NP-MRD: Showing NP-Card for (20s)-6,10,11-trimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaen-5-ol (NP0329444)

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Record Information

Version

2.0

Created at

2022-09-12 13:49:24 UTC

Updated at

2022-09-12 13:49:24 UTC

NP-MRD ID

NP0329444

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(20s)-6,10,11-trimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaen-5-ol

Description

3-Demethylisotylocrebrine 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. Based on a literature review very few articles have been published on 3-Demethylisotylocrebrine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122215492D          

 28 32  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
    4.4990   -1.1356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7793   -1.9115    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  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  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  2  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
  3 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  7 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
 26 27  1  0  0  0  0
 23 27  1  1  0  0  0
 27 28  1  0  0  0  0
  6 28  1  0  0  0  0
M  END

     RDKit          3D

 53 57  0  0  0  0  0  0  0  0999 V2000
   -1.8214    4.5120   -0.9514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7153    3.4205   -0.9961 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2344    2.1623   -0.7101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9203    1.9877   -0.3939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4556    0.7311   -0.1099 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8904    0.5575    0.1700 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4152   -0.6721    0.4203 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5686   -1.7533    0.3935 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0606   -3.0195    0.6434 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2622   -4.1413    0.6326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0668   -3.9858    0.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8527   -5.1198    0.3596 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6226   -2.7211    0.1087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9776   -2.7601   -0.1242 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8414   -2.8064    1.0464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8112   -1.6392    0.1208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3206   -0.3763   -0.1403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6356   -0.2026   -0.4600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0826    1.0941   -0.7453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4112    1.2538   -1.0634 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3131    0.1837   -1.1103 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8468   -0.8174    0.6973 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5317    0.3349   -0.0579 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0195    0.3182    0.1740 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3631    1.7902    0.1260 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0381    2.5197    0.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1003    1.5328    0.6011 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7561    1.7913    0.2025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4013    5.4748   -0.9402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2687    4.4974    0.0330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0976    4.5172   -1.7904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2051    2.8083   -0.3543 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1301   -3.0923    0.8622 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6828   -5.1140    0.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5021   -6.0365    0.5370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8724   -2.6494    0.7088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7790   -3.7908    1.5239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5056   -1.9749    1.6812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3359   -0.9627   -0.5573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9434   -0.6166   -1.7974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3201    0.4985   -1.3976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3867   -0.2572   -0.0909 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3308   -1.7174    0.2660 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0317   -0.7173    1.7872 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2549    0.2750   -1.1102 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4741   -0.2037   -0.7186 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2915   -0.1574    1.1219 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9042    2.0186   -0.8334 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9357    2.1280    1.0089 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0569    3.4322    0.7020 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7145    2.7238   -0.9745 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7502    2.3108   -0.7703 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2905    2.4307    1.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 19  2  0
 19 20  1  0
 20 21  1  0
 19 18  1  0
 18 17  2  0
 17  5  1  0
  5  4  2  0
  5  6  1  0
  6  7  2  0
  7 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  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  1  0
 14 15  1  0
 13 16  2  0
  4  3  1  0
 28  6  1  0
 16  8  1  0
 16 17  1  0
 27 23  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 21 40  1  0
 21 41  1  0
 21 42  1  0
 18 39  1  0
  4 32  1  0
 22 43  1  0
 22 44  1  0
 23 45  1  6
 24 46  1  0
 24 47  1  0
 25 48  1  0
 25 49  1  0
 26 50  1  0
 26 51  1  0
 28 52  1  0
 28 53  1  0
  9 33  1  0
 10 34  1  0
 12 35  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
M  END


  Mrv1652309122215492D          

 28 32  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
    4.4990   -1.1356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7793   -1.9115    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  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  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  2  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
  3 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  7 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
 26 27  1  0  0  0  0
 23 27  1  1  0  0  0
 27 28  1  0  0  0  0
  6 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0329444

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C23H25NO4/c1-26-20-10-16-17(11-21(20)27-2)22-14(6-7-19(25)23(22)28-3)15-9-13-5-4-8-24(13)12-18(15)16/h6-7,10-11,13,25H,4-5,8-9,12H2,1-3H3/t13-/m0/s1

> <INCHI_KEY>
IPEYRWVHYYVFAP-ZDUSSCGKSA-N

> <FORMULA>
C23H25NO4

> <MOLECULAR_WEIGHT>
379.456

> <EXACT_MASS>
379.178358289

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
42.437016598168725

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <JCHEM_LOGP>
3.366991909392045

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.770124177387062

> <JCHEM_PKA_STRONGEST_BASIC>
8.68030559236759

> <JCHEM_POLAR_SURFACE_AREA>
51.160000000000004

> <JCHEM_REFRACTIVITY>
109.39239999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-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  O   UNK     0       8.398  -2.120   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.921  -3.568   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.889  -3.026   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.413  -4.474   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.929  -4.746   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.452  -6.194   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.968  -6.465   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      10.961  -5.288   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.865  -3.661   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.872  -4.839   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.667  -4.889   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.095  -6.368   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.179  -7.232   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       1.395  -6.287   0.000  0.00  0.00           N+0
HETATM   28  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   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   17                                                  
CONECT    6    5    7   28                                                  
CONECT    7    6    8   22                                                  
CONECT    8    7    9   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13    8   17                                                  
CONECT   17   16    5   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18    3   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22    7   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   23   28                                                  
CONECT   28   27    6                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₅NO₄

Average Mass

379.4560 Da

Monoisotopic Mass

379.17836 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C23H25NO4/c1-26-20-10-16-17(11-21(20)27-2)22-14(6-7-19(25)23(22)28-3)15-9-13-5-4-8-24(13)12-18(15)16/h6-7,10-11,13,25H,4-5,8-9,12H2,1-3H3/t13-/m0/s1

InChI Key

IPEYRWVHYYVFAP-ZDUSSCGKSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 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
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
Phenol
N-alkylpyrrolidine
Pyrrolidine
Tertiary amine
Tertiary aliphatic amine
Organoheterocyclic compound
Azacycle
Ether
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxygen compound
Amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

8515128

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10339669

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (20s)-6,10,11-trimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaen-5-ol (NP0329444)

MOL for NP0329444 ((20s)-6,10,11-trimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaen-5-ol)

3D MOL for NP0329444 ((20s)-6,10,11-trimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaen-5-ol)

3D SDF for NP0329444 ((20s)-6,10,11-trimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaen-5-ol)

3D-SDF for NP0329444 ((20s)-6,10,11-trimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaen-5-ol)

PDB for NP0329444 ((20s)-6,10,11-trimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaen-5-ol)

3D PDB for NP0329444 ((20s)-6,10,11-trimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaen-5-ol)

SMILES for NP0329444 ((20s)-6,10,11-trimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaen-5-ol)

INCHI for NP0329444 ((20s)-6,10,11-trimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaen-5-ol)

Structure for NP0329444 ((20s)-6,10,11-trimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaen-5-ol)

3D Structure for NP0329444 ((20s)-6,10,11-trimethoxy-16-azapentacyclo[12.7.0.0²,⁷.0⁸,¹³.0¹⁶,²⁰]henicosa-1(14),2(7),3,5,8(13),9,11-heptaen-5-ol)