NP-MRD: Showing NP-Card for 2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione (NP0291025)

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Record Information

Version

2.0

Created at

2022-09-09 21:57:41 UTC

Updated at

2022-09-09 21:57:41 UTC

NP-MRD ID

NP0291025

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione

Description

2,15'-Dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]Heptadecane]-1',3',5',7'-tetraene-9',17'-dione belongs to the class of organic compounds known as pyridopyrimidines. Pyridopyrimidines are compounds containing a pyridopyrimidine, which consists of a pyridine fused to a pyrimidine. Pyridine is 6-membered ring consisting of five carbon atoms and a nitrogen atom. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions. 2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione is found in Scedosporium apiospermum. Based on a literature review very few articles have been published on 2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]Heptadecane]-1',3',5',7'-tetraene-9',17'-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092223572D          

 31 36  0  0  0  0            999 V2000
    3.3587    2.8851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3488    2.0601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5381    2.2131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1629    2.1937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4543    2.9655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6857    1.5555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4998    1.6890    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0225    1.0508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8366    1.1843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3594    0.5461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0680   -0.2258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2539   -0.3593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7311    0.2789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9170    0.1454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6256   -0.6265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3943    0.7836    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5802    0.6501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1347   -0.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3366    0.1648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2889    0.9884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0574    1.2883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4709    1.8684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3844   -0.6588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0787   -1.1043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6158   -0.9588    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0931   -0.3205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2690   -0.2819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1096    0.4511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3359    1.1455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1600    1.1069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5386    0.3739    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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
  6 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
 20 21  1  0  0  0  0
 17 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
 19 31  1  0  0  0  0
M  END

     RDKit          3D

 50 55  0  0  0  0  0  0  0  0999 V2000
    0.2553   -1.1804   -2.5579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2517   -1.9818   -1.3789 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0296   -3.4620   -1.7179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7174   -1.8036   -1.3149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5313   -2.5463   -1.9508 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2440   -0.7345   -0.4900 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5062   -0.2473   -0.6956 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0322    0.7304    0.0501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3048    1.2242   -0.1545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7696    2.2302    0.6572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9905    2.7580    1.6735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7378    2.2598    1.8620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2456    1.2454    1.0571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9735    0.7399    1.2487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3142    1.2702    2.2006 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4719   -0.2385    0.4873 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1401   -0.6723    0.7862 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8098    0.4957    0.6274 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1199   -0.2826    0.4789 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7835   -1.2846   -0.3944 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4644   -1.6769   -0.1125 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5765   -2.8835    0.6152 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6427   -0.7250    1.7576 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0351   -1.6511    2.6293 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7578   -0.1404    1.9831 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1093    0.7446    0.9068 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2247    1.5632    0.7495 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2931    2.3101   -0.4010 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3234    2.2792   -1.3790 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2434    1.4493   -1.1656 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1085    0.6667   -0.0272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5776   -1.0071   -3.2803 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7238   -0.2346   -2.2913 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0300   -1.7814   -3.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0499   -3.6795   -1.8424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4540   -4.0937   -0.9114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6208   -3.6926   -2.6358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8777    0.7818   -0.9602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7544    2.6176    0.5045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4221    3.5474    2.2718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1009    2.6399    2.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0669   -0.9841    1.8683 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6503    1.0746   -0.2861 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8544    1.1679    1.4972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3267   -3.0181    1.0227 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3821   -2.6190    2.6772 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0102    1.6058    1.5130 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1626    2.9560   -0.5365 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4000    2.8822   -2.2851 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4507    1.3811   -1.8947 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  6
 20 21  1  0
 21 22  1  1
 19 23  1  0
 23 24  1  0
 23 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 21  2  1  0
 31 26  1  0
 16  6  1  0
 21 17  1  0
 13  8  1  0
 31 19  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  9 38  1  0
 10 39  1  0
 11 40  1  0
 12 41  1  0
 17 42  1  1
 18 43  1  0
 18 44  1  0
 22 45  1  0
 24 46  1  0
 27 47  1  0
 28 48  1  0
 29 49  1  0
 30 50  1  0
M  END


  Mrv1652309092223572D          

 31 36  0  0  0  0            999 V2000
    3.3587    2.8851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3488    2.0601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5381    2.2131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1629    2.1937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4543    2.9655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6857    1.5555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4998    1.6890    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0225    1.0508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8366    1.1843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3594    0.5461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0680   -0.2258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2539   -0.3593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7311    0.2789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9170    0.1454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6256   -0.6265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3943    0.7836    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5802    0.6501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1347   -0.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3366    0.1648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2889    0.9884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0574    1.2883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4709    1.8684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3844   -0.6588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0787   -1.1043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6158   -0.9588    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0931   -0.3205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2690   -0.2819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1096    0.4511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3359    1.1455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1600    1.1069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5386    0.3739    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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
  6 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
 20 21  1  0  0  0  0
 17 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
 19 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0291025

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)C(=O)C2=NC3=CC=CC=C3C(=O)N2C2CC3(OC12O)C(O)=NC1=CC=CC=C31

> <INCHI_IDENTIFIER>
InChI=1S/C23H19N3O5/c1-21(2)17(27)18-24-14-9-5-3-7-12(14)19(28)26(18)16-11-22(31-23(16,21)30)13-8-4-6-10-15(13)25-20(22)29/h3-10,16,30H,11H2,1-2H3,(H,25,29)

> <INCHI_KEY>
BHSVORMFPXUPEG-UHFFFAOYSA-N

> <FORMULA>
C23H19N3O5

> <MOLECULAR_WEIGHT>
417.421

> <EXACT_MASS>
417.132470724

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
41.527841780309345

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0^{3,8}.0^{11,15}]heptadecane]-1',3',5',7'-tetraene-9',17'-dione

> <JCHEM_LOGP>
3.581925779958032

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.933102116831188

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.4073278748376987

> <JCHEM_PKA_STRONGEST_BASIC>
0.771220084248435

> <JCHEM_POLAR_SURFACE_AREA>
111.79

> <JCHEM_REFRACTIVITY>
112.97760000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0^{3,8}.0^{11,15}]heptadecane]-1',3',5',7'-tetraene-9',17'-dione

> <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       6.269   5.385   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.251   3.846   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.738   4.131   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.771   4.095   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       8.315   5.536   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       8.747   2.904   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      10.266   3.153   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      11.242   1.961   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.762   2.211   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.737   1.019   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.194  -0.421   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.674  -0.671   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.698   0.521   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.178   0.271   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.635  -1.169   0.000  0.00  0.00           O+0
HETATM   16  N   UNK     0       8.203   1.463   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       6.683   1.213   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.851  -0.083   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.362   0.308   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.273   1.845   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.707   2.405   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.612   3.488   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.451  -1.230   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.747  -2.061   0.000  0.00  0.00           O+0
HETATM   25  N   UNK     0       3.016  -1.790   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       2.040  -0.598   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.502  -0.526   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.205   0.842   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.627   2.138   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.165   2.066   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.872   0.698   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   21                                             
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   16                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8   14                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    6   17                                                  
CONECT   17   16   18   21                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   23   31                                             
CONECT   20   19   21                                                       
CONECT   21   20   17    2   22                                             
CONECT   22   21                                                            
CONECT   23   19   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   26   19                                                  
MASTER        0    0    0    0    0    0    0    0   31    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₁₉N₃O₅

Average Mass

417.4210 Da

Monoisotopic Mass

417.13247 Da

IUPAC Name

2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0^{3,8}.0^{11,15}]heptadecane]-1',3',5',7'-tetraene-9',17'-dione

Traditional Name

2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0^{3,8}.0^{11,15}]heptadecane]-1',3',5',7'-tetraene-9',17'-dione

CAS Registry Number

Not Available

SMILES

CC1(C)C(=O)C2=NC3=CC=CC=C3C(=O)N2C2CC3(OC12O)C(O)=NC1=CC=CC=C31

InChI Identifier

InChI=1S/C23H19N3O5/c1-21(2)17(27)18-24-14-9-5-3-7-12(14)19(28)26(18)16-11-22(31-23(16,21)30)13-8-4-6-10-15(13)25-20(22)29/h3-10,16,30H,11H2,1-2H3,(H,25,29)

InChI Key

BHSVORMFPXUPEG-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
Scedosporium apiospermum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyridopyrimidines. Pyridopyrimidines are compounds containing a pyridopyrimidine, which consists of a pyridine fused to a pyrimidine. Pyridine is 6-membered ring consisting of five carbon atoms and a nitrogen atom. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyridopyrimidines

Sub Class

Not Available

Direct Parent

Pyridopyrimidines

Alternative Parents

Substituents

Diazanaphthalene
3-alkylindole
Quinazoline
Pyridopyrimidine
Indole or derivatives
Aryl alkyl ketone
Aryl ketone
Pyrimidone
Benzenoid
Pyrimidine
Pyridine
Heteroaromatic compound
Cyclic carboximidic acid
Tetrahydrofuran
Lactam
Ketone
Hemiacetal
Oxacycle
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen 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	3.58	ChemAxon
pKa (Strongest Acidic)	2.41	ChemAxon
pKa (Strongest Basic)	0.77	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	111.79 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	112.98 m³·mol⁻¹	ChemAxon
Polarizability	41.53 Å³	ChemAxon
Number of Rings	6	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

162814944

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione (NP0291025)

MOL for NP0291025 (2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione)

3D MOL for NP0291025 (2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione)

3D SDF for NP0291025 (2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione)

3D-SDF for NP0291025 (2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione)

PDB for NP0291025 (2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione)

3D PDB for NP0291025 (2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione)

SMILES for NP0291025 (2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione)

INCHI for NP0291025 (2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione)

Structure for NP0291025 (2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione)

3D Structure for NP0291025 (2,15'-dihydroxy-16',16'-dimethyl-14'-oxa-2',10'-diazaspiro[indole-3,13'-tetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadecane]-1',3',5',7'-tetraene-9',17'-dione)