NP-MRD: Showing NP-Card for methyl (1s,12s,13s,14r,15e)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraene-13-carboxylate (NP0142919)

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Record Information

Version

2.0

Created at

2022-09-01 21:34:19 UTC

Updated at

2022-09-01 21:34:19 UTC

NP-MRD ID

NP0142919

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,12s,13s,14r,15e)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraene-13-carboxylate

Description

Methyl (1S,12S,13S,14R,15E)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]Octadeca-2(10),4(9),5,7-tetraene-13-carboxylate belongs to the class of organic compounds known as macroline alkaloids. These are alkaloids with a structure that is based on the tetracyclic macroline skeleton. The macroline skeleton arises by scission of the C-21 to N-4 bond of the akuammilan skeleton, and mostly occurs in bisindole alkaloids. Based on a literature review very few articles have been published on methyl (1S,12S,13S,14R,15E)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]Octadeca-2(10),4(9),5,7-tetraene-13-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309012223342D          

 25 29  0  0  1  0            999 V2000
   -1.4389   -0.5016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0850    0.2436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2627    0.3098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2871    0.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0821    0.6214    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8938    0.6568    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1650    0.1181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3854   -0.2352    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8279   -0.9407    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7294   -1.7598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0292   -2.0840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3895   -2.2547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2910   -3.0738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4501   -0.3360    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2834   -0.5597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0240   -0.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7490    0.6257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4038    1.1276    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0834    0.6599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8857    0.8521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4533    0.2534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2186   -0.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7861   -1.1363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4163   -0.7297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8487   -0.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  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
  8  7  1  6  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14  5  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
  6 17  1  6  0  0  0
 17 18  1  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
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 16 25  1  0  0  0  0
 19 25  1  0  0  0  0
M  END

     RDKit          3D

 47 51  0  0  0  0  0  0  0  0999 V2000
   -4.4094   -2.4049   -0.6230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6188   -2.5731    0.6149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5884   -1.7777    0.8283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7069   -1.8318    2.0242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4910   -1.1045    1.6381 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0703   -1.7130    0.3638 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9023   -1.1731   -0.7702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2520   -0.7371   -0.1791 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0307    0.5313    0.6596 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9853    1.7095   -0.1998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1360    1.5747   -1.4382 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7819    2.9749    0.2987 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7378    4.1204   -0.5361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7584    0.3054    1.4405 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4133    1.0220    0.8774 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5166    0.1407    0.4186 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3215   -1.1994    0.1558 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4889   -1.7347   -0.2388 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4654   -0.7962   -0.2501 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8139   -0.8265   -0.5706 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5856    0.3103   -0.4885 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9781    1.4882   -0.0763 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7854    2.6122   -0.0055 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6384    1.5118    0.2406 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8550    0.3702    0.1602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9058   -1.4168   -0.5662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7635   -2.4290   -1.5419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1388   -3.2374   -0.7711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8736   -3.3491    1.3612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4103   -2.8463    2.2984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1606   -1.2844    2.8795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1143   -2.7978    0.4640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1327   -2.0032   -1.4670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4195   -0.3474   -1.3062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0131   -0.5980   -0.9450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8912    0.5969    1.3568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7000    5.0320    0.0854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6928    4.1521   -1.1090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9062    4.0741   -1.2706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9431    0.7222    2.4746 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8769    1.7391    1.6094 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1467    1.6690   -0.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6143   -2.7244   -0.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2934   -1.7374   -0.8916 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6461    0.2936   -0.7390 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9165    3.2515   -0.8019 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1787    2.4410    0.5613 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 10  1  0
 10 11  2  0
 10  9  1  0
  9 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 17  6  1  0
  6  7  1  0
  7  8  1  0
  8  3  1  0
  3  4  1  0
  4  5  1  0
  3  2  2  0
  2  1  1  0
  8  9  1  0
  5 14  1  0
 25 16  1  0
  5  6  1  0
 25 19  1  0
 13 37  1  0
 13 38  1  0
 13 39  1  0
  9 36  1  1
 14 40  1  1
 15 41  1  0
 15 42  1  0
 18 43  1  0
 20 44  1  0
 21 45  1  0
 23 46  1  0
 24 47  1  0
  6 32  1  1
  7 33  1  0
  7 34  1  0
  8 35  1  6
  4 30  1  0
  4 31  1  0
  2 29  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
M  END


  Mrv1652309012223342D          

 25 29  0  0  1  0            999 V2000
   -1.4389   -0.5016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0850    0.2436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2627    0.3098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2871    0.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0821    0.6214    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8938    0.6568    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1650    0.1181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3854   -0.2352    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8279   -0.9407    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7294   -1.7598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0292   -2.0840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3895   -2.2547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2910   -3.0738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4501   -0.3360    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2834   -0.5597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0240   -0.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7490    0.6257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4038    1.1276    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0834    0.6599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8857    0.8521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4533    0.2534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2186   -0.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7861   -1.1363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4163   -0.7297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8487   -0.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  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
  8  7  1  6  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14  5  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
  6 17  1  6  0  0  0
 17 18  1  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
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 16 25  1  0  0  0  0
 19 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0142919

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H]1[C@@H]2CC3=C(NC4=CC=C(O)C=C34)[C@@H]3C[C@H]1\C(CN23)=C/C

> <INCHI_IDENTIFIER>
InChI=1S/C20H22N2O3/c1-3-10-9-22-16-8-14-13-6-11(23)4-5-15(13)21-19(14)17(22)7-12(10)18(16)20(24)25-2/h3-6,12,16-18,21,23H,7-9H2,1-2H3/b10-3-/t12-,16-,17-,18-/m0/s1

> <INCHI_KEY>
BAHKPCHVSKSQNO-SNIKXEHNSA-N

> <FORMULA>
C20H22N2O3

> <MOLECULAR_WEIGHT>
338.407

> <EXACT_MASS>
338.163042576

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
36.49806120416642

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,12S,13S,14R,15E)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0^{2,10}.0^{4,9}.0^{12,17}]octadeca-2(10),4,6,8-tetraene-13-carboxylate

> <ALOGPS_LOGP>
2.81

> <JCHEM_LOGP>
2.459577138666667

> <ALOGPS_LOGS>
-2.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.482323323720497

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.553208685469494

> <JCHEM_PKA_STRONGEST_BASIC>
5.923214684604878

> <JCHEM_POLAR_SURFACE_AREA>
65.56

> <JCHEM_REFRACTIVITY>
95.85520000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.14e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,12S,13S,14R,15E)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0^{2,10}.0^{4,9}.0^{12,17}]octadeca-2(10),4,6,8-tetraene-13-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 01-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.686  -0.936   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.025   0.455   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.490   0.578   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.536   1.770   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       2.020   1.160   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       3.535   1.226   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.175   0.220   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.719  -0.439   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.545  -1.756   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.362  -3.285   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.055  -3.890   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       2.594  -4.209   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.410  -5.738   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.707  -0.627   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.262  -1.045   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.645  -0.284   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.131   1.168   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       6.354   2.105   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       7.622   1.232   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.120   1.591   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.180   0.473   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.741  -1.003   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.801  -2.121   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.244  -1.362   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.184  -0.244   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   14                                                  
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12                                                            
CONECT   14    9    5   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16    6   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   16   19                                                  
MASTER        0    0    0    0    0    0    0    0   25    0   58    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1S,12S,13S,14R,15E)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0,.0,.0,]octadeca-2(10),4(9),5,7-tetraene-13-carboxylic acid	Generator

Chemical Formula

C₂₀H₂₂N₂O₃

Average Mass

338.4070 Da

Monoisotopic Mass

338.16304 Da

IUPAC Name

methyl (1S,12S,13S,14R,15E)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0^{2,10}.0^{4,9}.0^{12,17}]octadeca-2(10),4,6,8-tetraene-13-carboxylate

Traditional Name

methyl (1S,12S,13S,14R,15E)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0^{2,10}.0^{4,9}.0^{12,17}]octadeca-2(10),4,6,8-tetraene-13-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H]1[C@@H]2CC3=C(NC4=CC=C(O)C=C34)[C@@H]3C[C@H]1\C(CN23)=C/C

InChI Identifier

InChI=1S/C20H22N2O3/c1-3-10-9-22-16-8-14-13-6-11(23)4-5-15(13)21-19(14)17(22)7-12(10)18(16)20(24)25-2/h3-6,12,16-18,21,23H,7-9H2,1-2H3/b10-3-/t12-,16-,17-,18-/m0/s1

InChI Key

BAHKPCHVSKSQNO-SNIKXEHNSA-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 macroline alkaloids. These are alkaloids with a structure that is based on the tetracyclic macroline skeleton. The macroline skeleton arises by scission of the C-21 to N-4 bond of the akuammilan skeleton, and mostly occurs in bisindole alkaloids.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Macroline alkaloids

Sub Class

Not Available

Direct Parent

Macroline alkaloids

Alternative Parents

Substituents

Macroline skeleton
Sarpagine-skeleton
Vobasan skeleton
Beta-carboline
Pyridoindole
3-alkylindole
Hydroxyindole
Indole
Indole or derivatives
Piperidinecarboxylic acid
Quinuclidine
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
Benzenoid
Piperidine
Pyrrole
Methyl ester
Heteroaromatic compound
Amino acid or derivatives
Carboxylic acid ester
Tertiary aliphatic amine
Tertiary amine
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organopnictogen compound
Amine
Carbonyl group
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	2.81	ALOGPS
logP	2.46	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	9.55	ChemAxon
pKa (Strongest Basic)	5.92	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	65.56 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	95.86 m³·mol⁻¹	ChemAxon
Polarizability	36.5 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

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

163188788

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1s,12s,13s,14r,15e)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraene-13-carboxylate (NP0142919)

MOL for NP0142919 (methyl (1s,12s,13s,14r,15e)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraene-13-carboxylate)

3D MOL for NP0142919 (methyl (1s,12s,13s,14r,15e)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraene-13-carboxylate)

3D SDF for NP0142919 (methyl (1s,12s,13s,14r,15e)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraene-13-carboxylate)

3D-SDF for NP0142919 (methyl (1s,12s,13s,14r,15e)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraene-13-carboxylate)

PDB for NP0142919 (methyl (1s,12s,13s,14r,15e)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraene-13-carboxylate)

3D PDB for NP0142919 (methyl (1s,12s,13s,14r,15e)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraene-13-carboxylate)

SMILES for NP0142919 (methyl (1s,12s,13s,14r,15e)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraene-13-carboxylate)

INCHI for NP0142919 (methyl (1s,12s,13s,14r,15e)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraene-13-carboxylate)

Structure for NP0142919 (methyl (1s,12s,13s,14r,15e)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraene-13-carboxylate)

3D Structure for NP0142919 (methyl (1s,12s,13s,14r,15e)-15-ethylidene-7-hydroxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraene-13-carboxylate)