NP-MRD: Showing NP-Card for 9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol (NP0160604)

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Record Information

Version

2.0

Created at

2022-09-02 18:35:18 UTC

Updated at

2022-09-02 18:35:18 UTC

NP-MRD ID

NP0160604

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol

Description

Moschaminindolol belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. 9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol is found in Amberboa moschata. Based on a literature review very few articles have been published on Moschaminindolol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022220352D          

 27 30  0  0  0  0            999 V2000
    5.6368    4.7314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1489    4.0661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3288    4.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8410    3.4906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0209    3.5804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5331    2.9151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7130    3.0049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8654    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6902    2.1779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9892    2.9469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2861    1.6075    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3042    0.7827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7337    0.1867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9089    0.1687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5505   -0.5744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7330   -0.4632    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5862    0.3487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8846    0.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9098    1.6074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6365    1.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4170    2.7932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2949    1.5640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3129    0.7392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6886    4.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1765    5.0008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9966    4.9110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4844    5.5764    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  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  4  0  0  0
 12 13  1  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  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
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  2  0  0  0  0
 14 23  1  0  0  0  0
 17 23  1  0  0  0  0
  5 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
  3 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
    5.9727   -0.3054   -0.8592 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3045    0.1218    0.2870 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9271    0.1466    0.4457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0302   -0.2490   -0.5114 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6578   -0.2071   -0.3090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7870   -0.6727   -1.3877 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2203   -0.3555   -2.6692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6653   -0.7179   -1.1491 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8657   -1.8779   -0.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3052   -2.2963    0.4488 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8247   -2.5881    0.1539 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2507   -2.6532   -0.1561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9850   -1.6625    0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6365   -0.2552    0.4642 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6414    0.5942    0.9790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2953    1.8565    0.7407 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1163    1.8820    0.0965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4380    2.9880   -0.3378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2496    2.8632   -1.0034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7835    1.5545   -1.2049 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4252    1.5308   -1.8921 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4489    0.4345   -0.7749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6902    0.5825   -0.0836 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1818    0.2449    0.8884 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0814    0.6511    1.8722 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4383    0.6021    1.6521 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3121    1.0223    2.6738 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9437   -0.7695   -0.5175 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3972   -1.0994   -1.3401 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2724    0.5203   -1.5352 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4213   -0.6064   -1.4588 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1315   -1.8412   -1.4051 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8707   -1.0228   -3.3245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1686   -1.0880   -2.1349 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2447   -2.6735    1.3861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5873   -3.6668    0.1367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4488   -2.5413   -1.2379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0833   -1.8594    0.5045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8664   -1.9023    1.7766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5420    0.2858    1.4824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8860    2.6925    1.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8367    3.9847   -0.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7067    3.7149   -1.3505 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9343    2.3280   -2.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1274    0.3136    1.1536 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7248    1.0192    2.8445 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3055    0.9772    2.4890 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 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8 22  1  0
 22 23  2  0
 23 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  9  2  0
  9 10  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 26  3  1  0
  9  8  1  0
 20 22  1  0
 17 23  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
 24 45  1  0
 25 46  1  0
 27 47  1  0
  6 32  1  6
  7 33  1  0
  8 34  1  6
 13 38  1  0
 13 39  1  0
 12 36  1  0
 12 37  1  0
 10 35  1  0
 15 40  1  0
 16 41  1  0
 18 42  1  0
 19 43  1  0
 21 44  1  0
M  END


  Mrv1652309022220352D          

 27 30  0  0  0  0            999 V2000
    5.6368    4.7314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1489    4.0661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3288    4.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8410    3.4906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0209    3.5804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5331    2.9151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7130    3.0049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8654    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6902    2.1779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9892    2.9469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2861    1.6075    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3042    0.7827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7337    0.1867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9089    0.1687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5505   -0.5744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7330   -0.4632    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5862    0.3487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8846    0.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9098    1.6074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6365    1.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4170    2.7932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2949    1.5640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3129    0.7392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6886    4.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1765    5.0008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9966    4.9110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4844    5.5764    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  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  4  0  0  0
 12 13  1  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  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
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  2  0  0  0  0
 14 23  1  0  0  0  0
 17 23  1  0  0  0  0
  5 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
  3 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0160604

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC=C1O)C(O)C1C2=C3C(CCN=C1O)=CNC3=CC=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C20H20N2O5/c1-27-15-8-10(2-4-13(15)23)19(25)18-17-14(24)5-3-12-16(17)11(9-22-12)6-7-21-20(18)26/h2-5,8-9,18-19,22-25H,6-7H2,1H3,(H,21,26)

> <INCHI_KEY>
AGCOSKQDZBHXRQ-UHFFFAOYSA-N

> <FORMULA>
C20H20N2O5

> <MOLECULAR_WEIGHT>
368.389

> <EXACT_MASS>
368.137221752

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
37.56532669736749

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0^{4,14}]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol

> <ALOGPS_LOGP>
1.96

> <JCHEM_LOGP>
1.0282974678661514

> <ALOGPS_LOGS>
-3.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.822542785631226

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.8781244038319813

> <JCHEM_PKA_STRONGEST_BASIC>
5.555269651047343

> <JCHEM_POLAR_SURFACE_AREA>
118.30000000000001

> <JCHEM_REFRACTIVITY>
100.0593

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.72e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0^{4,14}]tetradeca-1,4,6,8(14),10-pentaene-7,10-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      10.522   8.832   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.611   7.590   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.080   7.758   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.170   6.516   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.639   6.683   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.728   5.441   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.198   5.609   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.349   4.032   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.888   4.065   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.446   5.501   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0       8.001   3.001   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       8.034   1.461   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.970   0.348   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.430   0.315   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.761  -1.072   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       3.235  -0.865   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       2.961   0.651   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.651   1.461   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.698   3.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.055   3.729   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.645   5.214   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.284   2.919   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.317   1.380   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.019   8.093   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.929   9.335   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.460   9.167   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.371  10.409   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   26                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   24                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   22                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   23                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20    8   23                                                  
CONECT   23   22   14   17                                                  
CONECT   24    5   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    3   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₀N₂O₅

Average Mass

368.3890 Da

Monoisotopic Mass

368.13722 Da

IUPAC Name

9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0^{4,14}]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol

Traditional Name

9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0^{4,14}]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC=C1O)C(O)C1C2=C3C(CCN=C1O)=CNC3=CC=C2O

InChI Identifier

InChI=1S/C20H20N2O5/c1-27-15-8-10(2-4-13(15)23)19(25)18-17-14(24)5-3-12-16(17)11(9-22-12)6-7-21-20(18)26/h2-5,8-9,18-19,22-25H,6-7H2,1H3,(H,21,26)

InChI Key

AGCOSKQDZBHXRQ-UHFFFAOYSA-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
Amberboa moschata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Hydroxyindole
Methoxyphenol
3-alkylindole
Indole
Indole or derivatives
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Heteroaromatic compound
Pyrrole
Secondary alcohol
Secondary carboxylic acid amide
Carboxamide group
Lactam
Organoheterocyclic compound
Carboxylic acid derivative
Azacycle
Ether
Aromatic alcohol
Hydrocarbon derivative
Alcohol
Organonitrogen compound
Organooxygen compound
Carbonyl group
Organic oxide
Organic oxygen compound
Organic nitrogen 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	1.96	ALOGPS
logP	1.03	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	2.88	ChemAxon
pKa (Strongest Basic)	5.56	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	118.3 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	100.06 m³·mol⁻¹	ChemAxon
Polarizability	37.57 Å³	ChemAxon
Number of Rings	4	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

101577561

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol (NP0160604)

MOL for NP0160604 (9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol)

3D MOL for NP0160604 (9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol)

3D SDF for NP0160604 (9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol)

3D-SDF for NP0160604 (9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol)

PDB for NP0160604 (9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol)

3D PDB for NP0160604 (9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol)

SMILES for NP0160604 (9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol)

INCHI for NP0160604 (9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol)

Structure for NP0160604 (9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol)

3D Structure for NP0160604 (9-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-3,11-diazatricyclo[6.5.1.0⁴,¹⁴]tetradeca-1,4,6,8(14),10-pentaene-7,10-diol)