NP-MRD: Showing NP-Card for (1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one (NP0317709)

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Record Information

Version

2.0

Created at

2022-09-11 17:44:26 UTC

Updated at

2022-09-11 17:44:26 UTC

NP-MRD ID

NP0317709

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one

Description

(1S,6R,7S,10S,15R,18S,19R,22S)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]Docos-13-en-4-one belongs to the class of organic compounds known as quinolidines. These are organic compounds containing a quinolidine or decahydroquinoline moiety, which is a bicyclic skeleton consisting of a piperidine fused to a cyclohexane ring. (1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one is found in Daphniphyllum oldhamii. Based on a literature review very few articles have been published on (1S,6R,7S,10S,15R,18S,19R,22S)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]Docos-13-en-4-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112219442D          

 25 30  0  0  1  0            999 V2000
    1.8384   -1.6007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6932   -0.7885    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2648   -0.1937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8758    0.5338    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0636    0.3886    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9508   -0.4287    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1728   -0.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2422    0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5318    1.0193    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2803    0.8741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8121    1.5048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318    2.2807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0636    2.9114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2803    2.4259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8121    1.7952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0924    2.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242    1.9404    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9045    2.7164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7167    2.8616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2485    2.2309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0730    2.2041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3024    1.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6195    0.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682    1.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561    1.3097    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  5  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  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 20 24  1  0  0  0  0
 24 25  1  0  0  0  0
 17 25  1  0  0  0  0
 25  4  1  6  0  0  0
M  END

     RDKit          3D

 56 61  0  0  0  0  0  0  0  0999 V2000
   -1.8990    4.0575   -0.0643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3509    2.8481    0.6159 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0697    2.3378   -0.0098 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0039    0.9857    0.4919 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2877    0.5025    0.7304 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2457    1.6241    0.4578 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6681    1.4076   -0.9511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2391    0.0244   -1.3659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7541   -0.6548   -0.0766 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9933   -1.2068    0.5593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7266   -2.1274    1.7140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8413   -3.2037    1.2369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8700   -4.3611    1.7487 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9766   -2.9416    0.2242 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7029   -1.6905   -0.3514 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5984   -1.9367   -1.8595 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6571   -1.2777    0.1685 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7045   -2.2257   -0.3376 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0957   -1.8436    0.0261 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3631   -0.4111   -0.4454 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7038    0.0952   -0.0548 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4148    1.0262    1.0892 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9566    1.2191    1.0978 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3459    0.4275    0.2489 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9283    0.1581   -0.1856 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9897    4.1119    0.1735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7077    4.0641   -1.1530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4197    4.9523    0.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2353    3.0256    1.6894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1397    2.3857   -1.1033 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7497    2.9586    0.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3606    0.1985    1.8146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0621    1.7001    1.1821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1785    2.1406   -1.6436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7642    1.5564   -1.1108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4748    0.0561   -2.1345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1240   -0.4976   -1.7849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6202   -1.7035   -0.1860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5828   -0.3402    0.9558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7056   -2.6095    1.9726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3732   -1.6318    2.6187 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0816   -1.2449   -2.3531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1897   -2.9748   -2.0388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6226   -1.9700   -2.3120 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6313   -1.3525    1.2751 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6636   -2.3746   -1.4355 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4929   -3.2206    0.1157 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7892   -2.5421   -0.4858 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3191   -1.8775    1.1064 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1873   -0.3677   -1.5410 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4259   -0.7022    0.2154 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1055    0.6858   -0.9294 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9753    1.9767    0.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7897    0.5252    2.0143 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4539    1.9381    1.7391 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9352    0.3005   -1.2926 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
  6  7  1  0
  7  8  1  0
  9  8  1  6
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  6
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
  6  2  1  0
 15  9  1  0
 25 17  1  0
 25  4  1  0
  9  5  1  0
 24 20  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  1
  3 30  1  0
  3 31  1  0
  5 32  1  1
  6 33  1  1
  7 34  1  0
  7 35  1  0
  8 36  1  0
  8 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  0
 11 41  1  0
 16 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  1
 18 46  1  0
 18 47  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  6
 21 51  1  0
 21 52  1  0
 22 53  1  0
 22 54  1  0
 23 55  1  0
 25 56  1  6
M  END


  Mrv1652309112219442D          

 25 30  0  0  1  0            999 V2000
    1.8384   -1.6007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6932   -0.7885    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2648   -0.1937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8758    0.5338    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0636    0.3886    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9508   -0.4287    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1728   -0.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2422    0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5318    1.0193    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2803    0.8741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8121    1.5048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318    2.2807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0636    2.9114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2803    2.4259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8121    1.7952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0924    2.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242    1.9404    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9045    2.7164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7167    2.8616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2485    2.2309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0730    2.2041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3024    1.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6195    0.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682    1.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561    1.3097    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  5  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  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 20 24  1  0  0  0  0
 24 25  1  0  0  0  0
 17 25  1  0  0  0  0
 25  4  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0317709

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CN2[C@H]3[C@@H]1CC[C@]31CCC(=O)O[C@]1(C)[C@H]1CC[C@@H]3CCC=C3[C@H]21

> <INCHI_IDENTIFIER>
InChI=1S/C22H31NO2/c1-13-12-23-19-16-5-3-4-14(16)6-7-17(19)21(2)22(11-9-18(24)25-21)10-8-15(13)20(22)23/h5,13-15,17,19-20H,3-4,6-12H2,1-2H3/t13-,14+,15-,17+,19+,20+,21-,22+/m1/s1

> <INCHI_KEY>
NGQSEZXJVMCXSC-XDZKTOJFSA-N

> <FORMULA>
C22H31NO2

> <MOLECULAR_WEIGHT>
341.495

> <EXACT_MASS>
341.235479242

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
39.16990962065732

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,6R,7S,10S,15R,18S,19R,22S)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0^{1,6}.0^{7,15}.0^{10,14}.0^{19,22}]docos-13-en-4-one

> <JCHEM_LOGP>
3.4301045203333347

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
11.883316986805168

> <JCHEM_POLAR_SURFACE_AREA>
29.540000000000003

> <JCHEM_REFRACTIVITY>
97.5873

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,6R,7S,10S,15R,18S,19R,22S)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0^{1,6}.0^{7,15}.0^{10,14}.0^{19,22}]docos-13-en-4-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       3.432  -2.988   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.161  -1.472   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.228  -0.362   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       3.501   0.996   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       1.985   0.725   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.775  -0.800   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.323  -0.214   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.452   1.105   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.993   1.903   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.523   1.632   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.516   2.809   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.993   4.257   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.985   5.435   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       0.523   4.528   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.516   3.351   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.039   4.799   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.032   3.622   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.555   5.071   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.071   5.342   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.064   4.164   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.603   4.114   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.031   2.635   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.756   1.771   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.541   2.716   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.025   2.445   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   25                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    2    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    5   10   15                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14    9   16   17                                             
CONECT   16   15                                                            
CONECT   17   15   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   20   25                                                  
CONECT   25   24   17    4                                                  
MASTER        0    0    0    0    0    0    0    0   25    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₁NO₂

Average Mass

341.4950 Da

Monoisotopic Mass

341.23548 Da

IUPAC Name

(1S,6R,7S,10S,15R,18S,19R,22S)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0^{1,6}.0^{7,15}.0^{10,14}.0^{19,22}]docos-13-en-4-one

Traditional Name

(1S,6R,7S,10S,15R,18S,19R,22S)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0^{1,6}.0^{7,15}.0^{10,14}.0^{19,22}]docos-13-en-4-one

CAS Registry Number

Not Available

SMILES

C[C@@H]1CN2[C@H]3[C@@H]1CC[C@]31CCC(=O)O[C@]1(C)[C@H]1CC[C@@H]3CCC=C3[C@H]21

InChI Identifier

InChI=1S/C22H31NO2/c1-13-12-23-19-16-5-3-4-14(16)6-7-17(19)21(2)22(11-9-18(24)25-21)10-8-15(13)20(22)23/h5,13-15,17,19-20H,3-4,6-12H2,1-2H3/t13-,14+,15-,17+,19+,20+,21-,22+/m1/s1

InChI Key

NGQSEZXJVMCXSC-XDZKTOJFSA-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

Species Name	Source	Reference
Daphniphyllum oldhamii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolidines. These are organic compounds containing a quinolidine or decahydroquinoline moiety, which is a bicyclic skeleton consisting of a piperidine fused to a cyclohexane ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolidines

Sub Class

Not Available

Direct Parent

Quinolidines

Alternative Parents

Substituents

Quinolidine
Indolizidine
Delta_valerolactone
Delta valerolactone
N-alkylpyrrolidine
Piperidine
Oxane
Pyrrolidine
Tertiary aliphatic amine
Tertiary amine
Lactone
Carboxylic acid ester
Amino acid or derivatives
Oxacycle
Azacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
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	3.43	ChemAxon
pKa (Strongest Basic)	11.88	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	29.54 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	97.59 m³·mol⁻¹	ChemAxon
Polarizability	39.17 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

162923742

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one (NP0317709)

MOL for NP0317709 ((1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

3D MOL for NP0317709 ((1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

3D SDF for NP0317709 ((1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

3D-SDF for NP0317709 ((1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

PDB for NP0317709 ((1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

3D PDB for NP0317709 ((1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

SMILES for NP0317709 ((1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

INCHI for NP0317709 ((1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

Structure for NP0317709 ((1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)

3D Structure for NP0317709 ((1s,6r,7s,10s,15r,18s,19r,22s)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴.0¹⁹,²²]docos-13-en-4-one)