NP-MRD: Showing NP-Card for (5r)-6-methyl-5-[(10s)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-10-yl]-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinoline (NP0184265)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 23:21:21 UTC

Updated at

2022-09-03 23:21:22 UTC

NP-MRD ID

NP0184265

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5r)-6-methyl-5-[(10s)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-10-yl]-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinoline

Description

(5R)-6-methyl-5-[(10S)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]Dodeca-1(9),2(6),7-trien-10-yl]-2H,5H,6H,7H,8H-[1,3]dioxolo[4,5-g]isoquinoline belongs to the class of organic compounds known as tetrahydroisoquinolines. These are tetrahydrogenated isoquinoline derivatives. Based on a literature review very few articles have been published on (5R)-6-methyl-5-[(10S)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]Dodeca-1(9),2(6),7-trien-10-yl]-2H,5H,6H,7H,8H-[1,3]dioxolo[4,5-g]isoquinoline.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042201212D          

 26 31  0  0  1  0            999 V2000
    8.4636    2.5034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2921    1.6964    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.9052    1.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7336    0.3374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9490    0.0825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7775   -0.7245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9929   -0.9795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3798   -0.4274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5513    0.3795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3359    0.6345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5074    1.4415    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8944    1.9935    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9806    2.8140    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2269    3.1495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6749    2.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0874    1.8220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6749    1.1075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8499    1.1075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4374    1.8220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8499    2.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2979    3.1495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5442    2.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6304    1.9935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6653   -0.8399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8368   -1.6469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6573   -1.7331    0.0000 O   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  1  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
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 19 23  1  0  0  0  0
  8 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  7 26  1  0  0  0  0
M  END

     RDKit          3D

 45 50  0  0  0  0  0  0  0  0999 V2000
    0.0627   -2.1660   -2.5611 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0966   -1.0422   -1.6344 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1964    0.1369   -2.3521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5801    1.3212   -1.5095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6697    0.9319   -0.5816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6708    1.8085   -0.2273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6948    1.4498    0.6385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7060    0.1734    1.1584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7015   -0.6976    0.7996 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6634   -0.3458   -0.0733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6038   -1.3039   -0.4349 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3239   -1.5865    0.7460 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1268   -2.6782    0.5189 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3613   -2.2237    0.0832 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5006   -0.8408    0.6212 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2435   -0.4544    1.0275 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0896    0.7927    1.5690 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1528    1.6382    1.7059 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4102    1.2539    1.3004 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5919    0.0004    0.7508 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9543   -0.1115    0.4363 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5864    1.1351    0.6292 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6455    1.9214    1.3304 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8307    0.0539    1.9993 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7164    1.1091    1.6701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8092    2.0863    1.1689 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0908   -3.1115   -1.9645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9506   -2.1540   -3.0410 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8464   -2.1101   -3.3228 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7077    0.4249   -2.9590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0120   -0.0155   -3.1130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9862    2.0896   -2.2341 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2516    1.8122   -1.0062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6475    2.8033   -0.6428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6936   -1.7059    1.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1433   -2.2906   -0.5806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2549   -1.7778    1.6659 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5013   -2.2325   -0.9961 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2015   -2.8197    0.5433 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0900    1.1058    1.8945 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0237    2.6461    2.1445 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8472    1.6355   -0.3260 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4902    1.0792    1.2427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3732    0.7836    0.8269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2923    1.4754    2.5354 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8 24  1  0
 24 25  1  0
 25 26  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 11  2  1  0
 16 12  1  0
 23 19  1  0
 10  5  1  0
 20 15  1  0
 26  7  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  6 34  1  0
 25 44  1  0
 25 45  1  0
  9 35  1  0
 11 36  1  6
 12 37  1  1
 14 38  1  0
 14 39  1  0
 17 40  1  0
 18 41  1  0
 22 42  1  0
 22 43  1  0
M  END


  Mrv1652309042201212D          

 26 31  0  0  1  0            999 V2000
    8.4636    2.5034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2921    1.6964    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.9052    1.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7336    0.3374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9490    0.0825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7775   -0.7245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9929   -0.9795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3798   -0.4274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5513    0.3795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3359    0.6345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5074    1.4415    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8944    1.9935    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9806    2.8140    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2269    3.1495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6749    2.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0874    1.8220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6749    1.1075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8499    1.1075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4374    1.8220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8499    2.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2979    3.1495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5442    2.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6304    1.9935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6653   -0.8399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8368   -1.6469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6573   -1.7331    0.0000 O   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  1  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
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 19 23  1  0  0  0  0
  8 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  7 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0184265

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1CCC2=CC3=C(OCO3)C=C2[C@@H]1[C@H]1OCC2=C1C=CC1=C2OCO1

> <INCHI_IDENTIFIER>
InChI=1S/C20H19NO5/c1-21-5-4-11-6-16-17(25-9-24-16)7-13(11)18(21)20-12-2-3-15-19(26-10-23-15)14(12)8-22-20/h2-3,6-7,18,20H,4-5,8-10H2,1H3/t18-,20+/m1/s1

> <INCHI_KEY>
AACMFFIUYXGCOC-QUCCMNQESA-N

> <FORMULA>
C20H19NO5

> <MOLECULAR_WEIGHT>
353.374

> <EXACT_MASS>
353.126322716

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
35.964948615683554

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5R)-6-methyl-5-[(10S)-3,5,11-trioxatricyclo[7.3.0.0^{2,6}]dodeca-1(9),2(6),7-trien-10-yl]-2H,5H,6H,7H,8H-[1,3]dioxolo[4,5-g]isoquinoline

> <JCHEM_LOGP>
2.749257075

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
7.182427432137947

> <JCHEM_POLAR_SURFACE_AREA>
49.39

> <JCHEM_REFRACTIVITY>
92.99520000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(5R)-6-methyl-5-[(10S)-3,5,11-trioxatricyclo[7.3.0.0^{2,6}]dodeca-1(9),2(6),7-trien-10-yl]-2H,5H,7H,8H-[1,3]dioxolo[4,5-g]isoquinoline

> <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      15.799   4.673   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      15.479   3.167   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      16.623   2.136   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.303   0.630   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.838   0.154   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.518  -1.352   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.053  -1.828   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.909  -0.798   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.229   0.708   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.694   1.184   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.014   2.691   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.869   3.721   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      13.030   5.253   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      11.624   5.879   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.593   4.735   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.363   3.401   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.593   2.067   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.053   2.067   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.283   3.401   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.053   4.735   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.023   5.879   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.616   5.253   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.777   3.721   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      10.575  -1.568   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      10.895  -3.074   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      12.427  -3.235   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   26                                                  
CONECT    8    7    9   24                                                  
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10    2   12                                                  
CONECT   12   11   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   12   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   15   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   19                                                       
CONECT   24    8   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    7                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₉NO₅

Average Mass

353.3740 Da

Monoisotopic Mass

353.12632 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CN1CCC2=CC3=C(OCO3)C=C2[C@@H]1[C@H]1OCC2=C1C=CC1=C2OCO1

InChI Identifier

InChI=1S/C20H19NO5/c1-21-5-4-11-6-16-17(25-9-24-16)7-13(11)18(21)20-12-2-3-15-19(26-10-23-15)14(12)8-22-20/h2-3,6-7,18,20H,4-5,8-10H2,1H3/t18-,20+/m1/s1

InChI Key

AACMFFIUYXGCOC-QUCCMNQESA-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 tetrahydroisoquinolines. These are tetrahydrogenated isoquinoline derivatives.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrahydroisoquinolines

Sub Class

Not Available

Direct Parent

Tetrahydroisoquinolines

Alternative Parents

Substituents

Tetrahydroisoquinoline
Benzodioxole
Isocoumaran
Aralkylamine
Benzenoid
Tertiary amine
Tertiary aliphatic amine
Acetal
Dialkyl ether
Ether
Oxacycle
Azacycle
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organic nitrogen compound
Amine
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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162898198

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5r)-6-methyl-5-[(10s)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-10-yl]-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinoline (NP0184265)

MOL for NP0184265 ((5r)-6-methyl-5-[(10s)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-10-yl]-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinoline)

3D MOL for NP0184265 ((5r)-6-methyl-5-[(10s)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-10-yl]-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinoline)

3D SDF for NP0184265 ((5r)-6-methyl-5-[(10s)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-10-yl]-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinoline)

3D-SDF for NP0184265 ((5r)-6-methyl-5-[(10s)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-10-yl]-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinoline)

PDB for NP0184265 ((5r)-6-methyl-5-[(10s)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-10-yl]-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinoline)

3D PDB for NP0184265 ((5r)-6-methyl-5-[(10s)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-10-yl]-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinoline)

SMILES for NP0184265 ((5r)-6-methyl-5-[(10s)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-10-yl]-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinoline)

INCHI for NP0184265 ((5r)-6-methyl-5-[(10s)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-10-yl]-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinoline)

Structure for NP0184265 ((5r)-6-methyl-5-[(10s)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-10-yl]-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinoline)

3D Structure for NP0184265 ((5r)-6-methyl-5-[(10s)-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1(9),2(6),7-trien-10-yl]-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinoline)