NP-MRD: Showing NP-Card for (20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol (NP0145280)

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Record Information

Version

2.0

Created at

2022-09-02 00:26:37 UTC

Updated at

2022-09-02 00:26:37 UTC

NP-MRD ID

NP0145280

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol

Description

Tylophoridicine E belongs to the class of organic compounds known as phenanthroindolizidines. These are aromatic polycyclic compounds containing the phenanthroindolizidine skeleton, which is structurally characterized by an indolizidine and a phenanthrene, where the indolizidine is fused to the second benzene ring of a phenanthrene. (20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol is found in Ideopsis similis. Based on a literature review very few articles have been published on tylophoridicine E.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022202262D          

 27 31  0  0  1  0            999 V2000
    5.0884   -4.8700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2763   -4.7248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9960   -3.9489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1838   -3.8037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9035   -3.0277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0914   -2.8825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8111   -2.1066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3429   -1.4759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0626   -0.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5945   -0.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4066   -0.2145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9384    0.4162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6869   -0.9904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1551   -1.6211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4354   -2.3970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2475   -2.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278   -3.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399   -3.4634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8717   -2.8327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9990   -1.9614    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7187   -1.1854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4672   -2.5921    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3574   -2.6189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5867   -3.4114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962   -3.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7475   -3.3680    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5596   -3.5132    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  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
  3 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 26  1  1  0  0  0
 26 27  1  0  0  0  0
  6 27  1  0  0  0  0
M  END

     RDKit          3D

 50 54  0  0  0  0  0  0  0  0999 V2000
    3.6742    3.5526   -0.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1307    2.2160   -0.0583 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2334    1.1806   -0.0182 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8528    1.4037    0.0345 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9891    0.3338    0.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3741    0.5238    0.1308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2695   -0.5186    0.1788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7454   -1.7922    0.1647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6217   -2.8686    0.2082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1637   -4.1768    0.1948 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1877   -4.4145    0.1370 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6473   -5.7494    0.1237 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0800   -3.3619    0.0927 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6279   -2.0633    0.1060 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4804   -0.9621    0.0609 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8314   -1.2045    0.0096 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6959   -0.1096   -0.0297 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0704   -0.3232   -0.0823 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5422   -1.6508   -0.0940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7419   -0.3733    0.2627 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3939   -0.7247   -0.9115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0584    1.0944    0.5196 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4756    1.4257    0.0473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3376    2.9119   -0.2546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8728    3.1081   -0.6155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2627    1.8405   -0.4015 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9094    1.9193    0.1223 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5330    4.2351    0.1324 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9808    3.6442    0.8287 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1036    3.8284   -0.9429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4938    2.4256    0.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6854   -2.6525    0.2505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8970   -4.9734    0.2308 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7647   -6.2084   -0.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1121   -3.5921    0.0486 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2559   -2.1829   -0.0019 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0775   -2.2425   -0.9183 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6303   -1.7280   -0.1023 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1642   -2.1218    0.8596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1226   -0.9147    1.1582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2859   -1.0912   -0.6394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9148    1.3631    1.5719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2221    1.2095    0.8113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6437    0.9002   -0.9018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6228    3.5371    0.6220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0147    3.1849   -1.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4301    3.9420   -0.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8557    3.3411   -1.7110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3323    2.5870   -0.5621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9054    2.2921    1.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 17  2  0
 17 18  1  0
 18 19  1  0
 17 16  1  0
 16 15  2  0
 15  5  1  0
  5  4  2  0
  5  6  1  0
  6  7  2  0
  7 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
  4  3  1  0
 27  6  1  0
 14  8  1  0
 14 15  1  0
 26 22  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 19 37  1  0
 19 38  1  0
 19 39  1  0
 16 36  1  0
  4 31  1  0
 20 40  1  1
 21 41  1  0
 22 42  1  1
 23 43  1  0
 23 44  1  0
 24 45  1  0
 24 46  1  0
 25 47  1  0
 25 48  1  0
 27 49  1  0
 27 50  1  0
  9 32  1  0
 10 33  1  0
 12 34  1  0
 13 35  1  0
M  END


  Mrv1652309022202262D          

 27 31  0  0  1  0            999 V2000
    5.0884   -4.8700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2763   -4.7248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9960   -3.9489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1838   -3.8037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9035   -3.0277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0914   -2.8825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8111   -2.1066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3429   -1.4759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0626   -0.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5945   -0.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4066   -0.2145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9384    0.4162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6869   -0.9904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1551   -1.6211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4354   -2.3970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2475   -2.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278   -3.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399   -3.4634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8717   -2.8327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9990   -1.9614    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7187   -1.1854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4672   -2.5921    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3574   -2.6189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5867   -3.4114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962   -3.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7475   -3.3680    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5596   -3.5132    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  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
  3 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 26  1  1  0  0  0
 26 27  1  0  0  0  0
  6 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0145280

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC)C=C2C(=C1)C1=C([C@H](O)[C@@H]3CCCN3C1)C1=CC=C(O)C=C21

> <INCHI_IDENTIFIER>
InChI=1S/C22H23NO4/c1-26-19-9-15-14-8-12(24)5-6-13(14)21-17(16(15)10-20(19)27-2)11-23-7-3-4-18(23)22(21)25/h5-6,8-10,18,22,24-25H,3-4,7,11H2,1-2H3/t18-,22+/m0/s1

> <INCHI_KEY>
SBVBOLGVLBCFIL-PGRDOPGGSA-N

> <FORMULA>
C22H23NO4

> <MOLECULAR_WEIGHT>
365.429

> <EXACT_MASS>
365.162708225

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
40.46876957137197

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(20S,21S)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0^{2,7}.0^{8,13}.0^{16,20}]henicosa-1(14),2,4,6,8,10,12-heptaene-5,21-diol

> <ALOGPS_LOGP>
3.26

> <JCHEM_LOGP>
2.7134909214025167

> <ALOGPS_LOGS>
-3.80

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.883794698750574

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.754686121978775

> <JCHEM_PKA_STRONGEST_BASIC>
8.266995260835847

> <JCHEM_POLAR_SURFACE_AREA>
62.160000000000004

> <JCHEM_REFRACTIVITY>
104.13669999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.78e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(20S,21S)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0^{2,7}.0^{8,13}.0^{16,20}]henicosa-1(14),2,4,6,8,10,12-heptaene-5,21-diol

> <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       9.498  -9.091   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.982  -8.820   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.459  -7.371   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.943  -7.100   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.420  -5.652   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.904  -5.381   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.381  -3.932   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.374  -2.755   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.850  -1.307   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.843  -0.129   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.359  -0.400   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.352   0.777   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.882  -1.849   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.889  -3.026   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.413  -4.474   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.929  -4.746   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.452  -6.194   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.968  -6.465   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      10.961  -5.288   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.865  -3.661   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.342  -2.213   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.872  -4.839   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.667  -4.889   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.095  -6.368   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.179  -7.232   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       1.395  -6.287   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       2.911  -6.558   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   15                                                  
CONECT    6    5    7   27                                                  
CONECT    7    6    8   20                                                  
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13    8   15                                                  
CONECT   15   14    5   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16    3   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20    7   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   26                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   22   27                                                  
CONECT   27   26    6                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₃NO₄

Average Mass

365.4290 Da

Monoisotopic Mass

365.16271 Da

IUPAC Name

(20S,21S)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0^{2,7}.0^{8,13}.0^{16,20}]henicosa-1(14),2,4,6,8,10,12-heptaene-5,21-diol

Traditional Name

(20S,21S)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0^{2,7}.0^{8,13}.0^{16,20}]henicosa-1(14),2,4,6,8,10,12-heptaene-5,21-diol

CAS Registry Number

Not Available

SMILES

COC1=C(OC)C=C2C(=C1)C1=C([C@H](O)[C@@H]3CCCN3C1)C1=CC=C(O)C=C21

InChI Identifier

InChI=1S/C22H23NO4/c1-26-19-9-15-14-8-12(24)5-6-13(14)21-17(16(15)10-20(19)27-2)11-23-7-3-4-18(23)22(21)25/h5-6,8-10,18,22,24-25H,3-4,7,11H2,1-2H3/t18-,22+/m0/s1

InChI Key

SBVBOLGVLBCFIL-PGRDOPGGSA-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
Ideopsis similis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthroindolizidines. These are aromatic polycyclic compounds containing the phenanthroindolizidine skeleton, which is structurally characterized by an indolizidine and a phenanthrene, where the indolizidine is fused to the second benzene ring of a phenanthrene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Phenanthroindolizidines

Direct Parent

Phenanthroindolizidines

Alternative Parents

Substituents

Phenanthroindolizidine
Phenanthrol
2-naphthol
Naphthalene
Tetrahydroisoquinoline
Indolizidine
Anisole
Phenol ether
Aralkylamine
Phenol
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
N-alkylpyrrolidine
Pyrrolidine
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
1,2-aminoalcohol
Organoheterocyclic compound
Azacycle
Ether
Alcohol
Organic nitrogen compound
Organic oxygen compound
Organonitrogen compound
Amine
Organooxygen compound
Hydrocarbon derivative
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	3.26	ALOGPS
logP	2.71	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	9.75	ChemAxon
pKa (Strongest Basic)	8.27	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	62.16 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	104.14 m³·mol⁻¹	ChemAxon
Polarizability	40.47 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

8082790

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9907138

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol (NP0145280)

MOL for NP0145280 ((20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol)

3D MOL for NP0145280 ((20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol)

3D SDF for NP0145280 ((20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol)

3D-SDF for NP0145280 ((20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol)

PDB for NP0145280 ((20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol)

3D PDB for NP0145280 ((20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol)

SMILES for NP0145280 ((20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol)

INCHI for NP0145280 ((20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol)

Structure for NP0145280 ((20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol)

3D Structure for NP0145280 ((20s,21s)-10,11-dimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaene-5,21-diol)