NP-MRD: Showing NP-Card for 7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide (NP0156479)

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Record Information

Version

2.0

Created at

2022-09-02 13:41:29 UTC

Updated at

2022-09-02 13:41:30 UTC

NP-MRD ID

NP0156479

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide

Description

7,9-Dibromo-N-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]Deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]Deca-2,6,8-triene-3-carboxamide belongs to the class of organic compounds known as isoxazolines. Isoxazolines are compounds containing a five-member unsaturated aliphatic ring, with an oxygen atom adjacent to a nitrogen atoms, and three carbon atoms. 7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide is found in Aplysina cavernicola. Based on a literature review very few articles have been published on 7,9-dibromo-N-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]Deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]Deca-2,6,8-triene-3-carboxamide.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309022215412D          

 40 43  0  0  0  0            999 V2000
   -2.6956   -9.1532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1805   -8.4857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8450   -7.7321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3299   -7.0646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1504   -7.1509    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -2.9944   -6.3110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4793   -5.6435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1739   -6.2247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6889   -6.8922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0245   -7.6458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5396   -8.3133    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -2.5864   -5.5102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0343   -4.8972    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2807   -5.2327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5662   -4.8202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5662   -3.9952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1483   -5.2327    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8628   -4.8202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5772   -5.2327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2917   -4.8202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0062   -5.2327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7206   -4.8202    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4351   -5.2327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4351   -6.0577    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1496   -4.8202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2358   -3.9997    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0428   -3.8282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4553   -4.5427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9402   -3.8752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7607   -3.9615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2456   -3.2940    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    8.0962   -4.7151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9167   -4.8014    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4016   -4.1339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6113   -5.3826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9469   -6.1363    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    6.7908   -5.2963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3059   -5.9638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9033   -5.1558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3669   -6.0532    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  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 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
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 28 37  1  0  0  0  0
 37 38  1  0  0  0  0
 28 39  1  0  0  0  0
 25 39  1  0  0  0  0
 14 40  1  0  0  0  0
  8 40  1  0  0  0  0
M  END


  Mrv1652309022215412D          

 40 43  0  0  0  0            999 V2000
   -2.6956   -9.1532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1805   -8.4857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8450   -7.7321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3299   -7.0646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1504   -7.1509    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -2.9944   -6.3110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4793   -5.6435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1739   -6.2247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6889   -6.8922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0245   -7.6458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5396   -8.3133    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -2.5864   -5.5102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0343   -4.8972    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2807   -5.2327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5662   -4.8202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5662   -3.9952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1483   -5.2327    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8628   -4.8202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5772   -5.2327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2917   -4.8202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0062   -5.2327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7206   -4.8202    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4351   -5.2327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4351   -6.0577    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1496   -4.8202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2358   -3.9997    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0428   -3.8282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4553   -4.5427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9402   -3.8752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7607   -3.9615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2456   -3.2940    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    8.0962   -4.7151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9167   -4.8014    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4016   -4.1339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6113   -5.3826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9469   -6.1363    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    6.7908   -5.2963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3059   -5.9638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9033   -5.1558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3669   -6.0532    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  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 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
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 28 37  1  0  0  0  0
 37 38  1  0  0  0  0
 28 39  1  0  0  0  0
 25 39  1  0  0  0  0
 14 40  1  0  0  0  0
  8 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0156479

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(Br)C(O)C2(CN=C(C2)C(=O)NCCCCNC(=O)C2=NOC3(C2)C=C(Br)C(OC)=C(Br)C3O)C=C1Br

> <INCHI_IDENTIFIER>
InChI=1S/C25H28Br4N4O7/c1-38-18-12(26)7-24(20(34)16(18)28)9-14(32-11-24)22(36)30-5-3-4-6-31-23(37)15-10-25(40-33-15)8-13(27)19(39-2)17(29)21(25)35/h7-8,20-21,34-35H,3-6,9-11H2,1-2H3,(H,30,36)(H,31,37)

> <INCHI_KEY>
TXXZXTFOPHJWJG-UHFFFAOYSA-N

> <FORMULA>
C25H28Br4N4O7

> <MOLECULAR_WEIGHT>
816.136

> <EXACT_MASS>
811.869151

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
66.79102040696702

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7,9-dibromo-N-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide

> <ALOGPS_LOGP>
3.59

> <JCHEM_LOGP>
0.7002943540000006

> <ALOGPS_LOGS>
-4.49

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.132231247520185

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.302206586344933

> <JCHEM_PKA_STRONGEST_BASIC>
2.0500628533421477

> <JCHEM_POLAR_SURFACE_AREA>
151.07

> <JCHEM_REFRACTIVITY>
165.3311

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.65e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7,9-dibromo-N-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.032 -17.086   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -5.937 -15.840   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.311 -14.433   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.216 -13.187   0.000  0.00  0.00           C+0
HETATM    5 Br   UNK     0      -7.747 -13.348   0.000  0.00  0.00          Br+0
HETATM    6  C   UNK     0      -5.589 -11.780   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -6.495 -10.535   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -4.058 -11.619   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.153 -12.865   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.779 -14.272   0.000  0.00  0.00           C+0
HETATM   11 Br   UNK     0      -2.874 -15.518   0.000  0.00  0.00          Br+0
HETATM   12  C   UNK     0      -4.828 -10.286   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -3.797  -9.141   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -2.391  -9.768   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.057  -8.998   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.057  -7.458   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0       0.277  -9.768   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       1.610  -8.998   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.944  -9.768   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.278  -8.998   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.612  -9.768   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       6.945  -8.998   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       8.279  -9.768   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.279 -11.308   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       9.613  -8.998   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       9.774  -7.466   0.000  0.00  0.00           N+0
HETATM   27  O   UNK     0      11.280  -7.146   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      12.050  -8.480   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.955  -7.234   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      14.487  -7.395   0.000  0.00  0.00           C+0
HETATM   31 Br   UNK     0      15.392  -6.149   0.000  0.00  0.00          Br+0
HETATM   32  C   UNK     0      15.113  -8.802   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      16.645  -8.963   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      17.550  -7.717   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      14.208 -10.047   0.000  0.00  0.00           C+0
HETATM   36 Br   UNK     0      14.834 -11.454   0.000  0.00  0.00          Br+0
HETATM   37  C   UNK     0      12.676  -9.887   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      11.771 -11.132   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      11.019  -9.624   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -2.552 -11.299   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   12   40                                             
CONECT    9    8   10                                                       
CONECT   10    9    3   11                                                  
CONECT   11   10                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   40                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   39                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   37   39                                             
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   35                                                  
CONECT   33   32   34                                                       
CONECT   34   33                                                            
CONECT   35   32   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   28   38                                                  
CONECT   38   37                                                            
CONECT   39   28   25                                                       
CONECT   40   14    8                                                       
MASTER        0    0    0    0    0    0    0    0   40    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₈Br₄N₄O₇

Average Mass

816.1360 Da

Monoisotopic Mass

811.86915 Da

IUPAC Name

7,9-dibromo-N-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide

Traditional Name

7,9-dibromo-N-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide

CAS Registry Number

Not Available

SMILES

COC1=C(Br)C(O)C2(CN=C(C2)C(=O)NCCCCNC(=O)C2=NOC3(C2)C=C(Br)C(OC)=C(Br)C3O)C=C1Br

InChI Identifier

InChI=1S/C25H28Br4N4O7/c1-38-18-12(26)7-24(20(34)16(18)28)9-14(32-11-24)22(36)30-5-3-4-6-31-23(37)15-10-25(40-33-15)8-13(27)19(39-2)17(29)21(25)35/h7-8,20-21,34-35H,3-6,9-11H2,1-2H3,(H,30,36)(H,31,37)

InChI Key

TXXZXTFOPHJWJG-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Aplysina cavernicola	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoxazolines. Isoxazolines are compounds containing a five-member unsaturated aliphatic ring, with an oxygen atom adjacent to a nitrogen atoms, and three carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azolines

Sub Class

Isoxazolines

Direct Parent

Isoxazolines

Alternative Parents

Substituents

Isoxazoline
Pyrroline
Bromohydrin
Carboxamide group
Halohydrin
Ketimine
Oxime ether
Secondary alcohol
Secondary carboxylic acid amide
Carboxylic acid derivative
Oxacycle
Azacycle
Bromoalkene
Haloalkene
Vinyl bromide
Vinyl halide
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Organonitrogen compound
Organobromide
Organohalogen compound
Hydrocarbon derivative
Organooxygen compound
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Alcohol
Organopnictogen compound
Imine
Organic oxide
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	3.59	ALOGPS
logP	0.7	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	12.3	ChemAxon
pKa (Strongest Basic)	2.05	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	151.07 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	165.33 m³·mol⁻¹	ChemAxon
Polarizability	66.79 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	Yes	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

162970741

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide (NP0156479)

MOL for NP0156479 (7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

3D MOL for NP0156479 (7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

3D SDF for NP0156479 (7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

3D-SDF for NP0156479 (7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

PDB for NP0156479 (7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

3D PDB for NP0156479 (7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

SMILES for NP0156479 (7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

INCHI for NP0156479 (7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

Structure for NP0156479 (7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

3D Structure for NP0156479 (7,9-dibromo-n-[4-({7,9-dibromo-10-hydroxy-8-methoxy-2-azaspiro[4.5]deca-2,6,8-trien-3-yl}formamido)butyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)