NP-MRD: Showing NP-Card for methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]octadecane-18-carboxylate (NP0233465)

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Record Information

Version

2.0

Created at

2022-09-06 15:04:47 UTC

Updated at

2022-09-06 15:04:47 UTC

NP-MRD ID

NP0233465

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]octadecane-18-carboxylate

Description

Methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]Octadecane-18-carboxylate belongs to the class of organic compounds known as indolines. Indolines are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole. Based on a literature review very few articles have been published on methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]Octadecane-18-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062217042D          

 26 29  0  0  0  0            999 V2000
   -1.5116    0.3421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6915    0.5597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0749    0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0276   -0.7079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7098   -1.1439    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6499   -1.9986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5151   -0.7825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3878   -0.6911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9886   -0.0744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9481    0.7496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7192    1.0428    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2364    0.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0601    0.3543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4323   -0.3820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9808   -1.0725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571   -1.0267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7848   -0.2904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3099    1.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4318    2.2664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4549    1.1990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8515    0.5620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2296   -0.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7865    0.6027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3266   -0.0782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8333    1.5726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9183    1.7773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  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
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 17  1  0  0  0  0
  9 17  1  0  0  0  0
 10 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
  3 21  1  0  0  0  0
 21 22  1  0  0  0  0
  7 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
    4.2949   -2.7770    0.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7421   -1.6983    1.2374 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9443   -0.7570    0.3611 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8388   -1.4846   -0.3145 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8292   -0.7293   -0.9133 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6026   -1.1740   -2.2980 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8497    0.6648   -0.8548 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5877    1.1619   -0.7119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4533    0.0431   -0.2477 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1277   -0.5026    1.0975 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3749   -0.5302    1.8825 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3643   -0.6348    0.8633 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7506   -0.2541    1.2941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6387   -0.3627    0.0710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8448   -0.6704   -1.1816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6851    0.2787   -1.3695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8918    0.4638   -0.1038 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0589    0.2032    1.8250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5031    1.2815    2.2455 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3632   -0.0349    2.1734 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3498    0.3914    1.1423 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6935    1.3176    0.1765 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7908    2.1542   -0.4390 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0096    1.9322   -0.2197 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5124    3.2198   -1.2850 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5324    4.0122   -1.8686 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3727   -2.9913    0.5530 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7140   -3.7139    0.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3192   -2.4168   -0.7527 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6102   -1.1919    1.6943 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1392   -2.2273    1.9804 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6276   -0.3640   -0.3972 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3806   -2.2193    0.4118 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3205   -2.1614   -1.0824 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0978   -2.1615   -2.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0267   -0.4167   -2.8508 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5758   -1.3452   -2.8122 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1909    1.0580   -1.8591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9968    1.5479   -1.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6456    1.9863    0.0222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4597   -0.7962   -1.0053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8533   -1.5958    1.0105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4534    0.4445    2.2981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2905   -1.6020    0.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1226   -0.8540    2.1422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7313    0.8323    1.5619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3128   -1.2356    0.2376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2828    0.5254   -0.0625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5439   -1.7180   -1.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5482   -0.4969   -2.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0763   -0.1229   -2.2041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1094    1.2646   -1.6518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9676    1.4562    0.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5990    0.5487    3.1109 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5108   -1.1086    2.4852 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2308    0.9232    1.6092 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1038    2.0492    0.7672 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5125    3.6341   -1.4580 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4257    5.0335   -1.4928 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5639    3.9206   -2.9630 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 21  3  1  0
 22  7  1  0
 10  9  1  0
 12 17  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  6
  4 33  1  0
  4 34  1  0
  6 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  6
  8 39  1  0
  8 40  1  0
  9 41  1  6
 17 53  1  1
 16 51  1  0
 16 52  1  0
 15 49  1  0
 15 50  1  0
 14 47  1  0
 14 48  1  0
 13 45  1  0
 13 46  1  0
 12 44  1  6
 11 43  1  0
 10 42  1  6
 20 54  1  0
 20 55  1  0
 21 56  1  1
 22 57  1  1
 26 58  1  0
 26 59  1  0
 26 60  1  0
M  END


  Mrv1652309062217042D          

 26 29  0  0  0  0            999 V2000
   -1.5116    0.3421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6915    0.5597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0749    0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0276   -0.7079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7098   -1.1439    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6499   -1.9986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5151   -0.7825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3878   -0.6911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9886   -0.0744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9481    0.7496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7192    1.0428    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2364    0.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0601    0.3543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4323   -0.3820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9808   -1.0725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571   -1.0267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7848   -0.2904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3099    1.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4318    2.2664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4549    1.1990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8515    0.5620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2296   -0.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7865    0.6027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3266   -0.0782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8333    1.5726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9183    1.7773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  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
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 17  1  0  0  0  0
  9 17  1  0  0  0  0
 10 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
  3 21  1  0  0  0  0
 21 22  1  0  0  0  0
  7 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0233465

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC1CN(C)C2CC3C4CCCCC4NC3C(=O)CC1C2C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C21H34N2O3/c1-4-12-11-23(2)17-9-15-13-7-5-6-8-16(13)22-20(15)18(24)10-14(12)19(17)21(25)26-3/h12-17,19-20,22H,4-11H2,1-3H3

> <INCHI_KEY>
SJBJYGYLCQECRD-UHFFFAOYSA-N

> <FORMULA>
C21H34N2O3

> <MOLECULAR_WEIGHT>
362.514

> <EXACT_MASS>
362.256942963

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
41.66935064182113

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0^{3,11}.0^{4,9}]octadecane-18-carboxylate

> <JCHEM_LOGP>
2.477918963999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.001105038866097

> <JCHEM_PKA_STRONGEST_BASIC>
10.16804330557422

> <JCHEM_POLAR_SURFACE_AREA>
58.64

> <JCHEM_REFRACTIVITY>
100.46779999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0^{3,11}.0^{4,9}]octadecane-18-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.822   0.639   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.291   1.045   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.140   0.266   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.051  -1.321   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       1.325  -2.135   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       1.213  -3.731   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.828  -1.461   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.457  -1.290   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.579  -0.139   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.503   1.399   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       6.943   1.947   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       7.908   0.747   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.446   0.661   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.140  -0.713   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.297  -2.002   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.760  -1.916   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.065  -0.542   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.312   2.428   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.539   4.231   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.716   2.238   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.590   1.049   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.295  -0.163   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.335   1.125   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.343  -0.146   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       3.422   2.936   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.714   3.318   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   22                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   17                                                  
CONECT   10    9   11   18                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12    9                                                  
CONECT   18   10   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20    3   22                                                  
CONECT   22   21    7   23                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Value	Source
Methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0,.0,]octadecane-18-carboxylic acid	Generator

Chemical Formula

C₂₁H₃₄N₂O₃

Average Mass

362.5140 Da

Monoisotopic Mass

362.25694 Da

IUPAC Name

methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0^{3,11}.0^{4,9}]octadecane-18-carboxylate

Traditional Name

methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0^{3,11}.0^{4,9}]octadecane-18-carboxylate

CAS Registry Number

Not Available

SMILES

CCC1CN(C)C2CC3C4CCCCC4NC3C(=O)CC1C2C(=O)OC

InChI Identifier

InChI=1S/C21H34N2O3/c1-4-12-11-23(2)17-9-15-13-7-5-6-8-16(13)22-20(15)18(24)10-14(12)19(17)21(25)26-3/h12-17,19-20,22H,4-11H2,1-3H3

InChI Key

SJBJYGYLCQECRD-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indolines. Indolines are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indolines

Direct Parent

Indolines

Alternative Parents

Substituents

Dihydroindole
Piperidinecarboxylic acid
Piperidine
Pyrrolidine
Methyl ester
Amino acid or derivatives
Carboxylic acid ester
Tertiary aliphatic amine
Tertiary amine
Ketone
Azacycle
Carboxylic acid derivative
Secondary aliphatic amine
Secondary amine
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Carbonyl group
Organic nitrogen compound
Organic oxide
Amine
Organonitrogen compound
Organooxygen compound
Organic oxygen compound
Organopnictogen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.48	ChemAxon
pKa (Strongest Acidic)	17	ChemAxon
pKa (Strongest Basic)	10.17	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	58.64 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	100.47 m³·mol⁻¹	ChemAxon
Polarizability	41.67 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

162996847

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]octadecane-18-carboxylate (NP0233465)

MOL for NP0233465 (methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]octadecane-18-carboxylate)

3D MOL for NP0233465 (methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]octadecane-18-carboxylate)

3D SDF for NP0233465 (methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]octadecane-18-carboxylate)

3D-SDF for NP0233465 (methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]octadecane-18-carboxylate)

PDB for NP0233465 (methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]octadecane-18-carboxylate)

3D PDB for NP0233465 (methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]octadecane-18-carboxylate)

SMILES for NP0233465 (methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]octadecane-18-carboxylate)

INCHI for NP0233465 (methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]octadecane-18-carboxylate)

Structure for NP0233465 (methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]octadecane-18-carboxylate)

3D Structure for NP0233465 (methyl 15-ethyl-17-methyl-12-oxo-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]octadecane-18-carboxylate)