NP-MRD: Showing NP-Card for (9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one (NP0201567)

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Record Information

Version

2.0

Created at

2022-09-04 20:38:33 UTC

Updated at

2022-09-04 20:38:34 UTC

NP-MRD ID

NP0201567

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one

Description

Lagerine belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. (9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one is found in Lagerstroemia indica. (9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one was first documented in 2009 (PMID: 19260657). Based on a literature review very few articles have been published on Lagerine (PMID: 21796576).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042222382D          

 31 35  0  0  1  0            999 V2000
    2.4609    0.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1913    0.3287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2244   -0.4956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5271   -0.9364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5602   -1.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2906   -2.1443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9880   -1.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9549   -0.8791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6522   -0.4383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8673   -1.6103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5928   -2.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0117   -2.6729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1857   -3.4812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9675   -3.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5782   -3.1820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3982   -2.3582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6642   -4.5613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0531   -5.1583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2179   -5.3097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1423   -6.1313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4230   -5.0080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8635   -4.3553    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2298   -3.5990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8180   -2.8611    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9807   -2.9074    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5551   -2.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7302   -2.2158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3309   -2.9377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7565   -3.6445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5814   -3.6293    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0252   -4.3463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
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  3  8  1  0  0  0  0
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  7 10  1  0  0  0  0
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  6 24  1  0  0  0  0
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 30 25  1  1  0  0  0
 30 31  1  0  0  0  0
 22 31  1  0  0  0  0
M  END

     RDKit          3D

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    0.4547    6.6617   -0.6659 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4455    5.6645   -0.5503 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0060    4.3721   -0.1937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3097    4.1059    0.0273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6884    2.8546    0.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2417    1.7487    0.5143 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2083   -2.9190   -0.3214 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2520   -2.4422    0.9582 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0622   -1.0444    1.1475 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1376   -4.4099   -0.5197 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6401   -4.8315   -0.3983 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7684   -3.8003   -1.0940 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6070   -4.1488   -2.3240 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3051   -2.7542   -0.4409 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2278   -1.5157   -0.4995 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1762   -0.8086    0.8429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5171    0.5815    0.9128 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9024    0.5968    0.3835 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8942    0.4067    1.3825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0055   -0.5220    1.0927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3809   -0.7043   -0.3367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5339    0.1074   -1.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0960   -0.0864   -0.8271 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7456   -1.5851   -0.8053 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1243   -0.7943    2.2434 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4077   -4.8117   -1.5020 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6428   -5.0872    0.1496 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3909   -4.7812    0.6754 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5201   -5.8315   -0.7817 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1054   -0.8180   -1.3129 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5703   -1.2491    1.5096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1202   -1.3132    1.3656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7405    0.7828    2.0452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2931    1.3839    1.7250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3588    0.0067    2.2961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8685   -1.5187    1.6105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9334   -0.1263    1.6085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4519   -0.4483   -0.5601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2880   -1.7802   -0.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7819    1.1640   -1.1475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6965   -0.2061   -2.3089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4760    0.3106   -1.6689 H   0  0  0  0  0  0  0  0  0  0  0  0
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 16 41  1  0
 15 40  1  0
M  END


  Mrv1652309042222382D          

 31 35  0  0  1  0            999 V2000
    2.4609    0.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1913    0.3287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2244   -0.4956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5271   -0.9364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5602   -1.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2906   -2.1443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9880   -1.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9549   -0.8791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6522   -0.4383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8673   -1.6103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5928   -2.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0117   -2.6729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0201567

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2[C@@H]3C[C@H](C[C@H]4CCCCN34)OC(=O)CCC3=CC=C(OC2=C1O)C=C3

> <INCHI_IDENTIFIER>
InChI=1S/C25H29NO5/c1-29-22-11-10-20-21-15-19(14-17-4-2-3-13-26(17)21)30-23(27)12-7-16-5-8-18(9-6-16)31-25(20)24(22)28/h5-6,8-11,17,19,21,28H,2-4,7,12-15H2,1H3/t17-,19+,21+/m1/s1

> <INCHI_KEY>
OBHAUUFTXJOWIW-LMNJBCLMSA-N

> <FORMULA>
C25H29NO5

> <MOLECULAR_WEIGHT>
423.509

> <EXACT_MASS>
423.204573038

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
45.40929100239637

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(9S,15R,17S)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1^{9,17}.0^{3,8}.0^{10,15}]heptacosa-1(24),3,5,7,22,25-hexaen-19-one

> <JCHEM_LOGP>
3.7544721315325784

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.968148400633645

> <JCHEM_PKA_STRONGEST_BASIC>
7.68052193025189

> <JCHEM_POLAR_SURFACE_AREA>
68.22999999999999

> <JCHEM_REFRACTIVITY>
116.90869999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(9S,15R,17S)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1^{9,17}.0^{3,8}.0^{10,15}]heptacosa-1(24),3,5,7,22,25-hexaen-19-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       4.594   1.329   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.957   0.614   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.019  -0.925   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.717  -1.748   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.779  -3.287   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.143  -4.003   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.444  -3.180   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.382  -1.641   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.684  -0.818   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       9.086  -3.006   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.440  -3.889   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.355  -4.989   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.680  -6.498   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.139  -7.015   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.279  -5.940   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.943  -4.402   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.573  -8.514   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.432  -9.629   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.873  -9.912   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.732 -11.445   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       6.390  -9.348   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.345  -8.130   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.029  -6.718   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.260  -5.341   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       3.697  -5.427   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       2.903  -4.108   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.363  -4.136   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.618  -5.484   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.412  -6.803   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.952  -6.775   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.780  -8.113   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   24                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
CONECT   17   14   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   31                                                  
CONECT   23   22   24                                                       
CONECT   24   23    6   25                                                  
CONECT   25   24   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   25   31                                                  
CONECT   31   30   22                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₉NO₅

Average Mass

423.5090 Da

Monoisotopic Mass

423.20457 Da

IUPAC Name

(9S,15R,17S)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1^{9,17}.0^{3,8}.0^{10,15}]heptacosa-1(24),3,5,7,22,25-hexaen-19-one

Traditional Name

(9S,15R,17S)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1^{9,17}.0^{3,8}.0^{10,15}]heptacosa-1(24),3,5,7,22,25-hexaen-19-one

CAS Registry Number

Not Available

SMILES

COC1=CC=C2[C@@H]3C[C@H](C[C@H]4CCCCN34)OC(=O)CCC3=CC=C(OC2=C1O)C=C3

InChI Identifier

InChI=1S/C25H29NO5/c1-29-22-11-10-20-21-15-19(14-17-4-2-3-13-26(17)21)30-23(27)12-7-16-5-8-18(9-6-16)31-25(20)24(22)28/h5-6,8-11,17,19,21,28H,2-4,7,12-15H2,1H3/t17-,19+,21+/m1/s1

InChI Key

OBHAUUFTXJOWIW-LMNJBCLMSA-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
Lagerstroemia indica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Diaryl ether
Quinolizidine
Anisole
Phenol ether
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Phenol
Aralkylamine
Piperidine
Benzenoid
Amino acid or derivatives
Carboxylic acid ester
Lactone
Tertiary aliphatic amine
Tertiary amine
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Oxacycle
Azacycle
Organoheterocyclic compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic nitrogen compound
Organic oxide
Amine
Carbonyl group
Organic oxygen 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	3.75	ChemAxon
pKa (Strongest Acidic)	8.97	ChemAxon
pKa (Strongest Basic)	7.68	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	68.23 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	116.91 m³·mol⁻¹	ChemAxon
Polarizability	45.41 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

C00047488

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

101473393

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lee I, Youn U, Kim H, Min B, Kim JS, Bae K: Biphenyl and biphenyl ether quinolizidine N-oxide alkaloids from Lagerstroemia indica L. Planta Med. 2011 Dec;77(18):2037-41. doi: 10.1055/s-0031-1280064. Epub 2011 Jul 27. [PubMed:21796576 ]
Kim HJ, Lee IS, Youn U, Chen QC, Ngoc TM, Ha do T, Liu H, Min BS, Lee JY, Seong RS, Bae K: Biphenylquinolizidine alkaloids from Lagerstroemia indica. J Nat Prod. 2009 Apr;72(4):749-52. doi: 10.1021/np800619g. [PubMed:19260657 ]
LOTUS database [Link]

Showing NP-Card for (9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one (NP0201567)

MOL for NP0201567 ((9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one)

3D MOL for NP0201567 ((9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one)

3D SDF for NP0201567 ((9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one)

3D-SDF for NP0201567 ((9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one)

PDB for NP0201567 ((9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one)

3D PDB for NP0201567 ((9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one)

SMILES for NP0201567 ((9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one)

INCHI for NP0201567 ((9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one)

Structure for NP0201567 ((9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one)

3D Structure for NP0201567 ((9s,15r,17s)-4-hydroxy-5-methoxy-2,18-dioxa-10-azapentacyclo[20.2.2.1⁹,¹⁷.0³,⁸.0¹⁰,¹⁵]heptacosa-1(24),3,5,7,22,25-hexaen-19-one)