NP-MRD: Showing NP-Card for 17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one (NP0201009)

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Record Information

Version

2.0

Created at

2022-09-04 19:58:50 UTC

Updated at

2022-09-04 19:58:51 UTC

NP-MRD ID

NP0201009

Secondary Accession Numbers

None

Natural Product Identification

Common Name

17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one

Description

17-Bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]Docosa-3,5,7,13,15(19),16-hexaen-11-one belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. 17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one is found in Securiflustra securifrons. 17-Bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]Docosa-3,5,7,13,15(19),16-hexaen-11-one is a strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171505132D          

 27 31  0  0  0  0            999 V2000
    2.0066   -2.9310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4764   -2.2528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1028   -2.7897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7420   -1.8485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0845   -2.3468    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.5461   -1.0105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8901   -0.4160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101   -1.2371    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0045   -1.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4025   -2.1324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2275   -2.1387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6455   -1.4274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2384   -0.7098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4135   -0.7035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1339   -0.0862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2138    0.7349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0194    0.9126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3492    1.6688    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4374    0.2013    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2797    0.3032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0307   -0.0783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3103   -0.8730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1344   -0.8349    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4253   -1.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2208   -1.8254    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.7809   -2.1222    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0918   -1.6685    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  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  7 19  1  0  0  0  0
 20 19  1  4  0  0  0
 20 21  2  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
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
  2 27  1  0  0  0  0
 22 27  2  0  0  0  0
M  END

     RDKit          3D

 47 51  0  0  0  0  0  0  0  0999 V2000
   -3.0302    2.0906   -1.0181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4401    1.0426   -0.0929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5575    1.5853    1.2862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1398   -0.2539   -0.3006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9909   -0.5522   -1.2876 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4020   -1.8116   -1.1653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6385   -2.6729   -2.3700 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -3.8060   -2.2856   -0.1070 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9857   -1.3479    0.4954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1742   -1.5140    1.6920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8947   -1.5184    1.9254 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2658   -1.3688    1.1810 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2237   -2.3941    0.7816 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5238   -3.4494    1.4163 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8232   -2.0295   -0.5062 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6657   -0.5300   -0.5449 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0577    0.0243   -0.3480 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0907    0.0582   -1.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2963    0.6174   -0.8769 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4172    1.1150    0.3947 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3770    1.0663    1.2744 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1417    0.5045    0.9119 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9290    0.3101    1.5705 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8813   -0.1521    0.6390 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0739    0.9746    0.5264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0271    0.8080   -0.5824 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9663   -0.8064   -1.3762 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -4.0714    2.2709   -0.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8781    1.8121   -2.0843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4741    3.0454   -0.8192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9341    2.5046    1.3718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6141    2.0009    1.3687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4822    0.8830    2.1108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3250    0.0768   -2.0768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8012   -1.6788    2.6194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6092   -1.7409    3.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4284   -2.5596   -1.3850 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9095   -2.3460   -0.4720 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3692   -0.1176   -1.5182 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0195   -0.3259   -2.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1266    0.6694   -1.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3623    1.5625    0.7218 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4437    1.4509    2.2833 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7432    0.4581    2.5785 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5036    1.9302    0.4536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5540    1.0563    1.5515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7288    1.5376   -1.3903 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2 26  1  0
 26 27  1  0
 26 25  1  0
 25 24  1  0
 24 23  1  1
 23 22  1  0
 22 21  2  0
 21 20  1  0
 20 19  2  0
 19 18  1  0
 18 17  2  0
 17 16  1  0
 16 15  1  0
 15 13  1  0
 13 14  2  0
 13 12  1  0
 12 11  1  0
 11 10  2  0
 10  9  1  0
  9  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
  4  2  1  0
 16 24  1  0
  8  9  1  0
 12 24  1  0
 17 22  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  3 32  1  0
  3 33  1  0
 26 47  1  6
 25 45  1  0
 25 46  1  0
 23 44  1  0
 21 43  1  0
 20 42  1  0
 19 41  1  0
 18 40  1  0
 16 39  1  6
 15 37  1  0
 15 38  1  0
 11 36  1  0
 10 35  1  0
  5 34  1  0
M  END


  Mrv1533004171505132D          

 27 31  0  0  0  0            999 V2000
    2.0066   -2.9310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4764   -2.2528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1028   -2.7897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7420   -1.8485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0845   -2.3468    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.5461   -1.0105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8901   -0.4160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101   -1.2371    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0045   -1.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4025   -2.1324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2275   -2.1387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6455   -1.4274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2384   -0.7098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4135   -0.7035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1339   -0.0862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2138    0.7349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0194    0.9126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3492    1.6688    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4374    0.2013    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2797    0.3032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0307   -0.0783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3103   -0.8730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1344   -0.8349    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4253   -1.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2208   -1.8254    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.7809   -2.1222    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0918   -1.6685    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  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  7 19  1  0  0  0  0
 20 19  1  4  0  0  0
 20 21  2  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
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
  2 27  1  0  0  0  0
 22 27  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0201009

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)C(Cl)CC23NC4=CC=CC=C4C2CC(=O)N3C=CC2=C1NC(Br)=N2

> <INCHI_IDENTIFIER>
InChI=1S/C20H20BrClN4O/c1-19(2)15(22)10-20-12(11-5-3-4-6-13(11)25-20)9-16(27)26(20)8-7-14-17(19)24-18(21)23-14/h3-8,12,15,25H,9-10H2,1-2H3,(H,23,24)

> <INCHI_KEY>
RIOWJYUGPBYKPY-UHFFFAOYSA-N

> <FORMULA>
C20H20BrClN4O

> <MOLECULAR_WEIGHT>
447.76

> <EXACT_MASS>
446.050902

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
41.587921897216084

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one

> <ALOGPS_LOGP>
4.50

> <JCHEM_LOGP>
3.8744259660000004

> <ALOGPS_LOGS>
-4.40

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.328384234207466

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.225642703312458

> <JCHEM_PKA_STRONGEST_BASIC>
4.023590662428676

> <JCHEM_POLAR_SURFACE_AREA>
61.02

> <JCHEM_REFRACTIVITY>
109.96170000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.80e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       3.746  -5.471   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.623  -4.205   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.792  -5.208   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.252  -3.450   0.000  0.00  0.00           C+0
HETATM    5 Cl   UNK     0       2.024  -4.381   0.000  0.00  0.00          Cl+0
HETATM    6  C   UNK     0       2.886  -1.886   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.661  -0.776   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       1.512  -2.309   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       0.008  -2.641   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.751  -3.980   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.291  -3.992   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.072  -2.665   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.312  -1.325   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.772  -1.313   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.250  -0.161   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.399   1.372   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.903   1.704   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.519   3.115   0.000  0.00  0.00           O+0
HETATM   19  N   UNK     0       2.683   0.376   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       4.255   0.566   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.657  -0.146   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.179  -1.630   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       7.718  -1.559   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       8.260  -3.000   0.000  0.00  0.00           C+0
HETATM   25 Br   UNK     0       9.745  -3.407   0.000  0.00  0.00          Br+0
HETATM   26  N   UNK     0       7.058  -3.961   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       5.771  -3.115   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   27                                             
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   15   19                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14    7   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17    7   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26    2   22                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₀BrClN₄O

Average Mass

447.7600 Da

Monoisotopic Mass

446.05090 Da

IUPAC Name

17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one

Traditional Name

17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one

CAS Registry Number

Not Available

SMILES

CC1(C)C(Cl)CC23NC4=CC=CC=C4C2CC(=O)N3C=CC2=C1NC(Br)=N2

InChI Identifier

InChI=1S/C20H20BrClN4O/c1-19(2)15(22)10-20-12(11-5-3-4-6-13(11)25-20)9-16(27)26(20)8-7-14-17(19)24-18(21)23-14/h3-8,12,15,25H,9-10H2,1-2H3,(H,23,24)

InChI Key

RIOWJYUGPBYKPY-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
Securiflustra securifrons	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting 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

Pyrroloindoles

Direct Parent

Pyrroloindoles

Alternative Parents

Substituents

Pyrroloindole
Indole
Dihydroindole
Aryl bromide
Aryl halide
Benzenoid
2-pyrrolidone
Pyrrolidone
Azole
Imidazole
Heteroaromatic compound
Tertiary carboxylic acid amide
Pyrrolidine
Pyrrole
Carboxamide group
Lactam
Azacycle
Carboxylic acid derivative
Organobromide
Organohalogen compound
Alkyl halide
Organooxygen compound
Hydrocarbon derivative
Alkyl chloride
Carbonyl group
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Amine
Organochloride
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	4.5	ALOGPS
logP	3.87	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	11.23	ChemAxon
pKa (Strongest Basic)	4.02	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	61.02 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	109.96 m³·mol⁻¹	ChemAxon
Polarizability	41.59 Å³	ChemAxon
Number of Rings	5	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

85218173

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one (NP0201009)

MOL for NP0201009 (17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one)

3D MOL for NP0201009 (17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one)

3D SDF for NP0201009 (17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one)

3D-SDF for NP0201009 (17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one)

PDB for NP0201009 (17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one)

3D PDB for NP0201009 (17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one)

SMILES for NP0201009 (17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one)

INCHI for NP0201009 (17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one)

Structure for NP0201009 (17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one)

3D Structure for NP0201009 (17-bromo-21-chloro-20,20-dimethyl-2,12,16,18-tetraazapentacyclo[10.10.0.0¹,⁹.0³,⁸.0¹⁵,¹⁹]docosa-3,5,7,13,15(19),16-hexaen-11-one)