NP-MRD: Showing NP-Card for (1s,11r,12s)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium (NP0155492)

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Record Information

Version

2.0

Created at

2022-09-02 12:33:42 UTC

Updated at

2022-09-02 12:33:42 UTC

NP-MRD ID

NP0155492

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,11r,12s)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium

Description

(1S,11R,12S)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]Icosa-2,4(8),9,13,15,17-hexaen-1-ium belongs to the class of organic compounds known as tetrahydroisoquinolines. These are tetrahydrogenated isoquinoline derivatives. Based on a literature review very few articles have been published on (1S,11R,12S)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]Icosa-2,4(8),9,13,15,17-hexaen-1-ium.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022214332D          

 25 29  0  0  1  0            999 V2000
    0.6322   -4.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4552   -4.1812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9164   -3.4971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7394   -3.5545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2006   -2.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388   -2.1290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0158   -2.0716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5546   -2.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7316   -2.6983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -1.4449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1230   -1.5023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4848   -2.2437    0.0000 N   0  3  2  0  0  0  0  0  0  0  0  0
    5.0149   -1.6116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2779   -2.4709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9774   -2.0336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7059   -2.4208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7349   -3.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0354   -3.6826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3069   -3.2954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5317   -3.5778    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3044   -4.3709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0236   -2.9278    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5280   -3.4725    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9892   -2.7884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4811   -2.1384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22  5  1  6  0  0  0
 12 22  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 16 25  1  0  0  0  0
M  CHG  1  12   1
M  END

     RDKit          3D

 45 49  0  0  0  0  0  0  0  0999 V2000
    5.3407   -1.2820    0.6945 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8968    0.0168    1.0022 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6501    0.5112    0.6818 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6868   -0.2186    0.0163 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4450    0.3014   -0.2925 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1676    1.5918    0.0797 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1067    2.3389    0.7418 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3609    1.8095    1.0521 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164    2.5622    1.7230 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1646    2.1377   -0.2562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5455    1.5367   -1.6110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6847    0.1260   -1.4552 N   0  0  2  0  0  4  0  0  0  0  0  0
   -1.1396   -0.4224   -2.7423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6952   -0.1557   -0.5004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9319    0.4479   -0.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7869    0.0190    0.7504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4408   -1.0542    1.5428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2281   -1.6556    1.2962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3555   -1.2222    0.2900 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0190   -1.7076   -0.1511 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2095   -2.8715   -0.8813 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4754   -0.5629   -1.0110 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4728   -1.2778    2.4563 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6267   -0.5801    2.0085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0371    0.4286    1.2060 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4557   -1.2811    0.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9256   -1.9717    1.4790 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0141   -1.5531   -0.3108 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9276   -1.2407   -0.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9098    3.3731    1.0504 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0771    3.5122    1.9828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9304    1.7558    0.4666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1718    3.2439   -0.2968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4910    1.9562   -1.9752 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2871    1.7820   -2.2943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0337    0.1725   -3.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5216   -1.4557   -2.5229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3421   -0.4087   -3.4896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2038    1.2973   -0.8681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9305   -2.5085    1.9108 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6788   -1.8391    0.6879 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6983   -3.2590   -1.0606 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0076   -0.9988   -1.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2331   -0.1744    2.8231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2318   -1.2192    1.3091 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 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  6
 12 22  1  0
 22 20  1  0
 20 21  1  0
 20 19  1  0
 19 18  2  0
 18 17  1  0
 17 16  2  0
 16 25  1  0
 25 24  1  0
 24 23  1  0
 16 15  1  0
 15 14  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8  3  1  0
 22  5  1  0
 14 19  1  0
 14 12  1  0
 23 17  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 13 36  1  0
 13 37  1  0
 13 38  1  0
 22 43  1  6
 20 41  1  1
 21 42  1  0
 18 40  1  0
 24 44  1  0
 24 45  1  0
 15 39  1  0
  7 30  1  0
  9 31  1  0
M  CHG  1  12   1
M  END


  Mrv1652309022214332D          

 25 29  0  0  1  0            999 V2000
    0.6322   -4.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4552   -4.1812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9164   -3.4971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7394   -3.5545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2006   -2.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388   -2.1290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0158   -2.0716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5546   -2.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7316   -2.6983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -1.4449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1230   -1.5023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4848   -2.2437    0.0000 N   0  3  2  0  0  0  0  0  0  0  0  0
    5.0149   -1.6116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2779   -2.4709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9774   -2.0336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7059   -2.4208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7349   -3.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0354   -3.6826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3069   -3.2954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5317   -3.5778    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3044   -4.3709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0236   -2.9278    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5280   -3.4725    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9892   -2.7884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4811   -2.1384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22  5  1  6  0  0  0
 12 22  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 16 25  1  0  0  0  0
M  CHG  1  12   1
M  END
> <DATABASE_ID>
NP0155492

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(CC[N@@+]3(C)[C@@H]2[C@H](O)C2=CC4=C(OCO4)C=C32)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C19H19NO5/c1-20-4-3-10-5-14(21)15(23-2)6-11(10)18(20)19(22)12-7-16-17(8-13(12)20)25-9-24-16/h5-8,18-19,22H,3-4,9H2,1-2H3/p+1/t18-,19+,20+/m0/s1

> <INCHI_KEY>
CVCLYISJHIEWIH-XUVXKRRUSA-O

> <FORMULA>
C19H20NO5

> <MOLECULAR_WEIGHT>
342.37

> <EXACT_MASS>
342.133599168

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
36.072065387897865

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
1

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,11R,12S)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0^{2,10}.0^{4,8}.0^{13,18}]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium

> <ALOGPS_LOGP>
1.54

> <JCHEM_LOGP>
-1.8600320274717448

> <ALOGPS_LOGS>
-4.39

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
11.974493702648441

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.84351002659565

> <JCHEM_PKA_STRONGEST_BASIC>
-4.142919481389305

> <JCHEM_POLAR_SURFACE_AREA>
68.15

> <JCHEM_REFRACTIVITY>
101.99980000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.52e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,11R,12S)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0^{2,10}.0^{4,8}.0^{13,18}]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium

> <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       1.180  -7.698   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.716  -7.805   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.577  -6.528   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.114  -6.635   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.974  -5.358   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.299  -3.974   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.763  -3.867   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.902  -5.144   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.366  -5.037   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.160  -2.697   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.696  -2.804   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       8.372  -4.188   0.000  0.00  0.00           N+1
HETATM   13  C   UNK     0       9.361  -3.008   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.852  -4.612   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.158  -3.796   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.518  -4.519   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.572  -6.058   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.266  -6.874   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.906  -6.151   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.459  -6.679   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.035  -8.159   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.511  -5.465   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      14.052  -6.482   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      14.913  -5.205   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.965  -3.992   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   22                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8                                                            
CONECT   10    6   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   22                                             
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   14   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20    5   12                                                  
CONECT   23   17   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   16                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₀NO₅

Average Mass

342.3700 Da

Monoisotopic Mass

342.13360 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(CC[N@@+]3(C)[C@@H]2[C@H](O)C2=CC4=C(OCO4)C=C32)C=C1O

InChI Identifier

InChI=1S/C19H19NO5/c1-20-4-3-10-5-14(21)15(23-2)6-11(10)18(20)19(22)12-7-16-17(8-13(12)20)25-9-24-16/h5-8,18-19,22H,3-4,9H2,1-2H3/p+1/t18-,19+,20+/m0/s1

InChI Key

CVCLYISJHIEWIH-XUVXKRRUSA-O

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 tetrahydroisoquinolines. These are tetrahydrogenated isoquinoline derivatives.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrahydroisoquinolines

Sub Class

Not Available

Direct Parent

Tetrahydroisoquinolines

Alternative Parents

Substituents

Tetrahydroisoquinoline
Indole or derivatives
Benzodioxole
Anisole
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
Alkyl aryl ether
Benzenoid
Quaternary ammonium salt
Secondary alcohol
1,2-aminoalcohol
Oxacycle
Azacycle
Ether
Acetal
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organic salt
Organooxygen compound
Organonitrogen compound
Amine
Alcohol
Organic cation
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source

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

163188143

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,12s)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium (NP0155492)

MOL for NP0155492 ((1s,11r,12s)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium)

3D MOL for NP0155492 ((1s,11r,12s)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium)

3D SDF for NP0155492 ((1s,11r,12s)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium)

3D-SDF for NP0155492 ((1s,11r,12s)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium)

PDB for NP0155492 ((1s,11r,12s)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium)

3D PDB for NP0155492 ((1s,11r,12s)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium)

SMILES for NP0155492 ((1s,11r,12s)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium)

INCHI for NP0155492 ((1s,11r,12s)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium)

Structure for NP0155492 ((1s,11r,12s)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium)

3D Structure for NP0155492 ((1s,11r,12s)-11,16-dihydroxy-15-methoxy-1-methyl-5,7-dioxa-1-azapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-1-ium)