NP-MRD: Showing NP-Card for 4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione (NP0151381)

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Record Information

Version

2.0

Created at

2022-09-02 07:41:17 UTC

Updated at

2022-09-02 07:41:17 UTC

NP-MRD ID

NP0151381

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione

Description

4-Chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]Hexadeca-1(15),4,11,13-tetraene-9,16-dione belongs to the class of organic compounds known as indoles and derivatives. These are organic compounds containing an indole, which is a bicyclic ring system made up of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. 4-Chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]Hexadeca-1(15),4,11,13-tetraene-9,16-dione is a strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241505292D          

 27 30  0  0  0  0            999 V2000
   -1.5079   -0.5743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6831   -0.5933    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2111   -1.2753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4892   -2.0520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6034   -1.0429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6242   -0.1953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1696    0.0806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2789    0.9128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3587    1.4527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1445    1.1636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3154    0.3339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1785    0.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2681    0.9453    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6026    1.4329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1387   -0.6316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3137   -0.6337    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1810   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0647   -1.3232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5090   -0.5787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.5677    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.0522    0.1424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7371    0.6024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0580    0.9674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3464    1.3849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3081   -1.5352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5132   -2.3343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7965   -2.1824    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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  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
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 12 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  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 17 25  1  0  0  0  0
  5 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
M  END

     RDKit          3D

 50 53  0  0  0  0  0  0  0  0999 V2000
   -2.5702    0.9040    2.0608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0628    0.6620    0.8592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5691   -0.4310    0.0161 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7908   -0.8415   -0.8563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3281   -1.6886    0.8174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7102   -2.5603    1.5099 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.1154   -2.2215    1.0553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0792   -1.5034    0.3849 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6850   -1.3605   -0.9946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5552   -2.0675   -1.9124 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5246   -0.0966   -0.9950 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0231    0.1851   -2.2927 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4682    0.9110   -3.1593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4880    0.9095   -0.5618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9907    2.1651   -0.3375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2108    3.2270    0.0796 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1256    3.0709    0.2920 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6727    1.8082    0.0736 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8970    0.7485   -0.3437 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7764   -0.4339   -0.5361 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0877    0.0272   -0.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1171   -0.6880    0.0559 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0158    1.3988    0.2550 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1227    2.2731    0.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3098   -1.6928    0.2337 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8082   -2.8700   -0.5463 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0085   -1.7297    1.5970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9784    1.7274    2.6339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7636    0.2723    2.4615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8645    1.3164    0.5293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2024    0.1166   -1.2408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5114   -1.4062   -0.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4281   -1.4199   -1.7106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0111   -3.0892    1.6878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1000   -0.5093    0.9670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5229    1.4261   -3.0315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9678    1.0376   -4.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0330    2.3975   -0.4877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6340    4.2122    0.2501 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7355    3.9147    0.6221 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8747   -0.6876   -1.6203 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3838    2.8963   -0.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7978    2.9087    1.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9706    1.6403    0.9827 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0485   -2.6169   -1.6056 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1031   -3.7432   -0.4946 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7733   -3.2660   -0.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2365   -0.7237    1.9696 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9754   -2.2722    1.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3478   -2.2370    2.3382 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 21  1  0
 21 22  2  0
 21 20  1  0
 20 19  1  0
 19 18  2  0
 18 17  1  0
 17 16  2  0
 16 15  1  0
 15 14  2  0
 14 11  1  0
 11 12  1  6
 12 13  2  3
 11  9  1  0
  9 10  2  0
  9  8  1  0
  8  7  1  0
  7  5  2  0
  5  6  1  0
  5  3  1  0
  3  4  1  0
  3  2  1  1
  2  1  2  3
  8 25  1  0
 25 26  1  0
 25 27  1  0
 18 23  1  0
  3 11  1  0
 25 20  1  0
 14 19  1  0
 24 42  1  0
 24 43  1  0
 24 44  1  0
 20 41  1  6
 17 40  1  0
 16 39  1  0
 15 38  1  0
 13 36  1  0
 13 37  1  0
  8 35  1  1
  7 34  1  0
  4 31  1  0
  4 32  1  0
  4 33  1  0
  2 30  1  0
  1 28  1  0
  1 29  1  0
 26 45  1  0
 26 46  1  0
 26 47  1  0
 27 48  1  0
 27 49  1  0
 27 50  1  0
M  END


  Mrv1533004241505292D          

 27 30  0  0  0  0            999 V2000
   -1.5079   -0.5743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6831   -0.5933    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2111   -1.2753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4892   -2.0520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6034   -1.0429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6242   -0.1953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1696    0.0806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2789    0.9128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3587    1.4527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1445    1.1636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3154    0.3339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1785    0.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2681    0.9453    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6026    1.4329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1387   -0.6316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3137   -0.6337    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1810   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0647   -1.3232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5090   -0.5787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.5677    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.0522    0.1424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7371    0.6024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0580    0.9674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3464    1.3849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3081   -1.5352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5132   -2.3343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7965   -2.1824    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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  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
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 12 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  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 17 25  1  0  0  0  0
  5 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0151381

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C(=O)C2C3=C1C=CC=C3C1(N=C)C(=O)C(C=C(Cl)C1(C)C=C)C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C22H23ClN2O2/c1-7-21(4)15(23)11-13-18(26)22(21,24-5)12-9-8-10-14-16(12)17(20(13,2)3)19(27)25(14)6/h7-11,13,17H,1,5H2,2-4,6H3

> <INCHI_KEY>
WLWKOTRIASYALY-UHFFFAOYSA-N

> <FORMULA>
C22H23ClN2O2

> <MOLECULAR_WEIGHT>
382.89

> <EXACT_MASS>
382.1448057

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
39.8754158398105

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione

> <ALOGPS_LOGP>
3.75

> <JCHEM_LOGP>
3.191509074

> <ALOGPS_LOGS>
-5.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.362091748730471

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.950089733854236

> <JCHEM_PKA_STRONGEST_BASIC>
3.480308063230881

> <JCHEM_POLAR_SURFACE_AREA>
49.74

> <JCHEM_REFRACTIVITY>
107.0763

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.29e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -2.815  -1.072   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      -1.275  -1.107   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      -0.394  -2.381   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.913  -3.830   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.126  -1.947   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.165  -0.365   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.317   0.150   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.521   1.704   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.670   2.712   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.136   2.172   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.455   0.623   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.067   0.234   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       4.234   1.765   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       2.992   2.675   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.992  -1.179   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.452  -1.183   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.071  -2.549   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.721  -2.470   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.550  -1.080   0.000  0.00  0.00           C+0
HETATM   20 Cl   UNK     0       8.090  -1.060   0.000  0.00  0.00          Cl+0
HETATM   21  C   UNK     0       5.697   0.266   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.976   1.124   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.708   1.806   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.380   2.585   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.442  -2.866   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.825  -4.357   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.487  -4.074   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   25                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    6   12                                                  
CONECT   12   11   13   15   21                                             
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   12   22   23                                             
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23                                                            
CONECT   25   17    5   26   27                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₃ClN₂O₂

Average Mass

382.8900 Da

Monoisotopic Mass

382.14481 Da

IUPAC Name

4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione

Traditional Name

4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione

CAS Registry Number

Not Available

SMILES

CN1C(=O)C2C3=C1C=CC=C3C1(N=C)C(=O)C(C=C(Cl)C1(C)C=C)C2(C)C

InChI Identifier

InChI=1S/C22H23ClN2O2/c1-7-21(4)15(23)11-13-18(26)22(21,24-5)12-9-8-10-14-16(12)17(20(13,2)3)19(27)25(14)6/h7-11,13,17H,1,5H2,2-4,6H3

InChI Key

WLWKOTRIASYALY-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indoles and derivatives. These are organic compounds containing an indole, which is a bicyclic ring system made up of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Not Available

Direct Parent

Indoles and derivatives

Alternative Parents

Substituents

Indole or derivatives
Cyclohexenone
Benzenoid
Tertiary carboxylic acid amide
Carboxamide group
Ketone
Lactam
Carboxylic acid derivative
Vinyl chloride
Vinyl halide
Azacycle
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Haloalkene
Chloroalkene
Organooxygen compound
Organonitrogen compound
Organochloride
Organohalogen compound
Hydrocarbon derivative
Carbonyl group
Organic nitrogen compound
Imine
Organic oxygen compound
Organopnictogen compound
Organic oxide
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	3.75	ALOGPS
logP	3.19	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	11.95	ChemAxon
pKa (Strongest Basic)	3.48	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	49.74 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	107.08 m³·mol⁻¹	ChemAxon
Polarizability	39.88 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione (NP0151381)

MOL for NP0151381 (4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione)

3D MOL for NP0151381 (4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione)

3D SDF for NP0151381 (4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione)

3D-SDF for NP0151381 (4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione)

PDB for NP0151381 (4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione)

3D PDB for NP0151381 (4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione)

SMILES for NP0151381 (4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione)

INCHI for NP0151381 (4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione)

Structure for NP0151381 (4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione)

3D Structure for NP0151381 (4-chloro-3-ethenyl-3,7,7,10-tetramethyl-2-(methylideneamino)-10-azatetracyclo[6.6.1.1²,⁶.0¹¹,¹⁵]hexadeca-1(14),4,11(15),12-tetraene-9,16-dione)