NP-MRD: Showing NP-Card for (1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol (NP0213276)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 12:13:12 UTC

Updated at

2022-09-05 12:13:12 UTC

NP-MRD ID

NP0213276

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol

Description

(1S,11R,13S)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Docosa-2(10),3,5(9),14,16,18-hexaen-11-ol belongs to the class of organic compounds known as rhoeadine alkaloids. These are alkaloids with a structure based on rhoeadine. They usually contain a benzazepine system fused with a six-membered hemiacetal or acetal. (1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol is found in Papaver glaucum. Based on a literature review very few articles have been published on (1S,11R,13S)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Docosa-2(10),3,5(9),14,16,18-hexaen-11-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052214132D          

 28 32  0  0  1  0            999 V2000
   -1.9941    0.3082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7376   -0.4759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9303   -0.6459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6738   -1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1335   -1.5999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6844   -0.9857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4279   -0.2016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3795   -0.0317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6359    0.7524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4433    0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5080   -1.0334    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8533   -0.2842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6748   -0.2086    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0201    0.5407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1510   -0.8823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8057   -1.6315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2819   -2.3052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1035   -2.2296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4488   -1.4804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9726   -0.8067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4661   -0.1456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2474   -0.4107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2366   -1.2356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9842   -1.7071    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7544   -2.4994    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3686   -3.0503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9917   -2.8138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2703   -2.4135    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  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
  6 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 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
 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
 24 16  1  6  0  0  0
 11 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
  5 28  1  0  0  0  0
M  END

     RDKit          3D

 51 55  0  0  0  0  0  0  0  0999 V2000
    6.0791    0.3418    1.1543 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4494    0.1026   -0.0866 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0533   -0.0034   -0.1069 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3273    0.1198    1.0305 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9545    0.0135    0.9977 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2499   -0.2189   -0.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9948   -0.3436   -1.3199 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3824   -0.2378   -1.2972 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1239   -0.3648   -2.4666 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4663   -0.6049   -3.7006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1634   -0.3722   -0.4952 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5505    0.8447   -1.1083 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7031    0.5548   -1.8562 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5984   -0.6178   -2.5727 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7807    0.3783   -0.8442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4503   -0.2888    0.3005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4548   -0.4521    1.2448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7321    0.0369    1.0388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0131    0.7068   -0.1419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0334    0.8817   -1.0944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6105    1.5856   -2.1628 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8127    2.2120   -1.6926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1712    1.3044   -0.6400 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0716   -0.8379    0.5630 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7745   -0.5752    1.9030 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5636   -1.7027    2.7524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0393    0.5905    2.2342 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4192    0.1852    2.3513 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9576   -0.5789    1.7776 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1602    0.5464    1.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6465    1.1949    1.7074 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8321    0.3061    1.9893 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5587   -0.5272   -2.2940 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7920    0.2513   -3.9357 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2493   -0.6595   -4.4786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8548   -1.5163   -3.6465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2104   -1.1205   -1.3403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9393    1.3837   -2.5576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2003   -1.3417   -2.2406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2726   -0.9685    2.1760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5233   -0.0890    1.7771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5714    2.2745   -2.4704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5264    3.1844   -1.2549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2242   -1.9585    0.4736 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2481   -2.3388    2.3336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3168   -1.3343    3.7671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4458   -2.3675    2.8514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3344    0.9793    3.2274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2023    1.3562    1.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0026    0.8933    2.9716 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4887   -0.8082    2.8623 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  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  6 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 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
 16 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
  8  3  1  0
 24 11  1  0
 28  5  1  0
 20 15  1  0
 23 19  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  4 32  1  0
  7 33  1  0
 10 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  6
 13 38  1  6
 14 39  1  0
 17 40  1  0
 18 41  1  0
 22 42  1  0
 22 43  1  0
 24 44  1  1
 26 45  1  0
 26 46  1  0
 26 47  1  0
 27 48  1  0
 27 49  1  0
 28 50  1  0
 28 51  1  0
M  END


  Mrv1652309052214132D          

 28 32  0  0  1  0            999 V2000
   -1.9941    0.3082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7376   -0.4759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9303   -0.6459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6738   -1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1335   -1.5999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6844   -0.9857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4279   -0.2016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3795   -0.0317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6359    0.7524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4433    0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5080   -1.0334    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8533   -0.2842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6748   -0.2086    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0201    0.5407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1510   -0.8823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8057   -1.6315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2819   -2.3052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1035   -2.2296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4488   -1.4804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9726   -0.8067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4661   -0.1456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2474   -0.4107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2366   -1.2356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9842   -1.7071    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7544   -2.4994    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3686   -3.0503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9917   -2.8138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2703   -2.4135    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  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
  6 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 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
 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
 24 16  1  6  0  0  0
 11 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
  5 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0213276

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C=C1OC)[C@@H]1O[C@@H](O)C3=C(C=CC4=C3OCO4)[C@@H]1N(C)CC2

> <INCHI_IDENTIFIER>
InChI=1S/C21H23NO6/c1-22-7-6-11-8-15(24-2)16(25-3)9-13(11)19-18(22)12-4-5-14-20(27-10-26-14)17(12)21(23)28-19/h4-5,8-9,18-19,21,23H,6-7,10H2,1-3H3/t18-,19-,21+/m0/s1

> <INCHI_KEY>
XYWRZQQANNOTTD-IRFCIJBXSA-N

> <FORMULA>
C21H23NO6

> <MOLECULAR_WEIGHT>
385.416

> <EXACT_MASS>
385.152537465

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
39.930584329730834

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,11R,13S)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0^{2,10}.0^{5,9}.0^{14,19}]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol

> <JCHEM_LOGP>
2.4464571343333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.25807530064381

> <JCHEM_PKA_STRONGEST_BASIC>
5.830233459398

> <JCHEM_POLAR_SURFACE_AREA>
69.62

> <JCHEM_REFRACTIVITY>
101.18459999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,11R,13S)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0^{2,10}.0^{5,9}.0^{14,19}]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.722   0.575   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.243  -0.888   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.737  -1.206   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.258  -2.669   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.249  -2.986   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.277  -1.840   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.799  -0.376   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.708  -0.059   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.187   1.405   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -2.694   1.722   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.815  -1.929   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.459  -0.530   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.993  -0.389   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.638   1.009   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.882  -1.647   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.237  -3.045   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.126  -4.303   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.660  -4.162   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.304  -2.763   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.415  -1.506   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.337  -0.272   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.795  -0.767   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.775  -2.306   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.704  -3.187   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       3.275  -4.666   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       4.421  -5.694   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.851  -5.252   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.505  -4.505   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   28                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    6   12   24                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   20                                                  
CONECT   16   15   17   24                                                  
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   16   11   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27    5                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₃NO₆

Average Mass

385.4160 Da

Monoisotopic Mass

385.15254 Da

IUPAC Name

(1S,11R,13S)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0^{2,10}.0^{5,9}.0^{14,19}]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol

Traditional Name

(1S,11R,13S)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0^{2,10}.0^{5,9}.0^{14,19}]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C=C1OC)[C@@H]1O[C@@H](O)C3=C(C=CC4=C3OCO4)[C@@H]1N(C)CC2

InChI Identifier

InChI=1S/C21H23NO6/c1-22-7-6-11-8-15(24-2)16(25-3)9-13(11)19-18(22)12-4-5-14-20(27-10-26-14)17(12)21(23)28-19/h4-5,8-9,18-19,21,23H,6-7,10H2,1-3H3/t18-,19-,21+/m0/s1

InChI Key

XYWRZQQANNOTTD-IRFCIJBXSA-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 glaucum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as rhoeadine alkaloids. These are alkaloids with a structure based on rhoeadine. They usually contain a benzazepine system fused with a six-membered hemiacetal or acetal.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Rhoeadine alkaloids

Sub Class

Not Available

Direct Parent

Rhoeadine alkaloids

Alternative Parents

Substituents

Rhoeadine-skeleton
Benzazepine
Benzopyran
Isochromane
2-benzopyran
Benzodioxole
Anisole
Alkyl aryl ether
Azepine
Aralkylamine
Benzenoid
Tertiary aliphatic amine
Tertiary amine
Hemiacetal
Acetal
Oxacycle
Azacycle
Organoheterocyclic compound
Ether
Organic nitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Amine
Organic oxygen compound
Organooxygen compound
Organonitrogen 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	2.45	ChemAxon
pKa (Strongest Acidic)	11.26	ChemAxon
pKa (Strongest Basic)	5.83	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	69.62 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	101.18 m³·mol⁻¹	ChemAxon
Polarizability	39.93 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

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

163055018

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol (NP0213276)

MOL for NP0213276 ((1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol)

3D MOL for NP0213276 ((1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol)

3D SDF for NP0213276 ((1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol)

3D-SDF for NP0213276 ((1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol)

PDB for NP0213276 ((1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol)

3D PDB for NP0213276 ((1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol)

SMILES for NP0213276 ((1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol)

INCHI for NP0213276 ((1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol)

Structure for NP0213276 ((1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol)

3D Structure for NP0213276 ((1s,11r,13s)-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14(19),15,17-hexaen-11-ol)