NP-MRD: Showing NP-Card for 6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid (NP0160255)

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Record Information

Version

2.0

Created at

2022-09-02 18:09:56 UTC

Updated at

2022-09-02 18:09:56 UTC

NP-MRD ID

NP0160255

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid

Description

Papaveroxidine belongs to the class of organic compounds known as benzylisoquinolines. These are organic compounds containing an isoquinoline to which a benzyl group is attached. 6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid is found in Papaver pseudo-orientale. 6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid was first documented in 1988 (PMID: 21401148). Based on a literature review very few articles have been published on Papaveroxidine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022220092D          

 34 37  0  0  1  0            999 V2000
    2.3685    6.3696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1136    5.5849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6656    4.9718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4107    4.1872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9627    3.5741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7697    3.7457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3217    3.1326    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1287    3.3041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6807    2.6910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4258    1.9064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4877    2.8625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3023    3.9266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.9354    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5349    1.5999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0246    4.5303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8316    4.7018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0865    5.4864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3836    4.0887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4726    5.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7275    5.9280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1755    6.5411    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
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 12  7  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 12 26  1  0  0  0  0
 26 27  1  0  0  0  0
  6 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 28 32  2  0  0  0  0
  3 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
M  END

     RDKit          3D

 61 64  0  0  0  0  0  0  0  0999 V2000
    4.8657   -0.4527    3.6934 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7343    0.2999    2.4790 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6230    0.0420    1.6444 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6878   -0.8910    1.9627 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6163   -1.1195    1.1233 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4216   -0.4275   -0.0825 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3552   -0.8499   -0.9749 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1342   -0.2579   -2.1841 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3514   -0.8622   -3.4598 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0772   -0.1313   -4.7059 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7813   -2.0325   -3.4434 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8801   -1.4212   -0.3411 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7691   -0.5953    0.4439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5821   -1.3423    1.3309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4408   -0.7540    2.1970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5350    0.6381    2.2227 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7694    1.4128    1.3807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8930    0.7591    0.4975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1903    1.6667   -0.3100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8232    2.1830   -1.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0861    2.7362    1.6426 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1475    2.8311    2.5491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3066    1.4949    2.9860 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4166   -2.8303    1.2026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5093   -3.1224   -0.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6134   -2.3665   -1.1095 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2958   -1.9497   -2.2723 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3689    0.5061   -0.3788 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2824    1.4102   -1.4679 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3699    1.6044   -2.2674 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3930    2.2619   -1.7484 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4640    0.7357    0.4825 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4397    1.6864    0.1885 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3127    3.0090    0.6863 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9946   -0.2811    4.3558 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8127   -0.2460    4.1920 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8289   -1.5368    3.4077 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8234   -1.4396    2.8928 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9070   -1.8754    1.4279 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8496   -1.8986   -1.3470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5664   -0.7185   -5.3997 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0639   -0.0295   -5.2354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2960    0.8876   -4.5403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4220   -2.1624    0.4544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0563   -1.3701    2.8694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4567    3.0435   -1.1116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0664    2.5839   -2.1388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4609    1.3874   -1.8849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9280    3.4810    3.4147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1078    3.0993    2.0343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3477   -3.3005    1.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5532   -3.2317    1.7112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4436   -4.2224   -0.4112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5579   -2.8356   -0.5780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4084   -2.2038   -2.2217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9689   -2.5181   -3.1745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2993   -0.8594   -2.3983 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7590    2.3199   -2.6759 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8581    3.7136    0.0329 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.7710    3.0404    1.7034 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
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  8  9  1  0
  9 10  1  0
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  7 12  1  0
 12 26  1  0
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 26 25  1  0
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 18 19  1  0
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 18 17  2  0
 17 21  1  0
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 23 16  1  0
 16 15  2  0
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 29 31  1  0
 29 30  2  0
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 32 33  1  0
 33 34  1  0
 32  3  1  0
 13 12  1  0
 16 17  1  0
 15 14  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  4 38  1  0
  5 39  1  0
  7 40  1  6
 10 41  1  0
 10 42  1  0
 10 43  1  0
 12 44  1  1
 27 55  1  0
 27 56  1  0
 27 57  1  0
 25 53  1  0
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 20 46  1  0
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 22 49  1  0
 22 50  1  0
 15 45  1  0
 31 58  1  0
 34 59  1  0
 34 60  1  0
 34 61  1  0
M  END


  Mrv1652309022220092D          

 34 37  0  0  1  0            999 V2000
    2.3685    6.3696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1136    5.5849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6656    4.9718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4107    4.1872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9627    3.5741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7697    3.7457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3217    3.1326    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1287    3.3041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6807    2.6910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4258    1.9064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4877    2.8625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3023    3.9266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.9354    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5349    1.5999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0246    4.5303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8316    4.7018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0865    5.4864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3836    4.0887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4726    5.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7275    5.9280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1755    6.5411    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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 25 26  1  0  0  0  0
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 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 28 32  2  0  0  0  0
  3 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0160255

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C([C@H](OC(C)=O)[C@@H]2N(C)CCC3=C2C(OC)=C2OCOC2=C3)C(C(O)=O)=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C24H27NO9/c1-12(26)34-20(14-6-7-15(29-3)21(30-4)18(14)24(27)28)19-17-13(8-9-25(19)2)10-16-22(23(17)31-5)33-11-32-16/h6-7,10,19-20H,8-9,11H2,1-5H3,(H,27,28)/t19-,20+/m1/s1

> <INCHI_KEY>
BHGUILBSZCQXQU-UXHICEINSA-N

> <FORMULA>
C24H27NO9

> <MOLECULAR_WEIGHT>
473.478

> <EXACT_MASS>
473.168581453

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
47.37891826376979

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-[(S)-(acetyloxy)[(5R)-4-methoxy-6-methyl-2H,5H,6H,7H,8H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid

> <ALOGPS_LOGP>
2.55

> <JCHEM_LOGP>
-0.35796916143042984

> <ALOGPS_LOGS>
-3.46

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.0615306591471008

> <JCHEM_PKA_STRONGEST_BASIC>
7.091284779948919

> <JCHEM_POLAR_SURFACE_AREA>
112.99000000000001

> <JCHEM_REFRACTIVITY>
119.71979999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.65e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-[(S)-(acetyloxy)[(5R)-4-methoxy-6-methyl-2H,5H,7H,8H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       4.421  11.890   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       3.945  10.425   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.976   9.281   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.500   7.816   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.530   6.672   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.037   6.992   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.067   5.847   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.574   6.168   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      10.604   5.023   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.128   3.559   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      12.110   5.343   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.924   5.923   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.298   7.330   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.126   4.089   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       7.591   1.303   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.925   2.073   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       8.925   3.613   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0      10.332   2.986   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.513   8.457   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.019   8.777   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       9.495  10.241   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      10.049   7.632   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       6.482   9.601   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       6.958  11.066   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.928  12.210   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   32                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   28                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7   13   26                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15   24                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18   21                                                  
CONECT   18   17   13   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   17   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   16                                                       
CONECT   24   14   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   12   27                                                  
CONECT   27   26                                                            
CONECT   28    6   29   32                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   28    3   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₇NO₉

Average Mass

473.4780 Da

Monoisotopic Mass

473.16858 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC=C([C@H](OC(C)=O)[C@@H]2N(C)CCC3=C2C(OC)=C2OCOC2=C3)C(C(O)=O)=C1OC

InChI Identifier

InChI=1S/C24H27NO9/c1-12(26)34-20(14-6-7-15(29-3)21(30-4)18(14)24(27)28)19-17-13(8-9-25(19)2)10-16-22(23(17)31-5)33-11-32-16/h6-7,10,19-20H,8-9,11H2,1-5H3,(H,27,28)/t19-,20+/m1/s1

InChI Key

BHGUILBSZCQXQU-UXHICEINSA-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
Papaver pseudo-orientale	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzylisoquinolines. These are organic compounds containing an isoquinoline to which a benzyl group is attached.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoquinolines and derivatives

Sub Class

Benzylisoquinolines

Direct Parent

Benzylisoquinolines

Alternative Parents

Substituents

Benzylisoquinoline
M-methoxybenzoic acid or derivatives
O-methoxybenzoic acid or derivatives
Benzyloxycarbonyl
Tetrahydroisoquinoline
Dimethoxybenzene
O-dimethoxybenzene
Benzodioxole
Benzoic acid or derivatives
Benzoic acid
Anisole
Methoxybenzene
Benzoyl
Phenoxy compound
Phenol ether
Aralkylamine
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Dicarboxylic acid or derivatives
Tertiary aliphatic amine
Tertiary amine
Amino acid
Amino acid or derivatives
Carboxylic acid ester
Oxacycle
Azacycle
Ether
Acetal
Carboxylic acid derivative
Carboxylic acid
Amine
Organonitrogen compound
Organooxygen compound
Organic oxygen compound
Organopnictogen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
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	2.55	ALOGPS
logS	-3.5	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

164607

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

189458

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Sariyar G, Shamma M: (-)-Papaveroxidine, A Modified Phthalideisoquinoline Alkaloid from Papaver Pseudo-orientale. J Nat Prod. 1988 Jul;51(4):802-3. doi: 10.1021/np50058a030. [PubMed:21401148 ]
LOTUS database [Link]

Showing NP-Card for 6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid (NP0160255)

MOL for NP0160255 (6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid)

3D MOL for NP0160255 (6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid)

3D SDF for NP0160255 (6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid)

3D-SDF for NP0160255 (6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid)

PDB for NP0160255 (6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid)

3D PDB for NP0160255 (6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid)

SMILES for NP0160255 (6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid)

INCHI for NP0160255 (6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid)

Structure for NP0160255 (6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid)

3D Structure for NP0160255 (6-[(s)-(acetyloxy)[(5r)-4-methoxy-6-methyl-2h,5h,7h,8h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]-2,3-dimethoxybenzoic acid)