NP-MRD: Showing NP-Card for (13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium (NP0200126)

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Record Information

Version

2.0

Created at

2022-09-04 18:54:02 UTC

Updated at

2022-09-04 18:54:02 UTC

NP-MRD ID

NP0200126

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium

Description

Coulteroberbinone belongs to the class of organic compounds known as protoberberine alkaloids and derivatives. These are alkaloids with a structure based on a protoberberine moiety, which consists of a 5,6-dihydrodibenzene moiety fused to a quinolizinium and forming 5,6-Dihydrodibenzo(a,g)quinolizinium skeleton. (13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium is found in Romneya coulteri. Based on a literature review very few articles have been published on Coulteroberbinone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042220542D          

 28 33  0  0  1  0            999 V2000
    2.1607   -2.7699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6394   -3.4418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2969   -4.1924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4756   -4.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1330   -5.0215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6117   -5.6934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4330   -5.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7755   -4.8643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5968   -4.7857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9394   -4.0352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4607   -3.3633    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7606   -3.9566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1032   -3.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9244   -3.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4031   -3.7994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0605   -4.5499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2393   -4.6285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8967   -5.3790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0755   -5.4576    0.0000 N   0  3  1  0  0  0  0  0  0  0  0  0
    4.5541   -6.1296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7329   -6.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9116   -6.2867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6685   -5.1077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3867   -4.7018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2227   -3.8933    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3134   -4.9276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1494   -4.1190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8677   -3.7132    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  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  2  0  0  0  0
  3  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
 10 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  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  7 22  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 15 25  1  0  0  0  0
  5 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  4 28  1  0  0  0  0
M  CHG  1  19   1
M  END

     RDKit          3D

 48 53  0  0  0  0  0  0  0  0999 V2000
    2.3017    2.0811   -1.8367 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1852    0.6622   -1.8630 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5241   -0.0046   -0.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8433   -0.3896   -0.5615 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2647   -1.0566    0.5701 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3595   -1.3401    1.5773 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0361   -0.9671    1.4723 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6311   -0.2931    0.3184 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2383    0.1215    0.1612 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4061   -0.3610   -1.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1581   -1.0013   -1.9942 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8202   -0.0319   -1.2324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5095   -0.1848   -2.4206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8466    0.1315   -2.5342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5211    0.6195   -1.4167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8216    0.7678   -0.2354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4772    0.4502   -0.1199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7984    0.6392    1.1882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6376   -0.2631    1.2365 N   0  0  1  0  0  4  0  0  0  0  0  0
   -1.1434   -1.6176    1.0729 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0087   -0.1992    2.5100 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0713   -1.2762    2.5673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7025    1.2643    0.7200 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9787    1.4102    0.1360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8463    1.0219   -1.2114 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6185   -1.3006    0.4018 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1318   -0.5671   -0.6950 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9578   -0.2385   -1.4050 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6339    2.5011   -2.7939 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0119    2.4196   -1.0595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3116    2.5448   -1.5737 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6900   -1.8723    2.4830 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2224    1.2346    0.1182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9992   -0.5621   -3.2941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4211    0.0273   -3.4413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3755    1.6816    1.2169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4465    0.4691    2.0503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4798   -2.2496    0.4543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2987   -2.0800    2.0918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1541   -1.6371    0.6063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425   -0.3061    3.3098 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5294    0.7791    2.5868 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6807   -2.2911    2.5326 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6126   -1.1287    3.5352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6630    0.7338    0.7124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3352    2.4776    0.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7837   -1.1927   -1.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6184    0.3743   -0.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4 28  1  0
 28 27  1  0
 27 26  1  0
 26  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 25  1  0
 25 24  1  0
 24 23  1  0
 23 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  6
 19 21  1  0
 21 22  1  0
  8  3  1  0
 19  9  1  0
  5  4  1  0
 22  7  1  0
 17 12  1  0
 16 15  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 27 47  1  0
 27 48  1  0
  6 32  1  0
  9 33  1  6
 13 34  1  0
 14 35  1  0
 24 45  1  0
 24 46  1  0
 18 36  1  0
 18 37  1  0
 20 38  1  0
 20 39  1  0
 20 40  1  0
 21 41  1  0
 21 42  1  0
 22 43  1  0
 22 44  1  0
M  CHG  1  19   1
M  END


  Mrv1652309042220542D          

 28 33  0  0  1  0            999 V2000
    2.1607   -2.7699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6394   -3.4418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2969   -4.1924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4756   -4.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1330   -5.0215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6117   -5.6934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4330   -5.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7755   -4.8643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5968   -4.7857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9394   -4.0352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4607   -3.3633    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7606   -3.9566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1032   -3.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9244   -3.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4031   -3.7994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0605   -4.5499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2393   -4.6285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8967   -5.3790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0755   -5.4576    0.0000 N   0  3  1  0  0  0  0  0  0  0  0  0
    4.5541   -6.1296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7329   -6.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9116   -6.2867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6685   -5.1077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3867   -4.7018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2227   -3.8933    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3134   -4.9276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1494   -4.1190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8677   -3.7132    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  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  2  0  0  0  0
  3  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
 10 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  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  7 22  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 15 25  1  0  0  0  0
  5 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  4 28  1  0  0  0  0
M  CHG  1  19   1
M  END
> <DATABASE_ID>
NP0200126

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2OCOC2=CC2=C1C1C(=O)C3=CC=C4OCOC4=C3C[N@+]1(C)CC2

> <INCHI_IDENTIFIER>
InChI=1S/C21H20NO6/c1-22-6-5-11-7-15-20(28-10-26-15)21(24-2)16(11)17(22)18(23)12-3-4-14-19(13(12)8-22)27-9-25-14/h3-4,7,17H,5-6,8-10H2,1-2H3/q+1/t17?,22-/m0/s1

> <INCHI_KEY>
SFKICQDFOFOUIY-UGNFMNBCSA-N

> <FORMULA>
C21H20NO6

> <MOLECULAR_WEIGHT>
382.391

> <EXACT_MASS>
382.128513788

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
38.96765631550007

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
1

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(13S)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{15,23}.0^{16,20}]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium

> <JCHEM_LOGP>
-1.9236039111384124

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
19.326886061605578

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.316871282662927

> <JCHEM_PKA_STRONGEST_BASIC>
-4.348670727546537

> <JCHEM_POLAR_SURFACE_AREA>
63.22000000000001

> <JCHEM_REFRACTIVITY>
110.02250000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(13S)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{15,23}.0^{16,20}]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       4.033  -5.170   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.927  -6.425   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.287  -7.826   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.754  -7.972   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.115  -9.373   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.009 -10.628   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.542 -10.481   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.181  -9.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.714  -8.933   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.353  -7.532   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.460  -6.278   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       8.886  -7.386   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.526  -5.985   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.059  -5.838   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.952  -7.092   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.313  -8.493   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.780  -8.640   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.141 -10.041   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       7.608 -10.188   0.000  0.00  0.00           N+1
HETATM   20  C   UNK     0       8.501 -11.442   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.968 -11.589   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.435 -11.735   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      12.448  -9.534   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      13.789  -8.777   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.482  -7.268   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       0.585  -9.198   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       0.279  -7.689   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.620  -6.931   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5   28                                                  
CONECT    5    4    6   26                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   22                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8   10   19                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   25                                                  
CONECT   16   15   17   23                                                  
CONECT   17   16   12   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18    9   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21    7                                                       
CONECT   23   16   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   15                                                       
CONECT   26    5   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27    4                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₀NO₆

Average Mass

382.3910 Da

Monoisotopic Mass

382.12851 Da

IUPAC Name

(13S)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{15,23}.0^{16,20}]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium

Traditional Name

(13S)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{15,23}.0^{16,20}]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium

CAS Registry Number

Not Available

SMILES

COC1=C2OCOC2=CC2=C1C1C(=O)C3=CC=C4OCOC4=C3C[N@+]1(C)CC2

InChI Identifier

InChI=1S/C21H20NO6/c1-22-6-5-11-7-15-20(28-10-26-15)21(24-2)16(11)17(22)18(23)12-3-4-14-19(13(12)8-22)27-9-25-14/h3-4,7,17H,5-6,8-10H2,1-2H3/q+1/t17?,22-/m0/s1

InChI Key

SFKICQDFOFOUIY-UGNFMNBCSA-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
Romneya coulteri	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as protoberberine alkaloids and derivatives. These are alkaloids with a structure based on a protoberberine moiety, which consists of a 5,6-dihydrodibenzene moiety fused to a quinolizinium and forming 5,6-Dihydrodibenzo(a,g)quinolizinium skeleton.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Protoberberine alkaloids and derivatives

Sub Class

Not Available

Direct Parent

Protoberberine alkaloids and derivatives

Alternative Parents

Substituents

Protoberberine skeleton
Tetrahydroprotoberberine skeleton
Isoquinolone
Tetrahydroisoquinoline
Benzodioxole
Anisole
Aryl alkyl ketone
Aryl ketone
Alkyl aryl ether
Aralkylamine
Benzenoid
Tetraalkylammonium salt
Quaternary ammonium salt
Ketone
Acetal
Ether
Oxacycle
Azacycle
Organoheterocyclic compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Aldehyde
Organopnictogen compound
Organooxygen compound
Organic nitrogen compound
Amine
Organic oxygen compound
Organic cation
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	-1.9	ChemAxon
pKa (Strongest Acidic)	17.32	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	63.22 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	110.02 m³·mol⁻¹	ChemAxon
Polarizability	38.97 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

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

101036654

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium (NP0200126)

MOL for NP0200126 ((13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium)

3D MOL for NP0200126 ((13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium)

3D SDF for NP0200126 ((13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium)

3D-SDF for NP0200126 ((13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium)

PDB for NP0200126 ((13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium)

3D PDB for NP0200126 ((13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium)

SMILES for NP0200126 ((13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium)

INCHI for NP0200126 ((13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium)

Structure for NP0200126 ((13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium)

3D Structure for NP0200126 ((13s)-3-methoxy-13-methyl-24-oxo-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.0²,¹⁰.0⁴,⁸.0¹⁵,²³.0¹⁶,²⁰]tetracosa-2(10),3,8,15,20,22-hexaen-13-ium)