NP-MRD: Showing NP-Card for methyl (2z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0⁴,⁸]decane-10-carboxylate (NP0172365)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 09:15:31 UTC

Updated at

2022-09-03 09:15:31 UTC

NP-MRD ID

NP0172365

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0⁴,⁸]decane-10-carboxylate

Description

Corialstonine belongs to the class of organic compounds known as quinolines and derivatives. Quinolines and derivatives are compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene. Based on a literature review very few articles have been published on Corialstonine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032211152D          

 30 34  0  0  0  0            999 V2000
    6.0730    1.8072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8242    1.0206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0186    0.8428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4345    1.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5867    1.3546    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7181    1.3350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4784    0.5082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1832   -0.0398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6974   -0.7066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0319   -1.4607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5461   -2.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7257   -2.0402    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3912   -1.2860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5708   -1.1987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2363   -0.4446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5841   -0.3572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0699   -1.0240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7221    0.2222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3875    0.9763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4328    1.0637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5425    0.1349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8770   -0.6192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9470   -0.5606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9219   -1.3852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1952   -1.7758    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6235   -1.8192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3502   -1.4287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7716   -0.0691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3189    0.2397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6060    0.5812    0.0000 C   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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  2  0  0  0  0
 21 22  1  0  0  0  0
  9 22  2  0  0  0  0
 13 22  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 28  1  0  0  0  0
  3 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  5 30  1  0  0  0  0
  8 30  1  0  0  0  0
M  END

     RDKit          3D

 56 60  0  0  0  0  0  0  0  0999 V2000
   -4.7328    1.9824   -1.4488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2776    0.8047   -0.6204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3420    0.9239    0.2774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6544    2.2138    0.5577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2096    2.0134    0.4259 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9515    1.7802   -0.9836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7235    0.4926   -1.0488 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6110   -0.1892    0.1592 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4781   -1.0821   -0.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1837   -2.4045   -0.4480 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1665   -3.2648   -0.9416 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3945   -2.8751   -1.2067 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7180   -1.5858   -0.9914 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9814   -1.1187   -1.2428 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3897    0.1793   -1.0426 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6766    0.6125   -1.3093 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7016   -0.1875   -1.8026 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4516    1.0511   -0.5567 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7122    2.3798   -0.3060 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7893    3.2994    0.1872 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1472    0.6101   -0.2869 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7562   -0.6852   -0.4922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8273   -1.0574    0.3918 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5360   -2.0552    1.5044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4674   -2.0773    2.1487 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5024   -2.9870    1.8267 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3233   -3.9590    2.8554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8647   -0.1667    1.1005 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8866    0.5150    2.0926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7350    0.8045    1.1371 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8732    2.8859   -0.8103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7450    1.7494   -1.8456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0802    2.1299   -2.3074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7622   -0.1717   -0.7956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8947    2.8780   -0.3292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9661    2.7663    1.4155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0798    2.3969   -1.2724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7865    2.1836   -1.6148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8230   -2.8612   -0.3322 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9070   -4.3197   -1.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7261   -1.8045   -1.6269 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7015    0.2736   -1.5637 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6786   -1.2366   -1.4825 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6521   -0.1896   -2.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3107    4.2964    0.2486 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3087    3.0162    1.1319 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0136    3.4530   -0.6157 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4386    1.2928    0.0973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2871   -1.5412   -0.4165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1482   -3.9092    3.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3214   -3.9084    3.3011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4011   -4.9533    2.3431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6045   -0.7577    1.6300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3021    1.3651    2.5977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6714   -0.2510    2.8438 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1081    1.2502    1.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
 26 24  1  0
 24 25  2  0
 24 23  1  0
 23 28  1  0
 28 29  1  0
 29 30  1  0
 30  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  6
  9 22  1  0
 22 21  2  0
 21 18  1  0
 18 19  1  0
 19 20  1  0
 18 15  2  0
 15 16  1  0
 16 17  1  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
 12 11  2  0
 11 10  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  8 23  1  0
 10  9  2  0
  3 28  1  0
  8 30  1  0
 13 22  1  0
 27 50  1  0
 27 51  1  0
 27 52  1  0
 23 49  1  6
 28 53  1  1
 29 54  1  0
 29 55  1  0
 30 56  1  1
  6 37  1  0
  6 38  1  0
 21 48  1  0
 20 45  1  0
 20 46  1  0
 20 47  1  0
 17 42  1  0
 17 43  1  0
 17 44  1  0
 14 41  1  0
 11 40  1  0
 10 39  1  0
  4 35  1  0
  4 36  1  0
  2 34  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
M  END


  Mrv1652309032211152D          

 30 34  0  0  0  0            999 V2000
    6.0730    1.8072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8242    1.0206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0186    0.8428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4345    1.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5867    1.3546    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7181    1.3350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4784    0.5082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1832   -0.0398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6974   -0.7066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0319   -1.4607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5461   -2.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7257   -2.0402    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3912   -1.2860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5708   -1.1987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2363   -0.4446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5841   -0.3572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0699   -1.0240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7221    0.2222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3875    0.9763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4328    1.0637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5425    0.1349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8770   -0.6192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9470   -0.5606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9219   -1.3852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1952   -1.7758    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6235   -1.8192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3502   -1.4287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7716   -0.0691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3189    0.2397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6060    0.5812    0.0000 C   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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  2  0  0  0  0
 21 22  1  0  0  0  0
  9 22  2  0  0  0  0
 13 22  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 28  1  0  0  0  0
  3 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  5 30  1  0  0  0  0
  8 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0172365

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1C2CC3N(COC13C1=C3C=C(OC)C(OC)=CC3=NC=C1)C\C2=C/C

> <INCHI_IDENTIFIER>
InChI=1S/C23H26N2O5/c1-5-13-11-25-12-30-23(20(25)9-14(13)21(23)22(26)29-4)16-6-7-24-17-10-19(28-3)18(27-2)8-15(16)17/h5-8,10,14,20-21H,9,11-12H2,1-4H3/b13-5+

> <INCHI_KEY>
TUICENXFLOTBCM-WLRTZDKTSA-N

> <FORMULA>
C23H26N2O5

> <MOLECULAR_WEIGHT>
410.47

> <EXACT_MASS>
410.184171945

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
43.27041673867158

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2Z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0^{4,8}]decane-10-carboxylate

> <ALOGPS_LOGP>
2.90

> <JCHEM_LOGP>
2.3621721656666668

> <ALOGPS_LOGS>
-3.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
5.664218332669457

> <JCHEM_POLAR_SURFACE_AREA>
70.12

> <JCHEM_REFRACTIVITY>
110.22199999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.92e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2Z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0^{4,8}]decane-10-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      11.336   3.373   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.872   1.905   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.368   1.573   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.278   2.871   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       6.695   2.529   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       5.074   2.492   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.626   0.949   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.942  -0.074   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.035  -1.319   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.660  -2.727   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.753  -3.971   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       3.221  -3.808   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       2.597  -2.401   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.066  -2.238   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.441  -0.830   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.090  -0.667   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -1.997  -1.912   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.348   0.415   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.723   1.823   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -0.808   1.986   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.879   0.252   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.504  -1.156   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.368  -1.046   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.321  -2.586   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.964  -3.315   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       8.631  -3.396   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.987  -2.667   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.907  -0.129   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.062   0.447   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.731   1.085   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   28                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   30                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   23   30                                             
CONECT    9    8   10   22                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   22                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22                                                       
CONECT   22   21    9   13                                                  
CONECT   23    8   24   28                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26                                                            
CONECT   28   23    3   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29    5    8                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₆N₂O₅

Average Mass

410.4700 Da

Monoisotopic Mass

410.18417 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)C1C2CC3N(COC13C1=C3C=C(OC)C(OC)=CC3=NC=C1)C\C2=C/C

InChI Identifier

InChI=1S/C23H26N2O5/c1-5-13-11-25-12-30-23(20(25)9-14(13)21(23)22(26)29-4)16-6-7-24-17-10-19(28-3)18(27-2)8-15(16)17/h5-8,10,14,20-21H,9,11-12H2,1-4H3/b13-5+

InChI Key

TUICENXFLOTBCM-WLRTZDKTSA-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 quinolines and derivatives. Quinolines and derivatives are compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Not Available

Direct Parent

Quinolines and derivatives

Alternative Parents

Substituents

Quinoline
Anisole
Phenol ether
Alkyl aryl ether
Azepane
Piperidine
Pyridine
Benzenoid
Oxazolidine
Heteroaromatic compound
Methyl ester
Hemiaminal
Carboxylic acid ester
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Oxacycle
Azacycle
Amine
Hydrocarbon derivative
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Organic oxide
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	2.9	ALOGPS
logS	-3.2	ALOGPS

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

4947294

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6443266

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0⁴,⁸]decane-10-carboxylate (NP0172365)

MOL for NP0172365 (methyl (2z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0⁴,⁸]decane-10-carboxylate)

3D MOL for NP0172365 (methyl (2z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0⁴,⁸]decane-10-carboxylate)

3D SDF for NP0172365 (methyl (2z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0⁴,⁸]decane-10-carboxylate)

3D-SDF for NP0172365 (methyl (2z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0⁴,⁸]decane-10-carboxylate)

PDB for NP0172365 (methyl (2z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0⁴,⁸]decane-10-carboxylate)

3D PDB for NP0172365 (methyl (2z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0⁴,⁸]decane-10-carboxylate)

SMILES for NP0172365 (methyl (2z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0⁴,⁸]decane-10-carboxylate)

INCHI for NP0172365 (methyl (2z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0⁴,⁸]decane-10-carboxylate)

Structure for NP0172365 (methyl (2z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0⁴,⁸]decane-10-carboxylate)

3D Structure for NP0172365 (methyl (2z)-7-(6,7-dimethoxyquinolin-4-yl)-2-ethylidene-6-oxa-4-azatricyclo[5.2.1.0⁴,⁸]decane-10-carboxylate)