NP-MRD: Showing NP-Card for methyl (2r)-2-[(2r,3e,7as,12bs,12cs)-3-ethylidene-1h,2h,4h,6h,7h,7ah,8h,12bh,12ch-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate (NP0274826)

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Record Information

Version

2.0

Created at

2022-09-08 22:21:08 UTC

Updated at

2022-09-08 22:21:09 UTC

NP-MRD ID

NP0274826

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2r)-2-[(2r,3e,7as,12bs,12cs)-3-ethylidene-1h,2h,4h,6h,7h,7ah,8h,12bh,12ch-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate

Description

Methyl (2R)-2-[(1S,2S,4R,5E,10S)-5-ethylidene-7,11-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁷]Heptadeca-12,14,16-trien-4-yl]-3-hydroxypropanoate belongs to the class of organic compounds known as quinolizines. Quinolizines are compounds containing a quinolizine moiety, which consists of two fused pyridine rings sharing a nitrogen atom. Based on a literature review very few articles have been published on methyl (2R)-2-[(1S,2S,4R,5E,10S)-5-ethylidene-7,11-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁷]Heptadeca-12,14,16-trien-4-yl]-3-hydroxypropanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092200212D          

 26 29  0  0  1  0            999 V2000
    2.0120   -1.7839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1420   -0.9692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9125   -0.6744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0424    0.1403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8129    0.4351    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9428    1.2499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7133    1.5447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3539    1.0248    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1689    1.1530    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.5427    0.4176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3394    0.2032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5520   -0.5939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9681   -1.1767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1714   -0.9623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9587   -0.1652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2240    0.2101    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4535   -0.0847    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3236   -0.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5531   -1.1943    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4232   -2.0090    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6526   -2.3038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5227   -3.1185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0638   -2.5288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8343   -2.2340    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9338   -3.3435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5744   -3.8634    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
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
 16 15  1  6  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17  5  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 20 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

 54 57  0  0  0  0  0  0  0  0999 V2000
   -3.4738    0.3168   -1.8523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1790   -0.3798   -1.9439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2704   -0.4418   -1.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0189   -1.1505   -1.2991 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0216   -0.1402   -1.3604 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5603    0.1929   -2.6214 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1953    1.5793   -2.5401 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0361    1.6753   -1.3127 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8007    0.4489   -1.1531 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8826    0.2080    0.2471 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7648   -0.5703    0.9641 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6949   -0.6771    2.3338 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7224    0.0079    3.0082 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8336    0.7927    2.2788 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8888    0.9101    0.9131 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1124    1.6371   -0.0927 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8098    0.9900   -0.4825 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0711    0.4465    0.7236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4050    0.1965    0.3057 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0448   -0.5984    1.3778 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4137   -1.9709    1.6077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1123   -2.5676    2.7076 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5137   -0.8280    1.0614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9733   -1.9226    0.7206 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3857    0.2583    1.1627 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7566    0.1889    0.9017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4251    1.2290   -1.2051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6688    0.7554   -2.8794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3381   -0.3184   -1.6569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9511   -0.9073   -2.8939 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1849   -1.9149   -0.5433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0207   -1.6858   -2.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7385    0.2793   -3.3666 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3274   -0.5118   -3.0018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7370    1.8096   -3.4715 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3695    2.3402   -2.4782 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7035    2.5367   -1.3020 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2021   -0.1277   -1.9182 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5505   -1.1284    0.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3905   -1.2906    2.8979 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6605   -0.0714    4.0934 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0907    1.3128    2.8764 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9047    2.6903    0.1732 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1601    1.7613   -0.9411 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1111    1.0738    1.6083 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5117   -0.5398    0.9242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8298    1.2257    0.2109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0460   -0.0910    2.3601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4073   -1.8300    1.9877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5615   -2.6621    0.7844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8094   -3.1686    2.3934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2424    0.9886    1.5343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1947   -0.8064    1.1346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0330    0.4492   -0.1406 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 25  1  0
 25 23  1  0
 23 24  2  0
 23 20  1  0
 20 21  1  0
 21 22  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
  3 19  1  0
 15 10  1  0
  5 17  1  0
 15 16  1  0
 26 52  1  0
 26 53  1  0
 26 54  1  0
 20 48  1  1
 21 49  1  0
 21 50  1  0
 22 51  1  0
 19 47  1  6
 18 45  1  0
 18 46  1  0
 17 44  1  6
 16 43  1  1
  8 37  1  6
  7 35  1  0
  7 36  1  0
  6 33  1  0
  6 34  1  0
  4 31  1  0
  4 32  1  0
  2 30  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  9 38  1  0
 11 39  1  0
 12 40  1  0
 13 41  1  0
 14 42  1  0
M  END


  Mrv1652309092200212D          

 26 29  0  0  1  0            999 V2000
    2.0120   -1.7839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1420   -0.9692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9125   -0.6744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0424    0.1403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8129    0.4351    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9428    1.2499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7133    1.5447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3539    1.0248    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1689    1.1530    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.5427    0.4176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3394    0.2032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5520   -0.5939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9681   -1.1767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1714   -0.9623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9587   -0.1652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2240    0.2101    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4535   -0.0847    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3236   -0.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5531   -1.1943    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4232   -2.0090    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6526   -2.3038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5227   -3.1185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0638   -2.5288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8343   -2.2340    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9338   -3.3435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5744   -3.8634    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
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
 16 15  1  6  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17  5  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 20 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>
NP0274826

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H](CO)[C@H]1C[C@H]2[C@@H]3[C@H](CCN2C\C1=C\C)NC1=CC=CC=C31

> <INCHI_IDENTIFIER>
InChI=1S/C21H28N2O3/c1-3-13-11-23-9-8-18-20(14-6-4-5-7-17(14)22-18)19(23)10-15(13)16(12-24)21(25)26-2/h3-7,15-16,18-20,22,24H,8-12H2,1-2H3/b13-3-/t15-,16-,18-,19-,20-/m0/s1

> <INCHI_KEY>
QLRORKBBLVDRPD-QAXFFASWSA-N

> <FORMULA>
C21H28N2O3

> <MOLECULAR_WEIGHT>
356.466

> <EXACT_MASS>
356.20999277

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.68055476891441

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2R)-2-[(2R,3E,7aS,12bS,12cS)-3-ethylidene-1H,2H,3H,4H,6H,7H,7aH,8H,12bH,12cH-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate

> <JCHEM_LOGP>
1.3242159019999988

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.2133269459755

> <JCHEM_PKA_STRONGEST_BASIC>
8.67278734560165

> <JCHEM_POLAR_SURFACE_AREA>
61.8

> <JCHEM_REFRACTIVITY>
103.74739999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2R)-2-[(2R,3E,7aS,12bS,12cS)-3-ethylidene-1H,2H,4H,6H,7H,7aH,8H,12bH,12cH-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       3.756  -3.330   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.998  -1.809   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.437  -1.259   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.679   0.262   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       7.117   0.812   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       7.360   2.333   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.798   2.883   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.994   1.913   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      11.515   2.152   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      12.213   0.779   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.700   0.379   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.097  -1.109   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.007  -2.196   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.520  -1.796   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.123  -0.308   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.752   0.392   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.313  -0.158   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.071  -1.679   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.632  -2.229   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.390  -3.750   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.952  -4.300   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.709  -5.821   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.586  -4.720   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.024  -4.170   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       7.343  -6.241   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.539  -7.212   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10   16                                                  
CONECT   16   15    8   17                                                  
CONECT   17   16    5   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18    3   20                                                  
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   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 (2R)-2-[(1S,2S,4R,5E,10S)-5-ethylidene-7,11-diazatetracyclo[8.7.0.0,.0,]heptadeca-12,14,16-trien-4-yl]-3-hydroxypropanoic acid	Generator

Chemical Formula

C₂₁H₂₈N₂O₃

Average Mass

356.4660 Da

Monoisotopic Mass

356.20999 Da

IUPAC Name

methyl (2R)-2-[(2R,3E,7aS,12bS,12cS)-3-ethylidene-1H,2H,3H,4H,6H,7H,7aH,8H,12bH,12cH-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate

Traditional Name

methyl (2R)-2-[(2R,3E,7aS,12bS,12cS)-3-ethylidene-1H,2H,4H,6H,7H,7aH,8H,12bH,12cH-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H](CO)[C@H]1C[C@H]2[C@@H]3[C@H](CCN2C\C1=C\C)NC1=CC=CC=C31

InChI Identifier

InChI=1S/C21H28N2O3/c1-3-13-11-23-9-8-18-20(14-6-4-5-7-17(14)22-18)19(23)10-15(13)16(12-24)21(25)26-2/h3-7,15-16,18-20,22,24H,8-12H2,1-2H3/b13-3-/t15-,16-,18-,19-,20-/m0/s1

InChI Key

QLRORKBBLVDRPD-QAXFFASWSA-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 quinolizines. Quinolizines are compounds containing a quinolizine moiety, which consists of two fused pyridine rings sharing a nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolizines

Sub Class

Not Available

Direct Parent

Quinolizines

Alternative Parents

Substituents

Quinolizidine
Quinolizine
Indole or derivatives
Dihydroindole
Beta-hydroxy acid
Aralkylamine
Secondary aliphatic/aromatic amine
Hydroxy acid
Piperidine
Benzenoid
Methyl ester
Amino acid or derivatives
Carboxylic acid ester
Tertiary aliphatic amine
Tertiary amine
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Azacycle
Secondary amine
Primary alcohol
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organopnictogen compound
Organic oxygen compound
Amine
Carbonyl group
Organic nitrogen compound
Alcohol
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	1.32	ChemAxon
pKa (Strongest Acidic)	15.21	ChemAxon
pKa (Strongest Basic)	8.67	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	61.8 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	103.75 m³·mol⁻¹	ChemAxon
Polarizability	38.68 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

163195337

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2r)-2-[(2r,3e,7as,12bs,12cs)-3-ethylidene-1h,2h,4h,6h,7h,7ah,8h,12bh,12ch-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate (NP0274826)

MOL for NP0274826 (methyl (2r)-2-[(2r,3e,7as,12bs,12cs)-3-ethylidene-1h,2h,4h,6h,7h,7ah,8h,12bh,12ch-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate)

3D MOL for NP0274826 (methyl (2r)-2-[(2r,3e,7as,12bs,12cs)-3-ethylidene-1h,2h,4h,6h,7h,7ah,8h,12bh,12ch-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate)

3D SDF for NP0274826 (methyl (2r)-2-[(2r,3e,7as,12bs,12cs)-3-ethylidene-1h,2h,4h,6h,7h,7ah,8h,12bh,12ch-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate)

3D-SDF for NP0274826 (methyl (2r)-2-[(2r,3e,7as,12bs,12cs)-3-ethylidene-1h,2h,4h,6h,7h,7ah,8h,12bh,12ch-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate)

PDB for NP0274826 (methyl (2r)-2-[(2r,3e,7as,12bs,12cs)-3-ethylidene-1h,2h,4h,6h,7h,7ah,8h,12bh,12ch-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate)

3D PDB for NP0274826 (methyl (2r)-2-[(2r,3e,7as,12bs,12cs)-3-ethylidene-1h,2h,4h,6h,7h,7ah,8h,12bh,12ch-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate)

SMILES for NP0274826 (methyl (2r)-2-[(2r,3e,7as,12bs,12cs)-3-ethylidene-1h,2h,4h,6h,7h,7ah,8h,12bh,12ch-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate)

INCHI for NP0274826 (methyl (2r)-2-[(2r,3e,7as,12bs,12cs)-3-ethylidene-1h,2h,4h,6h,7h,7ah,8h,12bh,12ch-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate)

Structure for NP0274826 (methyl (2r)-2-[(2r,3e,7as,12bs,12cs)-3-ethylidene-1h,2h,4h,6h,7h,7ah,8h,12bh,12ch-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate)

3D Structure for NP0274826 (methyl (2r)-2-[(2r,3e,7as,12bs,12cs)-3-ethylidene-1h,2h,4h,6h,7h,7ah,8h,12bh,12ch-indolo[3,2-a]quinolizin-2-yl]-3-hydroxypropanoate)