NP-MRD: Showing NP-Card for methyl (1r,9r,10s,12r)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate (NP0214152)

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Record Information

Version

2.0

Created at

2022-09-05 13:22:27 UTC

Updated at

2022-09-05 13:22:28 UTC

NP-MRD ID

NP0214152

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1r,9r,10s,12r)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate

Description

Tenuisine B belongs to the class of organic compounds known as indolecarboxylic acids. Indolecarboxylic acids are compounds containing a carboxylic acid group linked to an indole. Based on a literature review very few articles have been published on Tenuisine B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052215222D          

 31 36  0  0  1  0            999 V2000
   -1.2417    0.0285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5888   -0.4759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -0.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8273   -0.6670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2848    0.6549    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3817    1.2334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1940    1.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7251    1.7204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5374    1.5761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8185    0.8005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439    2.4960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9751    3.1273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6939    3.9029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6317    2.6403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1005    2.0090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8000    2.0327    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5182    2.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3990    2.5130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1506    2.0361    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7688    2.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4695    2.1680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2660    1.3425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4303    1.1544    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8181    0.4627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8858    0.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0975    1.0439    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8874    1.2970    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6519    1.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2522    1.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8042    2.3303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4388    1.3969    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
  3  5  1  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  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  2  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 19  1  6  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  5  1  1  0  0  0
 16 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 23 28  1  0  0  0  0
 27 29  1  1  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 16 31  1  1  0  0  0
M  END

     RDKit          3D

 57 62  0  0  0  0  0  0  0  0999 V2000
    1.8684    4.4173    1.8630 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7627    3.1006    1.3558 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5442    2.5017    1.0599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4734    3.2035    1.2703 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4217    1.1972    0.5564 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5791    0.3838    0.2486 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8810    0.7186   -0.0764 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8401   -0.2285   -0.3693 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1508    0.1098   -0.6965 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5027    1.4861   -0.7268 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4475   -1.5506   -0.3260 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4031   -2.5141   -0.6194 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1739   -3.8903   -0.6212 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1427   -1.9081   -0.0006 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1892   -0.9369    0.2926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2096   -0.9282    0.6871 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0430   -2.0622    0.3592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1632   -1.9369   -0.6291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2966   -1.1702   -0.1837 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5251   -1.7382   -0.6865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4626   -0.6289   -0.8745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7750    0.5039   -0.7859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3588    0.2109   -0.5366 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4339    0.5835   -1.6509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0129    0.6181   -1.1857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7272    0.3816    0.2160 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8626    0.3978    1.1925 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9405    1.1315    0.6558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0721    0.4658    2.3695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9875    1.1416    3.4173 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1787   -0.6124    2.1122 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9510    4.7015    1.7523 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2917    5.1422    1.2783 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6667    4.4691    2.9516 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1940    1.7678   -0.1112 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5754    1.6490   -0.8142 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9078    2.0369   -1.4975 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1928    1.9411    0.2578 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1330   -4.3790   -0.2809 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0357   -4.2777   -1.6686 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4021   -4.2342    0.0699 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8305   -2.9333    0.0350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4899   -2.4948    1.3005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3938   -2.9067   -0.0227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8625   -1.7650   -1.6661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5756   -3.0033   -0.6816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9150   -2.5411   -0.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2804   -2.1863   -1.6935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5289   -0.7618   -1.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2459    1.4757   -0.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5670   -0.0777   -2.5540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8197    1.5799   -2.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6696    1.6750   -1.4429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3066    0.0190   -1.8380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3303   -0.6409    1.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8287    1.1741    1.3246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7516    2.1225    0.2141 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
  3  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  8 11  2  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 23 22  1  6
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 29 31  1  0
 26  5  1  1
 15  6  1  0
 26 16  1  0
 16 31  1  1
 23 19  1  0
 28 23  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  7 35  1  0
 10 36  1  0
 10 37  1  0
 10 38  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 17 43  1  0
 17 44  1  0
 18 45  1  0
 18 46  1  0
 20 47  1  0
 20 48  1  0
 21 49  1  0
 22 50  1  0
 24 51  1  0
 24 52  1  0
 25 53  1  0
 25 54  1  0
 27 55  1  1
 28 56  1  0
 28 57  1  0
M  END


  Mrv1652309052215222D          

 31 36  0  0  1  0            999 V2000
   -1.2417    0.0285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5888   -0.4759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -0.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8273   -0.6670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2848    0.6549    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3817    1.2334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1940    1.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7251    1.7204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5374    1.5761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8185    0.8005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439    2.4960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9751    3.1273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6939    3.9029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6317    2.6403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1005    2.0090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8000    2.0327    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5182    2.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3990    2.5130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1506    2.0361    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7688    2.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4695    2.1680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2660    1.3425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4303    1.1544    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8181    0.4627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8858    0.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0975    1.0439    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8874    1.2970    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6519    1.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2522    1.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8042    2.3303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4388    1.3969    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
  3  5  1  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  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  2  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 19  1  6  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  5  1  1  0  0  0
 16 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 23 28  1  0  0  0  0
 27 29  1  1  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 16 31  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0214152

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)N1C2=CC(OC)=C(OC)C=C2[C@]23CCN4CC=C[C@]44CC[C@]12[C@H](C4)C(=O)O3

> <INCHI_IDENTIFIER>
InChI=1S/C23H26N2O6/c1-28-17-11-14-16(12-18(17)29-2)25(20(27)30-3)22-7-6-21-5-4-9-24(21)10-8-23(14,22)31-19(26)15(22)13-21/h4-5,11-12,15H,6-10,13H2,1-3H3/t15-,21-,22-,23-/m1/s1

> <INCHI_KEY>
XHJSBLSGHVGXNI-FNOORWRPSA-N

> <FORMULA>
C23H26N2O6

> <MOLECULAR_WEIGHT>
426.469

> <EXACT_MASS>
426.179086565

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
44.70168379551093

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,9R,10S,12R)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2^{9,12}.0^{1,9}.0^{2,7}.0^{12,16}]docosa-2,4,6,13-tetraene-8-carboxylate

> <JCHEM_LOGP>
1.6797165196666652

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.661406995926951

> <JCHEM_POLAR_SURFACE_AREA>
77.54

> <JCHEM_REFRACTIVITY>
111.02299999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,9R,10S,12R)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2^{9,12}.0^{1,9}.0^{2,7}.0^{12,16}]docosa-2,4,6,13-tetraene-8-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.318   0.053   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.099  -0.888   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.326  -0.304   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.544  -1.245   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0       0.532   1.223   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      -0.713   2.302   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.229   2.033   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.220   3.211   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -4.736   2.942   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -5.261   1.494   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.695   4.659   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -3.687   5.838   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -3.162   7.285   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.179   4.929   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.188   3.750   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.493   3.794   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.834   4.795   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.478   4.691   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       5.881   3.801   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       7.035   4.896   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.343   4.047   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.963   2.506   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.403   2.155   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.260   0.864   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.520   0.929   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.049   1.949   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.523   2.421   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.950   2.240   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.337   3.205   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       3.368   4.350   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       0.819   2.608   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   26                                                  
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15                                                       
CONECT   15   14    6   16                                                  
CONECT   16   15   17   26   31                                             
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   19   24   28                                             
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    5   16   27                                             
CONECT   27   26   28   29                                                  
CONECT   28   27   23                                                       
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   16                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₆N₂O₆

Average Mass

426.4690 Da

Monoisotopic Mass

426.17909 Da

IUPAC Name

methyl (1R,9R,10S,12R)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2^{9,12}.0^{1,9}.0^{2,7}.0^{12,16}]docosa-2,4,6,13-tetraene-8-carboxylate

Traditional Name

methyl (1R,9R,10S,12R)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2^{9,12}.0^{1,9}.0^{2,7}.0^{12,16}]docosa-2,4,6,13-tetraene-8-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)N1C2=CC(OC)=C(OC)C=C2[C@]23CCN4CC=C[C@]44CC[C@]12[C@H](C4)C(=O)O3

InChI Identifier

InChI=1S/C23H26N2O6/c1-28-17-11-14-16(12-18(17)29-2)25(20(27)30-3)22-7-6-21-5-4-9-24(21)10-8-23(14,22)31-19(26)15(22)13-21/h4-5,11-12,15H,6-10,13H2,1-3H3/t15-,21-,22-,23-/m1/s1

InChI Key

XHJSBLSGHVGXNI-FNOORWRPSA-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 indolecarboxylic acids. Indolecarboxylic acids are compounds containing a carboxylic acid group linked to an indole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indolecarboxylic acids and derivatives

Direct Parent

Indolecarboxylic acids

Alternative Parents

Substituents

Indolecarboxylic acid
Anisole
Phenol ether
Alkyl aryl ether
Aralkylamine
Gamma butyrolactone
Benzenoid
Oxolane
Carbamic acid ester
Pyrroline
Amino acid or derivatives
Carboxylic acid ester
Lactone
Tertiary aliphatic amine
Tertiary amine
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Oxacycle
Azacycle
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Amine
Carbonyl group
Organooxygen compound
Organic oxygen 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	1.68	ChemAxon
pKa (Strongest Basic)	9.66	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	77.54 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	111.02 m³·mol⁻¹	ChemAxon
Polarizability	44.7 Å³	ChemAxon
Number of Rings	6	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

C00026619

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

101354336

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1r,9r,10s,12r)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate (NP0214152)

MOL for NP0214152 (methyl (1r,9r,10s,12r)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

3D MOL for NP0214152 (methyl (1r,9r,10s,12r)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

3D SDF for NP0214152 (methyl (1r,9r,10s,12r)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

3D-SDF for NP0214152 (methyl (1r,9r,10s,12r)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

PDB for NP0214152 (methyl (1r,9r,10s,12r)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

3D PDB for NP0214152 (methyl (1r,9r,10s,12r)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

SMILES for NP0214152 (methyl (1r,9r,10s,12r)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

INCHI for NP0214152 (methyl (1r,9r,10s,12r)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

Structure for NP0214152 (methyl (1r,9r,10s,12r)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

3D Structure for NP0214152 (methyl (1r,9r,10s,12r)-4,5-dimethoxy-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)