NP-MRD: Showing NP-Card for 12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]docosa-3(11),4,6,8,21-pentaen-22-ol (NP0252789)

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Record Information

Version

2.0

Created at

2022-09-07 16:25:56 UTC

Updated at

2022-09-07 16:25:56 UTC

NP-MRD ID

NP0252789

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]docosa-3(11),4,6,8,21-pentaen-22-ol

Description

12,12,17-Trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]Docosa-3(11),4,6,8,21-pentaen-22-ol belongs to the class of organic compounds known as pyrroloquinolines. Pyrroloquinolines are compounds containing a pyrroloquinoline moiety, which consists of a pyrrole ring fused to a quinoline. Based on a literature review very few articles have been published on 12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]Docosa-3(11),4,6,8,21-pentaen-22-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072218252D          

 26 31  0  0  0  0            999 V2000
   -1.3679    0.2909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5513    0.1736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0668    0.7426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8557    0.4218    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6915    0.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3710    0.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1832    0.4813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8404   -0.0467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7212   -0.8631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4607   -1.2287    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0370   -0.6383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8613   -0.6716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3023    0.0257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9189    0.7562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0945    0.7895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6536    0.0922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9799   -1.2806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4793   -1.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3977   -1.8651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2825   -0.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4267   -1.1186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7416   -0.4940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1168   -0.5492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5313   -0.4972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0900   -1.1042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5901    0.2494    0.0000 N   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  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  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
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
  8 16  1  0  0  0  0
 11 16  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  4 22  1  0  0  0  0
 22 23  1  0  0  0  0
  2 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
  6 26  1  0  0  0  0
M  END

     RDKit          3D

 53 58  0  0  0  0  0  0  0  0999 V2000
    5.5057    0.6651    0.5919 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4395   -0.3600    0.2602 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2868   -0.2015    1.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4877    0.7793    0.6208 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1798    0.9847    1.1274 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1436    0.9428    0.0091 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1629    1.4515    0.4890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2998    0.5685    0.2425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1989   -0.7829   -0.0096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3971   -1.3384   -0.1975 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3020   -0.3419   -0.0680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6794   -0.4232   -0.1772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3931    0.7511   -0.0006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7538    1.9410    0.2708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3760    2.0018    0.3761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6510    0.8442    0.2035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8376   -1.3751   -0.0306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8300   -2.6335   -0.9101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4895   -1.8021    1.3488 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0884   -0.4028   -0.6625 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4893   -0.8995   -0.8601 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4195    0.2906   -0.7560 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8302    0.0018   -1.0922 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7985    1.3970   -1.5155 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3810    1.8870   -2.6547 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6953    1.8479   -1.0292 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.5368    0.2708    0.3913 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4615    0.9746    1.6527 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4084    1.5638   -0.0701 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8400   -1.3869    0.2759 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6610    0.2006    2.2256 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8226   -1.1650    1.4569 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1340    2.0465    1.5141 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9034    0.3565    1.9849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1237    1.6723    1.5936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3938    2.4543    0.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5844   -2.3592   -0.4058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2023   -1.3322   -0.3869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4703    0.7380   -0.0764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3254    2.8538    0.4069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8732    2.9479    0.5915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8581   -2.3191   -1.9765 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1582   -3.1119   -0.7480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6323   -3.3290   -0.6372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0007   -2.7959    1.5244 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5674   -1.9769    1.5411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9767   -1.1270    2.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3183   -0.2073   -1.7005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7494   -1.7212   -0.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6400   -1.3049   -1.9039 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8515   -0.9456   -1.7017 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3753    0.8202   -1.5887 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2758    2.3893   -2.5588 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  9 17  1  0
 17 18  1  0
 17 19  1  0
 17 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 22 24  1  0
 24 25  1  0
 24 26  2  0
 23  2  1  0
 22  4  1  0
 20  6  1  0
 26  6  1  0
 16  8  1  0
 16 11  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  6
  3 31  1  0
  3 32  1  0
  5 33  1  0
  5 34  1  0
  7 35  1  0
  7 36  1  0
 10 37  1  0
 12 38  1  0
 13 39  1  0
 14 40  1  0
 15 41  1  0
 18 42  1  0
 18 43  1  0
 18 44  1  0
 19 45  1  0
 19 46  1  0
 19 47  1  0
 20 48  1  6
 21 49  1  0
 21 50  1  0
 23 51  1  0
 23 52  1  0
 25 53  1  0
M  END


  Mrv1652309072218252D          

 26 31  0  0  0  0            999 V2000
   -1.3679    0.2909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5513    0.1736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0668    0.7426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8557    0.4218    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6915    0.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3710    0.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1832    0.4813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8404   -0.0467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7212   -0.8631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4607   -1.2287    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0370   -0.6383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8613   -0.6716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3023    0.0257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9189    0.7562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0945    0.7895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6536    0.0922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9799   -1.2806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4793   -1.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3977   -1.8651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2825   -0.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4267   -1.1186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7416   -0.4940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1168   -0.5492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5313   -0.4972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0900   -1.1042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5901    0.2494    0.0000 N   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  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  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
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
  8 16  1  0  0  0  0
 11 16  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  4 22  1  0  0  0  0
 22 23  1  0  0  0  0
  2 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
  6 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0252789

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CN2CC34CC5=C(NC6=CC=CC=C56)C(C)(C)C3CC2(C1)C(O)=N4

> <INCHI_IDENTIFIER>
InChI=1S/C22H27N3O/c1-13-8-22-10-17-20(2,3)18-15(14-6-4-5-7-16(14)23-18)9-21(17,24-19(22)26)12-25(22)11-13/h4-7,13,17,23H,8-12H2,1-3H3,(H,24,26)

> <INCHI_KEY>
YUPGACVQXOPMFV-UHFFFAOYSA-N

> <FORMULA>
C22H27N3O

> <MOLECULAR_WEIGHT>
349.478

> <EXACT_MASS>
349.215412501

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
40.72402807607879

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{15,19}]docosa-3(11),4,6,8,21-pentaen-22-ol

> <JCHEM_LOGP>
1.069796985986116

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
15.584590240333206

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.8146567589604925

> <JCHEM_PKA_STRONGEST_BASIC>
8.68023101353161

> <JCHEM_POLAR_SURFACE_AREA>
51.620000000000005

> <JCHEM_REFRACTIVITY>
102.63259999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{15,19}]docosa-3(11),4,6,8,21-pentaen-22-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.553   0.543   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.029   0.324   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.125   1.386   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       1.597   0.787   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       3.157   1.554   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.426   0.344   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.942   0.898   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.169  -0.087   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.946  -1.611   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       8.327  -2.294   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       9.402  -1.192   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.941  -1.254   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.764   0.048   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.049   1.412   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.510   1.474   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.687   0.172   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.563  -2.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.495  -3.616   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.476  -3.481   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.261  -1.408   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.663  -2.088   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.384  -0.922   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.218  -1.025   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.858  -0.928   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.901  -2.061   0.000  0.00  0.00           O+0
HETATM   26  N   UNK     0       2.968   0.466   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   22                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   20   26                                             
CONECT    7    6    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    8   11                                                  
CONECT   17    9   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17    6   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21    4   23   24                                             
CONECT   23   22    2                                                       
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    6                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₇N₃O

Average Mass

349.4780 Da

Monoisotopic Mass

349.21541 Da

IUPAC Name

12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{15,19}]docosa-3(11),4,6,8,21-pentaen-22-ol

Traditional Name

12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{15,19}]docosa-3(11),4,6,8,21-pentaen-22-ol

CAS Registry Number

Not Available

SMILES

CC1CN2CC34CC5=C(NC6=CC=CC=C56)C(C)(C)C3CC2(C1)C(O)=N4

InChI Identifier

InChI=1S/C22H27N3O/c1-13-8-22-10-17-20(2,3)18-15(14-6-4-5-7-16(14)23-18)9-21(17,24-19(22)26)12-25(22)11-13/h4-7,13,17,23H,8-12H2,1-3H3,(H,24,26)

InChI Key

YUPGACVQXOPMFV-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 pyrroloquinolines. Pyrroloquinolines are compounds containing a pyrroloquinoline moiety, which consists of a pyrrole ring fused to a quinoline.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Pyrroloquinolines

Direct Parent

Pyrroloquinolines

Alternative Parents

Substituents

Pyrroloquinoline
Carbazole
Alpha-amino acid amide
3-alkylindole
Azaspirodecane
Alpha-amino acid or derivatives
Indolizidine
Indole or derivatives
Indole
Aralkylamine
N-alkylpiperazine
Piperidinone
Delta-lactam
Benzenoid
N-alkylpyrrolidine
Piperidine
Piperazine
1,4-diazinane
Heteroaromatic compound
Pyrrolidine
Pyrrole
Tertiary aliphatic amine
Tertiary amine
Secondary carboxylic acid amide
Lactam
Carboxamide group
Amino acid or derivatives
Azacycle
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
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	1.07	ChemAxon
pKa (Strongest Acidic)	2.81	ChemAxon
pKa (Strongest Basic)	8.68	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	51.62 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	102.63 m³·mol⁻¹	ChemAxon
Polarizability	40.72 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

162815521

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]docosa-3(11),4,6,8,21-pentaen-22-ol (NP0252789)

MOL for NP0252789 (12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]docosa-3(11),4,6,8,21-pentaen-22-ol)

3D MOL for NP0252789 (12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]docosa-3(11),4,6,8,21-pentaen-22-ol)

3D SDF for NP0252789 (12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]docosa-3(11),4,6,8,21-pentaen-22-ol)

3D-SDF for NP0252789 (12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]docosa-3(11),4,6,8,21-pentaen-22-ol)

PDB for NP0252789 (12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]docosa-3(11),4,6,8,21-pentaen-22-ol)

3D PDB for NP0252789 (12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]docosa-3(11),4,6,8,21-pentaen-22-ol)

SMILES for NP0252789 (12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]docosa-3(11),4,6,8,21-pentaen-22-ol)

INCHI for NP0252789 (12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]docosa-3(11),4,6,8,21-pentaen-22-ol)

Structure for NP0252789 (12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]docosa-3(11),4,6,8,21-pentaen-22-ol)

3D Structure for NP0252789 (12,12,17-trimethyl-10,19,21-triazahexacyclo[13.5.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]docosa-3(11),4,6,8,21-pentaen-22-ol)