.00  0.00           H+0
HETATM   50  H   UNK     0       0.384   2.228   4.101  0.00  0.00           H+0
HETATM   51  H   UNK     0       2.425   1.087   4.899  0.00  0.00           H+0
HETATM   52  H   UNK     0       3.655  -0.458   3.390  0.00  0.00           H+0
HETATM   53  H   UNK     0       2.641  -1.044   0.079  0.00  0.00           H+0
CONECT    1    2   29   30   31                                             
CONECT    2   13    1    3                                                  
CONECT    3    4    5    2                                                  
CONECT    4    3   32                                                       
CONECT    5   11    6    3                                                  
CONECT    6    7    5   33   34                                             
CONECT    7    6    8   35   36                                             
CONECT    8    9   10    7   37                                             
CONECT    9    8   38   39   40                                             
CONECT   10    8   41   42   43                                             
CONECT   11   27   12    5                                                  
CONECT   12   11   13   19                                                  
CONECT   13    2   12   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   18   16   17                                             
CONECT   16   15   44   45   46                                             
CONECT   17   15   47   48   49                                             
CONECT   18   15   19                                                       
CONECT   19   20   12   18                                                  
CONECT   20   26   19   21                                                  
CONECT   21   20   22   50                                                  
CONECT   22   23   21   51                                                  
CONECT   23   22   24   52                                                  
CONECT   24   23   26   25                                                  
CONECT   25   24   53                                                       
CONECT   26   24   20   27                                                  
CONECT   27   11   28   26                                                  
CONECT   28   27                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    4                                                            
CONECT   33    6                                                            
CONECT   34    6                                                            
CONECT   35    7                                                            
CONECT   36    7                                                            
CONECT   37    8                                                            
CONECT   38    9                                                            
CONECT   39    9                                                            
CONECT   40    9                                                            
CONECT   41   10                                                            
CONECT   42   10                                                            
CONECT   43   10                                                            
CONECT   44   16                                                            
CONECT   45   16                                                            
CONECT   46   16                                                            
CONECT   47   17                                                            
CONECT   48   17                                                            
CONECT   49   17                                                            
CONECT   50   21                                                            
CONECT   51   22                                                            
CONECT   52   23                                                            
CONECT   53   25                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  112    0
END

RDKit          3D

53 56  0  0  0  0  0  0  0  0999 V2000
   -4.6151    2.3488   -1.4856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2630    1.7806   -1.1426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6100    0.8833   -2.0018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1773    0.5127   -3.1947 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3515    0.3208   -1.6918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7423   -0.6692   -2.6716 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1432    0.0290   -3.7113 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7401   -0.9369   -4.7517 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7215   -1.9303   -4.1277 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6111    2.1474    0.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9763    4.9970    1.2764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2761    2.9549    2.3830 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7749    2.0183    1.6536 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4362    1.3171    2.1331 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9098    1.5477    3.4348 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0628    0.9070    3.8899 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7522    0.0409    3.0456 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2859   -0.1818    1.7519 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0298   -1.0381    0.9835 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1196    0.4483    1.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6231    0.2090   -0.0792 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3587   -0.4088   -0.8429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3223    1.5392   -1.6951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5348    2.9984   -2.3633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0504    2.9419   -0.6762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9887    1.0160   -3.3612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5390   -1.2201   -3.1883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2108   -1.4551   -2.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4584    0.7832   -4.2361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9508    0.5821   -3.2158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0761   -1.5039   -5.2169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8457   -0.8111   -6.6219 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7480    0.5467   -6.3437 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2756    0.4473   -5.4496 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2195   -2.6006   -3.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1810   -2.5579   -4.8990 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5243   -1.4122   -3.5923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2549    4.4892    2.7487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8528    4.4732    3.8458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7268    2.9770    3.4752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4262    5.5861    2.0182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3139    4.8419    0.4170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8250    5.5890    0.9157 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3835    2.2285    4.1015 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4251    1.0875    4.8991 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6548   -0.4577    3.3899 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6410   -1.0445    0.0787 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 11  1  0
 22 23  2  0
  6  7  1  0
 23 24  1  0
 24 26  2  0
 12 11  2  0
 24 25  1  0
  8  9  1  0
 27 28  2  0
 11  5  1  0
  3  4  1  0
  5  6  1  0
  5  3  2  0
 13  2  2  0
  2  1  1  0
 12 13  1  0
  3  2  1  0
  8 10  1  0
  7  8  1  0
 26 20  1  0
 20 19  1  0
 20 21  2  0
 12 19  1  0
 13 14  1  0
 14 15  1  0
 15 18  1  0
 18 19  2  0
 26 27  1  0
 15 16  1  0
 21 22  1  0
 15 17  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  8 37  1  0
  9 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 10 43  1  0
 21 50  1  0
 22 51  1  0
 23 52  1  0
 25 53  1  0
  4 32  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 16 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 17 49  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₂₃H₂₅NO₄

Average Mass

379.4560 Da

Monoisotopic Mass

379.17836 Da

IUPAC Name

6,11-dihydroxy-12,15,15-trimethyl-10-(3-methylbutyl)-14-oxa-16-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2,4,6,9(17),10,12-heptaen-8-one

Traditional Name

6,11-dihydroxy-12,15,15-trimethyl-10-(3-methylbutyl)-14-oxa-16-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2,4,6,9(17),10,12-heptaen-8-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C2C(=O)C3=C4C(OC(N=C4C2=C([H])C([H])=C1[H])(C([H])([H])[H])C([H])([H])[H])=C(C(O[H])=C3C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C23H25NO4/c1-11(2)9-10-14-17-18-19(13-7-6-8-15(25)16(13)21(17)27)24-23(4,5)28-22(18)12(3)20(14)26/h6-8,11,25-26H,9-10H2,1-5H3

InChI Key

WMURTDFNFBXFFU-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Streptomyces spinoverrucosus	JEOL database	Hu, Y., et al, J. Nat. Prod. 75, 1759 (2012)

Chemical Taxonomy

Classification

Not classified

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	4.33	ALOGPS
logP	6.1	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	8.4	ChemAxon
pKa (Strongest Basic)	0.21	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	79.12 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	109.67 m³·mol⁻¹	ChemAxon
Polarizability	42.47 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

28666976

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

136236397

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Hu, Y., et al. (2012). Hu, Y., et al, J. Nat. Prod. 75, 1759 (2012). J. Nat. Prod..

Showing NP-Card for 5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+ (NP0037020)

MOL for NP0037020 (5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+)

3D MOL for NP0037020 (5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+)

3D SDF for NP0037020 (5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+)

3D-SDF for NP0037020 (5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+)

PDB for NP0037020 (5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+)

3D PDB for NP0037020 (5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+)

SMILES for NP0037020 (5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+)

INCHI for NP0037020 (5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+)

Structure for NP0037020 (5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+)

3D Structure for NP0037020 (5,8-dihydroxy-6-isopentyl-2,2,4-trimethylanthra[9,1-de][1,3]oxazin-7(2H)-+)