NP-MRD: Showing NP-Card for (11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one (NP0201632)

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Record Information

Version

2.0

Created at

2022-09-04 20:42:54 UTC

Updated at

2022-09-04 20:42:55 UTC

NP-MRD ID

NP0201632

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one

Description

Melicodenine D belongs to the class of organic compounds known as pyranoquinolines. These are polycyclic compounds containing a pyran ring fused to a quinoline moiety. Quinoline or benzo[b]pyridine is a bicyclic compound that consists of benzene fused to a pyridine. (11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one is found in Melicope denhamii. Based on a literature review very few articles have been published on Melicodenine D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042222422D          

 33 37  0  0  1  0            999 V2000
   -1.4277   -2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6756   -2.9412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0059   -2.4595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7462   -2.7987    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0381   -3.5703    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6990   -4.3223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1807   -4.9921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8416   -5.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0207   -5.8265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3185   -6.5785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1394   -6.6608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4610   -5.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2819   -5.2390    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7637   -4.5693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1219   -4.4047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8097   -3.2783    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6240   -3.4112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1462   -2.7726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9604   -2.9055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4827   -2.2669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2969   -2.3998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5889   -3.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0666   -3.8101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2524   -3.6771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7302   -4.3158    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0221   -5.0874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9159   -4.1829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3937   -4.8215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8542   -2.0010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0400   -1.8680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3123   -1.0893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3204   -1.4646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5178   -2.5067    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  2  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
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 15  2  0  0  0  0
  6 15  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  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
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 17 27  1  0  0  0  0
 27 28  2  0  0  0  0
 18 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33  4  1  6  0  0  0
 16 33  1  0  0  0  0
M  END

     RDKit          3D

 64 68  0  0  0  0  0  0  0  0999 V2000
   -1.7608    5.3111   -0.0404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0673    4.1338    0.1984 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0370    3.2941   -0.8903 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3307   -2.0284   -0.2020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1904   -3.1174   -0.4509 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8048   -4.0286   -1.4462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6836   -1.1189    0.7687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8707   -1.3193    1.4557 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3283   -0.4494    2.4695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8422   -0.0601    1.0067 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5660    1.0514    1.1206 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2632   -0.1492    0.6982 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2447   -0.1492   -0.2628 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9082   -1.2782   -0.6688 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8900   -1.2760   -1.6312 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5467   -2.4301   -2.0252 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2071   -3.6337   -1.4326 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2284   -3.6536   -0.4694 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5837   -2.4950   -0.0881 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6179   -2.4952    0.8583 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2923   -3.7878    1.4569 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9657   -1.3699    1.2540 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0866   -1.5368    2.1531 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5873    1.0540   -0.8561 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2563    2.2978   -0.2731 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3449    3.3407   -1.3651 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3146    2.6092    0.7620 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9240    2.3000    0.3939 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -1.2742    5.9076   -0.8442 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5338    3.7935   -1.7333 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0664    1.4323   -1.3728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3179    2.0223    1.3582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4270   -0.7117   -1.2298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8843   -2.5884   -1.6751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6137   -4.7853   -1.5427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8685   -4.5128   -1.1324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6886   -3.4534   -2.3900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5009   -0.1964    3.1920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0756   -1.0065    3.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8072    0.4608    2.0691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1460    0.6509    1.7853 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6731    1.1949    2.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1561   -0.3394   -2.0942 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3177   -2.3983   -2.7874 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7308   -4.5496   -1.7477 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9322   -4.5692    0.0185 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1529   -4.1447    2.0252 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3808   -3.6760    2.1146 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1317    2.9542   -2.3634 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.0000    3.4949    1.3144 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
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 33  4  1  0
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 15  6  1  0
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  1 34  1  0
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  3 37  1  0
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 16 50  1  1
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  7 41  1  0
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 11 43  1  0
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 14 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  0
M  END


  Mrv1652309042222422D          

 33 37  0  0  1  0            999 V2000
   -1.4277   -2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6756   -2.9412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0059   -2.4595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7462   -2.7987    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0381   -3.5703    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6990   -4.3223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1807   -4.9921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8416   -5.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0207   -5.8265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3185   -6.5785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4610   -5.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8097   -3.2783    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6240   -3.4112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1462   -2.7726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9604   -2.9055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4827   -2.2669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2969   -2.3998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5889   -3.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0666   -3.8101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2524   -3.6771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7302   -4.3158    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0221   -5.0874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9159   -4.1829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3937   -4.8215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0400   -1.8680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3123   -1.0893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3204   -1.4646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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 33  4  1  6  0  0  0
 16 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0201632

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC[C@@H]1[C@H]([C@@H]2[C@H]1C(C)(C)OC1=C2C(=O)N(C)C2=CC=CC=C12)C1=CC=C(OC)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C27H31NO5/c1-27(2)24-17(14-30-4)21(15-11-12-19(31-5)20(13-15)32-6)22(24)23-25(33-27)16-9-7-8-10-18(16)28(3)26(23)29/h7-13,17,21-22,24H,14H2,1-6H3/t17-,21-,22+,24+/m1/s1

> <INCHI_KEY>
KNXDILKOIQXPQV-INYSMAPRSA-N

> <FORMULA>
C27H31NO5

> <MOLECULAR_WEIGHT>
449.547

> <EXACT_MASS>
449.220223102

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
48.96167315076307

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(11R,12S,13R,14R)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0^{2,7}.0^{11,14}]hexadeca-1(10),2,4,6-tetraen-9-one

> <JCHEM_LOGP>
2.749394135999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.915415485704603

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3930054289483168

> <JCHEM_POLAR_SURFACE_AREA>
57.230000000000004

> <JCHEM_REFRACTIVITY>
127.26160000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(11R,12S,13R,14R)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0^{2,7}.0^{11,14}]hexadeca-1(10),2,4,6-tetraen-9-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      -2.665  -4.857   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.261  -5.490   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.011  -4.591   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.393  -5.224   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.938  -6.665   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.305  -8.068   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.204  -9.319   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.571 -10.722   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.039 -10.876   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.594 -12.280   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.127 -12.434   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.861  -9.626   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.393  -9.780   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -3.292  -8.529   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.228  -8.222   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.378  -6.119   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.898  -6.368   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.873  -5.176   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.393  -5.424   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.368  -4.232   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.888  -4.480   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.433  -5.920   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.458  -7.112   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.938  -6.864   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       6.963  -8.056   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       7.508  -9.496   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.443  -7.808   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.468  -9.000   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       5.328  -3.735   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.808  -3.487   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.316  -2.033   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.465  -2.734   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.833  -4.679   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   33                                                  
CONECT    5    4    6   16                                                  
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12    6                                                       
CONECT   16    5   17   33                                                  
CONECT   17   16   18   27                                                  
CONECT   18   17   19   29                                                  
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   17   28                                                  
CONECT   28   27                                                            
CONECT   29   18   30                                                       
CONECT   30   29   31   32   33                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   30    4   16                                                  
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₁NO₅

Average Mass

449.5470 Da

Monoisotopic Mass

449.22022 Da

IUPAC Name

(11R,12S,13R,14R)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0^{2,7}.0^{11,14}]hexadeca-1(10),2,4,6-tetraen-9-one

Traditional Name

(11R,12S,13R,14R)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0^{2,7}.0^{11,14}]hexadeca-1(10),2,4,6-tetraen-9-one

CAS Registry Number

Not Available

SMILES

COC[C@@H]1[C@H]([C@@H]2[C@H]1C(C)(C)OC1=C2C(=O)N(C)C2=CC=CC=C12)C1=CC=C(OC)C(OC)=C1

InChI Identifier

InChI=1S/C27H31NO5/c1-27(2)24-17(14-30-4)21(15-11-12-19(31-5)20(13-15)32-6)22(24)23-25(33-27)16-9-7-8-10-18(16)28(3)26(23)29/h7-13,17,21-22,24H,14H2,1-6H3/t17-,21-,22+,24+/m1/s1

InChI Key

KNXDILKOIQXPQV-INYSMAPRSA-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
Melicope denhamii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoquinolines. These are polycyclic compounds containing a pyran ring fused to a quinoline moiety. Quinoline or benzo[b]pyridine is a bicyclic compound that consists of benzene fused to a pyridine.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Quinolones and derivatives

Direct Parent

Pyranoquinolines

Alternative Parents

Substituents

Pyranoquinoline
Dihydroquinolone
Dihydroquinoline
Pyranopyridine
O-dimethoxybenzene
Dimethoxybenzene
Phenoxy compound
Anisole
Phenol ether
Methoxybenzene
Alkyl aryl ether
Pyridinone
Monocyclic benzene moiety
Pyran
Pyridine
Benzenoid
Heteroaromatic compound
Vinylogous ester
Lactam
Azacycle
Oxacycle
Ether
Dialkyl ether
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organic nitrogen 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	2.75	ChemAxon
pKa (Strongest Acidic)	18.92	ChemAxon
pKa (Strongest Basic)	-0.39	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	57.23 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	127.26 m³·mol⁻¹	ChemAxon
Polarizability	48.96 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

34250672

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

90675880

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one (NP0201632)

MOL for NP0201632 ((11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one)

3D MOL for NP0201632 ((11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one)

3D SDF for NP0201632 ((11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one)

3D-SDF for NP0201632 ((11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one)

PDB for NP0201632 ((11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one)

3D PDB for NP0201632 ((11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one)

SMILES for NP0201632 ((11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one)

INCHI for NP0201632 ((11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one)

Structure for NP0201632 ((11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one)

3D Structure for NP0201632 ((11r,12s,13r,14r)-12-(3,4-dimethoxyphenyl)-13-(methoxymethyl)-8,15,15-trimethyl-16-oxa-8-azatetracyclo[8.6.0.0²,⁷.0¹¹,¹⁴]hexadeca-1(10),2,4,6-tetraen-9-one)