NP-MRD: Showing NP-Card for (2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol (NP0282231)

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Record Information

Version

2.0

Created at

2022-09-09 08:59:07 UTC

Updated at

2022-09-09 08:59:07 UTC

NP-MRD ID

NP0282231

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol

Description

Petromindole belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene. (2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol was first documented in 2003 (PMID: 15369342). Based on a literature review very few articles have been published on Petromindole (PMID: 29336573).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092210592D          

 30 35  0  0  1  0            999 V2000
    6.9047    1.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0661    0.4111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8348    0.7105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2413    0.3927    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8129    1.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9881    1.0793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5917    0.3558    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1634    1.0609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0200   -0.3493    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6236   -1.0728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7988   -1.0912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3705   -0.3861    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9740   -1.1096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5457   -0.4045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8515   -1.1034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0409   -0.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7685   -0.1712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3067    0.4540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2022    1.2724    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9482    1.6247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5138    1.0241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1173    0.3006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3386    1.0425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7669    0.3374    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8448   -0.3308    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4484   -1.0544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.0980   -1.0175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.3192   -0.2756    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  4  5  1  6  0  0  0
  5  6  1  0  0  0  0
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  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
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 18 19  1  0  0  0  0
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 21 22  1  0  0  0  0
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  7 24  1  0  0  0  0
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  9 25  1  0  0  0  0
  4 25  1  0  0  0  0
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 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
  2 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END

     RDKit          3D

 69 74  0  0  0  0  0  0  0  0999 V2000
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    5.4431   -2.0975   -0.3846 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2156   -0.0464   -1.6609 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.3329    1.8881   -2.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5590    1.4245   -1.2272 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1358    0.2226   -0.8775 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3401    1.9229   -0.5049 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6598    0.6758   -0.0203 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8012   -0.6943    0.3270 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4893   -0.7882    1.6490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1108   -2.0316   -0.3764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5610   -2.2601   -0.5538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3698   -1.1442   -1.0691 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6516   -1.2388   -0.4697 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6173    1.0515    2.5596 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0904   -1.0739   -0.5046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0974   -2.3048    1.5359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0514   -0.8667    2.5546 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0415   -2.2364    0.8351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1991   -1.5595    2.4651 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8470    1.7322    2.0115 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7887    0.1976    3.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2007    0.6122    2.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0406   -2.4632    1.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0154   -3.0052   -0.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309092210592D          

 30 35  0  0  1  0            999 V2000
    6.9047    1.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0661    0.4111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3067    0.4540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2022    1.2724    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9482    1.6247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5138    1.0241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1173    0.3006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3386    1.0425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7669    0.3374    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    6.2732   -1.0359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4944   -0.2940    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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 29 30  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0282231

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)[C@H](O)CC[C@]2(C)[C@@H]1CC[C@@]1(C)[C@H]2CC[C@]2(C)[C@@H]1CC1=CNC3=CC=CC2=C13

> <INCHI_IDENTIFIER>
InChI=1S/C28H39NO/c1-25(2)20-9-13-28(5)21(27(20,4)14-11-23(25)30)10-12-26(3)18-7-6-8-19-24(18)17(16-29-19)15-22(26)28/h6-8,16,20-23,29-30H,9-15H2,1-5H3/t20-,21+,22+,23-,26+,27-,28+/m1/s1

> <INCHI_KEY>
DRNNQNUPQAJBQZ-DIADYQGESA-N

> <FORMULA>
C28H39NO

> <MOLECULAR_WEIGHT>
405.626

> <EXACT_MASS>
405.30316488

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
49.38721072404628

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,5R,6S,9R,11S,14S,15R)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0^{2,15}.0^{5,14}.0^{6,11}.0^{20,24}]tetracosa-1(24),17,20,22-tetraen-9-ol

> <JCHEM_LOGP>
6.334438719333331

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.489433390654742

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.516039674024068

> <JCHEM_PKA_STRONGEST_BASIC>
-0.835121834927616

> <JCHEM_POLAR_SURFACE_AREA>
36.019999999999996

> <JCHEM_REFRACTIVITY>
123.48119999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,5R,6S,9R,11S,14S,15R)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0^{2,15}.0^{5,14}.0^{6,11}.0^{20,24}]tetracosa-1(24),17,20,22-tetraen-9-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      12.889   2.278   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.190   0.767   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.625   1.326   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.650   0.733   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.851   2.049   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.311   2.015   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.571   0.664   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.772   1.980   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.371  -0.652   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.631  -2.003   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.091  -2.037   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.292  -0.721   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.551  -2.071   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.752  -0.755   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.456  -2.060   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.943  -1.773   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.435  -0.320   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.439   0.848   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       2.244   2.375   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       3.637   3.033   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.692   1.912   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.952   0.561   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.232   1.946   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.032   0.630   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.910  -0.618   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.170  -1.968   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.710  -1.934   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.250  -1.899   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      13.990  -0.549   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      15.529  -0.514   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   29                                             
CONECT    3    2                                                            
CONECT    4    2    5   25                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   24                                             
CONECT    8    7                                                            
CONECT    9    7   10   25                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   24                                             
CONECT   13   12                                                            
CONECT   14   12   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21   14   18                                                  
CONECT   23   21   24                                                       
CONECT   24   23    7   12                                                  
CONECT   25    9    4   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28    2   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₉NO

Average Mass

405.6260 Da

Monoisotopic Mass

405.30316 Da

IUPAC Name

(2R,5R,6S,9R,11S,14S,15R)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0^{2,15}.0^{5,14}.0^{6,11}.0^{20,24}]tetracosa-1(24),17,20,22-tetraen-9-ol

Traditional Name

(2R,5R,6S,9R,11S,14S,15R)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0^{2,15}.0^{5,14}.0^{6,11}.0^{20,24}]tetracosa-1(24),17,20,22-tetraen-9-ol

CAS Registry Number

Not Available

SMILES

CC1(C)[C@H](O)CC[C@]2(C)[C@@H]1CC[C@@]1(C)[C@H]2CC[C@]2(C)[C@@H]1CC1=CNC3=CC=CC2=C13

InChI Identifier

InChI=1S/C28H39NO/c1-25(2)20-9-13-28(5)21(27(20,4)14-11-23(25)30)10-12-26(3)18-7-6-8-19-24(18)17(16-29-19)15-22(26)28/h6-8,16,20-23,29-30H,9-15H2,1-5H3/t20-,21+,22+,23-,26+,27-,28+/m1/s1

InChI Key

DRNNQNUPQAJBQZ-DIADYQGESA-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 phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Not Available

Direct Parent

Phenanthrenes and derivatives

Alternative Parents

Substituents

Phenanthrene
3-alkylindole
Indole
Indole or derivatives
Isoindole or derivatives
Cyclic alcohol
Pyrrole
Heteroaromatic compound
Secondary alcohol
Organoheterocyclic compound
Azacycle
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Organic nitrogen 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	6.33	ChemAxon
pKa (Strongest Acidic)	17.52	ChemAxon
pKa (Strongest Basic)	-0.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	36.02 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	123.48 m³·mol⁻¹	ChemAxon
Polarizability	49.39 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	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

C00026510

Chemspider ID

154472

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

177411

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Dethe DH, Sau SK: Biomimetic Enantioselective Total Synthesis of (-)-Petromindole. Org Lett. 2018 Feb 2;20(3):632-635. doi: 10.1021/acs.orglett.7b03768. Epub 2018 Jan 16. [PubMed:29336573 ]
Xiong Q, Zhu X, Wilson WK, Ganesan A, Matsuda SP: Enzymatic synthesis of an indole diterpene by an oxidosqualene cyclase: mechanistic, biosynthetic, and phylogenetic implications. J Am Chem Soc. 2003 Jul 30;125(30):9002-3. doi: 10.1021/ja036322v. [PubMed:15369342 ]
LOTUS database [Link]

Showing NP-Card for (2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol (NP0282231)

MOL for NP0282231 ((2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol)

3D MOL for NP0282231 ((2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol)

3D SDF for NP0282231 ((2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol)

3D-SDF for NP0282231 ((2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol)

PDB for NP0282231 ((2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol)

3D PDB for NP0282231 ((2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol)

SMILES for NP0282231 ((2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol)

INCHI for NP0282231 ((2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol)

Structure for NP0282231 ((2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol)

3D Structure for NP0282231 ((2r,5r,6s,9r,11s,14s,15r)-2,6,10,10,14-pentamethyl-19-azahexacyclo[15.6.1.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²⁰,²⁴]tetracosa-1(24),17,20,22-tetraen-9-ol)