NP-MRD: Showing NP-Card for (2r,5s,6r,9s,10r,14s,16r)-3,9-dihydroxy-5-(1h-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0²,⁶.0²,¹⁰]henicosa-1(20),3,7,11,18-pentaen-17-one (NP0149636)

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Record Information

Version

2.0

Created at

2022-09-02 05:33:02 UTC

Updated at

2022-09-02 05:33:02 UTC

NP-MRD ID

NP0149636

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,5s,6r,9s,10r,14s,16r)-3,9-dihydroxy-5-(1h-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0²,⁶.0²,¹⁰]henicosa-1(20),3,7,11,18-pentaen-17-one

Description

Armochaetoglobin N belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position. Based on a literature review very few articles have been published on Armochaetoglobin N.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022207332D          

 38 43  0  0  1  0            999 V2000
    0.4966   -2.1651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3200   -2.1138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6873   -1.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2312   -0.6876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5107   -1.3238    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0236   -0.6776    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8022    0.1172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3798    0.7063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2427    1.5198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9741    1.9016    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5632    1.3240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3866    1.3752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8427    0.6878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4754   -0.0509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6520   -0.1022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1959    0.5852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7966   -0.9656    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7847   -1.6755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4078   -2.3027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9668   -2.0112    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7902   -1.9599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3678   -1.3709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1065   -1.7382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0697   -2.5961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2463   -2.6474    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5258   -3.2836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3493   -3.2323    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1586   -4.0223    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    4.3351   -4.0736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9679   -4.8123    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4240   -5.4998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1444   -4.8636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6883   -4.1761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0556   -3.4374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5995   -2.7500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7761   -2.8012    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4088   -3.5400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  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
  6 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 20 18  1  1  0  0  0
  5 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
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 21 25  1  0  0  0  0
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 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 34 33  1  4  0  0  0
 34 35  2  0  0  0  0
 36 35  1  1  0  0  0
 20 36  1  0  0  0  0
 36 37  1  0  0  0  0
  2 37  1  0  0  0  0
 37 38  1  6  0  0  0
M  END

     RDKit          3D

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    3.3425   -3.0584    0.3688 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8454    2.8912   -1.3787 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309022207332D          

 38 43  0  0  1  0            999 V2000
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    3.0556   -3.4374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5995   -2.7500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7761   -2.8012    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4088   -3.5400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  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
  6 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 20 18  1  1  0  0  0
  5 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  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
 21 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 34 33  1  4  0  0  0
 34 35  2  0  0  0  0
 36 35  1  1  0  0  0
 20 36  1  0  0  0  0
 36 37  1  0  0  0  0
  2 37  1  0  0  0  0
 37 38  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0149636

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC=C[C@H]2[C@H](O)C(C)=C(C)[C@H]3[C@H](CC4=CNC5=CC=CC=C45)N=C(O)[C@@]23C2=CC=C(N2)C(=O)[C@H](C)C1

> <INCHI_IDENTIFIER>
InChI=1S/C32H37N3O3/c1-17-8-7-10-23-30(37)20(4)19(3)28-26(15-21-16-33-24-11-6-5-9-22(21)24)35-31(38)32(23,28)27-13-12-25(34-27)29(36)18(2)14-17/h5-7,9-13,16-18,23,26,28,30,33-34,37H,8,14-15H2,1-4H3,(H,35,38)/t17-,18+,23-,26-,28-,30+,32+/m0/s1

> <INCHI_KEY>
KJMPCWQWZNLNTM-MUIYCEKNSA-N

> <FORMULA>
C32H37N3O3

> <MOLECULAR_WEIGHT>
511.666

> <EXACT_MASS>
511.283492063

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
57.45179891159725

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,5S,6R,9S,10R,14S,16R)-3,9-dihydroxy-5-[(1H-indol-3-yl)methyl]-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0^{2,6}.0^{2,10}]henicosa-1(20),3,7,11,18-pentaen-17-one

> <ALOGPS_LOGP>
5.42

> <JCHEM_LOGP>
4.345484554690948

> <ALOGPS_LOGS>
-5.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.353821212256985

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.1029525077726983

> <JCHEM_PKA_STRONGEST_BASIC>
5.500733317451698

> <JCHEM_POLAR_SURFACE_AREA>
101.47

> <JCHEM_REFRACTIVITY>
151.3975

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.77e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,5S,6R,9S,10R,14S,16R)-3,9-dihydroxy-5-(1H-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0^{2,6}.0^{2,10}]henicosa-1(20),3,7,11,18-pentaen-17-one

> <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       0.927  -4.041   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.464  -3.946   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.150  -2.567   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.298  -1.284   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.687  -2.471   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.644  -1.265   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.231   0.219   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.309   1.318   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.053   2.837   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       7.418   3.550   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       8.518   2.471   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.055   2.567   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.906   1.284   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.221  -0.095   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.684  -0.191   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.832   1.092   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       7.087  -1.802   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       7.065  -3.128   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.228  -4.298   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.538  -3.754   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.075  -3.659   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.153  -2.559   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.532  -3.245   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.464  -4.846   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       7.926  -4.942   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      10.315  -6.129   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      11.852  -6.034   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.629  -7.508   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.481  -8.792   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.092  -7.604   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.407  -8.983   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.258 -10.266   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.870  -9.079   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.018  -7.795   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.704  -6.416   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.852  -5.133   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.315  -5.229   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       2.630  -6.608   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   37                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   20                                                  
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8   10                                                       
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    6   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    5   21   36                                             
CONECT   21   20   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24   21                                                       
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   20   37                                                  
CONECT   37   36    2   38                                                  
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₃₇N₃O₃

Average Mass

511.6660 Da

Monoisotopic Mass

511.28349 Da

IUPAC Name

(2R,5S,6R,9S,10R,14S,16R)-3,9-dihydroxy-5-[(1H-indol-3-yl)methyl]-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0^{2,6}.0^{2,10}]henicosa-1(20),3,7,11,18-pentaen-17-one

Traditional Name

(2R,5S,6R,9S,10R,14S,16R)-3,9-dihydroxy-5-(1H-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0^{2,6}.0^{2,10}]henicosa-1(20),3,7,11,18-pentaen-17-one

CAS Registry Number

Not Available

SMILES

C[C@H]1CC=C[C@H]2[C@H](O)C(C)=C(C)[C@H]3[C@H](CC4=CNC5=CC=CC=C45)N=C(O)[C@@]23C2=CC=C(N2)C(=O)[C@H](C)C1

InChI Identifier

InChI=1S/C32H37N3O3/c1-17-8-7-10-23-30(37)20(4)19(3)28-26(15-21-16-33-24-11-6-5-9-22(21)24)35-31(38)32(23,28)27-13-12-25(34-27)29(36)18(2)14-17/h5-7,9-13,16-18,23,26,28,30,33-34,37H,8,14-15H2,1-4H3,(H,35,38)/t17-,18+,23-,26-,28-,30+,32+/m0/s1

InChI Key

KJMPCWQWZNLNTM-MUIYCEKNSA-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 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

3-alkylindoles

Alternative Parents

Substituents

3-alkylindole
Isoindole or derivatives
Aryl alkyl ketone
Aryl ketone
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Cyclic carboximidic acid
Pyrroline
Pyrrole
Secondary alcohol
Ketone
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Alcohol
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	5.42	ALOGPS
logP	4.35	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	3.1	ChemAxon
pKa (Strongest Basic)	5.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	101.47 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	151.4 m³·mol⁻¹	ChemAxon
Polarizability	57.45 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

139583116

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,5s,6r,9s,10r,14s,16r)-3,9-dihydroxy-5-(1h-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0²,⁶.0²,¹⁰]henicosa-1(20),3,7,11,18-pentaen-17-one (NP0149636)

MOL for NP0149636 ((2r,5s,6r,9s,10r,14s,16r)-3,9-dihydroxy-5-(1h-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0²,⁶.0²,¹⁰]henicosa-1(20),3,7,11,18-pentaen-17-one)

3D MOL for NP0149636 ((2r,5s,6r,9s,10r,14s,16r)-3,9-dihydroxy-5-(1h-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0²,⁶.0²,¹⁰]henicosa-1(20),3,7,11,18-pentaen-17-one)

3D SDF for NP0149636 ((2r,5s,6r,9s,10r,14s,16r)-3,9-dihydroxy-5-(1h-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0²,⁶.0²,¹⁰]henicosa-1(20),3,7,11,18-pentaen-17-one)

3D-SDF for NP0149636 ((2r,5s,6r,9s,10r,14s,16r)-3,9-dihydroxy-5-(1h-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0²,⁶.0²,¹⁰]henicosa-1(20),3,7,11,18-pentaen-17-one)

PDB for NP0149636 ((2r,5s,6r,9s,10r,14s,16r)-3,9-dihydroxy-5-(1h-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0²,⁶.0²,¹⁰]henicosa-1(20),3,7,11,18-pentaen-17-one)

3D PDB for NP0149636 ((2r,5s,6r,9s,10r,14s,16r)-3,9-dihydroxy-5-(1h-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0²,⁶.0²,¹⁰]henicosa-1(20),3,7,11,18-pentaen-17-one)

SMILES for NP0149636 ((2r,5s,6r,9s,10r,14s,16r)-3,9-dihydroxy-5-(1h-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0²,⁶.0²,¹⁰]henicosa-1(20),3,7,11,18-pentaen-17-one)

INCHI for NP0149636 ((2r,5s,6r,9s,10r,14s,16r)-3,9-dihydroxy-5-(1h-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0²,⁶.0²,¹⁰]henicosa-1(20),3,7,11,18-pentaen-17-one)

Structure for NP0149636 ((2r,5s,6r,9s,10r,14s,16r)-3,9-dihydroxy-5-(1h-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0²,⁶.0²,¹⁰]henicosa-1(20),3,7,11,18-pentaen-17-one)

3D Structure for NP0149636 ((2r,5s,6r,9s,10r,14s,16r)-3,9-dihydroxy-5-(1h-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0²,⁶.0²,¹⁰]henicosa-1(20),3,7,11,18-pentaen-17-one)